17-45299671-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299671
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299671
    reference: chr 17
allele count: 80
allele frequency: 6.666222251849877e-4
allele num: 120008
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000458907
  ensembl transcript: ENST00000576874
  gene symbol: MYL4
  hgvsc: ENST00000576874.1:c.488-75G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*90-75G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.488-75G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*274-75G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.488-75G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.199-75G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.488-75G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.488-75G>A
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2229
  bin: 3.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 21146
  bin: 2.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 4.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7835
  bin: 3.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21478
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2315
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2232
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 729
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 582
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 735
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 551
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8756
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

17-45299671-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299671
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299671
    reference: chr 17
allele count: 1
allele frequency: 8.332777814812346e-6
allele num: 120008
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.488-75G>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*274-75G>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.488-75G>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*90-75G>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.488-75G>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.488-75G>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000458907
  ensembl transcript: ENST00000576874
  gene symbol: MYL4
  hgvsc: ENST00000576874.1:c.488-75G>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.199-75G>C
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2315
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21146
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2232
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21478
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2229
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7835
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 582
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1095
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 735
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1303
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 729
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 551
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2769
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

17-45299677-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299677
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299677
    reference: chr 17
allele count: 14
allele frequency: 1.164086275422813e-4
allele num: 120266
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.488-69C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.199-69C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.488-69C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*274-69C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.488-69C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.488-69C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000458907
  ensembl transcript: ENST00000576874
  gene symbol: MYL4
  hgvsc: ENST00000576874.1:c.488-69C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*90-69C>T
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8019
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2216
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21923
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22749
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 454
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 670
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2702
  bin: 9.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

17-45299680-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299680
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299680
    reference: chr 17
allele count: 1
allele frequency: 8.309512730173502e-6
allele num: 120344
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.488-66G>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.488-66G>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*274-66G>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.488-66G>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.488-66G>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.199-66G>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*90-66G>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000458907
  ensembl transcript: ENST00000576874
  gene symbol: MYL4
  hgvsc: ENST00000576874.1:c.488-66G>C
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22994
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22395
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8106
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2234
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 607
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2580
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2448
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2691
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9133
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

17-45299681-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299681
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299681
    reference: chr 17
allele count: 1
allele frequency: 8.305233958440609e-6
allele num: 120406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*274-65G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000458907
  ensembl transcript: ENST00000576874
  gene symbol: MYL4
  hgvsc: ENST00000576874.1:c.488-65G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*90-65G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.488-65G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.488-65G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.488-65G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.199-65G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.488-65G>A
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22364
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23117
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2229
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8134
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38239
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2455
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 419
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1593
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP

17-45299682-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299682
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299682
    reference: chr 17
allele count: 1
allele frequency: 8.302751531857658e-6
allele num: 120442
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.488-64G>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*274-64G>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000458907
  ensembl transcript: ENST00000576874
  gene symbol: MYL4
  hgvsc: ENST00000576874.1:c.488-64G>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.199-64G>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*90-64G>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.488-64G>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.488-64G>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.488-64G>T
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22399
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23211
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8144
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2587
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 578
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2450
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

17-45299691-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299691
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299691
    reference: chr 17
allele count: 1
allele frequency: 8.281847845891375e-6
allele num: 120746
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.488-55G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.488-55G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.488-55G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*274-55G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000458907
  ensembl transcript: ENST00000576874
  gene symbol: MYL4
  hgvsc: ENST00000576874.1:c.488-55G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*90-55G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.199-55G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.488-55G>A
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2242
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23805
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8298
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22707
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2482
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 730
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

17-45299695-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299695
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299695
    reference: chr 17
allele count: 1
allele frequency: 8.274857672448034e-6
allele num: 120848
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*90-51C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000458907
  ensembl transcript: ENST00000576874
  gene symbol: MYL4
  hgvsc: ENST00000576874.1:c.488-51C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.488-51C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.199-51C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.488-51C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*274-51C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.488-51C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.488-51C>T
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2235
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23935
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22770
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8325
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39839
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2595
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

17-45299699-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299699
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299699
    reference: chr 17
allele count: 4
allele frequency: 3.307206402751596e-5
allele num: 120948
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.488-47T>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.488-47T>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000458907
  ensembl transcript: ENST00000576874
  gene symbol: MYL4
  hgvsc: ENST00000576874.1:c.488-47T>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*90-47T>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.488-47T>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.488-47T>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*274-47T>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.199-47T>C
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24015
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22798
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2233
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8352
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 582
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9423
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2698
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.75e1
  variant carriers: 0
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: T
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/17-45299703-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299703
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299703
    reference: chr 17
allele count: 2
allele frequency: 1.652482855490374e-5
allele num: 121030
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.488-43C>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*90-43C>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.488-43C>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*274-43C>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.488-43C>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.488-43C>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000458907
  ensembl transcript: ENST00000576874
  gene symbol: MYL4
  hgvsc: ENST00000576874.1:c.488-43C>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.199-43C>A
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2233
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24071
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22795
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8370
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 730
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum

17-45299704-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299704
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299704
    reference: chr 17
allele count: 2
allele frequency: 1.652346331791144e-5
allele num: 121040
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.488-42C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.488-42C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.488-42C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*90-42C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000458907
  ensembl transcript: ENST00000576874
  gene symbol: MYL4
  hgvsc: ENST00000576874.1:c.488-42C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*274-42C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.488-42C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.199-42C>T
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24106
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8368
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22800
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2495
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

17-45299705-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299705
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299705
    reference: chr 17
allele count: 1
allele frequency: 8.259820927082301e-6
allele num: 121068
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*90-41A>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.488-41A>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*274-41A>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.488-41A>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.488-41A>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000458907
  ensembl transcript: ENST00000576874
  gene symbol: MYL4
  hgvsc: ENST00000576874.1:c.488-41A>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.488-41A>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.199-41A>G
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22812
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24120
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8369
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 730
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2614
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: African
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

17-45299708-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299708
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299708
    reference: chr 17
allele count: 1
allele frequency: 8.25695648583932e-6
allele num: 121110
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.199-38T>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*274-38T>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.488-38T>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.488-38T>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000458907
  ensembl transcript: ENST00000576874
  gene symbol: MYL4
  hgvsc: ENST00000576874.1:c.488-38T>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*90-38T>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.488-38T>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.488-38T>C
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2236
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22833
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8371
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24150
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2502
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1596
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40190
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 582
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD

17-45299720-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299720
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299720
    reference: chr 17
allele count: 542
allele frequency: 4.470545538527524e-3
allele num: 121238
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*90-26C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.488-26C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.488-26C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.488-26C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.488-26C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*274-26C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000458907
  ensembl transcript: ENST00000576874
  gene symbol: MYL4
  hgvsc: ENST00000576874.1:c.488-26C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.199-26C>T
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 4.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.75e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 24093
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 6.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.25e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 22699
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 4.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 2216
  bin: 3.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 9.75e1
  variant carriers: 105
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 8306
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 21
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2561
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40144
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 705
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9403
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 13
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
population: African
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

17-45299721-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299721
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299721
    reference: chr 17
allele count: 1
allele frequency: 8.24715060946443e-6
allele num: 121254
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000458907
  ensembl transcript: ENST00000576874
  gene symbol: MYL4
  hgvsc: ENST00000576874.1:c.488-25G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*90-25G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.488-25G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.488-25G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*274-25G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.199-25G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.488-25G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.488-25G>A
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22738
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24320
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2232
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8428
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9501
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40410
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

17-45299725-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299725
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299725
    reference: chr 17
allele count: 1
allele frequency: 8.244294947896055e-6
allele num: 121296
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.488-21C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.488-21C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*90-21C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.488-21C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000458907
  ensembl transcript: ENST00000576874
  gene symbol: MYL4
  hgvsc: ENST00000576874.1:c.488-21C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*274-21C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.199-21C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.488-21C>T
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24354
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8422
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22756
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2485
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 721
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1562
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/17-45299734-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299734
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299734
    reference: chr 17
allele count: 2
allele frequency: 1.648070932972955e-5
allele num: 121354
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.488-12A>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.199-12A>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.488-12A>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000458907
  ensembl transcript: ENST00000576874
  gene symbol: MYL4
  hgvsc: ENST00000576874.1:c.488-12A>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.488-12A>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.488-12A>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*90-12A>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*274-12A>C
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24394
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22770
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8423
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2229
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1559
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 719
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2494
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ

17-45299741-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299741
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299741
    reference: chr 17
allele count: 33
allele frequency: 2.71904816835028e-4
allele num: 121366
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.488-5C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.488-5C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.488-5C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.488-5C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000458907
  ensembl transcript: ENST00000576874
  gene symbol: MYL4
  hgvsc: ENST00000576874.1:c.488-5C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*274-5C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.199-5C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*90-5C>T
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2229
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 24410
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8420
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22745
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 718
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40511
  bin: 6.25e1
  variant carriers: 0
hgvs: c.488-5C>T
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

17-45299742-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299742
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299742
    reference: chr 17
allele count: 494
allele frequency: 4.070265638389032e-3
allele num: 121368
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*90-4G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.488-4G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.199-4G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.488-4G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.488-4G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000458907
  ensembl transcript: ENST00000576874
  gene symbol: MYL4
  hgvsc: ENST00000576874.1:c.488-4G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*274-4G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.488-4G>A
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 6.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 22589
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 5.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 8340
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 4.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24289
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 4.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 2198
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 9.75e1
  variant carriers: 183
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 34
genotype quality: GenotypeQuality
  all individuals: 1523
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2457
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9453
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
hgvs: c.488-4G>A
num of homozygotes: 2
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

17-45299745-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299745
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299745
    reference: chr 17
allele count: 2
allele frequency: 1.647826516824309e-5
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.488-1G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.488-1G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*274-1G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*90-1G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.488-1G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000458907
  ensembl transcript: ENST00000576874
  gene symbol: MYL4
  hgvsc: ENST00000576874.1:c.488-1G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.488-1G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.199-1G>A
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22650
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24534
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8465
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1536
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2552
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.25e1
  variant carriers: 0
hgvs: c.488-1G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: African
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: VQSLOD

17-45299748-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299748
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299748
    reference: chr 17
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*276G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.490G>A
  hgvsp: ENSP00000347055.1:p.Glu164Lys
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000458907
  ensembl transcript: ENST00000576874
  gene symbol: MYL4
  hgvsc: ENST00000576874.1:c.490G>A
  hgvsp: ENSP00000458907.1:p.Glu164Lys
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.490G>A
  hgvsp: ENSP00000377096.1:p.Glu164Lys
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.490G>A
  hgvsp: ENSP00000442375.2:p.Glu164Lys
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.490G>A
  hgvsp: ENSP00000461570.1:p.Glu164Lys
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*92G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.201G>A
  hgvsp: ENSP00000461121.1:p.Glu68Lys
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: missense
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22649
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24538
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8464
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Glu164Lys
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ

17-45299748-GAGA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299748
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299745
    reference: chr 17
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*280_*282delAGA
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.494_496delAGA
  hgvsp: ENSP00000377096.1:p.Lys165del
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.494_496delAGA
  hgvsp: ENSP00000461570.1:p.Lys165del
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.494_496delAGA
  hgvsp: ENSP00000442375.2:p.Lys165del
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.205_207delAGA
  hgvsp: ENSP00000461121.1:p.Lys69del
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.494_496delAGA
  hgvsp: ENSP00000347055.1:p.Lys165del
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000458907
  ensembl transcript: ENST00000576874
  gene symbol: MYL4
  hgvsc: ENST00000576874.1:c.494_496delAGA
  hgvsp: ENSP00000458907.1:p.Lys165del
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*96_*98delAGA
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22649
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8464
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24538
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2484
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 548
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9557
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Lys165del
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: GAGA
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

17-45299757-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299757
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299757
    reference: chr 17
allele count: 3
allele frequency: 2.471576866040534e-5
allele num: 121380
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.499A>G
  hgvsp: ENSP00000377096.1:p.Thr167Ala
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.210A>G
  hgvsp: ENSP00000461121.1:p.Thr71Ala
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*285A>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*101A>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000458907
  ensembl transcript: ENST00000576874
  gene symbol: MYL4
  hgvsc: ENST00000576874.1:c.499A>G
  hgvsp: ENSP00000458907.1:p.Thr167Ala
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.499A>G
  hgvsp: ENSP00000442375.2:p.Thr167Ala
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.499A>G
  hgvsp: ENSP00000347055.1:p.Thr167Ala
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.499A>G
  hgvsp: ENSP00000461570.1:p.Thr167Ala
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22633
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8470
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24545
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1538
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40687
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr167Ala
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

17-45299769-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299769
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299769
    reference: chr 17
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.511G>A
  hgvsp: ENSP00000461570.1:p.Val171Met
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.511G>A
  hgvsp: ENSP00000347055.1:p.Val171Met
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.511G>A
  hgvsp: ENSP00000442375.2:p.Val171Met
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.511G>A
  hgvsp: ENSP00000377096.1:p.Val171Met
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.222G>A
  hgvsp: ENSP00000461121.1:p.Val75Met
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*113G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000458907
  ensembl transcript: ENST00000576874
  gene symbol: MYL4
  hgvsc: ENST00000576874.1:c.511G>A
  hgvsp: ENSP00000458907.1:p.Val171Met
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*297G>A
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22636
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24545
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8465
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2474
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2550
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Val171Met
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD

17-45299770-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299770
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299770
    reference: chr 17
allele count: 2
allele frequency: 1.647772211969417e-5
allele num: 121376
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.223T>C
  hgvsp: ENSP00000461121.1:p.Val75Ala
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*114T>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.512T>C
  hgvsp: ENSP00000347055.1:p.Val171Ala
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000458907
  ensembl transcript: ENST00000576874
  gene symbol: MYL4
  hgvsc: ENST00000576874.1:c.512T>C
  hgvsp: ENSP00000458907.1:p.Val171Ala
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*298T>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.512T>C
  hgvsp: ENSP00000461570.1:p.Val171Ala
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.512T>C
  hgvsp: ENSP00000442375.2:p.Val171Ala
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.512T>C
  hgvsp: ENSP00000377096.1:p.Val171Ala
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8466
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22633
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24547
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2473
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2548
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2599
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 9563
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Val171Ala
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/17-45299776-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299776
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299776
    reference: chr 17
allele count: 2
allele frequency: 1.64774506088418e-5
allele num: 121378
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*304A>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.518A>C
  hgvsp: ENSP00000442375.2:p.Gln173Pro
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.518A>C
  hgvsp: ENSP00000461570.1:p.Gln173Pro
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.518A>C
  hgvsp: ENSP00000347055.1:p.Gln173Pro
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*120A>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.518A>C
  hgvsp: ENSP00000377096.1:p.Gln173Pro
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.229A>C
  hgvsp: ENSP00000461121.1:p.Gln77Pro
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22624
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8459
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2223
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 548
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2474
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gln173Pro
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum

17-45299776-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299776
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299776
    reference: chr 17
allele count: 9
allele frequency: 7.41485277397881e-5
allele num: 121378
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.518A>G
  hgvsp: ENSP00000347055.1:p.Gln173Arg
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.518A>G
  hgvsp: ENSP00000442375.2:p.Gln173Arg
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.229A>G
  hgvsp: ENSP00000461121.1:p.Gln77Arg
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*304A>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*120A>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.518A>G
  hgvsp: ENSP00000377096.1:p.Gln173Arg
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.518A>G
  hgvsp: ENSP00000461570.1:p.Gln173Arg
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22624
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8459
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2223
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2474
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2548
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9561
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gln173Arg
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

17-45299780-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299780
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299780
    reference: chr 17
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*308G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.522G>A
  hgvsp: ENST00000354968.1:c.522G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*124G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.522G>A
  hgvsp: ENST00000393450.1:c.522G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.522G>A
  hgvsp: ENST00000536623.2:c.522G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.522G>A
  hgvsp: ENST00000572316.1:c.522G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.233G>A
  hgvsp: ENST00000570671.1:c.233G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24555
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22623
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8461
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40703
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Leu174Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

17-45299795-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299795
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299795
    reference: chr 17
allele count: 5
allele frequency: 4.120788554097712e-5
allele num: 121336
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.537G>A
  hgvsp: ENST00000536623.2:c.537G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*139G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.248G>A
  hgvsp: ENST00000570671.1:c.248G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.537G>A
  hgvsp: ENST00000393450.1:c.537G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*323G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.537G>A
  hgvsp: ENST00000354968.1:c.537G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.537G>A
  hgvsp: ENST00000572316.1:c.537G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24539
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2222
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8455
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22570
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 547
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2596
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1524
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2460
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu179Glu
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD

17-45299802-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299802
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299802
    reference: chr 17
allele count: 5
allele frequency: 4.121467902007979e-5
allele num: 121316
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.544A>G
  hgvsp: ENSP00000377096.1:p.Asn182Asp
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*146A>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.544A>G
  hgvsp: ENSP00000461570.1:p.Asn182Asp
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.255A>G
  hgvsp: ENSP00000461121.1:p.Asn86Asp
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*330A>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.544A>G
  hgvsp: ENSP00000442375.2:p.Asn182Asp
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.544A>G
  hgvsp: ENSP00000347055.1:p.Asn182Asp
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22539
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8457
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24527
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9520
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 697
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Asn182Asp
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

17-45299807-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299807
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299807
    reference: chr 17
allele count: 1
allele frequency: 8.244294947896055e-6
allele num: 121296
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.549C>T
  hgvsp: ENST00000536623.2:c.549C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*335C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.549C>T
  hgvsp: ENST00000354968.1:c.549C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.549C>T
  hgvsp: ENST00000572316.1:c.549C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*151C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.549C>T
  hgvsp: ENST00000393450.1:c.549C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.260C>T
  hgvsp: ENST00000570671.1:c.260C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22492
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24517
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8454
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 695
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1519
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2521
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gly183Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

17-45299808-TGCATCAATTATGAAGGTATTAAGCC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299808
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299783
    reference: chr 17
allele count: 1
allele frequency: 8.244974687927709e-6
allele num: 121286
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: splice donor
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2223
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8457
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24512
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22477
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2455
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9514
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
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: TGCATCAATTATGAAGGTATTAAGCC
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

17-45299814-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299814
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299814
    reference: chr 17
allele count: 286
allele frequency: 2.358996354278362e-3
allele num: 121238
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.556A>T
  hgvsp: ENSP00000347055.1:p.Asn186Tyr
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.556A>T
  hgvsp: ENSP00000377096.1:p.Asn186Tyr
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*158A>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.556A>T
  hgvsp: ENSP00000461570.1:p.Asn186Tyr
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.267A>T
  hgvsp: ENSP00000461121.1:p.Asn90Tyr
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.556A>T
  hgvsp: ENSP00000442375.2:p.Asn186Tyr
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*342A>T
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 4.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24458
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 5.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 3.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 8415
  bin: 3.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 9.75e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 22247
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 5.25e1
  variant carriers: 30
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 534
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asn186Tyr
num of homozygotes: 5
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

17-45299815-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299815
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299815
    reference: chr 17
allele count: 1
allele frequency: 8.249736008447729e-6
allele num: 121216
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*343A>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.557A>G
  hgvsp: ENSP00000377096.1:p.Asn186Ser
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.268A>G
  hgvsp: ENSP00000461121.1:p.Asn90Ser
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*159A>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.557A>G
  hgvsp: ENSP00000442375.2:p.Asn186Ser
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.557A>G
  hgvsp: ENSP00000461570.1:p.Asn186Ser
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.557A>G
  hgvsp: ENSP00000347055.1:p.Asn186Ser
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24561
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22230
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8464
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2445
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2502
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 538
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asn186Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP

17-45299833-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299833
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299833
    reference: chr 17
allele count: 6
allele frequency: 4.985376229726136e-5
allele num: 120352
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.565+10C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.276+10C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*351+10C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.565+10C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.565+10C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.565+10C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*167+10C>T
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2208
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23654
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19772
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8267
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2351
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2338
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2543
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 1714
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36908
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 624
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS

17-45299834-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299834
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299834
    reference: chr 17
allele count: 586
allele frequency: 4.872289477185047e-3
allele num: 120272
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*167+11G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.565+11G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.565+11G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.276+11G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*351+11G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.565+11G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.565+11G>A
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2536
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8143
  bin: 3.25e1
  variant carriers: 88
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 5.25e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 4.25e1
  variant carriers: 85
genotype depth: GenotypeDepth
  all individuals: 23483
  bin: 2.75e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 4.75e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19470
  bin: 2.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 2244
  bin: 3.75e1
  variant carriers: 92
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1015
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1835
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2289
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 635
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2363
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 2
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

17-45299835-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299835
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299835
    reference: chr 17
allele count: 24
allele frequency: 1.997636130578815e-4
allele num: 120142
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*167+12C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.565+12C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.276+12C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.565+12C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.565+12C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.565+12C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*351+12C>T
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23465
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19184
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8120
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2167
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2942
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2370
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 508
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2101
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 746
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2303
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

17-45299836-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299836
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299836
    reference: chr 17
allele count: 3
allele frequency: 2.497336174746936e-5
allele num: 120128
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.565+13G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*167+13G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*351+13G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.565+13G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.565+13G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.565+13G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.276+13G>A
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2966
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23523
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19141
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2157
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8091
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8784
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 788
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 753
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2134
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum

17-45299836-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299836
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299836
    reference: chr 17
allele count: 1
allele frequency: 8.324453915823122e-6
allele num: 120128
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.565+13G>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.565+13G>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.276+13G>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*167+13G>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.565+13G>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.565+13G>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*351+13G>C
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2966
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8091
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19141
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2157
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23523
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2358
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1186
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 788
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1453
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 753
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

17-45299840-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299840
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299840
    reference: chr 17
allele count: 3
allele frequency: 2.502043335390569e-5
allele num: 119902
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.565+17T>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*167+17T>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.565+17T>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.565+17T>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.276+17T>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.565+17T>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*351+17T>C
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22817
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18095
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7894
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4062
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2252
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2143
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1132
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2265
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2713
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34595
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1126
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS

17-45299842-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299842
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299842
    reference: chr 17
allele count: 9
allele frequency: 7.523951244795934e-5
allele num: 119618
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.565+19C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*167+19C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.565+19C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*351+19C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.276+19C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.565+19C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.565+19C>T
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2117
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21655
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 16489
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3621
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7648
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5622
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1801
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1634
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 552
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2228
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 590
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1430
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD

17-45299848-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299848
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299848
    reference: chr 17
allele count: 1
allele frequency: 8.382510729613734e-6
allele num: 119296
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.565+25A>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*167+25A>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.565+25A>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*351+25A>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.565+25A>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.565+25A>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.276+25A>G
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14530
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1977
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6401
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19553
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6791
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7774
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1029
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2996
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3935
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26713
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1333
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6489
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1924
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

17-45299852-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299852
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299852
    reference: chr 17
allele count: 1
allele frequency: 8.396728634523989e-6
allele num: 119094
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.276+29C>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.565+29C>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.565+29C>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.565+29C>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*167+29C>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.565+29C>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*351+29C>G
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6434
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8032
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19098
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14564
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1965
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6892
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 626
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3150
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27657
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1856
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4086
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1015
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

17-45299856-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299856
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299856
    reference: chr 17
allele count: 8
allele frequency: 6.73536741429245e-5
allele num: 118776
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.565+33C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.276+33C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.565+33C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.565+33C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*351+33C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.565+33C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*167+33C>T
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17137
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9929
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13033
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5985
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8876
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4986
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2982
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6008
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1776
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1492
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 641
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1568
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

17-45299857-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299857
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299857
    reference: chr 17
allele count: 1
allele frequency: 8.426161546369167e-6
allele num: 118678
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.565+34A>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*351+34A>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.276+34A>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.565+34A>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*167+34A>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.565+34A>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.565+34A>G
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5713
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12648
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9087
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15454
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12019
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1741
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 488
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3200
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1023
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2452
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5551
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5252
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ

17-45299860-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45299860
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45299860
    reference: chr 17
allele count: 1
allele frequency: 8.455515532782033e-6
allele num: 118266
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.276+37G>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.565+37G>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.565+37G>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*167+37G>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*351+37G>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.565+37G>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.565+37G>T
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9075
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1863
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13596
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11826
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15069
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5224
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5294
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6013
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17479
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2451
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3334
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1128
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1634
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

17-45300339-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45300339
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45300339
    reference: chr 17
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.566-41G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.566-41G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.566-41G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*352-41G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.277-41G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.566-41G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*168-41G>A
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7643
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4005
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3344
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18095
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2038
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16683
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3779
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5190
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20102
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10091
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

17-45300340-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45300340
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45300340
    reference: chr 17
allele count: 624
allele frequency: 5.142744115513945e-3
allele num: 121336
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.566-40C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*168-40C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.566-40C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.277-40C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.566-40C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.566-40C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*352-40C>T
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18110
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 5.75e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 4.75e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 5.25e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4005
  bin: 4.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 6.25e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 3324
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16681
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 9.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 3789
  bin: 9.75e1
  variant carriers: 171
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 6.75e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 7626
  bin: 3.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 8.25e1
  variant carriers: 23
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13089
  bin: 9.75e1
  variant carriers: 605
genotype quality: GenotypeQuality
  all individuals: 3723
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4014
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1721
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 19
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

17-45300346-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45300346
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45300346
    reference: chr 17
allele count: 3
allele frequency: 2.47222863170386e-5
allele num: 121348
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.566-34G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.566-34G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.566-34G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*168-34G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*352-34G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.566-34G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.277-34G>A
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2016
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4007
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16824
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3715
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7670
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18278
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3431
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2392
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

17-45300354-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45300354
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45300354
    reference: chr 17
allele count: 2
allele frequency: 1.648125257519571e-5
allele num: 121350
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*352-26G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.566-26G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.566-26G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.566-26G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*168-26G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.566-26G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.277-26G>A
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7672
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4009
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18320
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3715
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3427
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16831
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2016
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10182
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1735
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5215
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2392
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD

17-45300357-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45300357
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45300357
    reference: chr 17
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.566-23G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.566-23G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*352-23G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.566-23G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.566-23G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.277-23G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*168-23G>A
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18323
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4007
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16830
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7672
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3715
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3439
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4036
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3769
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20535
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum

http://identifiers.org/exac.variant/17-45300367-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45300367
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45300367
    reference: chr 17
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*168-13A>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.566-13A>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.566-13A>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*352-13A>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.277-13A>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.566-13A>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.566-13A>C
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16820
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3715
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7666
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18322
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4006
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12691
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2391
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20591
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4028
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: A
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff

17-45300376-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45300376
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45300376
    reference: chr 17
allele count: 39
allele frequency: 3.213420562595784e-4
allele num: 121366
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*168-4C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.566-4C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.566-4C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.566-4C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.277-4C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*352-4C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.566-4C>T
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18328
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 9.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7655
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16818
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4004
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3502
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20615
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12689
  bin: 9.75e1
  variant carriers: 39
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
hgvs: c.566-4C>T
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/17-45300380-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45300380
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45300380
    reference: chr 17
allele count: 4
allele frequency: 3.295707341188102e-5
allele num: 121370
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.566C>A
  hgvsp: ENSP00000442375.2:p.Ala189Asp
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.566C>A
  hgvsp: ENSP00000347055.1:p.Ala189Asp
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.566C>A
  hgvsp: ENSP00000377096.1:p.Ala189Asp
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.277C>A
  hgvsp: ENSP00000461121.1:p.Ala93Asp
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.566C>A
  hgvsp: ENSP00000461570.1:p.Ala189Asp
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*352C>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*168C>A
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18345
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3516
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4006
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7659
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16814
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3709
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20659
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3765
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1724
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ala189Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

17-45300381-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45300381
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45300381
    reference: chr 17
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.567C>T
  hgvsp: ENST00000393450.1:c.567C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*353C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.567C>T
  hgvsp: ENST00000354968.1:c.567C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.567C>T
  hgvsp: ENST00000536623.2:c.567C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*169C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.567C>T
  hgvsp: ENST00000572316.1:c.567C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.278C>T
  hgvsp: ENST00000570671.1:c.278C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3520
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16812
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18348
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7662
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3709
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4006
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2012
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20663
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2390
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10161
  bin: 6.75e1
  variant carriers: 0
hgvs: c.567C>T
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

17-45300398-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45300398
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45300398
    reference: chr 17
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.584T>C
  hgvsp: ENSP00000442375.2:p.Met195Thr
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.295T>C
  hgvsp: ENSP00000461121.1:p.Met99Thr
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.584T>C
  hgvsp: ENSP00000347055.1:p.Met195Thr
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*370T>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*186T>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.584T>C
  hgvsp: ENSP00000461570.1:p.Met195Thr
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.584T>C
  hgvsp: ENSP00000377096.1:p.Met195Thr
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2011
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3709
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7650
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3524
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16792
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4003
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18356
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3758
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4013
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12661
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Met195Thr
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD

17-45300404-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45300404
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45300404
    reference: chr 17
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*192G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.590G>A
  hgvsp: ENSP00000347055.1:p.Gly197Glu
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: incomplete_terminal_codon_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000442375
  ensembl transcript: ENST00000536623
  gene symbol: MYL4
  hgvsc: ENST00000536623.2:c.590G>A
  hgvsp: ENST00000536623.2:c.590G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.301G>A
  hgvsp: ENSP00000461121.1:p.Gly101Glu
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*376G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.590G>A
  hgvsp: ENSP00000377096.1:p.Gly197Glu
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.590G>A
  hgvsp: ENSP00000461570.1:p.Gly197Glu
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4001
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16770
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2011
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3538
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18331
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3708
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7637
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5186
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20702
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3995
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly197Glu
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

17-45300415-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45300415
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45300414
    reference: chr 17
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.*8delT
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.*8delT
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*204delT
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.*8delT
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.*8delT
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*388delT
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3708
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3534
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2012
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16705
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3994
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7620
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18259
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1715
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3966
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2381
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3731
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: GT
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD

17-45300422-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45300422
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45300422
    reference: chr 17
allele count: 2
allele frequency: 1.64883180266781e-5
allele num: 121298
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.*14A>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000460734
  ensembl transcript: ENST00000573747
  gene symbol: MYL4
  hgvsc: ENST00000573747.2:c.*210A>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.*14A>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*394A>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.*14A>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.*14A>G
  variant of: http://identifiers.org/hgnc/7585
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2002
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18121
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3989
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16586
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3708
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7592
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12641
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2374
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1715
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5119
  bin: 7.75e1
  variant carriers: 0
hgvs: c.*14A>G
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD

17-45300434-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45300434
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45300434
    reference: chr 17
allele count: 1
allele frequency: 8.248102936324645e-6
allele num: 121240
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.*15+11C>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.*26C>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.*15+11C>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.*15+11C>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*395+11C>G
  variant of: http://identifiers.org/hgnc/7585
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16084
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3708
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3609
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17424
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7494
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3951
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3819
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 415
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12620
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 19206
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 513
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5018
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 503
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

17-45300435-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45300435
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45300435
    reference: chr 17
allele count: 27
allele frequency: 2.226987792807654e-4
allele num: 121240
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.*15+12C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.*15+12C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*395+12C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.*27C>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.*15+12C>T
  variant of: http://identifiers.org/hgnc/7585
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3708
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3639
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16038
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7484
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3946
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17448
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3816
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19360
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12636
  bin: 9.75e1
  variant carriers: 26
genotype quality: GenotypeQuality
  all individuals: 5009
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9659
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2352
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1691
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3621
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ

17-45300445-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45300445
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45300445
    reference: chr 17
allele count: 1
allele frequency: 8.254639107178234e-6
allele num: 121144
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.*15+22T>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.*15+22T>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*395+22T>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.*15+22T>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.*37T>C
  variant of: http://identifiers.org/hgnc/7585
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1977
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7270
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14904
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16229
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2886
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3708
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3863
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3886
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 481
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4771
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3557
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3543
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 830
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1664
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1121
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1159
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 646
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 554
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD

17-45300446-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45300446
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45300446
    reference: chr 17
allele count: 3
allele frequency: 2.477086945751796e-5
allele num: 121110
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.*38G>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.*15+23G>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.*15+23G>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*395+23G>T
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.*15+23G>T
  variant of: http://identifiers.org/hgnc/7585
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14906
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7145
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3873
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14072
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4634
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4354
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1975
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3708
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1188
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2337
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 955
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3533
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 734
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 810
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1863
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 958
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7779
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 862
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4657
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS

17-45300448-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45300448
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45300448
    reference: chr 17
allele count: 4
allele frequency: 3.302728053372085e-5
allele num: 121112
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.*15+25T>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.*15+25T>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.*15+25T>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*395+25T>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.*40T>A
  variant of: http://identifiers.org/hgnc/7585
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7123
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3854
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4496
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13909
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14958
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4636
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1971
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3708
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4637
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12586
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 813
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1497
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3524
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 631
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1861
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1183
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2332
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 973
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: African
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD

17-45300454-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45300454
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45300454
    reference: chr 17
allele count: 1
allele frequency: 8.271572260455268e-6
allele num: 120896
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.*15+31C>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.*15+31C>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.*15+31C>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*395+31C>G
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.*46C>G
  variant of: http://identifiers.org/hgnc/7585
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6892
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12982
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7748
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5207
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1961
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3810
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3708
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1340
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1639
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2325
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7281
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4553
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1828
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1589
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12565
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3274
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 996
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

17-45300456-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45300456
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45300456
    reference: chr 17
allele count: 14
allele frequency: 1.160227404571296e-4
allele num: 120666
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.*48G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*395+33G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.*15+33G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.*15+33G>A
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.*15+33G>A
  variant of: http://identifiers.org/hgnc/7585
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12492
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9063
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5209
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11570
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3708
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6773
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3779
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4468
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11299
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1902
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7142
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2727
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1809
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3434
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 977
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3458
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2175
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 994
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

17-45300457-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45300457
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45300457
    reference: chr 17
allele count: 1
allele frequency: 8.298755186721992e-6
allele num: 120500
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000377096
  ensembl transcript: ENST00000393450
  gene symbol: MYL4
  hgvsc: ENST00000393450.1:c.*15+34G>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461121
  ensembl transcript: ENST00000570671
  gene symbol: MYL4
  hgvsc: ENST00000570671.1:c.*49G>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000347055
  ensembl transcript: ENST00000354968
  gene symbol: MYL4
  hgvsc: ENST00000354968.1:c.*15+34G>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000459035
  ensembl transcript: ENST00000571981
  gene symbol: MYL4
  hgvsc: ENST00000571981.1:c.*395+34G>C
  variant of: http://identifiers.org/hgnc/7585
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198336
  ensembl protein: ENSP00000461570
  ensembl transcript: ENST00000572316
  gene symbol: MYL4
  hgvsc: ENST00000572316.1:c.*15+34G>C
  variant of: http://identifiers.org/hgnc/7585
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3762
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10526
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12254
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5200
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3708
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6614
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10498
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5891
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1620
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 910
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2801
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 993
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4720
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1943
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12549
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2308
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2980
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7351
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

17-45331185-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45331185
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45331185
    reference: chr 17
allele count: 0
allele frequency: 0.0e0
allele num: 24
alternate allele: T
canonical: true
consequence: upstream gene
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  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: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1131
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
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  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 574
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: NaN
  allele num: 0
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: NaN
  allele num: 0
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 18
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: NaN
  allele num: 0
  num of homozygotes: 0
population: Latino
population: African
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

17-45331212-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45331212
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45331212
    reference: chr 17
allele count: 0
allele frequency: 0.0e0
allele num: 40
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000259207
  ensembl protein: ENSP00000452786
  ensembl transcript: ENST00000559488
  gene symbol: ITGB3
  hgvsc: ENST00000559488.1:c.-16G>T
  variant of: http://identifiers.org/hgnc/6156
canonical: true
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 8893
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 644
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8229
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 2
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: NaN
  allele num: 0
  num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

17-45331221-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45331221
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45331221
    reference: chr 17
allele count: 32
allele frequency: 2.222222222222222e-1
allele num: 144
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000259207
  ensembl protein: ENSP00000452786
  ensembl transcript: ENST00000559488
  gene symbol: ITGB3
  hgvsc: ENST00000559488.1:c.-7G>C
  variant of: http://identifiers.org/hgnc/6156
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000259207
  ensembl protein: ENSP00000461626
  ensembl transcript: ENST00000571680
  gene symbol: ITGB3
  hgvsc: ENST00000571680.1:c.-7G>C
  variant of: http://identifiers.org/hgnc/6156
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 7.5e0
  variant carriers: 143
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17036
  bin: 2.5e0
  variant carriers: 115
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 1.25e1
  variant carriers: 25
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 9.75e1
  variant carriers: 29
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 16242
  bin: 7.5e0
  variant carriers: 63
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 8.25e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 720
  bin: 2.25e1
  variant carriers: 26
genotype quality: GenotypeQuality
  all individuals: 784
  bin: 2.5e0
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 1.75e1
  variant carriers: 27
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 8.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 9.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 6.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 11
num of homozygotes: 2
population: East Asian
  type: Population
  allele count: 2
  allele frequency: 1.0e0
  allele num: 2
  num of homozygotes: 1
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

17-45331243-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45331243
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45331243
    reference: chr 17
allele count: 0
allele frequency: 0.0e0
allele num: 788
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000259207
  ensembl protein: ENSP00000461626
  ensembl transcript: ENST00000571680
  gene symbol: ITGB3
  hgvsc: ENST00000571680.1:c.16C>T
  hgvsp: ENSP00000461626.1:p.Arg6Trp
  variant of: http://identifiers.org/hgnc/6156
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000259207
  ensembl protein: ENSP00000452786
  ensembl transcript: ENST00000559488
  gene symbol: ITGB3
  hgvsc: ENST00000559488.1:c.16C>T
  hgvsp: ENSP00000452786.1:p.Arg6Trp
  variant of: http://identifiers.org/hgnc/6156
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30563
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5121
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 934
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 29514
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4598
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg6Trp
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 26
  num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

17-45331244-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45331244
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 45331244
    reference: chr 17
allele count: 3
allele frequency: 3.26797385620915e-3
allele num: 918
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000259207
  ensembl protein: ENSP00000461626
  ensembl transcript: ENST00000571680
  gene symbol: ITGB3
  hgvsc: ENST00000571680.1:c.17G>T
  hgvsp: ENSP00000461626.1:p.Arg6Leu
  variant of: http://identifiers.org/hgnc/6156
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000259207
  ensembl protein: ENSP00000452786
  ensembl transcript: ENST00000559488
  gene symbol: ITGB3
  hgvsc: ENST00000559488.1:c.17G>T
  hgvsp: ENSP00000452786.1:p.Arg6Leu
  variant of: http://identifiers.org/hgnc/6156
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31266
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5579
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 786
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30330
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5100
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg6Leu
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 18
  num of homozygotes: 0
population: European (Finnish)
reference allele: G

GenotypeQuality
all individuals: 328
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 634
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34711
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 903
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2597
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 866
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1575
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1303
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2426
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2769
bin: 9.75e1
variant carriers: 79

GenotypeQuality
all individuals: 1095
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

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

African
type: Population
allele count: 75
allele frequency: 7.305669199298656e-3
allele num: 10266
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.589095986886043e-5
allele num: 65884
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16372
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 9.0e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.601593e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.633e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.393e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.54e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.97e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.16e-1

GenotypeQuality
all individuals: 8756
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2597
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 903
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 866
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34711
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2426
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1575
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 634
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.703220191470844e-5
allele num: 11490
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65884
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16372
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 5.97e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.16e-1

QD
type: SiteQuality
SIO_000300: 1.393e1

DP
type: SiteQuality
SIO_000300: 1.601593e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 9.0e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.633e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 307
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 699
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37404
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 697
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 582
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1585
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2451
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 724
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2596
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9107
bin: 6.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 2.119606358819076e-4
allele num: 66050
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6576
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

VQSLOD
type: SiteQuality
SIO_000300: 6.6e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.299e0

MQRankSum
type: SiteQuality
SIO_000300: 9.53e-1

FS
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SIO_000300: 0.0e0

QD
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.77e-1

DP
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ReadPosRankSum
type: SiteQuality
SIO_000300: 3.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

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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bin: 4.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10288
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66074
num of homozygotes: 0

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

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

South Asian
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allele count: 1
allele frequency: 6.090133982947625e-5
allele num: 16420
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 896
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MQRankSum
type: SiteQuality
SIO_000300: -5.29e-1

MQ
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SIO_000300: 5.946e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -8.99e-1

BaseQRankSum
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SIO_000300: -5.29e-1

FS
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SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.313e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e0

VQSLOD
type: SiteQuality
SIO_000300: 4.81e-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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bin: 2.25e1
variant carriers: 0

Latino
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allele count: 1
allele frequency: 8.686587908269631e-5
allele num: 11512
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8576
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16430
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66110
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

VQSLOD
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SIO_000300: -1.918e0

FS
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ClippingRankSum
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ReadPosRankSum
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SIO_000300: -2.266e0

MQRankSum
type: SiteQuality
SIO_000300: 9.399999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.034e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.63498e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

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

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

South Asian
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allele count: 1
allele frequency: 6.086427267194157e-5
allele num: 16430
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66142
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.27e0

DP
type: SiteQuality
SIO_000300: 1.63663e6

VQSLOD
type: SiteQuality
SIO_000300: -7.825e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

FS
type: SiteQuality
SIO_000300: 3.617e0

MQRankSum
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SIO_000300: -4.65e-1

QD
type: SiteQuality
SIO_000300: 9.33e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.574e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.83e0

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66324
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.073858114674441e-5
allele num: 16464
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
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DP
type: SiteQuality
SIO_000300: 1.651245e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.835e0

VQSLOD
type: SiteQuality
SIO_000300: 3.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.95e-1

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.918e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e-2

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66372
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8600
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6604
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South Asian
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allele count: 1
allele frequency: 6.062810719049351e-5
allele num: 16494
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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MQ
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ReadPosRankSum
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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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South Asian
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Other
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European (Non-Finnish)
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Latino
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African
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East Asian
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allele num: 8610
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6604
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FS
type: SiteQuality
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QD
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ClippingRankSum
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DP
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ReadPosRankSum
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MQRankSum
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VQSLOD
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MQ
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BaseQRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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Latino
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East Asian
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allele frequency: 2.320724065908564e-4
allele num: 8618
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European (Finnish)
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European (Non-Finnish)
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Other
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VQSLOD
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DP
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QD
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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MQ
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FS
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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East Asian
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European (Non-Finnish)
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Latino
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European (Finnish)
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Other
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FS
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InbreedingCoeff
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DP
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MQRankSum
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BaseQRankSum
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QD
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MQ
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6606
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Latino
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European (Non-Finnish)
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allele num: 66524
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South Asian
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East Asian
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Other
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African
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QD
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ClippingRankSum
type: SiteQuality
SIO_000300: 5.14e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.2e-2

DP
type: SiteQuality
SIO_000300: 1.658545e6

MQRankSum
type: SiteQuality
SIO_000300: -9.340000000000001e-1

FS
type: SiteQuality
SIO_000300: 4.495e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.444e0

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 44
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2611
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9449
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 729
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2695
bin: 9.75e1
variant carriers: 1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -4.57e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.0e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.25e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.85e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -2.29e-1

DP
type: SiteQuality
SIO_000300: 1.659342e6

QD
type: SiteQuality
SIO_000300: 1.061e1

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

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

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

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

GenotypeQuality
all individuals: 563
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2464
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3121
bin: 9.75e1
variant carriers: 529

GenotypeQuality
all individuals: 1543
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.05057781779979e-4
allele num: 66630
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 23
allele frequency: 1.988587238457548e-3
allele num: 11566
num of homozygotes: 0

Other
type: Population
allele count: 5
allele frequency: 5.518763796909493e-3
allele num: 906
num of homozygotes: 0

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

African
type: Population
allele count: 506
allele frequency: 4.871943000192567e-2
allele num: 10386
num of homozygotes: 13

MQRankSum
type: SiteQuality
SIO_000300: 2.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.892e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.36e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.55e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.41e-2

FS
type: SiteQuality
SIO_000300: 1.325e0

DP
type: SiteQuality
SIO_000300: 1.684487e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.55e-1

QD
type: SiteQuality
SIO_000300: 1.255e1

MQ
type: SiteQuality
SIO_000300: 5.973e1

GenotypeQuality
all individuals: 21
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 572
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2483
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2666
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 721
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1562
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2584
bin: 7.75e1
variant carriers: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 9.28e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

DP
type: SiteQuality
SIO_000300: 1.663557e6

MQRankSum
type: SiteQuality
SIO_000300: 8.070000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.72e0

FS
type: SiteQuality
SIO_000300: 5.27e-1

QD
type: SiteQuality
SIO_000300: 1.102e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.16e-1

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

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

GenotypeQuality
all individuals: 15
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2667
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 9516
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40446
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2586
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 571
bin: 8.75e1
variant carriers: 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: 6610
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 1.724e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.03e-1

DP
type: SiteQuality
SIO_000300: 1.66387e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.375e1

MQ
type: SiteQuality
SIO_000300: 5.963e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.47e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.25e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.31e-1

GenotypeQuality
all individuals: 40505
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2591
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 28
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 572
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9520
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2669
bin: 9.75e1
variant carriers: 2

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 2
allele frequency: 2.312673450508788e-4
allele num: 8648
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 1.664752e6

MQRankSum
type: SiteQuality
SIO_000300: 3.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -7.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.63e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.66e0

VQSLOD
type: SiteQuality
SIO_000300: 1.78e0

FS
type: SiteQuality
SIO_000300: 8.34e-1

QD
type: SiteQuality
SIO_000300: 1.281e1

MQ
type: SiteQuality
SIO_000300: 5.947e1

GenotypeQuality
all individuals: 2588
bin: 7.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 569
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9520
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2492
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1558
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2694
bin: 9.75e1
variant carriers: 33

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

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

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

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

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

African
type: Population
allele count: 31
allele frequency: 2.981916121585225e-3
allele num: 10396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997961386257345e-5
allele num: 66712
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.199999999999999e-2

MQ
type: SiteQuality
SIO_000300: 5.968e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.07e0

VQSLOD
type: SiteQuality
SIO_000300: 2.02e0

FS
type: SiteQuality
SIO_000300: 2.548e0

QD
type: SiteQuality
SIO_000300: 1.167e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.49e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 1.66703e6

GenotypeQuality
all individuals: 3068
bin: 9.75e1
variant carriers: 491

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

GenotypeQuality
all individuals: 2530
bin: 7.75e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 546
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 689
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40385
bin: 6.25e1
variant carriers: 1

African
type: Population
allele count: 13
allele frequency: 1.250240430852087e-3
allele num: 10398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 403
allele frequency: 6.040892193308551e-3
allele num: 66712
num of homozygotes: 0

South Asian
type: Population
allele count: 14
allele frequency: 8.478682170542636e-4
allele num: 16512
num of homozygotes: 1

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

Latino
type: Population
allele count: 6
allele frequency: 5.182242183451373e-4
allele num: 11578
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 58
allele frequency: 8.769277290595706e-3
allele num: 6614
num of homozygotes: 1

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

FS
type: SiteQuality
SIO_000300: 5.39e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.09e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

DP
type: SiteQuality
SIO_000300: 1.694446e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 9.75e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.92e-1

QD
type: SiteQuality
SIO_000300: 1.192e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.79e-1

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

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 40687
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 548
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2482
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2600
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 699
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9558
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66712
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 8.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -6.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.63e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.74e-1

FS
type: SiteQuality
SIO_000300: 6.47e-1

DP
type: SiteQuality
SIO_000300: 1.665416e6

QD
type: SiteQuality
SIO_000300: 1.171e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.09e-1

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 40692
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2484
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1537
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2600
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 700
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2549
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 548
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9557
bin: 6.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498935755613514e-5
allele num: 66714
num of homozygotes: 0

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

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

East Asian
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ReadPosRankSum
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FS
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DP
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InbreedingCoeff
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VQSLOD
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QD
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ClippingRankSum
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MQRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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South Asian
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ClippingRankSum
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VQSLOD
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QD
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FS
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DP
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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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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African
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East Asian
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South Asian
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European (Finnish)
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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MQ
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DP
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FS
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MQRankSum
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QD
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ClippingRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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East Asian
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European (Non-Finnish)
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DP
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InbreedingCoeff
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QD
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BaseQRankSum
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ClippingRankSum
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FS
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MQ
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ReadPosRankSum
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MQRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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African
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Latino
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European (Non-Finnish)
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InbreedingCoeff
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FS
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MQ
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BaseQRankSum
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ClippingRankSum
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QD
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ReadPosRankSum
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MQRankSum
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VQSLOD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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FS
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ClippingRankSum
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MQ
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DP
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MQRankSum
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VQSLOD
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QD
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InbreedingCoeff
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BaseQRankSum
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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 (Finnish)
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East Asian
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VQSLOD
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FS
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MQRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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European (Non-Finnish)
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African
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BaseQRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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DP
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MQRankSum
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MQ
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GenotypeQuality
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European (Non-Finnish)
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MQ
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QD
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FS
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DP
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InbreedingCoeff
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MQRankSum
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VQSLOD
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European (Finnish)
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European (Non-Finnish)
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East Asian
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African
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FS
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.117e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.99e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.55e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.199999999999999e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.85e0

DP
type: SiteQuality
SIO_000300: 1.664014e6

QD
type: SiteQuality
SIO_000300: 1.428e1

GenotypeQuality
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bin: 9.75e1
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66676
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
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: 6606
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.605e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.401e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.8e-2

DP
type: SiteQuality
SIO_000300: 1.66333e6

VQSLOD
type: SiteQuality
SIO_000300: 5.38e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.42e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.362e1

MQ
type: SiteQuality
SIO_000300: 5.923e1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7.75e1
variant carriers: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
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: 1.499925003749813e-5
allele num: 66670
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -5.006e0

DP
type: SiteQuality
SIO_000300: 1.663142e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.04e0

QD
type: SiteQuality
SIO_000300: 8.2e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.884e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.504e0

MQ
type: SiteQuality
SIO_000300: 5.593e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.058e0

GenotypeQuality
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GenotypeQuality
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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: 281

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 275
allele frequency: 2.648815257175881e-2
allele num: 10382
num of homozygotes: 5

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.501665616278023e-5
allele num: 66642
num of homozygotes: 0

Latino
type: Population
allele count: 7
allele frequency: 6.055363321799307e-4
allele num: 11560
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.85e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.99e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.34e0

MQ
type: SiteQuality
SIO_000300: 5.977e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.1e-2

DP
type: SiteQuality
SIO_000300: 1.670876e6

QD
type: SiteQuality
SIO_000300: 1.353e1

FS
type: SiteQuality
SIO_000300: 7.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.85e-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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variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5008254539997e-5
allele num: 66630
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 3.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.72e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.654e0

VQSLOD
type: SiteQuality
SIO_000300: -2.113e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.77e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.129e1

DP
type: SiteQuality
SIO_000300: 1.660978e6

GenotypeQuality
all individuals: 584
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variant carriers: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16386
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10282
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6540
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.063991781980784e-5
allele num: 66196
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.84e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.23e0

DP
type: SiteQuality
SIO_000300: 1.622482e6

MQRankSum
type: SiteQuality
SIO_000300: -1.27e-1

QD
type: SiteQuality
SIO_000300: 1.385e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 1.168e0

GenotypeQuality
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variant carriers: 581

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
type: Population
allele count: 14
allele frequency: 1.362397820163488e-3
allele num: 10276
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 4.882216526302942e-4
allele num: 16386
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.168224299065421e-4
allele num: 8560
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.237136465324385e-3
allele num: 894
num of homozygotes: 0

Latino
type: Population
allele count: 68
allele frequency: 5.931612002791347e-3
allele num: 11464
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 12
allele frequency: 1.836547291092746e-3
allele num: 6534
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 481
allele frequency: 7.270473714441186e-3
allele num: 66158
num of homozygotes: 1

VQSLOD
type: SiteQuality
SIO_000300: 5.94e0

QD
type: SiteQuality
SIO_000300: 1.375e1

DP
type: SiteQuality
SIO_000300: 1.626076e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -5.7e-2

BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 2.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.34e-1

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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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66074
num of homozygotes: 0

African
type: Population
allele count: 19
allele frequency: 1.8504090377873e-3
allele num: 10268
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6532
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

Latino
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allele count: 3
allele frequency: 2.617801047120419e-4
allele num: 11460
num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 1.221597849987784e-4
allele num: 16372
num of homozygotes: 0

MQRankSum
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SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.609411e6

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e-1

InbreedingCoeff
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MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.87e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.62e-1

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

African
type: Population
allele count: 1
allele frequency: 9.742790335151988e-5
allele num: 10264
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16372
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6534
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.123595505617978e-3
allele num: 890
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11456
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.513683700653911e-5
allele num: 66064
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.1e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 7.87e-1

DP
type: SiteQuality
SIO_000300: 1.608552e6

FS
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 1.41e-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
all individuals: 654
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66064
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16372
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6534
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.729050279329609e-5
allele num: 11456
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.1e-1

DP
type: SiteQuality
SIO_000300: 1.608552e6

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.952e1

BaseQRankSum
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MQRankSum
type: SiteQuality
SIO_000300: 1.41e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.332e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.87e-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
all individuals: 502
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11424
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65926
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16358
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: 3
allele frequency: 2.923976608187135e-4
allele num: 10260
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8520
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MQRankSum
type: SiteQuality
SIO_000300: -1.6e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.278e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.671e0

DP
type: SiteQuality
SIO_000300: 1.586565e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.89e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.65e0

FS
type: SiteQuality
SIO_000300: 0.0e0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16336
num of homozygotes: 0

European (Non-Finnish)
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allele count: 6
allele frequency: 9.127141075177218e-5
allele num: 65738
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11396
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6518
num of homozygotes: 0

African
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allele count: 3
allele frequency: 2.927971891469842e-4
allele num: 10246
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.803e0

FS
type: SiteQuality
SIO_000300: 5.096e0

DP
type: SiteQuality
SIO_000300: 1.554058e6

VQSLOD
type: SiteQuality
SIO_000300: 1.89e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.36e-1

MQ
type: SiteQuality
SIO_000300: 5.939e1

QD
type: SiteQuality
SIO_000300: 1.079e1

GenotypeQuality
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variant carriers: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6494
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16288
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11364
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8466
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.524576167825345e-5
allele num: 65592
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

VQSLOD
type: SiteQuality
SIO_000300: -6.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.26e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.122e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.376e0

DP
type: SiteQuality
SIO_000300: 1.495297e6

QD
type: SiteQuality
SIO_000300: 9.119999999999999e0

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65486
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11334
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16266
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10192
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.183712121212121e-4
allele num: 8448
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.48e0

VQSLOD
type: SiteQuality
SIO_000300: 4.66e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.491e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.404e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.82e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.59e-1

QD
type: SiteQuality
SIO_000300: 1.627e1

DP
type: SiteQuality
SIO_000300: 1.483681e6

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 8
allele frequency: 7.870916961826052e-4
allele num: 10164
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65304
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11314
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8408
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6468
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.62e0

QD
type: SiteQuality
SIO_000300: 1.406e1

DP
type: SiteQuality
SIO_000300: 1.444236e6

MQRankSum
type: SiteQuality
SIO_000300: -1.37e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.364e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.6e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.4e-2

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16232
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6468
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.852691218130312e-5
allele num: 11296
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10160
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65254
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.416289e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.78e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.81e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.2e-1

QD
type: SiteQuality
SIO_000300: 1.892e1

MQRankSum
type: SiteQuality
SIO_000300: 1.8e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.21e0

MQ
type: SiteQuality
SIO_000300: 5.925e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
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African
type: Population
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: 11226
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8348
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.537941004583064e-5
allele num: 65022
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.4e-2

MQ
type: SiteQuality
SIO_000300: 5.895e1

FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 3.75e-1

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.388004e6

QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
type: Population
allele count: 0
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499520153550864e-5
allele num: 66688
num of homozygotes: 0

African
type: Population
allele count: 0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.198e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.1142e1

ReadPosRankSum
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SIO_000300: 1.35e0

VQSLOD
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DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
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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variant carriers: 0

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

Latino
type: Population
allele count: 28
allele frequency: 2.420051858254105e-3
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East Asian
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allele frequency: 1.155535012710885e-4
allele num: 8654
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European (Non-Finnish)
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allele count: 6
allele frequency: 8.997390756680563e-5
allele num: 66686
num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 1.212268153715602e-4
allele num: 16498
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Other
type: Population
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allele frequency: 1.101321585903084e-3
allele num: 908
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African
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allele frequency: 5.621756678839131e-2
allele num: 10406
num of homozygotes: 19

QD
type: SiteQuality
SIO_000300: 1.375e1

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.41e-1

BaseQRankSum
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InbreedingCoeff
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SIO_000300: 4.58e-2

VQSLOD
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MQ
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DP
type: SiteQuality
SIO_000300: 2.553247e6

ClippingRankSum
type: SiteQuality
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ReadPosRankSum
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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Other
type: Population
allele count: 0
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allele num: 908
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
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African
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allele frequency: 0.0e0
allele num: 10406
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
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European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.99895036737142e-5
allele num: 66690
num of homozygotes: 0

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

BaseQRankSum
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DP
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ReadPosRankSum
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.971e1

InbreedingCoeff
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SIO_000300: 1.0e-4

MQRankSum
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QD
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ClippingRankSum
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GenotypeQuality
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variant carriers: 2

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.49934029027228e-5
allele num: 66696
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
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allele frequency: 6.058403004967891e-5
allele num: 16506
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East Asian
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BaseQRankSum
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VQSLOD
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DP
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ClippingRankSum
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ReadPosRankSum
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FS
type: SiteQuality
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InbreedingCoeff
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MQ
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MQRankSum
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QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.499295331194339e-5
allele num: 66698
num of homozygotes: 0

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

Other
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South Asian
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VQSLOD
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ReadPosRankSum
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FS
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InbreedingCoeff
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QD
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ClippingRankSum
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MQRankSum
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DP
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MQ
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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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East Asian
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allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.499160470136723e-5
allele num: 66704
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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Other
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QD
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MQ
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MQRankSum
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BaseQRankSum
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DP
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ReadPosRankSum
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ClippingRankSum
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FS
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VQSLOD
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InbreedingCoeff
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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African
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allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

East Asian
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allele frequency: 4.391033048301364e-3
allele num: 8654
num of homozygotes: 0

South Asian
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Other
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allele num: 906
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Latino
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European (Non-Finnish)
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
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MQ
type: SiteQuality
SIO_000300: 5.964e1

DP
type: SiteQuality
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VQSLOD
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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FS
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.048e0

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

European (Non-Finnish)
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allele count: 4
allele frequency: 5.99592277251469e-5
allele num: 66712
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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East Asian
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Other
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allele frequency: 0.0e0
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South Asian
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.05e0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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European (Finnish)
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allele frequency: 0.0e0
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African
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allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

South Asian
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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MQ
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ClippingRankSum
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QD
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FS
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MQRankSum
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BaseQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8.643042350907519e-5
allele num: 11570
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele frequency: 3.000120004800192e-5
allele num: 66664
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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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South 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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 2.159e0

MQRankSum
type: SiteQuality
SIO_000300: 7.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.061e0

DP
type: SiteQuality
SIO_000300: 2.516084e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e0

BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.956e1

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -6.788999999999999e-1

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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variant carriers: 0

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

African
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allele frequency: 0.0e0
allele num: 10400
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Latino
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allele frequency: 0.0e0
allele num: 11552
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South Asian
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allele count: 1
allele frequency: 6.063545961678389e-5
allele num: 16492
num of homozygotes: 0

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.18e-1

FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

MQ
type: SiteQuality
SIO_000300: 5.86e1

DP
type: SiteQuality
SIO_000300: 2.495832e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.4e0

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 27
allele frequency: 1.637355973317162e-3
allele num: 16490
num of homozygotes: 0

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

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

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

Other
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allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.83e-1

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -4.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.9e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.517e0

DP
type: SiteQuality
SIO_000300: 2.495384e6

MQ
type: SiteQuality
SIO_000300: 5.968e1

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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bin: 9.25e1
variant carriers: 0

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

African
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allele frequency: 0.0e0
allele num: 10396
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East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50195253829979e-5
allele num: 66580
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.570000000000001e-1

FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.835e1

MQRankSum
type: SiteQuality
SIO_000300: 1.58e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.104e0

VQSLOD
type: SiteQuality
SIO_000300: -2.182e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.98e-1

DP
type: SiteQuality
SIO_000300: 2.458401e6

QD
type: SiteQuality
SIO_000300: 1.401e1

GenotypeQuality
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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: 8630
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African
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allele frequency: 0.0e0
allele num: 10398
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6602
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16474
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.506805275966709e-5
allele num: 66566
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.948e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

DP
type: SiteQuality
SIO_000300: 2.432339e6

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.909999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.18e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.92e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.54e-1

FS
type: SiteQuality
SIO_000300: 1.0453e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6598
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South Asian
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allele frequency: 0.0e0
allele num: 16474
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66562
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East Asian
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allele frequency: 0.0e0
allele num: 8636
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Latino
type: Population
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allele frequency: 3.466204506065858e-4
allele num: 11540
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.682e0

MQRankSum
type: SiteQuality
SIO_000300: 1.8e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.429925e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.19e-1

QD
type: SiteQuality
SIO_000300: 1.09e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.505706628120577e-5
allele num: 66414
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South Asian
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African
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allele frequency: 0.0e0
allele num: 10390
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Latino
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allele num: 11522
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Other
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East Asian
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allele num: 8616
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.394609e6

QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 8.61e-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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East Asian
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allele frequency: 3.492433061699651e-4
allele num: 8590
num of homozygotes: 0

South Asian
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allele frequency: 6.091617933723197e-5
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European (Non-Finnish)
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Latino
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allele num: 11486
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Other
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6592
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.55e-1

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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QD
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MQ
type: SiteQuality
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ReadPosRankSum
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.53e-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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Latino
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allele frequency: 0.0e0
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Other
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African
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European (Non-Finnish)
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European (Finnish)
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allele num: 6578
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East Asian
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South Asian
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InbreedingCoeff
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DP
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FS
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BaseQRankSum
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MQ
type: SiteQuality
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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VQSLOD
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QD
type: SiteQuality
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Latino
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African
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Other
type: Population
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InbreedingCoeff
type: SiteQuality
SIO_000300: -9.11e-2

ReadPosRankSum
type: SiteQuality
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FS
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ClippingRankSum
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MQRankSum
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MQ
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DP
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BaseQRankSum
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VQSLOD
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QD
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European (Finnish)
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Other
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South Asian
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European (Non-Finnish)
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FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
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DP
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InbreedingCoeff
type: SiteQuality
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MQ
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European (Finnish)
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South Asian
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allele frequency: 3.043478260869565e-1
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European (Non-Finnish)
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Latino
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Other
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African
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ClippingRankSum
type: SiteQuality
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MQ
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MQRankSum
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VQSLOD
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InbreedingCoeff
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DP
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FS
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BaseQRankSum
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QD
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ReadPosRankSum
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Latino
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East Asian
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
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European (Finnish)
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South Asian
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ReadPosRankSum
type: SiteQuality
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DP
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InbreedingCoeff
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VQSLOD
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MQ
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FS
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MQRankSum
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ClippingRankSum
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QD
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BaseQRankSum
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European (Finnish)
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num of homozygotes: 0