chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3170364426170364427GA51GENIChomozygous112371076
3170365122170365123G58GENIChomozygous127959696
3170365980170365981AG55GENIChomozygous111834356
3170366006170366007TA64GENIChomozygous111834358
3170366984170366985GT70GENIChomozygous112203739
3170367168170367171CCA46GENIChomozygous127959697
3170367205170367206GC56GENIChomozygous112371077
3170367605170367605C52GENIChomozygous127959698
3170367703170367704TA57GENIChomozygous111834364
3170367852170367853GA58GENIChomozygous111834366
3170369149170369150TC60GENIChomozygous111834368
3170369419170369419GGACACACAGGGCAGGAGCTGGGAGAGGGAGAATTCAGACTGGGAGGAGACACCTGCAGGAA51GENIChomozygous127959699
3170370834170370835CG55GENIChomozygous111834376
3170371347170371348AG57GENIChomozygous111834378
3170371396170371397TC58GENIChomozygous111834380
3170371669170371670GA49GENIChomozygous112371078
3170372273170372274AG72GENIChomozygous111834382
3170373273170373274AG50GENIChomozygous111834384
3170374367170374368AC58GENIChomozygous111834388
3170375409170375410TC64GENIChomozygous111834390
3170375495170375496AT50GENICpossibly homozygous112371079
3170377719170377720AG70GENIChomozygous111834394
3170377908170377909GA46GENIChomozygous112203765
3170379107170379107T60GENIChomozygous127959701
3170379541170379542CT64GENIChomozygous112371080
3170379834170379835GA66GENIChomozygous111834398