chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134790630447906305GA13GENIChomozygous114548465
134790858447908585AT20GENIChomozygous114548467
134790903547909036CT12GENIChomozygous114548468
134790985047909851GA28GENIChomozygous114548469
134791039647910397AG17GENIChomozygous114548470
134791053247910533CT25GENIChomozygous114548471
134791124547911246TC31GENIChomozygous114548472
134791150447911505CT23GENIChomozygous114548473
134791183147911832CT30GENIChomozygous114548474
134791280047912801AG18GENIChomozygous114548475
134791284247912843CT18GENIChomozygous114548476
134791303847913039CA19GENICpossibly homozygous114548477
134791317347913174CT15GENIChomozygous114548478
134791440947914410GA18GENIChomozygous114760408
134791460047914601TG7GENICpossibly homozygous114548479
134791474747914748TA11GENIChomozygous114548480
134791481247914813CT13GENIChomozygous114548481
134791508247915083AG9GENIChomozygous114548482
134791583147915832GA25GENIChomozygous114548483
134791621947916220GC25GENIChomozygous114548484
134791631047916311GC19GENIChomozygous114871690
134791653747916538TG13GENIChomozygous114720022
134791621747916218CA25GENIChomozygous114337868
134791618447916185GT24GENIChomozygous114337866