chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
54925533749255379GATGGGGAGGATGAGTATAGAGAGGAGGATGATGGGGAGGGT4GENIChomozygous141001916
54925571149255712AC27GENIChomozygous141003638
54925584549255846GA23GENIChomozygous137459044
54925593149255932CT27GENIChomozygous141003639
54925620349256204TA41GENIChomozygous137459045
54925630849256309TC40GENIChomozygous141003640
54925631549256316AC42GENIChomozygous141003641
54925652049256521TC36GENIChomozygous141003642
54925654349256544GT35GENIChomozygous141003643
54925770249257703TG13GENIChomozygous141003644
54925771749257718GT13GENIChomozygous141003645
54925797249257974CA34GENIChomozygous141001917
54925991949259951CAGGATCACAGGATCTCAGGATCACAGGATCC39GENIChomozygous141001918
54926109249261093CA38GENIChomozygous141003646
54926177649261777GA37GENIChomozygous141003647
54926208749262088CT45GENIChomozygous141003648
54926235349262354CT50GENIChomozygous137459052
54927121949271220TC38GENIChomozygous141003649
54927217049272171C13GENICpossibly homozygous141001919
54927392749273928GC30GENIChomozygous141003650
54927430749274308CT38GENIChomozygous141003651
54927434949274350CG35GENIChomozygous141003652
54927463849274639TC34GENIChomozygous141003653
54927627649276281CTTAA30GENIChomozygous141001920
54927848249278483TC44GENIChomozygous141003654
54927928549279286TA41GENIChomozygous141003655
54927937449279375GT43GENICpossibly homozygous141003656
54928346849283469AG47GENIChomozygous141003659
54927991949279920AG39GENIChomozygous141003657
54928134349281344CT40GENIChomozygous141003658
54928262749282628AC37GENIChomozygous137459059
54928499449284995TC53GENIChomozygous137459061
54928529549285296AG57GENIChomozygous141003660