chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1266050963266050964AC44GENIChomozygous108637474
1266051441266051442GT48GENICpossibly homozygous108637475
1266052451266052452GA69GENIChomozygous108637476
1266053709266053710CA29GENIChomozygous108637477
1266055639266055640GA43GENIChomozygous108637478
1266056737266056738GC37GENIChomozygous108637479
1266056762266056763GT49GENIChomozygous108637480
1266057629266057630CT45GENIChomozygous108637481
1266057650266057651TC52GENIChomozygous108637482
1266057701266057702AG60GENIChomozygous108637483
1266058549266058550GA44GENIChomozygous108637484
1266059060266059061GA34GENIChomozygous108637485