chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
588769678876968GA16GENIChomozygous928975606
588788498878850AG22GENIChomozygous928975607
588789358878936AC31GENIChomozygous928975608
588790788879079TC44GENIChomozygous928975609
588798118879812GA17GENIChomozygous928975610
588809308880931TC42GENIChomozygous928975611
588815008881501GT39GENIChomozygous928975612
588817318881732CT40GENIChomozygous928975613
588823498882350CG57GENIChomozygous928975614
588824028882403GA54GENIChomozygous928975615
588825578882558GC46GENIChomozygous928975616
588828818882882GA31GENIChomozygous928975617
588830988883099TC55GENIChomozygous928975618
588846728884673GA47GENIChomozygous928975619
588858208885821AT42GENIChomozygous928975620
588866998886700CT52GENIChomozygous928975621
588873948887395CT35GENIChomozygous928975622
588874668887467GT34GENIChomozygous928975623
588881568888157GA30GENIChomozygous928975624
588905418890542AC22GENIChomozygous928975625
588913638891364TC20GENIChomozygous928975626
588915168891517GC20GENIChomozygous928975627
588923948892395AG31GENIChomozygous928975628
588934038893404TA17GENICpossibly homozygous928975629
588934928893493GA16GENIChomozygous928975630
588936028893603TA29GENIChomozygous928975631
588938668893867TC28GENIChomozygous928975632