chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1245478671245478672CT45GENIChomozygous928178667
1245480598245480599AT24GENIChomozygous928178668
1245480625245480626CT25GENIChomozygous928178669
1245482925245482926TG59GENIChomozygous928178670
1245484741245484742AC61GENIChomozygous928178671
1245485884245485885CG30GENIChomozygous928178672
1245487389245487390TC30GENIChomozygous928178673
1245487458245487459GA37GENIChomozygous928178674
1245489679245489680GT37GENIChomozygous928178675
1245493519245493520TC13GENIChomozygous928178676
1245498236245498237GA18GENIChomozygous928178677
1245500482245500483AG38GENIChomozygous928178678
1245501182245501183TA51GENICpossibly homozygous928178679
1245501635245501636AT29GENIChomozygous928178680
1245502080245502081CT10GENIChomozygous928178681
1245503750245503751GA54GENIChomozygous928178682
1245507013245507014TC29GENIChomozygous928178683
1245508345245508346TC59GENIChomozygous928178684
1245508617245508618GA30GENIChomozygous928178685
1245509605245509606GA30GENIChomozygous928178686
1245510582245510583CT36GENIChomozygous928178687
1245515748245515749AG29GENIChomozygous928178688
1245516179245516180AG52GENIChomozygous928178689