chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1245478671245478672CT20GENIChomozygous875821448
1245480625245480626CT6GENIChomozygous875821449
1245482925245482926TG17GENIChomozygous875821450
1245484706245484707AG20GENIChomozygous875821451
1245484741245484742AC22GENIChomozygous875821452
1245485884245485885CG16GENIChomozygous875821453
1245487458245487459GA11GENIChomozygous875821454
1245489679245489680GT8GENIChomozygous875821455
1245492766245492767TC9GENIChomozygous875821456
1245500482245500483AG15GENIChomozygous875821457
1245501182245501183TA29GENIChomozygous875821458
1245501635245501636AT13GENIChomozygous875821459
1245503750245503751GA17GENIChomozygous875821460
1245504010245504011GA17GENIChomozygous875821461
1245507013245507014TC12GENIChomozygous875821462
1245508345245508346TC16GENICheterozygous875821463
1245508617245508618GA18GENIChomozygous875821464
1245509605245509606GA16GENIChomozygous875821465
1245509875245509876CT5GENIChomozygous875821466
1245510582245510583CT12GENIChomozygous875821467
1245514258245514259TC11GENIChomozygous875821468
1245515748245515749AG23GENIChomozygous875821469
1245516179245516180AG23GENIChomozygous875821470