chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1245478671245478672CT16GENIChomozygous891567500
1245480598245480599AT8GENIChomozygous891567501
1245480625245480626CT7GENIChomozygous891567502
1245482925245482926TG20GENIChomozygous891567503
1245484706245484707AG19GENIChomozygous891567504
1245484741245484742AC21GENIChomozygous891567505
1245487389245487390TC10GENIChomozygous891567506
1245487458245487459GA20GENIChomozygous891567507
1245489679245489680GT14GENIChomozygous891567508
1245492766245492767TC15GENIChomozygous891567509
1245492963245492964CG4GENIChomozygous893141723
1245493434245493435CA5GENICheterozygous890854437
1245500482245500483AG12GENIChomozygous891567510
1245501182245501183TA16GENICheterozygous891567511
1245501635245501636AT20GENIChomozygous891567512
1245501692245501693CT20GENIChomozygous891567513
1245503750245503751GA13GENIChomozygous891567514
1245504010245504011GA12GENIChomozygous891567515
1245507013245507014TC8GENIChomozygous891567516
1245508345245508346TC11GENIChomozygous891567517
1245508617245508618GA24GENIChomozygous891567518
1245509471245509472GA3GENICheterozygous891567519
1245509605245509606GA17GENIChomozygous891567520
1245509875245509876CT5GENIChomozygous891567521
1245510582245510583CT16GENIChomozygous891567522
1245514258245514259TC18GENIChomozygous891567523
1245515748245515749AG18GENIChomozygous891567524
1245516179245516180AG29GENIChomozygous891567525