chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
43461493034614931CT22GENIChomozygous816411778
43461708234617083TC19GENIChomozygous816411779
43461781934617820TC23GENIChomozygous816411780
43461803834618039TC23GENIChomozygous816411781
43461913934619140GA17GENIChomozygous816411782
43461947634619477GT16GENIChomozygous816411783
43462030134620302AG18GENIChomozygous816411784
43462032134620322CT14GENIChomozygous816411785
43462048134620482CT27GENIChomozygous816411786
43462055134620552TA14GENIChomozygous816411787
43462070434620705GA16GENIChomozygous816411788
43462070934620710CA17GENIChomozygous816411789
43462073734620738CT19GENIChomozygous816411790
43462114734621148AG16GENIChomozygous816411791
43462115234621155AAA---16GENIChomozygous816411792
43462131434621315GT16GENIChomozygous816411793
43462189634621897TC23GENIChomozygous816411794
43462243834622439CT20GENIChomozygous816411795
43462271834622719TTTG13GENIChomozygous816411796
43462276834622769GA18GENIChomozygous816411797
43462291534622916TC11GENIChomozygous816411798
43462308234623083A-9GENIChomozygous816411799
43462309034623091GA9GENIChomozygous816411800
43462356534623566AG19GENIChomozygous816411801
43462403534624036GA19GENIChomozygous816411802
43462423234624233TC18GENIChomozygous816411803