chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4150927701150927702CT20GENIChomozygous627738251
4150927963150927964AG31GENIChomozygous627738252
4150928969150928970AG31GENIChomozygous627738253
4150929723150929724CCAA18GENIChomozygous744109833
4150930668150930669CCT14GENICheterozygous744109834
4150930676150930677AT14GENIChomozygous627738254
4150930748150930749CT10GENIChomozygous627738255
4150932489150932490AG26GENIChomozygous627738256
4150933291150933295TGTG----11GENICheterozygous744109837
4150933293150933295TG--11GENICpossibly homozygous744109838
4150935670150935671GA21GENIChomozygous627738257
4150936222150936223AAAGCAGAGCAG14GENIChomozygous744109840
4150938908150938910TT--9GENICpossibly homozygous744109843
4150941363150941364GA17GENIChomozygous627738258
4150942267150942291AAAGAAAGAAAGAAAGAAAGAAAG------------------------11GENIChomozygous744109845
4150942601150942605AGGA----11GENIChomozygous744109848