chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108695134586951346CT37GENIChomozygous116948866
108695233286952333TC22GENIChomozygous116948868
108695269686952697TG28GENIChomozygous116668554
108695343586953436TC25GENIChomozygous116948870
108695357886953579GT28GENIChomozygous116948872
108695373286953733CG26GENICpossibly homozygous116948874
108695422386954224GA17GENICpossibly homozygous116948876
108695619586956196CG28GENIChomozygous116948878
108695848186958482GC16GENIChomozygous116948882
108695882186958822CT27GENICpossibly homozygous116948884
108695912286959123CA19GENIChomozygous117144402
108695933286959333AG20GENIChomozygous116668566
108695933486959335TC20GENIChomozygous116948886
108695980286959803CA17GENIChomozygous116948890
108695983786959838TC17GENICpossibly homozygous116948892
108695996086959961AT22GENICpossibly homozygous116948894
108696031186960312CT24GENIChomozygous116948896
108696118786961188TG25GENIChomozygous116668570
108696245986962460TA21GENIChomozygous116668574