chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
28180675181806752CT18GENICheterozygous59820088
28180745781807458AG17GENIChomozygous59820090
28180957781809578T-1GENIChomozygous58907433
28181281981812820GA20GENICpossibly homozygous59820091
28181368681813687A-2GENICheterozygous58907440
28181507581815076GA19GENICpossibly homozygous58907442
28181526181815262AG16GENICpossibly homozygous58907443
28181547481815475TC24GENIChomozygous58907444
28181596181815962CA13GENIChomozygous59820092
28181613781816138GA11GENICpossibly homozygous58907445
28181648181816482GC27GENICpossibly homozygous59820093
28181650481816505CT11GENIChomozygous58907450
28181716081817161CA8GENIChomozygous59820095
28181744381817444TC17GENIChomozygous59820096
28181780581817806AG9GENICheterozygous58907452
28181855381818554TA18GENICpossibly homozygous59820101
28182008181820082CT14GENIChomozygous59820102
28182052181820522CG17GENICpossibly homozygous59820104
28182124381821244TTA2GENIChomozygous59820105