chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
16139029861390299AG28GENIChomozygous108858148
16139032261390323AG22GENIChomozygous108122756
16139200761392008TC15GENIChomozygous108122758
16139879961398800GA19GENIChomozygous108122777
16139921361399214TA31GENIChomozygous108858151
16140084361400844AC12GENIChomozygous108122780
16140323561403236AT22GENIChomozygous108858152
16140412761404128TA7GENIChomozygous108858156
16140650461406505TA14GENIChomozygous108122785
16140837361408374TC16GENIChomozygous108122790
16140843861408439CA22GENIChomozygous108858157
16140951361409514AC24GENIChomozygous108858158
16140993861409939TC14GENIChomozygous120513877
16141211661412117AG14GENIChomozygous108122793
16141309461413095CT22GENIChomozygous108858160
16141503061415031GA9GENIChomozygous108858161
16141511961415120GA7GENIChomozygous108858162
16141538061415381TC5GENIChomozygous108122795
16142025161420252GA20GENIChomozygous108858163
16142029461420295GC24GENIChomozygous108858164
16142143161421432GC36GENICpossibly homozygous108858165
16142197561421976AG23GENIChomozygous108858166
16141765161417652CT8GENICheterozygous120847422
16142095561420956AG24GENICpossibly homozygous108122797
16142305861423059CT22GENICheterozygous108122798
16142454061424541TC10GENIChomozygous108122800