chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71241004612410047TC6GENICheterozygous53790877
71241116212411163CCGGCTGT4GENIChomozygous55071063
71241155612411557GA2GENICheterozygous54884983
71241170712411708GA6GENICheterozygous53790888
71241170812411709TG7GENICpossibly homozygous54630296
71241217912412180TC15GENIChomozygous53790889
71241239012412391AAG1GENIChomozygous54630298
71241302612413027CT18GENICpossibly homozygous53790892
71241400912414010AT12GENICheterozygous53790894
71241435912414362GGG---1GENIChomozygous53790895
71241634612416347GT1GENIChomozygous53790897
71241635912416360CA1GENIChomozygous53790898