chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
118305259083052591TG13GENIChomozygous50848654
118305261683052617TC21GENIChomozygous50848655
118305352883053529TC8GENICpossibly homozygous50848656
118305482283054823AAT9GENIChomozygous50848657
118305541583055416CT16GENIChomozygous50848658
118305711983057120CG15GENICpossibly homozygous50848660
118305743783057438CT17GENICpossibly homozygous50848661
118305856883058569CCTA1GENIChomozygous50848662
118306119683061197TC21GENICpossibly homozygous50848664
118306172183061722GC25GENICheterozygous50848665
118306289083062891GA14GENIChomozygous50848666
118306452983064530G-1GENIChomozygous50848667
118306453683064537GT1GENIChomozygous50848668
118306457583064576GA1GENIChomozygous50848673
118306456183064562GA1GENIChomozygous50848670
118306456583064566GA1GENIChomozygous50848671
118306457483064575GA1GENIChomozygous50848672
118306458383064584GA2GENIChomozygous50848674
118306461983064620GT14GENICpossibly homozygous50848675
118306610183066102CA4GENICheterozygous50848678
118306654083066541AG18GENIChomozygous50848679
118306881483068815GGT6GENICheterozygous50848680
118307132883071329GGTTT2GENICheterozygous50848682