chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3170400762170400763CT21GENICpossibly homozygous57785576
3170400837170400838G-19GENIChomozygous57785578
3170400971170400972AAT12GENICpossibly homozygous57785580
3170401577170401578T-4GENICheterozygous57785582
3170401586170401594TTTTTTTT--------4GENICheterozygous57785584
3170402349170402350GT4GENIChomozygous57785586
3170402351170402352GA4GENIChomozygous57785588
3170402402170402403CT3GENICheterozygous58049233
3170402440170402441AG10GENICheterozygous57785590
3170402858170402866TTTCCTTG--------6GENIChomozygous57785592
3170402936170402937TG16GENIChomozygous57785594
3170402961170402962GA21GENICpossibly homozygous57785596
3170403352170403367TGTTTTGTTTTGTTT---------------1GENIChomozygous57785598
3170404156170404157GA24GENIChomozygous57785600
3170405530170405531GA15GENIChomozygous57785608
3170406017170406018AAT4GENIChomozygous57785612
3170406326170406327G-2GENIChomozygous57785614
3170406483170406484CT3GENIChomozygous57785616
3170406594170406595G-7GENIChomozygous57785618
3170406768170406769CA20GENICheterozygous57785620
3170406769170406770GT21GENICheterozygous57785622
3170406825170406826GA24GENICpossibly homozygous57785624
3170407661170407662C-21GENICpossibly homozygous57785626
3170408397170408398TA17GENIChomozygous57785628
3170409702170409703CT17GENIChomozygous57785632
3170410525170410526GT16GENICpossibly homozygous57785634
3170411179170411180GC21GENICpossibly homozygous57785636
3170411229170411230TG16GENICpossibly homozygous57785638