chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3170400762170400763CT22GENIChomozygous57785576
3170400837170400838G-24GENIChomozygous57785578
3170400971170400972AAT20GENIChomozygous57785580
3170401577170401578T-15GENIChomozygous57785582
3170401586170401594TTTTTTTT--------17GENIChomozygous57785584
3170402349170402350GT10GENIChomozygous57785586
3170402351170402352GA10GENIChomozygous57785588
3170402402170402403CT8GENIChomozygous58049233
3170402440170402441AG11GENIChomozygous57785590
3170402858170402866TTTCCTTG--------11GENIChomozygous57785592
3170402936170402937TG19GENIChomozygous57785594
3170402961170402962GA20GENIChomozygous57785596
3170403352170403367TGTTTTGTTTTGTTT---------------3GENIChomozygous57785598
3170404156170404157GA33GENIChomozygous57785600
3170404222170404223CCAA17GENICpossibly homozygous57785602
3170404222170404223CCA17GENICheterozygous57785604
3170405530170405531GA29GENICpossibly homozygous57785608
3170405997170405998CCT10GENICheterozygous57785610
3170406017170406018AAT19GENIChomozygous57785612
3170406326170406327G-21GENIChomozygous57785614
3170406483170406484CT14GENICpossibly homozygous57785616
3170406594170406595G-21GENIChomozygous57785618
3170406768170406769CA19GENIChomozygous57785620
3170406769170406770GT19GENIChomozygous57785622
3170406825170406826GA19GENIChomozygous57785624
3170407661170407662C-22GENIChomozygous57785626
3170408397170408398TA25GENIChomozygous57785628
3170408576170408577CCA13GENICheterozygous57785630
3170409702170409703CT20GENIChomozygous57785632
3170410525170410526GT24GENIChomozygous57785634
3170411179170411180GC24GENIChomozygous57785636
3170411229170411230TG26GENIChomozygous57785638