chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3170400762170400763CT25GENIChomozygous57785576
3170400837170400838G-17GENIChomozygous57785578
3170400971170400972AAT19GENIChomozygous57785580
3170401577170401578T-8GENIChomozygous57785582
3170402349170402350GT11GENIChomozygous57785586
3170402351170402352GA11GENIChomozygous57785588
3170402367170402387ACACACACACACACACACAC--------------------11GENIChomozygous58632192
3170402402170402403CT10GENIChomozygous58049233
3170402440170402441AG14GENIChomozygous57785590
3170402858170402866TTTCCTTG--------14GENIChomozygous57785592
3170402936170402937TG18GENIChomozygous57785594
3170402961170402962GA16GENIChomozygous57785596
3170403352170403367TGTTTTGTTTTGTTT---------------6GENIChomozygous57785598
3170404156170404157GA15GENIChomozygous57785600
3170404222170404223CCA11GENIChomozygous57785604
3170404233170404234CA11GENIChomozygous57785606
3170405530170405531GA23GENIChomozygous57785608
3170406483170406484CT8GENIChomozygous57785616
3170406594170406595G-8GENIChomozygous57785618
3170406768170406769CA9GENIChomozygous57785620
3170406769170406770GT9GENIChomozygous57785622
3170406825170406826GA9GENIChomozygous57785624
3170407661170407662C-14GENIChomozygous57785626
3170408397170408398TA12GENIChomozygous57785628
3170408576170408577CCA6GENICheterozygous57785630
3170409702170409703CT25GENIChomozygous57785632
3170410525170410526GT13GENIChomozygous57785634
3170411179170411180GC19GENIChomozygous57785636
3170411229170411230TG13GENIChomozygous57785638