chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85787782557877826CT15GENIChomozygous52981823
85787795157877952GT34GENIChomozygous52981824
85787996057879961GA20GENICheterozygous52656881
85788004857880049GA35GENICheterozygous53182071
85788130457881305C-32GENIChomozygous52656885
85788233457882335GA31GENIChomozygous52981825
85788313157883132TC30GENIChomozygous52656887
85788395157883952CCA16GENIChomozygous52656889
85788493357884934GA31GENIChomozygous52981826
85788525857885259CT34GENIChomozygous52981827
85788528357885284AG31GENIChomozygous52981828
85788537257885373TC28GENIChomozygous52656891
85788595457885955CT22GENIChomozygous52656893
85788917457889175TC24GENIChomozygous52656895
85789115957891160AG19GENIChomozygous52656897
85789233257892333AAT20GENIChomozygous52981829
85789247357892474GA24GENIChomozygous52656901
85789258857892589CT20GENIChomozygous52656903
85789314657893147GA26GENIChomozygous52981830
85789416857894169T-23GENIChomozygous52981831
85789457757894578AC43GENIChomozygous52656909