chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1184184394184184395CT3GENICheterozygous60998679
1184184740184184741CT14GENIChomozygous60998680
1184185044184185045GC15GENIChomozygous60998681
1184185799184185800GA17GENIChomozygous60998682
1184185839184185840TTACGATGG4GENICheterozygous62027522
1184185966184185967T-1GENIChomozygous60998685
1184186294184186295GA27GENIChomozygous60998686
1184186369184186374CCGCC-----11GENIChomozygous60998688
1184186433184186434TC8GENIChomozygous60998689
1184187251184187252T-7GENICpossibly homozygous61567051
1184188059184188060CT10GENICpossibly homozygous60998692
1184188496184188497GA14GENIChomozygous62027523
1184188899184188900CCAGAGACAGAA2GENIChomozygous62181556