chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1221068459221068460TC24GENIChomozygous108543462
1221069809221069810AG29GENIChomozygous108543466
1221071971221071972AG40GENIChomozygous108543470
1221075946221075947CT13GENIChomozygous108543478
1221076783221076784AG28GENIChomozygous108543480
1221077741221077742CT26GENIChomozygous108994586
1221078222221078223AG18GENIChomozygous108543484
1221080823221080824GT20GENIChomozygous108543488
1221081352221081353TG17GENIChomozygous108543490
1221081607221081608AG15GENIChomozygous108543492
1221082401221082402AG19GENIChomozygous108543494
1221083686221083687AG26GENIChomozygous108543496
1221084139221084140GA18GENICpossibly homozygous108543498
1221084177221084178CT13GENIChomozygous108543500