chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1266051200266051201GA13GENIChomozygous120882127
1266051441266051442GT15GENIChomozygous108637475
1266051528266051529AG24GENIChomozygous109028135
1266052272266052274TG21GENIChomozygous131267901
1266052915266052916CT13GENIChomozygous109058218
1266053700266053702CC11GENIChomozygous131267902
1266053707266053708CG11GENIChomozygous120516194
1266054333266054334CA13GENIChomozygous109028136
1266055810266055811GC21GENIChomozygous120882128
1266056394266056395GA21GENIChomozygous109028137
1266057629266057630CT32GENIChomozygous108637481
1266057650266057651TC27GENIChomozygous108637482
1266057701266057702AG20GENIChomozygous108637483
1266058549266058550GA20GENIChomozygous108637484
1266059060266059061GA17GENIChomozygous108637485
1266053150266053151TG10GENICheterozygous133662160