chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1274339059274339060TA19GENICpossibly homozygous61226568
1274340009274340010AG16GENIChomozygous61226569
1274340034274340035TC26GENIChomozygous61226570
1274341049274341050TC26GENIChomozygous61226571
1274341558274341559GC25GENICpossibly homozygous61226572
1274342839274342840CT18GENICpossibly homozygous61226573
1274342900274342901GGA3GENICheterozygous61226574