chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1224959452224959453CT29GENICheterozygous773906619
1224960079224960080CT40GENICpossibly homozygous773906620
1224961163224961164TC28GENICpossibly homozygous773906621
1224962140224962141TC29GENIChomozygous773906622
1224969176224969177CT34GENIChomozygous773906623
1224969990224969991GA58GENIChomozygous773906624