chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1222700457222700458TG38GENICheterozygous109538044
1222712487222712488AG26GENICpossibly homozygous108547074
1222718971222718972GT32GENICpossibly homozygous109195646
1222718975222718976GT33GENICpossibly homozygous109195648
1222720945222720946TC49GENIChomozygous109538045