chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
153188868031888681GC98GENICheterozygous48272979
153188877531888776AG99GENICheterozygous48272981
153188893631888937CCTGGTTTGGGGGATTGTGGGTGAGCTGGGCCCCAAGGGT55GENICheterozygous49046101
153189780031897801AG18GENIChomozygous48272989
153189780131897802TG16GENIChomozygous48272990
153189780331897804TC15GENIChomozygous48272991
153189781731897818GA12GENIChomozygous48272992
153189782631897827TG6GENIChomozygous48272993
153190189331901895GT--25GENICpossibly homozygous48272996