chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1214127746214127747GC28GENIChomozygous974674958
1214128734214128735CT15GENIChomozygous974674959
1214128881214128882CG10GENIChomozygous974674960
1214130010214130011GA27GENIChomozygous974674961
1214131357214131358AG16GENIChomozygous974674962
1214132380214132381AG15GENIChomozygous974674963
1214132530214132531CT35GENIChomozygous974674964
1214132768214132769CG18GENIChomozygous974674965
1214135782214135783AG14GENIChomozygous974674966
1214136646214136647GA28GENIChomozygous974674967
1214138264214138265GT23GENIChomozygous974674968
1214139461214139462AT16GENIChomozygous974674969
1214141343214141344AG22GENIChomozygous974674970
1214142890214142891AG26GENIChomozygous974674971
1214146027214146028TC16GENIChomozygous974674972
1214146950214146951GA16GENIChomozygous974674973