chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108595604585956046CG17GENIChomozygous68926945
108595654885956549TA25GENIChomozygous68139155
108595767785957678TC25GENIChomozygous68139158
108596631785966318CT25GENIChomozygous68926947
108596962485969625TG43GENIChomozygous68139189
108597023685970237GA21GENIChomozygous68139192
108598023885980239CT25GENIChomozygous68926949
108598050585980506CT11GENIChomozygous68926951
108598139385981394AC9GENIChomozygous68139223
108598154985981550AG14GENIChomozygous68139226
108598920185989202CT33GENIChomozygous68926953
108599100485991005AG3GENIChomozygous68139266
108599150685991507AC7GENIChomozygous68926955
108599629785996298GT20GENICpossibly homozygous69144275
108600156886001569TC25GENIChomozygous68926957
108600442186004422AG37GENIChomozygous68926959
108600773886007739TC11GENIChomozygous68139293
108600923386009234CT28GENIChomozygous68926961
108601155786011558AG32GENIChomozygous68139299
108601432086014321AC33INTERGENIChomozygous68139308
108601470786014708GA7INTERGENIChomozygous69144279
108601506186015062AC8INTERGENIChomozygous69144284
108601684886016849GA12INTERGENIChomozygous69144288
108601730486017305GA12INTERGENICheterozygous69144292
108601773186017732GA10INTERGENIChomozygous69144296
108601664686016647AG5INTERGENIChomozygous68926967
108601401986014020CT31INTERGENIChomozygous68926963
108601584286015843CT43INTERGENIChomozygous68926965