chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
45608620356086204GA7GENICpossibly homozygous56905112
45608717456087175GA2GENIChomozygous56905114
45609008956090090TTA6GENIChomozygous56905131
45609061756090618AG5GENIChomozygous56905133
45609081856090819AG7GENIChomozygous56905135
45609148456091485CG7GENIChomozygous56905137
45609185156091852AG10GENIChomozygous56905139
45609195456091955AG17GENIChomozygous56905141
45609204456092045CT9GENIChomozygous56905143
45609215956092160TC7GENIChomozygous56905145
45609250256092503TTG3GENIChomozygous56905147
45609284956092850GT8GENICpossibly homozygous56905149
45609285056092851CT9GENICpossibly homozygous56905151
45609329956093300TC15GENIChomozygous56905153
45609345056093451AG8GENIChomozygous56905155
45609349956093500TC9GENIChomozygous56905157
45609377156093772GA13GENIChomozygous56905158
45609413456094135CT13GENICpossibly homozygous56905160
45609427656094277GA19GENIChomozygous56905161
45609437356094376AAG---5GENIChomozygous56905162
45609461156094612GT16GENIChomozygous56905164
45609494256094943GA7GENIChomozygous56905166
45609517856095179AT11GENIChomozygous56905167
45609536856095369CT12GENIChomozygous56905169
45609561956095620AG16GENICpossibly homozygous56905171
45609574256095743AG16GENIChomozygous56905173
45609586156095862TTGGCTGGTTCCTCAC1GENIChomozygous56905174
45609656856096569GC10GENIChomozygous56905178
45609677556096776GC6GENIChomozygous56905179
45609735356097354TC3GENIChomozygous56905180
45609754056097541AG8GENIChomozygous56905182
45609876056098761AATGT10GENIChomozygous56905186
45609881656098817AG10GENIChomozygous56905188
45609909856099099TTG4GENICheterozygous56905190