chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
45608560156085602CCA4GENIChomozygous58334902
45608560256085603CCACACA1GENIChomozygous58334903
45608620356086204GA12GENIChomozygous56905112
45608717456087175GA16GENIChomozygous56905114
45608792756087928AAGT5GENICheterozygous58587346
45609008956090090TTA21GENIChomozygous56905131
45609061756090618AG12GENIChomozygous56905133
45609081856090819AG21GENIChomozygous56905135
45609148456091485CG23GENIChomozygous56905137
45609185156091852AG20GENIChomozygous56905139
45609195456091955AG21GENIChomozygous56905141
45609204456092045CT28GENIChomozygous56905143
45609215956092160TC15GENIChomozygous56905145
45609250256092503TTG20GENIChomozygous56905147
45609284956092850GT21GENIChomozygous56905149
45609285056092851CT21GENIChomozygous56905151
45609329956093300TC18GENIChomozygous56905153
45609345056093451AG22GENIChomozygous56905155
45609349956093500TC29GENIChomozygous56905157
45609377156093772GA21GENIChomozygous56905158
45609413456094135CT22GENIChomozygous56905160
45609427656094277GA32GENIChomozygous56905161
45609437356094376AAG---21GENIChomozygous56905162
45609461156094612GT24GENIChomozygous56905164
45609494256094943GA26GENIChomozygous56905166
45609517856095179AT16GENIChomozygous56905167
45609536856095369CT27GENIChomozygous56905169
45609561956095620AG12GENIChomozygous56905171
45609574256095743AG27GENIChomozygous56905173
45609586156095862TTGGCTGGTTCCTCAC14GENIChomozygous56905174
45609656856096569GC36GENIChomozygous56905178
45609677556096776GC16GENIChomozygous56905179
45609735356097354TC18GENIChomozygous56905180
45609754056097541AG16GENIChomozygous56905182
45609876056098761AATGT21GENIChomozygous56905186
45609881656098817AG26GENIChomozygous56905188
45609909856099099TTG15GENIChomozygous56905190