chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
52557823025578230CTGGG42GENIChomozygous128160126
52557917225579173CT56GENIChomozygous119201129
52558043825580439AC54GENIChomozygous113696247
52558050925580510TC60GENIChomozygous113696249
52558095925580960CA50GENIChomozygous113696251
52558203625582036C69GENICpossibly homozygous128160127
52558259925582600AC48GENIChomozygous113696253
52558283625582837CG48GENIChomozygous113696255
52558323325583234CT55GENIChomozygous113696257
52558337125583372CT51GENIChomozygous113696259
52558345225583453TC36GENIChomozygous113696261
52558380725583808AT48GENIChomozygous113696263
52558390325583903A44GENIChomozygous128160134
52558391025583910C45GENIChomozygous128160135
52558391625583917C43GENIChomozygous128160136
52558392325583924C44GENIChomozygous128160137
52558392825583929C45GENIChomozygous128160138
52558394025583941C44GENIChomozygous128160139
52558396125583963CC44GENIChomozygous128160140
52558396525583965C43GENIChomozygous128160141
52558398425583985C43GENIChomozygous128160142
52558399225583993A46GENIChomozygous128160143
52558400025584000C43GENIChomozygous128160144
52558400725584007A42GENIChomozygous128160145
52558403925584039C49GENIChomozygous128160146
52558404125584041C48GENIChomozygous128160147
52558404525584045A49GENIChomozygous128160148
52558405525584056T49GENIChomozygous128160149
52558405925584060AC48GENIChomozygous113696265
52558413725584137TG47GENIChomozygous128160150
52558422925584230CA53GENIChomozygous113696267
52558424625584247TC56GENIChomozygous113696269
52558427725584278GA55GENIChomozygous113696271
52558025425580255CT49GENIChomozygous119146010