chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
34060104640601047GA49GENICpossibly homozygous774666139
34060144840601449TG56GENICheterozygous774666140
34060144940601450TC55GENICheterozygous774666141
34060146140601462CT65GENICheterozygous774666142
34060147840601479CT66GENICheterozygous774666143
34060149640601497GT71GENICheterozygous774666144
34060150240601503GA72GENICheterozygous774666145
34060150540601506CT74GENICheterozygous774666146
34060155540601556GA53GENICheterozygous774666147
34060155940601560GT55GENICheterozygous774666148
34060156240601563GA52GENICheterozygous774666149
34060157040601571GA48GENICheterozygous774666150
34060157340601574GA47GENICheterozygous774666151
34060157740601578TG49GENICheterozygous774666152
34060160540601606GT40GENICheterozygous774666153
34060162140601622TC39GENICheterozygous774666154
34060176640601767CT45GENICheterozygous774666155
34060177040601771TC45GENICheterozygous774666156
34060178840601789AC62GENICheterozygous774666157
34060179440601795CT65GENICheterozygous774666158
34060180240601803CT73GENICheterozygous774666159
34060185240601853CT76GENICheterozygous774666160
34060185340601854CG77GENICheterozygous774666161
34060190740601908TC74GENICheterozygous774666162
34060192540601926TC73GENICheterozygous774666163
34060194640601947GA69GENICheterozygous774666164
34060194840601949GA71GENICheterozygous774666165
34060196140601962TC79GENICheterozygous774666166
34060197240601973CT75GENICheterozygous774666167
34060197740601978AG74GENICheterozygous774666168
34060198240601983GA71GENICheterozygous774666169
34060199340601994TC58GENICheterozygous774666170
34060199440601995GA60GENICheterozygous774666171
34060266940602670GA44GENIChomozygous774666172
34060267940602680AG45GENICpossibly homozygous774666173
34060269640602697AG42GENIChomozygous774666174
34060269740602698AC42GENIChomozygous774666175
34060272440602725CG48GENIChomozygous774666176
34060272740602728CA51GENIChomozygous774666177
34060275940602760TG50GENIChomozygous774666178
34060303540603036CT43GENICpossibly homozygous774666179