chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1214124012214124013TC32GENIChomozygous885208149
1214124247214124248CT20GENIChomozygous885208150
1214124348214124349AG7GENICheterozygous885208151
1214124388214124389CA4GENICheterozygous885208152
1214124410214124411CA13GENICheterozygous885208153
1214126277214126278TC3GENICheterozygous885208154
1214126977214126978AC3GENICheterozygous885208155
1214127029214127030AT3GENICheterozygous885208156
1214127068214127069AT5GENICheterozygous885208157
1214127746214127747GC22GENIChomozygous885208158
1214129232214129233AC24GENIChomozygous885208159
1214130010214130011GA14GENIChomozygous885208160
1214131083214131084CG16GENIChomozygous885208161
1214131357214131358AG21GENIChomozygous885208162
1214132307214132308GC5GENICheterozygous885208163
1214132380214132381AG21GENIChomozygous885208164
1214132602214132603AT22GENIChomozygous885208165
1214132768214132769CG17GENIChomozygous885208166
1214132884214132885CT21GENIChomozygous885208167
1214134192214134193CT15GENICheterozygous885208168
1214138264214138265GT23GENIChomozygous885208169
1214140211214140212CT18GENICpossibly homozygous885208170
1214140827214140828GT22GENIChomozygous885208171
1214141343214141344AG13GENIChomozygous885208172
1214142493214142494GA22GENIChomozygous885208173
1214146027214146028TC18GENIChomozygous885208174
1214146950214146951GA19GENIChomozygous885208175