chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
117435204674352047TG115GENICheterozygous50832234
117435205274352053GT117GENICheterozygous50832235
117435205474352055GT112GENICheterozygous50832236
117435212074352121AG162GENICheterozygous50832237
117435223274352233CT140GENICheterozygous50832238
117435225874352259GC131GENICheterozygous50832239
117435232274352323TC86GENICheterozygous50832241
117435237174352372CT68GENICheterozygous50832245
117435254574352546TA81GENICheterozygous50832246
117435254974352550AT85GENICheterozygous50832247
117435259674352597GC77GENICheterozygous50832248
117435266374352664GA84GENICheterozygous50892715
117435267374352674TTCGA82GENICheterozygous50832249
117435281974352820AG138GENICheterozygous50832250
117435282774352828CT141GENICheterozygous50832251
117435288374352884TC122GENICheterozygous50832252
117435313174353132GA136GENICheterozygous50832253
117435316074353161CT122GENICheterozygous50832254
117435316874353169AC114GENICheterozygous50832255
117435317174353172GA112GENICheterozygous50832256
117435317774353178GC101GENICheterozygous50832257
117435318174353182GT104GENICheterozygous50832258
117435318574353186AT100GENICheterozygous50832259
117435324574353246AG89GENICheterozygous50832260
117435340574353406TC134GENICheterozygous50832261
117435340674353407TG137GENICheterozygous50832262
117435396774353968CT134GENICheterozygous50832263
117435417574354176CT119GENICheterozygous50832264
117435455274354553GGT8GENICheterozygous50832265
117435455974354560T-3GENIChomozygous50832266
117435456174354562C-2GENIChomozygous50832267
117435457374354574GT10GENICpossibly homozygous50892717
117435457874354579AAT4GENIChomozygous50832269
117435479074354791CG48GENICheterozygous50892719
117435479874354799GT57GENICheterozygous50892721
117435483174354832CT101GENICheterozygous50892723
117435483474354835CT105GENICheterozygous50892725
117435484174354842GT105GENICheterozygous50832270
117436730374367304TTA15GENIChomozygous50832273
117436732074367321G-7GENIChomozygous50832274