chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
154860367348603674CG23GENIChomozygous112503078
154860839748608398AT3GENIChomozygous113199921
154861080848610809GC17GENIChomozygous112503080
154861179748611798AG7GENIChomozygous112503082
154861268748612688TC26GENIChomozygous112503084
154863296548632966GC21GENIChomozygous112503086
154863360348633604AT10GENIChomozygous112503088
154864243248642433GA13GENIChomozygous112503090
154864243348642434GA13GENIChomozygous112503092
154864254948642550CT22GENIChomozygous112503094
154864417948644180AT14GENIChomozygous112503096
154865334848653349GT22GENIChomozygous112503100
154865671948656720AC25GENIChomozygous112503102
154865687448656875CG24GENIChomozygous112503104
154865782748657828TA10GENIChomozygous112503106
154865863548658636CT23GENIChomozygous112503108
154865886248658863CT16GENIChomozygous112503110
154866002448660025CT21GENIChomozygous112503112
154866128948661290CT19GENIChomozygous112503116
154866147648661477GC13GENIChomozygous112503117
154866325548663256CA6GENIChomozygous112503119
154866554548665546CT15GENIChomozygous112503121
154866563548665636CG23GENIChomozygous112503123
154866704448667045GA11GENIChomozygous112503125
154866858148668582GT17GENIChomozygous112503127
154866859848668599GA15GENIChomozygous112503129
154866860648668607GT14GENIChomozygous112503131
154866860748668608TA14GENIChomozygous112503133