chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
154861080848610809GC8GENIChomozygous112503080
154861179748611798AG22GENIChomozygous112503082
154861268748612688TC27GENIChomozygous112503084
154863296548632966GC12GENIChomozygous112503086
154863360348633604AT28GENIChomozygous112503088
154864243248642433GA16GENIChomozygous112503090
154864243348642434GA17GENIChomozygous112503092
154864254948642550CT25GENIChomozygous112503094
154864417948644180AT22GENIChomozygous112503096
154865334848653349GT23GENIChomozygous112503100
154865671948656720AC18GENIChomozygous112503102
154865687448656875CG25GENIChomozygous112503104
154865782748657828TA24GENIChomozygous112503106
154865863548658636CT22GENIChomozygous112503108
154865886248658863CT21GENIChomozygous112503110
154866002448660025CT19GENIChomozygous112503112
154866047848660479GC8GENIChomozygous112503114
154866128948661290CT29GENIChomozygous112503116
154866147648661477GC26GENIChomozygous112503117
154866325548663256CA17GENIChomozygous112503119
154866554548665546CT23GENIChomozygous112503121
154866704448667045GA28GENIChomozygous112503125
154866858148668582GT11GENIChomozygous112503127
154866859848668599GA11GENIChomozygous112503129
154866860648668607GT8GENIChomozygous112503131
154866860748668608TA8GENIChomozygous112503133