chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
148109320581093206T-10GENICheterozygous49016111
148109454381094544CT11GENIChomozygous49016114
148109605881096059G-16GENIChomozygous48809060
148109610281096103CT26GENIChomozygous49016115
148109623281096233TC25GENIChomozygous48809064
148109752481097525CCT15GENICheterozygous49016116
148109752481097525CCTT15GENICpossibly homozygous49016117
148109809681098097AT19GENIChomozygous48809069
148109827381098274TTC14GENIChomozygous48809071
148109351381093514CA18GENIChomozygous49572488
148109936081099361CG1GENIChomozygous49572489
148109373781093738GGA12GENICpossibly homozygous49345216