chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101461976314619764TC11GENIChomozygous116496775
101462229614622297AT23GENIChomozygous116496783
101462239214622393CT25GENIChomozygous116737098
101462380814623809CT13GENICheterozygous118030767
101462406814624069CA14GENICheterozygous118030775
101462408014624081TG16GENICheterozygous118030776
101462531914625320GC15GENIChomozygous116737100
101462574814625749TC14GENIChomozygous116496791
101462750514627506TC4GENIChomozygous126376085
101462767714627678AT13GENIChomozygous116737101
101463238814632389AC20GENIChomozygous116496809
101463265114632652CA26GENIChomozygous116737103
101463770514637706GA20GENIChomozygous116737104
101463926714639268GT27GENIChomozygous116737105