chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
146468709064687090C7GENIChomozygous129168144
146468724464687245G12GENIChomozygous129168145
146471248364712484T14GENICheterozygous129168166
146474110864741109GT26GENIChomozygous118700712
146474111564741116CT25GENIChomozygous118700713
146474111764741118AT25GENIChomozygous113481976
146474112764741128AT24GENIChomozygous118700714
146474113264741133AT24GENIChomozygous113481977
146474113464741135TG23GENIChomozygous114163722
146474114364741144AT22GENIChomozygous118700715
146474115264741153TG18GENIChomozygous113600168
146474115764741158AG17GENIChomozygous113747022
146474115864741159CT17GENIChomozygous113747024
146474116164741162CG15GENIChomozygous113747026
146474116364741164CT15GENIChomozygous113747028
146474117964741180TG12GENIChomozygous123925285
146474118064741181AC12GENIChomozygous123925286
146474118264741183AC12GENIChomozygous123925287
146474111064741111AT26GENIChomozygous114090903
146474116864741171ATC15GENIChomozygous130140923
146474117264741172AGT15GENIChomozygous130140924
146476787164767872A2GENIChomozygous130427758