chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106943498869434989C10GENIChomozygous128828381
106943528969435290CG21GENIChomozygous116625112
106943530369435304CG20GENIChomozygous116625114
106943651869436519GA17GENIChomozygous116625116
106943669069436691TG17GENIChomozygous116625118
106943681769436818TA14GENIChomozygous116625120
106943712869437129GC18GENIChomozygous116625122
106943777969437780AG10GENIChomozygous116625124
106943820369438204AG12GENIChomozygous116625126
106943866869438669AC16GENIChomozygous116625128
106943866969438670TC14GENIChomozygous116625130
106943882669438827TG14GENIChomozygous116625132
106943916769439168AT21GENIChomozygous116625134
106943921269439213TG24GENIChomozygous116625136
106943923269439233AG29GENIChomozygous116625138
106943927269439273TC22GENIChomozygous116625140
106943932569439326TG23GENIChomozygous116625142
106943952069439521GA14GENIChomozygous116625144