chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2078904017890402CG30GENIChomozygous109235885
2078919107891911GC26GENIChomozygous109085146
2078930047893005TC14GENIChomozygous109085150
2078937877893788CT20GENIChomozygous109085152
2078938867893887AT29GENIChomozygous109085154
2078939567893957CA19GENIChomozygous109085156
2078940197894020GA23GENIChomozygous109235886
2078940717894072CT24GENIChomozygous109235887
2078943247894325TC31GENIChomozygous109085158
2078944847894485CT21GENIChomozygous109329965
2078946297894630AG18GENIChomozygous109085161
2078949637894964GA18GENIChomozygous109235888
2078951677895168GA22GENIChomozygous109085163
2078975177897518CT40GENIChomozygous109235889
2078978787897879AG33GENIChomozygous109085171
2079015007901501TG3GENIChomozygous109572164
2079023507902351TC26GENIChomozygous109235890
2079024217902422GC25GENIChomozygous109235891
2079024417902442AG27GENIChomozygous109085184
2079025957902596TC35GENIChomozygous109085186