chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2078904017890402CG22GENIChomozygous109235885
2078919107891911GC18GENIChomozygous109085146
2078928057892806GA13GENIChomozygous109085148
2078930047893005TC12GENIChomozygous109085150
2078937877893788CT19GENIChomozygous109085152
2078938867893887AT30GENIChomozygous109085154
2078939567893957CA16GENIChomozygous109085156
2078940717894072CT26GENIChomozygous109235887
2078943247894325TC23GENIChomozygous109085158
2078944847894485CT20GENIChomozygous109329965
2078946297894630AG14GENIChomozygous109085161
2078975177897518CT9GENIChomozygous109235889
2078978787897879AG20GENIChomozygous109085171
2079023507902351TC14GENIChomozygous109235890
2079024217902422GC10GENIChomozygous109235891
2079024417902442AG10GENIChomozygous109085184
2079025957902596TC15GENIChomozygous109085186
2079054987905499GC7GENIChomozygous109085195