chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2034285453428546GT13GENIChomozygous109068774
2034292673429268AG40GENIChomozygous109417152
2034303413430342TA32GENIChomozygous109068782
2034304843430485GA34GENIChomozygous109068784
2034315253431526TA23GENIChomozygous109068788
2034320383432039TC23GENIChomozygous109068790
2034322033432204TC13GENIChomozygous109417153
2034330173433018TC25GENIChomozygous109068794
2034333443433345TC26GENIChomozygous109068796
2034348073434808GA19GENIChomozygous109417155
2034350913435092TC47GENIChomozygous109068800
2034358733435874TC28GENIChomozygous109068804
2034372933437294GA27GENIChomozygous109417157
2034375523437553TA10GENIChomozygous109417159
2034378183437819AG11GENIChomozygous109068808
2034379633437964AC22GENIChomozygous109068810
2034379673437968AG22GENIChomozygous109068812
2034379913437992TC21GENIChomozygous109417161
2034381053438106GC20GENIChomozygous109068814
2034381163438117AC17GENIChomozygous109068816
2034382973438298AG10GENIChomozygous109417169
2034383033438304GA9GENIChomozygous109417171
2034383083438309AG9GENIChomozygous109068818
2034383163438317TC8GENIChomozygous109417173
2034383253438326GT9GENIChomozygous109417175
2034381223438123AC19GENIChomozygous109328512
2034326713432672CT18GENIChomozygous109462983
2034380883438089GC17GENIChomozygous109328506
2034381193438120AC17GENIChomozygous109328509