chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
125040844050408441GC18GENIChomozygous118274615
125041009850410099TC52GENIChomozygous115352211
125041085350410854GT57GENIChomozygous115352213
125041106750411068CT29GENIChomozygous115352215
125041144850411449CG24GENICpossibly homozygous118274617
125041148550411486AT12GENIChomozygous118274618
125041152250411523GT9GENICpossibly homozygous118274619
125041162950411630CT9GENIChomozygous118274620
125041166750411668TC11GENICpossibly homozygous118306577
125041254350412544AG63GENIChomozygous115352218
125041313650413137GT35GENIChomozygous115352220
125041351050413511CT61GENIChomozygous115352222
125041426850414269AG24GENIChomozygous115352224