chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
186062046560620466TC34GENIChomozygous965450611
186062491860624919AG38GENIChomozygous965450612
186062580060625801TC19GENIChomozygous965450613
186062663260626633TC20GENIChomozygous965450614
186062748460627485TC54GENIChomozygous965450615
186062821960628220GA40GENIChomozygous965450616
186062829260628293GA37GENIChomozygous965450617
186062880060628801AG34GENIChomozygous965450618
186062902360629024TC28GENIChomozygous965450619
186062905260629053CT27GENIChomozygous965450620
186062924860629249GA25GENIChomozygous965450621
186063074960630750AT29GENIChomozygous965450622
186063094560630946CG43GENIChomozygous965450623
186063109760631098CT33GENIChomozygous965450624
186063147860631479CA45GENIChomozygous965450625
186063167060631671AG38GENIChomozygous965450626
186063192060631921GA29GENIChomozygous965450627
186063213660632137CT27GENIChomozygous965450628
186063215760632158GT25GENIChomozygous965450629
186063306660633067TC46GENIChomozygous965450630
186063366560633666GT43GENIChomozygous965450631