chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
186061949260619493AG8GENIChomozygous977510567
186062046560620466TC22GENIChomozygous977510568
186062056060620561GT18GENIChomozygous977510569
186062060360620604TC16GENIChomozygous977510570
186062580060625801TC11GENIChomozygous977510571
186062663260626633TC34GENIChomozygous977510572
186062748460627485TC20GENIChomozygous977510573
186062821960628220GA23GENIChomozygous977510574
186062880060628801AG19GENIChomozygous977510575
186062902360629024TC20GENIChomozygous977510576
186062905260629053CT17GENICpossibly homozygous977510577
186062924860629249GA27GENIChomozygous977510578
186063074960630750AT21GENIChomozygous977510579
186063094560630946CG18GENIChomozygous977510580
186063109760631098CT29GENIChomozygous977510581
186063147860631479CA26GENIChomozygous977510582
186063167060631671AG23GENIChomozygous977510583
186063213660632137CT23GENIChomozygous977510584
186063215760632158GT27GENIChomozygous977510585
186063306660633067TC30GENIChomozygous977510586
186063366560633666GT11GENICpossibly homozygous977510587