chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106377622363776224AG52GENIChomozygous781495273
106377820363778204CA52GENIChomozygous781495274
106377986863779869AC20GENIChomozygous781495275
106378004863780049GT55GENIChomozygous781495276
106378039763780398AC40GENIChomozygous781495277
106378056363780564GT24GENIChomozygous781495278
106378074563780746AT25GENIChomozygous781495279
106378078263780783CT17GENIChomozygous781495280
106378104263781043CG17GENIChomozygous781495281
106378110763781108AG45GENICpossibly homozygous781495282
106378119563781196CG13GENIChomozygous781495283
106378120663781207GT48GENIChomozygous781495284
106378148363781484GT30GENIChomozygous781495285
106378258663782587CG67GENICpossibly homozygous781495286
106378870963788710GC45GENICpossibly homozygous781495287
106378885563788856CT42GENIChomozygous781495288
106379054863790549AT44GENIChomozygous781495289
106379062063790621AC46GENIChomozygous781495290
106379067163790672TC49GENICpossibly homozygous781495291
106379087663790877AG34GENIChomozygous781495292
106379419663794197CT49GENIChomozygous781495293
106379449263794493AC49GENIChomozygous781495294
106379451963794520GC45GENIChomozygous781495295
106379453263794533GC49GENIChomozygous781495296
106379466163794662GT31GENIChomozygous781495297
106379474163794742GC46GENIChomozygous781495298
106379501463795015TC43GENICpossibly homozygous781495299