chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8111063992111063993CT33GENIChomozygous117172462
8111065209111065210GA33GENIChomozygous117172464
8111065654111065655TA19GENIChomozygous116646343
8111066551111066552AG20GENIChomozygous116646345
8111067863111067864GT14GENIChomozygous117172466
8111068881111068882TC15GENIChomozygous117172468
8111070608111070609TC30GENIChomozygous116646347
8111071177111071178GA19GENIChomozygous117172470
8111072446111072447TC23GENIChomozygous117172472
8111074146111074147CT24GENIChomozygous117172474
8111074255111074256CT10GENIChomozygous117172476
8111075082111075083AG12GENIChomozygous116873686
8111075926111075927TA17GENIChomozygous116873690
8111076872111076873AG30GENIChomozygous116873692
8111077894111077895GT20GENIChomozygous116873694
8111078087111078088AG12GENIChomozygous116646357
8111079238111079239CT13GENIChomozygous117172478
8111082212111082213GA18GENIChomozygous117172482
8111085578111085579AT17GENIChomozygous116873704
8111087416111087417TC27GENIChomozygous116646363
8111087462111087463CT40GENIChomozygous116646365
8111087785111087786CT22GENIChomozygous117172484
8111089766111089767GC10GENIChomozygous116646369
8111092196111092197CT18GENIChomozygous116646371
8111096469111096470GA21GENIChomozygous116646375
8111097126111097127CT15GENIChomozygous117172486
8111097690111097691AC8GENIChomozygous116873706
8111098916111098917GT33GENIChomozygous116646377
8111101896111101897AG27GENIChomozygous116646383
8111102594111102595TC25GENIChomozygous116646387
8111103273111103274TA13GENIChomozygous116646389
8111103525111103526AG9GENIChomozygous116646391
8111105692111105693AC26GENIChomozygous117172494
8111108040111108041TC21GENIChomozygous116646395
8111114821111114822AG16GENIChomozygous116646411
8111077769111077770GA7GENIChomozygous117930274