chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2045424074542408TC22GENIChomozygous109074694
2045424154542416AG21GENIChomozygous109074696
2045429564542957AG18GENIChomozygous109074698
2045449754544976CT30GENIChomozygous109074700
2045454404545441CT16GENIChomozygous109074702
2045455704545571AC4GENIChomozygous109465784
2045455774545578TA2GENIChomozygous109465785
2045455814545582TA2GENIChomozygous109465786
2045462514546252AG25GENIChomozygous109074704
2045472724547273GA16GENIChomozygous109418820
2045482334548234CA23GENIChomozygous109074708
2045487254548726CA13GENIChomozygous109465787
2045488414548842GT16GENIChomozygous109463078
2045490644549065GT24GENIChomozygous109074710
2045504644550465GC10GENIChomozygous109463080
2045509714550972AG13GENIChomozygous109074712
2045520764552077CA26GENIChomozygous109074716
2045530334553034GT16GENIChomozygous109074718
2045532514553252CT8GENIChomozygous109074720
2045543924554393TC7GENIChomozygous109074722
2045543934554394TG7GENIChomozygous109074724
2045548394554840GT22GENIChomozygous109074726
2045552674555268GA18GENIChomozygous109074728
2045555594555560GA27GENIChomozygous109418824
2045556664555667AG29GENIChomozygous109390042
2045557304555731AG44GENIChomozygous109233515
2045560454556046GA18GENIChomozygous109418826
2045572244557225CT9GENIChomozygous109329569
2045572664557267GC10GENIChomozygous109418828