chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
112052855820528559CCAT10GENIChomozygous50664667
112052969320529694TC18GENIChomozygous50664668
112052997120529972TG22GENIChomozygous50664669
112053004020530041CT16GENIChomozygous50664670
112053013720530140TAC---14GENIChomozygous50664671
112053019220530193AG17GENIChomozygous50664672
112053026020530261GT17GENIChomozygous50664673
112053041320530414TA11GENIChomozygous50664674
112053200720532008C-16GENIChomozygous50664676
112053205020532051CT12GENIChomozygous50664677
112053303720533038TC16GENIChomozygous50664678
112053367220533673GA18GENIChomozygous50664679
112053456220534563T-29GENIChomozygous50664680
112053517720535178TC14GENIChomozygous50664681
112053747320537474TC21GENIChomozygous50664682
112053758920537590GGA19GENIChomozygous50664683
112053864820538649AT11GENIChomozygous50664684
112053864920538650AC12GENIChomozygous50664685
112053874420538745CT12GENIChomozygous50664686
112053908420539085AAT12GENIChomozygous50664688
112053916620539167CT8GENIChomozygous50664689
112053924720539248CT14GENIChomozygous50664692
112053929520539296GC20GENIChomozygous50664693
112053965120539652AG15GENIChomozygous50664694
112053965420539655GC15GENIChomozygous50664695
112053985220539853GA25GENIChomozygous50664696
112053989520539896TC16GENIChomozygous50664697
112054008320540084TC12GENIChomozygous50664698
112054031220540313AG21GENIChomozygous50664699
112054088020540881TC19GENIChomozygous50664700
112054195720541958GGCA17GENIChomozygous50664701
112054203820542039TA21GENIChomozygous50664702
112054242920542430CT13GENIChomozygous50664703
112054286520542866CT19GENIChomozygous50664704
112054301520543016AG17GENIChomozygous50664705
112054338020543381CT23GENIChomozygous50664708
112054310320543108CGAAC-----20GENIChomozygous50664706
112054329420543295GA17GENIChomozygous50664707