chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101080915910809160T21GENIChomozygous128789536
101081045510810455T21GENIChomozygous128789537
101081230410812305GA27GENIChomozygous116734090
101081554810815549CT19GENIChomozygous116734091
101081630810816309TC33GENIChomozygous116493789
101081329910813300AG33GENIChomozygous116493783
101081499110814992GA20GENIChomozygous116493785
101081529410815295TC24GENIChomozygous116493787
101081355310813553T32GENIChomozygous131087111
101082018810820189TA36GENIChomozygous116734093
101081887110818872TC24GENIChomozygous116734092
101081935910819360AG39GENIChomozygous116913245
101081995410819955AG24GENIChomozygous118073741
101082088910820890CT35GENIChomozygous116734094
101082234510822346GT32GENIChomozygous116734095
101082333410823335TA27GENIChomozygous116734096
101082358810823589GA45GENIChomozygous116493799
101082593210825932G13GENIChomozygous131087112
101082593410825934TTTTTTTTTTTG7GENICheterozygous133757152
101082606110826062TC20GENIChomozygous116734097
101082644110826442CT22GENIChomozygous116493801
101082694510826946CT30GENIChomozygous116734098