chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101080915910809160T14GENIChomozygous128789536
101081045510810455T16GENIChomozygous128789537
101081230410812305GA22GENIChomozygous116734090
101081554810815549CT19GENIChomozygous116734091
101081630810816309TC22GENIChomozygous116493789
101081329910813300AG21GENIChomozygous116493783
101081499110814992GA19GENIChomozygous116493785
101081529410815295TC21GENIChomozygous116493787
101081355310813553T24GENIChomozygous131087111
101081887110818872TC25GENICpossibly homozygous116734092
101081935910819360AG27GENIChomozygous116913245
101081995410819955AG16GENIChomozygous118073741
101082018810820189TA24GENIChomozygous116734093
101082088910820890CT23GENIChomozygous116734094
101082234510822346GT21GENIChomozygous116734095
101082333410823335TA20GENIChomozygous116734096
101082358810823589GA33GENIChomozygous116493799
101082593110825931G10GENICheterozygous131901042
101082593210825932G10GENICheterozygous131087112
101082593410825934TTTTTTTTTTTG4GENICheterozygous133757152
101082606110826062TC19GENIChomozygous116734097
101082644110826442CT27GENIChomozygous116493801
101082694510826946CT22GENIChomozygous116734098