chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
99073346490733465GGT4GENIChomozygous717851837
99073349690733497GGT15GENIChomozygous717851838
99073521290735213GT5GENIChomozygous580182026
99073521390735214AT5GENIChomozygous580182027
99073573190735732AAGT8GENICheterozygous717851839
99073603090736031TTGGGA3GENIChomozygous717851840
99073603290736033TG3GENIChomozygous580182028
99073635590736356CG16GENIChomozygous580182029
99073637790736378AT14GENIChomozygous580182030
99073639590736396TG12GENIChomozygous579139941
99073673290736733TC16GENIChomozygous580182031
99073687890736879TG25GENICpossibly homozygous579139942
99073692190736922TG13GENIChomozygous579139943
99073693290736933TG7GENIChomozygous579139944
99073694690736947AG3GENIChomozygous579139945
99073695490736955TG3GENIChomozygous579139946
99073697190736972TA11GENICpossibly homozygous579139947
99073704190737042TA20GENICpossibly homozygous580182032
99073856290738563TC2GENIChomozygous580182033
99073982890739830AA--7GENIChomozygous717851841
99074127690741277TG13GENICheterozygous580182034
99074242490742426TT--5GENIChomozygous717851842
99074261090742611CT1GENIChomozygous580182035
99074261190742612CA1GENIChomozygous580182036
99074389790743898AC23GENIChomozygous580182037
99074517990745180AT15GENIChomozygous579139948
99074558690745587TG17GENIChomozygous579139949
99074575390745754TA8GENIChomozygous579139950
99074763590747638GTA---2GENICheterozygous717851843
99074879190748792GGT17GENICpossibly homozygous717851844
99074898990748990CT18GENIChomozygous579139951