chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
99073346490733465GGT14GENIChomozygous705476827
99073349690733497GGT16GENIChomozygous705476828
99073384490733846GT--5GENICheterozygous705476830
99073588290735884GT--14GENICheterozygous705476832
99073603090736031TTGGGA29GENIChomozygous705476836
99073603290736033TG30GENIChomozygous557855917
99073687890736879TG20GENIChomozygous556729747
99073692190736922TG24GENIChomozygous556729748
99073693290736933TG24GENIChomozygous556729749
99073694690736947AG22GENIChomozygous556729750
99073695490736955TG19GENIChomozygous556729751
99073697190736972TA23GENIChomozygous556729752
99073856290738563TC8GENIChomozygous557855918
99074061090740612AT--3GENIChomozygous705476837
99074145590741456AAAGG11GENIChomozygous705476838
99074242690742428AA--6GENICheterozygous705476839
99074258390742584CT17GENIChomozygous557855919
99074258590742586TC18GENIChomozygous557855920
99074259990742600CA21GENIChomozygous557855921
99074260190742602GT21GENIChomozygous557855922
99074260490742606CC--25GENIChomozygous705476840
99074261090742611CT25GENIChomozygous557855923
99074261190742612CA26GENIChomozygous557855924
99074280890742809AAG7GENIChomozygous705476841
99074769090747691TTAG17GENIChomozygous705476842
99074795090747951CT33GENIChomozygous557855925