chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
99073346490733465GGT24GENIChomozygous765633537
99073349690733497GGT27GENIChomozygous765633538
99073603090736031TTGGGA33GENIChomozygous765633539
99073603290736033TG33GENIChomozygous664212136
99073687890736879TG14GENIChomozygous664212137
99073692190736922TG14GENIChomozygous664212138
99073693290736933TG12GENIChomozygous664212139
99073694690736947AG13GENIChomozygous664212140
99073695490736955TG13GENIChomozygous664212141
99073697190736972TA12GENIChomozygous664212142
99073856290738563TC13GENIChomozygous664212143
99073880190738802C-3GENIChomozygous765633540
99073881790738818T-3GENIChomozygous765633541
99074061090740612AT--6GENIChomozygous765633542
99074145590741456AAAGG18GENIChomozygous765633543
99074242690742428AA--1GENIChomozygous765633544
99074258390742584CT9GENIChomozygous664212144
99074258590742586TC9GENIChomozygous664212145
99074259990742600CA13GENIChomozygous664212146
99074260190742602GT13GENIChomozygous664212147
99074260490742606CC--18GENIChomozygous765633545
99074261090742611CT20GENIChomozygous664212148
99074261190742612CA20GENIChomozygous664212149
99074280890742809AAG4GENIChomozygous765633546
99074769090747691TTAG11GENIChomozygous765633547
99074795090747951CT5GENIChomozygous664212150
99074956390749564GGT13GENICheterozygous765633548