chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
99073346490733465GGT18GENIChomozygous747809916
99073349690733497GGT23GENIChomozygous747809917
99073383190733832CCGT7GENICpossibly homozygous747809920
99073588190735882AAGT18GENICheterozygous747809922
99073588190735882AAGTGT18GENICheterozygous747809923
99073588290735884GT--18GENICheterozygous747809921
99073603090736031TTGGGA42GENIChomozygous747809925
99073603290736033TG42GENIChomozygous635018020
99073687890736879TG16GENIChomozygous635018021
99073692190736922TG22GENIChomozygous635018022
99073693290736933TG24GENIChomozygous635018023
99073694690736947AG26GENIChomozygous635018024
99073695490736955TG27GENIChomozygous635018025
99073697190736972TA30GENIChomozygous635018026
99073856290738563TC2GENIChomozygous635018027
99074145590741456AAAGG11GENIChomozygous747809926
99074242690742428AA--14GENICheterozygous747809927
99074258390742584CT14GENICpossibly homozygous635018028
99074258590742586TC14GENICpossibly homozygous635018029
99074259990742600CA18GENIChomozygous635018030
99074260190742602GT18GENIChomozygous635018031
99074260490742606CC--18GENIChomozygous747809928
99074261090742611CT20GENIChomozygous635018032
99074261190742612CA20GENIChomozygous635018033
99074280890742809AAG6GENIChomozygous747809929
99074769090747691T-7GENIChomozygous747809930
99074769390747702GTTGTTGTT---------8GENIChomozygous747809931
99074795090747951CT38GENIChomozygous635018034
99074867990748680CCGTGT4GENIChomozygous747809934