chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
99073346490733465GGT23GENIChomozygous750008610
99073349690733497GGT34GENIChomozygous750008611
99073383190733832CCGT11GENIChomozygous750008614
99073588190735882AAGT18GENICpossibly homozygous750008616
99073603090736031TTGGGA38GENIChomozygous750008619
99073603290736033TG38GENIChomozygous638455957
99073687890736879TG27GENIChomozygous638455958
99073692190736922TG23GENIChomozygous638455959
99073693290736933TG25GENIChomozygous638455960
99073694690736947AG27GENIChomozygous638455961
99073695490736955TG28GENIChomozygous638455962
99073697190736972TA27GENIChomozygous638455963
99073856290738563TC16GENIChomozygous638455964
99074145590741456AAAGG7GENIChomozygous750008620
99074242690742428AA--21GENICheterozygous750008621
99074258390742584CT27GENICpossibly homozygous638455965
99074258590742586TC29GENICpossibly homozygous638455966
99074259990742600CA30GENIChomozygous638455967
99074260190742602GT30GENIChomozygous638455968
99074260490742606CC--32GENIChomozygous750008622
99074261090742611CT32GENIChomozygous638455969
99074261190742612CA31GENIChomozygous638455970
99074280890742809AAG1GENIChomozygous750008623
99074769090747691T-2GENIChomozygous750008624
99074769390747702GTTGTTGTT---------2GENIChomozygous750008625
99074795090747951CT32GENIChomozygous638455971
99074867990748680CCGTGT15GENIChomozygous750008628