chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7119054689119054690CCGTGT17GENICpossibly homozygous749792520
7119054809119054817TATTTATT--------4GENIChomozygous749792522
7119055128119055129GGTTC19GENIChomozygous749792524
7119055234119055235GGA23GENIChomozygous749792525
7119056013119056014AC24GENIChomozygous638120971
7119056280119056281AG23GENIChomozygous638120972
7119057324119057325TC14GENIChomozygous638120973
7119057605119057606CA27GENIChomozygous638120974
7119058213119058214CCGTGTGT11GENICheterozygous749792527
7119058213119058214CCGTGTGTGTGT11GENICpossibly homozygous749792529
7119060355119060356TTTTTTG15GENIChomozygous749792531
7119060676119060680CCCT----27GENIChomozygous749792532
7119061805119061806CT28GENIChomozygous638120975
7119062366119062367AG30GENIChomozygous638120976
7119062556119062557AG24GENIChomozygous638120977
7119063659119063660TG22GENIChomozygous638120978
7119063859119063860TC22GENIChomozygous638120979
7119063979119064004TTTTTTTTTTTTTTTTTTTTTTTTT-------------------------21GENICheterozygous749792533
7119065285119065286CT35GENIChomozygous638120980
7119066563119066564AG15GENIChomozygous638120981
7119066575119066576CCGG15GENICheterozygous749792535
7119066575119066576CCGGG15GENICpossibly homozygous749792536
7119066602119066603CT15GENIChomozygous638120982
7119067033119067034CA35GENIChomozygous638120983