chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7119054689119054690CCGTGT17INTERGENICpossibly homozygous54232158
7119055128119055129GGTTC19INTERGENIChomozygous54080364
7119056013119056014AC24INTERGENIChomozygous54080365
7119056280119056281AG23INTERGENIChomozygous54080366
7119057324119057325TC14INTERGENIChomozygous54232164
7119058213119058214CCGTGTGTGTGT11INTERGENICpossibly homozygous55095542
7119060676119060680CCCT----27INTERGENIChomozygous54080373
7119061805119061806CT28INTERGENIChomozygous54750688
7119054809119054817TATTTATT--------4INTERGENIChomozygous55361603
7119058213119058214CCGTGTGT11INTERGENICheterozygous55361605
7119055234119055235GGA23INTERGENIChomozygous54750682
7119057605119057606CA27INTERGENIChomozygous54750684
7119060355119060356TTTTTTG15INTERGENIChomozygous54750686
7119062366119062367AG30INTERGENIChomozygous54750690
7119062556119062557AG24INTERGENIChomozygous54750692
7119063659119063660TG22INTERGENIChomozygous54080378
7119063859119063860TC22INTERGENIChomozygous54750694
7119063979119064004TTTTTTTTTTTTTTTTTTTTTTTTT-------------------------21INTERGENICheterozygous55878314
7119065285119065286CT35INTERGENIChomozygous54750696
7119066563119066564AG15INTERGENIChomozygous54750698
7119066575119066576CCGG15INTERGENICheterozygous54080381
7119066575119066576CCGGG15INTERGENICpossibly homozygous54586959
7119066602119066603CT15INTERGENIChomozygous54750700
7119067033119067034CA35INTERGENIChomozygous54750702