chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7119054689119054690CCGTGT6INTERGENICheterozygous54232158
7119054809119054817TATTTATT--------1INTERGENIChomozygous55361603
7119055128119055129GGTTC32INTERGENIChomozygous54080364
7119056013119056014AC21INTERGENIChomozygous54080365
7119058213119058214CCGTGTGT15INTERGENICheterozygous55361605
7119058660119058661CT48INTERGENICpossibly homozygous55878312
7119060332119060333CCT25INTERGENIChomozygous54232169
7119060638119060639TG12INTERGENIChomozygous54080372
7119060676119060680CCCT----20INTERGENIChomozygous54080373
7119060988119060989CT22INTERGENIChomozygous54080374
7119061805119061806CT17INTERGENIChomozygous54750688
7119062366119062367AG32INTERGENIChomozygous54750690
7119062556119062557AG45INTERGENIChomozygous54750692
7119063659119063660TG24INTERGENIChomozygous54080378
7119063979119064004TTTTTTTTTTTTTTTTTTTTTTTTT-------------------------6INTERGENICheterozygous55878314
7119065285119065286CT20INTERGENIChomozygous54750696
7119066563119066564AG9INTERGENIChomozygous54750698
7119066575119066576CCGGG5INTERGENIChomozygous54586959
7119067033119067034CA14INTERGENICpossibly homozygous54750702
7119058214119058216GT--15INTERGENICpossibly homozygous55030374