chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7119055128119055129GGTTC4GENIChomozygous717764075
7119056013119056014AC28GENICpossibly homozygous579944354
7119056280119056281AG4GENIChomozygous579944355
7119057367119057368T-15GENIChomozygous717764076
7119057935119057936AT26GENIChomozygous579944356
7119058484119058485AG27GENIChomozygous579944357
7119059885119059886GC13GENIChomozygous579944358
7119060638119060639TG14GENIChomozygous579944359
7119060676119060680CCCT----10GENIChomozygous717764077
7119060988119060989CT17GENICpossibly homozygous579944360
7119061761119061762TC17GENIChomozygous579944361
7119063659119063660TG7GENIChomozygous579944362
7119064563119064564GGT7GENIChomozygous717764078
7119066575119066576CCG3GENICheterozygous717764079
7119066575119066576CCGG3GENICheterozygous717764080