chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10110139141110139142A-16GENICpossibly homozygous52684191
10110139153110139154AG22GENICpossibly homozygous52814776
10110139500110139501CT35GENIChomozygous51601059
10110140004110140007AAA---14GENICpossibly homozygous51601060
10110140005110140007AA--14GENICheterozygous52969658
10110140154110140155AG18GENIChomozygous51601062
10110140346110140347A-10GENIChomozygous51601063
10110140635110140636AG4GENIChomozygous51601064
10110140738110140739GA2GENIChomozygous51601065
10110140784110140785GT1GENIChomozygous51601066
10110142723110142725AA--18INTERGENIChomozygous51601067
10110142859110142860TC28INTERGENIChomozygous51601068
10110145666110145667TC15GENIChomozygous51601069
10110146190110146191AG21GENIChomozygous51601070
10110147331110147332GA19GENIChomozygous51601073
10110147657110147658CA34GENIChomozygous51601074
10110147827110147828AC18GENIChomozygous51601075