chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
79183489191834892CT17GENIChomozygous54021791
79183550291835503TC21GENICpossibly homozygous54021793
79183575291835753GA27GENICpossibly homozygous54208395
79183578791835788CT20GENIChomozygous54021794
79183648391836484TA16GENIChomozygous54021797
79183763591837636TC9GENIChomozygous54021798
79183769891837699AG18GENICpossibly homozygous54021799
79184090991840910TC17GENICpossibly homozygous54021814
79184117091841171TC24GENICpossibly homozygous54021815
79184284891842849GT10GENIChomozygous54208397
79184361791843618TC19GENICpossibly homozygous54021827
79184503191845032TC17GENICheterozygous54208398
79184756191847562AG15GENIChomozygous54208399
79184908091849081TC7GENICheterozygous54208401
79185023591850236CCA3GENICheterozygous54988391
79185025791850258CA3GENICheterozygous54208402
79185057291850573GT16GENIChomozygous54208403