chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
79183383691833840TATG----10GENIChomozygous54988389
79183489191834892CT30GENIChomozygous54021791
79183550291835503TC30GENIChomozygous54021793
79183575291835753GA31GENIChomozygous54208395
79183578791835788CT33GENIChomozygous54021794
79183648391836484TA32GENIChomozygous54021797
79183763591837636TC29GENIChomozygous54021798
79183769891837699AG20GENIChomozygous54021799
79183792991837935ATATAT------3GENIChomozygous54208396
79184090991840910TC21GENIChomozygous54021814
79184117091841171TC26GENIChomozygous54021815
79184247791842478TC13GENICpossibly homozygous54021821
79184284891842849GT47GENIChomozygous54208397
79184361791843618TC31GENIChomozygous54021827
79184503191845032TC32GENIChomozygous54208398
79184756191847562AG25GENIChomozygous54208399
79184852591848527AC--5GENIChomozygous54208400
79184908091849081TC26GENIChomozygous54208401
79185023591850236CCA12GENIChomozygous54988391
79185025791850258CA12GENIChomozygous54208402
79185026291850263CA9GENICheterozygous54021850
79185057291850573GT29GENIChomozygous54208403