chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122395602723956028AG6GENIChomozygous115286245
122395666323956664TC11GENIChomozygous115286247
122395850823958509GA5GENIChomozygous115286249
122395905623959057GA6GENIChomozygous115286251
122396029523960296AC7GENIChomozygous115286253
122396167823961679TA4GENIChomozygous115510216
122396188023961881GT4GENIChomozygous115469778
122396412623964127GA2GENIChomozygous115286255
122396548923965490CT9GENIChomozygous115286259
122396854923968550CA8GENIChomozygous115286261
122396943723969438CT3GENIChomozygous115446259
122397533623975337AG4GENIChomozygous115469780
122397653823976539CT3GENIChomozygous115422070
122398204123982042CG3GENIChomozygous115286281
122398470823984709GC3GENIChomozygous115703399
122398472223984723AG3GENIChomozygous115703401
122398473323984734TA2GENIChomozygous115703403
122398605923986060AG7GENICpossibly homozygous115703405
122398635923986360TC2GENIChomozygous115469784