chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108876481288764812GG19GENIChomozygous128843485
108877303388773034TC11GENIChomozygous116674514
108877434888774349CT15GENIChomozygous116674516
108877599688775997GT17GENIChomozygous116674517
108877715788777158GA26GENIChomozygous116674519
108877939688779397T14GENIChomozygous128843489
108878047788780478CT25GENIChomozygous116674521
108878222788782228A17GENICpossibly homozygous128843490
108878275788782758AG22GENIChomozygous116674523
108878284188782842GA27GENIChomozygous116674525
108878415288784153CT19GENIChomozygous116674527
108878460788784608CT26GENIChomozygous116674529
108878684788786848AG18GENIChomozygous116674531
108878885188788852GC20GENIChomozygous116674533
108877722088777221TC19GENIChomozygous118007433
108877397988773981TG3GENIChomozygous129970351