chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7130446696130446697GC47GENIChomozygous115890242
7130446972130446973GT49GENICpossibly homozygous115890244
7130447504130447505GA46GENIChomozygous115890246
7130449854130449855AG41GENIChomozygous115890248
7130452601130452602TC50GENIChomozygous115890250