chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5107039382107039383GT8GENICheterozygous113954768
5107039506107039507TC11GENICpossibly homozygous114235662
5107039746107039747CT21GENICheterozygous114235663
5107039754107039755AC23GENICheterozygous114235664
5107039816107039817GA25GENICheterozygous113954771