chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5107039382107039383GT18GENIChomozygous113954768
5107039423107039424TC20GENIChomozygous114235660
5107039455107039456AC17GENIChomozygous114235661
5107039506107039507TC25GENIChomozygous114235662
5107039693107039694AG44GENIChomozygous113954770
5107039754107039755AC37GENICpossibly homozygous114235664
5107039816107039817GA28GENICpossibly homozygous113954771