chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
182231211822312119CT29GENIChomozygous977470236
182231263422312635TC31GENIChomozygous977470237
182231275622312757CT21GENIChomozygous977470238
182231309022313091TG30GENIChomozygous977470239
182231534522315346GT5GENICheterozygous977470240
182231581222315813TG39GENIChomozygous977470241
182231597422315975AC29GENIChomozygous977470242