chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3152752108152752109GA42GENICpossibly homozygous111781186
3152753578152753579CT39GENIChomozygous111781188
3152755595152755596CT34GENIChomozygous111781190
3152759373152759374CT52GENIChomozygous111781194
3152761705152761706TG47GENIChomozygous111781196
3152805934152805935GA21GENIChomozygous119652376
3152805935152805936CG21GENIChomozygous119652377
3152805950152805951AC15GENIChomozygous111781204
3152810364152810365GA8GENIChomozygous111781206