chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4104359642104359643GA28GENIChomozygous149554276
4104363501104363502TC22GENIChomozygous143136108
4104365470104365471GA17GENIChomozygous149554277
4104365593104365594TA14GENIChomozygous149554278
4104365657104365658AG13GENIChomozygous143136112
4104366296104366297AG17GENICpossibly homozygous143136114
4104366305104366306CT16GENICpossibly homozygous149554279
4104366533104366534GA19GENIChomozygous143136115
4104365999104366000TG14GENIChomozygous137186304
4104365918104365919TC23GENIChomozygous137186303
4104368328104368329AG12GENIChomozygous137186309