chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
118651724186517242G32GENICpossibly homozygous132158424
118651771086517711TC63GENIChomozygous116072778
118651796786517968TC69GENIChomozygous116072780
118651863086518631GA69GENIChomozygous116072782
118651871086518711AC55GENIChomozygous116072784
118651871386518714C55GENIChomozygous132158425
118651871586518716GA55GENIChomozygous116072786
118651871686518717TG55GENIChomozygous116072788
118651871886518719CG56GENIChomozygous116072790
118651970386519704TG57GENIChomozygous116072792