chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
118651724186517242G14GENICpossibly homozygous132158424
118651771086517711TC31GENIChomozygous116072778
118651796786517968TC24GENIChomozygous116072780
118651863086518631GA25GENIChomozygous116072782
118651871086518711AC26GENIChomozygous116072784
118651871386518714C26GENIChomozygous132158425
118651871586518716GA26GENIChomozygous116072786
118651871686518717TG26GENIChomozygous116072788
118651871886518719CG26GENIChomozygous116072790
118651970386519704TG19GENIChomozygous116072792