chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10109620956109620957CG26GENIChomozygous116718721
10109621176109621177CT24GENIChomozygous116718723
10109621565109621566TA27GENIChomozygous116718725
10109622042109622043TG31GENIChomozygous116718727
10109622112109622113TC24GENIChomozygous116718729
10109622187109622188CT27GENIChomozygous116718731
10109622202109622203GT31GENIChomozygous116718733
10109622373109622374GA24GENIChomozygous116718735
10109622747109622748AG15GENIChomozygous116718737
10109622803109622804AG14GENIChomozygous116718739
10109623005109623006GA19GENIChomozygous116718741
10109623609109623610CT22GENIChomozygous117136826
10109624580109624581AG14GENIChomozygous116718743
10109624600109624601CT15GENIChomozygous116718745
10109624800109624801TG31GENIChomozygous116718747
10109625094109625095GA33GENIChomozygous116718749