chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1167206725167206726CT23GENIChomozygous108357665
1167206950167206951AG25GENIChomozygous108357666
1167207061167207062TC17GENIChomozygous108357667
1167207097167207098GA18GENIChomozygous108357668
1167207316167207317AG13GENIChomozygous108357669
1167207317167207318AG13GENIChomozygous108357670
1167207394167207395GA13GENIChomozygous108357671
1167207940167207941TG18GENICpossibly homozygous108357672
1167207978167207979CT24GENIChomozygous109343177
1167208189167208190GA22GENIChomozygous109343179
1167208572167208573TC28GENIChomozygous108357673
1167209004167209005CT24GENIChomozygous109343181
1167209231167209232CT20GENIChomozygous109343183
1167209302167209303CT18GENIChomozygous108357675
1167209338167209339AG22GENIChomozygous108357676
1167209427167209428CT17GENIChomozygous108357677
1167210484167210485GT12GENIChomozygous120846218
1167211554167211555CG26GENIChomozygous109343185
1167211973167211974AG22GENIChomozygous109343187
1167210573167210574CT19GENIChomozygous108357678
1167211372167211373CT21GENIChomozygous108357679
1167210478167210479G12GENIChomozygous127453818