chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106377610663776107GC15GENIChomozygous958788727
106377622363776224AG15GENIChomozygous958788728
106377820363778204CA28GENIChomozygous958788729
106378014163780142TG21GENIChomozygous958788730
106378014463780145CT20GENIChomozygous958788731
106378019663780197TG20GENIChomozygous958788732
106378025263780253GT28GENIChomozygous958788733
106378025363780254TG26GENIChomozygous958788734
106378207463782075TC14GENIChomozygous958788735
106378294663782947CT30GENIChomozygous958788736
106378403763784038CG45GENIChomozygous958788737
106378485563784856GA37GENIChomozygous958788738
106378928963789290TC27GENIChomozygous958788739
106378943963789440GT28GENIChomozygous958788740
106379062063790621AC18GENIChomozygous958788741
106379067163790672TC25GENIChomozygous958788742
106379087663790877AG12GENIChomozygous958788743
106379279063792791CT17GENIChomozygous958788744
106379466163794662GT30GENIChomozygous958788745
106379483063794831TG27GENIChomozygous958788746
106379501463795015TC30GENIChomozygous958788747