chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1218818047218818048CT32GENICheterozygous109367657
1218826012218826013GT15GENICpossibly homozygous108993594
1218882538218882539AC10GENIChomozygous108539494
1218882690218882691AG6GENIChomozygous108539498
1218911864218911865CT22GENIChomozygous108539627
1218912930218912931AG25GENICpossibly homozygous108539635