chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4167778139167778140TC10GENIChomozygous113214938
4167787996167787997AG22GENICpossibly homozygous112942837
4167878448167878449TC20GENICheterozygous113474594
4167878453167878454TC19GENICheterozygous113474596
4167906937167906938AT26GENICheterozygous113474686
4167985903167985904TA37GENIChomozygous112943045
4167986014167986015TG43GENIChomozygous112943047