chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
77091721770917220TTT---16GENICpossibly homozygous53957665
77091721870917220TT--16GENICheterozygous53957667
77091742970917430CT20GENIChomozygous53957669
77091826170918262CG34GENIChomozygous53957671
77091850270918503AATCT41GENIChomozygous53957672
77091856970918570T-17GENICheterozygous55142026
77091858970918591GC--25GENICheterozygous54981796
77091859070918591CG23GENICheterozygous55357197