chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
183010647930106480AG9GENICpossibly homozygous46413704
183010740330107404GT9GENIChomozygous46413708
183010754630107547AC24GENICheterozygous46757025
183010755530107556TG23GENICheterozygous46757026
183010800930108010AT11GENIChomozygous46413709
183010822430108225AG28GENIChomozygous46413711