chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
142180522321805224CT22GENICpossibly homozygous113379848
142180552821805529AG10GENIChomozygous113581054
142180554021805541CT10GENIChomozygous113721630
142180590821805909AG27GENIChomozygous113379850
142180620821806209AG36GENIChomozygous113379852
142180658921806590TC16GENIChomozygous113379854
142180726321807264GA24GENIChomozygous113721632
142180730821807309CT25GENIChomozygous113721634
142180758221807583CG14GENIChomozygous113581058
142180769921807700AG10GENIChomozygous113379858