chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4105925045105925046TG12GENIChomozygous113364874
4105925089105925090TG11GENIChomozygous113364876
4105925125105925126AC11GENIChomozygous113364877
4105930397105930398AT20GENIChomozygous113364909
4105930464105930465AG27GENIChomozygous113364911
4105933893105933894AG21GENIChomozygous113364927
4105934150105934151AG28GENIChomozygous113364929
4105934215105934216GC31GENIChomozygous113364931
4105934605105934606GC38GENIChomozygous113364933
4105937186105937187TG24GENIChomozygous113364935
4105937259105937260TC16GENIChomozygous113364937