chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4105925045105925046TG21GENIChomozygous113364874
4105925089105925090TG13GENIChomozygous113364876
4105925125105925126AC12GENIChomozygous113364877
4105930397105930398AT20GENIChomozygous113364909
4105930464105930465AG24GENIChomozygous113364911
4105933893105933894AG23GENIChomozygous113364927
4105934150105934151AG17GENIChomozygous113364929
4105934215105934216GC20GENIChomozygous113364931
4105934605105934606GC21GENIChomozygous113364933
4105937186105937187TG12GENIChomozygous113364935
4105937259105937260TC4GENIChomozygous113364937
4105938557105938558CT20GENIChomozygous119437967