chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4105925045105925046TG4GENIChomozygous113364874
4105925125105925126AC6GENIChomozygous113364877
4105925211105925212GT7GENIChomozygous119399123
4105925364105925365CA3GENIChomozygous119399125
4105929373105929374TA2GENIChomozygous113545175
4105930290105930291CT3GENIChomozygous119399133
4105930464105930465AG5GENIChomozygous113364911
4105932888105932889TC6GENIChomozygous113364923
4105930317105930318CT4GENIChomozygous119586342
4105932110105932111CT2GENIChomozygous119624434
4105934150105934151AG5GENIChomozygous113364929
4105934605105934606GC2GENIChomozygous113364933
4105937186105937187TG8GENIChomozygous113364935
4105937641105937642GA2GENIChomozygous119399137
4105937649105937650CT3GENIChomozygous119399139
4105937877105937878TA10GENIChomozygous119399141
4105937989105937990CG9GENIChomozygous119399143
4105938767105938768GA4GENIChomozygous119399145