chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7142307157142307158CT19GENIChomozygous116097718
7142308425142308426CT12GENIChomozygous115941717
7142308713142308714GA12GENIChomozygous115941718
7142310471142310472TG8GENIChomozygous116097720
7142310811142310812AC10GENIChomozygous115941720
7142310892142310893GA13GENIChomozygous115941721
7142311316142311317AG13GENIChomozygous116097722
7142311727142311728CT14GENIChomozygous116097724
7142313489142313490CG17GENIChomozygous115941729
7142313528142313529TC21GENIChomozygous115941730
7142313902142313903AT7GENIChomozygous116097726
7142315146142315147TA21GENIChomozygous116097728
7142315308142315309AG20GENIChomozygous116097730
7142315783142315784CT15GENIChomozygous116097732
7142316042142316043CT15GENIChomozygous115941738
7142318487142318488GC11GENIChomozygous115941746
7142318518142318519TC12GENIChomozygous115941747
7142318531142318532TC12GENIChomozygous115941748