chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71294979112949792AG12GENIChomozygous115570738
71295007612950077GA18GENIChomozygous115570739
71295092112950922CT9GENIChomozygous115570740
71295110812951109AC19GENIChomozygous115570741
71295194912951950CG21GENIChomozygous115570742
71295534012955341CG20GENIChomozygous115570752
71295557012955571GA15GENIChomozygous115570753
71295588512955886TC19GENIChomozygous115570754
71295635312956354GA13GENIChomozygous115570755
71295889412958895GA7GENIChomozygous115570756
71295917512959176GA17GENIChomozygous115570757
71295963812959639TA10GENIChomozygous115570758
71296043912960440CT6GENIChomozygous115570759
71296118712961188AT8GENIChomozygous115570760
71296373512963736GA18GENIChomozygous115570761
71296569212965693CT18GENIChomozygous115570762
71296629912966300CT15GENIChomozygous115570763
71296778112967782TC3GENIChomozygous115570764
71296785112967852TC4GENIChomozygous115570765
71296790012967901AC9GENIChomozygous115570766
71296944012969441AG17GENIChomozygous115570767
71296951812969519AC13GENIChomozygous115570768
71296954012969541GA7GENIChomozygous115570769
71297058712970588AG17GENIChomozygous115570770
71297079812970799CT15GENIChomozygous115570771