chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71294979112949792AG11GENIChomozygous115570738
71295007612950077GA21GENIChomozygous115570739
71295092112950922CT8GENIChomozygous115570740
71295110812951109AC11GENIChomozygous115570741
71295194912951950CG11GENIChomozygous115570742
71295393412953935TC8GENIChomozygous115570747
71295410412954105CT3GENICheterozygous116003747
71295534012955341CG10GENIChomozygous115570752
71295557012955571GA13GENIChomozygous115570753
71295588512955886TC19GENIChomozygous115570754
71295635312956354GA15GENIChomozygous115570755
71295889412958895GA19GENIChomozygous115570756
71295917512959176GA16GENIChomozygous115570757
71295963812959639TA8GENIChomozygous115570758
71296043912960440CT6GENIChomozygous115570759
71296118712961188AT13GENIChomozygous115570760
71296373512963736GA5GENIChomozygous115570761
71296569212965693CT13GENIChomozygous115570762
71296778112967782TC7GENIChomozygous115570764
71296944012969441AG4GENIChomozygous115570767
71296951812969519AC5GENIChomozygous115570768
71296954012969541GA5GENIChomozygous115570769
71297058712970588AG4GENIChomozygous115570770
71297079812970799CT27GENIChomozygous115570771