chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
117714761771477CT60GENIChomozygous108024817
117719131771914AG22GENIChomozygous108024818
117736461773647AT38GENIChomozygous108024819
117746311774632AT60GENICpossibly homozygous108024820
117759851775986CT46GENIChomozygous108024821
117765721776573GA54GENIChomozygous108024822
117770021777003CT49GENIChomozygous108024823
117781131778114TC43GENIChomozygous108024824
117781291778130CT47GENIChomozygous108024825
117782351778236AT63GENIChomozygous108024826
117786291778630CT48GENIChomozygous108024827
117787061778707GA61GENIChomozygous108024828
117791751779176TG53GENIChomozygous108024829
117792651779266CT46GENIChomozygous108024830
117793321779333TC51GENIChomozygous108024831
117797571779758TG51GENIChomozygous108024832
117799041779905AG45GENIChomozygous108024833
117810811781082TC32GENIChomozygous108024834
117814471781448GC52GENIChomozygous108024835