chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
117714761771477CT52GENIChomozygous108024817
117719131771914AG35GENIChomozygous108024818
117736461773647AT57GENIChomozygous108024819
117746311774632AT64GENIChomozygous108024820
117759851775986CT54GENIChomozygous108024821
117765721776573GA39GENIChomozygous108024822
117770021777003CT57GENIChomozygous108024823
117781131778114TC51GENIChomozygous108024824
117781291778130CT51GENIChomozygous108024825
117782351778236AT53GENIChomozygous108024826
117786291778630CT49GENIChomozygous108024827
117787061778707GA51GENIChomozygous108024828
117791751779176TG49GENIChomozygous108024829
117792651779266CT52GENIChomozygous108024830
117793321779333TC58GENIChomozygous108024831
117797571779758TG50GENICpossibly homozygous108024832
117799041779905AG64GENIChomozygous108024833
117768711776874AAA61GENIChomozygous127346307
117798611779870TTATTTTAA54GENIChomozygous127346308
117801581780159TC12GENICheterozygous131584642
117801711780171TC12GENICheterozygous127346309
117801751780175TC12GENICheterozygous127346310
117804671780467AAGTTG52GENIChomozygous127346311
117810811781082TC45GENIChomozygous108024834
117814471781448GC50GENIChomozygous108024835