chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
144448128744481289TC18GENIChomozygous129152881
144448360044483601A13GENIChomozygous129152882
144448452044484522CA1GENIChomozygous129152883
144448452844484530GG3GENIChomozygous129152884
144448454644484546T3GENIChomozygous129152885
144448455244484553C4GENIChomozygous129152886
144448455844484559C4GENIChomozygous129152887
144448456744484568TG4GENIChomozygous113676807
144448456944484570CT4GENIChomozygous113676809
144448458344484584C4GENIChomozygous129152888
144448460744484608C6GENIChomozygous129152889
144448463844484639C10GENIChomozygous129152890
144448465844484658G10GENIChomozygous129152891
144448466644484668GC12GENIChomozygous129152892
144448467244484673C12GENIChomozygous129152893
144448467444484675C12GENIChomozygous129152894
144448471644484717C15GENIChomozygous129152895
144448471944484719G15GENIChomozygous129152896
144448473344484734A19GENIChomozygous129152897
144448474544484745T18GENIChomozygous129152898
144450067644500677GA19GENICheterozygous118691627
144450071944500720TC22GENICheterozygous130432679
144448929144489292TG17GENIChomozygous113995303
144449304044493041TG14GENIChomozygous113444686
144449356744493568AG22GENIChomozygous113444688