chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108682032986820330TC23GENIChomozygous116948778
108682090886820909CT6GENIChomozygous116948780
108682097586820976AG19GENIChomozygous116668192
108682124186821242CA3GENIChomozygous116668194
108682180986821810CA17GENIChomozygous116668198
108682246986822470GA20GENIChomozygous116948782
108682312586823126TC5GENIChomozygous116948784
108682318986823190AC5GENIChomozygous116948786
108682373886823739TG18GENIChomozygous116668200
108682535686825357CT18GENIChomozygous116668204
108682704986827050CA17GENIChomozygous116948788
108682751886827519AG18GENIChomozygous116668206
108682818886828189AG3GENIChomozygous116668208
108682879686828797GA16GENIChomozygous116948790
108682895086828951GA15GENIChomozygous116668210
108682924286829243AG12GENIChomozygous116668212
108683066886830669CT18GENIChomozygous116948792
108683170386831704GA23GENIChomozygous116948794
108683202686832027TC10GENIChomozygous116668216
108683231086832311TG8GENIChomozygous116668222