chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
142410964024109641GA18GENIChomozygous125908124
142410982124109822CA10GENIChomozygous125908126
142410985124109852TG17GENIChomozygous125946257
142410989224109893CA15GENIChomozygous125908128
142410998824109989CG10GENIChomozygous125908130
142411021224110213CT19GENIChomozygous125908132
142411603624116037CA9GENIChomozygous125946258
142411608824116089GC12GENIChomozygous125908134
142411653524116536AG17GENIChomozygous125908136
142411670824116709CT8GENIChomozygous125908138
142411704324117044TG10GENIChomozygous125908140
142411870824118709GC21GENIChomozygous125946259
142411943324119434AG7GENIChomozygous125946260
142411943624119437AT6GENIChomozygous125908142
142411955924119560CT8GENIChomozygous125946261
142411988624119887CT30GENIChomozygous125908144
142411991324119914TC18GENIChomozygous125946262
142412095924120960CT6GENIChomozygous125946264
142412123524121236CT10GENIChomozygous125908146
142412148524121486CT13GENIChomozygous125908148
142412329024123291CA20GENIChomozygous125908152
142412331124123312CG18GENIChomozygous125908154
142412386524123866GA21GENIChomozygous125946265
142412388924123890CG16GENIChomozygous125908156
142412524024125241AG15GENIChomozygous125908160