chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
142410379824103799AC13GENIChomozygous890588179
142410385724103858AT14GENIChomozygous890588178
142410426924104270AG18GENIChomozygous890588177
142410436524104366AG18GENIChomozygous890588176
142410441424104415CG22GENIChomozygous890588175
142410456224104563CT7GENIChomozygous890588174
142410471624104717CT17GENIChomozygous890588173
142410474024104741AG4GENIChomozygous890588172
142410961224109613AG28GENIChomozygous890588171
142410964024109641GA21GENIChomozygous890588170
142410982124109822CA16GENIChomozygous890588169
142410989224109893CA19GENIChomozygous890588168
142410998824109989CG11GENIChomozygous890588167
142411021224110213CT6GENIChomozygous890588166
142411603624116037CA11GENIChomozygous890588164
142411608824116089GC18GENIChomozygous890588163
142411653524116536AG15GENIChomozygous890588162
142411704324117044TG9GENIChomozygous890588161
142411943624119437AT15GENIChomozygous890588160
142411988624119887CT21GENIChomozygous890588159
142412028424120285CT4GENIChomozygous890588158
142412123524121236CT11GENIChomozygous890588157
142412148524121486CT20GENIChomozygous890588156
142412186724121868TA20GENIChomozygous890588155
142412329024123291CA16GENIChomozygous890588154
142412331124123312CG19GENIChomozygous890588153
142412388924123890CG14GENIChomozygous890588152
142412462624124627TC19GENIChomozygous890588151
142412524024125241AG18GENIChomozygous890588150