chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3122194745122194746CT21GENIChomozygous111690175
3122195519122195520AG44GENICpossibly homozygous111690176
3122195603122195604AG42GENIChomozygous111690177
3122196249122196250TG36GENIChomozygous111690178
3122196479122196480CT26GENIChomozygous111690179
3122197178122197179GA45GENIChomozygous111690180
3122197578122197579TC59GENIChomozygous111690181
3122197583122197584TC61GENIChomozygous111690182
3122198210122198211GA45GENIChomozygous111690183
3122198281122198282AG34GENIChomozygous111690184
3122199905122199906CT33GENIChomozygous111690185
3122201835122201836AG28GENIChomozygous111690186
3122202770122202771TC24GENIChomozygous111690187
3122204686122204687GA35GENIChomozygous111690188
3122205150122205151CT95GENIChomozygous111690189
3122205159122205160CG97GENIChomozygous111690190
3122205402122205403GC39GENIChomozygous119651398
3122205452122205453AG37GENIChomozygous111690191
3122205933122205934CG17GENIChomozygous111690192
3122206279122206280AG38GENIChomozygous111690193