Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:36129223-36129479 | Common:4; Rare:78 | ||||
chr18:36129772-36129943 | Common:1; Rare:71 | ||||
chr18:36187408-36187525 | Common:2; Rare:44 | ||||
chr18:36828748-36829148 | Common:3; Rare:148 | ||||
chr18:46104135-46104408 | Common:4; Rare:80; Clinvar (benign):1 | ||||
chr18:49813835-49814147 | Common:1; Rare:131 | ||||
chr18:50878984-50879223 | Common:4; Rare:78 | ||||
chr18:54269443-54269617 | Common:2; Rare:85 | ||||
chr18:54357860-54357961 | Common:4; Rare:29 | ||||
chr18:55589809-55589992 | Common:2; Rare:67 | ||||
chr18:56651231-56651371 | Common:2; Rare:31 | ||||
chr18:62186985-62187320 | Common:5; Rare:95 | ||||
chr18:63367138-63367326 | Common:1; Rare:68 | ||||
chr18:63422353-63422638 | Common:1; Rare:78 | ||||
chr18:68714981-68715254 | Common:5; Rare:123 |