| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:89525397-89525565 | Common:1; Rare:58 | ||||
| chr12:89525869-89526072 | Common:2; Rare:120 | ||||
| chr12:89708783-89709003 | Rare:169 | ||||
| chr12:89709288-89709804 | Common:3; Rare:328 | ||||
| chr12:92145616-92146400 | Common:8; Rare:370 | ||||
| chr12:92929121-92929566 | Common:4; Rare:248 | ||||
| chr12:93377688-93377997 | Rare:175 | ||||
| chr12:93441866-93442154 | Common:4; Rare:175 | ||||
| chr12:93677238-93677493 | Rare:79 | ||||
| chr12:94149199-94149535 | Common:1; Rare:79 | ||||
| chr12:94459823-94460062 | Common:4; Rare:125 | ||||
| chr12:95003651-95003839 | Common:6; Rare:137; Clinvar (benign):6 | ||||
| chr12:95072830-95073189 | Common:4; Rare:173 | ||||
| chr12:95073419-95073749 | Common:3; Rare:185 | ||||
| chr12:95217347-95217860 | Common:10; Rare:258 |