| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:89709433-89709845 | Common:2; Rare:218 | ||||
| chr12:92145799-92146089 | Common:4; Rare:101 | ||||
| chr12:92929073-92929587 | Common:3; Rare:246 | ||||
| chr12:93377728-93377932 | Rare:108 | ||||
| chr12:93441885-93442154 | Common:4; Rare:167 | ||||
| chr12:93570660-93571180 | Rare:209 | ||||
| chr12:93677212-93677511 | Common:2; Rare:99 | ||||
| chr12:94459751-94460073 | Common:5; Rare:157 | ||||
| chr12:95003665-95003839 | Common:6; Rare:129; Clinvar (benign):6 | ||||
| chr12:95072770-95073240 | Common:5; Rare:212 | ||||
| chr12:95073389-95073731 | Common:3; Rare:187 | ||||
| chr12:95217225-95217879 | Common:10; Rare:309 | ||||
| chr12:95218013-95218413 | Common:6; Rare:124 | ||||
| chr12:95473851-95474219 | Common:5; Rare:250 | ||||
| chr12:95790580-95791201 | Common:5; Rare:180 |