| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:89525405-89525721 | Common:1; Rare:78 | ||||
| chr12:89525969-89526132 | Rare:60 | ||||
| chr12:89708795-89708934 | Rare:56 | ||||
| chr12:92145815-92146217 | Common:3; Rare:132 | ||||
| chr12:92929069-92929665 | Common:3; Rare:172 | ||||
| chr12:93377727-93377929 | Rare:54 | ||||
| chr12:93441885-93442178 | Common:2; Rare:95 | ||||
| chr12:93467397-93467549 | Common:1; Rare:53 | ||||
| chr12:93570959-93571092 | Rare:36 | ||||
| chr12:93571738-93571912 | Common:7; Rare:67 | ||||
| chr12:94459812-94460025 | Common:3; Rare:58 | ||||
| chr12:95003605-95003816 | Common:3; Rare:88; Clinvar (benign):6 | ||||
| chr12:95073457-95073918 | Common:3; Rare:120 | ||||
| chr12:95217388-95217889 | Common:4; Rare:135 | ||||
| chr12:95474061-95474323 | Common:2; Rare:111 |