| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:89525397-89525665 | Common:1; Rare:64 | ||||
| chr12:89525995-89526231 | Rare:75 | ||||
| chr12:89708793-89709099 | Common:1; Rare:118 | ||||
| chr12:91111396-91111538 | Common:3; Rare:40 | ||||
| chr12:91111542-91111727 | Common:2; Rare:31 | ||||
| chr12:92145822-92146077 | Common:2; Rare:82 | ||||
| chr12:93377728-93377929 | Rare:54 | ||||
| chr12:93441855-93442271 | Common:6; Rare:146 | ||||
| chr12:93571761-93571902 | Common:6; Rare:57 | ||||
| chr12:93677322-93677390 | Rare:12 | ||||
| chr12:94459798-94460077 | Common:3; Rare:81 | ||||
| chr12:95003241-95003394 | Common:1; Rare:37 | ||||
| chr12:95003593-95003829 | Common:3; Rare:98; Clinvar (benign):6 | ||||
| chr12:95217378-95217746 | Common:4; Rare:100 | ||||
| chr12:96400556-96400689 | Rare:63 |