| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:92145896-92146206 | Common:1; Rare:83 | ||||
| chr12:92929094-92929440 | Common:2; Rare:107 | ||||
| chr12:93377728-93377956 | Rare:74 | ||||
| chr12:93441856-93442147 | Common:2; Rare:92 | ||||
| chr12:93571726-93571872 | Common:6; Rare:52 | ||||
| chr12:93677271-93677399 | Rare:27 | ||||
| chr12:94459797-94460047 | Common:3; Rare:70 | ||||
| chr12:95003605-95003829 | Common:3; Rare:93; Clinvar (benign):6 | ||||
| chr12:95073416-95073720 | Common:2; Rare:98 | ||||
| chr12:95217377-95217869 | Common:4; Rare:132 | ||||
| chr12:95473913-95474210 | Common:3; Rare:121 | ||||
| chr12:96399371-96399476 | Common:1; Rare:31 | ||||
| chr12:96400494-96400707 | Common:1; Rare:96 | ||||
| chr12:96489428-96489669 | Common:3; Rare:69 | ||||
| chr12:96907180-96907295 | Rare:43 |