| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:89526022-89526038 | Rare:6 | ||||
| chr12:89708824-89709099 | Common:1; Rare:107 | ||||
| chr12:92145797-92146215 | Common:4; Rare:143 | ||||
| chr12:93377709-93377950 | Rare:78 | ||||
| chr12:93467440-93467554 | Common:1; Rare:35 | ||||
| chr12:93571722-93571912 | Common:7; Rare:72 | ||||
| chr12:94459809-94460062 | Common:3; Rare:72 | ||||
| chr12:95003593-95003831 | Common:3; Rare:99; Clinvar (benign):6 | ||||
| chr12:95217377-95217774 | Common:4; Rare:111 | ||||
| chr12:95218113-95218276 | Common:2; Rare:44 | ||||
| chr12:95473997-95474210 | Common:2; Rare:99 | ||||
| chr12:95791128-95791276 | Rare:22 | ||||
| chr12:95858797-95859076 | Common:3; Rare:83 | ||||
| chr12:96035387-96035786 | Common:3; Rare:102 | ||||
| chr12:96907195-96907466 | Common:1; Rare:90 |