| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:92145843-92146144 | Common:1; Rare:87 | ||||
| chr12:93441880-93442178 | Common:2; Rare:96 | ||||
| chr12:93467432-93467531 | Common:1; Rare:31 | ||||
| chr12:93677287-93677381 | Rare:18 | ||||
| chr12:94459833-94460021 | Common:2; Rare:54 | ||||
| chr12:95003605-95003827 | Common:3; Rare:91; Clinvar (benign):6 | ||||
| chr12:95217384-95217746 | Common:4; Rare:99 | ||||
| chr12:95473863-95474330 | Common:3; Rare:177 | ||||
| chr12:96907180-96907285 | Rare:40 | ||||
| chr12:98515428-98515653 | Rare:77; Clinvar:1 | ||||
| chr12:98644974-98645305 | Common:2; Rare:98 | ||||
| chr12:100267060-100267246 | Common:1; Rare:94 | ||||
| chr12:101407738-101408045 | Common:2; Rare:76 | ||||
| chr12:102061958-102062215 | Rare:69 | ||||
| chr12:102120058-102120257 | Rare:79 |