| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:93377728-93377972 | Rare:80 | ||||
| chr12:93441876-93442193 | Common:2; Rare:101 | ||||
| chr12:93570827-93571305 | Common:1; Rare:112 | ||||
| chr12:93571738-93571900 | Common:6; Rare:62 | ||||
| chr12:93677344-93677412 | Rare:15 | ||||
| chr12:94459831-94460043 | Common:2; Rare:61 | ||||
| chr12:94615928-94616179 | Rare:47 | ||||
| chr12:95003593-95003820 | Common:3; Rare:94; Clinvar (benign):6 | ||||
| chr12:95073443-95073647 | Common:1; Rare:77 | ||||
| chr12:95217299-95217843 | Common:6; Rare:145 | ||||
| chr12:95473966-95474203 | Common:2; Rare:104 | ||||
| chr12:95548796-95548918 | Common:2; Rare:44 | ||||
| chr12:96035527-96035679 | Common:2; Rare:33 | ||||
| chr12:96400411-96400707 | Common:1; Rare:125 | ||||
| chr12:98515430-98516081 | Rare:229; Clinvar:10; Clinvar (benign):5 |