| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:88142066-88142368 | Rare:83; Clinvar:3 | ||||
| chr12:88580466-88580556 | Common:1; Rare:27 | ||||
| chr12:89352495-89352711 | Rare:61 | ||||
| chr12:89524757-89524869 | Common:1; Rare:21 | ||||
| chr12:89709296-89709409 | Common:2; Rare:54 | ||||
| chr12:92929290-92929537 | Rare:67 | ||||
| chr12:93377635-93377929 | Rare:90 | ||||
| chr12:93441880-93442178 | Common:2; Rare:96 | ||||
| chr12:93571755-93571890 | Common:6; Rare:51 | ||||
| chr12:94459859-94460003 | Common:2; Rare:40 | ||||
| chr12:95003670-95003830 | Common:3; Rare:60; Clinvar (benign):3 | ||||
| chr12:95217384-95217746 | Common:4; Rare:99 | ||||
| chr12:95473976-95474247 | Common:2; Rare:125 | ||||
| chr12:96907164-96907268 | Common:1; Rare:32 | ||||
| chr12:98515368-98515647 | Common:1; Rare:95; Clinvar:1 |