| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:89526022-89526052 | Rare:11 | ||||
| chr12:93377728-93377929 | Rare:54 | ||||
| chr12:93441880-93442193 | Common:2; Rare:100 | ||||
| chr12:94459832-94459992 | Common:2; Rare:45 | ||||
| chr12:94615991-94616166 | Rare:34 | ||||
| chr12:95003593-95003814 | Common:3; Rare:93; Clinvar (benign):6 | ||||
| chr12:95217367-95217769 | Common:5; Rare:109 | ||||
| chr12:95473997-95474218 | Common:2; Rare:105 | ||||
| chr12:96035380-96035470 | Common:1; Rare:22 | ||||
| chr12:96907185-96907295 | Rare:41 | ||||
| chr12:98515332-98515784 | Common:1; Rare:150; Clinvar:2 | ||||
| chr12:98593469-98593770 | Common:2; Rare:99; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:98644697-98644844 | Common:3; Rare:49 | ||||
| chr12:98644990-98645327 | Common:2; Rare:99 | ||||
| chr12:100267047-100267326 | Common:1; Rare:120 |