| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:93571746-93571902 | Common:6; Rare:61 | ||||
| chr12:94459814-94459955 | Common:1; Rare:38 | ||||
| chr12:95003615-95003833 | Common:3; Rare:89; Clinvar (benign):5 | ||||
| chr12:95217384-95217746 | Common:4; Rare:99 | ||||
| chr12:95474030-95474203 | Common:2; Rare:83 | ||||
| chr12:95858822-95859061 | Common:3; Rare:71 | ||||
| chr12:96035527-96035739 | Common:2; Rare:45 | ||||
| chr12:96907190-96907268 | Rare:26 | ||||
| chr12:98515470-98515870 | Rare:142; Clinvar:5; Clinvar (benign):1 | ||||
| chr12:98593484-98593793 | Common:2; Rare:102; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:98644705-98645293 | Common:7; Rare:172 | ||||
| chr12:100200674-100200876 | Common:1; Rare:68 | ||||
| chr12:100267065-100267383 | Common:1; Rare:129 | ||||
| chr12:100794805-100794880 | Rare:16 | ||||
| chr12:101280044-101280179 | Common:1; Rare:43 |