| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57604415-57604913 | Common:1; Rare:141 | ||||
| chr12:57605160-57605550 | Common:1; Rare:89 | ||||
| chr12:57614972-57615150 | Common:1; Rare:42 | ||||
| chr12:57632490-57632960 | Common:2; Rare:128 | ||||
| chr12:57633064-57633400 | Common:1; Rare:137 | ||||
| chr12:57693842-57694248 | Common:2; Rare:206 | ||||
| chr12:57694312-57694877 | Rare:159 | ||||
| chr12:57741960-57742400 | Rare:156 | ||||
| chr12:57744753-57745128 | Common:3; Rare:229 | ||||
| chr12:57745224-57745486 | Common:4; Rare:93 | ||||
| chr12:57751539-57752801 | Common:5; Rare:660; Clinvar:20; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr12:57754811-57755172 | Common:6; Rare:233 | ||||
| chr12:57755810-57756267 | Common:2; Rare:160 | ||||
| chr12:57765417-57765609 | Common:1; Rare:79; Clinvar:1 | ||||
| chr12:57770125-57770297 | Rare:26 |