| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:31631353-31631791 | Common:3; Rare:137 | ||||
| chr12:32039432-32040590 | Common:22; Rare:207 | ||||
| chr12:32054345-32054745 | Common:7; Rare:120 | ||||
| chr12:32107865-32108265 | Common:2; Rare:97 | ||||
| chr12:32456817-32456994 | Rare:51 | ||||
| chr12:32502757-32503157 | Rare:133 | ||||
| chr12:32561937-32562337 | Common:1; Rare:122 | ||||
| chr12:32785626-32786026 | Common:6; Rare:178 | ||||
| chr12:33265020-33265600 | Common:6; Rare:118 | ||||
| chr12:33383516-33383916 | Common:5; Rare:110 | ||||
| chr12:39064590-39065220 | Common:6; Rare:117 | ||||
| chr12:39394063-39394181 | Common:1; Rare:17 | ||||
| chr12:39443980-39444192 | Common:1; Rare:29 | ||||
| chr12:40310308-40310572 | Rare:71; Clinvar:6; Clinvar (pathogenic):2 | ||||
| chr12:40474689-40475184 | Common:6; Rare:186 |