| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53006096-53006499 | Common:4; Rare:148 | ||||
| chr12:53006885-53007040 | Rare:39 | ||||
| chr12:53079347-53079537 | Common:2; Rare:66 | ||||
| chr12:53097359-53097690 | Rare:68 | ||||
| chr12:53180549-53180750 | Common:2; Rare:83 | ||||
| chr12:53232179-53232422 | Common:2; Rare:54 | ||||
| chr12:53252016-53252255 | Common:3; Rare:85 | ||||
| chr12:53299314-53299855 | Common:4; Rare:199 | ||||
| chr12:53321236-53321456 | Common:1; Rare:83; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr12:53380114-53380275 | Common:3; Rare:70 | ||||
| chr12:53381183-53381256 | Rare:20 | ||||
| chr12:53441471-53441777 | Common:1; Rare:84 | ||||
| chr12:53451808-53452194 | Rare:98 | ||||
| chr12:53452258-53452374 | Rare:20 | ||||
| chr12:53467800-53468139 | Common:1; Rare:80 |