| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53299814-53299855 | Rare:20 | ||||
| chr12:53321226-53321415 | Common:1; Rare:67; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr12:53321486-53321638 | Common:1; Rare:50; Clinvar:3 | ||||
| chr12:53441454-53441775 | Common:1; Rare:90 | ||||
| chr12:53451809-53451924 | Rare:19 | ||||
| chr12:53452038-53452369 | Rare:83 | ||||
| chr12:53492972-53493251 | Common:3; Rare:72 | ||||
| chr12:53499436-53499536 | Rare:24 | ||||
| chr12:53501177-53501375 | Rare:45 | ||||
| chr12:53501514-53501633 | Rare:32 | ||||
| chr12:53625942-53626179 | Common:1; Rare:59 | ||||
| chr12:53626343-53626602 | Common:3; Rare:54 | ||||
| chr12:53676014-53676404 | Common:8; Rare:180 | ||||
| chr12:53727424-53727719 | Rare:65 | ||||
| chr12:54053641-54053885 | Rare:38 |