| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:12717284-12717401 | Rare:35 | ||||
| chr12:12725642-12726037 | Common:4; Rare:95 | ||||
| chr12:12891291-12891569 | Common:1; Rare:55 | ||||
| chr12:13000204-13000465 | Common:2; Rare:89 | ||||
| chr12:13197159-13197466 | Common:1; Rare:55 | ||||
| chr12:14365460-14365703 | Common:1; Rare:76 | ||||
| chr12:14774113-14774507 | Common:3; Rare:103 | ||||
| chr12:14774534-14774694 | Rare:65 | ||||
| chr12:14803354-14803699 | Common:3; Rare:95 | ||||
| chr12:14885734-14885909 | Common:3; Rare:40; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:14961251-14961426 | Common:1; Rare:31 | ||||
| chr12:15789308-15789547 | Common:1; Rare:85 | ||||
| chr12:15882298-15882818 | Common:1; Rare:163 | ||||
| chr12:15911236-15911408 | Common:5; Rare:70 | ||||
| chr12:19439338-19439816 | Common:3; Rare:177 |