| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:32390975-32391201 | Common:2; Rare:65 | ||||
| chr12:32398675-32398951 | Common:1; Rare:50 | ||||
| chr12:32437017-32437330 | Rare:37 | ||||
| chr12:32446422-32446693 | Rare:50 | ||||
| chr12:32755162-32755242 | Rare:25; Clinvar (pathogenic):1 | ||||
| chr12:32892047-32892295 | Rare:41 | ||||
| chr12:32893222-32893268 | Rare:7 | ||||
| chr12:32893584-32893854 | Common:1; Rare:44 | ||||
| chr12:32895775-32895975 | Common:1; Rare:43 | ||||
| chr12:32898040-32898179 | Common:1; Rare:28 | ||||
| chr12:32983403-32983723 | Common:1; Rare:63 | ||||
| chr12:32984109-32984324 | Common:2; Rare:53 | ||||
| chr12:32989114-32989224 | Common:1; Rare:24 | ||||
| chr12:38138784-38138993 | Common:2; Rare:59 | ||||
| chr12:38892137-38892466 | Common:1; Rare:54 |