| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6534616-6534872 | Common:3; Rare:103 | ||||
| chr12:6548788-6548920 | Rare:53 | ||||
| chr12:6568205-6568388 | Common:1; Rare:65 | ||||
| chr12:6606308-6606556 | Common:3; Rare:107 | ||||
| chr12:6688879-6689060 | Rare:58 | ||||
| chr12:6689222-6689742 | Common:3; Rare:140 | ||||
| chr12:6723844-6724172 | Common:1; Rare:70 | ||||
| chr12:6752932-6753191 | Common:6; Rare:79 | ||||
| chr12:6766165-6766360 | Common:1; Rare:42 | ||||
| chr12:6766442-6766748 | Rare:82 | ||||
| chr12:6821542-6821883 | Common:3; Rare:85 | ||||
| chr12:6851269-6851492 | Rare:47 | ||||
| chr12:6851902-6852179 | Rare:73 | ||||
| chr12:6867365-6867602 | Common:2; Rare:118; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6868884-6869387 | Rare:160; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):3 |