| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:33425591-33426177 | Common:2; Rare:133; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:33508391-33508587 | Common:3; Rare:39 | ||||
| chr6:33571070-33571143 | Common:1; Rare:14 | ||||
| chr6:33571292-33571537 | Rare:58 | ||||
| chr6:33585670-33585886 | Common:3; Rare:55 | ||||
| chr6:33585888-33586064 | Common:2; Rare:27 | ||||
| chr6:33633609-33633911 | Common:6; Rare:86 | ||||
| chr6:33904461-33904768 | Common:2; Rare:51 | ||||
| chr6:34182944-34183106 | Rare:21 | ||||
| chr6:34223962-34224346 | Common:5; Rare:112 | ||||
| chr6:34235740-34235810 | Common:1; Rare:23 | ||||
| chr6:34235872-34236010 | Common:1; Rare:55 | ||||
| chr6:34288739-34288790 | Rare:16 | ||||
| chr6:34317185-34317243 | Rare:11 | ||||
| chr6:34319232-34319288 | Rare:9 |