| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:49463174-49463434 | Common:1; Rare:75; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52284670-52284943 | Common:2; Rare:103 | ||||
| chr6:52995267-52995774 | Common:4; Rare:202 | ||||
| chr6:53065391-53065598 | Rare:67 | ||||
| chr6:53348878-53349085 | Common:2; Rare:89 | ||||
| chr6:53349146-53349222 | Rare:20 | ||||
| chr6:57046459-57046750 | Rare:104 | ||||
| chr6:57172240-57172777 | Common:1; Rare:155 | ||||
| chr6:57222266-57222376 | Rare:44 | ||||
| chr6:57317568-57317647 | Rare:22 | ||||
| chr6:70413147-70413448 | Common:1; Rare:93 | ||||
| chr6:73521193-73521407 | Rare:39 | ||||
| chr6:73521555-73521643 | Rare:23 | ||||
| chr6:73696095-73696218 | Rare:24 | ||||
| chr6:75284637-75285022 | Common:1; Rare:120 |