| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:55307906-55308146 | Common:2; Rare:102 | ||||
| chr5:55534962-55535172 | Common:1; Rare:72 | ||||
| chr5:55994898-55995204 | Rare:116 | ||||
| chr5:56909458-56909652 | Common:3; Rare:55 | ||||
| chr5:56909864-56910109 | Rare:65 | ||||
| chr5:56952098-56952419 | Rare:118 | ||||
| chr5:57173539-57174158 | Common:3; Rare:217 | ||||
| chr5:58459881-58460264 | Common:6; Rare:147 | ||||
| chr5:58581823-58582068 | Rare:35 | ||||
| chr5:58582114-58582407 | Common:1; Rare:55 | ||||
| chr5:58582908-58583218 | Common:2; Rare:81 | ||||
| chr5:58999850-59000113 | Rare:52 | ||||
| chr5:59039047-59039285 | Common:1; Rare:63; Clinvar (benign):1 | ||||
| chr5:59039300-59039414 | Common:1; Rare:27 | ||||
| chr5:59039423-59040011 | Common:6; Rare:151 |