| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:55534822-55534894 | Rare:7 | ||||
| chr5:55534944-55535189 | Common:1; Rare:82 | ||||
| chr5:55994807-55995163 | Rare:118 | ||||
| chr5:56909476-56909652 | Common:2; Rare:51 | ||||
| chr5:56952085-56952400 | Rare:116 | ||||
| chr5:56952446-56952619 | Common:2; Rare:48 | ||||
| chr5:57173528-57174125 | Common:3; Rare:213 | ||||
| chr5:58460030-58460192 | Common:4; Rare:68 | ||||
| chr5:59768111-59768331 | Rare:56 | ||||
| chr5:59768513-59768723 | Rare:52 | ||||
| chr5:60488061-60488197 | Rare:23 | ||||
| chr5:60700091-60700226 | Common:1; Rare:53 | ||||
| chr5:60844175-60844440 | Common:5; Rare:89 | ||||
| chr5:60945026-60945263 | Common:5; Rare:90; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr5:61162328-61162701 | Common:1; Rare:89 |