| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:43515111-43515306 | Common:3; Rare:80 | ||||
| chr5:43602542-43602741 | Common:2; Rare:38 | ||||
| chr5:43603086-43603277 | Rare:48 | ||||
| chr5:44808727-44808982 | Common:2; Rare:91 | ||||
| chr5:52787768-52787957 | Common:1; Rare:39 | ||||
| chr5:53109716-53109932 | Common:1; Rare:107; Clinvar:3 | ||||
| chr5:54310565-54310711 | Rare:42 | ||||
| chr5:55160090-55160212 | Rare:34 | ||||
| chr5:55307631-55308029 | Common:5; Rare:137 | ||||
| chr5:56909448-56909646 | Common:3; Rare:57 | ||||
| chr5:58460063-58460246 | Common:4; Rare:72 | ||||
| chr5:60700084-60700240 | Common:1; Rare:60 | ||||
| chr5:60945026-60945253 | Common:5; Rare:85; Clinvar:3; Clinvar (benign):5 | ||||
| chr5:61162350-61162568 | Common:1; Rare:57 | ||||
| chr5:62403870-62404060 | Common:3; Rare:62 |