| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:43515111-43515247 | Common:2; Rare:59 | ||||
| chr5:43556855-43556928 | Common:3; Rare:31 | ||||
| chr5:43603058-43603266 | Rare:54 | ||||
| chr5:44808761-44808965 | Common:2; Rare:64 | ||||
| chr5:52989216-52989406 | Common:4; Rare:50; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:53109725-53109899 | Common:1; Rare:89; Clinvar:2 | ||||
| chr5:54310549-54310711 | Rare:45 | ||||
| chr5:55160058-55160214 | Rare:39 | ||||
| chr5:55307627-55308061 | Common:5; Rare:156 | ||||
| chr5:55994879-55995152 | Rare:94 | ||||
| chr5:58460063-58460246 | Common:4; Rare:72 | ||||
| chr5:59768487-59768664 | Rare:43 | ||||
| chr5:60700067-60700226 | Common:1; Rare:64 | ||||
| chr5:60945028-60945245 | Common:5; Rare:84; Clinvar:3; Clinvar (benign):5 | ||||
| chr5:61162338-61162644 | Common:1; Rare:79 |