| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:43515133-43515252 | Common:2; Rare:43 | ||||
| chr5:43603052-43603280 | Rare:58 | ||||
| chr5:44389696-44389955 | Common:1; Rare:54 | ||||
| chr5:44808711-44808965 | Common:2; Rare:81 | ||||
| chr5:50665625-50665933 | Common:1; Rare:39 | ||||
| chr5:50667456-50667570 | Rare:34 | ||||
| chr5:50667768-50667904 | Common:1; Rare:40 | ||||
| chr5:52989216-52989377 | Common:4; Rare:43; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:53109730-53109909 | Common:1; Rare:87; Clinvar:2 | ||||
| chr5:54310487-54310711 | Rare:69 | ||||
| chr5:55233606-55233882 | Common:4; Rare:99 | ||||
| chr5:55307620-55308055 | Common:5; Rare:157 | ||||
| chr5:55534956-55535211 | Common:1; Rare:86 | ||||
| chr5:55994839-55995199 | Rare:129 | ||||
| chr5:56909452-56909638 | Common:2; Rare:52 |