| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:51383118-51383448 | Common:4; Rare:119 | ||||
| chr5:52787885-52788403 | Common:1; Rare:127 | ||||
| chr5:53109710-53109926 | Common:1; Rare:107; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr5:54310507-54310711 | Rare:65 | ||||
| chr5:54518232-54518409 | Common:1; Rare:70 | ||||
| chr5:55307627-55308035 | Common:5; Rare:143 | ||||
| chr5:55534613-55534840 | Common:3; Rare:72 | ||||
| chr5:55534844-55535162 | Common:1; Rare:95 | ||||
| chr5:55994803-55995196 | Rare:135 | ||||
| chr5:56952101-56952310 | Rare:77 | ||||
| chr5:57173611-57173888 | Common:2; Rare:100 | ||||
| chr5:59039056-59039203 | Common:1; Rare:46; Clinvar (benign):1 | ||||
| chr5:59039365-59039657 | Common:2; Rare:63 | ||||
| chr5:59039750-59039994 | Common:2; Rare:69 | ||||
| chr5:59768077-59768223 | Rare:29 |