| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:68216427-68216624 | Rare:41 | ||||
| chr5:68273949-68274020 | Rare:25 | ||||
| chr5:68275284-68275327 | Rare:10 | ||||
| chr5:68406978-68407125 | Rare:26 | ||||
| chr5:68443210-68443336 | Rare:17 | ||||
| chr5:69042722-69043078 | Common:1; Rare:62 | ||||
| chr5:69043239-69043311 | Common:1; Rare:13 | ||||
| chr5:69432982-69433023 | Rare:8; Clinvar (benign):1 | ||||
| chr5:70401358-70401517 | Common:2; Rare:12 | ||||
| chr5:71587830-71588017 | Rare:27 | ||||
| chr5:72108192-72108367 | Rare:41 | ||||
| chr5:72108906-72109141 | Rare:52 | ||||
| chr5:72301625-72301865 | Rare:41 | ||||
| chr5:72304734-72304767 | Rare:5 | ||||
| chr5:72452066-72452168 | Common:2; Rare:20 |