| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:69332767-69332851 | Rare:25 | ||||
| chr5:69369204-69369278 | Common:4; Rare:24 | ||||
| chr5:69369444-69369877 | Common:1; Rare:183 | ||||
| chr5:69560020-69560280 | Common:2; Rare:67 | ||||
| chr5:71455573-71455697 | Rare:36 | ||||
| chr5:71587192-71587426 | Common:1; Rare:74; Clinvar (benign):2 | ||||
| chr5:72816524-72816706 | Common:3; Rare:67 | ||||
| chr5:72847976-72848258 | Common:3; Rare:83 | ||||
| chr5:72955834-72956085 | Common:1; Rare:113 | ||||
| chr5:73446701-73446803 | Common:1; Rare:22 | ||||
| chr5:73448732-73448889 | Rare:36 | ||||
| chr5:73498288-73499080 | Common:4; Rare:239 | ||||
| chr5:73565352-73565418 | Rare:17 | ||||
| chr5:73565420-73565826 | Common:7; Rare:129 | ||||
| chr5:73625892-73626251 | Common:4; Rare:91 |