| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:52787823-52787987 | Common:1; Rare:31 | ||||
| chr5:52788024-52788426 | Common:1; Rare:100 | ||||
| chr5:52989201-52989369 | Common:4; Rare:46; Clinvar (benign):1 | ||||
| chr5:53109705-53109921 | Common:1; Rare:108; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr5:54310498-54310711 | Rare:67 | ||||
| chr5:55307625-55308049 | Common:5; Rare:152 | ||||
| chr5:55534611-55534840 | Common:3; Rare:72 | ||||
| chr5:55534956-55535179 | Common:1; Rare:77 | ||||
| chr5:55994782-55995196 | Common:1; Rare:137 | ||||
| chr5:57173548-57173903 | Common:2; Rare:128 | ||||
| chr5:58460052-58460200 | Common:4; Rare:60 | ||||
| chr5:59275568-59275631 | Rare:7 | ||||
| chr5:59275805-59275872 | Rare:10 | ||||
| chr5:59276006-59276176 | Common:4; Rare:24 | ||||
| chr5:59768513-59768740 | Rare:56 |