| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:964124-964254 | Common:1; Rare:18 | ||||
| chr5:997286-997612 | Common:2; Rare:63 | ||||
| chr5:1060366-1060657 | Common:5; Rare:83 | ||||
| chr5:1633921-1634062 | Common:2; Rare:49 | ||||
| chr5:1930935-1931209 | Common:3; Rare:71 | ||||
| chr5:6611753-6611997 | Common:5; Rare:62; Clinvar:2 | ||||
| chr5:8457531-8457765 | Common:2; Rare:87 | ||||
| chr5:10260570-10260852 | Common:2; Rare:52; Clinvar:2 | ||||
| chr5:10725254-10725305 | Rare:8 | ||||
| chr5:14011730-14011888 | Common:2; Rare:54 | ||||
| chr5:14145267-14145461 | Common:1; Rare:48 | ||||
| chr5:14186252-14186277 | Common:1; Rare:3 | ||||
| chr5:14207487-14207600 | Common:1; Rare:20 | ||||
| chr5:14358013-14358322 | Common:3; Rare:86 | ||||
| chr5:14713559-14713786 | Rare:60; Clinvar (benign):1 |