| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:52787823-52787957 | Common:1; Rare:23 | ||||
| chr5:52989218-52989408 | Common:4; Rare:50; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:53109711-53109913 | Common:1; Rare:104; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr5:54310513-54310711 | Rare:63 | ||||
| chr5:55307625-55308016 | Common:4; Rare:132 | ||||
| chr5:55994797-55995194 | Rare:135 | ||||
| chr5:56909800-56910081 | Common:3; Rare:71 | ||||
| chr5:57173548-57174141 | Common:2; Rare:204 | ||||
| chr5:57482800-57483082 | Rare:53 | ||||
| chr5:58460038-58460196 | Common:5; Rare:68 | ||||
| chr5:60700084-60700237 | Common:1; Rare:59 | ||||
| chr5:60945017-60945246 | Common:5; Rare:90; Clinvar:3; Clinvar (benign):5 | ||||
| chr5:61162338-61162637 | Common:1; Rare:77 | ||||
| chr5:62306367-62306485 | Rare:33; Clinvar (benign):2 | ||||
| chr5:62403507-62403516 |