| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:43483837-43483959 | Common:1; Rare:43 | ||||
| chr5:43515072-43515247 | Common:2; Rare:68 | ||||
| chr5:43603087-43603260 | Rare:42 | ||||
| chr5:44808730-44808965 | Common:2; Rare:77 | ||||
| chr5:50441244-50441444 | Common:3; Rare:61 | ||||
| chr5:52989181-52989419 | Common:4; Rare:66; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:53109725-53109906 | Common:1; Rare:91; Clinvar:2 | ||||
| chr5:54310507-54310711 | Rare:65 | ||||
| chr5:55307611-55308016 | Common:4; Rare:139 | ||||
| chr5:57173548-57174125 | Common:2; Rare:198 | ||||
| chr5:58460038-58460220 | Common:5; Rare:73 | ||||
| chr5:59767948-59768085 | Rare:24 | ||||
| chr5:59768634-59768761 | Rare:37 | ||||
| chr5:60488061-60488214 | Rare:24 | ||||
| chr5:60700114-60700237 | Common:1; Rare:43 |