| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:43515111-43515259 | Common:2; Rare:63 | ||||
| chr5:43602886-43603260 | Rare:91 | ||||
| chr5:44808727-44808965 | Common:2; Rare:78 | ||||
| chr5:50667776-50667924 | Common:1; Rare:49 | ||||
| chr5:52989157-52989409 | Common:4; Rare:68; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:53109734-53109889 | Common:1; Rare:74; Clinvar:2 | ||||
| chr5:54310535-54310711 | Rare:52 | ||||
| chr5:55307651-55308010 | Common:4; Rare:118 | ||||
| chr5:56909517-56909638 | Common:1; Rare:35 | ||||
| chr5:58460070-58460192 | Common:3; Rare:50 | ||||
| chr5:60700114-60700237 | Common:1; Rare:43 | ||||
| chr5:60945006-60945258 | Common:5; Rare:101; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr5:61162359-61162637 | Common:1; Rare:73 | ||||
| chr5:62412566-62412784 | Rare:71 | ||||
| chr5:64768553-64768978 | Common:5; Rare:113 |