| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:15855140-15855479 | Common:2; Rare:53 | ||||
| chr5:15902108-15902275 | Rare:28 | ||||
| chr5:16465145-16465271 | Rare:39 | ||||
| chr5:23951276-23951380 | Rare:49 | ||||
| chr5:25199030-25199214 | Common:1; Rare:44 | ||||
| chr5:32067407-32067663 | Common:4; Rare:52 | ||||
| chr5:34244735-34244889 | Rare:41 | ||||
| chr5:34918104-34918409 | Common:2; Rare:55 | ||||
| chr5:36875669-36876039 | Rare:87 | ||||
| chr5:37057083-37057329 | Rare:47; Clinvar (pathogenic):3 | ||||
| chr5:37304748-37304957 | Rare:49 | ||||
| chr5:38493734-38494107 | Common:3; Rare:75; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:38607676-38607722 | Common:1; Rare:13 | ||||
| chr5:38988646-38988744 | Rare:23 | ||||
| chr5:39072947-39073185 | Rare:46 |