| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:149960575-149960915 | Rare:114; Clinvar:7 | ||||
| chr5:150055290-150055552 | Common:2; Rare:54; Clinvar (pathogenic):1 | ||||
| chr5:150125987-150126281 | Common:2; Rare:43 | ||||
| chr5:150155268-150155370 | Common:1; Rare:14 | ||||
| chr5:150155475-150155902 | Common:1; Rare:100 | ||||
| chr5:150640553-150640800 | Rare:49 | ||||
| chr5:151026673-151027035 | Common:2; Rare:98 | ||||
| chr5:151036862-151037047 | Rare:44 | ||||
| chr5:151080954-151081174 | Common:1; Rare:71 | ||||
| chr5:151224046-151224149 | Common:2; Rare:31 | ||||
| chr5:151685183-151685267 | Common:1; Rare:14 | ||||
| chr5:151686627-151686846 | Rare:34 | ||||
| chr5:151686865-151687076 | Common:1; Rare:47 | ||||
| chr5:154038407-154038515 | Rare:21 | ||||
| chr5:154038882-154039015 | Common:1; Rare:47 |