| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:141418564-141418728 | Rare:51 | ||||
| chr5:141935982-141936088 | Common:1; Rare:23 | ||||
| chr5:142769766-142769878 | Rare:23 | ||||
| chr5:142770944-142771235 | Common:1; Rare:75 | ||||
| chr5:143167343-143167668 | Common:8; Rare:49 | ||||
| chr5:146482759-146482840 | Rare:24 | ||||
| chr5:147452035-147452247 | Rare:32 | ||||
| chr5:147459618-147459729 | Rare:23 | ||||
| chr5:148438439-148438542 | Common:1; Rare:29; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:149466709-149466895 | Common:3; Rare:35 | ||||
| chr5:149549444-149549675 | Rare:49 | ||||
| chr5:150778660-150778954 | Common:2; Rare:101 | ||||
| chr5:151674418-151674614 | Common:3; Rare:47 | ||||
| chr5:151790169-151790362 | Common:2; Rare:44 | ||||
| chr5:157312144-157312263 | Rare:17 |