| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:142012960-142013129 | Rare:54 | ||||
| chr5:142324979-142325236 | Rare:86 | ||||
| chr5:143404442-143404617 | Common:2; Rare:36 | ||||
| chr5:144170539-144170853 | Common:2; Rare:99 | ||||
| chr5:146182499-146182848 | Common:3; Rare:94 | ||||
| chr5:147234866-147235125 | Common:2; Rare:71 | ||||
| chr5:147782692-147782918 | Common:1; Rare:51 | ||||
| chr5:148383763-148384018 | Rare:71 | ||||
| chr5:149141400-149141851 | Common:1; Rare:110 | ||||
| chr5:149271664-149271926 | Common:2; Rare:88 | ||||
| chr5:149345332-149345559 | Common:1; Rare:81 | ||||
| chr5:149550906-149551096 | Rare:49 | ||||
| chr5:149551356-149551631 | Rare:65 | ||||
| chr5:149960575-149960863 | Rare:107; Clinvar:7 | ||||
| chr5:150055275-150055587 | Common:2; Rare:62; Clinvar (pathogenic):2 |