| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:141637323-141637468 | Common:1; Rare:33 | ||||
| chr5:141923632-141923904 | Common:1; Rare:81 | ||||
| chr5:141958167-141958303 | Rare:29 | ||||
| chr5:142012986-142013100 | Rare:37 | ||||
| chr5:142324965-142325190 | Rare:85 | ||||
| chr5:144170546-144170807 | Common:1; Rare:88 | ||||
| chr5:146182501-146182857 | Common:3; Rare:98 | ||||
| chr5:146878132-146878268 | Rare:41 | ||||
| chr5:146878692-146878764 | Common:1; Rare:20; Clinvar (benign):1 | ||||
| chr5:147055902-147056019 | Common:1; Rare:18 | ||||
| chr5:147234866-147235090 | Common:2; Rare:60 | ||||
| chr5:147509500-147509768 | Rare:91 | ||||
| chr5:147509930-147510263 | Common:1; Rare:60 | ||||
| chr5:147782629-147782934 | Common:4; Rare:68 | ||||
| chr5:148383777-148384021 | Rare:72 |