| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:141876037-141876246 | Rare:60 | ||||
| chr3:141876491-141876729 | Common:2; Rare:87 | ||||
| chr3:142447964-142448110 | Common:1; Rare:51 | ||||
| chr3:142578690-142578916 | Rare:82; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:142888856-142889265 | Common:4; Rare:98 | ||||
| chr3:143001434-143001631 | Common:3; Rare:72 | ||||
| chr3:143971751-143971847 | Common:1; Rare:44 | ||||
| chr3:146160975-146161388 | Common:2; Rare:125; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:146250802-146250898 | Common:1; Rare:25 | ||||
| chr3:146250966-146251233 | Common:2; Rare:63 | ||||
| chr3:146544458-146544797 | Common:5; Rare:80 | ||||
| chr3:146544813-146544927 | Rare:28 | ||||
| chr3:148991383-148991647 | Common:2; Rare:117; Clinvar (benign):1 | ||||
| chr3:149129549-149129711 | Common:1; Rare:68; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149377495-149377822 | Common:1; Rare:90 |