| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:146160996-146161302 | Common:1; Rare:101; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:146544545-146544827 | Common:4; Rare:66 | ||||
| chr3:149086478-149086720 | Rare:70 | ||||
| chr3:149129466-149129676 | Common:2; Rare:86; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:149377529-149377835 | Common:1; Rare:78 | ||||
| chr3:149812575-149812758 | Common:1; Rare:51 | ||||
| chr3:149813067-149813260 | Common:1; Rare:65 | ||||
| chr3:150603206-150603389 | Common:2; Rare:75 | ||||
| chr3:152268721-152268965 | Rare:97 | ||||
| chr3:152269443-152269678 | Rare:76 | ||||
| chr3:154324430-154324562 | Rare:50 | ||||
| chr3:155870361-155870711 | Common:1; Rare:103 | ||||
| chr3:156674373-156674647 | Common:3; Rare:78 | ||||
| chr3:157160099-157160328 | Rare:97 | ||||
| chr3:158672549-158672919 | Common:4; Rare:83 |