| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:150733525-150733573 | Rare:4 | ||||
| chr3:150736578-150736805 | Common:2; Rare:44 | ||||
| chr3:150740813-150741114 | Common:2; Rare:57 | ||||
| chr3:150761887-150761937 | Common:1; Rare:6 | ||||
| chr3:151770259-151770464 | Common:3; Rare:27 | ||||
| chr3:152349876-152349992 | Common:1; Rare:22 | ||||
| chr3:154140068-154140275 | Common:1; Rare:43 | ||||
| chr3:155890965-155891096 | Rare:20 | ||||
| chr3:157174912-157175269 | Common:3; Rare:159 | ||||
| chr3:160424708-160425018 | Common:2; Rare:84 | ||||
| chr3:160432025-160432478 | Common:4; Rare:125 | ||||
| chr3:169765047-169765267 | Rare:83; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr3:182895881-182895967 | Common:2; Rare:16 | ||||
| chr3:182981143-182981352 | Rare:47 | ||||
| chr3:185418816-185419037 | Common:1; Rare:29 |