| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:197029800-197029928 | Common:1; Rare:39 | ||||
| chr3:197736854-197737133 | Common:3; Rare:85 | ||||
| chr3:197749742-197749962 | Common:1; Rare:81 | ||||
| chr3:197949882-197950275 | Common:4; Rare:117; Clinvar (benign):2 | ||||
| chr3:197959986-197960242 | Common:1; Rare:91 | ||||
| chr4:499141-499313 | Common:2; Rare:65 | ||||
| chr4:663657-663725 | Rare:19 | ||||
| chr4:673842-673910 | Rare:27 | ||||
| chr4:674243-674573 | Common:2; Rare:154 | ||||
| chr4:932290-932487 | Common:2; Rare:76 | ||||
| chr4:1289662-1289906 | Common:1; Rare:77 | ||||
| chr4:2041875-2042011 | Common:1; Rare:51 | ||||
| chr4:2468878-2469167 | Common:4; Rare:108 | ||||
| chr4:2843679-2844011 | Common:3; Rare:123 | ||||
| chr4:2934767-2934910 | Common:1; Rare:66 |