| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:197091-197332 | Common:3; Rare:82 | ||||
| chr3:197517-198061 | Common:8; Rare:199 | ||||
| chr3:2098643-2098962 | Common:4; Rare:126 | ||||
| chr3:3126784-3126984 | Common:4; Rare:83; Clinvar (benign):1 | ||||
| chr3:3799813-3799877 | Common:1; Rare:19 | ||||
| chr3:4303270-4303405 | Common:1; Rare:56 | ||||
| chr3:4493167-4493532 | Rare:124; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:6860967-6861129 | Common:1; Rare:31 | ||||
| chr3:6862658-6862791 | Common:3; Rare:47 | ||||
| chr3:8501638-8501854 | Rare:76 | ||||
| chr3:9249588-9249742 | Common:1; Rare:37 | ||||
| chr3:9362978-9363105 | Common:1; Rare:49 | ||||
| chr3:9397432-9397678 | Rare:83 | ||||
| chr3:9749839-9750046 | Common:1; Rare:68 | ||||
| chr3:9769881-9769948 | Rare:24 |