| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52154376-52154521 | Common:1; Rare:38 | ||||
| chr3:52198019-52198169 | Rare:67 | ||||
| chr3:52230978-52231225 | Common:1; Rare:66 | ||||
| chr3:52239058-52239296 | Common:2; Rare:79 | ||||
| chr3:52278625-52278801 | Rare:63 | ||||
| chr3:52287755-52287859 | Common:2; Rare:44 | ||||
| chr3:52288012-52288093 | Rare:26 | ||||
| chr3:52410459-52410687 | Rare:55 | ||||
| chr3:52455455-52455638 | Common:2; Rare:63 | ||||
| chr3:52685544-52685654 | Rare:33 | ||||
| chr3:52685944-52686090 | Common:2; Rare:61 | ||||
| chr3:52705569-52706300 | Common:4; Rare:237 | ||||
| chr3:52770913-52771025 | Common:2; Rare:26 | ||||
| chr3:53130387-53130568 | Common:1; Rare:64; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:53347518-53347734 | Common:1; Rare:68 |