| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52278625-52278777 | Rare:54 | ||||
| chr3:52287727-52287859 | Common:2; Rare:49 | ||||
| chr3:52455427-52455733 | Common:2; Rare:100 | ||||
| chr3:52495247-52495435 | Common:2; Rare:55 | ||||
| chr3:52685555-52685831 | Common:2; Rare:68 | ||||
| chr3:52685937-52686214 | Common:2; Rare:105 | ||||
| chr3:52693107-52693247 | Common:1; Rare:46 | ||||
| chr3:52705768-52706177 | Common:2; Rare:143 | ||||
| chr3:52770913-52771031 | Common:2; Rare:27 | ||||
| chr3:53130398-53130568 | Common:1; Rare:59; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:53347518-53347734 | Common:1; Rare:68 | ||||
| chr3:53891802-53892063 | Common:3; Rare:85 | ||||
| chr3:56557076-56557234 | Common:2; Rare:61 | ||||
| chr3:57079252-57079375 | Common:2; Rare:43 | ||||
| chr3:57227615-57227936 | Common:4; Rare:106 |