| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52278608-52278791 | Rare:65 | ||||
| chr3:52287701-52287863 | Common:2; Rare:60 | ||||
| chr3:52455425-52455673 | Common:2; Rare:86 | ||||
| chr3:52484425-52484524 | Common:8; Rare:36 | ||||
| chr3:52495264-52495416 | Common:1; Rare:45 | ||||
| chr3:52685510-52686202 | Common:4; Rare:229 | ||||
| chr3:52705576-52706274 | Common:4; Rare:229 | ||||
| chr3:52770913-52771045 | Common:2; Rare:31 | ||||
| chr3:53130396-53130533 | Common:1; Rare:46; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:53234989-53235318 | Common:6; Rare:99 | ||||
| chr3:53347504-53347764 | Common:2; Rare:86 | ||||
| chr3:53891768-53892088 | Common:5; Rare:111 | ||||
| chr3:56557081-56557238 | Common:2; Rare:61 | ||||
| chr3:56801899-56802037 | Rare:52 | ||||
| chr3:57079235-57079373 | Common:2; Rare:46 |