| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52239079-52239284 | Common:2; Rare:72 | ||||
| chr3:52278334-52278791 | Rare:157 | ||||
| chr3:52287742-52287863 | Common:2; Rare:51 | ||||
| chr3:52288000-52288085 | Rare:31 | ||||
| chr3:52405674-52405819 | Rare:45; Clinvar:5; Clinvar (benign):10 | ||||
| chr3:52410351-52410687 | Rare:71 | ||||
| chr3:52455459-52455650 | Common:2; Rare:68 | ||||
| chr3:52536377-52536748 | Common:2; Rare:124 | ||||
| chr3:52685536-52686269 | Common:4; Rare:242 | ||||
| chr3:52692921-52693357 | Common:2; Rare:143 | ||||
| chr3:52693433-52693805 | Common:6; Rare:126 | ||||
| chr3:52705558-52706299 | Common:4; Rare:241 | ||||
| chr3:52770913-52771035 | Common:2; Rare:27 | ||||
| chr3:53130396-53130523 | Common:1; Rare:45; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:53229435-53229511 | Rare:26 |