| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:17577303-17577550 | Rare:227 | ||||
| chr4:17614055-17614455 | Common:5; Rare:115 | ||||
| chr4:17614541-17614686 | Common:4; Rare:126 | ||||
| chr4:17810624-17811056 | Common:7; Rare:254 | ||||
| chr4:18021728-18022045 | Common:4; Rare:183 | ||||
| chr4:20700256-20700495 | Common:2; Rare:194 | ||||
| chr4:22515010-22515510 | Common:7; Rare:188 | ||||
| chr4:22515886-22516200 | Common:10; Rare:203 | ||||
| chr4:22516280-22516620 | Common:6; Rare:130 | ||||
| chr4:23890024-23890129 | Rare:16 | ||||
| chr4:23890034-23890189 | Rare:24 | ||||
| chr4:24584443-24584682 | Rare:144 | ||||
| chr4:25154859-25155284 | Common:1; Rare:189; Clinvar:4 | ||||
| chr4:25159894-25160155 | Common:3; Rare:118 | ||||
| chr4:25160274-25160729 | Common:6; Rare:284; Clinvar:4; Clinvar (benign):2 |