| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:7192190-7192760 | Common:8; Rare:214 | ||||
| chr4:7939632-7940105 | Common:7; Rare:487 | ||||
| chr4:8010067-8010430 | Common:5; Rare:113 | ||||
| chr4:8010614-8011091 | Common:8; Rare:281 | ||||
| chr4:8158701-8159189 | Common:10; Rare:418 | ||||
| chr4:8199020-8199440 | Common:5; Rare:214 | ||||
| chr4:8428354-8428582 | Common:8; Rare:250 | ||||
| chr4:8440662-8440896 | Rare:243 | ||||
| chr4:8592480-8592940 | Common:10; Rare:178 | ||||
| chr4:10018760-10019170 | Common:3; Rare:135; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr4:10115670-10116126 | Common:7; Rare:197 | ||||
| chr4:10116249-10116484 | Rare:134 | ||||
| chr4:10116621-10117149 | Common:28; Rare:649 | ||||
| chr4:11428810-11429235 | Common:5; Rare:267 | ||||
| chr4:13484130-13484813 | Common:4; Rare:524 |