| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:44726547-44726642 | Rare:38 | ||||
| chr4:47463635-47463790 | Common:2; Rare:51 | ||||
| chr4:47485162-47485372 | Common:1; Rare:70 | ||||
| chr4:47838099-47838256 | Common:1; Rare:29 | ||||
| chr4:47914569-47914919 | Common:2; Rare:103 | ||||
| chr4:48016618-48016795 | Common:1; Rare:51 | ||||
| chr4:48269790-48269989 | Common:2; Rare:44 | ||||
| chr4:48780236-48780572 | Common:2; Rare:101 | ||||
| chr4:52038255-52038346 | Rare:35; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr4:52659238-52659439 | Common:1; Rare:68 | ||||
| chr4:53365997-53366222 | Rare:52 | ||||
| chr4:55395845-55395968 | Common:1; Rare:31; Clinvar:2 | ||||
| chr4:56387470-56387528 | Rare:15 | ||||
| chr4:56435473-56435764 | Common:5; Rare:106 | ||||
| chr4:56436033-56436315 | Rare:105 |