| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:148368360-148368659 | Common:2; Rare:63 | ||||
| chr4:148442224-148442713 | Rare:133; Clinvar:5; Clinvar (benign):3 | ||||
| chr4:148444599-148444696 | Common:1; Rare:23 | ||||
| chr4:150581808-150581976 | Rare:37 | ||||
| chr4:151015205-151015297 | Rare:30 | ||||
| chr4:151015709-151015955 | Rare:101 | ||||
| chr4:151099452-151099662 | Common:3; Rare:85 | ||||
| chr4:151408868-151409267 | Common:5; Rare:126 | ||||
| chr4:151760968-151761223 | Rare:85 | ||||
| chr4:152536039-152536424 | Common:3; Rare:143 | ||||
| chr4:152779730-152780158 | Common:2; Rare:111 | ||||
| chr4:152936177-152936385 | Common:3; Rare:53 | ||||
| chr4:153322418-153322722 | Common:2; Rare:60; Clinvar:1 | ||||
| chr4:155953828-155953907 | Rare:21 | ||||
| chr4:156971073-156971214 | Rare:21 |