| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:145180491-145180796 | Common:1; Rare:91 | ||||
| chr4:145619313-145619396 | Rare:36 | ||||
| chr4:145938773-145938980 | Rare:53 | ||||
| chr4:145938989-145939052 | Common:1; Rare:19 | ||||
| chr4:147480687-147481037 | Rare:58 | ||||
| chr4:147617190-147617498 | Common:1; Rare:71 | ||||
| chr4:147684079-147684302 | Common:1; Rare:87 | ||||
| chr4:148442412-148442712 | Rare:90; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:150581648-150581930 | Common:1; Rare:53 | ||||
| chr4:151015216-151015372 | Rare:42 | ||||
| chr4:151015707-151015849 | Rare:68 | ||||
| chr4:151099420-151099713 | Common:3; Rare:110 | ||||
| chr4:151408868-151409257 | Common:5; Rare:125 | ||||
| chr4:151760952-151761215 | Rare:98 | ||||
| chr4:152536053-152536378 | Common:2; Rare:124 |