| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:143336562-143336912 | Rare:79 | ||||
| chr4:143337236-143337371 | Rare:57 | ||||
| chr4:143513349-143513819 | Common:2; Rare:156 | ||||
| chr4:145098141-145098369 | Rare:80 | ||||
| chr4:145179999-145180140 | Rare:39 | ||||
| chr4:145619340-145619416 | Rare:27; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:147617145-147617479 | Common:1; Rare:77 | ||||
| chr4:147684081-147684242 | Common:1; Rare:59 | ||||
| chr4:148442375-148442712 | Rare:99; Clinvar:4; Clinvar (benign):2 | ||||
| chr4:151015210-151015330 | Rare:35 | ||||
| chr4:151015707-151015812 | Rare:41 | ||||
| chr4:151099412-151099713 | Common:3; Rare:111 | ||||
| chr4:151099867-151100123 | Rare:83 | ||||
| chr4:151408868-151409454 | Common:8; Rare:160 | ||||
| chr4:151760963-151761213 | Rare:89 |