| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:147617249-147617486 | Common:1; Rare:51 | ||||
| chr4:147684083-147684271 | Common:1; Rare:70 | ||||
| chr4:148442323-148442712 | Rare:110; Clinvar:4; Clinvar (benign):3 | ||||
| chr4:150581626-150581932 | Common:1; Rare:58 | ||||
| chr4:151015709-151015866 | Rare:75 | ||||
| chr4:151099396-151099713 | Common:3; Rare:114 | ||||
| chr4:151408885-151409209 | Common:5; Rare:106 | ||||
| chr4:152536053-152536413 | Common:3; Rare:137 | ||||
| chr4:152779730-152780169 | Common:2; Rare:113 | ||||
| chr4:152936823-152936954 | Common:1; Rare:30 | ||||
| chr4:153466078-153466410 | Common:3; Rare:134 | ||||
| chr4:154590627-154590976 | Common:3; Rare:80; Clinvar (benign):3 | ||||
| chr4:154612523-154612913 | Common:1; Rare:94; Clinvar:3 | ||||
| chr4:155953846-155953960 | Rare:29 | ||||
| chr4:158172369-158172617 | Rare:39 |