| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:136046830-136047419 | Common:4; Rare:149; Clinvar:3; Clinvar (benign):2 | ||||
| chr5:136053708-136054080 | Common:2; Rare:83 | ||||
| chr5:136058602-136058874 | Common:2; Rare:42 | ||||
| chr5:136132720-136132944 | Common:1; Rare:74 | ||||
| chr5:137736072-137736285 | Common:1; Rare:37 | ||||
| chr5:137754320-137754519 | Rare:68 | ||||
| chr5:138032736-138032815 | Common:1; Rare:13 | ||||
| chr5:138032984-138033260 | Common:1; Rare:91 | ||||
| chr5:138178615-138178739 | Rare:30 | ||||
| chr5:138178935-138179190 | Common:3; Rare:52 | ||||
| chr5:138213275-138213582 | Rare:81 | ||||
| chr5:138331731-138332142 | Common:2; Rare:105 | ||||
| chr5:138464940-138465180 | Rare:58 | ||||
| chr5:138542842-138543004 | Rare:48 | ||||
| chr5:138543032-138543618 | Common:3; Rare:179 |