| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:148991394-148991423 | Rare:11 | ||||
| chr3:148991431-148991643 | Common:2; Rare:94; Clinvar (benign):1 | ||||
| chr3:149129545-149129716 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149657903-149658212 | Common:1; Rare:66 | ||||
| chr3:149658526-149658661 | Rare:33 | ||||
| chr3:149813010-149813265 | Common:2; Rare:86 | ||||
| chr3:149968525-149968679 | Common:7; Rare:43 | ||||
| chr3:150407917-150408377 | Common:2; Rare:135 | ||||
| chr3:150408585-150408641 | Rare:20 | ||||
| chr3:150603147-150603360 | Common:2; Rare:82 | ||||
| chr3:150703735-150704013 | Common:2; Rare:144 | ||||
| chr3:150763145-150763266 | Rare:34 | ||||
| chr3:151384744-151384978 | Common:1; Rare:41 | ||||
| chr3:152267560-152267833 | Rare:52 | ||||
| chr3:152268122-152268395 | Common:1; Rare:38 |