| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:129278761-129278895 | Common:4; Rare:43 | ||||
| chr3:129316283-129316317 | Rare:17 | ||||
| chr3:129439876-129440158 | Common:1; Rare:88; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:129893580-129893891 | Rare:133 | ||||
| chr3:131026738-131026949 | Common:2; Rare:54 | ||||
| chr3:131381464-131381801 | Common:2; Rare:85 | ||||
| chr3:131502853-131503004 | Common:1; Rare:66 | ||||
| chr3:132660060-132660340 | Common:2; Rare:59 | ||||
| chr3:133661813-133662011 | Rare:47 | ||||
| chr3:134485404-134485773 | Rare:91 | ||||
| chr3:134485964-134486185 | Common:2; Rare:72 | ||||
| chr3:134650989-134651355 | Common:2; Rare:117 | ||||
| chr3:136752224-136752666 | Common:1; Rare:139 | ||||
| chr3:136862022-136862275 | Common:1; Rare:72 | ||||
| chr3:139389582-139389878 | Common:2; Rare:92 |