| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:80771170-80771413 | Common:2; Rare:69 | ||||
| chr3:81723846-81723882 | Rare:8 | ||||
| chr3:81760990-81761163 | Rare:40 | ||||
| chr3:81920997-81921060 | Rare:11 | ||||
| chr3:82080448-82080556 | Common:1; Rare:19 | ||||
| chr3:83942519-83942697 | Rare:30 | ||||
| chr3:85579359-85579446 | Common:1; Rare:19 | ||||
| chr3:86029764-86029919 | Common:1; Rare:32 | ||||
| chr3:86782350-86782610 | Common:2; Rare:56 | ||||
| chr3:86793810-86794063 | Common:1; Rare:46 | ||||
| chr3:86957484-86957535 | Rare:10 | ||||
| chr3:87085061-87085170 | Common:1; Rare:22 | ||||
| chr3:87089055-87089322 | Common:2; Rare:56 | ||||
| chr3:87089555-87089910 | Common:2; Rare:70 | ||||
| chr3:87262098-87262178 | Rare:21; Clinvar (pathogenic):3 |