| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:65597422-65597606 | Rare:35 | ||||
| chr3:66998013-66998318 | Rare:72 | ||||
| chr3:67654587-67654714 | Common:1; Rare:46 | ||||
| chr3:69052208-69052413 | Common:4; Rare:74 | ||||
| chr3:69542563-69542754 | Common:2; Rare:51 | ||||
| chr3:71725281-71725597 | Common:3; Rare:114 | ||||
| chr3:71755051-71755254 | Rare:54 | ||||
| chr3:72848374-72848563 | Rare:66 | ||||
| chr3:72996722-72997031 | Common:1; Rare:116 | ||||
| chr3:75785507-75785690 | Common:3; Rare:20 | ||||
| chr3:77039318-77039420 | Rare:17 | ||||
| chr3:79019025-79019054 | Rare:11 | ||||
| chr3:79767922-79768068 | Rare:24 | ||||
| chr3:81761642-81761736 | Common:1; Rare:36; Clinvar:1 | ||||
| chr3:87227237-87227401 | Common:1; Rare:49; Clinvar:1; Clinvar (benign):2 |