| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:28348787-28349196 | Common:4; Rare:129 | ||||
| chr3:29280837-29281102 | Common:3; Rare:55 | ||||
| chr3:31532371-31532648 | Common:3; Rare:78 | ||||
| chr3:31533016-31533224 | Rare:70; Clinvar (benign):2 | ||||
| chr3:31981607-31981808 | Common:1; Rare:53 | ||||
| chr3:32106425-32106720 | Common:3; Rare:75; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32502779-32502956 | Rare:47 | ||||
| chr3:32570707-32570950 | Common:1; Rare:112 | ||||
| chr3:33277289-33277482 | Common:2; Rare:52 | ||||
| chr3:33718050-33718295 | Rare:91 | ||||
| chr3:33798551-33798686 | Common:2; Rare:49 | ||||
| chr3:33798997-33799090 | Rare:31 | ||||
| chr3:36993072-36993098 | Rare:15 | ||||
| chr3:36993108-36993545 | Common:2; Rare:138; Clinvar:26; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr3:36993704-36993833 | Rare:53; Clinvar:1 |