| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:28348779-28349185 | Common:3; Rare:128 | ||||
| chr3:29280864-29281400 | Common:15; Rare:103 | ||||
| chr3:31532362-31532662 | Common:4; Rare:91 | ||||
| chr3:32106418-32106697 | Common:4; Rare:76; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32391727-32391922 | Common:3; Rare:57 | ||||
| chr3:32570684-32570937 | Rare:115 | ||||
| chr3:33097098-33097220 | Rare:41; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33218789-33218974 | Common:3; Rare:54 | ||||
| chr3:33277295-33277482 | Common:2; Rare:49 | ||||
| chr3:33440904-33441065 | Rare:29 | ||||
| chr3:33798520-33798686 | Common:2; Rare:60 | ||||
| chr3:36993078-36993563 | Common:2; Rare:165; Clinvar:27; Clinvar (benign):12; Clinvar (pathogenic):3 | ||||
| chr3:36993727-36993830 | Rare:39 | ||||
| chr3:37243166-37243358 | Common:1; Rare:49 | ||||
| chr3:38164974-38165272 | Common:1; Rare:73 |