| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:172750348-172751047 | Common:4; Rare:169 | ||||
| chr3:173397436-173397779 | Common:4; Rare:107 | ||||
| chr3:174440849-174441001 | Common:2; Rare:42 | ||||
| chr3:177196411-177196550 | Rare:38 | ||||
| chr3:177197128-177197393 | Rare:87 | ||||
| chr3:179071576-179071877 | Rare:82 | ||||
| chr3:179148028-179148190 | Common:3; Rare:59 | ||||
| chr3:179347598-179347779 | Common:1; Rare:44 | ||||
| chr3:179562658-179563003 | Rare:115 | ||||
| chr3:179604564-179604915 | Common:3; Rare:147 | ||||
| chr3:180602019-180602285 | Common:1; Rare:89 | ||||
| chr3:180679457-180679579 | Rare:27; Clinvar:3 | ||||
| chr3:180912331-180912736 | Common:4; Rare:131 | ||||
| chr3:180989618-180989804 | Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:180989805-180989898 | Rare:21 |