| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:25783380-25783640 | Common:2; Rare:83; Clinvar (benign):3 | ||||
| chr3:25790008-25790118 | Common:3; Rare:42 | ||||
| chr3:26622707-26622818 | Rare:22 | ||||
| chr3:28241441-28241659 | Common:1; Rare:71 | ||||
| chr3:28348626-28348749 | Rare:29 | ||||
| chr3:28348779-28349179 | Common:3; Rare:128 | ||||
| chr3:29280837-29281081 | Common:3; Rare:49 | ||||
| chr3:31532380-31532724 | Common:4; Rare:103 | ||||
| chr3:31981625-31981808 | Common:1; Rare:49 | ||||
| chr3:32106418-32106714 | Common:4; Rare:82; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32502749-32502889 | Rare:51 | ||||
| chr3:32570666-32570984 | Common:1; Rare:135 | ||||
| chr3:32685100-32685406 | Rare:88 | ||||
| chr3:33097098-33097267 | Rare:58; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33277312-33277509 | Common:2; Rare:59 |