| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:25592708-25592961 | Common:3; Rare:43 | ||||
| chr3:25781686-25782020 | Rare:55 | ||||
| chr3:25782306-25782349 | Rare:4 | ||||
| chr3:27360250-27360409 | Common:1; Rare:30 | ||||
| chr3:27483196-27483346 | Common:1; Rare:35 | ||||
| chr3:30644895-30645187 | Common:3; Rare:58; Clinvar (benign):2 | ||||
| chr3:31241723-31241757 | Rare:9 | ||||
| chr3:32401903-32402028 | Rare:22 | ||||
| chr3:32436270-32436561 | Common:2; Rare:42 | ||||
| chr3:32439121-32439262 | Common:1; Rare:20 | ||||
| chr3:32455824-32456107 | Common:3; Rare:49 | ||||
| chr3:32457989-32458151 | Common:2; Rare:25 | ||||
| chr3:32502136-32502257 | Rare:21 | ||||
| chr3:32577924-32578003 | Common:1; Rare:9 | ||||
| chr3:32781547-32781788 | Common:1; Rare:70 |