| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:152269501-152269759 | Common:2; Rare:78 | ||||
| chr3:152269836-152270054 | Common:4; Rare:54 | ||||
| chr3:155870323-155870732 | Common:2; Rare:118 | ||||
| chr3:156674362-156674659 | Common:3; Rare:89 | ||||
| chr3:157160072-157160315 | Rare:103 | ||||
| chr3:158105739-158105878 | Common:5; Rare:70; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:158672559-158672598 | Rare:9 | ||||
| chr3:158801993-158802206 | Common:2; Rare:95 | ||||
| chr3:160399196-160399539 | Rare:104; Clinvar:6 | ||||
| chr3:160565256-160565842 | Common:3; Rare:194 | ||||
| chr3:160755312-160755684 | Common:1; Rare:115 | ||||
| chr3:160755922-160756345 | Common:1; Rare:105 | ||||
| chr3:160756665-160756811 | Common:3; Rare:56 | ||||
| chr3:167734466-167734605 | Rare:34 | ||||
| chr3:167734849-167735107 | Common:2; Rare:85 |