| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:157174870-157175253 | Common:3; Rare:169 | ||||
| chr3:167811074-167811334 | Rare:37 | ||||
| chr3:169765058-169765207 | Rare:65; Clinvar (pathogenic):1 | ||||
| chr3:171775830-171776204 | Common:2; Rare:70 | ||||
| chr3:181056653-181056715 | Rare:7 | ||||
| chr3:181699430-181699618 | Rare:29 | ||||
| chr3:181699622-181699787 | Common:1; Rare:28 | ||||
| chr3:181712675-181712961 | Rare:80; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr3:181717817-181718037 | Common:2; Rare:43 | ||||
| chr3:183447414-183447723 | Common:2; Rare:79 | ||||
| chr3:194583888-194584020 | Common:10; Rare:48 | ||||
| chr3:195657920-195658126 | Common:12; Rare:36 | ||||
| chr3:195990227-195990419 | Rare:24 | ||||
| chr3:197627833-197628032 | Common:6; Rare:75 | ||||
| chr3:197850988-197850993 |