| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:21751067-21751251 | Common:1; Rare:60 | ||||
| chr3:23805812-23806066 | Common:1; Rare:51 | ||||
| chr3:23916848-23917359 | Rare:174 | ||||
| chr3:25428098-25428398 | Rare:67 | ||||
| chr3:25663552-25663899 | Common:1; Rare:69 | ||||
| chr3:25664878-25665069 | Common:1; Rare:63 | ||||
| chr3:25783377-25783634 | Common:2; Rare:85; Clinvar (benign):3 | ||||
| chr3:25789962-25790138 | Common:5; Rare:74 | ||||
| chr3:26622707-26622765 | Rare:15 | ||||
| chr3:26623550-26623863 | Common:1; Rare:57 | ||||
| chr3:27484399-27484660 | Common:2; Rare:86 | ||||
| chr3:28241441-28241672 | Common:1; Rare:78 | ||||
| chr3:28348592-28349179 | Common:3; Rare:176 | ||||
| chr3:31532371-31532733 | Common:4; Rare:112 | ||||
| chr3:32106425-32106670 | Common:3; Rare:61; Clinvar:2; Clinvar (benign):1 |