| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:179652620-179652841 | Common:2; Rare:42 | ||||
| chr3:179652859-179653149 | Common:1; Rare:81 | ||||
| chr3:179653382-179653627 | Common:3; Rare:74 | ||||
| chr3:179653653-179653710 | Common:1; Rare:28 | ||||
| chr3:180601946-180602402 | Common:1; Rare:146 | ||||
| chr3:180602404-180602553 | Rare:38 | ||||
| chr3:180912283-180912766 | Common:4; Rare:155 | ||||
| chr3:180989466-180989514 | Rare:7 | ||||
| chr3:180989609-180989957 | Rare:122; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:182793254-182793672 | Common:4; Rare:111 | ||||
| chr3:182793678-182793968 | Common:2; Rare:83 | ||||
| chr3:182980380-182980652 | Rare:104 | ||||
| chr3:182980780-182980817 | Common:2; Rare:9 | ||||
| chr3:183098897-183099060 | Common:1; Rare:34 | ||||
| chr3:183099432-183099773 | Common:2; Rare:107; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 |