| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:39153531-39153750 | Common:3; Rare:69 | ||||
| chr3:39383243-39383437 | Common:2; Rare:34; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:39383547-39383653 | Rare:25; Clinvar:1 | ||||
| chr3:40309491-40309880 | Common:9; Rare:132 | ||||
| chr3:40457204-40457388 | Common:3; Rare:91 | ||||
| chr3:40477094-40477203 | Common:1; Rare:30 | ||||
| chr3:40505936-40506137 | Rare:44 | ||||
| chr3:40524832-40524904 | Common:1; Rare:14 | ||||
| chr3:42581881-42582138 | Common:3; Rare:80 | ||||
| chr3:42582256-42582316 | Rare:13 | ||||
| chr3:42600328-42600709 | Common:3; Rare:152 | ||||
| chr3:42804427-42804631 | Common:2; Rare:59 | ||||
| chr3:43690574-43691010 | Common:7; Rare:179; Clinvar:7; Clinvar (benign):3 | ||||
| chr3:44338095-44338190 | Common:2; Rare:35 | ||||
| chr3:44338698-44338809 | Common:3; Rare:40 |