| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:11272247-11272413 | Common:1; Rare:32 | ||||
| chr3:11643707-11644016 | Common:2; Rare:76 | ||||
| chr3:11719419-11719595 | Rare:57 | ||||
| chr3:12004240-12004402 | Common:2; Rare:49 | ||||
| chr3:12158848-12158959 | Rare:36 | ||||
| chr3:12484158-12484560 | Common:5; Rare:116; Clinvar:3; Clinvar (benign):2 | ||||
| chr3:12545509-12545641 | Common:2; Rare:25 | ||||
| chr3:12664080-12664330 | Common:1; Rare:68; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:12796572-12796744 | Common:5; Rare:53 | ||||
| chr3:12841481-12841882 | Common:2; Rare:129 | ||||
| chr3:13480018-13480330 | Common:2; Rare:77 | ||||
| chr3:14124742-14125119 | Common:4; Rare:111; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178569-14178875 | Common:2; Rare:158; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14402333-14402628 | Common:1; Rare:80 | ||||
| chr3:14651442-14651818 | Rare:109 |