| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:25783390-25783621 | Common:2; Rare:76; Clinvar (benign):3 | ||||
| chr3:25789928-25790106 | Common:3; Rare:66 | ||||
| chr3:28241472-28241661 | Common:1; Rare:64 | ||||
| chr3:28348618-28348741 | Rare:27 | ||||
| chr3:28348787-28349188 | Common:4; Rare:125 | ||||
| chr3:29280864-29280891 | Common:1; Rare:6 | ||||
| chr3:29280997-29281102 | Common:1; Rare:18 | ||||
| chr3:31532380-31532656 | Common:4; Rare:77 | ||||
| chr3:32106404-32106712 | Common:4; Rare:86; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32502779-32502902 | Rare:40 | ||||
| chr3:32570655-32570914 | Rare:123 | ||||
| chr3:33277347-33277487 | Common:1; Rare:36 | ||||
| chr3:33798435-33798690 | Common:2; Rare:83 | ||||
| chr3:33799014-33799231 | Rare:70 | ||||
| chr3:36993077-36993586 | Common:2; Rare:179; Clinvar:34; Clinvar (benign):15; Clinvar (pathogenic):4 |