| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:25783388-25783621 | Common:2; Rare:78; Clinvar (benign):3 | ||||
| chr3:25789901-25790118 | Common:4; Rare:78 | ||||
| chr3:28241441-28241768 | Common:2; Rare:109 | ||||
| chr3:28348578-28348865 | Common:1; Rare:76 | ||||
| chr3:28348868-28349188 | Common:3; Rare:102 | ||||
| chr3:29280868-29281388 | Common:15; Rare:100 | ||||
| chr3:29281391-29281661 | Common:1; Rare:59 | ||||
| chr3:30606291-30606592 | Common:1; Rare:79; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:31532375-31532656 | Common:4; Rare:80 | ||||
| chr3:31533085-31533293 | Common:1; Rare:58; Clinvar (benign):1 | ||||
| chr3:32106418-32106720 | Common:4; Rare:82; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32502779-32502889 | Rare:38 | ||||
| chr3:32570655-32570956 | Common:1; Rare:136 | ||||
| chr3:33097078-33097258 | Rare:61; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:33114357-33114524 | Common:1; Rare:65; Clinvar:4; Clinvar (benign):4 |