| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:43690616-43690993 | Common:6; Rare:157; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:43691555-43691670 | Common:1; Rare:18 | ||||
| chr3:44338703-44338800 | Common:3; Rare:36 | ||||
| chr3:44477618-44477758 | Common:1; Rare:32 | ||||
| chr3:44510588-44510661 | Common:2; Rare:23 | ||||
| chr3:44584669-44584981 | Rare:63 | ||||
| chr3:44624888-44625087 | Common:2; Rare:60 | ||||
| chr3:44712563-44712704 | Common:1; Rare:49 | ||||
| chr3:44761565-44761810 | Common:3; Rare:99 | ||||
| chr3:44861757-44861918 | Common:2; Rare:72 | ||||
| chr3:44974994-44975278 | Common:3; Rare:38 | ||||
| chr3:44976024-44976317 | Common:5; Rare:116 | ||||
| chr3:45146274-45146517 | Common:2; Rare:82 | ||||
| chr3:45594012-45594277 | Rare:93 | ||||
| chr3:45689180-45689459 | Common:1; Rare:93 |