| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48989703-48989953 | Rare:116 | ||||
| chr3:48990128-48990311 | Rare:71 | ||||
| chr3:48990320-48990490 | Rare:116 | ||||
| chr3:48990670-48990880 | Common:1; Rare:73 | ||||
| chr3:48990888-48991013 | Rare:43 | ||||
| chr3:49007177-49007448 | Common:4; Rare:175 | ||||
| chr3:49007680-49008250 | Common:5; Rare:222 | ||||
| chr3:49018517-49018620 | Rare:44 | ||||
| chr3:49021481-49021845 | Rare:145; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:49022058-49022361 | Rare:171; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr3:49024976-49025501 | Common:1; Rare:204 | ||||
| chr3:49029357-49029573 | Common:4; Rare:291 | ||||
| chr3:49093449-49093670 | Rare:80 | ||||
| chr3:49093981-49094148 | Rare:72 | ||||
| chr3:49094184-49094700 | Common:2; Rare:193 |