| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:38496045-38496370 | Common:2; Rare:99 | ||||
| chr3:39051924-39052085 | Common:1; Rare:58 | ||||
| chr3:39107503-39107725 | Common:3; Rare:74 | ||||
| chr3:39153508-39153750 | Common:3; Rare:76 | ||||
| chr3:39383272-39383452 | Common:2; Rare:33; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:39383530-39383724 | Rare:44; Clinvar:2 | ||||
| chr3:39406541-39406761 | Common:6; Rare:97 | ||||
| chr3:40309456-40309890 | Common:9; Rare:142 | ||||
| chr3:40457201-40457436 | Common:5; Rare:110 | ||||
| chr3:40477059-40477193 | Common:1; Rare:34 | ||||
| chr3:40505932-40506132 | Rare:44 | ||||
| chr3:40524815-40525013 | Common:1; Rare:58 | ||||
| chr3:41199685-41199761 | Rare:21 | ||||
| chr3:41199823-41200155 | Common:2; Rare:92 | ||||
| chr3:41224697-41225207 | Common:1; Rare:97; Clinvar:1; Clinvar (pathogenic):2 |