| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:37176280-37176387 | Rare:35 | ||||
| chr3:37243172-37243418 | Common:1; Rare:58 | ||||
| chr3:38024490-38024667 | Common:1; Rare:66 | ||||
| chr3:39051939-39052027 | Common:1; Rare:32 | ||||
| chr3:39107555-39107704 | Common:3; Rare:46 | ||||
| chr3:39383257-39383443 | Common:2; Rare:35; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:39383582-39383700 | Rare:26; Clinvar:1 | ||||
| chr3:39406427-39406764 | Common:7; Rare:132 | ||||
| chr3:40309486-40309803 | Common:9; Rare:110 | ||||
| chr3:40457225-40457370 | Common:2; Rare:69 | ||||
| chr3:40505930-40506123 | Rare:44 | ||||
| chr3:40524815-40524965 | Common:1; Rare:40 | ||||
| chr3:42581900-42582137 | Common:3; Rare:73 | ||||
| chr3:42600372-42600777 | Common:2; Rare:155 | ||||
| chr3:42773206-42773321 | Common:1; Rare:40 |