| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9891059-9891321 | Common:1; Rare:55 | ||||
| chr3:9933457-9933923 | Common:3; Rare:183; Clinvar:4 | ||||
| chr3:9933951-9934123 | Rare:37 | ||||
| chr3:9952372-9952536 | Rare:31 | ||||
| chr3:9986724-9987166 | Common:4; Rare:125 | ||||
| chr3:9987333-9987538 | Rare:55 | ||||
| chr3:9987574-9987607 | Common:1; Rare:5 | ||||
| chr3:10026250-10026556 | Common:1; Rare:89 | ||||
| chr3:10115440-10115754 | Common:4; Rare:113 | ||||
| chr3:10115829-10116037 | Common:1; Rare:44 | ||||
| chr3:10141636-10142134 | Common:3; Rare:219; Clinvar:55; Clinvar (benign):47; Clinvar (pathogenic):7 | ||||
| chr3:10164813-10164940 | Rare:45 | ||||
| chr3:10248173-10248509 | Common:5; Rare:97 | ||||
| chr3:10248814-10248862 | Common:1; Rare:9 | ||||
| chr3:10248917-10248954 | Rare:6 |