| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:43690782-43690938 | Common:1; Rare:67; Clinvar:5; Clinvar (benign):1 | ||||
| chr3:44338676-44338804 | Common:3; Rare:47 | ||||
| chr3:44624941-44625088 | Common:2; Rare:44 | ||||
| chr3:44761590-44761794 | Common:3; Rare:73 | ||||
| chr3:44861759-44861926 | Common:2; Rare:76 | ||||
| chr3:44976116-44976311 | Common:3; Rare:85 | ||||
| chr3:45689150-45689459 | Common:2; Rare:104 | ||||
| chr3:46407049-46407259 | Rare:37 | ||||
| chr3:46979569-46979852 | Common:1; Rare:68; Clinvar:1 | ||||
| chr3:47163947-47164236 | Common:1; Rare:77 | ||||
| chr3:47380816-47381079 | Rare:82 | ||||
| chr3:48088837-48089063 | Rare:76 | ||||
| chr3:48301358-48301495 | Common:1; Rare:33 | ||||
| chr3:48440043-48440276 | Common:1; Rare:72 | ||||
| chr3:48473015-48473280 | Common:2; Rare:56 |