| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:42906349-42906354 | Rare:1 | ||||
| chr3:43286459-43286662 | Common:2; Rare:88 | ||||
| chr3:43690817-43690950 | Common:1; Rare:60; Clinvar:5; Clinvar (benign):1 | ||||
| chr3:43691554-43691621 | Common:1; Rare:13 | ||||
| chr3:44338384-44338518 | Common:1; Rare:48 | ||||
| chr3:44338709-44338797 | Common:3; Rare:31 | ||||
| chr3:44477628-44477746 | Common:1; Rare:25 | ||||
| chr3:44510606-44510754 | Common:1; Rare:31 | ||||
| chr3:44624935-44625095 | Common:2; Rare:45 | ||||
| chr3:44761594-44761804 | Common:3; Rare:76 | ||||
| chr3:44861772-44861927 | Common:2; Rare:69 | ||||
| chr3:44976118-44976289 | Common:2; Rare:72 | ||||
| chr3:45689180-45689468 | Common:1; Rare:97 | ||||
| chr3:45796465-45796687 | Common:2; Rare:65; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:45842064-45842208 | Rare:35 |