| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:39383258-39383432 | Common:1; Rare:32; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:39383582-39383680 | Rare:23; Clinvar:1 | ||||
| chr3:39406555-39406762 | Common:6; Rare:88 | ||||
| chr3:40309440-40309808 | Common:9; Rare:124 | ||||
| chr3:40457209-40457402 | Common:3; Rare:98 | ||||
| chr3:40524839-40525004 | Rare:44 | ||||
| chr3:41199290-41199580 | Common:1; Rare:133 | ||||
| chr3:42581913-42582126 | Common:2; Rare:66 | ||||
| chr3:42600422-42600709 | Common:2; Rare:109 | ||||
| chr3:42773206-42773351 | Common:1; Rare:42 | ||||
| chr3:42804427-42804663 | Common:2; Rare:71 | ||||
| chr3:43690818-43690950 | Common:1; Rare:60; Clinvar:5; Clinvar (benign):1 | ||||
| chr3:44338720-44338800 | Common:2; Rare:29 | ||||
| chr3:44477625-44477752 | Common:1; Rare:28 | ||||
| chr3:44510606-44510656 | Common:1; Rare:11 |