| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:28349015-28349179 | Common:2; Rare:48 | ||||
| chr3:29280831-29281407 | Common:15; Rare:113 | ||||
| chr3:31981624-31981774 | Rare:41 | ||||
| chr3:33277295-33277489 | Common:2; Rare:50 | ||||
| chr3:33798520-33798692 | Common:2; Rare:63 | ||||
| chr3:36993117-36993543 | Common:2; Rare:132; Clinvar:26; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr3:37243166-37243361 | Common:1; Rare:49 | ||||
| chr3:38024518-38024667 | Common:1; Rare:59 | ||||
| chr3:39051956-39052039 | Common:1; Rare:31 | ||||
| chr3:39107555-39107725 | Common:3; Rare:52 | ||||
| chr3:39153515-39153742 | Common:3; Rare:74 | ||||
| chr3:40309491-40309873 | Common:9; Rare:130 | ||||
| chr3:42581932-42582204 | Common:3; Rare:72 | ||||
| chr3:42600372-42600720 | Common:2; Rare:138 | ||||
| chr3:42773206-42773332 | Common:1; Rare:40 |