| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:39051956-39052040 | Common:1; Rare:31 | ||||
| chr3:39107617-39107649 | Rare:8 | ||||
| chr3:39383267-39383415 | Rare:28; Clinvar:1 | ||||
| chr3:40309526-40309807 | Common:7; Rare:96 | ||||
| chr3:40457204-40457388 | Common:3; Rare:91 | ||||
| chr3:40524832-40524890 | Common:1; Rare:10 | ||||
| chr3:41962069-41962224 | Common:2; Rare:32 | ||||
| chr3:42581907-42582139 | Common:3; Rare:72 | ||||
| chr3:42600370-42600709 | Common:2; Rare:134 | ||||
| chr3:42804427-42804646 | Common:2; Rare:65 | ||||
| chr3:42936334-42936422 | Common:1; Rare:28 | ||||
| chr3:43621919-43622312 | Common:2; Rare:115; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:43690817-43690953 | Common:1; Rare:61; Clinvar:5; Clinvar (benign):1 | ||||
| chr3:44338106-44338158 | Common:1; Rare:18 | ||||
| chr3:44338714-44338807 | Common:3; Rare:30 |