| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:39180858-39180935 | Rare:14 | ||||
| chr3:39208602-39208690 | Rare:15 | ||||
| chr3:39384211-39384479 | Common:7; Rare:72 | ||||
| chr3:39639452-39639599 | Common:1; Rare:24 | ||||
| chr3:40453039-40453091 | Rare:10 | ||||
| chr3:40453094-40453481 | Common:7; Rare:90 | ||||
| chr3:40593444-40593656 | Rare:36 | ||||
| chr3:40615667-40615882 | Rare:54 | ||||
| chr3:40616009-40616044 | Rare:4 | ||||
| chr3:41681586-41681788 | Common:1; Rare:73; Clinvar (benign):1 | ||||
| chr3:41941673-41941961 | Common:2; Rare:39 | ||||
| chr3:41961396-41961442 | Common:2; Rare:12 | ||||
| chr3:42015283-42015431 | Rare:33 | ||||
| chr3:42025650-42025887 | Common:1; Rare:57 | ||||
| chr3:42036529-42036682 | Rare:26 |