| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:177051597-177051690 | Rare:20; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:177055617-177055861 | Rare:40 | ||||
| chr3:177057758-177057899 | Common:1; Rare:25 | ||||
| chr3:177068698-177068725 | Rare:4 | ||||
| chr3:177070274-177070435 | Rare:37 | ||||
| chr3:177070737-177070755 | Rare:4 | ||||
| chr3:177070787-177070905 | Common:5; Rare:32 | ||||
| chr3:177071041-177071146 | Common:2; Rare:28 | ||||
| chr3:177191125-177191374 | Rare:48 | ||||
| chr3:177193703-177194020 | Common:7; Rare:79 | ||||
| chr3:177195105-177195372 | Common:2; Rare:59 | ||||
| chr3:177211272-177211423 | Common:1; Rare:35 | ||||
| chr3:177211637-177211791 | Common:1; Rare:19 | ||||
| chr3:177211951-177212186 | Common:1; Rare:50 | ||||
| chr3:177250287-177250439 | Common:2; Rare:22 |