| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:23806372-23806558 | Common:1; Rare:45 | ||||
| chr3:23806894-23807114 | Common:1; Rare:67 | ||||
| chr3:23810331-23810577 | Rare:77 | ||||
| chr3:23811357-23811513 | Common:1; Rare:40 | ||||
| chr3:23916855-23917359 | Rare:171 | ||||
| chr3:23917607-23917794 | Common:2; Rare:46 | ||||
| chr3:23945129-23945359 | Common:7; Rare:85 | ||||
| chr3:24494688-24494921 | Rare:61 | ||||
| chr3:25664231-25664732 | Common:3; Rare:141 | ||||
| chr3:25664809-25665082 | Common:4; Rare:83 | ||||
| chr3:25783338-25783640 | Common:2; Rare:106; Clinvar (benign):3 | ||||
| chr3:25789957-25790123 | Common:4; Rare:66 | ||||
| chr3:26622711-26622809 | Rare:20 | ||||
| chr3:27484366-27484735 | Common:3; Rare:119 | ||||
| chr3:28241441-28241791 | Common:2; Rare:120 |