| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:123585023-123585317 | Common:1; Rare:91 | ||||
| chr3:123585489-123585590 | Rare:20 | ||||
| chr3:123692314-123692464 | Rare:34 | ||||
| chr3:123700785-123701341 | Common:2; Rare:143; Clinvar:15; Clinvar (benign):10 | ||||
| chr3:123701436-123701558 | Rare:44; Clinvar:7 | ||||
| chr3:123961194-123961483 | Common:3; Rare:118 | ||||
| chr3:124730374-124730473 | Common:2; Rare:53; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:125055633-125055814 | Common:2; Rare:45 | ||||
| chr3:125211632-125211707 | Rare:10 | ||||
| chr3:125212698-125212784 | Common:2; Rare:24 | ||||
| chr3:125357215-125357340 | Common:1; Rare:38 | ||||
| chr3:125375113-125375443 | Rare:89 | ||||
| chr3:125520120-125520297 | Rare:69 | ||||
| chr3:125595252-125595398 | Common:2; Rare:45 | ||||
| chr3:125595522-125595690 | Rare:55 |