| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:122661058-122661176 | Rare:24 | ||||
| chr3:123299537-123299719 | Common:1; Rare:35 | ||||
| chr3:123618640-123619064 | Rare:112; Clinvar:7; Clinvar (benign):3 | ||||
| chr3:123638994-123639306 | Common:1; Rare:54 | ||||
| chr3:124077842-124077927 | Common:1; Rare:14 | ||||
| chr3:124286617-124286656 | Rare:9 | ||||
| chr3:125310968-125311117 | Common:1; Rare:24 | ||||
| chr3:125374467-125374555 | Rare:17 | ||||
| chr3:125766424-125766529 | Rare:41 | ||||
| chr3:125915899-125916165 | Common:5; Rare:75 | ||||
| chr3:125916420-125916671 | Common:7; Rare:76 | ||||
| chr3:125990499-125990615 | Common:3; Rare:41 | ||||
| chr3:126057354-126057447 | Rare:20 | ||||
| chr3:126247403-126247435 | Common:1; Rare:7 | ||||
| chr3:126433995-126434299 | Common:1; Rare:89 |