| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:122564437-122564467 | Rare:9 | ||||
| chr3:122793780-122793908 | Common:3; Rare:36 | ||||
| chr3:123201658-123201970 | Common:1; Rare:85 | ||||
| chr3:123585028-123585324 | Common:1; Rare:92 | ||||
| chr3:123585489-123585646 | Rare:28 | ||||
| chr3:123700966-123701347 | Rare:72; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:123961194-123961483 | Common:3; Rare:118 | ||||
| chr3:124584571-124584718 | Rare:30 | ||||
| chr3:124730340-124730468 | Common:3; Rare:69; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:125375129-125375448 | Rare:89 | ||||
| chr3:125520118-125520300 | Rare:69 | ||||
| chr3:126084099-126084297 | Common:1; Rare:83 | ||||
| chr3:126180568-126180682 | Common:1; Rare:26 | ||||
| chr3:126704071-126704313 | Common:2; Rare:80 | ||||
| chr3:127598223-127598458 | Common:3; Rare:68 |