| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:122793682-122793937 | Common:4; Rare:73 | ||||
| chr3:122794928-122795069 | Rare:50 | ||||
| chr3:123201703-123202020 | Common:2; Rare:94 | ||||
| chr3:123585043-123585300 | Common:1; Rare:78 | ||||
| chr3:123585491-123585598 | Rare:19 | ||||
| chr3:124730340-124730485 | Common:3; Rare:83; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:125375218-125375409 | Rare:53 | ||||
| chr3:125520170-125520291 | Rare:32 | ||||
| chr3:126083990-126084212 | Common:2; Rare:73 | ||||
| chr3:127598212-127598458 | Common:3; Rare:73 | ||||
| chr3:127672805-127673011 | Common:3; Rare:99 | ||||
| chr3:128052149-128052539 | Common:3; Rare:132 | ||||
| chr3:128123921-128124199 | Common:1; Rare:75 | ||||
| chr3:128153365-128153483 | Rare:32 | ||||
| chr3:128725979-128726255 | Common:1; Rare:90; Clinvar:3; Clinvar (benign):1 |