| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:121834987-121835231 | Common:3; Rare:81; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122383192-122383323 | Common:1; Rare:41 | ||||
| chr3:122384054-122384247 | Rare:72 | ||||
| chr3:122416039-122416233 | Common:1; Rare:61 | ||||
| chr3:122514848-122515015 | Common:2; Rare:49 | ||||
| chr3:122564252-122564436 | Common:2; Rare:57 | ||||
| chr3:122793762-122793948 | Common:3; Rare:50 | ||||
| chr3:123201838-123201970 | Common:1; Rare:42 | ||||
| chr3:123585035-123585317 | Common:1; Rare:85 | ||||
| chr3:123585489-123585582 | Rare:16 | ||||
| chr3:123700957-123701352 | Rare:75; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:124730340-124730487 | Common:3; Rare:84; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:125375120-125375391 | Rare:69 | ||||
| chr3:125520120-125520307 | Rare:72 | ||||
| chr3:126704071-126704302 | Common:2; Rare:76 |