| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:37861580-37862120 | Common:3; Rare:189 | ||||
| chr3:37990623-37990842 | Common:2; Rare:69 | ||||
| chr3:37998923-37999240 | Common:10; Rare:256 | ||||
| chr3:38024350-38024716 | Common:3; Rare:324 | ||||
| chr3:38024840-38025351 | Common:15; Rare:268 | ||||
| chr3:38136937-38137609 | Common:3; Rare:439 | ||||
| chr3:38138524-38138779 | Common:6; Rare:187; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr3:38139178-38139595 | Rare:115 | ||||
| chr3:38164727-38165270 | Common:3; Rare:254 | ||||
| chr3:38165354-38165865 | Common:4; Rare:358 | ||||
| chr3:38346485-38347014 | Common:3; Rare:220 | ||||
| chr3:38453701-38454028 | Common:2; Rare:198 | ||||
| chr3:38454234-38454607 | Common:2; Rare:193 | ||||
| chr3:38496192-38496757 | Common:3; Rare:425 | ||||
| chr3:38649626-38649914 | Common:8; Rare:157 |