| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:69052216-69052413 | Common:4; Rare:74 | ||||
| chr3:69080342-69080456 | Rare:50 | ||||
| chr3:69084853-69085203 | Common:3; Rare:94 | ||||
| chr3:69542310-69542805 | Common:4; Rare:121 | ||||
| chr3:69866043-69866310 | Rare:52; Clinvar (benign):1 | ||||
| chr3:69936128-69936854 | Common:1; Rare:162; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:69937327-69937732 | Common:1; Rare:76 | ||||
| chr3:72996699-72997071 | Common:2; Rare:135 | ||||
| chr3:76310624-76310777 | Rare:31 | ||||
| chr3:76310805-76311175 | Common:1; Rare:74 | ||||
| chr3:77039964-77040162 | Common:1; Rare:50 | ||||
| chr3:79018988-79019066 | Rare:29 | ||||
| chr3:81761504-81761784 | Common:8; Rare:98; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:87227186-87227404 | Common:1; Rare:74; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:88058186-88058735 | Common:2; Rare:154 |