| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:157159843-157160295 | Common:1; Rare:170 | ||||
| chr3:158110338-158110387 | Common:1; Rare:13 | ||||
| chr3:158644246-158644653 | Common:6; Rare:117; Clinvar (benign):6 | ||||
| chr3:158672528-158672722 | Common:2; Rare:53 | ||||
| chr3:158801997-158802170 | Common:2; Rare:81 | ||||
| chr3:159764303-159764589 | Common:1; Rare:81 | ||||
| chr3:160399175-160399317 | Rare:39; Clinvar:2 | ||||
| chr3:160399520-160399669 | Rare:30 | ||||
| chr3:160565284-160565842 | Common:3; Rare:187 | ||||
| chr3:160755453-160755666 | Common:1; Rare:80 | ||||
| chr3:167734804-167735226 | Common:3; Rare:140; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735611-167735721 | Rare:26 | ||||
| chr3:168094782-168094992 | Common:1; Rare:38 | ||||
| chr3:169773331-169773424 | Rare:29 | ||||
| chr3:169966706-169966858 | Rare:65 |