| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:143001407-143001621 | Common:3; Rare:81 | ||||
| chr3:146544537-146544858 | Common:4; Rare:75 | ||||
| chr3:149129545-149129711 | Common:1; Rare:69; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149377628-149377776 | Common:1; Rare:37 | ||||
| chr3:150603162-150603342 | Common:2; Rare:68 | ||||
| chr3:152268721-152268958 | Rare:93 | ||||
| chr3:156674376-156674635 | Common:3; Rare:73 | ||||
| chr3:157160145-157160285 | Rare:57 | ||||
| chr3:158105755-158105872 | Common:5; Rare:61; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:160399213-160399353 | Rare:43; Clinvar:2 | ||||
| chr3:169773347-169773405 | Rare:16 | ||||
| chr3:172711051-172711350 | Common:1; Rare:78 | ||||
| chr3:179604620-179604827 | Common:1; Rare:70 | ||||
| chr3:180989659-180989793 | Rare:57; Clinvar:1 | ||||
| chr3:184298947-184299279 | Common:3; Rare:102 |