| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:11225866-11225991 | Rare:20 | ||||
| chr3:12484375-12484520 | Common:1; Rare:44; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:12664105-12664310 | Common:1; Rare:53; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:14124713-14125160 | Common:4; Rare:131; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178559-14178859 | Common:2; Rare:157; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14402435-14402625 | Rare:47 | ||||
| chr3:14651483-14651833 | Rare:110 | ||||
| chr3:14947233-14947583 | Common:4; Rare:159 | ||||
| chr3:15206073-15206294 | Common:1; Rare:91 | ||||
| chr3:15206441-15206583 | Rare:61 | ||||
| chr3:15427471-15427627 | Common:1; Rare:57 | ||||
| chr3:15601413-15601804 | Common:4; Rare:161; Clinvar:1 | ||||
| chr3:15859777-15860092 | Common:4; Rare:97 | ||||
| chr3:16264845-16265243 | Common:2; Rare:137 | ||||
| chr3:16513511-16513855 | Common:4; Rare:85 |