| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:12664040-12664274 | Common:2; Rare:62; Clinvar:1; Clinvar (benign):5 | ||||
| chr3:13420222-13420458 | Common:1; Rare:68 | ||||
| chr3:13480060-13480339 | Common:1; Rare:66 | ||||
| chr3:14124723-14125099 | Common:4; Rare:110; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178532-14178863 | Common:2; Rare:172; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14402284-14402722 | Common:2; Rare:107 | ||||
| chr3:14651486-14651833 | Rare:108 | ||||
| chr3:14947170-14947559 | Common:5; Rare:165 | ||||
| chr3:14948024-14948208 | Rare:81 | ||||
| chr3:14948354-14948637 | Common:2; Rare:76 | ||||
| chr3:15032500-15032794 | Rare:67 | ||||
| chr3:15065184-15065186 | |||||
| chr3:15206015-15206279 | Rare:97 | ||||
| chr3:15427460-15427640 | Common:1; Rare:65 | ||||
| chr3:15601473-15601816 | Common:4; Rare:144; Clinvar:2 |