| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:15206057-15206269 | Rare:82 | ||||
| chr3:15427505-15427623 | Rare:39 | ||||
| chr3:15601509-15601790 | Common:4; Rare:117; Clinvar:1 | ||||
| chr3:15601831-15602010 | Common:1; Rare:91; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr3:15795951-15796131 | Common:2; Rare:27 | ||||
| chr3:16264921-16265243 | Common:2; Rare:92 | ||||
| chr3:16512862-16513026 | Common:1; Rare:33 | ||||
| chr3:16513492-16513873 | Common:4; Rare:95 | ||||
| chr3:17742596-17742963 | Common:4; Rare:129 | ||||
| chr3:19946953-19947427 | Common:6; Rare:176 | ||||
| chr3:20186161-20186485 | Common:3; Rare:105 | ||||
| chr3:23916973-23917181 | Rare:72 | ||||
| chr3:25790012-25790126 | Common:4; Rare:44 | ||||
| chr3:28349015-28349157 | Common:1; Rare:41 | ||||
| chr3:31981634-31981808 | Common:1; Rare:44 |