| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:147423303-147423470 | Rare:45 | ||||
| chr3:147939937-147940054 | Common:1; Rare:21 | ||||
| chr3:148079206-148079453 | Rare:40 | ||||
| chr3:149971786-149971811 | Rare:6 | ||||
| chr3:150408869-150409002 | Rare:40 | ||||
| chr3:156817011-156817088 | Rare:25 | ||||
| chr3:157089114-157089280 | Rare:68 | ||||
| chr3:157174851-157175253 | Common:3; Rare:174 | ||||
| chr3:165192661-165192788 | Common:1; Rare:22 | ||||
| chr3:168249318-168249693 | Common:2; Rare:81 | ||||
| chr3:169619269-169619385 | Rare:30 | ||||
| chr3:169764995-169765258 | Common:1; Rare:102; Clinvar:7; Clinvar (pathogenic):3 | ||||
| chr3:179230181-179230263 | Rare:11 | ||||
| chr3:181056616-181056719 | Common:1; Rare:10 | ||||
| chr3:181417799-181417987 | Rare:20 |