| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:141875961-141876227 | Rare:70 | ||||
| chr3:141876491-141876682 | Common:1; Rare:73 | ||||
| chr3:141876970-141877265 | Common:4; Rare:87 | ||||
| chr3:141921755-141922030 | Common:1; Rare:52 | ||||
| chr3:142028570-142028687 | Common:1; Rare:14 | ||||
| chr3:142149349-142149669 | Common:2; Rare:92 | ||||
| chr3:142225491-142225629 | Common:3; Rare:50 | ||||
| chr3:142429739-142429887 | Rare:30 | ||||
| chr3:142429966-142430079 | Common:1; Rare:17 | ||||
| chr3:142447945-142448145 | Common:1; Rare:74 | ||||
| chr3:142578700-142578976 | Rare:107; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:142596205-142596485 | Common:4; Rare:70 | ||||
| chr3:142656601-142656921 | Common:2; Rare:54 | ||||
| chr3:142888868-142889049 | Common:3; Rare:57 | ||||
| chr3:142963976-142964067 | Common:2; Rare:25 |