| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:164841192-164841523 | Rare:95 | ||||
| chr2:164841762-164841870 | Rare:26 | ||||
| chr2:164841873-164841888 | Rare:5 | ||||
| chr2:165794116-165794323 | Common:2; Rare:59; Clinvar:6; Clinvar (benign):1 | ||||
| chr2:168456578-168456616 | Rare:11 | ||||
| chr2:169479368-169479547 | Common:3; Rare:66; Clinvar (benign):1 | ||||
| chr2:169584321-169584640 | Common:1; Rare:123 | ||||
| chr2:169584703-169584816 | Rare:30 | ||||
| chr2:169694333-169694597 | Common:5; Rare:92 | ||||
| chr2:170928929-170929331 | Common:4; Rare:122 | ||||
| chr2:171160292-171160560 | Rare:99 | ||||
| chr2:171433906-171434234 | Common:3; Rare:85 | ||||
| chr2:171434736-171434839 | Common:1; Rare:22 | ||||
| chr2:171687964-171688019 | Common:1; Rare:10 | ||||
| chr2:171894210-171894584 | Common:2; Rare:138; Clinvar:1 |