| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:176002229-176002416 | Common:3; Rare:81 | ||||
| chr2:176002766-176002939 | Common:1; Rare:20 | ||||
| chr2:176116596-176116789 | Common:2; Rare:41 | ||||
| chr2:176117051-176117369 | Rare:112; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:176122260-176122343 | Rare:25 | ||||
| chr2:176129586-176129747 | Rare:88 | ||||
| chr2:176130492-176130776 | Common:2; Rare:157 | ||||
| chr2:176136072-176136236 | Rare:52 | ||||
| chr2:176188501-176188678 | Common:1; Rare:69 | ||||
| chr2:176188956-176189081 | Common:2; Rare:38 | ||||
| chr2:176269317-176269596 | Common:2; Rare:97 | ||||
| chr2:177212526-177212835 | Common:3; Rare:127 | ||||
| chr2:177213153-177213295 | Rare:63 | ||||
| chr2:177231989-177232033 | Rare:6 | ||||
| chr2:177263432-177263687 | Common:1; Rare:61 |