| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:174395605-174395795 | Common:2; Rare:63 | ||||
| chr2:174487037-174487409 | Common:2; Rare:91 | ||||
| chr2:175168122-175168497 | Common:2; Rare:99 | ||||
| chr2:175181629-175181740 | Common:4; Rare:55 | ||||
| chr2:176002232-176002389 | Common:2; Rare:67 | ||||
| chr2:176116593-176116824 | Common:2; Rare:55 | ||||
| chr2:176129586-176129730 | Rare:84 | ||||
| chr2:176130451-176130813 | Common:2; Rare:189 | ||||
| chr2:176188493-176188678 | Common:1; Rare:72 | ||||
| chr2:176188952-176189081 | Common:2; Rare:39 | ||||
| chr2:177212434-177212821 | Common:4; Rare:155 | ||||
| chr2:177263436-177263636 | Common:1; Rare:42 | ||||
| chr2:177264578-177264892 | Common:2; Rare:93 | ||||
| chr2:177392638-177393070 | Common:3; Rare:147; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:177552728-177552855 | Common:1; Rare:50 |