| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:175181450-175181834 | Common:6; Rare:122 | ||||
| chr2:176002207-176002416 | Common:4; Rare:88 | ||||
| chr2:176269350-176269530 | Common:1; Rare:72 | ||||
| chr2:177212365-177212821 | Common:5; Rare:181 | ||||
| chr2:177213160-177213295 | Rare:60 | ||||
| chr2:177263402-177263736 | Common:2; Rare:78 | ||||
| chr2:177264589-177264905 | Common:2; Rare:92 | ||||
| chr2:177392627-177392876 | Common:1; Rare:84; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:177552761-177553068 | Common:4; Rare:94 | ||||
| chr2:177618699-177619018 | Common:7; Rare:89 | ||||
| chr2:178194322-178194651 | Common:2; Rare:97 | ||||
| chr2:178450698-178450897 | Common:1; Rare:68 | ||||
| chr2:178451081-178451387 | Common:6; Rare:89; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:178478515-178478659 | Common:1; Rare:45 | ||||
| chr2:179050034-179050169 | Rare:31 |