| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:174395616-174395911 | Common:4; Rare:184 | ||||
| chr2:174487045-174487409 | Common:4; Rare:162 | ||||
| chr2:175167670-175167840 | Rare:116 | ||||
| chr2:175168058-175168578 | Common:4; Rare:271 | ||||
| chr2:175181561-175181846 | Common:7; Rare:153 | ||||
| chr2:176002229-176002422 | Common:6; Rare:156 | ||||
| chr2:176160370-176160975 | Common:6; Rare:294 | ||||
| chr2:176188501-176188699 | Common:3; Rare:151 | ||||
| chr2:177212365-177212892 | Common:10; Rare:371 | ||||
| chr2:177213045-177213445 | Rare:195 | ||||
| chr2:177263400-177263753 | Common:3; Rare:159 | ||||
| chr2:177264535-177265331 | Common:8; Rare:334 | ||||
| chr2:177392627-177392930 | Common:1; Rare:99; Clinvar:5; Clinvar (benign):2 | ||||
| chr2:177393070-177393320 | Common:1; Rare:97 | ||||
| chr2:177552650-177552890 | Common:2; Rare:125 |