| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:177552680-177552855 | Common:3; Rare:140 | ||||
| chr2:177552910-177553240 | Common:9; Rare:159 | ||||
| chr2:177618633-177618809 | Common:3; Rare:171 | ||||
| chr2:177618838-177619050 | Common:8; Rare:99 | ||||
| chr2:178072667-178072994 | Common:2; Rare:187 | ||||
| chr2:178073060-178073430 | Rare:93 | ||||
| chr2:178112288-178112687 | Common:2; Rare:122 | ||||
| chr2:178194268-178194656 | Common:4; Rare:249 | ||||
| chr2:178450608-178450981 | Common:3; Rare:280; Clinvar:1 | ||||
| chr2:178451031-178451438 | Common:23; Rare:348; Clinvar:13; Clinvar (benign):12 | ||||
| chr2:178478510-178478808 | Common:3; Rare:186 | ||||
| chr2:178480153-178480573 | Common:7; Rare:287 | ||||
| chr2:178481005-178481261 | Common:2; Rare:72 | ||||
| chr2:179263733-179264384 | Common:11; Rare:256 | ||||
| chr2:179264464-179264717 | Common:2; Rare:131 |