| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:175168311-175168570 | Common:1; Rare:66 | ||||
| chr2:175181654-175181767 | Common:3; Rare:48 | ||||
| chr2:176002225-176002414 | Common:3; Rare:82 | ||||
| chr2:176188529-176188668 | Common:1; Rare:51 | ||||
| chr2:176269378-176269470 | Common:1; Rare:30 | ||||
| chr2:177212426-177212809 | Common:4; Rare:154 | ||||
| chr2:177263410-177263651 | Common:1; Rare:52 | ||||
| chr2:177264563-177264863 | Common:2; Rare:88 | ||||
| chr2:177392672-177393029 | Common:2; Rare:130; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:177552750-177552841 | Common:1; Rare:32 | ||||
| chr2:178450731-178450902 | Rare:60 | ||||
| chr2:178451090-178451378 | Common:6; Rare:85; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:179264503-179264886 | Common:4; Rare:141 | ||||
| chr2:180980287-180980545 | Common:1; Rare:85 | ||||
| chr2:181891635-181892269 | Common:6; Rare:249 |