| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:176116603-176116789 | Common:2; Rare:40 | ||||
| chr2:176188524-176188668 | Common:1; Rare:51 | ||||
| chr2:177212414-177212802 | Common:4; Rare:159 | ||||
| chr2:177392672-177393059 | Common:2; Rare:136; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:178451090-178451310 | Common:5; Rare:68; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:178478504-178478662 | Common:1; Rare:49 | ||||
| chr2:180980284-180980545 | Common:1; Rare:85 | ||||
| chr2:181891627-181892036 | Common:4; Rare:172 | ||||
| chr2:183124252-183124464 | Common:4; Rare:71 | ||||
| chr2:186486118-186486354 | Common:3; Rare:79 | ||||
| chr2:186590265-186590437 | Rare:69 | ||||
| chr2:188293005-188293064 | Rare:7 | ||||
| chr2:189179701-189179838 | Rare:15; Clinvar:1 | ||||
| chr2:189441172-189441529 | Common:2; Rare:112 | ||||
| chr2:189783979-189784104 | Common:2; Rare:43; Clinvar (benign):1 |