| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:178450731-178450897 | Rare:56 | ||||
| chr2:178451090-178451363 | Common:6; Rare:82; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:178478538-178478666 | Common:1; Rare:40 | ||||
| chr2:179264508-179264861 | Common:4; Rare:132 | ||||
| chr2:180980274-180980545 | Common:1; Rare:86 | ||||
| chr2:181457210-181458097 | Common:3; Rare:308 | ||||
| chr2:181458103-181458278 | Common:1; Rare:56 | ||||
| chr2:181891871-181892281 | Common:2; Rare:153 | ||||
| chr2:182866474-182866723 | Common:1; Rare:64 | ||||
| chr2:182867158-182867233 | Rare:18 | ||||
| chr2:183124252-183124460 | Common:4; Rare:71 | ||||
| chr2:186485959-186486364 | Common:3; Rare:116 | ||||
| chr2:186589988-186590034 | Rare:9 | ||||
| chr2:186590039-186590455 | Rare:141 | ||||
| chr2:187554314-187554390 | Rare:13 |