| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27890639-27890829 | Rare:55 | ||||
| chr2:28392626-28392917 | Rare:104 | ||||
| chr2:28751704-28752134 | Common:2; Rare:178 | ||||
| chr2:28870238-28870447 | Rare:92 | ||||
| chr2:30146855-30147028 | Common:2; Rare:52 | ||||
| chr2:31414635-31414957 | Common:2; Rare:67; Clinvar (benign):1 | ||||
| chr2:32039751-32039854 | Rare:32 | ||||
| chr2:32165743-32165918 | Common:1; Rare:69 | ||||
| chr2:32627945-32628139 | Rare:63 | ||||
| chr2:33599222-33599434 | Common:1; Rare:80 | ||||
| chr2:36966575-36966803 | Common:2; Rare:87 | ||||
| chr2:37084262-37084558 | Common:4; Rare:108 | ||||
| chr2:37231451-37231726 | Common:5; Rare:142; Clinvar (benign):4 | ||||
| chr2:37279852-37280162 | Common:2; Rare:82 | ||||
| chr2:37324714-37325091 | Common:1; Rare:135 |