| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:176002214-176002420 | Common:4; Rare:86 | ||||
| chr2:176116616-176116797 | Rare:41 | ||||
| chr2:176129581-176129748 | Rare:91 | ||||
| chr2:176188524-176188668 | Common:1; Rare:51 | ||||
| chr2:177212416-177212857 | Common:4; Rare:172 | ||||
| chr2:177263528-177263849 | Common:2; Rare:84 | ||||
| chr2:177264533-177264874 | Common:2; Rare:99 | ||||
| chr2:177392672-177392823 | Rare:43; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:178451090-178451365 | Common:6; Rare:82; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:178478538-178478659 | Common:1; Rare:35 | ||||
| chr2:179264508-179264857 | Common:4; Rare:130 | ||||
| chr2:181891665-181892267 | Common:6; Rare:234 | ||||
| chr2:182716204-182716328 | Rare:48 | ||||
| chr2:186485994-186486360 | Common:3; Rare:106 | ||||
| chr2:186589857-186590034 | Rare:47 |