| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:168140357-168140689 | Common:3; Rare:69 | ||||
| chr2:169705587-169705631 | Rare:6 | ||||
| chr2:169810854-169811324 | Rare:122 | ||||
| chr2:171752004-171752254 | Common:2; Rare:50 | ||||
| chr2:171766927-171767047 | Common:1; Rare:26 | ||||
| chr2:171772202-171772378 | Common:1; Rare:41 | ||||
| chr2:174429760-174429823 | Rare:12 | ||||
| chr2:175140851-175140996 | Rare:13 | ||||
| chr2:176201071-176201135 | Common:1; Rare:9 | ||||
| chr2:176637544-176637752 | Common:2; Rare:72 | ||||
| chr2:176637886-176638068 | Common:2; Rare:40 | ||||
| chr2:178413862-178413993 | Rare:39 | ||||
| chr2:178437675-178437793 | Rare:22 | ||||
| chr2:178523010-178523253 | Rare:77 | ||||
| chr2:178613029-178613239 | Common:1; Rare:55; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):1 |