| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:183038228-183038760 | Common:8; Rare:266 | ||||
| chr2:183078601-183078812 | Rare:73 | ||||
| chr2:183124252-183124463 | Common:8; Rare:138 | ||||
| chr2:183124770-183125060 | Common:4; Rare:100 | ||||
| chr2:186485944-186486382 | Common:6; Rare:202 | ||||
| chr2:186589788-186590367 | Rare:278 | ||||
| chr2:187554290-187554525 | Rare:88 | ||||
| chr2:189440990-189441516 | Common:5; Rare:231 | ||||
| chr2:189762540-189762990 | Rare:138 | ||||
| chr2:189763040-189763400 | Common:9; Rare:114 | ||||
| chr2:189783953-189784136 | Common:8; Rare:127; Clinvar:2; Clinvar (benign):4 | ||||
| chr2:189784268-189784564 | Common:6; Rare:170; Clinvar:14; Clinvar (benign):4 | ||||
| chr2:190319749-190319983 | Common:4; Rare:82; Clinvar (benign):4 | ||||
| chr2:190343455-190343719 | Common:4; Rare:116 | ||||
| chr2:190343730-190344260 | Common:6; Rare:227 |