| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27380553-27380887 | Common:2; Rare:126; Clinvar:6 | ||||
| chr2:27489673-27489953 | Rare:70; Clinvar (benign):1 | ||||
| chr2:27582965-27583112 | Rare:54 | ||||
| chr2:27628954-27629073 | Common:1; Rare:57 | ||||
| chr2:27663358-27663469 | Rare:30 | ||||
| chr2:27663491-27663911 | Rare:141 | ||||
| chr2:27771652-27772009 | Common:1; Rare:109 | ||||
| chr2:27890348-27890836 | Common:1; Rare:136 | ||||
| chr2:28751694-28752175 | Common:2; Rare:202 | ||||
| chr2:28870267-28870454 | Rare:70 | ||||
| chr2:30146600-30147023 | Common:5; Rare:134 | ||||
| chr2:31138035-31138270 | Common:3; Rare:62 | ||||
| chr2:31234009-31234164 | Rare:39 | ||||
| chr2:32011020-32011125 | Rare:35 | ||||
| chr2:32039282-32039908 | Rare:186 |