| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:186485704-186485851 | Rare:20 | ||||
| chr2:186485862-186486370 | Common:3; Rare:133 | ||||
| chr2:186589712-186589791 | Rare:19 | ||||
| chr2:186589823-186590164 | Rare:107 | ||||
| chr2:186590251-186590372 | Rare:41 | ||||
| chr2:186693922-186694063 | Rare:62 | ||||
| chr2:187448225-187448407 | Rare:28 | ||||
| chr2:189440920-189441185 | Common:2; Rare:77 | ||||
| chr2:189441362-189441784 | Common:3; Rare:152 | ||||
| chr2:189674434-189674547 | Common:1; Rare:30 | ||||
| chr2:189674554-189674806 | Common:2; Rare:56 | ||||
| chr2:189762446-189762958 | Rare:151 | ||||
| chr2:189763134-189763262 | Common:1; Rare:22 | ||||
| chr2:189783524-189783578 | Rare:10 | ||||
| chr2:189783896-189784222 | Common:5; Rare:105; Clinvar:1; Clinvar (benign):2 |