| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:183124250-183124470 | Common:4; Rare:75 | ||||
| chr2:186485987-186486457 | Common:3; Rare:136 | ||||
| chr2:186589894-186590355 | Rare:141 | ||||
| chr2:187554306-187554657 | Common:2; Rare:64 | ||||
| chr2:188291672-188291780 | Common:1; Rare:18 | ||||
| chr2:188291838-188292083 | Common:4; Rare:84 | ||||
| chr2:188292556-188292869 | Common:2; Rare:71 | ||||
| chr2:189441102-189441529 | Common:2; Rare:136 | ||||
| chr2:189580736-189581059 | Common:2; Rare:103; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:189783965-189784112 | Common:3; Rare:54; Clinvar (benign):1 | ||||
| chr2:189784271-189784537 | Common:4; Rare:97; Clinvar:8; Clinvar (benign):2 | ||||
| chr2:190343860-190344038 | Rare:35 | ||||
| chr2:190469378-190469499 | Rare:18 | ||||
| chr2:190534696-190534879 | Common:1; Rare:59 | ||||
| chr2:190648469-190648935 | Common:6; Rare:154 |