| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:51982851-51982986 | Rare:27 | ||||
| chr3:51983012-51983561 | Common:2; Rare:124 | ||||
| chr3:51995820-51996010 | Common:2; Rare:73 | ||||
| chr3:52154304-52154558 | Common:3; Rare:84; Clinvar (benign):1 | ||||
| chr3:52154691-52155059 | Common:4; Rare:81 | ||||
| chr3:52197881-52198263 | Common:1; Rare:126 | ||||
| chr3:52225593-52225871 | Rare:54 | ||||
| chr3:52239031-52239366 | Common:2; Rare:99 | ||||
| chr3:52239572-52239675 | Rare:23 | ||||
| chr3:52245338-52245500 | Rare:16 | ||||
| chr3:52245647-52245806 | Common:1; Rare:48 | ||||
| chr3:52246086-52246147 | Rare:9 | ||||
| chr3:52277686-52277840 | Common:1; Rare:44 | ||||
| chr3:52278108-52278246 | Common:1; Rare:31 | ||||
| chr3:52278344-52278469 | Rare:54 |