| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27356391-27357265 | Common:3; Rare:278 | ||||
| chr2:27369811-27369924 | Rare:44; Clinvar:1 | ||||
| chr2:27370185-27370745 | Common:2; Rare:225 | ||||
| chr2:27371097-27371332 | Common:1; Rare:68 | ||||
| chr2:27379892-27380018 | Common:3; Rare:23 | ||||
| chr2:27380686-27380977 | Common:1; Rare:108; Clinvar:2 | ||||
| chr2:27408804-27409140 | Common:1; Rare:69 | ||||
| chr2:27409475-27409864 | Rare:132 | ||||
| chr2:27428263-27428323 | Common:1; Rare:9 | ||||
| chr2:27428383-27428795 | Common:1; Rare:149 | ||||
| chr2:27428952-27429346 | Common:3; Rare:107 | ||||
| chr2:27489681-27490015 | Common:1; Rare:84; Clinvar (benign):1 | ||||
| chr2:27582771-27583278 | Rare:161 | ||||
| chr2:27628798-27629161 | Common:1; Rare:150 | ||||
| chr2:27663358-27663975 | Common:1; Rare:209 |