| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:231464138-231464272 | Rare:42 | ||||
| chr2:231464399-231465071 | Common:4; Rare:216 | ||||
| chr2:231483121-231483186 | Common:1; Rare:12 | ||||
| chr2:231706399-231706708 | Common:2; Rare:75 | ||||
| chr2:231706794-231707042 | Rare:59 | ||||
| chr2:231707329-231707620 | Rare:80 | ||||
| chr2:231707676-231707845 | Common:1; Rare:58 | ||||
| chr2:231708329-231708571 | Rare:96 | ||||
| chr2:231710227-231710518 | Common:3; Rare:154 | ||||
| chr2:231781191-231781769 | Common:4; Rare:168 | ||||
| chr2:231782026-231782197 | Rare:38 | ||||
| chr2:231786172-231786535 | Common:3; Rare:104 | ||||
| chr2:231960913-231961274 | Common:3; Rare:61 | ||||
| chr2:231961376-231961565 | Common:1; Rare:30 | ||||
| chr2:231961569-231961860 | Common:1; Rare:95; Clinvar:4 |