| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:231681060-231681363 | Rare:80 | ||||
| chr2:231687317-231687614 | Rare:69 | ||||
| chr2:231739079-231739479 | Rare:136 | ||||
| chr2:231745544-231746081 | Common:3; Rare:108 | ||||
| chr2:232259940-232260420 | Common:3; Rare:90 | ||||
| chr2:232282070-232282974 | Common:7; Rare:261 | ||||
| chr2:232667982-232668382 | Common:5; Rare:88 | ||||
| chr2:232669069-232669469 | Common:1; Rare:81 | ||||
| chr2:232902104-232902504 | Common:4; Rare:129 | ||||
| chr2:233716796-233717196 | Common:6; Rare:84 | ||||
| chr2:233767495-233767895 | Common:6; Rare:111; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr2:233768153-233768325 | Rare:50; Clinvar:9; Clinvar (pathogenic):1 | ||||
| chr2:234335227-234335627 | Common:1; Rare:100 | ||||
| chr2:234363250-234363650 | Common:6; Rare:80 | ||||
| chr2:234366810-234367268 | Common:12; Rare:157 |