| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:111120744-111120945 | Common:4; Rare:165 | ||||
| chr2:111122446-111122691 | Common:3; Rare:177 | ||||
| chr2:111884091-111884266 | Rare:97 | ||||
| chr2:112055089-112055299 | Common:3; Rare:49 | ||||
| chr2:112255004-112255161 | Common:2; Rare:129 | ||||
| chr2:112275366-112275654 | Common:2; Rare:194 | ||||
| chr2:112481922-112482294 | Common:3; Rare:221 | ||||
| chr2:112542088-112542517 | Common:4; Rare:268 | ||||
| chr2:112584354-112584659 | Common:2; Rare:166 | ||||
| chr2:112584710-112585030 | Common:1; Rare:94 | ||||
| chr2:112644980-112645570 | Common:1; Rare:151 | ||||
| chr2:112645661-112645984 | Common:4; Rare:234 | ||||
| chr2:112646230-112646388 | Common:3; Rare:102 | ||||
| chr2:112764063-112764267 | Common:2; Rare:64 | ||||
| chr2:112764581-112764859 | Common:3; Rare:152; Clinvar (pathogenic):2 |