| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:27270644-27270880 | Common:1; Rare:86 | ||||
| chr13:27424437-27424742 | Common:5; Rare:103 | ||||
| chr13:27450025-27450367 | Common:3; Rare:109 | ||||
| chr13:27450369-27450768 | Common:4; Rare:143 | ||||
| chr13:27619993-27620044 | Rare:11 | ||||
| chr13:27620426-27620865 | Common:3; Rare:145 | ||||
| chr13:27621620-27621972 | Common:7; Rare:146; Clinvar:5; Clinvar (benign):6 | ||||
| chr13:27919822-27920056 | Common:3; Rare:66 | ||||
| chr13:28100515-28100717 | Common:2; Rare:47 | ||||
| chr13:28137954-28138385 | Common:4; Rare:112 | ||||
| chr13:28139033-28139340 | Common:1; Rare:82 | ||||
| chr13:28495102-28495365 | Common:1; Rare:76 | ||||
| chr13:28659031-28659218 | Common:1; Rare:85; Clinvar (pathogenic):1 | ||||
| chr13:28718665-28718848 | Common:2; Rare:47 | ||||
| chr13:28718909-28719200 | Common:1; Rare:74 |