| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:27620005-27620054 | Rare:13 | ||||
| chr13:27620443-27620907 | Common:3; Rare:152 | ||||
| chr13:27621613-27621970 | Common:7; Rare:148; Clinvar:5; Clinvar (benign):6 | ||||
| chr13:27919816-27920043 | Common:2; Rare:61 | ||||
| chr13:28137919-28138602 | Common:7; Rare:180 | ||||
| chr13:28138786-28138898 | Rare:21 | ||||
| chr13:28139030-28139341 | Common:1; Rare:83 | ||||
| chr13:28495110-28495358 | Common:1; Rare:72 | ||||
| chr13:28658864-28659394 | Common:3; Rare:177; Clinvar (pathogenic):1 | ||||
| chr13:28659486-28659859 | Common:1; Rare:91 | ||||
| chr13:28718632-28719218 | Common:3; Rare:148 | ||||
| chr13:29594793-29595220 | Common:2; Rare:104 | ||||
| chr13:29595436-29595914 | Common:3; Rare:152 | ||||
| chr13:29850242-29850480 | Common:3; Rare:69 | ||||
| chr13:29850544-29850707 | Common:1; Rare:71 |