| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:48037513-48037789 | Common:1; Rare:114 | ||||
| chr13:48037914-48038116 | Common:5; Rare:63 | ||||
| chr13:48233064-48233227 | Common:1; Rare:55 | ||||
| chr13:48303665-48303918 | Rare:84; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr13:48975785-48975930 | Common:1; Rare:54 | ||||
| chr13:48976544-48976662 | Common:1; Rare:41 | ||||
| chr13:49110228-49110387 | Common:2; Rare:43 | ||||
| chr13:49247807-49247976 | Rare:48 | ||||
| chr13:49248314-49248337 | Rare:6 | ||||
| chr13:49401216-49401549 | Common:2; Rare:64 | ||||
| chr13:49444005-49444484 | Common:1; Rare:153 | ||||
| chr13:49495942-49496041 | Rare:27 | ||||
| chr13:49585527-49585628 | Common:1; Rare:31 | ||||
| chr13:49628395-49628484 | Common:1; Rare:19 | ||||
| chr13:49691267-49691563 | Common:2; Rare:106 |