| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:48304119-48304213 | Common:2; Rare:18 | ||||
| chr13:48411924-48412034 | Rare:37; Clinvar (pathogenic):1 | ||||
| chr13:48412366-48412404 | Rare:13 | ||||
| chr13:48492528-48492695 | Common:1; Rare:44 | ||||
| chr13:48532605-48532928 | Common:4; Rare:115 | ||||
| chr13:48532992-48533223 | Common:2; Rare:74 | ||||
| chr13:48975515-48976306 | Common:2; Rare:223 | ||||
| chr13:48976326-48976821 | Common:3; Rare:148 | ||||
| chr13:49110181-49110386 | Common:3; Rare:69 | ||||
| chr13:49110706-49110878 | Rare:37 | ||||
| chr13:49247820-49247996 | Rare:56 | ||||
| chr13:49248173-49248227 | Common:1; Rare:13 | ||||
| chr13:49248450-49248673 | Rare:39 | ||||
| chr13:49443876-49444385 | Common:2; Rare:161 | ||||
| chr13:49445125-49445285 | Common:2; Rare:34 |