| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:46553432-46553598 | Common:1; Rare:53 | ||||
| chr13:46797103-46797337 | Common:3; Rare:79 | ||||
| chr13:48001267-48001383 | Common:1; Rare:55; Clinvar:3; Clinvar (benign):2 | ||||
| chr13:48037668-48037789 | Common:1; Rare:64 | ||||
| chr13:48095053-48095120 | Rare:41 | ||||
| chr13:48233060-48233475 | Common:3; Rare:144 | ||||
| chr13:48303664-48304011 | Common:1; Rare:119; Clinvar:12; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr13:48476317-48476497 | Rare:21 | ||||
| chr13:48492611-48492743 | Rare:34 | ||||
| chr13:48492774-48493026 | Common:2; Rare:40 | ||||
| chr13:48533044-48533110 | Common:2; Rare:20 | ||||
| chr13:48975659-48976051 | Common:2; Rare:116 | ||||
| chr13:48976147-48976249 | Rare:29 | ||||
| chr13:48976540-48976845 | Common:1; Rare:87 | ||||
| chr13:49247830-49248035 | Rare:60 |