| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:45120379-45120560 | Common:2; Rare:59 | ||||
| chr13:45341040-45341617 | Common:4; Rare:259 | ||||
| chr13:46052627-46052821 | Common:2; Rare:49 | ||||
| chr13:46182151-46182422 | Common:3; Rare:47 | ||||
| chr13:46211801-46212030 | Common:2; Rare:71 | ||||
| chr13:46387207-46387352 | Rare:35 | ||||
| chr13:46552994-46553304 | Common:2; Rare:98 | ||||
| chr13:48001178-48001405 | Common:1; Rare:105; Clinvar:5; Clinvar (benign):11 | ||||
| chr13:48037607-48037767 | Rare:69 | ||||
| chr13:48037938-48038116 | Common:5; Rare:49 | ||||
| chr13:48233046-48233475 | Common:5; Rare:147 | ||||
| chr13:48303656-48303880 | Rare:74; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr13:48533038-48533110 | Common:2; Rare:23 | ||||
| chr13:48975599-48975937 | Common:2; Rare:107 | ||||
| chr13:48976531-48976828 | Common:1; Rare:87 |