| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:45341040-45341617 | Common:4; Rare:259 | ||||
| chr13:45464808-45465247 | Common:1; Rare:128 | ||||
| chr13:46052684-46052859 | Common:2; Rare:49 | ||||
| chr13:46797098-46797305 | Common:3; Rare:75 | ||||
| chr13:48001034-48001060 | Rare:6 | ||||
| chr13:48001265-48001389 | Common:1; Rare:60; Clinvar:3; Clinvar (benign):2 | ||||
| chr13:48037658-48037818 | Common:2; Rare:80; Clinvar:2 | ||||
| chr13:48037956-48038141 | Common:3; Rare:44 | ||||
| chr13:48233097-48233473 | Common:2; Rare:131 | ||||
| chr13:48303674-48303894 | Rare:73; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr13:48975830-48975952 | Rare:45 | ||||
| chr13:48976399-48976837 | Common:3; Rare:137 | ||||
| chr13:49247806-49248115 | Rare:89 | ||||
| chr13:49443955-49444479 | Common:1; Rare:165 | ||||
| chr13:49585485-49585616 | Common:1; Rare:44 |