| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:109265841-109265982 | Common:3; Rare:29 | ||||
| chr13:109266905-109266942 | Rare:9 | ||||
| chr13:109267622-109267664 | Rare:4 | ||||
| chr13:109271689-109271735 | Rare:13 | ||||
| chr13:109412506-109412807 | Rare:70 | ||||
| chr13:109587126-109587267 | Common:1; Rare:28 | ||||
| chr13:109787417-109787528 | Common:1; Rare:39 | ||||
| chr13:109836667-109836989 | Common:1; Rare:67 | ||||
| chr13:110012170-110012471 | Common:3; Rare:46 | ||||
| chr13:110094630-110094975 | Common:2; Rare:81 | ||||
| chr13:110137830-110137896 | Common:1; Rare:10 | ||||
| chr13:110137902-110137950 | Rare:6 | ||||
| chr13:110138369-110138786 | Common:2; Rare:99 | ||||
| chr13:110186317-110186549 | Common:2; Rare:69; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr13:110206274-110206444 | Common:2; Rare:22 |