| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:44989428-44989607 | Rare:69 | ||||
| chr13:45120358-45120569 | Common:2; Rare:66 | ||||
| chr13:45341036-45341628 | Common:4; Rare:266 | ||||
| chr13:45418340-45418544 | Rare:61 | ||||
| chr13:45464721-45465039 | Common:1; Rare:80 | ||||
| chr13:46052709-46052795 | Common:1; Rare:23 | ||||
| chr13:46896857-46896950 | Rare:24 | ||||
| chr13:48001246-48001405 | Common:1; Rare:74; Clinvar:3; Clinvar (benign):4 | ||||
| chr13:48037610-48037771 | Rare:68 | ||||
| chr13:48037932-48038124 | Common:5; Rare:54 | ||||
| chr13:48303692-48303890 | Rare:60; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr13:48533038-48533127 | Common:2; Rare:30 | ||||
| chr13:48975786-48975928 | Common:1; Rare:53 | ||||
| chr13:48976426-48976662 | Common:3; Rare:84 | ||||
| chr13:49247807-49247976 | Rare:48 |