| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:21670946-21671170 | Common:1; Rare:81; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:23579179-23579400 | Common:5; Rare:77 | ||||
| chr13:23889294-23889619 | Common:1; Rare:107 | ||||
| chr13:23979690-23979850 | Common:2; Rare:38 | ||||
| chr13:24160577-24160771 | Rare:59 | ||||
| chr13:24512739-24512849 | Common:3; Rare:33 | ||||
| chr13:24922795-24923082 | Common:2; Rare:92; Clinvar:1 | ||||
| chr13:25172139-25172308 | Rare:20 | ||||
| chr13:25287362-25287584 | Common:2; Rare:66 | ||||
| chr13:25301250-25301706 | Common:2; Rare:132 | ||||
| chr13:26221787-26221932 | Rare:36 | ||||
| chr13:26557472-26557781 | Common:4; Rare:125 | ||||
| chr13:27251245-27251617 | Common:6; Rare:112 | ||||
| chr13:27424509-27424753 | Common:2; Rare:83 | ||||
| chr13:27450119-27450214 | Common:3; Rare:28 |