| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:21176405-21176709 | Common:2; Rare:133 | ||||
| chr13:23889338-23889484 | Common:1; Rare:55 | ||||
| chr13:24512739-24512844 | Common:3; Rare:31 | ||||
| chr13:24922790-24922974 | Rare:50; Clinvar:1 | ||||
| chr13:25301492-25301714 | Common:1; Rare:83 | ||||
| chr13:26221798-26221983 | Rare:57 | ||||
| chr13:27251245-27251632 | Common:6; Rare:118 | ||||
| chr13:27424514-27424726 | Common:2; Rare:68 | ||||
| chr13:27450529-27450685 | Common:2; Rare:58 | ||||
| chr13:28658902-28659187 | Common:1; Rare:114; Clinvar (pathogenic):1 | ||||
| chr13:30306808-30307197 | Common:7; Rare:103 | ||||
| chr13:30307372-30307583 | Common:2; Rare:76 | ||||
| chr13:30617748-30618000 | Common:1; Rare:86 | ||||
| chr13:33285703-33285913 | Rare:49 | ||||
| chr13:35855656-35855715 | Rare:12 |