| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:110264051-110264244 | Common:3; Rare:30 | ||||
| chr13:110312680-110312999 | Common:2; Rare:67 | ||||
| chr13:110313898-110314080 | Common:1; Rare:31 | ||||
| chr13:110441998-110442201 | Common:3; Rare:28 | ||||
| chr13:110447234-110447500 | Common:2; Rare:47 | ||||
| chr13:110448278-110448585 | Common:1; Rare:51 | ||||
| chr13:110473276-110473470 | Common:1; Rare:32 | ||||
| chr13:110485597-110485756 | Common:2; Rare:44; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr13:110508169-110508355 | Rare:36; Clinvar:1 | ||||
| chr13:110527444-110527694 | Common:2; Rare:58 | ||||
| chr13:110555848-110556033 | Common:2; Rare:33 | ||||
| chr13:110560695-110560845 | Common:2; Rare:28 | ||||
| chr13:110716364-110716397 | Rare:8 | ||||
| chr13:110716416-110716438 | Rare:4 | ||||
| chr13:110716444-110716452 | Rare:1 |