| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:46052374-46052511 | Rare:37 | ||||
| chr13:46052594-46052908 | Common:17; Rare:473 | ||||
| chr13:46052921-46053324 | Common:2; Rare:133 | ||||
| chr13:46181700-46182080 | Common:3; Rare:95 | ||||
| chr13:46182115-46182571 | Common:15; Rare:261 | ||||
| chr13:46211003-46211403 | Common:8; Rare:92 | ||||
| chr13:46211680-46212100 | Common:11; Rare:505 | ||||
| chr13:46438110-46438470 | Common:2; Rare:96 | ||||
| chr13:46552889-46553299 | Common:9; Rare:356 | ||||
| chr13:46553546-46553946 | Common:2; Rare:114 | ||||
| chr13:46796427-46796827 | Common:4; Rare:185 | ||||
| chr13:46797007-46797430 | Common:17; Rare:514 | ||||
| chr13:46797721-46798121 | Rare:81 | ||||
| chr13:48001160-48001560 | Common:9; Rare:450; Clinvar:16; Clinvar (benign):29 | ||||
| chr13:48036912-48038240 | Common:61; Rare:1561; Clinvar:8 |