| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:51453026-51453372 | Rare:130 | ||||
| chr13:51804110-51804199 | Common:2; Rare:30 | ||||
| chr13:52012090-52012418 | Common:2; Rare:108; Clinvar:1 | ||||
| chr13:52159559-52159726 | Common:1; Rare:26 | ||||
| chr13:52455344-52455507 | Common:3; Rare:53 | ||||
| chr13:52652626-52652929 | Common:3; Rare:97 | ||||
| chr13:60163887-60164055 | Common:1; Rare:40 | ||||
| chr13:60397171-60397372 | Common:4; Rare:73 | ||||
| chr13:72727600-72727938 | Common:4; Rare:121 | ||||
| chr13:72781853-72782261 | Common:1; Rare:147 | ||||
| chr13:75636013-75636353 | Common:2; Rare:81 | ||||
| chr13:76992038-76992181 | Rare:68; Clinvar:9; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr13:77027137-77027293 | Common:5; Rare:49 | ||||
| chr13:77918692-77918975 | Common:2; Rare:61 | ||||
| chr13:77919397-77919592 | Common:1; Rare:73; Clinvar:1; Clinvar (benign):1 |