| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:93496396-93496728 | Common:4; Rare:86 | ||||
| chr10:93702384-93702726 | Common:5; Rare:109 | ||||
| chr10:93893912-93894063 | Rare:66 | ||||
| chr10:94362858-94363059 | Common:3; Rare:84 | ||||
| chr10:94402302-94402502 | Rare:54 | ||||
| chr10:94545695-94545892 | Common:4; Rare:68 | ||||
| chr10:95290911-95291133 | Common:2; Rare:84 | ||||
| chr10:95656623-95656909 | Common:1; Rare:83; Clinvar:6; Clinvar (benign):2 | ||||
| chr10:95907741-95907967 | Common:3; Rare:67 | ||||
| chr10:96044073-96044421 | Common:2; Rare:98 | ||||
| chr10:96129555-96129737 | Common:1; Rare:46 | ||||
| chr10:96129946-96130327 | Common:4; Rare:135 | ||||
| chr10:96130459-96130657 | Rare:54 | ||||
| chr10:96831983-96832319 | Rare:128 | ||||
| chr10:97401263-97401469 | Rare:76 |