| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:89327639-89327949 | Common:2; Rare:58 | ||||
| chr10:89414514-89414619 | Common:1; Rare:27 | ||||
| chr10:89644939-89645288 | Common:5; Rare:148 | ||||
| chr10:91163274-91163393 | Common:1; Rare:30 | ||||
| chr10:91410246-91410453 | Common:2; Rare:73 | ||||
| chr10:91798350-91798541 | Common:1; Rare:82 | ||||
| chr10:91923653-91923861 | Common:1; Rare:84 | ||||
| chr10:92291051-92291403 | Common:5; Rare:110 | ||||
| chr10:92573989-92574135 | Common:1; Rare:50 | ||||
| chr10:92592938-92593149 | Common:2; Rare:62 | ||||
| chr10:92689695-92689987 | Common:3; Rare:102 | ||||
| chr10:94362901-94362903 | |||||
| chr10:95290903-95291178 | Common:2; Rare:115 | ||||
| chr10:95693862-95694188 | Common:5; Rare:109; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr10:95907805-95907962 | Common:3; Rare:51 |