| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:45727116-45727307 | Common:3; Rare:73 | ||||
| chr10:45972352-45972634 | Common:2; Rare:90 | ||||
| chr10:46030530-46030746 | Common:1; Rare:68 | ||||
| chr10:46398234-46398389 | Common:3; Rare:57 | ||||
| chr10:48306407-48306731 | Common:2; Rare:132 | ||||
| chr10:49941915-49942134 | Rare:69 | ||||
| chr10:50067822-50067999 | Common:4; Rare:81 | ||||
| chr10:50623209-50623512 | Common:2; Rare:70 | ||||
| chr10:50623872-50624084 | Common:1; Rare:84 | ||||
| chr10:50624861-50624977 | Common:1; Rare:45 | ||||
| chr10:50625163-50625256 | Common:1; Rare:27 | ||||
| chr10:50739910-50739982 | Rare:14 | ||||
| chr10:51074382-51074524 | Rare:22 | ||||
| chr10:52771583-52771852 | Common:3; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:56361214-56361518 | Common:7; Rare:114 |