| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:102502604-102502845 | Rare:75 | ||||
| chr10:102644283-102644547 | Common:1; Rare:74 | ||||
| chr10:102644946-102645163 | Rare:43 | ||||
| chr10:102714271-102714669 | Common:2; Rare:129 | ||||
| chr10:102776078-102776224 | Common:1; Rare:23 | ||||
| chr10:102854061-102854299 | Common:1; Rare:82 | ||||
| chr10:102918112-102918322 | Common:1; Rare:72 | ||||
| chr10:103140216-103140299 | Rare:11 | ||||
| chr10:103193243-103193527 | Common:5; Rare:82; Clinvar (benign):1 | ||||
| chr10:103350930-103351219 | Common:2; Rare:113 | ||||
| chr10:103367873-103367981 | Common:2; Rare:17 | ||||
| chr10:103396411-103396715 | Rare:106 | ||||
| chr10:103452242-103452446 | Rare:64 | ||||
| chr10:103917493-103917854 | Rare:93 | ||||
| chr10:103918120-103918478 | Common:4; Rare:101 |