| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:100343158-100343341 | Common:4; Rare:32 | ||||
| chr10:100347944-100348162 | Rare:68 | ||||
| chr10:100373391-100373710 | Common:2; Rare:69 | ||||
| chr10:100373984-100374258 | Rare:48 | ||||
| chr10:100381060-100381267 | Common:1; Rare:35 | ||||
| chr10:100566142-100566364 | Common:1; Rare:42 | ||||
| chr10:101201277-101201337 | Common:1; Rare:7 | ||||
| chr10:101694597-101694657 | Common:2; Rare:22; Clinvar:2; Clinvar (benign):3 | ||||
| chr10:101781492-101781772 | Rare:57 | ||||
| chr10:102109015-102109037 | Rare:6 | ||||
| chr10:102119625-102119918 | Common:1; Rare:53 | ||||
| chr10:102121352-102121695 | Common:1; Rare:51 | ||||
| chr10:102449504-102449958 | Common:6; Rare:94 | ||||
| chr10:102643510-102643689 | Common:1; Rare:44 | ||||
| chr10:107913678-107913943 | Common:3; Rare:92 |