| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:70170410-70170826 | Common:4; Rare:118 | ||||
| chr10:70233259-70234180 | Common:10; Rare:229; Clinvar (benign):1 | ||||
| chr10:70381888-70382093 | Common:1; Rare:44 | ||||
| chr10:70382515-70382902 | Common:5; Rare:143 | ||||
| chr10:70403907-70404272 | Common:1; Rare:124 | ||||
| chr10:70404688-70404793 | Common:3; Rare:33 | ||||
| chr10:70478293-70478422 | Rare:37 | ||||
| chr10:70478439-70478580 | Common:1; Rare:34 | ||||
| chr10:70478627-70479030 | Common:1; Rare:132 | ||||
| chr10:70815813-70816127 | Rare:106 | ||||
| chr10:70816157-70816748 | Common:1; Rare:114 | ||||
| chr10:70887868-70888176 | Common:1; Rare:60 | ||||
| chr10:70888193-70888383 | Common:3; Rare:38 | ||||
| chr10:70888423-70888752 | Common:2; Rare:93; Clinvar:5; Clinvar (benign):2 | ||||
| chr10:71212352-71212797 | Common:2; Rare:127 |