| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:124792154-124792207 | Rare:11 | ||||
| chr10:124801638-124801902 | Rare:86 | ||||
| chr10:124802207-124802315 | Rare:28 | ||||
| chr10:125158565-125158678 | Common:1; Rare:37 | ||||
| chr10:125158714-125158891 | Rare:48 | ||||
| chr10:125159350-125159516 | Common:1; Rare:67 | ||||
| chr10:125160187-125160347 | Common:1; Rare:53 | ||||
| chr10:125160458-125160769 | Common:1; Rare:43 | ||||
| chr10:125160848-125160963 | Rare:33 | ||||
| chr10:125160965-125161332 | Common:4; Rare:133 | ||||
| chr10:125161348-125161664 | Common:1; Rare:88 | ||||
| chr10:125719076-125719283 | Common:1; Rare:40 | ||||
| chr10:125719369-125719815 | Common:1; Rare:163 | ||||
| chr10:125823184-125823625 | Common:2; Rare:159; Clinvar:1; Clinvar (benign):2 | ||||
| chr10:125896409-125896608 | Common:3; Rare:12 |