| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:100969212-100969556 | Common:3; Rare:87 | ||||
| chr10:100987090-100987599 | Common:1; Rare:185; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:100999668-100999946 | Common:1; Rare:81 | ||||
| chr10:101031102-101031533 | Common:1; Rare:98 | ||||
| chr10:101588127-101588335 | Rare:89 | ||||
| chr10:101817909-101817977 | Common:1; Rare:22 | ||||
| chr10:101818065-101818762 | Common:1; Rare:202 | ||||
| chr10:102056089-102056368 | Common:1; Rare:67 | ||||
| chr10:102114944-102115128 | Common:2; Rare:54 | ||||
| chr10:102120448-102120565 | Common:1; Rare:43 | ||||
| chr10:102394315-102394582 | Common:1; Rare:72 | ||||
| chr10:102395553-102395729 | Common:1; Rare:49 | ||||
| chr10:102396104-102396291 | Rare:58; Clinvar (benign):1 | ||||
| chr10:102421483-102421597 | Rare:37 | ||||
| chr10:102432544-102432835 | Common:2; Rare:86 |