| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:13586786-13587095 | Common:3; Rare:110 | ||||
| chr10:14604235-14604685 | Common:7; Rare:176 | ||||
| chr10:14837794-14838412 | Common:4; Rare:202 | ||||
| chr10:14838449-14838549 | Rare:32 | ||||
| chr10:14838591-14839012 | Common:1; Rare:134 | ||||
| chr10:14878210-14878455 | Rare:77 | ||||
| chr10:14878496-14878917 | Common:2; Rare:130 | ||||
| chr10:14879088-14879260 | Common:1; Rare:62 | ||||
| chr10:14879492-14879753 | Rare:69 | ||||
| chr10:14953474-14953921 | Common:4; Rare:117; Clinvar (pathogenic):1 | ||||
| chr10:14953985-14954513 | Common:3; Rare:145 | ||||
| chr10:14959205-14959460 | Common:2; Rare:72 | ||||
| chr10:14959506-14959828 | Common:1; Rare:99 | ||||
| chr10:14959909-14960173 | Common:2; Rare:52 | ||||
| chr10:15088764-15088923 | Common:1; Rare:56 |