| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:58267088-58267173 | Rare:17 | ||||
| chr10:58384213-58384393 | Common:3; Rare:27 | ||||
| chr10:59880951-59881214 | Common:4; Rare:46 | ||||
| chr10:59885547-59885785 | Rare:44 | ||||
| chr10:59904926-59905399 | Common:2; Rare:83 | ||||
| chr10:59905735-59905861 | Rare:30 | ||||
| chr10:59908511-59908730 | Common:1; Rare:46 | ||||
| chr10:60074025-60074090 | Rare:21; Clinvar:1 | ||||
| chr10:60074114-60074273 | Rare:46; Clinvar:3 | ||||
| chr10:60074314-60074624 | Common:1; Rare:63; Clinvar:3 | ||||
| chr10:60074732-60074847 | Common:1; Rare:30; Clinvar:4; Clinvar (benign):1 | ||||
| chr10:60236944-60237216 | Common:1; Rare:56 | ||||
| chr10:61286713-61286979 | Common:2; Rare:49 | ||||
| chr10:61867897-61868021 | Common:1; Rare:29 | ||||
| chr10:61896981-61897343 | Common:2; Rare:74 |