| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:17228954-17229026 | Common:1; Rare:20 | ||||
| chr10:17643894-17644279 | Common:2; Rare:114 | ||||
| chr10:18651570-18651693 | Common:1; Rare:47 | ||||
| chr10:24208746-24209184 | Common:2; Rare:125 | ||||
| chr10:27154315-27154486 | Rare:46 | ||||
| chr10:27155165-27155412 | Common:6; Rare:101; Clinvar:5; Clinvar (benign):6 | ||||
| chr10:27240478-27240675 | Common:2; Rare:59 | ||||
| chr10:27242058-27242217 | Common:1; Rare:67 | ||||
| chr10:28532515-28532890 | Common:4; Rare:148 | ||||
| chr10:28533021-28533160 | Rare:46 | ||||
| chr10:29735768-29735944 | Common:2; Rare:31 | ||||
| chr10:29736688-29736717 | Rare:3 | ||||
| chr10:30059491-30059651 | Common:1; Rare:61 | ||||
| chr10:31031820-31032039 | Common:2; Rare:82 | ||||
| chr10:31318302-31318552 | Common:3; Rare:58 |