| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:27154332-27154526 | Rare:57 | ||||
| chr10:27155124-27155439 | Common:7; Rare:123; Clinvar:5; Clinvar (benign):7 | ||||
| chr10:27240381-27240529 | Rare:49 | ||||
| chr10:27240560-27240898 | Common:2; Rare:85 | ||||
| chr10:27241846-27242414 | Common:3; Rare:188 | ||||
| chr10:27504022-27504370 | Rare:153; Clinvar:4; Clinvar (benign):1 | ||||
| chr10:27998480-27998820 | Common:1; Rare:83 | ||||
| chr10:27998893-27999166 | Common:3; Rare:67 | ||||
| chr10:28532621-28532832 | Common:1; Rare:89 | ||||
| chr10:28532923-28533137 | Common:1; Rare:71 | ||||
| chr10:28677322-28677581 | Common:4; Rare:120 | ||||
| chr10:29735384-29735524 | Rare:38 | ||||
| chr10:29735780-29735999 | Common:3; Rare:43 | ||||
| chr10:29736933-29737129 | Common:2; Rare:60 | ||||
| chr10:30349220-30349443 | Common:12; Rare:102 |