| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:27155170-27155395 | Common:4; Rare:83; Clinvar:5; Clinvar (benign):4 | ||||
| chr10:27240342-27240596 | Rare:75 | ||||
| chr10:27240605-27240897 | Common:2; Rare:77 | ||||
| chr10:27241837-27242241 | Common:2; Rare:139 | ||||
| chr10:28532515-28532909 | Common:4; Rare:154 | ||||
| chr10:28533002-28533214 | Rare:83 | ||||
| chr10:28677245-28677537 | Common:6; Rare:133 | ||||
| chr10:29735787-29735984 | Common:3; Rare:38 | ||||
| chr10:30059501-30059636 | Common:1; Rare:48 | ||||
| chr10:30434056-30434222 | Common:1; Rare:35 | ||||
| chr10:31031838-31032037 | Common:1; Rare:77 | ||||
| chr10:31318233-31318888 | Common:6; Rare:166 | ||||
| chr10:31319022-31319256 | Common:2; Rare:70 | ||||
| chr10:31928714-31928913 | Common:3; Rare:79 | ||||
| chr10:32378684-32378895 | Common:1; Rare:26 |