| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:27504126-27504351 | Rare:119; Clinvar:4; Clinvar (benign):1 | ||||
| chr10:30349336-30349421 | Common:9; Rare:25 | ||||
| chr10:31319005-31319258 | Common:2; Rare:73 | ||||
| chr10:31319825-31320135 | Common:2; Rare:113 | ||||
| chr10:31928769-31928892 | Common:2; Rare:51 | ||||
| chr10:32056368-32056587 | Common:2; Rare:87 | ||||
| chr10:32378716-32378854 | Rare:21 | ||||
| chr10:32446014-32446239 | Common:1; Rare:105 | ||||
| chr10:32958151-32958537 | Common:3; Rare:147 | ||||
| chr10:35090314-35090670 | Rare:107 | ||||
| chr10:35126639-35127001 | Common:3; Rare:115 | ||||
| chr10:35642276-35642460 | Common:2; Rare:63 | ||||
| chr10:37857586-37857726 | Common:2; Rare:55 | ||||
| chr10:38010639-38010756 | Common:1; Rare:56 | ||||
| chr10:42782684-42782833 | Rare:40 |