| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:17643866-17644253 | Common:2; Rare:118 | ||||
| chr10:18651571-18651732 | Common:1; Rare:66 | ||||
| chr10:18659254-18659362 | Common:1; Rare:38 | ||||
| chr10:21533955-21534280 | Common:2; Rare:117 | ||||
| chr10:22316282-22316438 | Rare:65 | ||||
| chr10:25016451-25016640 | Common:4; Rare:68 | ||||
| chr10:25016971-25017034 | Common:2; Rare:20 | ||||
| chr10:26438051-26438208 | Common:1; Rare:41 | ||||
| chr10:26438242-26438439 | Common:1; Rare:41 | ||||
| chr10:26697605-26697775 | Common:1; Rare:47; Clinvar (benign):1 | ||||
| chr10:26860801-26861316 | Common:6; Rare:147 | ||||
| chr10:27100483-27100578 | Common:2; Rare:30; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:27154323-27154486 | Rare:45 | ||||
| chr10:27155194-27155412 | Common:6; Rare:91; Clinvar:3; Clinvar (benign):6 | ||||
| chr10:27240571-27240646 | Common:2; Rare:20 |