| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:17201023-17201569 | Common:9; Rare:146 | ||||
| chr10:17201670-17201943 | Common:2; Rare:55 | ||||
| chr10:17228090-17228290 | Common:1; Rare:48 | ||||
| chr10:17229043-17229310 | Common:2; Rare:50 | ||||
| chr10:17230180-17231448 | Common:4; Rare:452; Clinvar:2 | ||||
| chr10:17617296-17617539 | Common:4; Rare:85 | ||||
| chr10:17643860-17644309 | Common:2; Rare:140 | ||||
| chr10:18140985-18141429 | Common:6; Rare:177; Clinvar:2; Clinvar (benign):2 | ||||
| chr10:18651543-18651752 | Common:1; Rare:88 | ||||
| chr10:18659132-18659559 | Common:3; Rare:134 | ||||
| chr10:19815680-19815849 | Rare:49 | ||||
| chr10:19816268-19816628 | Common:6; Rare:77 | ||||
| chr10:21145570-21146190 | Common:5; Rare:114 | ||||
| chr10:21174081-21174318 | Rare:71 | ||||
| chr10:21174557-21174957 | Common:9; Rare:99 |