| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:7787950-7788222 | Common:1; Rare:113 | ||||
| chr10:7818372-7818520 | Common:1; Rare:30 | ||||
| chr10:12195817-12196241 | Rare:115 | ||||
| chr10:14837987-14838355 | Common:2; Rare:100 | ||||
| chr10:14878657-14878886 | Common:2; Rare:66 | ||||
| chr10:15860455-15860572 | Rare:34 | ||||
| chr10:16817358-16817678 | Common:4; Rare:110 | ||||
| chr10:18651578-18651730 | Common:1; Rare:60 | ||||
| chr10:27154321-27154474 | Rare:42 | ||||
| chr10:27155227-27155386 | Common:3; Rare:56; Clinvar:2; Clinvar (benign):3 | ||||
| chr10:31319042-31319230 | Common:2; Rare:58 | ||||
| chr10:32958151-32958527 | Common:2; Rare:142 | ||||
| chr10:35090323-35090388 | Rare:16 | ||||
| chr10:35126671-35126978 | Common:3; Rare:92 | ||||
| chr10:35127053-35127131 | Rare:29 |