| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:14837971-14838415 | Common:4; Rare:132 | ||||
| chr10:14878606-14878914 | Common:2; Rare:98 | ||||
| chr10:14953985-14954198 | Rare:75 | ||||
| chr10:15097293-15097385 | Common:1; Rare:49 | ||||
| chr10:15860455-15860581 | Rare:36 | ||||
| chr10:17228481-17228675 | Common:1; Rare:55 | ||||
| chr10:17228930-17229410 | Common:5; Rare:110 | ||||
| chr10:17230538-17230710 | Rare:74; Clinvar:1 | ||||
| chr10:17643871-17644286 | Common:2; Rare:125 | ||||
| chr10:18340594-18340723 | Common:3; Rare:29; Clinvar (benign):2 | ||||
| chr10:18651571-18651693 | Common:1; Rare:47 | ||||
| chr10:18659221-18659663 | Common:2; Rare:153 | ||||
| chr10:19816263-19816653 | Common:6; Rare:84 | ||||
| chr10:21173769-21173960 | Common:3; Rare:55; Clinvar (benign):1 | ||||
| chr10:21497248-21497410 | Common:1; Rare:33 |