| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:171434692-171434806 | Rare:30 | ||||
| chr2:171522244-171522538 | Common:3; Rare:72 | ||||
| chr2:171687343-171687579 | Common:2; Rare:39 | ||||
| chr2:171687691-171687960 | Rare:77 | ||||
| chr2:171688103-171688311 | Common:1; Rare:46 | ||||
| chr2:171894211-171894326 | Rare:56; Clinvar:1 | ||||
| chr2:171922249-171922689 | Common:1; Rare:142 | ||||
| chr2:171999818-172000020 | Common:1; Rare:80 | ||||
| chr2:172102901-172103053 | Common:1; Rare:37 | ||||
| chr2:172427106-172427474 | Common:6; Rare:75 | ||||
| chr2:172427500-172427801 | Common:4; Rare:82; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:172487756-172488227 | Common:2; Rare:117; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:172555520-172555687 | Common:1; Rare:39 | ||||
| chr2:172555848-172556223 | Common:3; Rare:149 | ||||
| chr2:172927906-172928180 | Common:2; Rare:39 |