| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:30464274-30464367 | Rare:26 | ||||
| chr13:30464482-30464670 | Common:3; Rare:68 | ||||
| chr13:30464680-30464994 | Common:3; Rare:107 | ||||
| chr13:30465045-30465157 | Rare:23 | ||||
| chr13:30465651-30465706 | Rare:10 | ||||
| chr13:30465739-30466432 | Common:3; Rare:189 | ||||
| chr13:30616947-30617280 | Rare:70 | ||||
| chr13:30617315-30617724 | Rare:125 | ||||
| chr13:30617726-30618018 | Common:1; Rare:95 | ||||
| chr13:31161774-31162050 | Rare:125 | ||||
| chr13:31162422-31162695 | Common:1; Rare:78 | ||||
| chr13:31199849-31200057 | Common:1; Rare:80 | ||||
| chr13:31200270-31200636 | Common:2; Rare:103 | ||||
| chr13:32031009-32031168 | Rare:33 | ||||
| chr13:32314992-32315292 | Common:1; Rare:52; Clinvar (benign):1 |