| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:8457590-8457730 | Common:1; Rare:37 | ||||
| chr5:96340344-96340573 | Rare:44 | ||||
| chr5:150778671-150778863 | Rare:74 | ||||
| chr5:159100325-159100526 | Common:3; Rare:62 | ||||
| chr5:180831560-180831679 | Common:2; Rare:51 | ||||
| chr5:181207514-181207751 | Common:5; Rare:64 | ||||
| chr6:57961366-57961653 | Common:2; Rare:83 | ||||
| chr6:85678729-85678971 | Rare:81 | ||||
| chr6:129478393-129478721 | Common:3; Rare:77; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:16989939-16990250 | Common:2; Rare:63 | ||||
| chr7:39733327-39733602 | Common:2; Rare:53 | ||||
| chr7:45768945-45769158 | Common:2; Rare:68 | ||||
| chr7:65750922-65751074 | Common:2; Rare:55 | ||||
| chr7:66493512-66493734 | Common:4; Rare:94 | ||||
| chr7:66592328-66592449 | Common:2; Rare:43 |