| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:44107430-44107785 | Common:3; Rare:113 | ||||
| chr7:44107802-44108093 | Common:3; Rare:99; Clinvar (pathogenic):1 | ||||
| chr7:44467579-44467861 | Common:3; Rare:50 | ||||
| chr7:44986592-44986766 | Common:2; Rare:87 | ||||
| chr7:45768887-45769121 | Common:3; Rare:67 | ||||
| chr7:64463692-64463876 | Common:1; Rare:50 | ||||
| chr7:65081205-65081416 | Common:3; Rare:72 | ||||
| chr7:65750910-65751089 | Common:2; Rare:75 | ||||
| chr7:65770719-65770936 | Common:6; Rare:69 | ||||
| chr7:66493509-66493737 | Common:4; Rare:95 | ||||
| chr7:66592295-66592578 | Common:2; Rare:93 | ||||
| chr7:66654296-66654568 | Common:2; Rare:85 | ||||
| chr7:66731310-66731432 | Common:1; Rare:23 | ||||
| chr7:66844894-66845065 | Common:2; Rare:72 | ||||
| chr7:67302391-67302696 | Common:5; Rare:98 |