| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:44999958-45000299 | Common:1; Rare:81 | ||||
| chr7:45111665-45111816 | Common:1; Rare:56 | ||||
| chr7:47979463-47979758 | Rare:116 | ||||
| chr7:48088331-48088662 | Common:2; Rare:77 | ||||
| chr7:48089006-48089369 | Common:5; Rare:91 | ||||
| chr7:48089444-48089571 | Common:2; Rare:30 | ||||
| chr7:50450306-50450453 | Common:1; Rare:59 | ||||
| chr7:55572322-55572632 | Common:1; Rare:111 | ||||
| chr7:56051380-56051941 | Common:1; Rare:200; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:56106393-56106713 | Common:9; Rare:112 | ||||
| chr7:64882432-64882700 | Common:2; Rare:56 | ||||
| chr7:64903119-64903319 | Common:2; Rare:57 | ||||
| chr7:65006633-65006876 | Common:3; Rare:74 | ||||
| chr7:66114767-66114969 | Common:1; Rare:91 | ||||
| chr7:66115183-66115353 | Rare:40 |