| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:44490589-44490723 | Common:1; Rare:53 | ||||
| chr7:44573881-44574078 | Common:3; Rare:62 | ||||
| chr7:44582169-44582542 | Common:1; Rare:142 | ||||
| chr7:44606428-44606652 | Common:1; Rare:74 | ||||
| chr7:44748307-44748591 | Common:2; Rare:69 | ||||
| chr7:44796389-44796790 | Common:3; Rare:155 | ||||
| chr7:44999613-44999747 | Common:2; Rare:53 | ||||
| chr7:45111672-45111818 | Common:1; Rare:56 | ||||
| chr7:45921264-45921411 | Rare:40 | ||||
| chr7:47539586-47539839 | Common:2; Rare:48 | ||||
| chr7:47979507-47979707 | Rare:81 | ||||
| chr7:48089004-48089269 | Common:4; Rare:64 | ||||
| chr7:50450306-50450432 | Common:1; Rare:51 | ||||
| chr7:56051434-56051845 | Common:1; Rare:158; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:56064236-56064356 | Rare:85 |