| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:30594709-30594950 | Common:4; Rare:109; Clinvar:6; Clinvar (benign):7 | ||||
| chr7:32495247-32495617 | Common:1; Rare:93 | ||||
| chr7:33062704-33062955 | Common:3; Rare:104 | ||||
| chr7:33129234-33129570 | Common:5; Rare:94 | ||||
| chr7:35800725-35801252 | Common:2; Rare:200 | ||||
| chr7:37916689-37917068 | Common:2; Rare:97 | ||||
| chr7:39566306-39566450 | Common:1; Rare:71 | ||||
| chr7:39623503-39623763 | Rare:86 | ||||
| chr7:40134581-40135020 | Rare:138; Clinvar:1 | ||||
| chr7:41703060-41703268 | Common:1; Rare:28 | ||||
| chr7:42932137-42932470 | Rare:133 | ||||
| chr7:43729451-43729567 | Common:1; Rare:39 | ||||
| chr7:43869481-43869605 | Rare:40 | ||||
| chr7:43926382-43926498 | Rare:36 | ||||
| chr7:44104626-44104915 | Common:1; Rare:94 |