| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:16645707-16645976 | Rare:90 | ||||
| chr7:22822783-22822936 | Common:2; Rare:58 | ||||
| chr7:23531964-23532083 | Rare:49 | ||||
| chr7:26201426-26201805 | Common:2; Rare:184 | ||||
| chr7:27740092-27740199 | Common:3; Rare:29 | ||||
| chr7:30594761-30594914 | Common:1; Rare:74; Clinvar:4; Clinvar (benign):3 | ||||
| chr7:32495281-32495548 | Rare:64 | ||||
| chr7:33062741-33062905 | Common:3; Rare:71 | ||||
| chr7:35800936-35801255 | Common:2; Rare:134 | ||||
| chr7:39623547-39623752 | Rare:74 | ||||
| chr7:40134842-40135016 | Rare:62; Clinvar:1 | ||||
| chr7:41703069-41703270 | Common:1; Rare:28 | ||||
| chr7:42932151-42932389 | Rare:88 | ||||
| chr7:43869475-43869663 | Rare:60 | ||||
| chr7:44796565-44796721 | Common:2; Rare:76 |