| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:6401633-6401925 | Common:1; Rare:66 | ||||
| chr7:6447778-6448081 | Common:2; Rare:124 | ||||
| chr7:6483966-6483999 | Rare:6 | ||||
| chr7:6484071-6484449 | Common:2; Rare:140 | ||||
| chr7:6577335-6577513 | Common:1; Rare:63 | ||||
| chr7:6706895-6707016 | Rare:61 | ||||
| chr7:7968592-7968803 | Common:2; Rare:70 | ||||
| chr7:10940017-10940224 | Common:1; Rare:97; Clinvar (benign):3 | ||||
| chr7:16645508-16646189 | Common:3; Rare:244 | ||||
| chr7:17299154-17299264 | Rare:41 | ||||
| chr7:17940322-17940384 | Rare:22 | ||||
| chr7:19116729-19116914 | Rare:48; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr7:19117627-19117934 | Common:1; Rare:69 | ||||
| chr7:19708784-19708902 | Rare:40 | ||||
| chr7:20330557-20330719 | Common:2; Rare:35 |