| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:30594709-30594949 | Common:4; Rare:107; Clinvar:6; Clinvar (benign):7 | ||||
| chr7:30771280-30771472 | Common:1; Rare:59 | ||||
| chr7:32490273-32490507 | Common:2; Rare:77 | ||||
| chr7:32495247-32495591 | Common:1; Rare:88 | ||||
| chr7:32495894-32495930 | Rare:11 | ||||
| chr7:33062701-33062923 | Common:3; Rare:94 | ||||
| chr7:33063122-33063195 | Rare:21 | ||||
| chr7:33109270-33109651 | Common:2; Rare:113; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:33129346-33129587 | Common:3; Rare:56 | ||||
| chr7:33905304-33905625 | Common:3; Rare:68; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:35253998-35254302 | Common:1; Rare:104 | ||||
| chr7:35254578-35254719 | Rare:25 | ||||
| chr7:35694868-35695216 | Common:3; Rare:87 | ||||
| chr7:35800585-35800694 | Rare:26 | ||||
| chr7:35800940-35801264 | Common:2; Rare:138 |