| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:90245083-90245243 | Rare:52 | ||||
| chr7:90346596-90346733 | Common:3; Rare:59 | ||||
| chr7:90595855-90596016 | Common:6; Rare:53 | ||||
| chr7:90596256-90596469 | Rare:69 | ||||
| chr7:91880672-91880813 | Common:1; Rare:39 | ||||
| chr7:91940839-91940979 | Common:3; Rare:47; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:92134432-92134899 | Common:5; Rare:136 | ||||
| chr7:92245876-92245974 | Rare:29; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:92246121-92246488 | Common:3; Rare:144 | ||||
| chr7:92528439-92528826 | Common:4; Rare:122; Clinvar:3; Clinvar (benign):2 | ||||
| chr7:92833919-92834089 | Rare:43 | ||||
| chr7:93232138-93232379 | Common:2; Rare:52 | ||||
| chr7:94394632-94394928 | Common:1; Rare:47; Clinvar (benign):1 | ||||
| chr7:94656083-94656374 | Common:2; Rare:76; Clinvar:3; Clinvar (benign):3 | ||||
| chr7:95596162-95596230 | Rare:26 |