| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:99010933-99011088 | Common:1; Rare:30 | ||||
| chr7:99017244-99017482 | Rare:46 | ||||
| chr7:99031612-99031684 | Rare:13 | ||||
| chr7:99033129-99033273 | Common:1; Rare:38 | ||||
| chr7:99037159-99037316 | Common:1; Rare:39 | ||||
| chr7:99038293-99038438 | Rare:50 | ||||
| chr7:99041323-99041394 | Rare:23 | ||||
| chr7:99126090-99126375 | Common:1; Rare:49 | ||||
| chr7:99273273-99273448 | Common:2; Rare:46 | ||||
| chr7:99403413-99403662 | Rare:58 | ||||
| chr7:99650087-99650347 | Rare:67 | ||||
| chr7:99665367-99665720 | Rare:44 | ||||
| chr7:99667031-99667132 | Rare:24 | ||||
| chr7:99979370-99979408 | Rare:10 | ||||
| chr7:99980613-99980766 | Rare:26 |