| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:16645690-16646122 | Common:2; Rare:150 | ||||
| chr7:17940412-17940595 | Common:2; Rare:90 | ||||
| chr7:20217365-20217815 | Common:1; Rare:97 | ||||
| chr7:22220173-22220345 | Common:2; Rare:31 | ||||
| chr7:23105678-23105858 | Common:2; Rare:100; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:23181891-23182068 | Rare:70 | ||||
| chr7:23470362-23470563 | Rare:60 | ||||
| chr7:23531948-23532093 | Common:1; Rare:58 | ||||
| chr7:24980114-24980324 | Common:4; Rare:89 | ||||
| chr7:25125251-25125443 | Rare:79; Clinvar:3 | ||||
| chr7:26200683-26200948 | Common:1; Rare:142 | ||||
| chr7:26201139-26201464 | Common:1; Rare:130 | ||||
| chr7:26201492-26201554 | Rare:22 | ||||
| chr7:26201570-26201800 | Common:2; Rare:124 | ||||
| chr7:27095933-27096224 | Rare:83 |