| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:125903099-125903221 | Common:1; Rare:23 | ||||
| chr11:126062820-126062934 | Common:2; Rare:35 | ||||
| chr11:126062946-126062994 | Rare:18 | ||||
| chr11:126062999-126063045 | Rare:19 | ||||
| chr11:126211347-126211448 | Common:1; Rare:32 | ||||
| chr11:126211546-126211856 | Rare:143 | ||||
| chr11:126212007-126212036 | Rare:6 | ||||
| chr11:126212038-126212095 | Rare:14 | ||||
| chr11:126268318-126268471 | Rare:35 | ||||
| chr11:126268508-126268668 | Common:2; Rare:44 | ||||
| chr11:126268731-126269286 | Common:2; Rare:225; Clinvar:4; Clinvar (benign):7 | ||||
| chr11:126269370-126269679 | Common:1; Rare:68 | ||||
| chr11:126282927-126283078 | Common:2; Rare:39 | ||||
| chr11:126283234-126283337 | Common:1; Rare:29 | ||||
| chr11:126283442-126283601 | Common:1; Rare:29 |