| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:124762287-124762422 | Rare:33 | ||||
| chr11:124800406-124800466 | Rare:20 | ||||
| chr11:124954015-124954213 | Common:4; Rare:51 | ||||
| chr11:125063152-125063344 | Common:3; Rare:59 | ||||
| chr11:125164551-125164768 | Rare:38 | ||||
| chr11:125592506-125592932 | Common:6; Rare:138 | ||||
| chr11:125625864-125625962 | Rare:34 | ||||
| chr11:125887454-125887727 | Common:2; Rare:83 | ||||
| chr11:125903179-125903354 | Rare:44 | ||||
| chr11:126211623-126211819 | Rare:90 | ||||
| chr11:126266188-126266491 | Rare:104 | ||||
| chr11:126268793-126269192 | Common:1; Rare:154; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:126304008-126304081 | Rare:38 | ||||
| chr11:126355545-126355778 | Rare:62 | ||||
| chr11:130069624-130069970 | Common:2; Rare:127 |