| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:123083125-123083453 | Common:2; Rare:55 | ||||
| chr11:124673704-124673932 | Common:4; Rare:72 | ||||
| chr11:124762251-124762413 | Rare:44 | ||||
| chr11:124800406-124800457 | Rare:17 | ||||
| chr11:125063164-125063305 | Common:2; Rare:40 | ||||
| chr11:125592543-125592900 | Common:6; Rare:117 | ||||
| chr11:126211623-126211809 | Rare:85 | ||||
| chr11:126265364-126265541 | Rare:45 | ||||
| chr11:126268775-126269192 | Common:1; Rare:160; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:126283024-126283131 | Rare:43 | ||||
| chr11:126303967-126304069 | Rare:58 | ||||
| chr11:128522251-128522559 | Common:1; Rare:93 | ||||
| chr11:128692795-128692978 | Rare:45 | ||||
| chr11:129895535-129895661 | Common:2; Rare:46 | ||||
| chr11:130002818-130003033 | Common:1; Rare:43 |