| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:123062082-123062295 | Common:3; Rare:86 | ||||
| chr11:123062418-123062666 | Common:4; Rare:116 | ||||
| chr11:123741658-123741799 | Common:1; Rare:36 | ||||
| chr11:124673715-124673935 | Common:4; Rare:65 | ||||
| chr11:124800406-124800485 | Rare:31 | ||||
| chr11:124953989-124954225 | Common:4; Rare:63 | ||||
| chr11:125164607-125164759 | Rare:28 | ||||
| chr11:125496145-125496355 | Rare:55 | ||||
| chr11:125592471-125592904 | Common:6; Rare:147 | ||||
| chr11:125625871-125626008 | Rare:44 | ||||
| chr11:125904288-125904514 | Rare:72 | ||||
| chr11:126211625-126211822 | Rare:92 | ||||
| chr11:126268829-126269209 | Common:2; Rare:144; Clinvar:2; Clinvar (benign):4 | ||||
| chr11:126303989-126304081 | Rare:53 | ||||
| chr11:129895535-129895703 | Common:2; Rare:61 |