| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:123062397-123062666 | Common:4; Rare:124 | ||||
| chr11:124673715-124673935 | Common:4; Rare:65 | ||||
| chr11:124762251-124762416 | Rare:44 | ||||
| chr11:124800406-124800466 | Rare:20 | ||||
| chr11:124897797-124897885 | Common:2; Rare:16 | ||||
| chr11:124953989-124954135 | Common:3; Rare:42 | ||||
| chr11:125495435-125495536 | Common:4; Rare:42 | ||||
| chr11:125592489-125592913 | Common:6; Rare:140 | ||||
| chr11:125625871-125625935 | Rare:24 | ||||
| chr11:125887480-125887737 | Common:2; Rare:82 | ||||
| chr11:126211641-126211809 | Rare:77 | ||||
| chr11:126268756-126269207 | Common:2; Rare:175; Clinvar:2; Clinvar (benign):4 | ||||
| chr11:126283013-126283134 | Common:1; Rare:49 | ||||
| chr11:126303877-126304104 | Rare:101 | ||||
| chr11:126355504-126355771 | Common:2; Rare:77 |