| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:124896593-124896937 | Common:4; Rare:94 | ||||
| chr11:124897136-124897422 | Common:4; Rare:74; Clinvar (pathogenic):1 | ||||
| chr11:124897764-124898050 | Common:4; Rare:71 | ||||
| chr11:124935972-124936121 | Common:2; Rare:35; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:124936294-124936473 | Rare:31 | ||||
| chr11:124953980-124954144 | Common:3; Rare:48 | ||||
| chr11:125063144-125063314 | Common:2; Rare:46 | ||||
| chr11:125496178-125496466 | Rare:64 | ||||
| chr11:125592451-125592917 | Common:6; Rare:158 | ||||
| chr11:125625871-125625959 | Rare:32 | ||||
| chr11:125887495-125887727 | Common:2; Rare:72 | ||||
| chr11:126062712-126063037 | Common:7; Rare:109 | ||||
| chr11:126211623-126211822 | Rare:92 | ||||
| chr11:126266023-126266184 | Common:1; Rare:60 | ||||
| chr11:126266219-126266491 | Rare:92 |