| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:124876417-124876735 | Common:1; Rare:64; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:124953941-124954241 | Common:5; Rare:83 | ||||
| chr11:125111675-125112004 | Common:3; Rare:70 | ||||
| chr11:125164494-125164759 | Rare:50 | ||||
| chr11:125495397-125495528 | Common:4; Rare:53 | ||||
| chr11:125495539-125495612 | Rare:20 | ||||
| chr11:125495869-125496456 | Common:2; Rare:104 | ||||
| chr11:125569269-125569575 | Common:2; Rare:86 | ||||
| chr11:125592569-125592963 | Common:6; Rare:124; Clinvar (benign):1 | ||||
| chr11:125625574-125625773 | Common:1; Rare:55 | ||||
| chr11:125625861-125626594 | Common:3; Rare:214 | ||||
| chr11:125887467-125887764 | Common:2; Rare:97 | ||||
| chr11:125903167-125903354 | Rare:47 | ||||
| chr11:125904215-125904534 | Common:1; Rare:95 | ||||
| chr11:126062802-126063037 | Common:3; Rare:83 |