| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:123062069-123062336 | Common:3; Rare:112 | ||||
| chr11:124673715-124673940 | Common:4; Rare:66 | ||||
| chr11:125569254-125569523 | Common:1; Rare:82 | ||||
| chr11:125592513-125592918 | Common:6; Rare:133 | ||||
| chr11:125625864-125626003 | Rare:45 | ||||
| chr11:126211644-126211812 | Rare:78 | ||||
| chr11:126268814-126269132 | Common:1; Rare:116; Clinvar:1 | ||||
| chr11:126303984-126304083 | Rare:56 | ||||
| chr11:126355521-126355771 | Common:2; Rare:72 | ||||
| chr11:130069624-130069990 | Common:2; Rare:131 | ||||
| chr11:130448465-130448647 | Rare:46 | ||||
| chr11:131911303-131911486 | Common:1; Rare:68 | ||||
| chr11:134223930-134224127 | Common:2; Rare:57 | ||||
| chr11:134253290-134253586 | Common:2; Rare:101; Clinvar (benign):1 | ||||
| chr12:389249-389371 | Rare:45 |