| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:119057048-119057466 | Common:3; Rare:159 | ||||
| chr11:123062123-123062367 | Rare:90 | ||||
| chr11:124673712-124673947 | Common:5; Rare:68 | ||||
| chr11:125592524-125592904 | Common:6; Rare:124 | ||||
| chr11:125625639-125625731 | Rare:27 | ||||
| chr11:125625875-125625990 | Rare:38 | ||||
| chr11:125887468-125887737 | Common:2; Rare:83 | ||||
| chr11:126211641-126211804 | Rare:75 | ||||
| chr11:126268805-126269207 | Common:2; Rare:157; Clinvar:2; Clinvar (benign):4 | ||||
| chr11:126355548-126355747 | Rare:48 | ||||
| chr11:130448341-130448668 | Rare:78 | ||||
| chr11:134253298-134253586 | Common:2; Rare:94; Clinvar (benign):1 | ||||
| chr12:2877051-2877260 | Rare:63 | ||||
| chr12:2890700-2890938 | Common:1; Rare:96 | ||||
| chr12:4538443-4538930 | Common:3; Rare:110 |