| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:113875512-113875793 | Common:4; Rare:107 | ||||
| chr11:114296280-114296549 | Rare:51 | ||||
| chr11:114400456-114400713 | Common:2; Rare:109 | ||||
| chr11:117199023-117199435 | Common:6; Rare:129 | ||||
| chr11:119018281-119018538 | Common:8; Rare:110 | ||||
| chr11:119018640-119018795 | Common:5; Rare:68 | ||||
| chr11:119057099-119057437 | Common:3; Rare:133 | ||||
| chr11:121292615-121292798 | Rare:61; Clinvar:3 | ||||
| chr11:126211645-126211809 | Rare:76 | ||||
| chr11:126268829-126269154 | Common:1; Rare:116; Clinvar:1 | ||||
| chr11:131911348-131911460 | Common:1; Rare:46 | ||||
| chr11:134253306-134253572 | Common:2; Rare:84; Clinvar (benign):1 | ||||
| chr12:389261-389340 | Rare:28 | ||||
| chr12:6493793-6494093 | Common:2; Rare:94 | ||||
| chr12:6970648-6970952 | Common:3; Rare:95 |