| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111911970-111912158 | Common:3; Rare:35 | ||||
| chr11:111912611-111912813 | Common:1; Rare:44 | ||||
| chr11:111913128-111913281 | Rare:44 | ||||
| chr11:111926956-111927347 | Common:10; Rare:73 | ||||
| chr11:111937115-111937217 | Common:5; Rare:39 | ||||
| chr11:111977097-111977350 | Common:4; Rare:55 | ||||
| chr11:112025328-112025464 | Rare:30; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:112073954-112074349 | Common:2; Rare:87 | ||||
| chr11:112086710-112086928 | Rare:95; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr11:112167260-112167398 | Common:1; Rare:39 | ||||
| chr11:112226314-112226691 | Common:1; Rare:154; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr11:112961239-112961463 | Rare:105 | ||||
| chr11:113314448-113314930 | Common:4; Rare:165 | ||||
| chr11:113773668-113773847 | Common:1; Rare:56 | ||||
| chr11:113875485-113875815 | Common:4; Rare:123 |