| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:34105493-34105724 | Common:2; Rare:76 | ||||
| chr11:34438774-34439028 | Common:2; Rare:87; Clinvar (benign):1 | ||||
| chr11:34916292-34916719 | Common:11; Rare:174; Clinvar:7; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr11:36510229-36510372 | Rare:43 | ||||
| chr11:43358885-43358983 | Rare:54 | ||||
| chr11:43880752-43880863 | Common:1; Rare:20 | ||||
| chr11:46120951-46121294 | Common:2; Rare:55 | ||||
| chr11:46617173-46617590 | Common:5; Rare:117 | ||||
| chr11:46700553-46700839 | Common:1; Rare:74 | ||||
| chr11:46700944-46701059 | Common:1; Rare:36 | ||||
| chr11:46846235-46846414 | Common:1; Rare:50 | ||||
| chr11:47176846-47177131 | Common:1; Rare:116 | ||||
| chr11:47185360-47185608 | Common:2; Rare:51 | ||||
| chr11:47214814-47215011 | Common:1; Rare:47 | ||||
| chr11:47248785-47248938 | Rare:61 |