| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:30322944-30323179 | Common:2; Rare:68 | ||||
| chr11:31509600-31509787 | Common:1; Rare:56 | ||||
| chr11:32091424-32091449 | Rare:7 | ||||
| chr11:33161440-33161657 | Common:6; Rare:58 | ||||
| chr11:33257122-33257427 | Common:3; Rare:98 | ||||
| chr11:33257466-33257732 | Common:1; Rare:62 | ||||
| chr11:33722721-33722844 | Common:1; Rare:22 | ||||
| chr11:33736375-33736605 | Common:2; Rare:72 | ||||
| chr11:34052145-34052523 | Common:4; Rare:173 | ||||
| chr11:34438812-34439016 | Common:2; Rare:69; Clinvar (benign):1 | ||||
| chr11:34916292-34916669 | Common:10; Rare:154; Clinvar:5; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35943969-35944110 | Common:2; Rare:46 | ||||
| chr11:36510236-36510377 | Rare:40 | ||||
| chr11:43358813-43358979 | Rare:79 | ||||
| chr11:44066183-44066349 | Common:1; Rare:44 |