| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:72223594-72223644 | Rare:6 | ||||
| chr11:72223684-72223995 | Rare:77 | ||||
| chr11:72224023-72224267 | Common:3; Rare:64 | ||||
| chr11:72224737-72224875 | Rare:38 | ||||
| chr11:72225078-72225176 | Common:1; Rare:15 | ||||
| chr11:72225500-72225836 | Common:1; Rare:72 | ||||
| chr11:72434148-72434388 | Rare:95; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:72434404-72434861 | Common:4; Rare:123; Clinvar (benign):1 | ||||
| chr11:72752251-72752653 | Common:3; Rare:103 | ||||
| chr11:72752672-72752796 | Rare:17 | ||||
| chr11:72780981-72781078 | Rare:26 | ||||
| chr11:72781153-72781419 | Rare:70 | ||||
| chr11:72781465-72781610 | Rare:26 | ||||
| chr11:72781652-72782035 | Common:1; Rare:103 | ||||
| chr11:72782323-72782470 | Common:1; Rare:18 |