| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:36510236-36510377 | Rare:40 | ||||
| chr11:36594349-36594646 | Common:2; Rare:52 | ||||
| chr11:43311758-43312064 | Common:2; Rare:99 | ||||
| chr11:43358779-43359260 | Rare:191 | ||||
| chr11:43644168-43644256 | Rare:15 | ||||
| chr11:43880686-43880965 | Common:2; Rare:72 | ||||
| chr11:44726426-44726471 | Rare:12 | ||||
| chr11:45917816-45918190 | Common:1; Rare:97; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:45918792-45918897 | Rare:33 | ||||
| chr11:46380733-46381310 | Common:5; Rare:142 | ||||
| chr11:46381967-46382139 | Common:1; Rare:67 | ||||
| chr11:46594001-46594133 | Common:2; Rare:28 | ||||
| chr11:46617119-46617585 | Common:5; Rare:131 | ||||
| chr11:46700562-46700818 | Common:1; Rare:65 | ||||
| chr11:46846149-46846449 | Common:1; Rare:96 |