| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:33258105-33258380 | Rare:100 | ||||
| chr11:33736384-33736605 | Common:2; Rare:68 | ||||
| chr11:34051588-34051741 | Rare:64 | ||||
| chr11:34052126-34052613 | Common:4; Rare:218 | ||||
| chr11:34105481-34105735 | Common:2; Rare:84 | ||||
| chr11:34357996-34358285 | Common:2; Rare:76 | ||||
| chr11:34438769-34439079 | Common:2; Rare:103; Clinvar (benign):1 | ||||
| chr11:34632483-34632566 | Rare:11 | ||||
| chr11:34916242-34916462 | Common:5; Rare:87; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr11:34916465-34916813 | Common:10; Rare:131; Clinvar:4; Clinvar (benign):11 | ||||
| chr11:35138954-35139187 | Common:1; Rare:54 | ||||
| chr11:35525581-35525816 | Rare:57 | ||||
| chr11:35943886-35944131 | Common:3; Rare:80 | ||||
| chr11:36510222-36510382 | Rare:51 | ||||
| chr11:43358855-43358983 | Rare:60 |