| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:78139581-78139796 | Common:3; Rare:87; Clinvar:2 | ||||
| chr11:78188614-78188939 | Common:2; Rare:102 | ||||
| chr11:83071797-83072083 | Common:4; Rare:80 | ||||
| chr11:83193636-83193759 | Common:1; Rare:56 | ||||
| chr11:83285898-83286130 | Common:3; Rare:106 | ||||
| chr11:85628338-85628613 | Common:6; Rare:84 | ||||
| chr11:86302131-86302475 | Common:2; Rare:80 | ||||
| chr11:88337693-88337892 | Common:3; Rare:94; Clinvar:4; Clinvar (benign):2 | ||||
| chr11:90223018-90223156 | Common:1; Rare:52 | ||||
| chr11:93741456-93741687 | Common:5; Rare:94 | ||||
| chr11:94493786-94494011 | Common:3; Rare:65; Clinvar (benign):1 | ||||
| chr11:94973545-94973711 | Rare:49 | ||||
| chr11:95089731-95089883 | Common:3; Rare:63 | ||||
| chr11:95790398-95790603 | Common:1; Rare:71 | ||||
| chr11:95923976-95924134 | Rare:64; Clinvar (benign):1 |