| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:74949068-74949294 | Common:6; Rare:59 | ||||
| chr11:76381092-76381353 | Common:3; Rare:79 | ||||
| chr11:76444619-76445088 | Common:1; Rare:114 | ||||
| chr11:76783042-76783388 | Common:10; Rare:113 | ||||
| chr11:77637725-77637877 | Common:1; Rare:54 | ||||
| chr11:77820941-77821216 | Common:1; Rare:85 | ||||
| chr11:78079584-78079723 | Common:2; Rare:51 | ||||
| chr11:78139587-78139815 | Common:3; Rare:89; Clinvar:2 | ||||
| chr11:78188586-78188912 | Common:2; Rare:106 | ||||
| chr11:83071784-83072124 | Common:4; Rare:95 | ||||
| chr11:83193621-83193786 | Common:1; Rare:75 | ||||
| chr11:83286344-83286479 | Rare:27 | ||||
| chr11:85627265-85627397 | Rare:23 | ||||
| chr11:85628339-85628658 | Common:6; Rare:107 | ||||
| chr11:85647954-85648036 | Common:1; Rare:24; Clinvar:1; Clinvar (benign):1 |