| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:76860660-76860972 | Common:4; Rare:100 | ||||
| chr11:77473564-77473815 | Common:1; Rare:87 | ||||
| chr11:77637592-77637868 | Common:1; Rare:91 | ||||
| chr11:77820567-77820792 | Rare:82 | ||||
| chr11:77820931-77821210 | Common:1; Rare:85 | ||||
| chr11:78063756-78063893 | Rare:30 | ||||
| chr11:78079635-78079942 | Common:2; Rare:104 | ||||
| chr11:78139581-78139815 | Common:3; Rare:92; Clinvar:2 | ||||
| chr11:78188568-78188944 | Common:3; Rare:120 | ||||
| chr11:78417688-78418074 | Common:3; Rare:160 | ||||
| chr11:78574761-78574972 | Common:2; Rare:85; Clinvar (benign):1 | ||||
| chr11:83035540-83035682 | Rare:19 | ||||
| chr11:83071406-83071471 | Rare:13 | ||||
| chr11:83071735-83072116 | Common:4; Rare:107 | ||||
| chr11:83193607-83193830 | Common:1; Rare:101 |