| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:73982821-73982898 | Common:6; Rare:23 | ||||
| chr11:74170861-74171427 | Common:3; Rare:179 | ||||
| chr11:74592492-74592668 | Common:1; Rare:62 | ||||
| chr11:74748673-74748871 | Common:3; Rare:48 | ||||
| chr11:74949055-74949294 | Common:6; Rare:64 | ||||
| chr11:75351602-75351866 | Common:3; Rare:78 | ||||
| chr11:76381101-76381364 | Common:4; Rare:83 | ||||
| chr11:76444654-76444919 | Rare:58 | ||||
| chr11:76783041-76783396 | Common:10; Rare:114 | ||||
| chr11:76783909-76784193 | Common:4; Rare:64 | ||||
| chr11:77637710-77637858 | Common:1; Rare:56 | ||||
| chr11:77820815-77821224 | Common:2; Rare:117 | ||||
| chr11:78139587-78139809 | Common:3; Rare:88; Clinvar:2 | ||||
| chr11:78188592-78188964 | Common:3; Rare:116 | ||||
| chr11:78574779-78574950 | Common:2; Rare:65; Clinvar (benign):1 |