| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:74398359-74398558 | Common:3; Rare:49 | ||||
| chr11:74592492-74592660 | Common:1; Rare:59 | ||||
| chr11:74949124-74949328 | Common:3; Rare:60 | ||||
| chr11:75561807-75562156 | Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:75562159-75562324 | Common:1; Rare:43; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:76381101-76381364 | Common:4; Rare:83 | ||||
| chr11:76444606-76445099 | Common:1; Rare:120 | ||||
| chr11:76783045-76783366 | Common:9; Rare:107 | ||||
| chr11:77473564-77473771 | Common:1; Rare:74 | ||||
| chr11:77637592-77637887 | Common:1; Rare:91 | ||||
| chr11:77820988-77821189 | Common:1; Rare:63 | ||||
| chr11:78079683-78079942 | Common:2; Rare:82 | ||||
| chr11:78139585-78139779 | Common:3; Rare:77; Clinvar:2 | ||||
| chr11:78188603-78188925 | Common:2; Rare:99 | ||||
| chr11:78574768-78574985 | Common:2; Rare:84; Clinvar (benign):1 |