| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:70398465-70398596 | Common:1; Rare:42 | ||||
| chr11:71448338-71448673 | Common:4; Rare:88; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71928956-71929064 | Common:1; Rare:37 | ||||
| chr11:72041856-72042099 | Common:1; Rare:57 | ||||
| chr11:72080479-72080634 | Rare:33; Clinvar:2 | ||||
| chr11:72103210-72103509 | Rare:84 | ||||
| chr11:73760956-73761292 | Common:3; Rare:105 | ||||
| chr11:73876799-73877024 | Common:4; Rare:58 | ||||
| chr11:74170866-74171421 | Common:3; Rare:176 | ||||
| chr11:74592504-74592648 | Common:1; Rare:51 | ||||
| chr11:74949082-74949307 | Common:6; Rare:62 | ||||
| chr11:76444661-76444987 | Rare:68 | ||||
| chr11:76783119-76783365 | Common:8; Rare:85 | ||||
| chr11:77637718-77637858 | Common:1; Rare:56 | ||||
| chr11:77820966-77821201 | Common:1; Rare:71 |