| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:73787752-73787974 | Common:1; Rare:54 | ||||
| chr11:73876634-73876714 | Rare:34 | ||||
| chr11:73876794-73877036 | Common:4; Rare:68 | ||||
| chr11:74170825-74171348 | Common:3; Rare:168 | ||||
| chr11:74398231-74398534 | Common:3; Rare:68 | ||||
| chr11:74398708-74398844 | Rare:41 | ||||
| chr11:74467547-74467743 | Common:4; Rare:49 | ||||
| chr11:74493304-74493375 | Rare:30; Clinvar (pathogenic):1 | ||||
| chr11:74493722-74493858 | Rare:51 | ||||
| chr11:74592500-74592659 | Common:1; Rare:59 | ||||
| chr11:74949055-74949306 | Common:6; Rare:71 | ||||
| chr11:74988614-74988956 | Rare:75 | ||||
| chr11:75150997-75151126 | Rare:24 | ||||
| chr11:75351593-75351803 | Common:2; Rare:60 | ||||
| chr11:75351985-75352174 | Common:2; Rare:38 |