| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:73876804-73877036 | Common:4; Rare:62 | ||||
| chr11:73982829-73983039 | Common:6; Rare:54 | ||||
| chr11:74170831-74171427 | Common:3; Rare:192 | ||||
| chr11:74398380-74398558 | Common:3; Rare:39 | ||||
| chr11:74493711-74493805 | Rare:32 | ||||
| chr11:74592480-74592659 | Common:1; Rare:60 | ||||
| chr11:74949055-74949335 | Common:6; Rare:85 | ||||
| chr11:74988614-74988956 | Rare:75 | ||||
| chr11:75151028-75151116 | Rare:17 | ||||
| chr11:75159722-75159866 | Common:1; Rare:28 | ||||
| chr11:75351593-75351894 | Common:3; Rare:89 | ||||
| chr11:75561997-75562308 | Common:1; Rare:75; Clinvar:4; Clinvar (benign):2 | ||||
| chr11:75719794-75720024 | Common:3; Rare:66 | ||||
| chr11:76380858-76381364 | Common:4; Rare:168 | ||||
| chr11:76444578-76445092 | Common:1; Rare:126 |