| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:74493585-74493866 | Common:1; Rare:114; Clinvar (pathogenic):1 | ||||
| chr11:74592450-74592659 | Common:1; Rare:70 | ||||
| chr11:74696974-74697215 | Common:3; Rare:59 | ||||
| chr11:74748818-74749505 | Common:8; Rare:232 | ||||
| chr11:74948637-74948702 | Rare:12 | ||||
| chr11:74948954-74949429 | Common:8; Rare:147 | ||||
| chr11:74949932-74950032 | Rare:24 | ||||
| chr11:74988617-74989174 | Rare:143 | ||||
| chr11:75351612-75351912 | Common:3; Rare:87 | ||||
| chr11:75399408-75399637 | Common:5; Rare:100 | ||||
| chr11:75399957-75400029 | Rare:14 | ||||
| chr11:75400377-75400489 | Rare:43 | ||||
| chr11:75400932-75401289 | Common:1; Rare:78 | ||||
| chr11:75525809-75526202 | Common:2; Rare:119 | ||||
| chr11:75562019-75562357 | Common:1; Rare:82; Clinvar:4; Clinvar (benign):2 |