| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:74170828-74171436 | Common:4; Rare:195 | ||||
| chr11:74398367-74398586 | Common:3; Rare:57 | ||||
| chr11:74398695-74398968 | Rare:82 | ||||
| chr11:74493013-74493458 | Common:1; Rare:160; Clinvar (pathogenic):1 | ||||
| chr11:74493650-74493758 | Common:1; Rare:46 | ||||
| chr11:74592473-74592730 | Common:1; Rare:74 | ||||
| chr11:74748603-74748962 | Common:3; Rare:116 | ||||
| chr11:74749255-74749555 | Common:4; Rare:87 | ||||
| chr11:74949003-74949441 | Common:8; Rare:139 | ||||
| chr11:74988684-74989072 | Rare:102 | ||||
| chr11:74989379-74989447 | Common:1; Rare:6 | ||||
| chr11:75100397-75100620 | Rare:38 | ||||
| chr11:75399394-75399637 | Common:5; Rare:103 | ||||
| chr11:75562002-75562359 | Common:1; Rare:83; Clinvar:4; Clinvar (benign):2 | ||||
| chr11:75562508-75562968 | Common:1; Rare:101 |