| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:73760612-73760834 | Common:2; Rare:53 | ||||
| chr11:73761026-73761371 | Common:4; Rare:97 | ||||
| chr11:73876778-73877038 | Common:5; Rare:73 | ||||
| chr11:74170849-74171092 | Common:1; Rare:71 | ||||
| chr11:74171140-74171474 | Common:2; Rare:110 | ||||
| chr11:74592492-74592664 | Common:1; Rare:61 | ||||
| chr11:74949055-74949335 | Common:6; Rare:85 | ||||
| chr11:75351608-75351777 | Common:2; Rare:51 | ||||
| chr11:75562063-75562192 | Rare:28; Clinvar:4; Clinvar (benign):1 | ||||
| chr11:75562194-75562313 | Common:1; Rare:33; Clinvar (benign):1 | ||||
| chr11:76444560-76445088 | Common:1; Rare:133 | ||||
| chr11:76783041-76783396 | Common:10; Rare:114 | ||||
| chr11:77637664-77637877 | Common:1; Rare:75 | ||||
| chr11:77820704-77820758 | Rare:22 | ||||
| chr11:77820854-77821218 | Common:1; Rare:106 |