| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:34105471-34105719 | Common:2; Rare:84 | ||||
| chr11:34620933-34621103 | Common:1; Rare:30 | ||||
| chr11:34916318-34916683 | Common:10; Rare:148; Clinvar:4; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35139018-35139177 | Common:1; Rare:33 | ||||
| chr11:35943917-35944110 | Common:3; Rare:64 | ||||
| chr11:36510249-36510360 | Rare:30 | ||||
| chr11:46846239-46846412 | Common:1; Rare:48 | ||||
| chr11:47186408-47186572 | Rare:41 | ||||
| chr11:47269555-47269680 | Common:1; Rare:42 | ||||
| chr11:47270018-47270166 | Common:1; Rare:52 | ||||
| chr11:47565540-47565620 | Common:2; Rare:13 | ||||
| chr11:47578944-47579087 | Rare:74; Clinvar:2 | ||||
| chr11:47642472-47642839 | Rare:131 | ||||
| chr11:57427070-57427262 | Common:1; Rare:57 | ||||
| chr11:57530682-57530852 | Common:1; Rare:41 |