| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66268404-66268682 | Common:3; Rare:81 | ||||
| chr11:66289076-66289427 | Common:1; Rare:88 | ||||
| chr11:66345036-66345203 | Common:1; Rare:49 | ||||
| chr11:66347596-66347823 | Common:5; Rare:58 | ||||
| chr11:66371745-66371857 | Common:1; Rare:26 | ||||
| chr11:66466706-66466956 | Rare:77 | ||||
| chr11:66480232-66480450 | Common:1; Rare:57 | ||||
| chr11:66491652-66491711 | Rare:23 | ||||
| chr11:66510547-66510687 | Common:1; Rare:65; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr11:66593044-66593264 | Common:1; Rare:78 | ||||
| chr11:66616396-66616649 | Common:1; Rare:69 | ||||
| chr11:66677766-66678018 | Common:1; Rare:102 | ||||
| chr11:66744650-66744801 | Common:1; Rare:58 | ||||
| chr11:66843320-66843523 | Common:6; Rare:103 | ||||
| chr11:67119078-67119278 | Rare:65 |