| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65444017-65444766 | Common:9; Rare:153 | ||||
| chr11:65445231-65445257 | Rare:6 | ||||
| chr11:65455117-65455296 | Rare:82 | ||||
| chr11:65472141-65472319 | Rare:26 | ||||
| chr11:65477434-65477646 | Common:2; Rare:69 | ||||
| chr11:65489361-65489421 | Rare:14 | ||||
| chr11:65493943-65494088 | Common:2; Rare:28 | ||||
| chr11:65497388-65497837 | Common:1; Rare:196 | ||||
| chr11:65498096-65498284 | Rare:120 | ||||
| chr11:65526000-65526277 | Rare:94; Clinvar (pathogenic):1 | ||||
| chr11:65640663-65640860 | Rare:36 | ||||
| chr11:66211022-66211186 | Rare:38; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:67372917-67373062 | Rare:34 | ||||
| chr11:67441153-67441308 | Rare:59 | ||||
| chr11:67490640-67490819 | Rare:46; Clinvar:2; Clinvar (pathogenic):2 |