| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67288459-67288607 | Rare:29 | ||||
| chr11:67353258-67353377 | Rare:42 | ||||
| chr11:67373591-67373697 | Rare:23 | ||||
| chr11:67401506-67401735 | Common:1; Rare:78 | ||||
| chr11:67401789-67402027 | Common:1; Rare:90 | ||||
| chr11:67428341-67428537 | Rare:67 | ||||
| chr11:67443457-67443710 | Common:2; Rare:87 | ||||
| chr11:67469122-67469407 | Common:3; Rare:100 | ||||
| chr11:67482720-67483161 | Common:2; Rare:98; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:67508048-67508505 | Common:1; Rare:104 | ||||
| chr11:68004051-68004231 | Common:1; Rare:58 | ||||
| chr11:68030432-68030744 | Common:3; Rare:78; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68271930-68272102 | Common:2; Rare:78 | ||||
| chr11:68460530-68460773 | Common:3; Rare:92 | ||||
| chr11:68903728-68903920 | Common:3; Rare:80; Clinvar (benign):3 |