| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67428353-67428561 | Rare:80 | ||||
| chr11:67443770-67443899 | Rare:29 | ||||
| chr11:67464616-67464909 | Rare:166 | ||||
| chr11:67468210-67468340 | Common:2; Rare:21 | ||||
| chr11:67469147-67469453 | Common:3; Rare:108 | ||||
| chr11:67482920-67483061 | Rare:30; Clinvar (pathogenic):1 | ||||
| chr11:67504235-67504685 | Common:4; Rare:168 | ||||
| chr11:67505293-67505505 | Rare:50 | ||||
| chr11:67505618-67506114 | Common:2; Rare:123 | ||||
| chr11:67507785-67507929 | Rare:39 | ||||
| chr11:67508155-67508464 | Common:1; Rare:60 | ||||
| chr11:67508662-67508795 | Common:2; Rare:55 | ||||
| chr11:67583551-67583862 | Common:2; Rare:90 | ||||
| chr11:67606730-67606975 | Common:1; Rare:79; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:67629211-67629611 | Common:2; Rare:128 |