| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67356921-67357098 | Rare:31 | ||||
| chr11:67401741-67402076 | Common:3; Rare:123 | ||||
| chr11:67428295-67428537 | Rare:84 | ||||
| chr11:67438367-67438617 | Common:1; Rare:92 | ||||
| chr11:67443458-67443572 | Common:1; Rare:35 | ||||
| chr11:67464546-67464837 | Rare:156 | ||||
| chr11:67482936-67483154 | Rare:50; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:67507794-67507892 | Rare:23 | ||||
| chr11:67508043-67508496 | Common:1; Rare:104 | ||||
| chr11:67611900-67612206 | Common:2; Rare:114; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr11:68038881-68039101 | Rare:67; Clinvar:1 | ||||
| chr11:68061951-68062271 | Rare:62 | ||||
| chr11:68271871-68272134 | Common:2; Rare:108 | ||||
| chr11:68460223-68460399 | Common:3; Rare:64 | ||||
| chr11:68460538-68460793 | Common:3; Rare:97 |