| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:58578121-58578138 | Rare:5 | ||||
| chr11:58578354-58578519 | Common:2; Rare:64 | ||||
| chr11:59142705-59142968 | Common:1; Rare:47 | ||||
| chr11:59668999-59669316 | Rare:109 | ||||
| chr11:60906504-60906792 | Rare:73 | ||||
| chr11:60913981-60914244 | Common:1; Rare:65 | ||||
| chr11:60952291-60952512 | Rare:49 | ||||
| chr11:61333028-61333251 | Rare:74 | ||||
| chr11:61361832-61361964 | Common:1; Rare:32 | ||||
| chr11:61362255-61362417 | Common:1; Rare:46; Clinvar:7 | ||||
| chr11:61429916-61430149 | Common:1; Rare:103; Clinvar:1; Clinvar (benign):3 | ||||
| chr11:61792564-61792947 | Common:5; Rare:105 | ||||
| chr11:61816134-61816330 | Rare:54 | ||||
| chr11:61840440-61840676 | Common:1; Rare:49 | ||||
| chr11:61967311-61967564 | Common:1; Rare:94; Clinvar:1 |