| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:34052126-34052523 | Common:4; Rare:177 | ||||
| chr11:34438547-34438731 | Common:1; Rare:43 | ||||
| chr11:34438769-34439084 | Common:2; Rare:104; Clinvar (benign):1 | ||||
| chr11:34916248-34916683 | Common:11; Rare:174; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr11:35138949-35139188 | Common:1; Rare:55 | ||||
| chr11:36510229-36510372 | Rare:43 | ||||
| chr11:36567816-36568038 | Common:1; Rare:33; Clinvar:1 | ||||
| chr11:36594440-36594592 | Common:2; Rare:27 | ||||
| chr11:36598225-36598508 | Common:1; Rare:57 | ||||
| chr11:43358847-43359096 | Rare:100 | ||||
| chr11:45804290-45804475 | Common:1; Rare:38 | ||||
| chr11:45804955-45805118 | Common:1; Rare:33 | ||||
| chr11:45847172-45847514 | Common:2; Rare:139 | ||||
| chr11:46617136-46617600 | Common:5; Rare:131 | ||||
| chr11:46700555-46700818 | Common:1; Rare:68 |