| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:61342066-61342816 | Common:5; Rare:583 | ||||
| chr11:61361048-61361448 | Common:2; Rare:74 | ||||
| chr11:61361453-61361853 | Rare:80 | ||||
| chr11:61361775-61362080 | Common:12; Rare:348; Clinvar:10 | ||||
| chr11:61362090-61362481 | Common:12; Rare:510; Clinvar:53; Clinvar (benign):5 | ||||
| chr11:61362489-61363256 | Common:1; Rare:189 | ||||
| chr11:61367881-61368281 | Common:2; Rare:153; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr11:61391981-61392430 | Common:8; Rare:158; Clinvar:2 | ||||
| chr11:61392430-61392690 | Common:6; Rare:174; Clinvar:10; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr11:61429110-61429590 | Common:21; Rare:653 | ||||
| chr11:61429805-61430529 | Common:10; Rare:869; Clinvar:15; Clinvar (benign):38 | ||||
| chr11:61488880-61489310 | Common:7; Rare:80 | ||||
| chr11:61509230-61509620 | Common:2; Rare:229 | ||||
| chr11:61680160-61680440 | Common:1; Rare:85 | ||||
| chr11:61752330-61752710 | Common:7; Rare:201 |