| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:61967580-61967783 | Common:2; Rare:80; Clinvar:3 | ||||
| chr11:62545566-62545885 | Common:1; Rare:70 | ||||
| chr11:62577296-62577411 | Rare:24 | ||||
| chr11:62591511-62591837 | Rare:105 | ||||
| chr11:62599177-62599426 | Rare:62 | ||||
| chr11:62646563-62646891 | Common:2; Rare:124; Clinvar (pathogenic):1 | ||||
| chr11:62653262-62653436 | Common:1; Rare:60 | ||||
| chr11:62665075-62665418 | Common:5; Rare:156 | ||||
| chr11:62678864-62679186 | Rare:108 | ||||
| chr11:62706232-62706426 | Common:2; Rare:89; Clinvar (benign):4 | ||||
| chr11:62727913-62728138 | Common:5; Rare:44 | ||||
| chr11:62787253-62787432 | Common:2; Rare:132 | ||||
| chr11:62831653-62831824 | Common:1; Rare:41 | ||||
| chr11:62832015-62832244 | Rare:83 | ||||
| chr11:62855879-62856161 | Rare:106 |