| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67482914-67483157 | Rare:56; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:68030611-68030764 | Common:1; Rare:36; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68038919-68039083 | Rare:50; Clinvar:1 | ||||
| chr11:68271930-68272134 | Common:2; Rare:89 | ||||
| chr11:68903784-68903920 | Common:3; Rare:63; Clinvar (benign):3 | ||||
| chr11:69641364-69641415 | Rare:14 | ||||
| chr11:70398460-70398640 | Common:1; Rare:62 | ||||
| chr11:71448299-71448633 | Common:3; Rare:94; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:72080408-72080493 | Common:1; Rare:25; Clinvar:2 | ||||
| chr11:72080499-72080809 | Common:1; Rare:69; Clinvar:5 | ||||
| chr11:73308719-73308906 | Rare:66 | ||||
| chr11:73760196-73760337 | Rare:29 | ||||
| chr11:73760642-73760734 | Common:2; Rare:23 | ||||
| chr11:73787851-73787957 | Common:1; Rare:32 | ||||
| chr11:73876803-73877032 | Common:4; Rare:60 |