| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:59552858-59553083 | Common:1; Rare:26 | ||||
| chr11:59560898-59561142 | Common:2; Rare:56 | ||||
| chr11:60285445-60285519 | Rare:13 | ||||
| chr11:61313860-61314114 | Rare:74 | ||||
| chr11:61346141-61346427 | Common:1; Rare:82 | ||||
| chr11:61437794-61438034 | Common:2; Rare:75; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr11:62571539-62571902 | Common:1; Rare:69 | ||||
| chr11:62630393-62630639 | Rare:82 | ||||
| chr11:64181663-64181777 | Rare:24 | ||||
| chr11:64258678-64258974 | Common:1; Rare:92 | ||||
| chr11:64265048-64265226 | Rare:55 | ||||
| chr11:64320657-64321068 | Common:1; Rare:163 | ||||
| chr11:64835346-64835498 | Common:1; Rare:48 | ||||
| chr11:65418705-65419034 | Common:2; Rare:62 | ||||
| chr11:65420026-65420187 | Rare:38 |