| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47347649-47347906 | Common:1; Rare:75; Clinvar:15; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr11:47349764-47350081 | Common:4; Rare:121; Clinvar:28; Clinvar (benign):21; Clinvar (pathogenic):6 | ||||
| chr11:47351757-47352033 | Common:1; Rare:52 | ||||
| chr11:57778585-57778834 | Rare:43 | ||||
| chr11:61313950-61314103 | Rare:48 | ||||
| chr11:63872169-63872370 | Common:1; Rare:31 | ||||
| chr11:64242553-64242628 | Common:1; Rare:17 | ||||
| chr11:65420019-65420163 | Rare:36 | ||||
| chr11:65421200-65421483 | Rare:58 | ||||
| chr11:65422655-65423041 | Common:3; Rare:115 | ||||
| chr11:65423137-65423452 | Common:1; Rare:75 | ||||
| chr11:65424690-65425027 | Common:2; Rare:68 | ||||
| chr11:65425379-65425649 | Rare:51 | ||||
| chr11:65425928-65426098 | Rare:32 | ||||
| chr11:65427170-65427425 | Rare:45 |