| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47553024-47553341 | Common:2; Rare:116 | ||||
| chr11:47565490-47565661 | Common:3; Rare:37 | ||||
| chr11:47578931-47579098 | Rare:89; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47642407-47642852 | Rare:148 | ||||
| chr11:47715344-47715452 | Common:1; Rare:32 | ||||
| chr11:47848314-47848398 | Rare:44 | ||||
| chr11:55883155-55883266 | Rare:17 | ||||
| chr11:55885573-55886098 | Common:4; Rare:166 | ||||
| chr11:57324890-57325270 | Common:1; Rare:114 | ||||
| chr11:57335748-57335971 | Common:4; Rare:52 | ||||
| chr11:57427070-57427232 | Common:1; Rare:49 | ||||
| chr11:57530675-57530829 | Common:1; Rare:36 | ||||
| chr11:57657424-57657794 | Common:4; Rare:94 | ||||
| chr11:57667731-57667831 | Common:4; Rare:25 | ||||
| chr11:57712013-57712621 | Common:10; Rare:201 |