| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18322443-18322582 | Common:2; Rare:52 | ||||
| chr11:27506758-27506838 | Common:1; Rare:36 | ||||
| chr11:31509600-31509784 | Common:1; Rare:56 | ||||
| chr11:34916356-34916669 | Common:8; Rare:124; Clinvar:4; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr11:46846276-46846412 | Common:1; Rare:37 | ||||
| chr11:47565552-47565620 | Common:2; Rare:11 | ||||
| chr11:47578974-47579085 | Rare:58; Clinvar:2 | ||||
| chr11:57712308-57712614 | Common:3; Rare:84 | ||||
| chr11:59142804-59142864 | Rare:10 | ||||
| chr11:61333045-61333207 | Rare:56 | ||||
| chr11:61361880-61362055 | Common:2; Rare:39; Clinvar:2 | ||||
| chr11:61362291-61362397 | Common:1; Rare:31; Clinvar:5 | ||||
| chr11:61429961-61430152 | Common:1; Rare:80; Clinvar:1; Clinvar (benign):3 | ||||
| chr11:61792581-61792908 | Common:5; Rare:80 | ||||
| chr11:62665167-62665309 | Common:3; Rare:55 |