| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:57427027-57427236 | Common:1; Rare:64 | ||||
| chr11:57460604-57460721 | Rare:37 | ||||
| chr11:57499626-57499819 | Rare:57 | ||||
| chr11:57514833-57515034 | Common:2; Rare:40 | ||||
| chr11:57515679-57515847 | Common:1; Rare:31 | ||||
| chr11:57530673-57530824 | Common:1; Rare:36 | ||||
| chr11:57567607-57567736 | Rare:44 | ||||
| chr11:57597464-57597755 | Rare:65; Clinvar:4; Clinvar (benign):1 | ||||
| chr11:57711997-57712652 | Common:10; Rare:220 | ||||
| chr11:57741255-57741612 | Common:1; Rare:137 | ||||
| chr11:58578090-58578508 | Common:4; Rare:133 | ||||
| chr11:58731874-58732029 | Rare:27 | ||||
| chr11:58927437-58927756 | Common:5; Rare:58 | ||||
| chr11:58939345-58939550 | Common:2; Rare:34 | ||||
| chr11:59142689-59142951 | Common:1; Rare:46 |