| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:993895-994109 | Common:2; Rare:63 | ||||
| chr11:1307308-1307531 | Common:1; Rare:52 | ||||
| chr11:1753427-1753899 | Common:4; Rare:193; Clinvar:12; Clinvar (benign):22; Clinvar (pathogenic):2 | ||||
| chr11:1792905-1792916 | |||||
| chr11:2378001-2378136 | Common:3; Rare:36 | ||||
| chr11:2397707-2397765 | Rare:13 | ||||
| chr11:2945497-2945833 | Common:1; Rare:95 | ||||
| chr11:3779045-3779254 | Rare:67 | ||||
| chr11:3904497-3904784 | Common:5; Rare:80 | ||||
| chr11:3972752-3972796 | Rare:8 | ||||
| chr11:4076529-4076710 | Rare:28 | ||||
| chr11:4197921-4198204 | Common:3; Rare:58 | ||||
| chr11:4723852-4723864 | Rare:1 | ||||
| chr11:4986367-4986505 | Rare:26 | ||||
| chr11:6423657-6423925 | Rare:37 |