| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:133308835-133308976 | Rare:67 | ||||
| chr11:208688-208787 | Rare:31 | ||||
| chr11:695724-695817 | Rare:31 | ||||
| chr11:832874-833020 | Common:7; Rare:53 | ||||
| chr11:842497-842886 | Common:7; Rare:160 | ||||
| chr11:1838684-1839009 | Common:2; Rare:87; Clinvar:1 | ||||
| chr11:6481309-6481539 | Common:4; Rare:99 | ||||
| chr11:6603597-6603806 | Common:2; Rare:63 | ||||
| chr11:8682658-8682803 | Common:2; Rare:64 | ||||
| chr11:10541145-10541312 | Rare:64 | ||||
| chr11:10858030-10858223 | Common:2; Rare:50 | ||||
| chr11:16738466-16738698 | Common:3; Rare:49 | ||||
| chr11:17077618-17077854 | Common:2; Rare:99 | ||||
| chr11:18322108-18322295 | Common:3; Rare:69; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:18634336-18634566 | Common:2; Rare:73 |