| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:69048728-69049000 | Common:6; Rare:100 | ||||
| chr11:69640861-69641230 | Rare:78 | ||||
| chr11:69641267-69641508 | Rare:66 | ||||
| chr11:69675290-69675517 | Rare:62 | ||||
| chr11:69704611-69704776 | Rare:42 | ||||
| chr11:70203029-70203403 | Common:4; Rare:133 | ||||
| chr11:70270447-70270775 | Common:2; Rare:132 | ||||
| chr11:70371352-70371535 | Common:5; Rare:18 | ||||
| chr11:70398003-70398014 | |||||
| chr11:70398269-70398622 | Common:4; Rare:123 | ||||
| chr11:70662260-70662358 | Rare:26 | ||||
| chr11:70662387-70662516 | Common:2; Rare:38 | ||||
| chr11:71252484-71252622 | Common:1; Rare:41 | ||||
| chr11:71448276-71448697 | Common:4; Rare:117; Clinvar:4; Clinvar (benign):1 | ||||
| chr11:71452987-71453281 | Common:3; Rare:82 |