| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65921067-65921542 | Common:1; Rare:143 | ||||
| chr11:66002102-66002397 | Common:3; Rare:88; Clinvar:5; Clinvar (benign):3 | ||||
| chr11:66002418-66002521 | Rare:26; Clinvar:1 | ||||
| chr11:66260982-66261177 | Common:2; Rare:34 | ||||
| chr11:66288987-66289418 | Common:1; Rare:112 | ||||
| chr11:66347576-66347834 | Common:5; Rare:63 | ||||
| chr11:66466702-66466921 | Rare:64 | ||||
| chr11:66479963-66480043 | Rare:13 | ||||
| chr11:66480224-66480458 | Common:1; Rare:63 | ||||
| chr11:66593057-66593299 | Common:1; Rare:79 | ||||
| chr11:66616403-66616679 | Common:2; Rare:82 | ||||
| chr11:66638430-66638773 | Common:3; Rare:140 | ||||
| chr11:66677769-66677981 | Common:1; Rare:81 | ||||
| chr11:66686424-66686806 | Common:2; Rare:90 | ||||
| chr11:66744658-66744919 | Common:3; Rare:98 |