| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67401780-67402076 | Common:3; Rare:111 | ||||
| chr11:67428156-67428531 | Rare:112 | ||||
| chr11:67469212-67469407 | Common:1; Rare:63 | ||||
| chr11:67482941-67483154 | Rare:48; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:67508078-67508369 | Common:1; Rare:67 | ||||
| chr11:68030381-68030744 | Common:3; Rare:101; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68038925-68039053 | Rare:38; Clinvar:1 | ||||
| chr11:68271895-68272031 | Common:1; Rare:65 | ||||
| chr11:68903778-68903938 | Common:4; Rare:77; Clinvar (benign):6 | ||||
| chr11:69675309-69675488 | Rare:50 | ||||
| chr11:70398331-70398608 | Common:2; Rare:96 | ||||
| chr11:71448338-71448690 | Common:4; Rare:94; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71928915-71929058 | Common:1; Rare:47 | ||||
| chr11:72041056-72041295 | Common:1; Rare:42 | ||||
| chr11:72041846-72042065 | Common:2; Rare:50 |