| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:69641002-69641178 | Rare:33 | ||||
| chr11:69675309-69675529 | Rare:59 | ||||
| chr11:70398421-70398591 | Common:2; Rare:61 | ||||
| chr11:71448338-71448673 | Common:4; Rare:88; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71787334-71787539 | Common:12; Rare:81 | ||||
| chr11:71928568-71929058 | Common:1; Rare:134 | ||||
| chr11:72041014-72041331 | Common:1; Rare:63 | ||||
| chr11:72041846-72042041 | Common:2; Rare:38 | ||||
| chr11:72080475-72080853 | Common:1; Rare:85; Clinvar:6 | ||||
| chr11:72103222-72103509 | Rare:81 | ||||
| chr11:72434490-72434721 | Common:4; Rare:63; Clinvar (benign):1 | ||||
| chr11:72814064-72814124 | Common:1; Rare:19 | ||||
| chr11:72814154-72814458 | Common:3; Rare:90 | ||||
| chr11:73598063-73598283 | Common:2; Rare:58 | ||||
| chr11:73876767-73877036 | Common:5; Rare:76 |