| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:68038919-68039060 | Rare:42; Clinvar:1 | ||||
| chr11:68271895-68272134 | Common:2; Rare:100 | ||||
| chr11:68903800-68903943 | Common:4; Rare:63; Clinvar (benign):6 | ||||
| chr11:69048714-69048950 | Common:5; Rare:84 | ||||
| chr11:69640972-69641267 | Common:1; Rare:64 | ||||
| chr11:69675307-69675478 | Rare:47 | ||||
| chr11:70398425-70398604 | Common:2; Rare:66 | ||||
| chr11:71448352-71448621 | Common:2; Rare:71; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:72041846-72041895 | Common:1; Rare:9 | ||||
| chr11:72080471-72080819 | Common:1; Rare:76; Clinvar:5 | ||||
| chr11:72752382-72752610 | Common:3; Rare:64 | ||||
| chr11:72814314-72814429 | Rare:35 | ||||
| chr11:73876800-73877036 | Common:4; Rare:65 | ||||
| chr11:74170937-74171419 | Common:3; Rare:158 | ||||
| chr11:74949060-74949328 | Common:6; Rare:80 |