| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:28108134-28108414 | Common:1; Rare:82 | ||||
| chr11:30016943-30017112 | Rare:47 | ||||
| chr11:30322971-30323191 | Common:2; Rare:62 | ||||
| chr11:30584004-30584159 | Rare:41 | ||||
| chr11:30586115-30586244 | Common:1; Rare:47 | ||||
| chr11:31369731-31369901 | Rare:51 | ||||
| chr11:31509561-31509940 | Common:1; Rare:140 | ||||
| chr11:31817926-31818081 | Common:2; Rare:45 | ||||
| chr11:32583663-32583918 | Rare:93 | ||||
| chr11:32588712-32589091 | Common:2; Rare:102 | ||||
| chr11:33161449-33161648 | Common:6; Rare:52 | ||||
| chr11:33736384-33736605 | Common:2; Rare:68 | ||||
| chr11:34051617-34051741 | Rare:54 | ||||
| chr11:34105529-34105724 | Common:2; Rare:67 | ||||
| chr11:34438776-34439034 | Common:2; Rare:88; Clinvar (benign):1 |