| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:28107817-28107876 | Rare:12 | ||||
| chr11:28108065-28108478 | Common:3; Rare:121 | ||||
| chr11:28110219-28110405 | Rare:48 | ||||
| chr11:30322893-30323258 | Common:5; Rare:97 | ||||
| chr11:30323293-30323464 | Common:2; Rare:53 | ||||
| chr11:31369692-31369974 | Rare:76 | ||||
| chr11:31370095-31370158 | Rare:13 | ||||
| chr11:31509522-31510052 | Common:3; Rare:197 | ||||
| chr11:32090753-32091002 | Common:2; Rare:66 | ||||
| chr11:32091019-32091213 | Common:2; Rare:58 | ||||
| chr11:32091409-32091791 | Common:1; Rare:103 | ||||
| chr11:32091807-32091920 | Common:1; Rare:25 | ||||
| chr11:32091940-32092057 | Common:1; Rare:25 | ||||
| chr11:32400289-32400589 | Common:2; Rare:45 | ||||
| chr11:32434568-32434883 | Common:1; Rare:98; Clinvar:9; Clinvar (benign):10 |