| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:19713313-19713569 | Common:1; Rare:50 | ||||
| chr11:20387392-20387694 | Common:8; Rare:94 | ||||
| chr11:22625515-22625611 | Rare:50; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:22625813-22626006 | Common:3; Rare:66; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:22829327-22829422 | Common:1; Rare:23 | ||||
| chr11:26572134-26572466 | Rare:56 | ||||
| chr11:26994055-26994181 | Common:1; Rare:20 | ||||
| chr11:27363194-27363382 | Rare:76 | ||||
| chr11:27506725-27506875 | Common:1; Rare:70 | ||||
| chr11:28108115-28108421 | Common:1; Rare:94 | ||||
| chr11:30016943-30017103 | Rare:42 | ||||
| chr11:30322983-30323164 | Common:1; Rare:52 | ||||
| chr11:31369713-31369882 | Rare:52 | ||||
| chr11:31509575-31509790 | Common:1; Rare:67 | ||||
| chr11:32583628-32583929 | Rare:106 |