| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:20387410-20387758 | Common:8; Rare:114 | ||||
| chr11:22625518-22625609 | Rare:46; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:22625813-22626004 | Common:2; Rare:66; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:26994055-26994168 | Common:1; Rare:17 | ||||
| chr11:27363128-27363289 | Rare:71 | ||||
| chr11:27506751-27506868 | Common:1; Rare:50 | ||||
| chr11:28108120-28108414 | Common:1; Rare:89 | ||||
| chr11:30322912-30323183 | Common:3; Rare:78 | ||||
| chr11:31369769-31369887 | Rare:40 | ||||
| chr11:31509575-31509787 | Common:1; Rare:65 | ||||
| chr11:32091424-32091449 | Rare:7 | ||||
| chr11:33039610-33039762 | Common:1; Rare:31 | ||||
| chr11:33161429-33161648 | Common:6; Rare:60 | ||||
| chr11:33257182-33257439 | Common:3; Rare:87 | ||||
| chr11:33258136-33258346 | Rare:82 |