| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:20364118-20364221 | Rare:24 | ||||
| chr11:20387516-20387765 | Common:3; Rare:78 | ||||
| chr11:22625518-22625609 | Rare:46; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:22625808-22626015 | Common:3; Rare:70; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:26994049-26994092 | Rare:6 | ||||
| chr11:26994099-26994188 | Common:1; Rare:17 | ||||
| chr11:27506738-27506877 | Common:1; Rare:59 | ||||
| chr11:28108130-28108421 | Common:1; Rare:87 | ||||
| chr11:30322875-30323186 | Common:3; Rare:89 | ||||
| chr11:31369737-31369882 | Rare:45 | ||||
| chr11:31509575-31509806 | Common:1; Rare:76 | ||||
| chr11:32583673-32583929 | Rare:92 | ||||
| chr11:33015792-33015935 | Common:1; Rare:57 | ||||
| chr11:33039607-33040051 | Common:3; Rare:116 | ||||
| chr11:33161449-33161657 | Common:6; Rare:55 |