| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:22625806-22626021 | Common:3; Rare:73; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:22829322-22829395 | Common:1; Rare:18 | ||||
| chr11:22829784-22830091 | Common:3; Rare:97 | ||||
| chr11:24496750-24496994 | Common:2; Rare:66 | ||||
| chr11:27363002-27363288 | Common:1; Rare:130 | ||||
| chr11:27506721-27506927 | Common:1; Rare:87 | ||||
| chr11:28108072-28108421 | Common:2; Rare:103 | ||||
| chr11:30322924-30323186 | Common:3; Rare:76 | ||||
| chr11:30586091-30586525 | Common:2; Rare:133 | ||||
| chr11:31369735-31369912 | Rare:53 | ||||
| chr11:31509526-31509949 | Common:2; Rare:154 | ||||
| chr11:32583663-32583929 | Rare:95 | ||||
| chr11:33015784-33015935 | Common:1; Rare:59 | ||||
| chr11:33039452-33039681 | Common:1; Rare:57 | ||||
| chr11:33039685-33040020 | Common:2; Rare:89 |