Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:46382160-46382700 | Common:1; Rare:267 | ||||
chr11:46593516-46594250 | Common:9; Rare:397 | ||||
chr11:46594344-46594744 | Common:3; Rare:60 | ||||
chr11:46616162-46617007 | Common:1; Rare:246 | ||||
chr11:46617058-46618180 | Common:38; Rare:1239 | ||||
chr11:46700401-46701161 | Common:23; Rare:916 | ||||
chr11:46718400-46718770 | Common:1; Rare:58 | ||||
chr11:46826703-46827105 | Rare:115 | ||||
chr11:46845400-46845910 | Common:4; Rare:176 | ||||
chr11:46846155-46846555 | Common:7; Rare:484 | ||||
chr11:46918440-46918950 | Common:3; Rare:106; Clinvar:3; Clinvar (benign):2 | ||||
chr11:46936482-46937020 | Common:6; Rare:299 | ||||
chr11:47176059-47176459 | Common:1; Rare:181 | ||||
chr11:47176795-47177226 | Common:4; Rare:874 | ||||
chr11:47177321-47177670 | Rare:147 |