Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:112446914-112447230 | Common:3; Rare:68 | ||||
chr10:119178792-119178895 | Common:2; Rare:41 | ||||
chr10:119892552-119892772 | Common:3; Rare:83 | ||||
chr10:125719453-125719721 | Rare:83 | ||||
chr10:125823169-125823561 | Common:2; Rare:131; Clinvar:1; Clinvar (benign):2 | ||||
chr10:132331817-132332183 | Common:13; Rare:112 | ||||
chr10:133308837-133308961 | Rare:57 | ||||
chr11:207343-207717 | Common:8; Rare:128 | ||||
chr11:208746-208843 | Rare:40 | ||||
chr11:236333-236523 | Common:6; Rare:57 | ||||
chr11:236919-237064 | Common:1; Rare:57 | ||||
chr11:777474-777593 | Rare:50 | ||||
chr11:832858-833018 | Common:7; Rare:58 | ||||
chr11:842515-842978 | Common:8; Rare:183 | ||||
chr11:843964-844147 | Common:1; Rare:44 |