Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:55546798-55547018 | Common:2; Rare:76 | ||||
chr4:55853481-55853795 | Rare:88 | ||||
chr4:55948636-55948976 | Common:2; Rare:71 | ||||
chr4:56387425-56387524 | Rare:35 | ||||
chr4:56435475-56435973 | Common:6; Rare:163 | ||||
chr4:56435994-56436327 | Rare:118 | ||||
chr4:56467542-56467679 | Common:2; Rare:61; Clinvar (benign):4 | ||||
chr4:56977570-56977753 | Common:1; Rare:72 | ||||
chr4:57110371-57110537 | Common:1; Rare:53 | ||||
chr4:67545423-67545724 | Common:2; Rare:73 | ||||
chr4:67701111-67701368 | Common:4; Rare:121 | ||||
chr4:70688185-70688624 | Common:2; Rare:114 | ||||
chr4:70902167-70902378 | Common:5; Rare:78 | ||||
chr4:73258510-73258887 | Common:1; Rare:104 | ||||
chr4:73869159-73869555 | Common:4; Rare:131 |