Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:38664843-38665122 | Common:1; Rare:77 | ||||
chr4:38667224-38667555 | Rare:67 | ||||
chr4:38868329-38868446 | Rare:23 | ||||
chr4:52712213-52712518 | Common:4; Rare:79 | ||||
chr4:52713570-52713767 | Rare:29 | ||||
chr4:52954916-52955123 | Rare:42 | ||||
chr4:52996284-52996589 | Common:3; Rare:52 | ||||
chr4:54231865-54232052 | Common:2; Rare:42 | ||||
chr4:54232940-54233174 | Common:5; Rare:57 | ||||
chr4:54727829-54728112 | Common:1; Rare:73; Clinvar:8; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
chr4:71186558-71186765 | Common:1; Rare:55 | ||||
chr4:72569353-72569473 | Rare:36 | ||||
chr4:76306533-76306772 | Rare:70 | ||||
chr4:77058505-77058825 | Common:5; Rare:70 | ||||
chr4:77820243-77820380 | Rare:55 |