Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:88592268-88592562 | Common:1; Rare:90 | ||||
chr4:88592955-88593290 | Common:3; Rare:82 | ||||
chr4:88697612-88697910 | Common:3; Rare:136 | ||||
chr4:89057150-89057288 | Rare:33 | ||||
chr4:89111301-89111641 | Common:4; Rare:121 | ||||
chr4:89836836-89837263 | Common:3; Rare:133; Clinvar:5; Clinvar (benign):1 | ||||
chr4:89837469-89837593 | Rare:26 | ||||
chr4:89838256-89838533 | Common:3; Rare:51 | ||||
chr4:90127272-90127700 | Common:1; Rare:132 | ||||
chr4:90127766-90127793 | Rare:4 | ||||
chr4:92303666-92303810 | Rare:28 | ||||
chr4:92303938-92304291 | Rare:103 | ||||
chr4:92304426-92304709 | Common:1; Rare:55 | ||||
chr4:94207514-94208090 | Common:4; Rare:184 | ||||
chr4:94451777-94451968 | Common:3; Rare:63 |