Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:17810681-17811020 | Common:3; Rare:104 | ||||
chr4:25160450-25160704 | Common:3; Rare:69; Clinvar:2; Clinvar (benign):1 | ||||
chr4:30720245-30720415 | Common:1; Rare:44 | ||||
chr4:37826497-37826728 | Common:6; Rare:80 | ||||
chr4:38867596-38867826 | Common:2; Rare:84 | ||||
chr4:39458857-39459065 | Common:3; Rare:116 | ||||
chr4:39527405-39527763 | Common:2; Rare:91 | ||||
chr4:39527959-39527987 | Rare:4 | ||||
chr4:39638834-39639204 | Common:1; Rare:142 | ||||
chr4:39697987-39698174 | Common:1; Rare:76 | ||||
chr4:44726498-44726639 | Common:1; Rare:51 | ||||
chr4:47463647-47463883 | Common:3; Rare:70 | ||||
chr4:52659188-52659437 | Common:1; Rare:85 | ||||
chr4:55546871-55546996 | Common:2; Rare:51 | ||||
chr4:56387449-56387522 | Rare:25 |