Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:183504522-183504785 | Common:1; Rare:88 | ||||
chr4:183659049-183659394 | Common:1; Rare:105 | ||||
chr4:184474504-184474812 | Rare:68 | ||||
chr4:184649403-184649805 | Common:4; Rare:131 | ||||
chr4:185203910-185204201 | Common:2; Rare:95 | ||||
chr4:185425883-185426014 | Common:2; Rare:47 | ||||
chr4:186723802-186723911 | Common:2; Rare:39 | ||||
chr4:189940657-189940991 | Common:11; Rare:120 | ||||
chr5:218123-218362 | Common:3; Rare:97; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
chr5:443095-443275 | Common:9; Rare:81 | ||||
chr5:612189-612358 | Rare:68 | ||||
chr5:892540-892990 | Common:5; Rare:144 | ||||
chr5:1799784-1799986 | Common:7; Rare:95 | ||||
chr5:1801300-1801447 | Common:4; Rare:71; Clinvar:3; Clinvar (benign):1 | ||||
chr5:6378498-6378699 | Rare:81 |