Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:1799791-1799977 | Common:4; Rare:89 | ||||
chr5:1801300-1801432 | Common:4; Rare:57; Clinvar:1; Clinvar (benign):1 | ||||
chr5:6378498-6378686 | Rare:75 | ||||
chr5:6632982-6633398 | Common:8; Rare:134; Clinvar:10; Clinvar (benign):4 | ||||
chr5:7869000-7869204 | Common:2; Rare:103; Clinvar (benign):1 | ||||
chr5:9546052-9546313 | Common:6; Rare:60 | ||||
chr5:10249874-10250404 | Common:19; Rare:246; Clinvar:4; Clinvar (benign):2 | ||||
chr5:10353597-10353910 | Common:3; Rare:114 | ||||
chr5:16465524-16465876 | Rare:95 | ||||
chr5:31532045-31532356 | Common:3; Rare:87 | ||||
chr5:33440632-33441122 | Common:7; Rare:139 | ||||
chr5:33891992-33892394 | Rare:96 | ||||
chr5:34656243-34656480 | Common:1; Rare:65 | ||||
chr5:34915472-34915775 | Common:1; Rare:87 | ||||
chr5:36151885-36152174 | Rare:91 |