Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:218114-218369 | Common:3; Rare:107; Clinvar:7; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
chr5:443095-443263 | Common:8; Rare:75 | ||||
chr5:892535-892901 | Common:5; Rare:107 | ||||
chr5:1799785-1799988 | Common:7; Rare:96 | ||||
chr5:1801300-1801447 | Common:4; Rare:71; Clinvar:3; Clinvar (benign):1 | ||||
chr5:7868987-7869204 | Common:2; Rare:112; Clinvar (benign):1 | ||||
chr5:9546052-9546376 | Common:7; Rare:75 | ||||
chr5:10249869-10250170 | Common:16; Rare:142 | ||||
chr5:10250187-10250427 | Common:3; Rare:115; Clinvar:5; Clinvar (benign):2 | ||||
chr5:10353573-10353950 | Common:3; Rare:147 | ||||
chr5:16465715-16465889 | Rare:29 | ||||
chr5:16936235-16936480 | Common:3; Rare:73 | ||||
chr5:31532052-31532382 | Common:3; Rare:98 | ||||
chr5:32174277-32174379 | Common:1; Rare:38 | ||||
chr5:32711102-32711344 | Rare:38 |