Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:179820669-179820984 | Common:6; Rare:114; Clinvar:2; Clinvar (benign):2 | ||||
chr5:179823915-179824323 | Common:1; Rare:162; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr5:179858796-179859052 | Rare:135 | ||||
chr5:180071629-180071839 | Common:2; Rare:87 | ||||
chr5:180291884-180292197 | Common:2; Rare:116 | ||||
chr5:180802762-180802961 | Common:6; Rare:82 | ||||
chr5:180803803-180804022 | Common:3; Rare:53 | ||||
chr5:180809819-180809932 | Common:4; Rare:26 | ||||
chr5:180810083-180810223 | Common:1; Rare:34 | ||||
chr5:180815532-180815805 | Common:2; Rare:55 | ||||
chr5:180861127-180861332 | Common:2; Rare:80 | ||||
chr5:181040110-181040299 | Rare:35 | ||||
chr5:181223116-181223313 | Rare:68 | ||||
chr5:181223566-181223768 | Common:3; Rare:43 | ||||
chr5:181243680-181243875 | Common:2; Rare:62 |