Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:186723767-186723914 | Common:5; Rare:60 | ||||
chr4:189940605-189941004 | Common:16; Rare:139 | ||||
chr5:218134-218381 | Common:3; Rare:106; Clinvar:10; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
chr5:612215-612353 | Rare:55 | ||||
chr5:892640-892907 | Common:5; Rare:89 | ||||
chr5:1799791-1799992 | Common:4; Rare:94 | ||||
chr5:1801300-1801460 | Common:4; Rare:80; Clinvar:3; Clinvar (benign):1 | ||||
chr5:5422332-5422655 | Common:2; Rare:102 | ||||
chr5:6378498-6378663 | Rare:67 | ||||
chr5:6633034-6633318 | Common:5; Rare:82; Clinvar:7; Clinvar (benign):2 | ||||
chr5:7868991-7869204 | Common:2; Rare:109; Clinvar (benign):1 | ||||
chr5:9546074-9546361 | Common:7; Rare:68 | ||||
chr5:10250224-10250377 | Common:2; Rare:85; Clinvar:3; Clinvar (benign):2 | ||||
chr5:10353564-10353901 | Common:4; Rare:133 | ||||
chr5:10441812-10441911 | Rare:30 |