Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:42528428-42528532 | Common:2; Rare:33 | ||||
chr19:43527156-43527276 | Common:5; Rare:56; Clinvar:4; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
chr19:43575438-43575563 | Common:2; Rare:50 | ||||
chr19:43670109-43670324 | Common:2; Rare:58 | ||||
chr19:43754890-43755090 | Common:3; Rare:77 | ||||
chr19:44025231-44025412 | Common:1; Rare:40 | ||||
chr19:44071948-44072166 | Common:1; Rare:54 | ||||
chr19:44094113-44094399 | Common:1; Rare:67 | ||||
chr19:44113157-44113434 | Common:3; Rare:61 | ||||
chr19:44141511-44141636 | Common:1; Rare:17 | ||||
chr19:44164923-44165133 | Common:1; Rare:51 | ||||
chr19:44212441-44212575 | Rare:34 | ||||
chr19:44448428-44448598 | Rare:60 | ||||
chr19:44643792-44644040 | Rare:65 | ||||
chr19:44955237-44955404 | Common:2; Rare:48 |