Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:41363801-41363983 | Common:1; Rare:65; Clinvar:1 | ||||
chr19:41860080-41860278 | Common:1; Rare:76; Clinvar:2; Clinvar (benign):1 | ||||
chr19:42075816-42076199 | Rare:105 | ||||
chr19:42220128-42220349 | Common:2; Rare:62 | ||||
chr19:42268236-42268570 | Rare:68 | ||||
chr19:42302332-42302498 | Rare:51 | ||||
chr19:43465540-43465780 | Common:1; Rare:76 | ||||
chr19:43527173-43527310 | Common:4; Rare:55; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
chr19:43577066-43577185 | Common:1; Rare:25 | ||||
chr19:43619582-43619818 | Common:3; Rare:77 | ||||
chr19:43754898-43755094 | Common:3; Rare:72 | ||||
chr19:43901782-43901911 | Common:2; Rare:27 | ||||
chr19:44002819-44002976 | Common:4; Rare:38 | ||||
chr19:44094166-44094420 | Common:1; Rare:65 | ||||
chr19:44113129-44113451 | Common:4; Rare:73 |