Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:11089159-11089516 | Rare:54; Clinvar:9; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr19:11197524-11197666 | Common:1; Rare:48 | ||||
chr19:11559205-11559407 | Common:1; Rare:61 | ||||
chr19:12610723-12610941 | Rare:74 | ||||
chr19:12666743-12666822 | Rare:25; Clinvar:1 | ||||
chr19:14529265-14529660 | Common:1; Rare:164 | ||||
chr19:16661045-16661185 | Common:1; Rare:43 | ||||
chr19:17215245-17215398 | Common:2; Rare:51 | ||||
chr19:17405577-17405822 | Common:5; Rare:39 | ||||
chr19:17794977-17795180 | Common:2; Rare:38 | ||||
chr19:18173542-18173830 | Rare:55 | ||||
chr19:18323027-18323336 | Common:3; Rare:104 | ||||
chr19:18919352-18919740 | Common:2; Rare:133 | ||||
chr19:19033482-19033614 | Common:2; Rare:45 | ||||
chr19:19192122-19192259 | Common:1; Rare:42 |