Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:7533858-7534179 | Common:3; Rare:80; Clinvar (benign):1 | ||||
chr19:7629539-7629826 | Common:5; Rare:101; Clinvar (benign):1 | ||||
chr19:8321338-8321653 | Common:2; Rare:135 | ||||
chr19:8390063-8390412 | Common:1; Rare:98 | ||||
chr19:9621192-9621525 | Common:3; Rare:92 | ||||
chr19:9827838-9827947 | Common:1; Rare:38 | ||||
chr19:10653842-10654046 | Common:1; Rare:73 | ||||
chr19:10928551-10928851 | Common:2; Rare:96 | ||||
chr19:11197489-11197644 | Common:1; Rare:45 | ||||
chr19:12610750-12610954 | Rare:75 | ||||
chr19:12666688-12666825 | Rare:56; Clinvar:4 | ||||
chr19:12696583-12696675 | Rare:42 | ||||
chr19:12940412-12940652 | Rare:75 | ||||
chr19:13150225-13150475 | Common:2; Rare:85 | ||||
chr19:13764473-13764561 | Common:1; Rare:31 |