Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:6416776-6417019 | Common:1; Rare:85 | ||||
chr19:6424461-6424668 | Common:2; Rare:47 | ||||
chr19:6424808-6424831 | Rare:5 | ||||
chr19:6501291-6501554 | Common:1; Rare:60; Clinvar:1; Clinvar (benign):2 | ||||
chr19:6502198-6502423 | Rare:64; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr19:6737525-6737852 | Common:4; Rare:108 | ||||
chr19:7394977-7395215 | Common:6; Rare:75 | ||||
chr19:7488988-7489104 | Rare:53 | ||||
chr19:7515884-7516240 | Rare:82 | ||||
chr19:7522452-7522679 | Common:1; Rare:78; Clinvar:2 | ||||
chr19:7534084-7534213 | Common:3; Rare:36; Clinvar (benign):1 | ||||
chr19:7535514-7535740 | Common:3; Rare:75; Clinvar:2 | ||||
chr19:7595707-7596035 | Common:3; Rare:116 | ||||
chr19:7629520-7629874 | Common:5; Rare:127; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr19:7680706-7680919 | Common:2; Rare:74 |