Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:45771567-45771814 | Common:1; Rare:114; Clinvar (benign):1 | ||||
chr19:45777403-45777778 | Common:1; Rare:150; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr19:45779444-45779738 | Common:2; Rare:99 | ||||
chr19:45782216-45782417 | Common:1; Rare:82 | ||||
chr19:45863119-45863385 | Common:3; Rare:83 | ||||
chr19:46296838-46297069 | Common:4; Rare:86 | ||||
chr19:46298120-46298473 | Common:5; Rare:85 | ||||
chr19:46346951-46347163 | Common:3; Rare:74 | ||||
chr19:46495846-46495983 | Rare:42 | ||||
chr19:46600913-46601411 | Common:5; Rare:172; Clinvar (benign):1 | ||||
chr19:46745820-46746071 | Common:3; Rare:54 | ||||
chr19:46788555-46788617 | Rare:12 | ||||
chr19:47112151-47112618 | Common:2; Rare:153 | ||||
chr19:47113103-47113414 | Common:2; Rare:83 | ||||
chr19:47256472-47256577 | Rare:39 |