Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:19776378-19776591 | Common:2; Rare:58 | ||||
chr19:20423687-20423745 | Common:1; Rare:18 | ||||
chr19:23762849-23763011 | Common:2; Rare:53 | ||||
chr19:27793338-27793477 | Common:3; Rare:36 | ||||
chr19:27793667-27794066 | Common:1; Rare:101 | ||||
chr19:33037348-33037534 | Common:1; Rare:40 | ||||
chr19:34860562-34860736 | Common:1; Rare:38 | ||||
chr19:35115044-35115078 | Rare:6 | ||||
chr19:36142725-36142959 | Rare:53 | ||||
chr19:36797290-36797546 | Rare:55 | ||||
chr19:38709977-38710329 | Common:1; Rare:84; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
chr19:38717788-38718059 | Rare:66; Clinvar (benign):1 | ||||
chr19:39403759-39403924 | Rare:27 | ||||
chr19:42287363-42287592 | Rare:75; Clinvar:1 | ||||
chr19:43361849-43362222 | Common:4; Rare:130 |