Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:22839526-22839795 | Common:1; Rare:51 | ||||
chr14:22930434-22930733 | Common:2; Rare:62 | ||||
chr14:24259218-24259543 | Rare:71 | ||||
chr14:31229679-31229845 | Rare:30 | ||||
chr14:31992072-31992365 | Common:1; Rare:58 | ||||
chr14:32203246-32203583 | Common:13; Rare:150 | ||||
chr14:32203586-32203661 | Rare:30 | ||||
chr14:34800383-34800535 | Rare:29 | ||||
chr14:35374600-35374618 | Common:1; Rare:4 | ||||
chr14:35402158-35402671 | Common:4; Rare:146; Clinvar:3; Clinvar (benign):2 | ||||
chr14:45232799-45233084 | Common:1; Rare:64 | ||||
chr14:49633888-49634053 | Common:1; Rare:67; Clinvar:7; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr14:49862284-49862559 | Common:1; Rare:63 | ||||
chr14:49862639-49862705 | Rare:30 | ||||
chr14:49862707-49863048 | Common:1; Rare:154 |