Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:48011210-48011610 | Common:4; Rare:171 | ||||
chr14:49633949-49634092 | Common:1; Rare:65; Clinvar:9; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr14:49634262-49634536 | Common:1; Rare:136; Clinvar:10; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr14:49861705-49861940 | Common:1; Rare:63 | ||||
chr14:49862839-49863044 | Rare:80 | ||||
chr14:49868104-49868340 | Common:1; Rare:46 | ||||
chr14:50003245-50003692 | Common:5; Rare:187 | ||||
chr14:50311417-50311567 | Common:1; Rare:46 | ||||
chr14:50335300-50335720 | Common:1; Rare:107 | ||||
chr14:50336020-50336490 | Common:2; Rare:133 | ||||
chr14:50667313-50667713 | Common:3; Rare:205 | ||||
chr14:50943440-50943770 | Common:3; Rare:65 | ||||
chr14:51006447-51007115 | Common:4; Rare:158 | ||||
chr14:51093636-51094036 | Common:5; Rare:159 | ||||
chr14:51139089-51139489 | Common:6; Rare:102 |