Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:48413064-48413208 | Rare:20 | ||||
chr13:52194408-52194542 | Rare:37 | ||||
chr13:73497533-73497769 | Rare:40 | ||||
chr13:73611104-73611188 | Rare:14 | ||||
chr13:109148297-109148550 | Common:1; Rare:47 | ||||
chr13:109265126-109265419 | Common:4; Rare:68 | ||||
chr13:109272007-109272217 | Common:6; Rare:46 | ||||
chr14:22980676-22980894 | Common:1; Rare:48 | ||||
chr14:49633956-49634064 | Common:1; Rare:43; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr14:49862651-49863044 | Common:1; Rare:181 | ||||
chr14:51397173-51397335 | Common:1; Rare:41 | ||||
chr14:68547614-68547815 | Common:1; Rare:25 | ||||
chr14:70698439-70698609 | Common:2; Rare:19 | ||||
chr14:73246009-73246106 | Rare:40 | ||||
chr14:75222113-75222372 | Common:2; Rare:48 |