Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:49633956-49634092 | Common:1; Rare:60; Clinvar:8; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr14:49853800-49853930 | Rare:30 | ||||
chr14:49862645-49863036 | Common:1; Rare:181 | ||||
chr14:49864846-49865128 | Rare:61 | ||||
chr14:49868119-49868394 | Common:1; Rare:62 | ||||
chr14:49970752-49970977 | Rare:46 | ||||
chr14:49993001-49993216 | Rare:35 | ||||
chr14:50001230-50001619 | Common:3; Rare:75 | ||||
chr14:50065014-50065131 | Rare:23 | ||||
chr14:50335419-50335589 | Common:1; Rare:60 | ||||
chr14:50920600-50920787 | Common:2; Rare:43; Clinvar:2; Clinvar (benign):1 | ||||
chr14:51561206-51561495 | Common:2; Rare:51 | ||||
chr14:51596524-51596718 | Rare:41 | ||||
chr14:51922631-51922974 | Common:2; Rare:55 | ||||
chr14:54367246-54367425 | Rare:26 |