Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:36524559-36524727 | Common:1; Rare:33 | ||||
chr14:36524847-36525060 | Rare:51 | ||||
chr14:41605318-41605420 | Common:2; Rare:24 | ||||
chr14:44962738-44962790 | Rare:12 | ||||
chr14:49633848-49634094 | Common:1; Rare:96; Clinvar:12; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
chr14:49775060-49775303 | Rare:48 | ||||
chr14:49799649-49799804 | Rare:32 | ||||
chr14:49853834-49854113 | Rare:45 | ||||
chr14:49862632-49863064 | Common:1; Rare:190 | ||||
chr14:49868119-49868453 | Common:3; Rare:74 | ||||
chr14:50335419-50335739 | Common:5; Rare:86 | ||||
chr14:52010987-52011089 | Common:1; Rare:39 | ||||
chr14:53217826-53217929 | Common:1; Rare:22 | ||||
chr14:55581028-55581319 | Common:6; Rare:77 | ||||
chr14:60642276-60642444 | Common:1; Rare:44 |