Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:24818188-24818403 | Common:3; Rare:43 | ||||
chr14:31944515-31944837 | Common:3; Rare:62 | ||||
chr14:32203267-32203583 | Common:13; Rare:134 | ||||
chr14:32572447-32572586 | Rare:29 | ||||
chr14:34764869-34765192 | Rare:78 | ||||
chr14:34874112-34874231 | Common:1; Rare:33 | ||||
chr14:35335585-35335750 | Rare:36 | ||||
chr14:35341694-35341853 | Common:4; Rare:29 | ||||
chr14:35402012-35402102 | Rare:37; Clinvar:1; Clinvar (benign):1 | ||||
chr14:37554297-37554344 | Rare:14 | ||||
chr14:37554513-37554703 | Common:5; Rare:24 | ||||
chr14:37555942-37556228 | Common:6; Rare:33 | ||||
chr14:37567060-37567212 | Rare:30 | ||||
chr14:37598406-37598513 | Rare:26 | ||||
chr14:39175863-39176149 | Common:4; Rare:71 |