Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:24242580-24242770 | Common:1; Rare:46; Clinvar:1; Clinvar (benign):2 | ||||
chr14:24271453-24271659 | Common:1; Rare:60 | ||||
chr14:24299736-24299850 | Common:4; Rare:31 | ||||
chr14:24429852-24429968 | Rare:26 | ||||
chr14:24442663-24443023 | Common:5; Rare:116 | ||||
chr14:30559006-30559216 | Common:3; Rare:79 | ||||
chr14:30622190-30622365 | Common:1; Rare:77 | ||||
chr14:31025622-31025662 | Rare:12 | ||||
chr14:31207639-31207906 | Common:2; Rare:92 | ||||
chr14:31420524-31420777 | Common:4; Rare:73 | ||||
chr14:31561089-31561503 | Common:4; Rare:114; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr14:32076672-32077040 | Common:3; Rare:111 | ||||
chr14:34462205-34462602 | Common:1; Rare:136 | ||||
chr14:34539626-34539882 | Common:1; Rare:71 | ||||
chr14:34629944-34630260 | Common:5; Rare:126 |