Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:50312152-50312376 | Rare:98 | ||||
chr14:50532438-50532798 | Common:4; Rare:110 | ||||
chr14:50560091-50560178 | Rare:18 | ||||
chr14:50668301-50668556 | Common:3; Rare:92 | ||||
chr14:50944399-50944546 | Common:3; Rare:58; Clinvar:1; Clinvar (benign):2 | ||||
chr14:51240012-51240284 | Common:2; Rare:90 | ||||
chr14:51651627-51651988 | Common:4; Rare:104 | ||||
chr14:52707055-52707232 | Common:1; Rare:79 | ||||
chr14:55027085-55027295 | Common:2; Rare:58 | ||||
chr14:55411792-55411872 | Rare:38 | ||||
chr14:55580096-55580299 | Common:2; Rare:91 | ||||
chr14:57268782-57269115 | Common:2; Rare:100 | ||||
chr14:58298084-58298386 | Rare:82 | ||||
chr14:58427158-58427435 | Rare:59 | ||||
chr14:58427468-58427733 | Rare:82 |