Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:96363283-96363556 | Common:1; Rare:92 | ||||
chr14:96502301-96502595 | Common:1; Rare:126 | ||||
chr14:99480728-99481013 | Common:2; Rare:110 | ||||
chr14:100239650-100239904 | Common:2; Rare:94 | ||||
chr14:100323189-100323448 | Common:2; Rare:67 | ||||
chr14:100375323-100375755 | Common:4; Rare:73 | ||||
chr14:100376259-100376511 | Common:3; Rare:80 | ||||
chr14:101809686-101810034 | Rare:83 | ||||
chr14:102083523-102083983 | Common:4; Rare:193 | ||||
chr14:102139663-102139932 | Rare:96 | ||||
chr14:102362849-102363092 | Rare:111 | ||||
chr14:103333924-103334258 | Common:3; Rare:143 | ||||
chr14:103385366-103385439 | Common:1; Rare:28 | ||||
chr14:103528981-103529243 | Common:1; Rare:73 | ||||
chr14:103562620-103563053 | Common:8; Rare:171; Clinvar (benign):5 |