Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:81170401-81170482 | Rare:20 | ||||
chr14:81219339-81219504 | Rare:37 | ||||
chr14:90264818-90265149 | Rare:67 | ||||
chr14:90383258-90383512 | Common:2; Rare:80 | ||||
chr14:95516614-95516744 | Common:2; Rare:26 | ||||
chr14:96039022-96039395 | Common:2; Rare:95 | ||||
chr14:100825953-100826216 | Rare:65 | ||||
chr14:101559964-101560166 | Rare:45 | ||||
chr14:101948057-101948381 | Common:2; Rare:96 | ||||
chr14:102010075-102010312 | Common:1; Rare:64; Clinvar (benign):5 | ||||
chr14:103533180-103533414 | Common:1; Rare:55 | ||||
chr14:103552436-103552737 | Common:1; Rare:56 | ||||
chr14:104957469-104957650 | Common:2; Rare:53 | ||||
chr14:106422173-106422317 | Common:4; Rare:45 | ||||
chr15:22494645-22494902 | Common:1; Rare:33 |