Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:50686756-50686903 | Common:3; Rare:66 | ||||
chr15:50908579-50908775 | Common:2; Rare:84; Clinvar (benign):2 | ||||
chr15:51622828-51623094 | Common:3; Rare:100 | ||||
chr15:51971738-51971841 | Rare:46 | ||||
chr15:52019089-52019259 | Common:1; Rare:87 | ||||
chr15:52179885-52179929 | Common:1; Rare:23 | ||||
chr15:52179936-52179980 | Rare:16 | ||||
chr15:52679326-52679519 | Common:1; Rare:66 | ||||
chr15:55196852-55196978 | Common:3; Rare:39 | ||||
chr15:55319108-55319247 | Common:2; Rare:37 | ||||
chr15:55408234-55408521 | Common:3; Rare:67 | ||||
chr15:55993551-55993796 | Common:1; Rare:79 | ||||
chr15:56918421-56918837 | Common:3; Rare:143 | ||||
chr15:58770981-58771323 | Common:3; Rare:136 | ||||
chr15:58933048-58933389 | Common:1; Rare:113 |