Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:228103049-228103526 | Common:2; Rare:188 | ||||
chr1:228109172-228109666 | Rare:132 | ||||
chr1:228139769-228140411 | Common:4; Rare:189 | ||||
chr1:228140509-228140633 | Common:1; Rare:28 | ||||
chr1:228165385-228165854 | Rare:143; Clinvar (benign):2 | ||||
chr1:228165922-228166328 | Common:2; Rare:177; Clinvar:5; Clinvar (benign):7; Clinvar (pathogenic):5 | ||||
chr1:228174534-228174570 | Rare:8 | ||||
chr1:228213530-228213864 | Common:2; Rare:104 | ||||
chr1:228406713-228407214 | Common:6; Rare:109 | ||||
chr1:228416357-228416459 | Rare:26 | ||||
chr1:228416598-228416836 | Common:1; Rare:47 | ||||
chr1:228457285-228457711 | Common:2; Rare:159 | ||||
chr1:228457742-228458195 | Common:2; Rare:225 | ||||
chr1:228458507-228458736 | Common:5; Rare:74 | ||||
chr1:228487030-228487463 | Common:4; Rare:129 |