Input Chromosomal region, for example: chr1:1000-10000 to view the enhancers around this region



Chrom. Start End TF Name Source Predicted site? Tissue/Cell line id More
chr20 35239893 35239908 FOXP1 JASPAR yes 113973800
chr20 35239894 35239909 FOXP1 JASPAR yes 113973801
chr20 35239895 35239910 FOXP1 JASPAR yes 113973802
chr20 35239895 35239916 IRF1 JASPAR yes 113973803
chr20 35239896 35239911 FOXP1 JASPAR yes 113973804
chr20 35239896 35239917 IRF1 JASPAR yes 113973805
chr20 35239897 35239912 FOXP1 JASPAR yes 113973806
chr20 35239897 35239918 IRF1 JASPAR yes 113973807
chr20 35239898 35239913 FOXP1 JASPAR yes 113973808
chr20 35239898 35239919 IRF1 JASPAR yes 113973809
chr20 35239899 35239914 FOXP1 JASPAR yes 113973810
chr20 35239899 35239920 IRF1 JASPAR yes 113973811
chr20 35239900 35239915 FOXP1 JASPAR yes 113973812
chr20 35239900 35239921 IRF1 JASPAR yes 113973813
chr20 35239901 35239916 FOXP1 JASPAR yes 113973814
chr20 35239902 35239917 FOXP1 JASPAR yes 113973815
chr20 35239902 35239923 IRF1 JASPAR yes 113973816
chr20 35239903 35239918 FOXP1 JASPAR yes 113973817
chr20 35239903 35239924 IRF1 JASPAR yes 113973818
chr20 35239904 35239919 FOXP1 JASPAR yes 113973819
chr20 35239907 35239922 STAT2 JASPAR yes 113973820
chr20 35239914 35239929 RUNX2 JASPAR yes 113973821
chr20 35239915 35239924 RUNX2 JASPAR yes 113973822
chr20 35239915 35239925 RUNX3 JASPAR yes 113973823
chr20 35239915 35239926 RUNX1 JASPAR yes 113973824
chr20 35239933 35239943 SMAD3 JASPAR yes 113973825
chr20 35239944 35239947 MYB TRANSFAC yes 113973826
chr20 35239949 35239967 NFYA JASPAR yes 113973827
chr20 35239951 35239962 CDX2 JASPAR yes 113973828
chr20 35239952 35239963 HOXA10 JASPAR yes 113973829
chr20 35239953 35239957 H1TF2 TRANSFAC yes 113973830
chr20 35239953 35239957 NFE TRANSFAC yes 113973831
chr20 35239953 35239957 SRF TRANSFAC yes 113973832
chr20 35239953 35239962 CDX1 JASPAR yes 113973833
chr20 35239953 35239963 HOXA13 JASPAR yes 113973834
chr20 35239953 35239963 HOXB13 JASPAR yes 113973835
chr20 35239953 35239963 HOXD13 JASPAR yes 113973836

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More

Blank TSI value indicates lack of sufficient expression for calculation
Chrom Start End Strand Gene Name Ensembl ID TSS TSI of Normal tissues TSI of Cancer tissues Distance between enhancer and TSS id More
chr20 35169887 35178228 + MYL9 ENSG00000101335.5 35169887 0.92 1.0 18458 29994
chr20 35201891 35222353 + TGIF2 ENSG00000118707.5 35201891 0.75 0.98 18459 61998
chr20 35202956 35240787 + TGIF2-C20orf24 ENSG00000259399.1 35202956 0.91 0.83 18460 63063
chr20 35234137 35240960 + C20orf24 ENSG00000101084.12 35234137 0.73 0.88 18461 94244
chr20 35240721 35274619 - SLA2 ENSG00000101082.9 35274619 0.94 1.0 18462 65367


Blank TSI value indicates lack of sufficient expression for calculation
Chrom Start End Strand miRNA Name miRBase ID TSS Score TSI of Normal tissues TSI of Cancer tissues id More

No results