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
chr4 2389743 2389747 H4TF2 TRANSFAC yes 49190386
chr4 2389743 2389747 H4TF2 TRANSFAC yes 87852950
chr4 2389754 2389759 SP1 TRANSFAC yes 49190387
chr4 2389754 2389759 SP1 TRANSFAC yes 87852951
chr4 2389795 2389805 EVX1 JASPAR yes 49190388
chr4 2389795 2389805 MEOX1 JASPAR yes 49190389
chr4 2389795 2389805 EVX1 JASPAR yes 87852952
chr4 2389795 2389805 MEOX1 JASPAR yes 87852953
chr4 2389796 2389806 POU6F2 JASPAR yes 49190390
chr4 2389796 2389806 POU6F2 JASPAR yes 87852954
chr4 2389801 2389815 GLIS3 JASPAR yes 49190391
chr4 2389801 2389815 GLIS3 JASPAR yes 87852955
chr4 2389804 2389820 ZNF143 JASPAR yes 49190392
chr4 2389804 2389820 ZNF143 JASPAR yes 87852956
chr4 2389836 2389856 ESR1 JASPAR yes 49190393
chr4 2389836 2389856 ESR1 JASPAR yes 87852957
chr4 2389840 2389855 AR JASPAR yes 49190394
chr4 2389840 2389855 AR JASPAR yes 87852958
chr4 2389846 2389856 SP1 JASPAR yes 49190395
chr4 2389846 2389856 SP1 JASPAR yes 87852959
chr4 2389849 2389855 NFE2 TRANSFAC yes 49190396
chr4 2389849 2389855 NFE2 TRANSFAC yes 87852960
chr4 2389855 2389865 SP1 JASPAR yes 49190397
chr4 2389855 2389865 SP1 JASPAR yes 87852961
chr4 2389882 2389887 GATA2 JASPAR yes 49190398
chr4 2389882 2389887 GATA2 JASPAR yes 87852962
chr4 2389882 2389896 EBF1 JASPAR yes 49190399
chr4 2389882 2389896 EBF1 JASPAR yes 87852963
chr4 2389908 2389922 TCF7L2 JASPAR yes 49190400
chr4 2389908 2389922 TCF7L2 JASPAR yes 87852964
chr4 2389912 2389918 TCF1 TRANSFAC yes 49190401
chr4 2389912 2389918 TCF1 TRANSFAC yes 87852965
chr4 2389912 2389919 TCF4 TRANSFAC yes 49190402
chr4 2389912 2389919 TCF4 TRANSFAC yes 87852966
chr4 2389925 2389933 HOXA5 JASPAR yes 49190403
chr4 2389925 2389933 HOXA5 JASPAR yes 87852967
chr4 2389965 2389977 HNF1B JASPAR yes 49190404
chr4 2389965 2389977 HNF1B JASPAR yes 87852968
chr4 2389992 2390004 IRF1 JASPAR yes 49190405
chr4 2389992 2390004 IRF1 JASPAR yes 87852969

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr4 2389730 rs3135096 A G no 7351877
chr4 2389800 rs3135095 A G 7351878
chr4 2389863 rs3135094 C T
7351879
chr4 2389869 rs80226020 C T no 7351880
chr4 2389870 rs117527882 G A no 7351881
chr4 2389932 rs149338384 T C
7351882
chr4 2389959 rs7438668 C T no 7351883

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
chr4 2271309 2420390 - ZFYVE28 ENSG00000159733.9 2420390 0.71 1.0 4471 69624
chr4 2451700 2464668 + RP11-503N18.3 ENSG00000249428.1 2451700 0.92 1.0 4472 38314
chr4 2463947 2627047 + RNF4 ENSG00000063978.11 2463947 0.69 0.99 4473 26067


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