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
chr7 104618635 104618650 HNF4A JASPAR yes 16920776
chr7 104618635 104618650 HNF4A JASPAR yes 26108607
chr7 104618641 104618652 ESRRA JASPAR yes 16920777
chr7 104618641 104618652 ESRRB JASPAR yes 16920778
chr7 104618641 104618652 ESRRA JASPAR yes 26108608
chr7 104618641 104618652 ESRRB JASPAR yes 26108609
chr7 104618642 104618650 NR4A2 JASPAR yes 16920779
chr7 104618642 104618650 NR4A2 JASPAR yes 26108610
chr7 104618643 104618653 RORA JASPAR yes 16920780
chr7 104618643 104618653 RORA JASPAR yes 26108611
chr7 104618652 104618669 ESR1 JASPAR yes 16920781
chr7 104618652 104618669 ESR1 JASPAR yes 26108612
chr7 104618655 104618666 NRL JASPAR yes 16920782
chr7 104618655 104618666 NRL JASPAR yes 26108613
chr7 104618728 104618731 MYB TRANSFAC yes 16920783
chr7 104618728 104618731 MYB TRANSFAC yes 26108614
chr7 104618736 104618743 NKX3-1 JASPAR yes 16920784
chr7 104618736 104618743 NKX3-1 JASPAR yes 26108615
chr7 104618737 104618745 FOXC1 JASPAR yes 16920785
chr7 104618737 104618745 FOXC1 JASPAR yes 26108616
chr7 104618760 104618766 TCF4 TRANSFAC yes 16920786
chr7 104618760 104618766 TCF4 TRANSFAC yes 26108617
chr7 104618779 104618791 PROX1 JASPAR yes 16920787
chr7 104618779 104618791 PROX1 JASPAR yes 26108618
chr7 104618786 104618801 HNF1A JASPAR yes 16920788
chr7 104618786 104618801 HNF1A JASPAR yes 26108619
chr7 104618787 104618800 HNF1B JASPAR yes 16920789
chr7 104618787 104618800 HNF1B JASPAR yes 26108620
chr7 104618790 104618805 LEF1 JASPAR yes 16920790
chr7 104618790 104618805 LEF1 JASPAR yes 26108621
chr7 104618791 104618806 MEF2C JASPAR yes 16920791
chr7 104618791 104618806 MEF2C JASPAR yes 26108622
chr7 104618792 104618805 POU3F3 JASPAR yes 16920792
chr7 104618792 104618805 POU3F3 JASPAR yes 26108623
chr7 104618793 104618805 POU2F1 JASPAR yes 16920793
chr7 104618793 104618805 POU2F1 JASPAR yes 26108624
chr7 104618807 104618820 DUXA JASPAR yes 16920794
chr7 104618807 104618820 DUXA JASPAR yes 26108625
chr7 104618810 104618815 MYB TRANSFAC yes 16920795
chr7 104618810 104618815 MYB TRANSFAC yes 26108626
chr7 104618819 104618827 RHOXF1 JASPAR yes 16920796
chr7 104618819 104618827 RHOXF1 JASPAR yes 26108627
chr7 104618826 104618830 YY1 TRANSFAC yes 16920797
chr7 104618826 104618830 YY1 TRANSFAC yes 26108628
chr7 104618829 104618835 TCF1 TRANSFAC yes 16920798
chr7 104618829 104618835 TCF1 TRANSFAC yes 26108629
chr7 104618843 104618854 NFKB1 JASPAR yes 16920799
chr7 104618843 104618854 NFKB1 JASPAR yes 26108630
chr7 104618844 104618854 NFKB1 JASPAR yes 16920800
chr7 104618844 104618854 NFKB1 JASPAR yes 26108631
chr7 104618852 104618863 TBX20 JASPAR yes 16920801
chr7 104618852 104618863 TBX20 JASPAR yes 26108632
chr7 104618858 104618872 NR2F1 JASPAR yes 16920802
chr7 104618858 104618872 NR2F1 JASPAR yes 26108633
chr7 104618860 104618873 JUN JASPAR yes 16920803
chr7 104618860 104618873 JUN JASPAR yes 26108634
chr7 104618862 104618877 JUND JASPAR yes 16920804
chr7 104618862 104618877 JUND JASPAR yes 26108635
chr7 104618864 104618872 CREB1 JASPAR yes 16920805
chr7 104618864 104618872 CREB1 JASPAR yes 26108636
chr7 104618867 104618871 ESR1 TRANSFAC yes 16920806
chr7 104618867 104618871 ESR1 TRANSFAC yes 26108637
chr7 104618886 104618890 ESR1 TRANSFAC yes 16920807
chr7 104618886 104618890 ESR1 TRANSFAC yes 26108638
chr7 104618901 104618922 IRF1 JASPAR yes 16920808
chr7 104618901 104618922 IRF1 JASPAR yes 26108639
chr7 104618917 104618921 YY1 TRANSFAC yes 16920809
chr7 104618917 104618921 YY1 TRANSFAC yes 26108640
chr7 104618943 104618954 NFE2L2 JASPAR yes 16920810
chr7 104618943 104618954 NFE2L2 JASPAR yes 26108641
chr7 104618962 104618977 FOXP1 JASPAR yes 16920811
chr7 104618962 104618977 FOXP1 JASPAR yes 26108642
chr7 104618963 104618978 FOXP1 JASPAR yes 16920812
chr7 104618963 104618978 FOXP1 JASPAR yes 26108643
chr7 104618967 104618982 FOXP1 JASPAR yes 16920813
chr7 104618967 104618982 FOXP1 JASPAR yes 26108644

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr7 104618886 rs148568217 T C
10000315

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
chr7 104654626 104754808 + KMT2E ENSG00000005483.15 104654626 0.78 0.99 7734 64352


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