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
chr11 56970711 56970715 YY1 TRANSFAC yes 38989797
chr11 56970711 56970715 YY1 TRANSFAC yes 114073125
chr11 56970731 56970735 H4TF2 TRANSFAC yes 38989798
chr11 56970731 56970735 H4TF2 TRANSFAC yes 114073126
chr11 56970739 56970743 YY1 TRANSFAC yes 38989799
chr11 56970739 56970743 YY1 TRANSFAC yes 114073127
chr11 56970767 56970786 REST JASPAR yes 38989800
chr11 56970767 56970786 REST JASPAR yes 114073128
chr11 56970807 56970812 GATA2 JASPAR yes 38989801
chr11 56970807 56970812 GATA2 JASPAR yes 114073129
chr11 56970810 56970815 GATA2 JASPAR yes 38989802
chr11 56970810 56970815 GATA2 JASPAR yes 114073130
chr11 56970843 56970846 MYB TRANSFAC yes 38989803
chr11 56970843 56970846 MYB TRANSFAC yes 114073131
chr11 56970849 56970861 NHLH1 JASPAR yes 38989804
chr11 56970849 56970861 NHLH1 JASPAR yes 114073132
chr11 56970850 56970860 NHLH1 JASPAR yes 38989805
chr11 56970850 56970860 NHLH1 JASPAR yes 114073133
chr11 56970856 56970861 TFAP2A TRANSFAC yes 38989806
chr11 56970856 56970861 TFAP2A TRANSFAC yes 114073134
chr11 56970856 56970862 MZF1 JASPAR yes 38989807
chr11 56970856 56970862 MZF1 JASPAR yes 114073135
chr11 56970859 56970876 BCL6B JASPAR yes 38989808
chr11 56970859 56970876 BCL6B JASPAR yes 114073136
chr11 56970871 56970886 AR JASPAR yes 38989809
chr11 56970871 56970886 AR JASPAR yes 114073137
chr11 56970880 56970886 NFIC JASPAR yes 38989810
chr11 56970880 56970886 NFIC JASPAR yes 114073138
chr11 56970882 56970892 TEAD1 JASPAR yes 38989811
chr11 56970882 56970892 TEAD4 JASPAR yes 38989812
chr11 56970882 56970892 TEAD1 JASPAR yes 114073139
chr11 56970882 56970892 TEAD4 JASPAR yes 114073140
chr11 56970883 56970891 TEAD3 JASPAR yes 38989813
chr11 56970883 56970891 TEAD3 JASPAR yes 114073141
chr11 56970886 56970891 ETS2 TRANSFAC yes 38989814
chr11 56970886 56970891 ETS2 TRANSFAC yes 114073142

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr11 56970769 rs185043751 C T
2007647
chr11 56970799 rs138474255 C T no 2007648

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
chr11 56949221 56959191 + LRRC55 ENSG00000183908.5 56949221 0.92 0.0 10833 78509
chr11 57001051 57004709 - APLNR ENSG00000134817.9 57004709 0.92 0.99 10834 66177


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