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
chr15 40162586 40162590 YY1 TRANSFAC yes 70510891
chr15 40162617 40162632 JUND JASPAR yes 70510892
chr15 40162619 40162633 ATF7 JASPAR yes 70510893
chr15 40162619 40162633 BATF3 JASPAR yes 70510894
chr15 40162620 40162632 JDP2 JASPAR yes 70510895
chr15 40162620 40162635 JUND JASPAR yes 70510896
chr15 40162621 40162634 JUN JASPAR yes 70510897
chr15 40162622 40162629 JUN TRANSFAC yes 70510898
chr15 40162628 40162632 YY1 TRANSFAC yes 70510899
chr15 40162636 40162641 GATA2 JASPAR yes 70510900
chr15 40162639 40162642 MYB TRANSFAC yes 70510901
chr15 40162639 40162648 RUNX2 JASPAR yes 70510902
chr15 40162639 40162649 RUNX3 JASPAR yes 70510903
chr15 40162639 40162650 RUNX1 JASPAR yes 70510904
chr15 40162687 40162697 CUX1 JASPAR yes 70510905
chr15 40162687 40162697 CUX2 JASPAR yes 70510906
chr15 40162694 40162697 MYB TRANSFAC yes 70510907
chr15 40162702 40162706 YY1 TRANSFAC yes 70510908
chr15 40162724 40162735 FOXB1 JASPAR yes 70510909
chr15 40162728 40162735 NKX3-1 JASPAR yes 70510910
chr15 40162746 40162749 MYB TRANSFAC yes 70510911
chr15 40162766 40162769 MYB TRANSFAC yes 70510912
chr15 40162769 40162781 YY1 JASPAR yes 70510913
chr15 40162823 40162827 H1TF2 TRANSFAC yes 70510914
chr15 40162823 40162827 NFE TRANSFAC yes 70510915
chr15 40162823 40162827 SRF TRANSFAC yes 70510916
chr15 40162847 40162851 TEAD2 TRANSFAC yes 70510917
chr15 40162848 40162856 OTX2 JASPAR yes 70510918
chr15 40162859 40162871 TEAD1 JASPAR yes 70510919
chr15 40162871 40162876 SP1 TRANSFAC yes 70510920
chr15 40162883 40162900 ZNF410 JASPAR yes 70510921
chr15 40162909 40162920 NFE2L2 JASPAR yes 70510922
chr15 40162911 40162927 SOX8 JASPAR yes 70510923
chr15 40162915 40162929 POU4F1 JASPAR yes 70510924
chr15 40162915 40162931 POU4F2 JASPAR yes 70510925
chr15 40162915 40162931 POU4F3 JASPAR yes 70510926
chr15 40162934 40162938 NFE TRANSFAC yes 70510927

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr15 40162605 rs17719200 G A no 3909179
chr15 40162610 rs118172022 C G no 3909180
chr15 40162636 rs7497058 A G
3909181
chr15 40162717 rs1369884 T C no 3909182
chr15 40162766 rs1369885 C A
3909183
chr15 40162929 rs150980294 G A 3909184

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
chr15 39892232 40075031 - FSIP1 ENSG00000150667.6 40075031 0.82 0.97 13796 12449
chr15 40091233 40213093 - GPR176 ENSG00000166073.4 40213093 0.76 0.97 13797 49861
chr15 40226347 40327797 + EIF2AK4 ENSG00000128829.7 40226347 0.85 0.99 13798 36607


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