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 107594643 107594655 TEAD1 JASPAR yes 26113813
chr7 107594645 107594655 TEAD1 JASPAR yes 26113814
chr7 107594645 107594655 TEAD4 JASPAR yes 26113815
chr7 107594646 107594654 TEAD3 JASPAR yes 26113816
chr7 107594682 107594692 RELA JASPAR yes 26113817
chr7 107594684 107594695 ELK4 JASPAR yes 26113818
chr7 107594685 107594697 EHF JASPAR yes 26113819
chr7 107594685 107594697 ELF1 JASPAR yes 26113820
chr7 107594686 107594694 FEV JASPAR yes 26113821
chr7 107594686 107594695 ELK4 JASPAR yes 26113822
chr7 107594687 107594693 ETS1 JASPAR yes 26113823
chr7 107594698 107594703 ETS2 TRANSFAC yes 26113824
chr7 107594708 107594718 NKX2-3 JASPAR yes 26113825
chr7 107594709 107594718 NKX2-8 JASPAR yes 26113826
chr7 107594710 107594724 SPI1 JASPAR yes 26113827
chr7 107594717 107594732 STAT1 JASPAR yes 26113828
chr7 107594719 107594730 STAT1 JASPAR yes 26113829
chr7 107594719 107594730 STAT3 JASPAR yes 26113830
chr7 107594724 107594736 NHLH1 JASPAR yes 26113831
chr7 107594725 107594735 NHLH1 JASPAR yes 26113832
chr7 107594752 107594761 ZEB1 JASPAR yes 26113833
chr7 107594753 107594763 ID4 JASPAR yes 26113834
chr7 107594754 107594763 SNAI2 JASPAR yes 26113835
chr7 107594755 107594760 USF2 TRANSFAC yes 26113836
chr7 107594770 107594791 IRF1 JASPAR yes 26113837
chr7 107594771 107594792 IRF1 JASPAR yes 26113838
chr7 107594773 107594794 IRF1 JASPAR yes 26113839
chr7 107594774 107594795 IRF1 JASPAR yes 26113840
chr7 107594775 107594790 FOXP1 JASPAR yes 26113841
chr7 107594775 107594796 IRF1 JASPAR yes 26113842
chr7 107594776 107594791 FOXP1 JASPAR yes 26113843
chr7 107594777 107594792 FOXP1 JASPAR yes 26113844
chr7 107594778 107594793 FOXP1 JASPAR yes 26113845
chr7 107594779 107594794 FOXP1 JASPAR yes 26113846
chr7 107594780 107594795 FOXP1 JASPAR yes 26113847
chr7 107594781 107594796 FOXP1 JASPAR yes 26113848
chr7 107594782 107594797 FOXP1 JASPAR yes 26113849

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr7 107594717 rs73195553 A G 10016696
chr7 107594745 rs139914895 T C no 10016697

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 107531415 107572175 + DLD ENSG00000091140.8 107531415 0.71 0.99 7754 36779
chr7 107564244 107643700 - LAMB1 ENSG00000091136.9 107643700 0.89 0.99 7755 51097


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