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 101690851 101690872 ZNF263 JASPAR yes 16825764
chr7 101690851 101690872 ZNF263 JASPAR yes 26106151
chr7 101690852 101690873 ZNF263 JASPAR yes 16825765
chr7 101690852 101690873 ZNF263 JASPAR yes 26106152
chr7 101690856 101690877 ZNF263 JASPAR yes 16825766
chr7 101690856 101690877 ZNF263 JASPAR yes 26106153
chr7 101690858 101690864 MAZ TRANSFAC yes 16825767
chr7 101690858 101690864 MAZ TRANSFAC yes 26106154
chr7 101690858 101690869 E2F6 JASPAR yes 16825768
chr7 101690858 101690869 E2F6 JASPAR yes 26106155
chr7 101690860 101690868 SP1 TRANSFAC yes 16825769
chr7 101690860 101690868 SP1 TRANSFAC yes 26106156
chr7 101690860 101690881 ZNF263 JASPAR yes 16825770
chr7 101690860 101690881 ZNF263 JASPAR yes 26106157
chr7 101690862 101690868 MAZ TRANSFAC yes 16825771
chr7 101690862 101690868 MAZ TRANSFAC yes 26106158
chr7 101690862 101690873 E2F6 JASPAR yes 16825772
chr7 101690862 101690873 E2F6 JASPAR yes 26106159
chr7 101690864 101690872 SP1 TRANSFAC yes 16825773
chr7 101690864 101690872 SP1 TRANSFAC yes 26106160
chr7 101690864 101690885 ZNF263 JASPAR yes 16825774
chr7 101690864 101690885 ZNF263 JASPAR yes 26106161
chr7 101690866 101690872 MAZ TRANSFAC yes 16825775
chr7 101690866 101690872 MAZ TRANSFAC yes 26106162
chr7 101690868 101690889 ZNF263 JASPAR yes 16825776
chr7 101690868 101690889 ZNF263 JASPAR yes 26106163
chr7 101690872 101690893 ZNF263 JASPAR yes 16825777
chr7 101690872 101690893 ZNF263 JASPAR yes 26106164
chr7 101690873 101690885 PBX1 JASPAR yes 16825778
chr7 101690873 101690885 PBX1 JASPAR yes 26106165
chr7 101690877 101690889 PBX1 JASPAR yes 16825779
chr7 101690877 101690889 PBX1 JASPAR yes 26106166
chr7 101690881 101690893 PBX1 JASPAR yes 16825780
chr7 101690881 101690893 PBX1 JASPAR yes 26106167
chr7 101690886 101690903 BCL6B JASPAR yes 16825781
chr7 101690886 101690903 BCL6B JASPAR yes 26106168

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr7 101690871 rs561322266 G T 9991193
chr7 101690875 rs150429649 T G
9991194

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

No results

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