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
chr3 134309763 134309776 ZBTB18 JASPAR yes 71055157
chr3 134309764 134309776 NHLH1 JASPAR yes 71055158
chr3 134309765 134309775 FIGLA JASPAR yes 71055159
chr3 134309765 134309775 MSC JASPAR yes 71055160
chr3 134309765 134309775 MYF6 JASPAR yes 71055161
chr3 134309765 134309775 NHLH1 JASPAR yes 71055162
chr3 134309765 134309775 TFAP4 JASPAR yes 71055163
chr3 134309765 134309777 TAL1 JASPAR yes 71055164
chr3 134309789 134309793 YY1 TRANSFAC yes 71055165
chr3 134309794 134309798 NFE TRANSFAC yes 71055166
chr3 134309795 134309800 GATA2 JASPAR yes 71055167
chr3 134309804 134309814 NFKB1 JASPAR yes 71055168
chr3 134309804 134309815 NFKB1 JASPAR yes 71055169
chr3 134309813 134309819 SOX10 JASPAR yes 71055170
chr3 134309824 134309830 SOX10 JASPAR yes 71055171
chr3 134309834 134309847 ELF3 JASPAR yes 71055172
chr3 134309835 134309846 ELF5 JASPAR yes 71055173
chr3 134309835 134309847 EHF JASPAR yes 71055174
chr3 134309835 134309847 ELF1 JASPAR yes 71055175
chr3 134309835 134309847 ELF4 JASPAR yes 71055176
chr3 134309835 134309848 ELF1 JASPAR yes 71055177
chr3 134309844 134309855 STAT3 JASPAR yes 71055178
chr3 134309864 134309879 HNF4A JASPAR yes 71055179
chr3 134309865 134309880 HNF4G JASPAR yes 71055180
chr3 134309871 134309875 NFE TRANSFAC yes 71055181
chr3 134309904 134309915 FOSL2 JASPAR yes 71055182
chr3 134309905 134309911 YY1 JASPAR yes 71055183
chr3 134309905 134309916 NFE2 JASPAR yes 71055184
chr3 134309932 134309943 ESRRB JASPAR yes 71055185
chr3 134309946 134309961 AR JASPAR yes 71055186
chr3 134309975 134309987 PBX1 JASPAR yes 71055187
chr3 134309989 134309992 MYB TRANSFAC yes 71055188
chr3 134309996 134310001 GATA2 JASPAR yes 71055189
chr3 134310011 134310019 FEV JASPAR yes 71055190
chr3 134310121 134310125 YY1 TRANSFAC yes 71055191
chr3 134310135 134310145 MSC JASPAR yes 71055192
chr3 134310135 134310147 GRHL1 JASPAR yes 71055193
chr3 134310138 134310144 PTF TRANSFAC yes 71055194

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr3 134309848 rs115752682 C T
7047989
chr3 134309858 rs574615851 C T no 7047990
chr3 134309913 rs148586038 C T
7047991
chr3 134309963 rs193220381 T C no 7047992
chr3 134309977 rs13088413 T C
7047993
chr3 134310085 rs115862035 T G no 7047994

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
chr3 134316643 134979309 + EPHB1 ENSG00000154928.12 134316643 0.8 0.97 4105 93518
chr3 134321980 134370478 - KY ENSG00000174611.7 134370478 0.86 1.0 4106 39683


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