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
chr14 53598795 53598807 INSM1 JASPAR yes 107549952
chr14 53598799 53598809 HOXB13 JASPAR yes 107549953
chr14 53598799 53598809 HOXD13 JASPAR yes 107549954
chr14 53598811 53598832 ZNF263 JASPAR yes 107549955
chr14 53598818 53598839 ZNF263 JASPAR yes 107549956
chr14 53598819 53598825 MZF1 JASPAR yes 107549957
chr14 53598822 53598843 ZNF263 JASPAR yes 107549958
chr14 53598827 53598842 PRDM1 JASPAR yes 107549959
chr14 53598842 53598848 TBP TRANSFAC yes 107549960
chr14 53598856 53598866 MSC JASPAR yes 107549961
chr14 53598865 53598871 MZF1 JASPAR yes 107549962
chr14 53598882 53598885 MYB TRANSFAC yes 107549963
chr14 53598901 53598912 FOXH1 JASPAR yes 107549964
chr14 53598903 53598907 YY1 TRANSFAC yes 107549965
chr14 53598925 53598940 RUNX2 JASPAR yes 107549966
chr14 53598928 53598940 GLI2 JASPAR yes 107549967
chr14 53598934 53598938 ESR1 TRANSFAC yes 107549968
chr14 53598980 53598984 NFE TRANSFAC yes 107549969
chr14 53598993 53599001 NR4A2 JASPAR yes 107549970
chr14 53599037 53599048 USF1 JASPAR yes 107549971

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr14 53598922 rs11620755 C T no 3545892
chr14 53598965 rs143406039 G A no 3545893
chr14 53598966 rs11157950 T C no 3545894
chr14 53599024 rs11157951 G A,T no 3545895

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
chr14 53510686 53620000 - DDHD1 ENSG00000100523.10 53620000 0.81 0.99 13324 79062


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