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
chr12 112809865 112809877 SRF JASPAR yes 82478608
chr12 112809865 112809877 SRF JASPAR yes 123788849
chr12 112809869 112809879 MEF2A JASPAR yes 82478609
chr12 112809869 112809879 MEF2A JASPAR yes 123788850
chr12 112809870 112809874 TEAD2 TRANSFAC yes 82478610
chr12 112809870 112809874 TEAD2 TRANSFAC yes 123788851
chr12 112809870 112809875 TBP TRANSFAC yes 82478611
chr12 112809870 112809875 TBP TRANSFAC yes 123788852
chr12 112809880 112809891 FOXH1 JASPAR yes 82478612
chr12 112809880 112809891 FOXH1 JASPAR yes 123788853
chr12 112809892 112809900 FOXL1 JASPAR yes 82478613
chr12 112809892 112809900 FOXL1 JASPAR yes 123788854
chr12 112809902 112809923 IRF1 JASPAR yes 82478614
chr12 112809902 112809923 IRF1 JASPAR yes 123788855
chr12 112809904 112809925 IRF1 JASPAR yes 82478615
chr12 112809904 112809925 IRF1 JASPAR yes 123788856
chr12 112809905 112809920 FOXP1 JASPAR yes 82478616
chr12 112809905 112809920 FOXP1 JASPAR yes 123788857
chr12 112809905 112809926 IRF1 JASPAR yes 82478617
chr12 112809905 112809926 IRF1 JASPAR yes 123788858
chr12 112809907 112809922 FOXP1 JASPAR yes 82478618
chr12 112809907 112809922 FOXP1 JASPAR yes 123788859
chr12 112809908 112809923 FOXP1 JASPAR yes 82478619
chr12 112809908 112809923 FOXP1 JASPAR yes 123788860
chr12 112809909 112809924 FOXP1 JASPAR yes 82478620
chr12 112809909 112809924 FOXP1 JASPAR yes 123788861
chr12 112809909 112809930 IRF1 JASPAR yes 82478621
chr12 112809909 112809930 IRF1 JASPAR yes 123788862
chr12 112809910 112809925 FOXP1 JASPAR yes 82478622
chr12 112809910 112809925 FOXP1 JASPAR yes 123788863
chr12 112809911 112809926 FOXP1 JASPAR yes 82478623
chr12 112809911 112809926 FOXP1 JASPAR yes 123788864
chr12 112809912 112809927 FOXP1 JASPAR yes 82478624
chr12 112809912 112809927 FOXP1 JASPAR yes 123788865
chr12 112809913 112809928 FOXP1 JASPAR yes 82478625
chr12 112809913 112809928 FOXP1 JASPAR yes 123788866

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr12 112809865 rs115831901 G A
2905127
chr12 112809908 rs538069859 C CT
2905128
chr12 112809908 rs541181560 C CT
2905129

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
chr12 112597992 112819896 - HECTD4 ENSG00000173064.6 112819896 0.73 1.0 12550 90029
chr12 112842994 112856642 - RPL6 ENSG00000089009.11 112856642 0.63 0.99 12551 53283
chr12 112856155 112947717 + PTPN11 ENSG00000179295.11 112856155 0.56 0.99 12552 53770


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
chr12 112601069 112601086 - hsa-miR-6861-3p MIMAT0027624 112820234 0.01661586864615082 0.0 0.0 336