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
chr16 69351854 69351869 FOXP1 JASPAR yes 49387615
chr16 69351855 69351870 FOXP1 JASPAR yes 49387616
chr16 69351855 69351876 IRF1 JASPAR yes 49387617
chr16 69351856 69351871 FOXP1 JASPAR yes 49387618
chr16 69351856 69351877 IRF1 JASPAR yes 49387619
chr16 69351857 69351872 FOXP1 JASPAR yes 49387620
chr16 69351857 69351878 IRF1 JASPAR yes 49387621
chr16 69351858 69351873 FOXP1 JASPAR yes 49387622
chr16 69351858 69351879 IRF1 JASPAR yes 49387623
chr16 69351859 69351874 FOXP1 JASPAR yes 49387624
chr16 69351859 69351880 IRF1 JASPAR yes 49387625
chr16 69351860 69351875 FOXP1 JASPAR yes 49387626
chr16 69351860 69351881 IRF1 JASPAR yes 49387627
chr16 69351861 69351876 FOXP1 JASPAR yes 49387628
chr16 69351861 69351882 IRF1 JASPAR yes 49387629
chr16 69351862 69351877 FOXP1 JASPAR yes 49387630
chr16 69351862 69351883 IRF1 JASPAR yes 49387631
chr16 69351863 69351878 FOXP1 JASPAR yes 49387632
chr16 69351863 69351884 IRF1 JASPAR yes 49387633
chr16 69351864 69351879 FOXP1 JASPAR yes 49387634
chr16 69351866 69351881 FOXP1 JASPAR yes 49387635
chr16 69351870 69351884 SPI1 JASPAR yes 49387636
chr16 69351877 69351892 HSF1 JASPAR yes 49387637
chr16 69351878 69351891 HSF1 JASPAR yes 49387638
chr16 69351878 69351891 HSF2 JASPAR yes 49387639
chr16 69351878 69351891 HSF4 JASPAR yes 49387640
chr16 69351887 69351897 NHLH1 JASPAR yes 49387641
chr16 69351894 69351903 SOX9 JASPAR yes 49387642
chr16 69351904 69351925 IRF1 JASPAR yes 49387643
chr16 69351906 69351921 STAT2 JASPAR yes 49387644
chr16 69351909 69351924 FOXP1 JASPAR yes 49387645
chr16 69351910 69351925 FOXP1 JASPAR yes 49387646
chr16 69351911 69351926 FOXP1 JASPAR yes 49387647
chr16 69351912 69351927 FOXP1 JASPAR yes 49387648
chr16 69351913 69351928 FOXP1 JASPAR yes 49387649

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr16 69351910 rs71148992 CT C 4505261
chr16 69351910 rs764204248 CT C 4505262

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
chr16 69333585 69354614 + RP11-343C2.11 ENSG00000260914.2 69333585 0.94 0.79 15000 81731
chr16 69345259 69358949 + VPS4A ENSG00000132612.14 69345259 0.55 1.0 15001 93405
chr16 69354043 69373570 - COG8 ENSG00000213380.9 69373570 0.67 0.99 15002 78359
chr16 69362524 69364498 - PDF ENSG00000258429.1 69364498 0.82 0.97 15003 87431
chr16 69362547 69368774 - RP11-343C2.12 ENSG00000272617.1 69368774 0.92 0.75 15004 83155
chr16 69368994 69390209 - RP11-343C2.9 ENSG00000260371.1 69390209 0.99 0.95 15005 61720
chr16 69369179 69385633 - RP11-343C2.7 ENSG00000259900.1 69385633 1.0 1.0 15006 66296
chr16 69373333 69377014 + NIP7 ENSG00000132603.9 69373333 0.77 0.99 15007 78596
chr16 69377151 69385712 - TMED6 ENSG00000157315.4 69385712 0.98 0.95 15008 66217
chr16 69389464 69442474 - TERF2 ENSG00000132604.6 69442474 0.71 1.0 15009 9455


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