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
chr13 111568628 111568632 YY1 TRANSFAC yes 19344155
chr13 111568633 111568637 YY1 TRANSFAC yes 19344156
chr13 111568636 111568649 POU2F2 JASPAR yes 19344157
chr13 111568636 111568650 POU1F1 JASPAR yes 19344158
chr13 111568637 111568649 POU3F1 JASPAR yes 19344159
chr13 111568637 111568649 POU3F2 JASPAR yes 19344160
chr13 111568637 111568650 POU3F3 JASPAR yes 19344161
chr13 111568638 111568642 YY1 TRANSFAC yes 19344162
chr13 111568642 111568654 MEF2B JASPAR yes 19344163
chr13 111568642 111568654 MEF2D JASPAR yes 19344164
chr13 111568644 111568652 FOXL1 JASPAR yes 19344165
chr13 111568667 111568678 ELF5 JASPAR yes 19344166
chr13 111568667 111568680 ELF1 JASPAR yes 19344167
chr13 111568667 111568681 SPI1 JASPAR yes 19344168
chr13 111568667 111568681 SPIC JASPAR yes 19344169
chr13 111568668 111568675 SPI1 JASPAR yes 19344170
chr13 111568668 111568676 FEV JASPAR yes 19344171
chr13 111568670 111568675 ETS2 TRANSFAC yes 19344172
chr13 111568683 111568697 XBP1 JASPAR yes 19344173
chr13 111568684 111568698 CREB3 JASPAR yes 19344174
chr13 111568689 111568694 ATF1 TRANSFAC yes 19344175
chr13 111568693 111568701 HOXA5 JASPAR yes 19344176
chr13 111568698 111568703 MYB TRANSFAC yes 19344177
chr13 111568707 111568717 GBX2 JASPAR yes 19344178
chr13 111568707 111568717 MNX1 JASPAR yes 19344179
chr13 111568708 111568716 BARX1 JASPAR yes 19344180
chr13 111568708 111568716 EN1 JASPAR yes 19344181
chr13 111568708 111568716 ISL2 JASPAR yes 19344182
chr13 111568708 111568716 MSX1 JASPAR yes 19344183
chr13 111568708 111568716 MSX2 JASPAR yes 19344184
chr13 111568708 111568716 PDX1 JASPAR yes 19344185
chr13 111568723 111568728 ETS2 TRANSFAC yes 19344186
chr13 111568762 111568773 HOXA10 JASPAR yes 19344187
chr13 111568763 111568773 HOXD13 JASPAR yes 19344188
chr13 111568765 111568779 IRF7 JASPAR yes 19344189
chr13 111568771 111568792 IRF1 JASPAR yes 19344190
chr13 111568775 111568789 STAT1 JASPAR yes 19344191
chr13 111568775 111568790 STAT2 JASPAR yes 19344192
chr13 111568787 111568799 HNF1B JASPAR yes 19344193
chr13 111568795 111568798 MYB TRANSFAC yes 19344194
chr13 111568796 111568810 SPI1 JASPAR yes 19344195
chr13 111568796 111568810 SPIC JASPAR yes 19344196
chr13 111568797 111568803 SOX10 JASPAR yes 19344197
chr13 111568802 111568807 ETS2 TRANSFAC yes 19344198
chr13 111568810 111568820 HMBOX1 JASPAR yes 19344199
chr13 111568810 111568822 HNF1B JASPAR yes 19344200
chr13 111568811 111568819 LBX1 JASPAR yes 19344201
chr13 111568812 111568815 MYB TRANSFAC yes 19344202
chr13 111568821 111568832 FOXP2 JASPAR yes 19344203
chr13 111568822 111568830 FOXO3 JASPAR yes 19344204
chr13 111568823 111568830 FOXD2 JASPAR yes 19344205
chr13 111568823 111568830 FOXI1 JASPAR yes 19344206
chr13 111568823 111568830 FOXL1 JASPAR yes 19344207
chr13 111568823 111568830 FOXO4 JASPAR yes 19344208
chr13 111568823 111568830 FOXO6 JASPAR yes 19344209
chr13 111568823 111568830 FOXP3 JASPAR yes 19344210
chr13 111568823 111568831 FOXD1 JASPAR yes 19344211
chr13 111568823 111568831 FOXG1 JASPAR yes 19344212
chr13 111568823 111568831 FOXO3 JASPAR yes 19344213
chr13 111568851 111568862 FOXA1 JASPAR yes 19344214
chr13 111568858 111568868 MYF6 JASPAR yes 19344215
chr13 111568858 111568868 NEUROG2 JASPAR yes 19344216
chr13 111568860 111568864 YY1 TRANSFAC yes 19344217
chr13 111568885 111568891 HiNF-A TRANSFAC yes 19344218
chr13 111568910 111568915 TFAP2A TRANSFAC yes 19344219
chr13 111568910 111568916 MZF1 JASPAR yes 19344220
chr13 111568912 111568917 ETS2 TRANSFAC yes 19344221
chr13 111568925 111568929 YY1 TRANSFAC yes 19344222
chr13 111568954 111568964 NFATC3 JASPAR yes 19344223
chr13 111568956 111568963 NFATC2 JASPAR yes 19344224
chr13 111568959 111568973 JUN JASPAR yes 19344225
chr13 111568964 111568973 JDP2 JASPAR yes 19344226
chr13 111568978 111568982 NFE TRANSFAC yes 19344227
chr13 111568978 111568983 GATA1 TRANSFAC yes 19344228
chr13 111568978 111568984 GATA3 JASPAR yes 19344229

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr13 111568652 rs149859266 A ATG 3398636
chr13 111568702 rs10693206 G GAACTTT
3398637
chr13 111568702 rs113599494 G GAACTTT
3398638
chr13 111568729 rs565206585 G A no 3398639
chr13 111568824 rs150752511 G A 3398640
chr13 111568907 rs192102867 A G no 3398641
chr13 111568989 rs55808575 C T no 3398642

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
chr13 111521578 111522162 - LINC00346 ENSG00000255874.1 111522162 0.76 1.0 13025 53544
chr13 111530887 111567416 - ANKRD10 ENSG00000088448.10 111567416 0.78 1.0 13026 98798


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