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
chr11 3792619 3792624 GATA2 JASPAR yes 114033158
chr11 3792628 3792643 PRDM1 JASPAR yes 114033159
chr11 3792629 3792633 YY1 TRANSFAC yes 114033160
chr11 3792671 3792692 IRF1 JASPAR yes 114033161
chr11 3792681 3792691 NFATC3 JASPAR yes 114033162
chr11 3792690 3792705 HSF1 JASPAR yes 114033163
chr11 3792691 3792703 TEAD1 JASPAR yes 114033164
chr11 3792691 3792704 HSF1 JASPAR yes 114033165
chr11 3792691 3792704 HSF2 JASPAR yes 114033166
chr11 3792691 3792704 HSF4 JASPAR yes 114033167
chr11 3792693 3792703 TEAD1 JASPAR yes 114033168
chr11 3792693 3792703 TEAD4 JASPAR yes 114033169
chr11 3792694 3792702 TEAD3 JASPAR yes 114033170
chr11 3792703 3792715 E2F8 JASPAR yes 114033171
chr11 3792704 3792716 INSM1 JASPAR yes 114033172
chr11 3792727 3792742 LEF1 JASPAR yes 114033173

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr11 3792657 rs7931756 G T no 1811472
chr11 3792666 rs554914000 C CA no 1811473
chr11 3792691 rs169346 T C 1811474

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
chr11 3686817 3692614 - CHRNA10 ENSG00000129749.3 3692614 0.75 0.99 10432 3
chr11 3692313 3819022 - NUP98 ENSG00000110713.11 3819022 0.64 1.0 10433 73720
chr11 3818954 3847601 + PGAP2 ENSG00000148985.15 3818954 0.67 1.0 10434 73788
chr11 3848208 3862213 - RHOG ENSG00000177105.9 3862213 0.83 1.0 10435 30529
chr11 3875757 4114439 + STIM1 ENSG00000167323.5 3875757 0.66 1.0 10436 16985


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