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 68776296 68776501 FOSL2 UCSC Txn Factor no Conserved 107985241
chr11 68776295 68776300 SP1 TRANSFAC yes 39497513
chr11 68776295 68776300 SP1 TRANSFAC yes 114093183
chr11 68776299 68776303 ESR1 TRANSFAC yes 39497514
chr11 68776299 68776303 ESR1 TRANSFAC yes 114093184
chr11 68776334 68776344 NFATC3 JASPAR yes 39497515
chr11 68776334 68776344 NFATC3 JASPAR yes 114093185
chr11 68776336 68776343 NFATC2 JASPAR yes 39497516
chr11 68776336 68776343 NFATC2 JASPAR yes 114093186
chr11 68776353 68776359 SP1 TRANSFAC yes 39497517
chr11 68776353 68776359 SP1 TRANSFAC yes 114093187
chr11 68776378 68776392 JUN JASPAR yes 39497518
chr11 68776378 68776392 JUN JASPAR yes 114093188
chr11 68776381 68776392 FOSL2 JASPAR yes 39497519
chr11 68776381 68776392 JUNB JASPAR yes 39497520
chr11 68776381 68776392 FOSL2 JASPAR yes 114093189
chr11 68776381 68776392 JUNB JASPAR yes 114093190
chr11 68776382 68776393 FOS JASPAR yes 39497521
chr11 68776382 68776393 FOSL1 JASPAR yes 39497522
chr11 68776382 68776393 JUND JASPAR yes 39497523
chr11 68776382 68776393 NFE2 JASPAR yes 39497524
chr11 68776382 68776393 FOS JASPAR yes 114093191
chr11 68776382 68776393 FOSL1 JASPAR yes 114093192
chr11 68776382 68776393 JUND JASPAR yes 114093193
chr11 68776382 68776393 NFE2 JASPAR yes 114093194
chr11 68776383 68776392 JDP2 JASPAR yes 39497525
chr11 68776383 68776392 JDP2 JASPAR yes 114093195
chr11 68776383 68776394 FOSL2 JASPAR yes 39497526
chr11 68776383 68776394 JUNB JASPAR yes 39497527
chr11 68776383 68776394 FOSL2 JASPAR yes 114093196
chr11 68776383 68776394 JUNB JASPAR yes 114093197
chr11 68776383 68776397 JUN JASPAR yes 39497528
chr11 68776383 68776397 JUN JASPAR yes 114093198
chr11 68776501 68776511 SREBF1 JASPAR yes 39497529
chr11 68776501 68776511 SREBF2 JASPAR yes 39497530
chr11 68776501 68776511 SREBF1 JASPAR yes 114093199
chr11 68776501 68776511 SREBF2 JASPAR yes 114093200

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr11 68776413 rs528525759 C G
2068890
chr11 68776451 rs142380197 C T
2068891
chr11 68776459 rs185907614 C T
2068892
chr11 68776479 rs151329295 C T
2068893

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 68747490 68748455 - MRGPRD ENSG00000172938.3 68748455 0.91 0.0 11180 72163
chr11 68771863 68780877 - MRGPRF ENSG00000172935.8 68780877 0.91 1.0 11181 95668
chr11 68816365 68858072 + TPCN2 ENSG00000162341.11 68816365 0.67 1.0 11182 60180


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