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
chr8 1910267 1910282 HNF4A JASPAR yes 42789356
chr8 1910267 1910282 HNF4A JASPAR yes 68306656
chr8 1910268 1910282 RXRB JASPAR yes 42789357
chr8 1910268 1910282 RXRB JASPAR yes 68306657
chr8 1910268 1910283 HNF4G JASPAR yes 42789358
chr8 1910268 1910283 HNF4G JASPAR yes 68306658
chr8 1910280 1910293 SMAD2 JASPAR yes 42789359
chr8 1910280 1910293 SMAD2 JASPAR yes 68306659
chr8 1910284 1910288 NFE TRANSFAC yes 42789360
chr8 1910284 1910288 NFE TRANSFAC yes 68306660
chr8 1910300 1910308 EHF JASPAR yes 42789361
chr8 1910300 1910308 EHF JASPAR yes 68306661
chr8 1910314 1910319 ETS2 TRANSFAC yes 42789362
chr8 1910314 1910319 ETS2 TRANSFAC yes 68306662
chr8 1910336 1910350 MTF1 JASPAR yes 42789363
chr8 1910336 1910350 MTF1 JASPAR yes 68306663
chr8 1910353 1910373 ESR1 JASPAR yes 42789364
chr8 1910353 1910373 ESR1 JASPAR yes 68306664
chr8 1910358 1910373 ESR2 JASPAR yes 42789365
chr8 1910358 1910373 ESR2 JASPAR yes 68306665
chr8 1910359 1910363 LFA1 TRANSFAC yes 42789366
chr8 1910359 1910363 LFA1 TRANSFAC yes 68306666
chr8 1910378 1910383 MYC TRANSFAC yes 42789367
chr8 1910378 1910383 MYC TRANSFAC yes 68306667

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr8 1910295 rs143982005 C T no 10229098
chr8 1910334 rs562100840 G A no 10229099

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
chr8 1922044 1955102 + KBTBD11 ENSG00000176595.3 1922044 0.92 1.0 8073 88336
chr8 1993155 2113475 + MYOM2 ENSG00000036448.5 1993155 0.98 1.0 8074 17225


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