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
chr17 48996389 48996394 MYC TRANSFAC yes 21254959
chr17 48996389 48996394 MYC TRANSFAC yes 54733955
chr17 48996432 48996436 H4TF2 TRANSFAC yes 21254960
chr17 48996432 48996436 H4TF2 TRANSFAC yes 54733956
chr17 48996439 48996460 ZNF263 JASPAR yes 21254961
chr17 48996439 48996460 ZNF263 JASPAR yes 54733957
chr17 48996441 48996452 E2F4 JASPAR yes 21254962
chr17 48996441 48996452 E2F6 JASPAR yes 21254963
chr17 48996441 48996452 E2F4 JASPAR yes 54733958
chr17 48996441 48996452 E2F6 JASPAR yes 54733959
chr17 48996442 48996453 E2F1 JASPAR yes 21254964
chr17 48996442 48996453 E2F1 JASPAR yes 54733960
chr17 48996461 48996473 FOXI1 JASPAR yes 21254965
chr17 48996461 48996473 FOXI1 JASPAR yes 54733961
chr17 48996462 48996473 FOXP2 JASPAR yes 21254966
chr17 48996462 48996473 FOXP2 JASPAR yes 54733962
chr17 48996467 48996478 FLI1 JASPAR yes 21254967
chr17 48996467 48996478 FLI1 JASPAR yes 54733963
chr17 48996468 48996472 YY1 TRANSFAC yes 21254968
chr17 48996468 48996472 YY1 TRANSFAC yes 54733964
chr17 48996469 48996477 FEV JASPAR yes 21254969
chr17 48996469 48996477 FEV JASPAR yes 54733965

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr17 48996391 rs116702743 A G
4926953
chr17 48996429 rs187291655 A C no 4926954
chr17 48996454 rs77531496 G C
4926955

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
chr17 48912011 48919709 + WFIKKN2 ENSG00000173714.7 48912011 1.0 1.0 16045 15634
chr17 48939584 48945339 - TOB1 ENSG00000141232.4 48945339 0.81 1.0 16046 48962


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