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
chr6 132811271 132811282 ETV2 JASPAR yes 70436282
chr6 132811271 132811282 ETV2 JASPAR yes 105314804
chr6 132811272 132811283 FLI1 JASPAR yes 70436283
chr6 132811272 132811283 FLI1 JASPAR yes 105314805
chr6 132811285 132811289 LFA1 TRANSFAC yes 70436284
chr6 132811285 132811289 LFA1 TRANSFAC yes 105314806
chr6 132811315 132811321 MZF1 JASPAR yes 70436285
chr6 132811315 132811321 MZF1 JASPAR yes 105314807
chr6 132811355 132811376 ZNF263 JASPAR yes 70436286
chr6 132811355 132811376 ZNF263 JASPAR yes 105314808
chr6 132811357 132811362 ETS2 TRANSFAC yes 70436287
chr6 132811357 132811362 ETS2 TRANSFAC yes 105314809
chr6 132811357 132811368 FLI1 JASPAR yes 70436288
chr6 132811357 132811368 FLI1 JASPAR yes 105314810
chr6 132811359 132811367 EHF JASPAR yes 70436289
chr6 132811359 132811367 EHF JASPAR yes 105314811
chr6 132811363 132811371 MEIS2 JASPAR yes 70436290
chr6 132811363 132811371 MEIS3 JASPAR yes 70436291
chr6 132811363 132811371 MEIS2 JASPAR yes 105314812
chr6 132811363 132811371 MEIS3 JASPAR yes 105314813
chr6 132811364 132811368 NFE TRANSFAC yes 70436292
chr6 132811364 132811368 NFE TRANSFAC yes 105314814
chr6 132811369 132811375 ZNF354C JASPAR yes 70436293
chr6 132811369 132811375 ZNF354C JASPAR yes 105314815
chr6 132811371 132811380 NKX2-8 JASPAR yes 70436294
chr6 132811371 132811380 NKX2-8 JASPAR yes 105314816
chr6 132811383 132811387 H1TF2 TRANSFAC yes 70436295
chr6 132811383 132811387 NFE TRANSFAC yes 70436296
chr6 132811383 132811387 SRF TRANSFAC yes 70436297
chr6 132811383 132811387 H1TF2 TRANSFAC yes 105314817
chr6 132811383 132811387 NFE TRANSFAC yes 105314818
chr6 132811383 132811387 SRF TRANSFAC yes 105314819
chr6 132811473 132811484 BATF JASPAR yes 70436298
chr6 132811473 132811484 BATF JASPAR yes 105314820
chr6 132811478 132811482 YY1 TRANSFAC yes 70436299
chr6 132811478 132811482 YY1 TRANSFAC yes 105314821

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr6 132811314 rs7772611 A G no 9341210
chr6 132811325 rs12193914 C T no 9341211
chr6 132811360 rs7772758 C T 9341212
chr6 132811377 rs114989856 C T
9341213
chr6 132811422 rs549256008 T C no 9341214

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
chr6 132617194 132722684 - MOXD1 ENSG00000079931.10 132722684 0.95 0.98 6959 11404
chr6 132767006 132834337 - STX7 ENSG00000079950.9 132834337 0.82 0.99 6960 77153
chr6 132873832 132874860 + TAAR8 ENSG00000146385.1 132873832 0.0 0.0 6961 37658
chr6 132891461 132892498 + TAAR6 ENSG00000146383.7 132891461 0.98 0.0 6962 20029
chr6 132909731 132910877 - TAAR5 ENSG00000135569.3 132910877 0.0 0.0 6963 613


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