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 74764385 74764400 FOXP1 JASPAR yes 21300221
chr17 74764386 74764401 FOXP1 JASPAR yes 21300222
chr17 74764386 74764407 IRF1 JASPAR yes 21300223
chr17 74764387 74764402 FOXP1 JASPAR yes 21300224
chr17 74764387 74764408 IRF1 JASPAR yes 21300225
chr17 74764388 74764403 FOXP1 JASPAR yes 21300226
chr17 74764388 74764409 IRF1 JASPAR yes 21300227
chr17 74764389 74764404 FOXP1 JASPAR yes 21300228
chr17 74764389 74764410 IRF1 JASPAR yes 21300229
chr17 74764390 74764405 FOXP1 JASPAR yes 21300230
chr17 74764391 74764406 FOXP1 JASPAR yes 21300231
chr17 74764391 74764412 IRF1 JASPAR yes 21300232
chr17 74764392 74764407 FOXP1 JASPAR yes 21300233
chr17 74764395 74764410 PRDM1 JASPAR yes 21300234
chr17 74764395 74764410 STAT2 JASPAR yes 21300235
chr17 74764399 74764417 NR3C1 JASPAR yes 21300236
chr17 74764406 74764422 POU4F3 JASPAR yes 21300237
chr17 74764408 74764412 YY1 TRANSFAC yes 21300238
chr17 74764435 74764446 RUNX1 JASPAR yes 21300239
chr17 74764451 74764461 SP1 JASPAR yes 21300240
chr17 74764452 74764457 SP1 TRANSFAC yes 21300241
chr17 74764453 74764458 SP1 TRANSFAC yes 21300242
chr17 74764453 74764459 SP1 TRANSFAC yes 21300243
chr17 74764487 74764502 FOXP1 JASPAR yes 21300244
chr17 74764488 74764497 SRY JASPAR yes 21300245
chr17 74764488 74764499 FOXP2 JASPAR yes 21300246
chr17 74764488 74764500 FOXC2 JASPAR yes 21300247
chr17 74764489 74764500 FOXC1 JASPAR yes 21300248
chr17 74764490 74764501 FOXA1 JASPAR yes 21300249
chr17 74764500 74764506 TBP TRANSFAC yes 21300250
chr17 74764519 74764527 LBX1 JASPAR yes 21300251
chr17 74764521 74764536 HNF1A JASPAR yes 21300252
chr17 74764522 74764535 HNF1B JASPAR yes 21300253
chr17 74764554 74764566 BHLHE23 JASPAR yes 21300254
chr17 74764555 74764565 OLIG1 JASPAR yes 21300255
chr17 74764555 74764565 OLIG2 JASPAR yes 21300256
chr17 74764555 74764565 OLIG3 JASPAR yes 21300257
chr17 74764555 74764570 MEF2A JASPAR yes 21300258
chr17 74764557 74764569 MEF2A JASPAR yes 21300259
chr17 74764558 74764568 MEF2A JASPAR yes 21300260
chr17 74764559 74764563 YY1 TRANSFAC yes 21300261
chr17 74764574 74764585 FOXA1 JASPAR yes 21300262
chr17 74764574 74764585 FOXH1 JASPAR yes 21300263
chr17 74764574 74764589 FOXA1 JASPAR yes 21300264
chr17 74764575 74764586 FOXC1 JASPAR yes 21300265
chr17 74764575 74764587 FOXC2 JASPAR yes 21300266
chr17 74764578 74764586 FOXG1 JASPAR yes 21300267
chr17 74764581 74764597 SOX8 JASPAR yes 21300268
chr17 74764583 74764587 YY1 TRANSFAC yes 21300269
chr17 74764622 74764626 YY1 TRANSFAC yes 21300270
chr17 74764636 74764640 H4TF2 TRANSFAC yes 21300271
chr17 74764649 74764662 POU3F3 JASPAR yes 21300272
chr17 74764657 74764672 LEF1 JASPAR yes 21300273
chr17 74764671 74764682 NFKB1 JASPAR yes 21300274
chr17 74764674 74764688 STAT1 JASPAR yes 21300275
chr17 74764676 74764691 FOXP1 JASPAR yes 21300276
chr17 74764679 74764696 BCL6B JASPAR yes 21300277
chr17 74764680 74764695 STAT1 JASPAR yes 21300278
chr17 74764682 74764693 STAT1 JASPAR yes 21300279
chr17 74764682 74764693 STAT3 JASPAR yes 21300280
chr17 74764699 74764709 ALX3 JASPAR yes 21300281
chr17 74764699 74764709 GSX2 JASPAR yes 21300282
chr17 74764699 74764709 MIXL1 JASPAR yes 21300283
chr17 74764699 74764709 MNX1 JASPAR yes 21300284
chr17 74764700 74764708 ISX JASPAR yes 21300285
chr17 74764700 74764708 LMX1A JASPAR yes 21300286
chr17 74764700 74764708 LMX1B JASPAR yes 21300287
chr17 74764700 74764708 NKX6-1 JASPAR yes 21300288
chr17 74764700 74764708 NKX6-2 JASPAR yes 21300289
chr17 74764700 74764708 PRRX1 JASPAR yes 21300290
chr17 74764700 74764708 RAX2 JASPAR yes 21300291
chr17 74764700 74764708 SHOX JASPAR yes 21300292
chr17 74764700 74764708 UNCX JASPAR yes 21300293
chr17 74764700 74764708 VAX1 JASPAR yes 21300294
chr17 74764710 74764714 YY1 TRANSFAC yes 21300295

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr17 74764416 rs182922334 A G 5066726
chr17 74764457 rs187263289 G A
5066727
chr17 74764496 rs554883296 T C 5066728
chr17 74764547 rs77684571 C T no 5066729
chr17 74764579 rs16969272 A T 5066730

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 74668633 74707098 - MXRA7 ENSG00000182534.9 74707098 0.66 0.99 16290 42713
chr17 74708919 74722866 - JMJD6 ENSG00000070495.10 74722866 0.54 1.0 16291 58481
chr17 74722912 74730018 + METTL23 ENSG00000181038.9 74722912 0.54 0.99 16292 58527
chr17 74729060 74734604 + RP11-318A15.7 ENSG00000267168.1 74729060 1.0 0.96 16293 64675
chr17 74730197 74733456 - SRSF2 ENSG00000161547.10 74733456 0.67 0.99 16294 69071
chr17 74731947 74777531 + MFSD11 ENSG00000092931.7 74731947 0.67 1.0 16295 67562
chr17 74864538 74946475 + MGAT5B ENSG00000167889.8 74864538 0.87 1.0 16296 194


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