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
chr1 26101399 26101419 TP63 JASPAR yes 118254077
chr1 26101408 26101412 NFE TRANSFAC yes 118254078
chr1 26101413 26101428 FOXP1 JASPAR yes 118254079
chr1 26101416 26101430 IRF7 JASPAR yes 118254080
chr1 26101418 26101424 TCF4 TRANSFAC yes 118254081
chr1 26101433 26101448 FOXP1 JASPAR yes 118254082
chr1 26101435 26101450 LEF1 JASPAR yes 118254083
chr1 26101436 26101450 GATA2 JASPAR yes 118254084
chr1 26101436 26101451 FOXP1 JASPAR yes 118254085
chr1 26101440 26101448 GATA3 JASPAR yes 118254086
chr1 26101464 26101469 MYC TRANSFAC yes 118254087
chr1 26101470 26101484 TCF7L2 JASPAR yes 118254088
chr1 26101474 26101480 TCF1 TRANSFAC yes 118254089
chr1 26101492 26101496 TEAD2 TRANSFAC yes 118254090
chr1 26101495 26101506 ETV2 JASPAR yes 118254091
chr1 26101496 26101504 FEV JASPAR yes 118254092
chr1 26101498 26101505 SPIB JASPAR yes 118254093
chr1 26101510 26101518 DLX6 JASPAR yes 118254094
chr1 26101510 26101518 MSX1 JASPAR yes 118254095
chr1 26101514 26101521 NKX3-1 JASPAR yes 118254096
chr1 26101515 26101523 FOXC1 JASPAR yes 118254097
chr1 26101517 26101532 TFAP2A JASPAR yes 118254098
chr1 26101518 26101532 TLX1 JASPAR yes 118254099
chr1 26101525 26101530 SP1 TRANSFAC yes 118254100
chr1 26101527 26101546 CTCF JASPAR yes 118254101
chr1 26101538 26101548 NFATC3 JASPAR yes 118254102
chr1 26101557 26101562 SP1 TRANSFAC yes 118254103
chr1 26101572 26101581 SNAI2 JASPAR yes 118254104
chr1 26101572 26101582 ID4 JASPAR yes 118254105
chr1 26101572 26101582 TCF3 JASPAR yes 118254106
chr1 26101572 26101582 TCF4 JASPAR yes 118254107
chr1 26101616 26101631 AR JASPAR yes 118254108
chr1 26101624 26101645 REST JASPAR yes 118254109
chr1 26101625 26101644 REST JASPAR yes 118254110
chr1 26101702 26101714 CREB1 JASPAR yes 118254111
chr1 26101714 26101726 NHLH1 JASPAR yes 118254112
chr1 26101715 26101725 NHLH1 JASPAR yes 118254113

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr1 26101408 rs150644578 A G
175939
chr1 26101577 rs72877404 G A,C 175940
chr1 26101594 rs181798438 G A no 175941
chr1 26101691 rs138881875 C T no 175942
chr1 26101723 rs187233967 G A
175943
chr1 26101727 rs373057123 G A no 175944

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
chr1 26126667 26144713 + SEPN1 ENSG00000162430.12 26126667 0.64 1.0 347 75100
chr1 26137961 26150235 + RP1-317E23.6 ENSG00000255054.3 26137961 0.91 0.99 348 63806
chr1 26145131 26159432 + MTFR1L ENSG00000117640.13 26145131 0.69 1.0 349 56636
chr1 26145212 26147288 - AL020996.1 ENSG00000223474.2 26147288 0.74 1.0 350 54479
chr1 26158414 26185903 - AUNIP ENSG00000127423.6 26185903 0.86 0.99 351 15864
chr1 26187701 26197744 - PAQR7 ENSG00000182749.5 26197744 0.83 1.0 352 4023


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