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
chr16 4900346 4900360 GATA2 JASPAR yes 49332127
chr16 4900348 4900356 GATA3 JASPAR yes 49332128
chr16 4900348 4900356 GATA5 JASPAR yes 49332129
chr16 4900358 4900373 FOXP1 JASPAR yes 49332130
chr16 4900359 4900370 FOXP2 JASPAR yes 49332131
chr16 4900360 4900368 FOXD1 JASPAR yes 49332132
chr16 4900360 4900368 FOXG1 JASPAR yes 49332133
chr16 4900360 4900368 FOXO3 JASPAR yes 49332134
chr16 4900361 4900368 FOXD2 JASPAR yes 49332135
chr16 4900361 4900368 FOXI1 JASPAR yes 49332136
chr16 4900361 4900368 FOXL1 JASPAR yes 49332137
chr16 4900361 4900368 FOXO4 JASPAR yes 49332138
chr16 4900361 4900368 FOXO6 JASPAR yes 49332139
chr16 4900361 4900368 FOXP3 JASPAR yes 49332140
chr16 4900394 4900404 NFIA JASPAR yes 49332141
chr16 4900396 4900402 NFIC JASPAR yes 49332142
chr16 4900398 4900402 H1TF2 TRANSFAC yes 49332143
chr16 4900398 4900402 NFE TRANSFAC yes 49332144
chr16 4900398 4900402 SRF TRANSFAC yes 49332145
chr16 4900402 4900416 PAX6 JASPAR yes 49332146
chr16 4900408 4900419 ESRRB JASPAR yes 49332147
chr16 4900413 4900421 EHF JASPAR yes 49332148
chr16 4900418 4900436 NFYA JASPAR yes 49332149
chr16 4900421 4900437 NFYA JASPAR yes 49332150
chr16 4900424 4900439 NFYB JASPAR yes 49332151
chr16 4900427 4900437 HMBOX1 JASPAR yes 49332152
chr16 4900433 4900436 MYB TRANSFAC yes 49332153
chr16 4900434 4900445 NRL JASPAR yes 49332154
chr16 4900474 4900478 NFE TRANSFAC yes 49332155
chr16 4900512 4900516 YY1 TRANSFAC yes 49332156
chr16 4900517 4900537 RREB1 JASPAR yes 49332157
chr16 4900537 4900552 TFAP2A JASPAR yes 49332158
chr16 4900539 4900544 GATA2 JASPAR yes 49332159
chr16 4900557 4900562 H4TF1 TRANSFAC yes 49332160
chr16 4900567 4900580 NFKB1 JASPAR yes 49332161
chr16 4900567 4900580 NFKB2 JASPAR yes 49332162
chr16 4900568 4900579 NFKB1 JASPAR yes 49332163
chr16 4900569 4900579 REL JASPAR yes 49332164
chr16 4900581 4900584 MYB TRANSFAC yes 49332165
chr16 4900592 4900610 TP73 JASPAR yes 49332166

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr16 4900351 rs559276894 A G 4279345
chr16 4900415 rs74003516 C G,T
4279346
chr16 4900477 rs183481699 A G,T
4279347
chr16 4900526 rs185911158 C G
4279348
chr16 4900621 rs139893802 G T no 4279349

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
chr16 4798240 4817625 - ZNF500 ENSG00000103199.9 4817625 0.6 1.0 14509 17294
chr16 4827670 4838522 - SEPT12 ENSG00000140623.9 4838522 0.85 1.0 14510 38191
chr16 4838398 4846492 + SMIM22 ENSG00000267795.1 4838398 0.97 1.0 14511 38067
chr16 4846969 4852951 - ROGDI ENSG00000067836.8 4852951 0.7 1.0 14512 52620
chr16 4853204 4897343 - GLYR1 ENSG00000140632.12 4897343 0.72 0.99 14513 97012
chr16 4896666 4932361 + UBN1 ENSG00000118900.10 4896666 0.59 1.0 14514 96335


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