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
chr12 69312048 69312062 GATA2 JASPAR yes 82429568
chr12 69312048 69312063 FOXP1 JASPAR yes 82429569
chr12 69312052 69312060 GATA3 JASPAR yes 82429570
chr12 69312076 69312087 PROP1 JASPAR yes 82429571
chr12 69312077 69312081 YY1 TRANSFAC yes 82429572
chr12 69312078 69312088 HOXA13 JASPAR yes 82429573
chr12 69312078 69312088 HOXB13 JASPAR yes 82429574
chr12 69312078 69312088 HOXD13 JASPAR yes 82429575
chr12 69312078 69312089 HOXA10 JASPAR yes 82429576
chr12 69312079 69312088 CDX1 JASPAR yes 82429577
chr12 69312079 69312089 MNX1 JASPAR yes 82429578
chr12 69312079 69312090 CDX2 JASPAR yes 82429579
chr12 69312106 69312110 YY1 TRANSFAC yes 82429580
chr12 69312163 69312172 NKX3-2 JASPAR yes 82429581
chr12 69312191 69312196 GATA2 JASPAR yes 82429582
chr12 69312194 69312209 ZIC3 JASPAR yes 82429583
chr12 69312232 69312238 JUN TRANSFAC yes 82429584
chr12 69312247 69312252 H4TF1 TRANSFAC yes 82429585
chr12 69312262 69312266 NFE TRANSFAC yes 82429586
chr12 69312264 69312285 IRF1 JASPAR yes 82429587
chr12 69312287 69312290 MYB TRANSFAC yes 82429588

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr12 69312110 rs147160321 T C
2714097
chr12 69312176 rs78416315 C A no 2714098
chr12 69312178 rs569960722 C T no 2714099
chr12 69312183 rs140344807 G A no 2714100
chr12 69312278 rs117259045 T A
2714101
chr12 69312301 rs141145355 C G no 2714102

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
chr12 69235977 69365350 - CPM ENSG00000135678.7 69365350 0.92 0.99 12318 46972


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