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 858852 858862 TBX21 JASPAR yes 49325503
chr16 858852 858863 TBX20 JASPAR yes 49325504
chr16 858852 858863 TBX2 JASPAR yes 49325505
chr16 858852 858865 EOMES JASPAR yes 49325506
chr16 858852 858866 JUN JASPAR yes 49325507
chr16 858853 858861 MGA JASPAR yes 49325508
chr16 858853 858861 TBX15 JASPAR yes 49325509
chr16 858853 858861 TBX1 JASPAR yes 49325510
chr16 858853 858861 TBX4 JASPAR yes 49325511
chr16 858853 858861 TBX5 JASPAR yes 49325512
chr16 858853 858863 TBR1 JASPAR yes 49325513
chr16 858855 858866 FOSL2 JASPAR yes 49325514
chr16 858855 858866 JUNB JASPAR yes 49325515
chr16 858856 858867 FOS JASPAR yes 49325516
chr16 858856 858867 FOSL1 JASPAR yes 49325517
chr16 858856 858867 JUND JASPAR yes 49325518
chr16 858857 858864 JUN TRANSFAC yes 49325519
chr16 858921 858935 GLIS2 JASPAR yes 49325520
chr16 858929 858934 SP1 TRANSFAC yes 49325521
chr16 858931 858952 REST JASPAR yes 49325522
chr16 858935 858939 NFE TRANSFAC yes 49325523
chr16 858939 858950 ESRRA JASPAR yes 49325524
chr16 858942 858963 ZNF263 JASPAR yes 49325525
chr16 858943 858947 LFA1 TRANSFAC yes 49325526
chr16 858948 858961 ELF1 JASPAR yes 49325527
chr16 858948 858969 ZNF263 JASPAR yes 49325528
chr16 858951 858957 PEA3 TRANSFAC yes 49325529
chr16 858953 858968 PRDM1 JASPAR yes 49325530
chr16 858995 859006 E2F6 JASPAR yes 49325531
chr16 858996 859017 IRF1 JASPAR yes 49325532
chr16 858998 859019 IRF1 JASPAR yes 49325533
chr16 858999 859020 IRF1 JASPAR yes 49325534
chr16 859000 859021 IRF1 JASPAR yes 49325535
chr16 859001 859016 FOXP1 JASPAR yes 49325536
chr16 859001 859022 IRF1 JASPAR yes 49325537
chr16 859003 859018 FOXP1 JASPAR yes 49325538
chr16 859004 859019 FOXP1 JASPAR yes 49325539
chr16 859005 859020 FOXP1 JASPAR yes 49325540
chr16 859006 859021 FOXP1 JASPAR yes 49325541
chr16 859007 859022 FOXP1 JASPAR yes 49325542
chr16 859008 859023 FOXP1 JASPAR yes 49325543

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr16 858834 rs142733227 G A no 4249402
chr16 858935 rs115341944 C T
4249403
chr16 858984 rs147387219 G C no 4249404
chr16 859004 rs200060841 CTTTTT C 4249405

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 765115 769655 + METRN ENSG00000103260.4 765115 0.82 1.0 14363 6282
chr16 770581 772601 + FAM173A ENSG00000103254.5 770581 0.56 1.0 14364 11748
chr16 772582 776954 - CCDC78 ENSG00000162004.12 776954 0.89 0.99 14365 18121
chr16 776936 785525 + HAGHL ENSG00000103253.13 776936 0.78 1.0 14366 18103
chr16 779753 791329 - NARFL ENSG00000103245.9 791329 0.59 1.0 14367 32496
chr16 810762 818865 + MSLN ENSG00000102854.10 810762 0.98 1.0 14368 51929
chr16 819428 833370 - MSLNL ENSG00000162006.5 833370 0.96 1.0 14369 74537
chr16 834974 838397 - RPUSD1 ENSG00000007376.3 838397 0.63 1.0 14370 79564
chr16 838046 850737 + CHTF18 ENSG00000127586.12 838046 0.8 1.0 14371 79213
chr16 848041 850733 - GNG13 ENSG00000127588.4 850733 0.97 1.0 14372 91900
chr16 855443 863861 + PRR25 ENSG00000167945.1 855443 0.78 0.91 14373 96610


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