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
chr14 78144886 78144901 FOXP1 JASPAR yes 107588047
chr14 78144887 78144902 FOXP1 JASPAR yes 107588048
chr14 78144888 78144903 FOXP1 JASPAR yes 107588049
chr14 78144888 78144909 IRF1 JASPAR yes 107588050
chr14 78144889 78144904 FOXP1 JASPAR yes 107588051
chr14 78144889 78144910 IRF1 JASPAR yes 107588052
chr14 78144890 78144905 FOXP1 JASPAR yes 107588053
chr14 78144892 78144907 FOXP1 JASPAR yes 107588054
chr14 78144893 78144908 STAT2 JASPAR yes 107588055
chr14 78144894 78144909 FOXP1 JASPAR yes 107588056
chr14 78144897 78144908 FOXP2 JASPAR yes 107588057
chr14 78144907 78144913 SOX10 JASPAR yes 107588058
chr14 78144913 78144916 MYB TRANSFAC yes 107588059
chr14 78144946 78144950 H1TF2 TRANSFAC yes 107588060
chr14 78144946 78144950 NFE TRANSFAC yes 107588061
chr14 78144946 78144950 SRF TRANSFAC yes 107588062
chr14 78144949 78144960 FOXC1 JASPAR yes 107588063
chr14 78144950 78144954 YY1 TRANSFAC yes 107588064
chr14 78144952 78144967 FOXP1 JASPAR yes 107588065
chr14 78144952 78144973 IRF1 JASPAR yes 107588066
chr14 78144953 78144966 POU2F2 JASPAR yes 107588067
chr14 78144956 78144970 IRF7 JASPAR yes 107588068
chr14 78144961 78144965 YY1 TRANSFAC yes 107588069
chr14 78144963 78144978 MEF2C JASPAR yes 107588070
chr14 78144972 78144976 TEAD2 TRANSFAC yes 107588071
chr14 78145003 78145013 ALX3 JASPAR yes 107588072
chr14 78145003 78145013 LBX2 JASPAR yes 107588073
chr14 78145003 78145013 MIXL1 JASPAR yes 107588074
chr14 78145004 78145012 LHX9 JASPAR yes 107588075
chr14 78145004 78145012 SHOX JASPAR yes 107588076
chr14 78145038 78145050 PROX1 JASPAR yes 107588077
chr14 78145061 78145066 GATA2 JASPAR yes 107588078

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr14 78144888 rs558714460 CAAA C
3680580
chr14 78144888 rs577702127 CAAA C
3680581
chr14 78144905 rs201612724 C A 3680582
chr14 78144906 rs76902647 A G 3680583
chr14 78144954 rs541308059 T A 3680584
chr14 78145060 rs138596359 G A,C no 3680585

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
chr14 77972340 78083116 - SPTLC2 ENSG00000100596.2 78083116 0.79 1.0 13525 38230
chr14 78138747 78174363 - ALKBH1 ENSG00000100601.5 78174363 0.59 1.0 13526 70708
chr14 78174414 78227447 + SLIRP ENSG00000119705.5 78174414 0.93 0.98 13527 70657
chr14 78183942 78227550 - SNW1 ENSG00000100603.9 78227550 0.58 0.99 13528 17521
chr14 78227173 78236085 + C14orf178 ENSG00000197734.4 78227173 0.84 1.0 13529 17898
chr14 78227711 78228033 - AC008372.1 ENSG00000268208.1 78228033 0.0 0.0 13530 17038


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