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
chr10 99113811 99113830 REST JASPAR yes 21141074
chr10 99113821 99113831 NFKB1 JASPAR yes 21141075
chr10 99113827 99113833 MZF1 JASPAR yes 21141076
chr10 99113873 99113890 RXRA JASPAR yes 21141077
chr10 99113874 99113878 LFA1 TRANSFAC yes 21141078
chr10 99113874 99113894 ESR1 JASPAR yes 21141079
chr10 99113876 99113887 ESRRA JASPAR yes 21141080
chr10 99113876 99113887 ESRRB JASPAR yes 21141081
chr10 99113877 99113895 ESR2 JASPAR yes 21141082
chr10 99113878 99113886 NR4A2 JASPAR yes 21141083
chr10 99113878 99113895 ESR1 JASPAR yes 21141084
chr10 99113879 99113894 ESR2 JASPAR yes 21141085
chr10 99113879 99113899 ESR1 JASPAR yes 21141086
chr10 99113880 99113884 ESR1 TRANSFAC yes 21141087
chr10 99113883 99113901 ESR2 JASPAR yes 21141088
chr10 99113888 99113891 MYB TRANSFAC yes 21141089
chr10 99113891 99113902 FOS JASPAR yes 21141090
chr10 99113891 99113902 FOSL1 JASPAR yes 21141091
chr10 99113891 99113902 JUND JASPAR yes 21141092
chr10 99113891 99113902 NFE2 JASPAR yes 21141093
chr10 99113892 99113903 FOSL2 JASPAR yes 21141094
chr10 99113892 99113903 JUNB JASPAR yes 21141095
chr10 99113892 99113906 JUN JASPAR yes 21141096
chr10 99113930 99113940 SMAD3 JASPAR yes 21141097
chr10 99113951 99113957 MZF1 JASPAR yes 21141098
chr10 99113987 99114002 IRF9 JASPAR yes 21141099
chr10 99113988 99113998 RUNX3 JASPAR yes 21141100
chr10 99113989 99113998 RUNX2 JASPAR yes 21141101
chr10 99114006 99114026 TP63 JASPAR yes 21141102
chr10 99114015 99114027 GRHL1 JASPAR yes 21141103
chr10 99114018 99114024 PTF TRANSFAC yes 21141104
chr10 99114021 99114029 FOXO3 JASPAR yes 21141105
chr10 99114022 99114032 NFATC3 JASPAR yes 21141106
chr10 99114023 99114030 NFATC2 JASPAR yes 21141107
chr10 99114024 99114042 SRF JASPAR yes 21141108
chr10 99114028 99114032 YY1 TRANSFAC yes 21141109
chr10 99114030 99114041 STAT1 JASPAR yes 21141110
chr10 99114030 99114041 STAT3 JASPAR yes 21141111

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr10 99113878 rs11189158 C T 1603755
chr10 99113910 rs17112653 A G no 1603756
chr10 99113964 rs11189159 G A no 1603757
chr10 99114041 rs184186639 T C 1603758

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
chr10 98757795 99052413 - ARHGAP19-SLIT1 ENSG00000269891.1 99052413 0.93 0.95 10068 38609
chr10 98978996 99052413 - ARHGAP19 ENSG00000213390.6 99052413 0.79 1.0 10070 38609
chr10 99079022 99081672 + FRAT1 ENSG00000165879.7 99079022 0.85 0.99 10071 65218
chr10 99092255 99094458 - FRAT2 ENSG00000181274.5 99094458 0.85 0.99 10072 80654
chr10 99116115 99161127 - RRP12 ENSG00000052749.9 99161127 0.75 1.0 10073 52916
chr10 99179228 99185831 - AL355490.1 ENSG00000224474.2 99185831 0.78 1.0 10074 28212
chr10 99185917 99193198 + PGAM1 ENSG00000171314.8 99185917 0.9 0.98 10075 28126
chr10 99195899 99205774 - EXOSC1 ENSG00000171311.8 99205774 0.74 1.0 10076 8269
chr10 99205927 99217127 + ZDHHC16 ENSG00000171307.14 99205927 0.71 0.99 10077 8116


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