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 90957951 90958227 EGR1 UCSC Txn Factor no Conserved 108118135
chr14 90957920 90957935 STAT2 JASPAR yes 107595833
chr14 90957920 90957935 STAT2 JASPAR yes 117223916
chr14 90957921 90957935 STAT1 JASPAR yes 107595834
chr14 90957921 90957935 STAT1 JASPAR yes 117223917
chr14 90957923 90957944 ZNF263 JASPAR yes 107595835
chr14 90957923 90957944 ZNF263 JASPAR yes 117223918
chr14 90957924 90957945 ZNF263 JASPAR yes 107595836
chr14 90957924 90957945 ZNF263 JASPAR yes 117223919
chr14 90957943 90957955 SRF JASPAR yes 107595837
chr14 90957943 90957955 SRF JASPAR yes 117223920
chr14 90957946 90957950 TEAD2 TRANSFAC yes 107595838
chr14 90957946 90957950 TEAD2 TRANSFAC yes 117223921
chr14 90957956 90957968 TEAD1 JASPAR yes 107595839
chr14 90957956 90957968 TEAD1 JASPAR yes 117223922
chr14 90957958 90957968 TEAD4 JASPAR yes 107595840
chr14 90957958 90957968 TEAD4 JASPAR yes 117223923
chr14 90957959 90957967 TEAD3 JASPAR yes 107595841
chr14 90957959 90957967 TEAD3 JASPAR yes 117223924
chr14 90957960 90957975 MAFK JASPAR yes 107595842
chr14 90957960 90957975 MAFK JASPAR yes 117223925
chr14 90957990 90958009 RFX2 JASPAR yes 107595843
chr14 90957990 90958009 RFX2 JASPAR yes 117223926
chr14 90957991 90958012 REST JASPAR yes 107595844
chr14 90957991 90958012 REST JASPAR yes 117223927
chr14 90957992 90958007 RFX5 JASPAR yes 107595845
chr14 90957992 90958007 RFX5 JASPAR yes 117223928
chr14 90957993 90957998 MYC TRANSFAC yes 107595846
chr14 90957993 90957998 MYC TRANSFAC yes 117223929
chr14 90957994 90958010 RFX2 JASPAR yes 107595847
chr14 90957994 90958010 RFX3 JASPAR yes 107595848
chr14 90957994 90958010 RFX4 JASPAR yes 107595849
chr14 90957994 90958010 RFX5 JASPAR yes 107595850
chr14 90957994 90958010 RFX2 JASPAR yes 117223930
chr14 90957994 90958010 RFX3 JASPAR yes 117223931
chr14 90957994 90958010 RFX4 JASPAR yes 117223932
chr14 90957994 90958010 RFX5 JASPAR yes 117223933
chr14 90957995 90958014 RFX2 JASPAR yes 107595851
chr14 90957995 90958014 RFX2 JASPAR yes 117223934
chr14 90958023 90958033 NFATC3 JASPAR yes 107595852
chr14 90958023 90958033 NFATC3 JASPAR yes 117223935
chr14 90958038 90958057 RFX2 JASPAR yes 107595853
chr14 90958038 90958057 RFX2 JASPAR yes 117223936
chr14 90958040 90958055 RFX5 JASPAR yes 107595854
chr14 90958040 90958055 RFX5 JASPAR yes 117223937
chr14 90958042 90958052 NFIA JASPAR yes 107595855
chr14 90958042 90958052 NFIA JASPAR yes 117223938
chr14 90958043 90958052 NFIX JASPAR yes 107595856
chr14 90958043 90958052 NFIX JASPAR yes 117223939
chr14 90958044 90958050 NFIC JASPAR yes 107595857
chr14 90958044 90958050 NFIC JASPAR yes 117223940
chr14 90958063 90958073 SP1 JASPAR yes 107595858
chr14 90958063 90958073 SP1 JASPAR yes 117223941
chr14 90958064 90958074 SP1 JASPAR yes 107595859
chr14 90958064 90958074 SP1 JASPAR yes 117223942
chr14 90958074 90958080 SP1 TRANSFAC yes 107595860
chr14 90958074 90958080 SP1 TRANSFAC yes 117223943
chr14 90958092 90958097 SP1 TRANSFAC yes 107595861
chr14 90958092 90958097 SP1 TRANSFAC yes 117223944
chr14 90958123 90958128 SP1 TRANSFAC yes 107595862
chr14 90958123 90958128 SP1 TRANSFAC yes 117223945
chr14 90958137 90958141 NFE TRANSFAC yes 107595863
chr14 90958137 90958141 NFE TRANSFAC yes 117223946
chr14 90958148 90958158 SP1 JASPAR yes 107595864
chr14 90958148 90958158 SP1 JASPAR yes 117223947
chr14 90958153 90958162 SP1 TRANSFAC yes 107595865
chr14 90958153 90958162 SP1 TRANSFAC yes 117223948
chr14 90958154 90958164 SP1 JASPAR yes 107595866
chr14 90958154 90958164 SP1 JASPAR yes 117223949
chr14 90958156 90958162 NFE2 TRANSFAC yes 107595867
chr14 90958156 90958162 NFE2 TRANSFAC yes 117223950
chr14 90958157 90958167 GCM2 JASPAR yes 107595868
chr14 90958157 90958167 GCM2 JASPAR yes 117223951

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr14 90957934 rs143337681 C A 3724119
chr14 90958078 rs530250329 C G,T
3724120
chr14 90958097 rs148389487 G A
3724121

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 90862846 90874605 + CALM1 ENSG00000198668.6 90862846 0.65 0.99 13557 4927


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