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
chr7 475919 475925 SOX10 JASPAR yes 12393550
chr7 475919 475925 SOX10 JASPAR yes 26008273
chr7 475923 475943 TP53 JASPAR yes 12393551
chr7 475923 475943 TP53 JASPAR yes 26008274
chr7 475925 475945 TP63 JASPAR yes 12393552
chr7 475925 475945 TP63 JASPAR yes 26008275
chr7 475928 475943 TP53 JASPAR yes 12393553
chr7 475928 475943 TP53 JASPAR yes 26008276
chr7 475929 475940 NFE2L2 JASPAR yes 12393554
chr7 475929 475940 NFE2L2 JASPAR yes 26008277
chr7 475977 475986 SP1 TRANSFAC yes 12393555
chr7 475977 475986 SP1 TRANSFAC yes 26008278
chr7 475977 475996 PAX5 JASPAR yes 12393556
chr7 475977 475996 PAX5 JASPAR yes 26008279
chr7 475978 475984 SP1 TRANSFAC yes 12393557
chr7 475978 475984 SP1 TRANSFAC yes 26008280
chr7 475978 475988 SP1 JASPAR yes 12393558
chr7 475978 475988 SP1 JASPAR yes 26008281
chr7 475979 475986 SP1 TRANSFAC yes 12393559
chr7 475979 475986 SP1 TRANSFAC yes 26008282
chr7 475980 475985 SP1 TRANSFAC yes 12393560
chr7 475980 475985 SP1 TRANSFAC yes 26008283
chr7 475980 475986 SP1 TRANSFAC yes 12393561
chr7 475980 475986 SP1 TRANSFAC yes 26008284
chr7 475988 476002 TLX1 JASPAR yes 12393562
chr7 475988 476002 TLX1 JASPAR yes 26008285

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr7 475962 rs147357079 C T no 9561597

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
chr7 536895 559933 - PDGFA ENSG00000197461.9 559933 0.72 1.0 7149 16063


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