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 91697881 91697891 RORA JASPAR yes 107597508
chr14 91697881 91697891 RORA JASPAR yes 117277771
chr14 91697883 91697898 NR2C2 JASPAR yes 107597509
chr14 91697883 91697898 NR2C2 JASPAR yes 117277772
chr14 91697884 91697898 RXRB JASPAR yes 107597510
chr14 91697884 91697898 RXRG JASPAR yes 107597511
chr14 91697884 91697898 RXRB JASPAR yes 117277773
chr14 91697884 91697898 RXRG JASPAR yes 117277774
chr14 91697886 91697890 ESR1 TRANSFAC yes 107597512
chr14 91697886 91697890 ESR1 TRANSFAC yes 117277775
chr14 91697921 91697928 SPIB JASPAR yes 107597513
chr14 91697921 91697928 SPIB JASPAR yes 117277776
chr14 91697937 91697942 TFAP2A TRANSFAC yes 107597514
chr14 91697937 91697942 TFAP2A TRANSFAC yes 117277777
chr14 91697937 91697943 MZF1 JASPAR yes 107597515
chr14 91697937 91697943 MZF1 JASPAR yes 117277778
chr14 91697945 91697949 YY1 TRANSFAC yes 107597516
chr14 91697945 91697949 YY1 TRANSFAC yes 117277779
chr14 91697982 91697997 RUNX2 JASPAR yes 107597517
chr14 91697982 91697997 RUNX2 JASPAR yes 117277780
chr14 91698002 91698015 ELF1 JASPAR yes 107597518
chr14 91698002 91698015 ELF1 JASPAR yes 117277781
chr14 91698003 91698006 MYB TRANSFAC yes 107597519
chr14 91698003 91698006 MYB TRANSFAC yes 117277782
chr14 91698004 91698015 ELF5 JASPAR yes 107597520
chr14 91698004 91698015 ELF5 JASPAR yes 117277783
chr14 91698005 91698015 GABPA JASPAR yes 107597521
chr14 91698005 91698015 GABPA JASPAR yes 117277784
chr14 91698022 91698033 FOXA1 JASPAR yes 107597522
chr14 91698022 91698033 FOXA1 JASPAR yes 117277785
chr14 91698022 91698037 FOXA1 JASPAR yes 107597523
chr14 91698022 91698037 FOXA1 JASPAR yes 117277786
chr14 91698023 91698034 FOXB1 JASPAR yes 107597524
chr14 91698023 91698034 FOXC1 JASPAR yes 107597525
chr14 91698023 91698034 FOXB1 JASPAR yes 117277787
chr14 91698023 91698034 FOXC1 JASPAR yes 117277788
chr14 91698024 91698035 FOXP2 JASPAR yes 107597526
chr14 91698024 91698035 FOXP2 JASPAR yes 117277789
chr14 91698025 91698033 FOXO3 JASPAR yes 107597527
chr14 91698025 91698033 FOXO3 JASPAR yes 117277790
chr14 91698026 91698033 FOXD2 JASPAR yes 107597528
chr14 91698026 91698033 FOXI1 JASPAR yes 107597529
chr14 91698026 91698033 FOXL1 JASPAR yes 107597530
chr14 91698026 91698033 FOXO4 JASPAR yes 107597531
chr14 91698026 91698033 FOXO6 JASPAR yes 107597532
chr14 91698026 91698033 FOXP3 JASPAR yes 107597533
chr14 91698026 91698033 FOXD2 JASPAR yes 117277791
chr14 91698026 91698033 FOXI1 JASPAR yes 117277792
chr14 91698026 91698033 FOXL1 JASPAR yes 117277793
chr14 91698026 91698033 FOXO4 JASPAR yes 117277794
chr14 91698026 91698033 FOXO6 JASPAR yes 117277795
chr14 91698026 91698033 FOXP3 JASPAR yes 117277796
chr14 91698026 91698034 FOXD1 JASPAR yes 107597534
chr14 91698026 91698034 FOXO3 JASPAR yes 107597535
chr14 91698026 91698034 FOXD1 JASPAR yes 117277797
chr14 91698026 91698034 FOXO3 JASPAR yes 117277798
chr14 91698026 91698040 SPI1 JASPAR yes 107597536
chr14 91698026 91698040 SPIC JASPAR yes 107597537
chr14 91698026 91698040 SPI1 JASPAR yes 117277799
chr14 91698026 91698040 SPIC JASPAR yes 117277800
chr14 91698027 91698040 ELF1 JASPAR yes 107597538
chr14 91698027 91698040 ELF1 JASPAR yes 117277801
chr14 91698029 91698040 ELF5 JASPAR yes 107597539
chr14 91698029 91698040 ELF5 JASPAR yes 117277802
chr14 91698030 91698040 GABPA JASPAR yes 107597540
chr14 91698030 91698040 GABPA JASPAR yes 117277803
chr14 91698067 91698081 POU4F1 JASPAR yes 107597541
chr14 91698067 91698081 POU4F1 JASPAR yes 117277804
chr14 91698067 91698083 POU4F2 JASPAR yes 107597542
chr14 91698067 91698083 POU4F3 JASPAR yes 107597543
chr14 91698067 91698083 POU4F2 JASPAR yes 117277805
chr14 91698067 91698083 POU4F3 JASPAR yes 117277806
chr14 91698085 91698094 VENTX JASPAR yes 107597544
chr14 91698085 91698094 VENTX JASPAR yes 117277807

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr14 91697872 rs531508218 G T no 3729978

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 91698876 91720269 - GPR68 ENSG00000119714.6 91720269 0.78 1.0 13561 77817
chr14 91709103 91717426 + CTD-2547L24.3 ENSG00000258875.1 91709103 0.9 1.0 13562 88983


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