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
chr13 111048883 111048889 YY1 JASPAR yes 19342915
chr13 111048883 111048889 YY1 JASPAR yes 60347457
chr13 111048885 111048898 ZBTB18 JASPAR yes 19342916
chr13 111048885 111048898 ZBTB18 JASPAR yes 60347458
chr13 111048941 111048956 LEF1 JASPAR yes 19342917
chr13 111048941 111048956 LEF1 JASPAR yes 60347459
chr13 111048942 111048956 TCF7L2 JASPAR yes 19342918
chr13 111048942 111048956 TCF7L2 JASPAR yes 60347460
chr13 111048944 111048951 TCF4 TRANSFAC yes 19342919
chr13 111048944 111048951 TCF4 TRANSFAC yes 60347461
chr13 111048945 111048951 LEF1 TRANSFAC yes 19342920
chr13 111048945 111048951 TCF4 TRANSFAC yes 19342921
chr13 111048945 111048951 LEF1 TRANSFAC yes 60347462
chr13 111048945 111048951 TCF4 TRANSFAC yes 60347463
chr13 111048952 111048963 NFE2 JASPAR yes 19342922
chr13 111048952 111048963 NFE2 JASPAR yes 60347464
chr13 111048953 111048962 JDP2 JASPAR yes 19342923
chr13 111048953 111048962 JDP2 JASPAR yes 60347465
chr13 111048959 111048976 ESR1 JASPAR yes 19342924
chr13 111048959 111048976 ESR1 JASPAR yes 60347466
chr13 111048959 111048980 ZNF263 JASPAR yes 19342925
chr13 111048959 111048980 ZNF263 JASPAR yes 60347467
chr13 111048965 111048975 SP1 JASPAR yes 19342926
chr13 111048965 111048975 SP1 JASPAR yes 60347468
chr13 111048968 111048973 SP1 TRANSFAC yes 19342927
chr13 111048968 111048973 SP1 TRANSFAC yes 60347469
chr13 111048979 111048982 MYB TRANSFAC yes 19342928
chr13 111048979 111048982 MYB TRANSFAC yes 60347470
chr13 111048994 111048999 TFAP2A TRANSFAC yes 19342929
chr13 111048994 111048999 TFAP2A TRANSFAC yes 60347471
chr13 111048994 111049000 MZF1 JASPAR yes 19342930
chr13 111048994 111049000 MZF1 JASPAR yes 60347472
chr13 111049010 111049020 GSX2 JASPAR yes 19342931
chr13 111049010 111049020 GSX2 JASPAR yes 60347473
chr13 111049010 111049021 HOXA10 JASPAR yes 19342932
chr13 111049010 111049021 HOXC11 JASPAR yes 19342933
chr13 111049010 111049021 HOXD12 JASPAR yes 19342934
chr13 111049010 111049021 HOXA10 JASPAR yes 60347474
chr13 111049010 111049021 HOXC11 JASPAR yes 60347475
chr13 111049010 111049021 HOXD12 JASPAR yes 60347476
chr13 111049011 111049019 NKX6-1 JASPAR yes 19342935
chr13 111049011 111049019 NKX6-1 JASPAR yes 60347477
chr13 111049011 111049021 HOXC10 JASPAR yes 19342936
chr13 111049011 111049021 HOXD11 JASPAR yes 19342937
chr13 111049011 111049021 HOXC10 JASPAR yes 60347478
chr13 111049011 111049021 HOXD11 JASPAR yes 60347479
chr13 111049013 111049017 YY1 TRANSFAC yes 19342938
chr13 111049013 111049017 YY1 TRANSFAC yes 60347480
chr13 111049052 111049067 STAT1 JASPAR yes 19342939
chr13 111049052 111049067 STAT1 JASPAR yes 60347481
chr13 111049054 111049065 STAT1 JASPAR yes 19342940
chr13 111049054 111049065 STAT1 JASPAR yes 60347482
chr13 111049059 111049073 JUN JASPAR yes 19342941
chr13 111049059 111049073 JUN JASPAR yes 60347483
chr13 111049060 111049066 HiNF-A TRANSFAC yes 19342942
chr13 111049060 111049066 HiNF-A TRANSFAC yes 60347484
chr13 111049061 111049072 BATF JASPAR yes 19342943
chr13 111049061 111049072 BATF JASPAR yes 60347485
chr13 111049062 111049073 FOSL2 JASPAR yes 19342944
chr13 111049062 111049073 JUNB JASPAR yes 19342945
chr13 111049062 111049073 FOSL2 JASPAR yes 60347486
chr13 111049062 111049073 JUNB JASPAR yes 60347487
chr13 111049063 111049074 FOS JASPAR yes 19342946
chr13 111049063 111049074 FOSL1 JASPAR yes 19342947
chr13 111049063 111049074 FOS JASPAR yes 60347488
chr13 111049063 111049074 FOSL1 JASPAR yes 60347489
chr13 111049064 111049075 NFE2L2 JASPAR yes 19342948
chr13 111049064 111049075 NFE2L2 JASPAR yes 60347490

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr13 111048889 rs369455015 C G
3394173
chr13 111048894 rs9583490 T C
3394174
chr13 111048937 rs186408663 T G no 3394175
chr13 111048938 rs536994614 T C no 3394176
chr13 111049009 rs149428589 C G no 3394177
chr13 111049075 rs578077715 G A
3394178
chr13 111049109 rs55912318 C CG no 3394179
chr13 111049109 rs78286938 C CG no 3394180

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
chr13 110801318 110959496 - COL4A1 ENSG00000187498.10 110959496 0.85 0.93 13019 10608
chr13 110958159 111165374 + COL4A2 ENSG00000134871.13 110958159 0.78 0.91 13020 9271


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