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
chr16 389801 389822 ZNF263 JASPAR yes 9107053
chr16 389801 389822 ZNF263 JASPAR yes 49324889
chr16 389830 389834 H4TF2 TRANSFAC yes 9107055
chr16 389830 389834 H4TF2 TRANSFAC yes 49324890
chr16 389838 389841 MYB TRANSFAC yes 9107056
chr16 389838 389841 MYB TRANSFAC yes 49324891
chr16 389847 389862 TFAP2C JASPAR yes 9107057
chr16 389847 389862 TFAP2C JASPAR yes 49324892
chr16 389848 389860 INSM1 JASPAR yes 9107058
chr16 389848 389860 TFAP2A JASPAR yes 9107059
chr16 389848 389860 TFAP2B JASPAR yes 9107060
chr16 389848 389860 TFAP2C JASPAR yes 9107061
chr16 389848 389860 INSM1 JASPAR yes 49324893
chr16 389848 389860 TFAP2A JASPAR yes 49324894
chr16 389848 389860 TFAP2B JASPAR yes 49324895
chr16 389848 389860 TFAP2C JASPAR yes 49324896
chr16 389849 389858 TFAP2A JASPAR yes 9107062
chr16 389849 389858 TFAP2A JASPAR yes 49324897
chr16 389863 389877 PLAG1 JASPAR yes 9107063
chr16 389863 389877 PLAG1 JASPAR yes 49324898
chr16 389885 389896 ETV2 JASPAR yes 9107064
chr16 389885 389896 ETV2 JASPAR yes 49324899
chr16 389886 389896 ERF JASPAR yes 9107065
chr16 389886 389896 ETS1 JASPAR yes 9107066
chr16 389886 389896 ERF JASPAR yes 49324900
chr16 389886 389896 ETS1 JASPAR yes 49324901
chr16 389886 389897 ELK4 JASPAR yes 9107067
chr16 389886 389897 FLI1 JASPAR yes 9107068
chr16 389886 389897 ELK4 JASPAR yes 49324902
chr16 389886 389897 FLI1 JASPAR yes 49324903
chr16 389888 389903 HNF4G JASPAR yes 9107069
chr16 389888 389903 HNF4G JASPAR yes 49324904
chr16 389889 389903 NR2F1 JASPAR yes 9107070
chr16 389889 389903 NR2F1 JASPAR yes 49324905
chr16 389889 389904 HNF4A JASPAR yes 9107071
chr16 389889 389904 HNF4A JASPAR yes 49324906
chr16 389911 389921 SP1 JASPAR yes 9107072
chr16 389911 389921 SP1 JASPAR yes 49324907
chr16 389929 389948 REST JASPAR yes 9107073
chr16 389929 389948 REST JASPAR yes 49324908
chr16 389930 389934 LFA1 TRANSFAC yes 9107074
chr16 389930 389934 LFA1 TRANSFAC yes 49324909

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr16 389827 rs574322466 CA C no 4245476
chr16 389870 rs576713538 T TG
4245477
chr16 389879 rs537257895 C A no 4245478

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
chr16 299546 319942 + ITFG3 ENSG00000269881.1 299546 0.97 0.95 14338 9730
chr16 318300 325980 - RGS11 ENSG00000076344.11 325980 0.76 0.98 14339 36164
chr16 318726 333003 + ARHGDIG ENSG00000242173.4 318726 0.98 0.93 14340 28910
chr16 333152 337215 + PDIA2 ENSG00000185615.11 333152 1.0 0.91 14341 43336
chr16 337440 402673 - AXIN1 ENSG00000103126.10 402673 0.57 1.0 14342 87273
chr16 417384 420527 - MRPL28 ENSG00000086504.11 420527 0.65 0.99 14343 69419
chr16 420773 437113 - TMEM8A ENSG00000129925.6 437113 0.77 1.0 14344 52833
chr16 446725 460367 + NME4 ENSG00000103202.8 446725 0.55 0.99 14345 43221
chr16 451826 462487 + DECR2 ENSG00000242612.2 451826 0.94 1.0 14346 38120
chr16 475619 573011 + RAB11FIP3 ENSG00000090565.11 475619 0.88 0.99 14347 14327


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