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
chr11 61742735 61742914 FOXA1 UCSC Txn Factor no Conserved 107973404
chr11 61742603 61742616 POU2F2 JASPAR yes 39174596
chr11 61742603 61742616 POU2F2 JASPAR yes 114079346
chr11 61742663 61742669 NFE2 TRANSFAC yes 39174597
chr11 61742663 61742669 NFE2 TRANSFAC yes 114079347
chr11 61742678 61742689 NFKB1 JASPAR yes 39174598
chr11 61742678 61742689 NFKB1 JASPAR yes 114079348
chr11 61742681 61742691 NFATC3 JASPAR yes 39174599
chr11 61742681 61742691 NFATC3 JASPAR yes 114079349
chr11 61742691 61742697 SOX10 JASPAR yes 39174600
chr11 61742691 61742697 SOX10 JASPAR yes 114079350
chr11 61742737 61742754 ESR1 JASPAR yes 39174601
chr11 61742737 61742754 ESR1 JASPAR yes 114079351
chr11 61742738 61742753 ESR2 JASPAR yes 39174602
chr11 61742738 61742753 ESR2 JASPAR yes 114079352
chr11 61742752 61742773 ZNF263 JASPAR yes 39174603
chr11 61742752 61742773 ZNF263 JASPAR yes 114079353
chr11 61742760 61742780 RREB1 JASPAR yes 39174604
chr11 61742760 61742780 RREB1 JASPAR yes 114079354
chr11 61742765 61742775 ZNF740 JASPAR yes 39174605
chr11 61742765 61742775 ZNF740 JASPAR yes 114079355
chr11 61742782 61742796 NR2F1 JASPAR yes 39174606
chr11 61742782 61742796 NR2F1 JASPAR yes 114079356
chr11 61742790 61742805 FOXA1 JASPAR yes 39174607
chr11 61742790 61742805 FOXA1 JASPAR yes 114079357
chr11 61742791 61742806 FOXP1 JASPAR yes 39174608
chr11 61742791 61742806 FOXP1 JASPAR yes 114079358
chr11 61742792 61742803 FOXP2 JASPAR yes 39174609
chr11 61742792 61742803 FOXP2 JASPAR yes 114079359
chr11 61742792 61742806 FOXF2 JASPAR yes 39174610
chr11 61742792 61742806 FOXF2 JASPAR yes 114079360
chr11 61742794 61742805 FOXA1 JASPAR yes 39174611
chr11 61742794 61742805 FOXA1 JASPAR yes 114079361
chr11 61742795 61742803 GATA3 JASPAR yes 39174612
chr11 61742795 61742803 GATA3 JASPAR yes 114079362
chr11 61742810 61742831 ZNF263 JASPAR yes 39174613
chr11 61742810 61742831 ZNF263 JASPAR yes 114079363
chr11 61742818 61742829 E2F6 JASPAR yes 39174614
chr11 61742818 61742829 E2F6 JASPAR yes 114079364
chr11 61742819 61742830 TBX20 JASPAR yes 39174615
chr11 61742819 61742830 TBX20 JASPAR yes 114079365
chr11 61742821 61742829 TBX15 JASPAR yes 39174616
chr11 61742821 61742829 TBX15 JASPAR yes 114079366
chr11 61742827 61742848 REST JASPAR yes 39174617
chr11 61742827 61742848 REST JASPAR yes 114079367
chr11 61742828 61742847 REST JASPAR yes 39174618
chr11 61742828 61742847 REST JASPAR yes 114079368
chr11 61742830 61742840 ID4 JASPAR yes 39174619
chr11 61742830 61742840 TCF3 JASPAR yes 39174620
chr11 61742830 61742840 TCF4 JASPAR yes 39174621
chr11 61742830 61742840 ID4 JASPAR yes 114079369
chr11 61742830 61742840 TCF3 JASPAR yes 114079370
chr11 61742830 61742840 TCF4 JASPAR yes 114079371
chr11 61742832 61742837 USF2 TRANSFAC yes 39174622
chr11 61742832 61742837 USF2 TRANSFAC yes 114079372
chr11 61742841 61742856 AR JASPAR yes 39174623
chr11 61742841 61742856 AR JASPAR yes 114079373
chr11 61742875 61742892 ZNF410 JASPAR yes 39174624
chr11 61742875 61742892 ZNF410 JASPAR yes 114079374
chr11 61742894 61742897 MYB TRANSFAC yes 39174625
chr11 61742894 61742897 MYB TRANSFAC yes 114079375
chr11 61742899 61742913 NR2F1 JASPAR yes 39174626
chr11 61742899 61742913 NR2F1 JASPAR yes 114079376
chr11 61742930 61742941 ETV2 JASPAR yes 39174627
chr11 61742930 61742941 ETV2 JASPAR yes 114079377
chr11 61742935 61742950 RFX5 JASPAR yes 39174628
chr11 61742935 61742950 RFX5 JASPAR yes 114079378
chr11 61742954 61742960 NFE2 TRANSFAC yes 39174629
chr11 61742954 61742960 NFE2 TRANSFAC yes 114079379
chr11 61742986 61742992 TCF4 TRANSFAC yes 39174630
chr11 61742986 61742992 TCF4 TRANSFAC yes 114079380
chr11 61742986 61743001 FOXP1 JASPAR yes 39174631
chr11 61742986 61743001 FOXP1 JASPAR yes 114079381
chr11 61742987 61742998 FOXP2 JASPAR yes 39174632
chr11 61742987 61742998 FOXP2 JASPAR yes 114079382
chr11 61742996 61743003 MEIS1 JASPAR yes 39174633
chr11 61742996 61743003 MEIS1 JASPAR yes 114079383

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr11 61742716 rs182838004 C T no 2028063
chr11 61742733 rs80172518 C T no 2028064
chr11 61742736 rs10897192 G A
2028065
chr11 61742738 rs77895954 A G 2028066
chr11 61742812 rs148316075 C A,G 2028067
chr11 61742818 rs116451482 C A 2028068
chr11 61742823 rs75074494 C T 2028069
chr11 61742842 rs540326714 A T
2028070
chr11 61742875 rs115857955 C T 2028071
chr11 61742966 rs195446 C T no 2028072
chr11 61742972 rs117832375 C T no 2028073
chr11 61742985 rs530427754 T C no 2028074

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
chr11 61640991 61659523 - FADS3 ENSG00000221968.4 61659523 0.7 1.0 10947 16917
chr11 61664773 61687741 - RAB3IL1 ENSG00000167994.7 61687741 0.81 1.0 10948 45135
chr11 61717293 61732987 + BEST1 ENSG00000167995.11 61717293 0.82 1.0 10949 74687
chr11 61727190 61735132 - FTH1 ENSG00000167996.11 61735132 0.62 0.99 10950 92526
chr11 61735453 61736755 + AP003733.1 ENSG00000269089.1 61735453 0.8 1.0 10951 92847


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