EnhancerDB
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  3. TCF7L2[chr16:89037679-89042618]
Chromosome characteristics of TCF7L2[chr16:89037679-89042618]
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Enhancers possibly regulated by TCF7L2[chr16:89037679-89042618]
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Chrom Start End Enhancer ID Tissues that enhancer appears More
chr16 89029754 89041849 enh47986
Blood (OCI-LY7) Blood (GM12878) Peripheral Blood (MM.1S) Thymus Stomach
chr16 89038174 89038503 vista23533
VISTA
chr16 89039891 89040100 vista23534
VISTA
chr16 89040833 89040974 vista23535
VISTA
SNP sites on TCF7L2[chr16:89037679-89042618]
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Chrom Position dbSNP ID Reference Allele Alternative Allele id More
chr16 89037760 rs570991228 C CGCCT 4670651
chr16 89037984 rs370541129 G C 4670652
chr16 89038036 rs77712900 C T 4670653
chr16 89038037 rs118058794 G A 4670654
chr16 89038038 rs573991802 G A 4670655
chr16 89038114 rs73256250 G C 4670656
chr16 89038155 rs566883794 A C 4670657
chr16 89038168 rs546955357 C T 4670658
chr16 89038220 rs113826479 A C 4670659
chr16 89038265 rs116126905 G A 4670660
chr16 89038342 rs74033232 T A 4670661
chr16 89038355 rs7200905 G A 4670662
chr16 89038427 rs530530482 C T 4670663
chr16 89038455 rs548634795 C A 4670664
chr16 89038713 rs547311983 G A 4670665
chr16 89038729 rs113523370 C T 4670666
chr16 89038745 rs114227586 G A,C 4670667
chr16 89038747 rs569437504 G C,T 4670668
chr16 89038800 rs116363590 G C 4670669
chr16 89038865 rs112615485 C T 4670670
chr16 89038880 rs13333659 G T 4670671
chr16 89038940 rs182747382 T C 4670672
chr16 89039002 rs114031998 C G,T 4670673
chr16 89039117 rs185633466 G T 4670674
chr16 89039174 rs150534980 C T 4670675
chr16 89039227 rs549111243 G A 4670676
chr16 89039391 rs187644297 A C 4670677
chr16 89039417 rs149655780 C T 4670678
chr16 89039421 rs147850452 C T 4670679
chr16 89039457 rs11859859 A T 4670680
chr16 89039477 rs115102807 C A 4670681
chr16 89039496 rs568665224 C A,T 4670682
chr16 89039542 rs80211567 C T 4670683
chr16 89039598 rs75396238 C G 4670684
chr16 89039707 rs112379645 G A 4670685
chr16 89039720 rs76133836 C T 4670686
chr16 89039813 rs376904050 C T 4670687
chr16 89039856 rs11859986 A G 4670688
chr16 89040027 rs548442750 G A 4670689
chr16 89040141 rs192305953 C T 4670690
chr16 89040180 rs542110295 T TGGCC 4670691
chr16 89040197 rs147623543 C T 4670692
chr16 89040215 rs575048798 TGGGCTCCAGCCA T 4670693
chr16 89040302 rs184512169 G A 4670694
chr16 89040317 rs35148767 T TG 4670695
chr16 89040322 rs564297161 C T 4670696
chr16 89040329 rs13330216 C T 4670697
chr16 89040387 rs537872388 C G,T 4670698
chr16 89040404 rs149085471 G A 4670699
chr16 89040461 rs527546699 C G 4670700
chr16 89040532 rs11862139 T C 4670701
chr16 89040605 rs535449830 CTCT C 4670702
chr16 89040629 rs556164397 G A,C 4670703
chr16 89040637 rs192665649 A C 4670704
chr16 89040642 rs577903646 G A 4670705
chr16 89040649 rs376287225 C A 4670706
chr16 89040767 rs184751319 G A,T 4670707
chr16 89040792 rs553787821 CAG C 4670708
chr16 89040872 rs565511425 C T 4670709
chr16 89040978 rs112253959 C A,T 4670710
chr16 89041014 rs541132260 C T 4670711
chr16 89041059 rs564366072 C T 4670712
chr16 89041111 rs9922717 C T 4670713
chr16 89041165 rs4782492 G A 4670714
chr16 89041320 rs116057573 T A 4670715
chr16 89041372 rs553178975 A G 4670716
chr16 89041424 rs545421016 C T 4670717
chr16 89041547 rs62045814 G C 4670718
chr16 89041555 rs4782491 G A 4670719
chr16 89041559 rs62045815 G A 4670720
chr16 89041563 rs4782490 T C,G 4670721
chr16 89041618 rs4782488 C T 4670722
chr16 89041695 rs569276700 G A,T 4670723
chr16 89041716 rs146387844 A G 4670724
chr16 89041742 rs567885643 G A,C 4670725
chr16 89041754 rs181711161 C T 4670726
chr16 89041790 rs185803887 C T 4670727
chr16 89041791 rs543773177 G A 4670728
chr16 89041793 rs555461254 C T 4670729
chr16 89041794 rs138297369 G A,T 4670730
chr16 89041818 rs559459226 G A 4670731
chr16 89041833 rs117826371 G A 4670732
chr16 89041846 rs562974032 T C 4670733
chr16 89041854 rs117572341 G A 4670734
chr16 89041878 rs115140361 A G 4670735
chr16 89041913 rs4782487 C T 4670736
chr16 89041931 rs116547555 C T 4670737
chr16 89041944 rs143956988 A G 4670738
chr16 89041965 rs116122895 C T 4670739
chr16 89041966 rs577395161 G A 4670740
chr16 89041971 rs544741141 G A 4670741
chr16 89042031 rs190809953 G A 4670742
chr16 89042067 rs79128326 C G 4670743
chr16 89042083 rs532741720 G A,T 4670744
chr16 89042091 rs551140197 G A 4670745
chr16 89042121 rs182256317 G A,T 4670746
chr16 89042152 rs566830650 G A 4670747
chr16 89042155 rs148625106 C T 4670748
chr16 89042194 rs144222561 G T 4670749
chr16 89042301 rs78258274 G C 4670750
chr16 89042334 rs7193421 T A,G 4670751
chr16 89042348 rs113629998 G C 4670752
chr16 89042367 rs7201599 C T 4670753
chr16 89042368 rs139435727 G A 4670754
chr16 89042455 rs534191985 T G 4670755
chr16 89042497 rs145322635 C G,T 4670756
chr16 89042510 rs73256262 C T 4670757
chr16 89042511 rs183165345 G A 4670758
chr16 89042570 rs572796704 C A,G,T 4670759
chr16 89042571 rs78654464 G A 4670760
chr16 89042615 rs7202173 C A,G 4670761
Genes possibly regulated by TCF7L2[chr16:89037679-89042618]
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Details of Genes
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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 to TFBS id More
chr16 88941266 89043612 - CBFA2T3 ENSG00000129993.10 89043612 0.96 0.99 994 15169
Expression level of Genes
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miRNAs possibly regulated by TCF7L2[chr16:89037679-89042618]
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Details of miRNAs
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Blank TSI value indicates lack of sufficient expression for calculation
Chrom Start End strand miRNA Name miRBase ID TSS TSI of Normal tissues TSI of Cancer tissues Distance to TFBS id More
Expression level of miRNAs
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No results