EnhancerDB
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Chromosome characteristics of TCF7L2[chr1:8088588-8098693]
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Enhancers possibly regulated by TCF7L2[chr1:8088588-8098693]
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Chrom Start End Enhancer ID Tissues that enhancer appears More
chr1 8089365 8111955 enh11459
Brain (SK-N-MC) Astrocyte Colon (HCT116) Pancreas Uterus Epithelial (MCF-7) Bone (Osteoblast) Thyroid Pancreas (Panc1) Prostate (PC-3) Cervix (HeLa-S3) Large Intestine Esophagus Placenta Lung (PC-9) Breast Muscle (Myoblast) Muscle (Myotube) Liver (HepG2) Prostate (RWPE1) Muscle (A673)
SNP sites on TCF7L2[chr1:8088588-8098693]
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Chrom Position dbSNP ID Reference Allele Alternative Allele id More
chr1 8088891 rs370838150 TTAA T 50612
chr1 8088896 rs114623662 G A 50613
chr1 8088949 rs11800783 G A 50614
chr1 8088967 rs183219321 C T 50615
chr1 8089038 rs12021543 A C 50616
chr1 8089107 rs536126680 G A 50617
chr1 8089201 rs199666249 A AT 50618
chr1 8089456 rs12058555 T C 50619
chr1 8089576 rs12021731 A G 50620
chr1 8089697 rs367803696 G A 50621
chr1 8089799 rs147113825 TAC T 50622
chr1 8089799 rs774830287 TAC T 50623
chr1 8089800 rs12057543 A G 50624
chr1 8089805 rs546709099 C T 50625
chr1 8089874 rs529297803 G A 50626
chr1 8089959 rs569929773 C T 50627
chr1 8090030 rs182147269 A G 50628
chr1 8090138 rs12063453 G A 50629
chr1 8090287 rs138464628 A G 50630
chr1 8090434 rs143040734 G A 50631
chr1 8090534 rs373046572 C T 50632
chr1 8090535 rs145950364 G A 50633
chr1 8090551 rs192509027 G T 50634
chr1 8090559 rs138377825 T C 50635
chr1 8090615 rs225126 A G 50636
chr1 8090822 rs144470675 G A 50637
chr1 8090939 rs368314664 G A 50638
chr1 8091015 rs185714396 G A 50639
chr1 8091025 rs148457941 C T 50640
chr1 8091585 rs375177098 A C 50641
chr1 8091799 rs367894523 G A 50642
chr1 8091810 rs185363930 C T 50643
chr1 8091897 rs72856335 G A 50644
chr1 8091917 rs144498407 T G 50645
chr1 8091963 rs72856336 T A 50646
chr1 8092091 rs151046838 G A 50647
chr1 8092106 rs139689662 G A 50648
chr1 8092251 rs550945490 G A 50649
chr1 8092275 rs79134628 T A 50650
chr1 8092372 rs11801089 T C 50651
chr1 8092480 rs145738467 C T 50652
chr1 8092587 rs118010018 A T 50653
chr1 8092749 rs77542255 A T 50654
chr1 8092888 rs117649092 G A 50655
chr1 8093004 rs225127 G A 50656
chr1 8093006 rs141157193 T TA 50657
chr1 8093053 rs527293174 A G 50658
chr1 8093100 rs538575678 G A 50659
chr1 8093123 rs539097493 G A 50660
chr1 8093154 rs554987003 G A 50661
chr1 8093167 rs112798356 TA T 50662
chr1 8093195 rs225128 C T 50663
chr1 8093372 rs74053419 G A,T 50664
chr1 8093401 rs571002101 CAG C 50665
chr1 8093432 rs72634234 T C 50666
chr1 8093480 rs187361097 C G 50667
chr1 8093577 rs77561349 C T 50668
chr1 8093595 rs560969692 T C 50669
chr1 8093633 rs115181339 T A 50670
chr1 8093671 rs143392835 G C 50671
chr1 8093687 rs75519712 T G 50672
chr1 8094164 rs225129 T A 50673
chr1 8094193 rs573127698 GCA G 50674
chr1 8094200 rs11799555 T G 50675
chr1 8094268 rs7513370 C A 50676
chr1 8094286 rs150259844 TAGAA T 50677
chr1 8094641 rs11577776 G A 50678
chr1 8094673 rs7525435 A G 50679
chr1 8094717 rs113711530 TA T 50680
chr1 8094854 rs11121070 C T 50681
chr1 8094978 rs12745223 C T 50682
chr1 8095032 rs115118262 G A 50683
chr1 8095127 rs532831502 G A 50684
chr1 8095185 rs186756662 G A 50685
chr1 8095312 rs225130 G A 50686
chr1 8095360 rs11121071 C A 50687
chr1 8095383 rs190914291 G A 50688
chr1 8095439 rs536441251 A G 50689
chr1 8095451 rs554843610 C A 50690
chr1 8095468 rs150327790 C T 50691
chr1 8095486 rs225131 T C 50692
chr1 8095500 rs225132 T G 50693
chr1 8095575 rs137967918 G A 50694
chr1 8095815 rs11121072 C T 50695
chr1 8095849 rs147201391 A G 50696
chr1 8095863 rs372691016 CAG C 50697
chr1 8095900 rs528486808 G A 50698
chr1 8096005 rs374180471 C T 50699
chr1 8096134 rs558693879 A G 50700
chr1 8096160 rs542352268 A ACGTATATATATATATACG 50701
chr1 8096173 rs534603843 T C 50702
chr1 8096179 rs552729284 T C 50703
chr1 8096213 rs111559438 C T 50704
chr1 8096253 rs142253396 T C 50705
chr1 8096305 rs563508681 T C 50706
chr1 8096332 rs151242975 T C 50707
chr1 8096663 rs569827130 G A 50708
chr1 8096762 rs193266833 G A,T 50709
chr1 8096774 rs184190987 G A 50710
chr1 8096803 rs200842921 GA G 50711
chr1 8096852 rs191678471 G A 50712
chr1 8096959 rs184140137 A G 50713
chr1 8097019 rs188099892 T G 50714
chr1 8097143 rs116764098 G T 50715
chr1 8097145 rs7522911 C T 50716
chr1 8097726 rs528155857 G T 50717
chr1 8097801 rs184573276 C G 50718
chr1 8097819 rs190252533 G A 50719
chr1 8097884 rs113399029 G A 50720
chr1 8098089 rs375296229 T C,G 50721
chr1 8098200 rs114856263 G A,T 50722
chr1 8098462 rs225133 G A 50723
chr1 8098509 rs12062908 A G 50724
chr1 8098555 rs181201772 C G,T 50725
chr1 8098657 rs116593615 T G 50726
Genes possibly regulated by TCF7L2[chr1:8088588-8098693]
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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
Expression level of Genes
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No results
miRNAs possibly regulated by TCF7L2[chr1:8088588-8098693]
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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