EnhancerDB
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  3. TCF7L2[chr17:2688374-2693226]
Chromosome characteristics of TCF7L2[chr17:2688374-2693226]
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Enhancers possibly regulated by TCF7L2[chr17:2688374-2693226]
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Chrom Start End Enhancer ID Tissues that enhancer appears More
chr17 2687493 2699555 enh52404
Cervix (HeLa-S3) Prostate (RWPE1) Large Intestine Blood (T-cell) Stomach
chr17 2692899 2693294 vista23731
VISTA
SNP sites on TCF7L2[chr17:2688374-2693226]
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Chrom Position dbSNP ID Reference Allele Alternative Allele id More
chr17 2688524 rs77118776 C G 4703920
chr17 2688527 rs56943334 C G,T 4703921
chr17 2688671 rs8070218 G T 4703922
chr17 2688695 rs11419211 G GA 4703923
chr17 2688695 rs558860326 G GA 4703924
chr17 2688990 rs147368136 G A,C 4703925
chr17 2689115 rs116164565 T A 4703926
chr17 2689193 rs374525671 C CT 4703927
chr17 2689193 rs376291459 C CT,CTT,CTTT 4703928
chr17 2689264 rs9944498 C T 4703929
chr17 2689265 rs373785952 G A 4703930
chr17 2689271 rs139876813 C T 4703931
chr17 2689272 rs531372535 C T 4703932
chr17 2689298 rs190180533 C T 4703933
chr17 2689349 rs35539899 C G 4703934
chr17 2689440 rs570702364 C T 4703935
chr17 2689442 rs539618685 G C 4703936
chr17 2689503 rs367896958 T C 4703937
chr17 2689585 rs557404706 A G,T 4703938
chr17 2689818 rs537404039 CG C 4703939
chr17 2689922 rs186074360 T C 4703940
chr17 2689934 rs35938193 AT A 4703941
chr17 2689934 rs574442084 AT A 4703942
chr17 2689934 rs58758851 ATT A 4703943
chr17 2689934 rs796229033 AT A 4703944
chr17 2689934 rs797004500 ATT A 4703945
chr17 2689948 rs564437734 T A 4703946
chr17 2689980 rs566901328 C T 4703947
chr17 2690042 rs111794606 C T 4703948
chr17 2690214 rs178582 T A,G 4703949
chr17 2690277 rs373338165 G A 4703950
chr17 2690327 rs555820884 C T 4703951
chr17 2690360 rs146076117 C T 4703952
chr17 2690564 rs113457559 C T 4703953
chr17 2690577 rs527316630 G A,C 4703954
chr17 2690719 rs143695559 A T 4703955
chr17 2690789 rs187677253 A G 4703956
chr17 2690831 rs115160986 T C 4703957
chr17 2690843 rs190909239 C T 4703958
chr17 2690876 rs372730913 T G 4703959
chr17 2690884 rs541583201 T TG 4703960
chr17 2690963 rs182521676 G T 4703961
chr17 2690996 rs146807246 G C 4703962
chr17 2691112 rs140309570 C T 4703963
chr17 2691141 rs572863171 A G 4703964
chr17 2691264 rs12600882 C A,T 4703965
chr17 2691328 rs144989154 A G 4703966
chr17 2691362 rs187136371 A G 4703967
chr17 2691463 rs145917008 TAGTC T 4703968
chr17 2691779 rs146130265 C T 4703969
chr17 2691793 rs9906052 T C 4703970
chr17 2691812 rs112408457 G A 4703971
chr17 2691841 rs56188113 C T 4703972
chr17 2692047 rs114684716 G T 4703973
chr17 2692129 rs201930551 C T 4703974
chr17 2692189 rs1124039 C A 4703975
chr17 2692321 rs1124040 G A,C 4703976
chr17 2692357 rs137976908 T A 4703977
chr17 2692401 rs376335565 G C 4703978
chr17 2692722 rs72817353 C T 4703979
chr17 2692747 rs573521156 G A,C 4703980
chr17 2692825 rs178581 C T 4703981
chr17 2692901 rs546111176 TA T 4703982
chr17 2692945 rs188854783 G T 4703983
chr17 2692992 rs547364389 C G,T 4703984
chr17 2693035 rs372021918 C G 4703985
chr17 2693066 rs141675636 A G 4703986
Genes possibly regulated by TCF7L2[chr17:2688374-2693226]
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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[chr17:2688374-2693226]
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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