Chrom Start End Enhancer ID Tissues that enhancer appears More
chr19 1028160 1028923 vista28131

Chrom Position dbSNP ID Reference Allele Alternative Allele id More
chr19 1025788 rs544684727 G A 5370777
chr19 1025848 rs12977691 T C 5370778
chr19 1025865 rs12979724 G A 5370779
chr19 1025897 rs71174339 T TTTAC 5370780
chr19 1025897 rs71307182 T TTTAC 5370781
chr19 1026006 rs76160910 C A 5370782
chr19 1026075 rs78615531 T C 5370783
chr19 1026264 rs564195995 TC T 5370784
chr19 1026314 rs140606971 C T 5370785
chr19 1026317 rs144242821 A G 5370786
chr19 1026318 rs10422209 C G 5370787
chr19 1026346 rs559497987 T C 5370788
chr19 1026360 rs578187799 G C 5370789
chr19 1026471 rs538598630 G A 5370790
chr19 1026477 rs4807440 G T 5370791
chr19 1026617 rs370451484 C G,T 5370792
chr19 1026622 rs528317691 C G,T 5370793
chr19 1026653 rs532321155 C A 5370794
chr19 1026736 rs374427898 C A 5370795
chr19 1026844 rs147767045 C G 5370796
chr19 1026848 rs116087737 C G 5370797
chr19 1026927 rs12973333 G A 5370798
chr19 1026957 rs143841422 T TC 5370799
chr19 1026961 rs561919584 C CA 5370800
chr19 1026964 rs571874121 C A,G 5370801
chr19 1027063 rs369570220 G A 5370802
chr19 1027286 rs12980170 G T 5370803
chr19 1027343 rs12980370 G T 5370804
chr19 1027371 rs373441144 T A 5370805
chr19 1027388 rs561297473 G A 5370806
chr19 1027501 rs73920546 C T 5370807
chr19 1027610 rs34697645 G A 5370808
chr19 1027640 rs139106846 G A 5370809
chr19 1027644 rs188731717 G T 5370810
chr19 1027735 rs149909932 C A 5370811
chr19 1027792 rs533679718 G T 5370812
chr19 1027797 rs7253254 A C 5370813
chr19 1027872 rs192976751 G C 5370814
chr19 1028032 rs35981894 C T 5370815
chr19 1028143 rs540415868 G C 5370816
chr19 1028149 rs75364577 G A 5370817
chr19 1028175 rs532556422 C T 5370818
chr19 1028291 rs62131169 G C 5370819
chr19 1028297 rs144928319 G T 5370820
chr19 1028403 rs201243630 AG A 5370821
chr19 1028434 rs79064007 C G 5370822
chr19 1028535 rs558330906 G A,C 5370823
chr19 1028871 rs574372299 C G 5370824
chr19 1028873 rs541748730 T G 5370825

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
chr19 1026298 1039068 + CNN2 ENSG00000064666.10 1026298 0.77 1.0 537 16730


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

No results