Chrom Start End Enhancer ID Tissues that enhancer appears More
chr17 77776510 77776898 vista26281
chr17 77778056 77778248 vista26282
chr17 77778301 77778701 vista26283

Chrom Position dbSNP ID Reference Allele Alternative Allele id More
chr17 77771548 rs8082452 T C,G 5096784
chr17 77771560 rs531965883 G C 5096785
chr17 77771562 rs550674488 A C 5096786
chr17 77771564 rs529726470 A C 5096787
chr17 77771591 rs548865797 TC T 5096788
chr17 77772068 rs9905914 G A 5096789
chr17 77772187 rs9906169 G C 5096790
chr17 77772452 rs192945400 G C 5096791
chr17 77772458 rs376218803 GA G 5096792
chr17 77772459 rs559923351 A G 5096793
chr17 77772607 rs374470533 C T 5096794
chr17 77772747 rs141784169 TTC T 5096795
chr17 77772966 rs549983631 C G 5096796
chr17 77772985 rs56150471 C T 5096797
chr17 77773240 rs545963907 A AGAGCG 5096798
chr17 77773318 rs1105820 T C 5096799
chr17 77773330 rs117056514 C G 5096800
chr17 77773349 rs147348596 G A 5096801
chr17 77773441 rs377554474 C G 5096802
chr17 77773601 rs75488081 C T 5096803
chr17 77773837 rs77877768 C T 5096804
chr17 77773876 rs870681 A C 5096805
chr17 77774185 rs117742856 C T 5096806
chr17 77774363 rs531490469 G A 5096807
chr17 77774505 rs566062429 A G 5096808
chr17 77775227 rs528792105 G C 5096809
chr17 77775339 rs529251936 G A 5096810
chr17 77775471 rs183946677 T C 5096811
chr17 77775616 rs533311374 C A 5096812
chr17 77775768 rs530893422 C T 5096813
chr17 77776086 rs539387844 A T 5096814
chr17 77776093 rs189408187 G A 5096815
chr17 77776101 rs576233137 T C 5096816
chr17 77776123 rs371421925 G T 5096817
chr17 77776147 rs144361139 G A 5096818
chr17 77776379 rs193281518 G C 5096819
chr17 77776429 rs559569859 G A 5096820
chr17 77776561 rs577971737 G C 5096821
chr17 77776605 rs77489244 G A 5096822
chr17 77776612 rs530955781 G A 5096823
chr17 77776702 rs34125910 GC G 5096824
chr17 77776702 rs397857948 GC G 5096825
chr17 77776798 rs546996291 C T 5096826
chr17 77776835 rs9897277 C T 5096827
chr17 77777125 rs12946718 C A 5096828
chr17 77777154 rs114925139 C T 5096829
chr17 77777155 rs544611843 CT C 5096830
chr17 77777202 rs143934410 C T 5096831
chr17 77777560 rs140493366 A AC 5096832
chr17 77777562 rs185288616 C A 5096833
chr17 77777593 rs115610288 T C 5096834
chr17 77777650 rs140532783 G T 5096835
chr17 77777656 rs530489797 T C 5096836
chr17 77777830 rs28494747 C G 5096837
chr17 77777852 rs59361837 C T 5096838
chr17 77777857 rs113060189 C T 5096839
chr17 77777940 rs144255988 T G 5096840
chr17 77778051 rs185197075 G A 5096841
chr17 77778226 rs9911735 G C 5096842
chr17 77778227 rs9896202 T C 5096843
chr17 77778403 rs116434465 T C 5096844
chr17 77778455 rs151065686 C T 5096845
chr17 77778461 rs141015675 C A,T 5096846
chr17 77778712 rs9890723 G A 5096847
chr17 77778726 rs546314718 GCTTA G 5096848
chr17 77778879 rs190795068 G T 5096849
chr17 77778982 rs141417759 C T 5096850
chr17 77779097 rs75686797 C T 5096851
chr17 77779104 rs187251434 G A 5096852
chr17 77779177 rs147016291 G A,C 5096853

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
chr17 77765931 77775482 - CBX8 ENSG00000141570.6 77775482 0.83 1.0 3715 16327


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