Chrom Start End Enhancer ID Tissues that enhancer appears More
chr11 65782974 65783337 vista10645

Chrom Position dbSNP ID Reference Allele Alternative Allele id More
chr11 65778540 rs138006882 C T 2050436
chr11 65778758 rs11227377 T C 2050437
chr11 65778763 rs11227378 G A 2050438
chr11 65778808 rs114318641 G C 2050439
chr11 65778834 rs559185098 T C 2050440
chr11 65778922 rs72930984 C T 2050441
chr11 65779173 rs371076526 AAG A 2050442
chr11 65779173 rs533222503 AAG A 2050443
chr11 65779248 rs551729486 G A 2050444
chr11 65779330 rs75154345 C T 2050445
chr11 65779523 rs200759724 G T 2050446
chr11 65779533 rs148357805 C T 2050447
chr11 65779590 rs1131544 C A,T 2050448
chr11 65779825 rs190751510 G A 2050449
chr11 65779883 rs377647173 C A 2050450
chr11 65779961 rs12223658 C T 2050451
chr11 65780243 rs72930985 G A,T 2050452
chr11 65780539 rs575454336 G A,C 2050453
chr11 65780654 rs554278099 G A,T 2050454
chr11 65780675 rs367894852 G A 2050455
chr11 65780702 rs9667817 A G 2050456
chr11 65780881 rs188986260 G A 2050457
chr11 65780912 rs186658608 G T 2050458
chr11 65780938 rs139763518 C T 2050459
chr11 65780962 rs189042368 G A,T 2050460
chr11 65781036 rs528103934 C T 2050461
chr11 65781054 rs74707968 G A 2050462
chr11 65781084 rs537957069 A AGCT 2050463
chr11 65781191 rs187098379 A T 2050464
chr11 65781195 rs632578 C A 2050465
chr11 65781242 rs632640 C G,T 2050466
chr11 65781304 rs535696770 ACT A 2050467
chr11 65781341 rs142760959 C T 2050468
chr11 65781369 rs73498411 G A 2050469
chr11 65781459 rs12785292 G A 2050470
chr11 65781551 rs545657477 C T 2050471
chr11 65781589 rs11604021 C T 2050472
chr11 65781768 rs75038923 C T 2050473
chr11 65781769 rs182991083 G A 2050474
chr11 65781775 rs7933510 A G 2050475
chr11 65781799 rs372028889 T C 2050476
chr11 65781824 rs149806349 C T 2050477
chr11 65781852 rs535340874 G C 2050478
chr11 65781858 rs144745547 C G,T 2050479
chr11 65781869 rs148655964 C T 2050480
chr11 65781870 rs377596879 G A 2050481
chr11 65781898 rs557456324 T C 2050482
chr11 65781902 rs577261991 T C 2050483
chr11 65781991 rs113898544 G A 2050484
chr11 65782022 rs572652595 C A 2050485
chr11 65782028 rs541740729 C T 2050486
chr11 65782053 rs58833868 A AC 2050487
chr11 65782090 rs7933764 T C 2050488
chr11 65782118 rs147838706 A T 2050489
chr11 65782209 rs141485759 G A 2050490
chr11 65782497 rs685334 C T 2050491
chr11 65782574 rs61895578 C T 2050492
chr11 65782604 rs145014911 G C 2050493
chr11 65782605 rs147570813 G A 2050494
chr11 65782622 rs684546 G T 2050495
chr11 65782636 rs112746775 C A 2050496
chr11 65782651 rs77273262 G A 2050497
chr11 65782730 rs113377204 G A 2050498
chr11 65782768 rs6591195 C T 2050499
chr11 65782770 rs561796728 G GC 2050500
chr11 65782856 rs529116582 C G 2050501
chr11 65783120 rs138476969 G A 2050502
chr11 65783143 rs141786826 CTG C 2050503
chr11 65783185 rs137997131 T TCCTGGGC 2050504

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
chr11 65779312 65780976 + CST6 ENSG00000175315.2 65779312 0.92 1.0 816 11099


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