Chrom Start End Enhancer ID Tissues that enhancer appears More
chr19 996390 996745 vista28129

Chrom Position dbSNP ID Reference Allele Alternative Allele id More
chr19 992948 rs139719986 G A 5370449
chr19 993164 rs544237617 G A 5370450
chr19 993295 rs150928207 C T 5370451
chr19 993313 rs2240153 G A 5370452
chr19 993316 rs191800817 C T 5370453
chr19 993346 rs113136716 A G 5370454
chr19 993363 rs139533248 G A 5370455
chr19 993380 rs553923964 G A 5370456
chr19 993397 rs116615905 T G 5370457
chr19 993417 rs557756527 C T 5370458
chr19 993424 rs73497105 C T 5370459
chr19 993429 rs79454716 C G 5370460
chr19 993494 rs149686393 C T 5370461
chr19 993568 rs74531697 A G 5370462
chr19 993654 rs546424756 T C 5370463
chr19 993708 rs117251899 G C 5370464
chr19 993730 rs3216949 G GC 5370465
chr19 993730 rs397770114 G GC 5370466
chr19 993757 rs373038165 A AC 5370467
chr19 993757 rs554969470 A AC 5370468
chr19 993790 rs113974452 C T 5370469
chr19 993853 rs72971640 C G 5370470
chr19 993868 rs7245515 C T 5370471
chr19 993986 rs181862253 C T 5370472
chr19 994020 rs201195680 G T 5370473
chr19 994074 rs139898299 G T 5370474
chr19 994101 rs73918298 C A 5370475
chr19 994135 rs548856093 T C 5370476
chr19 994198 rs145086348 G A,T 5370477
chr19 994248 rs200235925 G A 5370478
chr19 994348 rs200438163 C T 5370479
chr19 994498 rs539462169 T G 5370480
chr19 994531 rs118012496 T C 5370481
chr19 994544 rs3177032 A G 5370482
chr19 994556 rs60103115 C T 5370483
chr19 994643 rs370167431 A G 5370484
chr19 994666 rs546836187 C A,T 5370485
chr19 994688 rs571033565 C G 5370486
chr19 994697 rs143675316 C T 5370487
chr19 994759 rs56220038 G A,C 5370488
chr19 994795 rs72971641 G A,C 5370489
chr19 994800 rs8109453 A G 5370490
chr19 994813 rs8106918 G T 5370491
chr19 994814 rs8109460 A G 5370492
chr19 994828 rs115565727 C T 5370493
chr19 994950 rs116303157 A G 5370494
chr19 995112 rs10414650 C T 5370495
chr19 995158 rs530931999 C T 5370496
chr19 995159 rs549458041 C T 5370497
chr19 995282 rs10425117 A G 5370498
chr19 995297 rs56252150 G A 5370499
chr19 995404 rs554648698 G A 5370500
chr19 995421 rs55710267 C T 5370501
chr19 995479 rs543013644 TCCTA T 5370502
chr19 995520 rs72971646 G A 5370503
chr19 995555 rs561418104 T C 5370504
chr19 995640 rs56078743 A G 5370505
chr19 995676 rs56101664 T C,G 5370506
chr19 995682 rs116318459 G A 5370507
chr19 995687 rs141826467 C T 5370508
chr19 995719 rs116523793 T C 5370509
chr19 995729 rs150223567 C T 5370510
chr19 995735 rs75876097 G A 5370511
chr19 995783 rs117509593 A T 5370512
chr19 995801 rs558623296 C T 5370513
chr19 995815 rs57950827 A G 5370514
chr19 995862 rs556475332 C G,T 5370515
chr19 995918 rs72971649 G A,C 5370516
chr19 995943 rs7248806 T G 5370517
chr19 995985 rs199629976 A AG 5370518
chr19 995987 rs78708781 G A,C 5370519
chr19 996034 rs72971653 G A,C 5370520
chr19 996041 rs548887461 C G,T 5370521
chr19 996148 rs7252019 T C 5370522
chr19 996252 rs114466389 C T 5370523
chr19 996311 rs573143391 G A 5370524
chr19 996319 rs7245730 G T 5370525
chr19 996347 rs532507736 G A 5370526
chr19 996437 rs11882989 C T 5370527
chr19 996549 rs7246039 G A 5370528
chr19 996566 rs34707868 A AC 5370529
chr19 996571 rs139807519 C T 5370530
chr19 996651 rs115004497 G A 5370531
chr19 996665 rs73918299 A G 5370532
chr19 996712 rs78547816 C A 5370533
chr19 996803 rs549668003 G GT 5370534
chr19 996929 rs143886778 C A 5370535
chr19 996933 rs7258555 C G 5370536
chr19 996942 rs74783476 C T 5370537
chr19 997023 rs142042666 C T 5370538
chr19 997058 rs549890277 G A 5370539
chr19 997067 rs143472607 A C 5370540
chr19 997101 rs62134170 A G 5370541
chr19 997114 rs111678277 G A,C,T 5370542
chr19 997166 rs112747304 C T 5370543
chr19 997223 rs191352679 C G,T 5370544
chr19 997224 rs62134171 T A,G 5370545
chr19 997274 rs537891170 C T 5370546
chr19 997315 rs146842780 G A,C 5370547
chr19 997437 rs113581266 G A 5370548
chr19 997555 rs112413375 A C 5370549
chr19 997599 rs192003223 G A 5370550
chr19 997656 rs35251115 CAAA C 5370551
chr19 997656 rs577418908 CAAA C 5370552
chr19 997656 rs771365838 CAAA C 5370553

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 999601 999952 + AC004528.1 ENSG00000269169.1 999601 0.0 0.0 1918 16727
chr19 1000418 1009731 + GRIN3B ENSG00000116032.5 1000418 0.81 1.0 2735 16728


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