Chrom Start End Enhancer ID Tissues that enhancer appears More
chr16 88969235 88997095 enh16904
chr16 88969739 88970176 vista23530

Chrom Position dbSNP ID Reference Allele Alternative Allele id More
chr16 88970063 rs115789514 C T 4669590
chr16 88970067 rs34558819 TG T 4669591
chr16 88970067 rs558492520 TG T 4669592
chr16 88970067 rs766953766 TG T 4669593
chr16 88970077 rs556457491 G C 4669594
chr16 88970099 rs199576024 T TGG 4669595
chr16 88970178 rs74035890 G A 4669596
chr16 88970223 rs180759242 C G 4669597
chr16 88970294 rs114025956 G A 4669598
chr16 88970317 rs544425470 T C 4669599
chr16 88970374 rs537070603 G A 4669600
chr16 88970480 rs149617988 G A 4669601
chr16 88970487 rs115043217 A C 4669602
chr16 88970513 rs115897737 G A 4669603
chr16 88970516 rs190860392 C T 4669604
chr16 88970543 rs535994693 A T 4669605
chr16 88970555 rs183054522 C T 4669606
chr16 88970556 rs187297328 C A,T 4669607
chr16 88970566 rs2968474 G A 4669608
chr16 88970585 rs144323315 C T 4669609
chr16 88970586 rs190251917 G A 4669610
chr16 88970598 rs115298978 C T 4669611
chr16 88970609 rs41476048 T A 4669612
chr16 88970667 rs148638735 G C 4669613
chr16 88970673 rs573066659 C CT 4669614
chr16 88970684 rs79068777 T C 4669615
chr16 88970712 rs74750667 G A 4669616
chr16 88970768 rs550206662 T G 4669617
chr16 88970776 rs475796 C G 4669618
chr16 88970787 rs144263109 C T 4669619
chr16 88970811 rs559178778 A C,G 4669620
chr16 88970818 rs561795 A G 4669621
chr16 88970875 rs572236971 G A 4669622
chr16 88970879 rs114887799 G A 4669623
chr16 88970881 rs116043490 A G 4669624
chr16 88970919 rs187878543 C T 4669625
chr16 88970944 rs562812 G A 4669626
chr16 88970991 rs577499357 C T 4669627
chr16 88971086 rs13330003 G T 4669628
chr16 88971105 rs570095065 A T 4669629
chr16 88971120 rs115619284 G A 4669630
chr16 88971131 rs568297637 C G,T 4669631
chr16 88971134 rs535763599 A G 4669632
chr16 88971141 rs74035891 G C 4669633
chr16 88971198 rs545976933 G A 4669634
chr16 88971199 rs73254243 C A,G 4669635
chr16 88971296 rs535214206 C T 4669636
chr16 88971299 rs9923835 G A 4669637
chr16 88971300 rs559572080 G A 4669638
chr16 88971310 rs6500507 C G 4669639
chr16 88971360 rs6500508 T C 4669640
chr16 88971403 rs6500509 T C 4669641
chr16 88971463 rs184135044 G A,T 4669642
chr16 88971473 rs117458677 C G,T 4669643
chr16 88971551 rs540583507 G C 4669644
chr16 88971560 rs553200875 G A 4669645
chr16 88971608 rs189207976 G A 4669646
chr16 88971617 rs577233419 G A 4669647
chr16 88971658 rs117781438 C T 4669648
chr16 88971683 rs117558576 A G 4669649
chr16 88971739 rs562738346 G GA 4669650
chr16 88971741 rs574697184 C A,T 4669651
chr16 88971747 rs541486193 A C 4669652
chr16 88971756 rs151019161 C T 4669653
chr16 88971757 rs112909909 G A 4669654
chr16 88971850 rs573394385 G C 4669655
chr16 88971879 rs552534268 T G 4669656
chr16 88971886 rs563061034 T C 4669657
chr16 88971935 rs113430518 C G 4669658
chr16 88971940 rs575150882 C T 4669659
chr16 88971970 rs7195662 A G 4669660
chr16 88971975 rs115929739 A G 4669661
chr16 88971978 rs7186718 C T 4669662
chr16 88971998 rs545510230 C A 4669663
chr16 88972138 rs569811237 A G 4669664
chr16 88972170 rs145542134 C A 4669665
chr16 88972196 rs184638299 G C 4669666
chr16 88972254 rs528422795 C G 4669667
chr16 88972289 rs560588204 G GACCCATGGCTGCCCTGGAC 4669668
chr16 88972289 rs577221417 G C 4669669
chr16 88972345 rs140872013 CGTGGGTCCACCCCACAGCCACAGCAGGAGGCTG C 4669670
chr16 88972398 rs181489259 C T 4669671
chr16 88972405 rs150408628 C CT 4669672
chr16 88972421 rs184967757 T C 4669673
chr16 88972430 rs35777274 C T 4669674
chr16 88972448 rs114343497 G A 4669675
chr16 88972472 rs369885125 A AG 4669676
chr16 88972472 rs545728368 A AG 4669677
chr16 88972491 rs563649076 C T 4669678
chr16 88972539 rs141304213 C A,T 4669679
chr16 88972554 rs488251 G A 4669680
chr16 88972591 rs117482119 C G 4669681
chr16 88972629 rs78085058 G A 4669682
chr16 88972659 rs74541677 G C 4669683
chr16 88972671 rs145079992 C A 4669684
chr16 88972725 rs8045542 G A,C 4669685
chr16 88972728 rs114659811 G A 4669686
chr16 88972737 rs540535976 C T 4669687
chr16 88972753 rs138853740 C T 4669688
chr16 88972805 rs191001705 T C 4669689
chr16 88972836 rs138123374 T TGCTCCCC 4669690
chr16 88972836 rs372452492 T TGCTCCCC 4669691
chr16 88972852 rs72815507 C T 4669692
chr16 88972853 rs115151903 G A,T 4669693
chr16 88972860 rs117336969 G A,T 4669694
chr16 88972884 rs149591775 GAAT G 4669695
chr16 88972884 rs370177066 GAAT G 4669696
chr16 88972957 rs114852028 A G 4669697
chr16 88972965 rs8045905 G C 4669698
chr16 88972976 rs79644196 G A 4669699
chr16 88973007 rs560892488 C T 4669700
chr16 88973034 rs115126588 G A 4669701
chr16 88973054 rs141985035 C T 4669702
chr16 88973069 rs532308147 C G 4669703
chr16 88973103 rs8062621 C T 4669704
chr16 88973104 rs374889053 C T 4669705
chr16 88973119 rs75320646 C A 4669706
chr16 88973129 rs8046274 G A 4669707
chr16 88973167 rs567200215 G A,T 4669708
chr16 88973189 rs145619122 C G 4669709
chr16 88973220 rs75469892 C G,T 4669710
chr16 88973240 rs73254246 G A 4669711
chr16 88973326 rs141974126 G A,C 4669712
chr16 88973338 rs73254249 T C 4669713
chr16 88973356 rs78201826 G A 4669714
chr16 88973360 rs76620267 G A,C 4669715
chr16 88973440 rs150669141 C T 4669716
chr16 88973465 rs560207634 A G 4669717

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

No results

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