Chrom Start End Enhancer ID Tissues that enhancer appears More
chr17 4437372 4437692 vista23789

Chrom Position dbSNP ID Reference Allele Alternative Allele id More
chr17 4437166 rs113678833 A C,G 4713711
chr17 4437200 rs145277159 C A 4713712
chr17 4437212 rs575852271 G A 4713713
chr17 4437214 rs4790202 C T 4713714
chr17 4437224 rs555171118 C T 4713715
chr17 4437237 rs74378371 G A,T 4713716
chr17 4437239 rs115646227 G A,T 4713717
chr17 4437272 rs73972613 G A 4713718
chr17 4437448 rs547903885 G A,C 4713719
chr17 4437458 rs114110265 C T 4713720
chr17 4437472 rs549616511 C G,T 4713721
chr17 4437477 rs58472777 G C 4713722
chr17 4437535 rs200905138 C CGGCTGG 4713723
chr17 4437567 rs78555253 A T 4713724
chr17 4437592 rs139545659 C T 4713725
chr17 4437629 rs149722380 G A 4713726
chr17 4437655 rs577155377 ATGGGAGCACCC A 4713727
chr17 4437711 rs145587766 C A,T 4713728
chr17 4437712 rs75154008 G A 4713729
chr17 4437791 rs56788731 T A 4713730
chr17 4437900 rs144113398 G GCCAGGC 4713731
chr17 4437912 rs140818425 G A,T 4713732
chr17 4437925 rs35082251 C T 4713733
chr17 4437926 rs114310965 G A 4713734
chr17 4437937 rs74599522 C G 4713735
chr17 4437943 rs79327088 C T 4713736
chr17 4437953 rs12943653 C G 4713737
chr17 4437962 rs564101870 G A,C 4713738
chr17 4437971 rs370366600 T G 4713739
chr17 4438013 rs531735764 C G,T 4713740
chr17 4438014 rs548631884 G A,C 4713741
chr17 4438019 rs556744539 TG T 4713742
chr17 4438036 rs371529728 GCA G 4713743
chr17 4438036 rs534003444 G A 4713744
chr17 4438062 rs8066779 A G 4713745
chr17 4438066 rs79695397 G A,C,T 4713746
chr17 4438075 rs193045155 G A 4713747
chr17 4438095 rs554976035 C T 4713748
chr17 4438100 rs77354906 CCA C 4713749
chr17 4438125 rs185003102 A C 4713750
chr17 4438132 rs577754445 G A,C 4713751
chr17 4438176 rs543690500 C G 4713752
chr17 4438177 rs115404296 A G 4713753
chr17 4438184 rs6502795 G C 4713754
chr17 4438230 rs377645268 C T 4713755
chr17 4438287 rs73335846 G C 4713756
chr17 4438371 rs138517870 TAAGGCTGGCACTCCA T 4713757
chr17 4438371 rs34835089 TAAGGCTGGCACTCCA T 4713758
chr17 4438371 rs775256697 TAAGGCTGGCACTCCA T 4713759
chr17 4438409 rs115533758 C T 4713760
chr17 4438410 rs559607173 G A,C 4713761
chr17 4438444 rs541460211 G A 4713762
chr17 4438471 rs564399192 G C 4713763
chr17 4438568 rs183749026 C A,T 4713764
chr17 4438604 rs557770249 G A 4713765
chr17 4438605 rs72830097 G C 4713766
chr17 4438614 rs114738549 G C 4713767
chr17 4438657 rs118097965 G A,T 4713768
chr17 4438679 rs552988662 G A,T 4713769
chr17 4438704 rs72830098 C G 4713770
chr17 4438716 rs189269136 T C 4713771
chr17 4438735 rs192728386 C T 4713772
chr17 4438754 rs569231692 G A 4713773
chr17 4438787 rs148169311 C T 4713774
chr17 4438947 rs536035880 A G 4713775
chr17 4438982 rs190070156 G A 4713776
chr17 4439057 rs542771480 G A 4713777
chr17 4439072 rs141119499 C T 4713778
chr17 4439137 rs150243635 G A 4713779
chr17 4439147 rs143171433 GGGA G 4713780
chr17 4439152 rs1076073 G A 4713781
chr17 4439204 rs12450809 G C 4713782
chr17 4439253 rs573972734 A T 4713783

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