Chrom Start End Enhancer ID Tissues that enhancer appears More
chr14 100071651 100072022 vista19060

Chrom Position dbSNP ID Reference Allele Alternative Allele id More
chr14 100071612 rs527505479 G A 3783678
chr14 100071706 rs202039988 AGGCGG A 3783679
chr14 100071808 rs550150329 C G 3783680
chr14 100071848 rs555475369 G A 3783681
chr14 100071856 rs565809104 A T 3783682
chr14 100072249 rs185957200 G A 3783683
chr14 100072314 rs142155357 T TG 3783684
chr14 100072319 rs527360032 T G 3783685
chr14 100072363 rs539549768 C A 3783686
chr14 100072441 rs79610145 C G 3783687
chr14 100072608 rs192035966 C G 3783688
chr14 100072755 rs151204955 GCA G 3783689
chr14 100072779 rs11160531 G C 3783690
chr14 100072784 rs144200913 G A 3783691
chr14 100072806 rs573984329 G GA 3783692
chr14 100072877 rs114736626 G A 3783693
chr14 100072907 rs113348312 G A 3783694
chr14 100072999 rs12433803 G A 3783695
chr14 100073006 rs190465653 A G 3783696
chr14 100073091 rs2895810 G A 3783697
chr14 100073097 rs61984365 G A 3783698
chr14 100073182 rs182696161 C G 3783699
chr14 100073216 rs4619332 C G,T 3783700
chr14 100073258 rs147809079 C A,T 3783701
chr14 100073273 rs139519421 G A,T 3783702
chr14 100073347 rs550503712 C T 3783703
chr14 100073386 rs34010063 G T 3783704
chr14 100073411 rs186354212 C T 3783705
chr14 100073462 rs76385130 C T 3783706
chr14 100073463 rs144827611 G A 3783707
chr14 100073549 rs77923492 T C 3783708
chr14 100073589 rs151293219 C G 3783709
chr14 100073598 rs140619170 A G 3783710
chr14 100073710 rs150490439 C T 3783711
chr14 100073719 rs12437096 T G 3783712
chr14 100073864 rs12434036 G C 3783713
chr14 100074000 rs8005317 T C 3783714
chr14 100074033 rs8004370 G C 3783715
chr14 100074046 rs114635561 C T 3783716
chr14 100074099 rs112233650 G A 3783717
chr14 100074257 rs577791801 A AAT 3783718
chr14 100074273 rs187750815 T C 3783719
chr14 100074389 rs2022745 C T 3783720
chr14 100074390 rs149148927 G A,T 3783721
chr14 100074459 rs74483388 C T 3783722
chr14 100074493 rs570949499 G T 3783723
chr14 100074501 rs79863097 A T 3783724
chr14 100074533 rs58891081 G A 3783725
chr14 100074561 rs200400802 AGAG A 3783726
chr14 100074633 rs192595737 G A 3783727
chr14 100074667 rs2022744 G A 3783728
chr14 100074786 rs148042420 G A 3783729
chr14 100074826 rs141725763 C T 3783730
chr14 100074938 rs115464598 A T 3783731
chr14 100074991 rs17098887 G A 3783732
chr14 100075113 rs142703900 G A 3783733
chr14 100075114 rs183311278 C G,T 3783734
chr14 100075132 rs538442099 C T 3783735
chr14 100075164 rs187679256 A G 3783736
chr14 100075334 rs4243726 C T 3783737
chr14 100075339 rs147340367 G A 3783738
chr14 100075350 rs139581945 G T 3783739
chr14 100075390 rs12432708 T G 3783740

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