Chrom Start End Enhancer ID Tissues that enhancer appears More
chr16 89902939 89911515 enh16910
chr16 89904172 89904600 vista23589

Chrom Position dbSNP ID Reference Allele Alternative Allele id More
chr16 89904502 rs77668804 G A 4679899
chr16 89904669 rs561070601 C A 4679900
chr16 89904679 rs112976246 C G 4679901
chr16 89904834 rs142382996 G A,C 4679902
chr16 89904852 rs570158000 A G 4679903
chr16 89904946 rs567891262 A T 4679904
chr16 89904950 rs535296633 C A 4679905
chr16 89904961 rs117973878 G A 4679906
chr16 89904971 rs72811601 G A 4679907
chr16 89905115 rs62056065 C G 4679908
chr16 89905128 rs370566622 C T 4679909
chr16 89905221 rs527932243 GC G 4679910
chr16 89905263 rs145043974 G A 4679911
chr16 89905336 rs147558234 C T 4679912
chr16 89905428 rs80294481 T G 4679913
chr16 89905487 rs140635976 C G,T 4679914
chr16 89905521 rs35051452 G A 4679915
chr16 89905529 rs34562649 C T 4679916
chr16 89905781 rs11368696 C CA 4679917
chr16 89905781 rs537824236 C CA,CAA 4679918
chr16 89905848 rs9928396 T C 4679919
chr16 89905857 rs34043061 T A 4679920
chr16 89905859 rs191303806 G A 4679921
chr16 89905880 rs112626584 G C 4679922
chr16 89905888 rs115563842 C T 4679923
chr16 89905925 rs9935541 G C,T 4679924
chr16 89905926 rs148878724 G A 4679925
chr16 89906027 rs73268499 C T 4679926
chr16 89906062 rs151278976 C T 4679927
chr16 89906131 rs556094437 G A 4679928
chr16 89906174 rs73268501 C T 4679929
chr16 89906246 rs571048224 G A 4679930
chr16 89906274 rs532683861 C T 4679931
chr16 89906277 rs188510760 G A 4679932
chr16 89906320 rs112544894 CTG C 4679933
chr16 89906320 rs371799913 CTG C 4679934
chr16 89906461 rs74033892 T C 4679935
chr16 89906563 rs62056066 G A 4679936
chr16 89906581 rs145653684 C A,G,T 4679937
chr16 89906688 rs8056619 C G,T 4679938
chr16 89906720 rs181542417 C T 4679939
chr16 89906727 rs371160462 G A 4679940
chr16 89906800 rs143106090 G A 4679941
chr16 89906807 rs530314835 G A 4679942
chr16 89906837 rs572734180 T G 4679943
chr16 89906864 rs150274116 A G 4679944
chr16 89906876 rs113715290 T C 4679945
chr16 89906879 rs190295257 G A,C 4679946
chr16 89906892 rs571860879 T C 4679947
chr16 89906893 rs534034806 G A,C 4679948
chr16 89906894 rs8055746 G T 4679949
chr16 89906899 rs560198882 C T 4679950
chr16 89906904 rs181942928 G A 4679951
chr16 89906920 rs560678251 G C 4679952
chr16 89906931 rs527928994 C T 4679953
chr16 89906936 rs113892241 A G 4679954
chr16 89906937 rs144766880 T A 4679955
chr16 89907002 rs567933260 C A,G,T 4679956
chr16 89907044 rs10708235 AT A 4679957
chr16 89907044 rs752579011 AT A 4679958
chr16 89907082 rs547246990 C T 4679959
chr16 89907129 rs139592082 C T 4679960
chr16 89907145 rs375479132 G A 4679961
chr16 89907164 rs182251041 C T 4679962
chr16 89907168 rs532484164 C T 4679963
chr16 89907193 rs143496972 G A 4679964
chr16 89907205 rs6500458 A G 4679965
chr16 89907343 rs531455483 C G 4679966
chr16 89907493 rs79284621 G T 4679967
chr16 89907520 rs538328720 A T 4679968
chr16 89907526 rs7205642 T A 4679969
chr16 89907528 rs190149419 G A 4679970

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