Chrom Start End Enhancer ID Tissues that enhancer appears More
chr14 104683866 104698135 enh47819

Chrom Position dbSNP ID Reference Allele Alternative Allele id More
chr14 104694104 rs147446472 A G 3820027
chr14 104694119 rs533131094 C T 3820028
chr14 104694333 rs187172831 T C 3820029
chr14 104694358 rs12050370 A G 3820030
chr14 104694424 rs551165431 G A 3820031
chr14 104694502 rs539605431 C T 3820032
chr14 104694547 rs570061553 T C 3820033
chr14 104694548 rs79801821 G T 3820034
chr14 104694608 rs372325441 A G 3820035
chr14 104694618 rs74087248 C T 3820036
chr14 104694639 rs558235839 T C 3820037
chr14 104694688 rs148672794 C A,T 3820038
chr14 104694714 rs111606173 G A 3820039
chr14 104694777 rs11850370 C T 3820040
chr14 104694949 rs114039592 C A 3820041
chr14 104695123 rs74839431 C T 3820042
chr14 104695152 rs80245549 G C 3820043
chr14 104695217 rs11851356 C T 3820044
chr14 104695228 rs566068275 G A 3820045
chr14 104695294 rs559272644 A G 3820046
chr14 104695315 rs73362244 G A 3820047
chr14 104695334 rs543910589 C T 3820048
chr14 104695624 rs564518536 A G 3820049
chr14 104695636 rs11628649 C T 3820050
chr14 104695639 rs550227489 C T 3820051
chr14 104695667 rs28363958 C A 3820052
chr14 104695740 rs118150168 C T 3820053
chr14 104695766 rs575460484 TA T 3820054
chr14 104695775 rs571651392 T C 3820055
chr14 104695778 rs537555977 G C 3820056
chr14 104695835 rs182424629 C G 3820057
chr14 104695915 rs79464297 C T 3820058
chr14 104695920 rs112253764 G GC 3820059
chr14 104695935 rs150397876 TGTG T 3820060
chr14 104696012 rs146409564 C T 3820061
chr14 104696026 rs74087250 G A 3820062
chr14 104696094 rs537404776 C A,T 3820063
chr14 104696108 rs550946269 C T 3820064
chr14 104696121 rs78788865 G A 3820065
chr14 104696280 rs115264504 G A 3820066
chr14 104696371 rs75287271 T C 3820067
chr14 104696380 rs117590845 C T 3820068
chr14 104696383 rs77829952 G C 3820069
chr14 104696393 rs185692015 C T 3820070
chr14 104696452 rs111523239 C T 3820071
chr14 104696489 rs112308978 A G 3820072
chr14 104696490 rs138319807 G A 3820073
chr14 104696755 rs74087251 C T 3820074
chr14 104696772 rs73362248 G A 3820075
chr14 104696819 rs143339920 G A 3820076
chr14 104696881 rs113523375 C T 3820077
chr14 104696934 rs545666805 T C 3820078
chr14 104696953 rs7142792 C T 3820079
chr14 104697049 rs79446706 G A 3820080
chr14 104697055 rs374987588 C T 3820081
chr14 104697065 rs559535677 G A 3820082
chr14 104697073 rs145442989 CAG C 3820083
chr14 104697073 rs36125573 CAG C 3820084
chr14 104697278 rs73362249 C A,T 3820085
chr14 104697604 rs73362251 T C 3820086
chr14 104697777 rs73362252 G T 3820087
chr14 104697847 rs185572927 C T 3820088
chr14 104697903 rs373647236 C T 3820089
chr14 104697916 rs190280910 T C 3820090
chr14 104697958 rs72717026 C A,G,T 3820091

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