Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs144214859 1.000 0.080 2 68397478 downstream gene variant G/A snv 1.7E-02 1
rs148048756 1.000 0.080 8 612963 downstream gene variant A/G snv 7.3E-03 1
rs1775148 1.000 0.080 1 205788696 downstream gene variant C/A;T snv 1
rs201158093 1.000 0.080 16 82145289 downstream gene variant AAAAAA/-;AAA;AAAA;AAAAA;AAAAAAA delins 0.45 1
rs34925593 1.000 0.080 2 173369819 downstream gene variant T/A;C snv 1
rs74702681 1.000 0.080 2 66425753 downstream gene variant C/T snv 1.5E-02 1
rs9287719 1.000 0.080 2 10570604 downstream gene variant C/T snv 0.60 1
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs4073 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs689466 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 33
rs7799039 0.649 0.560 7 128238730 upstream gene variant G/A;C snv 33
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 23
rs2295080 0.695 0.320 1 11262571 upstream gene variant G/C;T snv 20
rs16260 0.716 0.440 16 68737131 upstream gene variant C/A snv 0.24 19