Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs116855380 1.000 0.040 20 47491550 downstream gene variant A/G snv 2.8E-02 1
rs35206230 1.000 0.040 15 74805439 downstream gene variant C/T snv 0.43 1
rs4764133 1.000 0.040 12 14911429 downstream gene variant C/G;T snv 1
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
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
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs1800587 0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs763110 0.653 0.560 1 172658358 upstream gene variant C/T snv 0.49 30
rs2057768 0.925 0.120 16 27310774 upstream gene variant C/A;G;T snv 4
rs11564299 0.925 0.040 18 28180064 upstream gene variant A/G snv 0.17 2
rs10980705 1.000 0.040 9 111040905 upstream gene variant C/T snv 0.18 1
rs1564861 1.000 0.040 8 118953670 upstream gene variant A/C snv 0.43 1
rs62435998 1.000 0.040 6 44727469 upstream gene variant C/T snv 0.28 1
rs62435999 1.000 0.040 6 44727536 upstream gene variant T/G snv 0.28 1
rs904571820 0.851 0.160 6 151842664 start lost A/G snv 4.0E-06 5
rs7775228 0.790 0.360 6 32690302 TF binding site variant T/C snv 0.15 7
rs4931462 1.000 0.040 12 31225008 TF binding site variant T/G snv 0.65 1
rs532464664 0.882 0.040 22 41238083 frameshift variant -/GCCCGCGC delins 4.8E-03 1.2E-02 3
rs3783553 0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs2082940 0.763 0.480 3 186856375 3 prime UTR variant T/A;C snv 10
rs2929970 0.827 0.200 8 133228894 3 prime UTR variant G/A snv 0.52 5
rs6976 0.851 0.080 3 52694788 3 prime UTR variant C/T snv 0.38 0.33 4