geneid | 4835 |
---|---|
ensemblid | ENSG00000124588.22 |
hgncid | 7856 |
symbol | NQO2 |
name | N-ribosyldihydronicotinamide:quinone reductase 2 |
refseq_nuc | NM_000904.6 |
refseq_prot | NP_000895.2 |
ensembl_nuc | ENST00000380455.11 |
ensembl_prot | ENSP00000369822.4 |
mane_status | MANE Select |
chr | chr6 |
start | 2999894 |
end | 3019755 |
strand | + |
ver | v1.2 |
region | chr6:2999894-3019755 |
region5000 | chr6:2994894-3024755 |
regionname0 | NQO2_chr6_2999894_3019755 |
regionname5000 | NQO2_chr6_2994894_3024755 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 231 | 311 | 87 | 56 | 130 | 12 | 26 | 105 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
a0002 | 1/1 | 231 | 117 | 1 | 20 | 79 | 2 | 13 | 60 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
a0003 | 0/0 | 231 | 7 | 5 | 1 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
a0004 | 0/0 | 231 | 6 | 1 | 2 | 0 | 1 | 2 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
a0005 | 0/0 | 231 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
a0006 | 0/0 | 231 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
a0007 | 0/0 | 231 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
a0008 | 0/0 | 231 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 696 | 218 | 43 | 49 | 95 | 8 | 23 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
c0002 | 1/1 | 696 | 117 | 1 | 20 | 79 | 2 | 13 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
c0003 | 0/0 | 696 | 83 | 39 | 7 | 33 | 1 | 3 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
c0004 | 0/0 | 696 | 7 | 5 | 1 | 0 | 1 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
c0005 | 0/0 | 696 | 6 | 3 | 0 | 0 | 3 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
c0006 | 0/0 | 696 | 6 | 1 | 2 | 0 | 1 | 2 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
c0007 | 0/0 | 696 | 2 | 0 | 1 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
c0008 | 0/0 | 696 | 2 | 0 | 0 | 2 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
c0009 | 0/0 | 696 | 2 | 2 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
c0010 | 0/0 | 696 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
c0011 | 0/0 | 696 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
c0012 | 0/0 | 696 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 378 | 276 | 53 | 47 | 138 | 10 | 26 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
t0002 | 0/0 | 378 | 101 | 24 | 13 | 53 | 2 | 9 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
t0003 | 0/0 | 378 | 40 | 3 | 9 | 19 | 2 | 7 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
t0004 | 0/0 | 378 | 27 | 12 | 11 | 2 | 2 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
t0005 | 0/0 | 378 | 2 | 2 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/1 | 38 | 0 | 3 | 29 | 0 | 5 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0002 | 0/0 | 14 | 0 | 2 | 10 | 1 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0003 | 0/0 | 13 | 1 | 1 | 8 | 0 | 3 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0004 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0005 | 0/0 | 7 | 0 | 1 | 5 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0006 | 0/0 | 6 | 1 | 2 | 2 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0007 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0008 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0009 | 0/0 | 5 | 1 | 0 | 4 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0013 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0014 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0019 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0022 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0023 | 1/0 | 3 | 0 | 0 | 2 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0025 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0026 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0028 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0033 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0037 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0042 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0048 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0053 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 696 | 218 | 43 | 49 | 95 | 8 | 23 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
a0001c0003 | 0/0 | 696 | 83 | 39 | 7 | 33 | 1 | 3 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
a0001c0005 | 0/0 | 696 | 6 | 3 | 0 | 0 | 3 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
a0001c0008 | 0/0 | 696 | 2 | 0 | 0 | 2 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
a0001c0009 | 0/0 | 696 | 2 | 2 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
a0002c0002 | 1/1 | 696 | 117 | 1 | 20 | 79 | 2 | 13 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
a0003c0004 | 0/0 | 696 | 7 | 5 | 1 | 0 | 1 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
a0004c0006 | 0/0 | 696 | 6 | 1 | 2 | 0 | 1 | 2 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
a0005c0007 | 0/0 | 696 | 2 | 0 | 1 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
a0006c0012 | 0/0 | 696 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
a0007c0011 | 0/0 | 696 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
a0008c0010 | 0/0 | 696 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1073 | 124 | 22 | 23 | 64 | 4 | 11 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
a0001c0001t0002 | 0/0 | 1073 | 26 | 5 | 6 | 10 | 0 | 5 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
a0001c0001t0003 | 0/0 | 1073 | 40 | 3 | 9 | 19 | 2 | 7 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
a0001c0001t0004 | 0/0 | 1073 | 27 | 12 | 11 | 2 | 2 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
a0001c0001t0005 | 0/0 | 1073 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
a0001c0003t0001 | 0/0 | 1073 | 29 | 25 | 3 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
a0001c0003t0002 | 0/0 | 1073 | 53 | 13 | 4 | 32 | 1 | 3 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
a0001c0003t0005 | 0/0 | 1073 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
a0001c0005t0001 | 0/0 | 1073 | 3 | 0 | 0 | 0 | 3 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
a0001c0005t0002 | 0/0 | 1073 | 3 | 3 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
a0001c0008t0001 | 0/0 | 1073 | 2 | 0 | 0 | 2 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
a0001c0009t0002 | 0/0 | 1073 | 2 | 2 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
a0002c0002t0001 | 1/1 | 1073 | 105 | 1 | 18 | 70 | 2 | 12 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
a0002c0002t0002 | 0/0 | 1073 | 12 | 0 | 2 | 9 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
a0003c0004t0001 | 0/0 | 1073 | 6 | 5 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
a0003c0004t0002 | 0/0 | 1073 | 1 | 0 | 0 | 0 | 1 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
a0004c0006t0001 | 0/0 | 1073 | 4 | 0 | 1 | 0 | 1 | 2 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
a0004c0006t0002 | 0/0 | 1073 | 2 | 1 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
a0005c0007t0001 | 0/0 | 1073 | 2 | 0 | 1 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
a0006c0012t0002 | 0/0 | 1073 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
a0007c0011t0001 | 0/0 | 1073 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
a0008c0010t0002 | 0/0 | 1073 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | copy fasta | chr6 | 2994894 | 3024755 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0006 | 0/0 | 5 | 1 | 2 | 1 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0008 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0002g0014 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0002g0042 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0003g0009 | 0/0 | 5 | 1 | 0 | 4 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0003g0013 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0003g0025 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0003g0026 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0004g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0004g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0004g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0004g0037 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0004g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0004g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0004g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0004g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0004g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0004g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0004g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0001t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0001g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0001g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0002g0002 | 0/0 | 14 | 0 | 2 | 10 | 1 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0002g0004 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0002g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0003t0005g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0005t0001g0022 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0005t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0005t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0005t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0008t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0008t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0001c0009t0002g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0001g0001 | 0/1 | 38 | 0 | 3 | 29 | 0 | 5 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0001g0003 | 0/0 | 13 | 1 | 1 | 8 | 0 | 3 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0001g0007 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0001g0023 | 1/0 | 3 | 0 | 0 | 2 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0001g0028 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0001g0048 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0001g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0001g0053 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0002g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0002c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0003c0004t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0003c0004t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0003c0004t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0003c0004t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0003c0004t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0003c0004t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0003c0004t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0004c0006t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0004c0006t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0004c0006t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0004c0006t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0004c0006t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0004c0006t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0005c0007t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0005c0007t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0006c0012t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0007c0011t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
a0008c0010t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0003 | c0004 | t0002 | g0226 | EUR | GBR | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0160 | EUR | GBR | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG00140 | hp1 | a0004 | c0006 | t0001 | g0067 | EUR | GBR | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0053 | EUR | GBR | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | FIN | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG00280 | hp2 | a0001 | c0003 | t0002 | g0002 | EUR | FIN | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG00323 | hp1 | a0002 | c0002 | t0001 | g0053 | EUR | FIN | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG00323 | hp2 | a0001 | c0005 | t0001 | g0022 | EUR | FIN | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG00408 | hp1 | a0001 | c0003 | t0002 | g0197 | EAS | CHS | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | CHS | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG00438 | hp2 | a0001 | c0003 | t0002 | g0002 | EAS | CHS | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG00544 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | CHS | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG00558 | hp2 | a0002 | c0002 | t0002 | g0199 | EAS | CHS | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0282 | EAS | CHS | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG00609 | hp1 | a0002 | c0002 | t0001 | g0265 | EAS | CHS | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG00609 | hp2 | a0001 | c0008 | t0001 | g0102 | EAS | CHS | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG00621 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | CHS | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0159 | AMR | PUR | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0025 | AMR | PUR | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | CHS | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG00733 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | PUR | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG00735 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | PUR | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0154 | AMR | PUR | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0057 | AMR | PUR | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG00741 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | PUR | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01070 | hp2 | a0001 | c0003 | t0001 | g0069 | AMR | PUR | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0052 | AMR | PUR | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0026 | AMR | PUR | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01081 | hp1 | a0001 | c0001 | t0004 | g0093 | AMR | PUR | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01081 | hp2 | a0004 | c0006 | t0001 | g0258 | AMR | PUR | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0145 | AMR | PUR | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01106 | hp1 | a0001 | c0001 | t0004 | g0092 | AMR | PUR | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01109 | hp1 | a0003 | c0004 | t0001 | g0130 | AMR | PUR | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01109 | hp2 | a0001 | c0001 | t0004 | g0227 | AMR | PUR | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01167 | hp1 | a0001 | c0001 | t0004 | g0044 | AMR | PUR | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01167 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01169 | hp2 | a0001 | c0001 | t0004 | g0044 | AMR | PUR | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0183 | AMR | PUR | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01192 | hp2 | a0001 | c0003 | t0002 | g0205 | AMR | PUR | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01243 | hp1 | a0001 | c0003 | t0001 | g0144 | AMR | PUR | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01243 | hp2 | a0001 | c0003 | t0002 | g0149 | AMR | PUR | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0163 | AMR | CLM | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01255 | hp2 | a0001 | c0001 | t0004 | g0020 | AMR | CLM | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01256 | hp1 | a0002 | c0002 | t0001 | g0263 | AMR | CLM | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01256 | hp2 | a0001 | c0001 | t0004 | g0255 | AMR | CLM | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01257 | hp1 | a0001 | c0003 | t0001 | g0245 | AMR | CLM | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01257 | hp2 | a0002 | c0002 | t0001 | g0243 | AMR | CLM | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0026 | AMR | CLM | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | CLM | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | CLM | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01358 | hp1 | a0001 | c0001 | t0004 | g0020 | AMR | CLM | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01361 | hp1 | a0002 | c0002 | t0002 | g0150 | AMR | CLM | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0028 | AMR | CLM | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01496 | hp1 | a0001 | c0001 | t0004 | g0020 | AMR | CLM | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01515 | hp1 | a0001 | c0005 | t0001 | g0022 | EUR | IBS | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0111 | EUR | IBS | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01516 | hp1 | a0001 | c0001 | t0004 | g0037 | EUR | IBS | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0026 | EUR | IBS | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | IBS | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01517 | hp2 | a0001 | c0001 | t0004 | g0037 | EUR | IBS | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01884 | hp2 | a0001 | c0003 | t0001 | g0012 | AFR | ACB | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01891 | hp1 | a0001 | c0003 | t0002 | g0169 | AFR | ACB | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01891 | hp2 | a0001 | c0003 | t0001 | g0024 | AFR | ACB | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0262 | AMR | PEL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0172 | AMR | PEL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01943 | hp2 | a0001 | c0001 | t0004 | g0174 | AMR | PEL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01952 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | PEL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0281 | AMR | PEL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01978 | hp2 | a0005 | c0007 | t0001 | g0005 | AMR | PEL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01981 | hp2 | a0002 | c0002 | t0001 | g0052 | AMR | PEL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0153 | AMR | PEL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02004 | hp1 | a0002 | c0002 | t0002 | g0151 | AMR | PEL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02004 | hp2 | a0004 | c0006 | t0002 | g0056 | AMR | PEL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02015 | hp2 | a0002 | c0002 | t0002 | g0208 | EAS | KHV | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02027 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | KHV | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02040 | hp2 | a0007 | c0011 | t0001 | g0006 | EAS | KHV | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02055 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | ACB | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02056 | hp1 | a0006 | c0012 | t0002 | g0188 | EAS | KHV | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0168 | EAS | KHV | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | KHV | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02071 | hp2 | a0002 | c0002 | t0001 | g0275 | EAS | KHV | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02080 | hp2 | a0002 | c0002 | t0001 | g0266 | EAS | KHV | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02083 | hp1 | a0001 | c0003 | t0002 | g0184 | EAS | KHV | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02132 | hp1 | a0002 | c0002 | t0001 | g0274 | EAS | KHV | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | KHV | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02135 | hp1 | a0002 | c0002 | t0001 | g0278 | EAS | KHV | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02145 | hp2 | a0001 | c0003 | t0001 | g0061 | AFR | ACB | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02148 | hp1 | a0001 | c0003 | t0002 | g0002 | AMR | PEL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02155 | hp1 | a0001 | c0003 | t0002 | g0195 | EAS | CDX | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CDX | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02165 | hp1 | a0001 | c0003 | t0002 | g0045 | EAS | CDX | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0256 | EAS | CDX | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02257 | hp2 | a0001 | c0003 | t0002 | g0221 | AFR | ACB | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | ACB | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02258 | hp2 | a0001 | c0005 | t0002 | g0203 | AFR | ACB | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02273 | hp2 | a0001 | c0003 | t0002 | g0002 | AMR | PEL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | ACB | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02280 | hp2 | a0001 | c0003 | t0001 | g0070 | AFR | ACB | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0280 | AMR | PEL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0146 | AMR | PEL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02300 | hp2 | a0001 | c0001 | t0004 | g0178 | AMR | PEL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02451 | hp1 | a0001 | c0003 | t0002 | g0213 | AFR | ACB | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02451 | hp2 | a0001 | c0001 | t0004 | g0021 | AFR | ACB | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0267 | EAS | KHV | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02572 | hp2 | a0001 | c0003 | t0001 | g0116 | AFR | GWD | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0156 | SAS | PJL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02615 | hp1 | a0001 | c0009 | t0002 | g0038 | AFR | GWD | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02615 | hp2 | a0001 | c0003 | t0001 | g0011 | AFR | GWD | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02647 | hp1 | a0001 | c0003 | t0005 | g0223 | AFR | GWD | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02647 | hp2 | a0001 | c0001 | t0005 | g0225 | AFR | GWD | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02717 | hp2 | a0001 | c0003 | t0002 | g0218 | AFR | GWD | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02723 | hp1 | a0001 | c0003 | t0001 | g0012 | AFR | GWD | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0167 | SAS | PJL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0202 | AFR | GWD | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02809 | hp2 | a0001 | c0003 | t0001 | g0137 | AFR | GWD | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | GWD | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02886 | hp1 | a0001 | c0003 | t0001 | g0133 | AFR | GWD | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02886 | hp2 | a0001 | c0003 | t0002 | g0215 | AFR | GWD | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02895 | hp1 | a0001 | c0003 | t0002 | g0204 | AFR | GWD | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02895 | hp2 | a0001 | c0003 | t0002 | g0047 | AFR | GWD | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02896 | hp1 | a0001 | c0003 | t0002 | g0047 | AFR | GWD | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0021 | AFR | GWD | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02922 | hp1 | a0001 | c0003 | t0001 | g0011 | AFR | ESN | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02922 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | ESN | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02965 | hp1 | a0001 | c0003 | t0002 | g0220 | AFR | ESN | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02965 | hp2 | a0001 | c0005 | t0002 | g0214 | AFR | ESN | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | ESN | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02970 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | ESN | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02976 | hp1 | a0001 | c0003 | t0001 | g0024 | AFR | ESN | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02976 | hp2 | a0001 | c0003 | t0001 | g0012 | AFR | ESN | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0161 | SAS | PJL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0206 | AFR | GWD | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03098 | hp1 | a0003 | c0004 | t0001 | g0273 | AFR | MSL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03098 | hp2 | a0001 | c0003 | t0001 | g0117 | AFR | MSL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0222 | AFR | ESN | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03139 | hp1 | a0001 | c0003 | t0001 | g0143 | AFR | ESN | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03139 | hp2 | a0001 | c0003 | t0001 | g0039 | AFR | ESN | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03195 | hp1 | a0003 | c0004 | t0001 | g0129 | AFR | ESN | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03195 | hp2 | a0001 | c0003 | t0001 | g0012 | AFR | ESN | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0279 | SAS | PJL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | MSL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03453 | hp2 | a0001 | c0003 | t0001 | g0039 | AFR | MSL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03486 | hp1 | a0003 | c0004 | t0001 | g0253 | AFR | MSL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03486 | hp2 | a0001 | c0003 | t0002 | g0219 | AFR | MSL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03490 | hp1 | a0001 | c0003 | t0002 | g0193 | SAS | PJL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0158 | SAS | PJL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0155 | SAS | PJL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03491 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03492 | hp1 | a0001 | c0003 | t0002 | g0002 | SAS | PJL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03516 | hp1 | a0001 | c0001 | t0004 | g0134 | AFR | ESN | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03516 | hp2 | a0001 | c0001 | t0004 | g0060 | AFR | ESN | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03540 | hp2 | a0001 | c0003 | t0001 | g0011 | AFR | GWD | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0021 | AFR | MSL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03579 | hp2 | a0001 | c0003 | t0001 | g0118 | AFR | MSL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0148 | SAS | PJL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03669 | hp2 | a0004 | c0006 | t0001 | g0087 | SAS | PJL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | STU | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03688 | hp2 | a0002 | c0002 | t0002 | g0147 | SAS | STU | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0164 | SAS | PJL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0054 | SAS | PJL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03710 | hp1 | a0001 | c0003 | t0002 | g0182 | SAS | PJL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0097 | SAS | BEB | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | BEB | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03927 | hp1 | a0002 | c0002 | t0001 | g0048 | SAS | BEB | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG04184 | hp1 | a0004 | c0006 | t0001 | g0101 | SAS | BEB | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG04184 | hp2 | a0002 | c0002 | t0001 | g0003 | SAS | BEB | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG04199 | hp1 | a0005 | c0007 | t0001 | g0086 | SAS | STU | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0040 | SAS | STU | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0260 | SAS | STU | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG04204 | hp2 | a0002 | c0002 | t0001 | g0003 | SAS | STU | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG04228 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | STU | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0040 | SAS | STU | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18522 | hp1 | a0001 | c0003 | t0002 | g0217 | AFR | YRI | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | YRI | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHB | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18612 | hp2 | a0001 | c0003 | t0002 | g0002 | EAS | CHB | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHB | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0115 | AFR | YRI | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18906 | hp2 | a0001 | c0003 | t0001 | g0250 | AFR | YRI | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18939 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18940 | hp1 | a0001 | c0003 | t0002 | g0063 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18940 | hp2 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18941 | hp2 | a0001 | c0003 | t0002 | g0191 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18942 | hp2 | a0001 | c0003 | t0002 | g0209 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0254 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18945 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18947 | hp1 | a0002 | c0002 | t0001 | g0271 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18949 | hp2 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18950 | hp1 | a0001 | c0003 | t0002 | g0002 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0244 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18951 | hp2 | a0001 | c0003 | t0002 | g0194 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18953 | hp1 | a0001 | c0003 | t0002 | g0192 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18953 | hp2 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18956 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18957 | hp1 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18959 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18961 | hp2 | a0002 | c0002 | t0001 | g0277 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18962 | hp2 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18963 | hp2 | a0002 | c0002 | t0001 | g0246 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0272 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18965 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18966 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18968 | hp1 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18969 | hp1 | a0001 | c0003 | t0002 | g0002 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18969 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18972 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18973 | hp1 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18974 | hp2 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18980 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18980 | hp2 | a0001 | c0001 | t0004 | g0252 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18981 | hp1 | a0002 | c0002 | t0001 | g0264 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18982 | hp1 | a0001 | c0003 | t0002 | g0002 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18985 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18986 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18986 | hp2 | a0001 | c0003 | t0002 | g0142 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18990 | hp1 | a0001 | c0001 | t0004 | g0251 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18990 | hp2 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18991 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18994 | hp1 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18994 | hp2 | a0002 | c0002 | t0002 | g0201 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18995 | hp1 | a0001 | c0003 | t0002 | g0187 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18995 | hp2 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18997 | hp1 | a0002 | c0002 | t0001 | g0249 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18997 | hp2 | a0002 | c0002 | t0001 | g0261 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18999 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18999 | hp2 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19000 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19001 | hp1 | a0001 | c0003 | t0002 | g0045 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19001 | hp2 | a0002 | c0002 | t0001 | g0269 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0268 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19002 | hp2 | a0001 | c0003 | t0002 | g0002 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19003 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19004 | hp1 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19007 | hp1 | a0002 | c0002 | t0002 | g0200 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19007 | hp2 | a0001 | c0003 | t0002 | g0002 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19009 | hp2 | a0001 | c0003 | t0002 | g0002 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19011 | hp2 | a0001 | c0003 | t0002 | g0002 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19012 | hp2 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0152 | AFR | LWK | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19030 | hp2 | a0001 | c0001 | t0004 | g0127 | AFR | LWK | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19043 | hp1 | a0003 | c0004 | t0001 | g0113 | AFR | LWK | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19043 | hp2 | a0001 | c0003 | t0001 | g0210 | AFR | LWK | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19056 | hp2 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19057 | hp1 | a0001 | c0003 | t0001 | g0276 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19060 | hp1 | a0002 | c0002 | t0001 | g0247 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19063 | hp1 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19063 | hp2 | a0002 | c0002 | t0002 | g0139 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19065 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19067 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19067 | hp2 | a0001 | c0008 | t0001 | g0103 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19070 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19070 | hp2 | a0002 | c0002 | t0002 | g0165 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19074 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19075 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19078 | hp1 | a0002 | c0002 | t0002 | g0166 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19078 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19079 | hp1 | a0001 | c0003 | t0002 | g0189 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19080 | hp1 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19080 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19082 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19083 | hp1 | a0001 | c0003 | t0002 | g0190 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19084 | hp1 | a0002 | c0002 | t0001 | g0104 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19085 | hp2 | a0001 | c0003 | t0002 | g0002 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19087 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19088 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19091 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19240 | hp1 | a0001 | c0003 | t0001 | g0024 | AFR | YRI | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA19240 | hp2 | a0001 | c0003 | t0001 | g0114 | AFR | YRI | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA20129 | hp1 | a0004 | c0006 | t0002 | g0055 | AFR | ASW | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA20129 | hp2 | a0001 | c0003 | t0002 | g0211 | AFR | ASW | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0085 | EUR | TSI | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA20805 | hp2 | a0001 | c0005 | t0001 | g0022 | EUR | TSI | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0180 | SAS | GIH | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | GIH | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0025 | AMR | CLM | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG01123 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | CLM | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02109 | hp2 | a0003 | c0004 | t0001 | g0128 | AFR | ACB | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02486 | hp1 | a0001 | c0003 | t0002 | g0216 | AFR | ACB | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02486 | hp2 | a0001 | c0005 | t0002 | g0207 | AFR | ACB | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | ACB | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG02559 | hp2 | a0001 | c0003 | t0001 | g0011 | AFR | ACB | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03471 | hp1 | a0001 | c0009 | t0002 | g0038 | AFR | MSL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG03471 | hp2 | a0001 | c0003 | t0001 | g0132 | AFR | MSL | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG06807 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | USA | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | USA | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18955 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA18955 | hp2 | a0008 | c0010 | t0002 | g0181 | EAS | JPT | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | USA | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA20300 | hp2 | a0001 | c0001 | t0004 | g0175 | AFR | USA | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | LWK | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | LWK | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0001 | REF | REF | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0023 | REF | REF | NQO2_chr6_2994894_3024755 | NQO2 | chr6 | 2994894 | 3024755 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:3010064
|
A | G | 1 | a0003 | 7 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(4): Show |
missense_variant | MODERATE | c.47A>G | p.Lys16Arg | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 3/7 | 324/1073 | 47/696 | 16/231 | chr6 | 3010064 | ||
chr6:3010103
|
A | G | 1 | a0004 | 6 | HG00140.hp1 HG01081.hp2 HG02004.hp2 others(3): Show |
missense_variant | MODERATE | c.86A>G | p.Glu29Gly | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 3/7 | 363/1073 | 86/696 | 29/231 | chr6 | 3010103 | ||
chr6:3010156
|
C | T | 7 | a0001a0003a0004others(4): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
missense_variant | MODERATE | c.139C>T | p.Leu47Phe | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 3/7 | 416/1073 | 139/696 | 47/231 | chr6 | 3010156 | ||
chr6:3012544
|
G | A | 1 | a0005 | 2 | HG01978.hp2 HG04199.hp1 |
missense_variant&splice_region_variant | MODERATE | c.173G>A | p.Gly58Asp | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/7 | 450/1073 | 173/696 | 58/231 | chr6 | 3012544 | ||
chr6:3019510
|
T | C | 1 | a0006 | 1 | HG02056.hp1 | missense_variant | MODERATE | c.551T>C | p.Val184Ala | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 7/7 | 828/1073 | 551/696 | 184/231 | chr6 | 3019510 | ||
chr6:3019629
|
A | G | 1 | a0007 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.670A>G | p.Thr224Ala | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 7/7 | 947/1073 | 670/696 | 224/231 | chr6 | 3019629 | ||
chr6:3019647
|
G | C | 1 | a0008 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.688G>C | p.Gly230Arg | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 7/7 | 965/1073 | 688/696 | 230/231 | chr6 | 3019647 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:3015556
|
A | G | 10 | a0001c0001a0001c0003a0001c0008others(7): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
synonymous_variant | LOW | c.330A>G | p.Pro110Pro | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 5/7 | 607/1073 | 330/696 | 110/231 | chr6 | 3015556 | ||
chr6:3015631
|
C | T | 3 | a0001c0003a0004c0006a0006c0012 | 90 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(87): Show |
synonymous_variant | LOW | c.405C>T | p.Ser135Ser | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 5/7 | 682/1073 | 405/696 | 135/231 | chr6 | 3015631 | ||
chr6:3016904
|
C | T | 2 | a0001c0009a0003c0004 | 9 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(6): Show |
synonymous_variant | LOW | c.438C>T | p.Ser146Ser | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/7 | 715/1073 | 438/696 | 146/231 | chr6 | 3016904 | ||
chr6:3016937
|
G | C | 1 | a0001c0008 | 2 | HG00609.hp2 NA19067.hp2 |
synonymous_variant | LOW | c.471G>C | p.Thr157Thr | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/7 | 748/1073 | 471/696 | 157/231 | chr6 | 3016937 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:3000040
|
G | A | 2 | a0001c0001t0005a0001c0003t0005 | 2 | HG02647.hp1 HG02647.hp2 |
5_prime_UTR_variant | MODIFIER | c.-131G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/7 | 6513 | chr6 | 3000040 | |||||
chr6:3000069
|
A | C | 12 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(9): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
5_prime_UTR_variant | MODIFIER | c.-102A>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/7 | 6484 | chr6 | 3000069 | |||||
chr6:3019693
|
G | C | 2 | a0001c0001t0003a0001c0001t0004 | 67 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*38G>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 7/7 | 38 | chr6 | 3019693 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:3000098
|
C | T | 69 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0049others(66): Show | 139 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.-86+13C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3000098 | ||||||
chr6:3000103
|
G | A | 69 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0049others(66): Show | 139 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.-86+18G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3000103 | ||||||
chr6:3000199
|
C | T | 1 | a0003c0004t0002g0226 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-86+114C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3000199 | ||||||
chr6:3000255
|
G | T | 5 | a0001c0001t0002g0222a0001c0001t0002g0224a0001c0001t0005g0225others(2): Show | 6 | HG02647.hp1 HG02647.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-86+170G>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3000255 | ||||||
chr6:3000284
|
T | TC | 4 | a0001c0001t0002g0054a0001c0001t0002g0057a0004c0006t0002g0055others(1): Show | 4 | HG00741.hp1 HG02004.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.-86+200dupC | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 3000284 | |||||
chr6:3000371
|
A | T | 1 | a0001c0003t0002g0221 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-86+286A>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3000371 | ||||||
chr6:3000380
|
A | AG | 10 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0002g0064others(7): Show | 11 | HG00621.hp2 HG01109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-86+300dupG | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 3000380 | |||||
chr6:3000382
|
G | T | 9 | a0001c0003t0002g0213a0001c0003t0002g0215a0001c0003t0002g0216others(6): Show | 9 | HG02257.hp2 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-86+297G>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3000382 | ||||||
chr6:3000527
|
G | GA | 14 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0049others(11): Show | 21 | HG00639.hp2 HG02027.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.-86+453dupA | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 3000527 | |||||
chr6:3000527
|
GA | G | 106 | a0001c0001t0001g0014a0001c0001t0001g0041a0001c0001t0001g0212others(103): Show | 152 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.-86+453delA | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 3000527 | |||||
chr6:3000529
|
A | G | 1 | a0001c0001t0001g0212 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-86+444A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3000529 | ||||||
chr6:3000543
|
C | CT | 102 | a0001c0001t0001g0014a0001c0001t0001g0041a0001c0001t0001g0138others(99): Show | 146 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.-86+470dupT | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 3000543 | |||||
chr6:3000555
|
T | C | 3 | a0001c0001t0002g0057a0004c0006t0002g0055a0004c0006t0002g0056 | 3 | HG00741.hp1 HG02004.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-86+470T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3000555 | ||||||
chr6:3000598
|
G | A | 52 | a0001c0001t0001g0014a0001c0001t0001g0041a0001c0001t0002g0014others(49): Show | 69 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.-86+513G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3000598 | ||||||
chr6:3000623
|
C | G | 2 | a0001c0001t0003g0026a0001c0003t0002g0182 | 4 | HG01074.hp2 HG01261.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-86+538C>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3000623 | ||||||
chr6:3000744
|
G | A | 59 | a0001c0001t0001g0014a0001c0001t0001g0029a0001c0001t0001g0041others(56): Show | 81 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.-86+659G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3000744 | ||||||
chr6:3000852
|
C | CT | 57 | a0001c0001t0001g0014a0001c0001t0001g0041a0001c0001t0002g0014others(54): Show | 78 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.-86+777dupT | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 3000852 | |||||
chr6:3000956
|
C | G | 1 | a0001c0001t0001g0212 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-86+871C>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3000956 | ||||||
chr6:3001024
|
G | A | 74 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(71): Show | 105 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.-86+939G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3001024 | ||||||
chr6:3001034
|
G | A | 3 | a0001c0001t0002g0222a0001c0001t0002g0224a0001c0003t0005g0223 | 3 | HG02647.hp1 HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-86+949G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3001034 | ||||||
chr6:3001090
|
CT | C | 217 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(214): Show | 306 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.-86+1021delT | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 3001090 | |||||
chr6:3001097
|
T | C | 6 | a0001c0001t0004g0021a0001c0001t0004g0060a0001c0001t0004g0115others(3): Show | 11 | HG02451.hp2 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-86+1012T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3001097 | ||||||
chr6:3001120
|
A | G | 239 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(236): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.-86+1035A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3001120 | ||||||
chr6:3001121
|
C | T | 11 | a0001c0001t0002g0206a0001c0003t0002g0213a0001c0003t0002g0215others(8): Show | 11 | HG02257.hp2 HG02451.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-86+1036C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3001121 | ||||||
chr6:3001183
|
G | A | 4 | a0001c0003t0001g0012a0001c0003t0001g0061a0001c0003t0001g0116others(1): Show | 7 | HG01884.hp2 HG02145.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-86+1098G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3001183 | ||||||
chr6:3001197
|
C | T | 56 | a0001c0001t0001g0014a0001c0001t0001g0041a0001c0001t0002g0014others(53): Show | 76 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.-86+1112C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3001197 | ||||||
chr6:3001215
|
G | T | 1 | a0001c0001t0003g0179 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-86+1130G>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3001215 | ||||||
chr6:3001234
|
T | C | 32 | a0001c0001t0002g0185a0001c0001t0002g0198a0001c0001t0003g0065others(29): Show | 54 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.-86+1149T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3001234 | ||||||
chr6:3001244
|
T | C | 1 | a0001c0003t0001g0118 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-86+1159T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3001244 | ||||||
chr6:3001247
|
A | G | 1 | a0001c0003t0001g0118 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-86+1162A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3001247 | ||||||
chr6:3001306
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-86+1221G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3001306 | ||||||
chr6:3001360
|
G | C | 3 | a0001c0001t0002g0057a0004c0006t0002g0055a0004c0006t0002g0056 | 3 | HG00741.hp1 HG02004.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-86+1275G>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3001360 | ||||||
chr6:3001445
|
T | G | 2 | a0001c0001t0004g0015a0001c0001t0004g0134 | 5 | HG02280.hp1 HG02922.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-86+1360T>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3001445 | ||||||
chr6:3001497
|
AT | A | 3 | a0001c0001t0002g0057a0004c0006t0002g0055a0004c0006t0002g0056 | 3 | HG00741.hp1 HG02004.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-86+1413delT | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3001497 | ||||||
chr6:3001757
|
C | T | 1 | a0001c0003t0002g0205 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-86+1672C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3001757 | ||||||
chr6:3001916
|
C | T | 1 | a0002c0002t0001g0280 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-86+1831C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3001916 | ||||||
chr6:3001951
|
A | C | 1 | a0001c0001t0001g0135 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-86+1866A>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3001951 | ||||||
chr6:3002004
|
T | C | 219 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(216): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.-86+1919T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3002004 | ||||||
chr6:3002060
|
A | G | 1 | a0001c0003t0001g0133 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-86+1975A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3002060 | ||||||
chr6:3002089
|
C | G | 40 | a0001c0001t0002g0057a0001c0001t0002g0185a0001c0001t0002g0198others(37): Show | 66 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.-86+2004C>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3002089 | ||||||
chr6:3002293
|
C | A | 3 | a0001c0003t0002g0205a0001c0003t0002g0211a0001c0005t0002g0203 | 3 | HG01192.hp2 HG02258.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-86+2208C>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3002293 | ||||||
chr6:3002401
|
C | G | 2 | a0001c0001t0001g0110a0001c0001t0001g0111 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-86+2316C>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3002401 | ||||||
chr6:3002453
|
C | T | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG00733.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.-86+2368C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3002453 | ||||||
chr6:3002575
|
G | A | 1 | a0004c0006t0001g0067 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-86+2490G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3002575 | ||||||
chr6:3002609
|
G | A | 1 | a0003c0004t0001g0253 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-86+2524G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3002609 | ||||||
chr6:3002741
|
T | C | 219 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(216): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.-86+2656T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3002741 | ||||||
chr6:3002762
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-86+2677C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3002762 | ||||||
chr6:3002808
|
T | C | 1 | a0001c0003t0001g0133 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-86+2723T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3002808 | ||||||
chr6:3002826
|
C | T | 219 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(216): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.-86+2741C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3002826 | ||||||
chr6:3002956
|
A | G | 32 | a0001c0001t0002g0185a0001c0001t0002g0198a0001c0001t0003g0065others(29): Show | 55 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.-86+2871A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3002956 | ||||||
chr6:3002986
|
G | A | 1 | a0002c0002t0001g0254 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-86+2901G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3002986 | ||||||
chr6:3003203
|
C | T | 5 | a0001c0003t0001g0012a0001c0003t0001g0061a0001c0003t0001g0116others(2): Show | 8 | HG01884.hp2 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.-86+3118C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3003203 | ||||||
chr6:3003222
|
T | C | 6 | a0001c0001t0001g0010a0001c0001t0001g0030a0001c0001t0001g0068others(3): Show | 10 | HG01070.hp2 HG02148.hp2 NA18939.hp2 others(7): Show |
intron_variant | MODIFIER | c.-86+3137T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3003222 | ||||||
chr6:3003317
|
G | A | 10 | a0001c0003t0001g0024a0001c0003t0001g0070a0001c0003t0001g0143others(7): Show | 12 | HG01891.hp2 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.-85-3151G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3003317 | ||||||
chr6:3003328
|
C | T | 10 | a0001c0003t0001g0024a0001c0003t0001g0070a0001c0003t0001g0143others(7): Show | 12 | HG01891.hp2 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.-85-3140C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3003328 | ||||||
chr6:3003334
|
A | G | 10 | a0001c0003t0001g0024a0001c0003t0001g0070a0001c0003t0001g0143others(7): Show | 12 | HG01891.hp2 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.-85-3134A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3003334 | ||||||
chr6:3003342
|
A | T | 10 | a0001c0003t0001g0024a0001c0003t0001g0070a0001c0003t0001g0143others(7): Show | 12 | HG01891.hp2 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.-85-3126A>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3003342 | ||||||
chr6:3003347
|
A | G | 10 | a0001c0003t0001g0024a0001c0003t0001g0070a0001c0003t0001g0143others(7): Show | 12 | HG01891.hp2 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.-85-3121A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3003347 | ||||||
chr6:3003396
|
C | G | 43 | a0001c0001t0001g0014a0001c0001t0001g0131a0001c0001t0002g0014others(40): Show | 56 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.-85-3072C>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3003396 | ||||||
chr6:3003403
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-85-3065C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3003403 | ||||||
chr6:3003466
|
G | A | 5 | a0001c0001t0001g0018a0001c0001t0001g0071a0001c0001t0001g0072others(2): Show | 7 | NA18952.hp2 NA18960.hp2 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.-85-3002G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3003466 | ||||||
chr6:3003476
|
C | T | 73 | a0001c0001t0001g0014a0001c0001t0001g0041a0001c0001t0001g0105others(70): Show | 99 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.-85-2992C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3003476 | ||||||
chr6:3003541
|
C | A | 151 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(148): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.-85-2927C>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3003541 | ||||||
chr6:3003551
|
T | C | 1 | a0001c0003t0002g0205 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-85-2917T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3003551 | ||||||
chr6:3003606
|
C | T | 2 | a0001c0001t0001g0099a0001c0001t0002g0145 | 2 | HG00280.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.-85-2862C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3003606 | ||||||
chr6:3003680
|
T | C | 175 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(172): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.-85-2788T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3003680 | ||||||
chr6:3003681
|
T | C | 175 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(172): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.-85-2787T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3003681 | ||||||
chr6:3003683
|
T | C | 175 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(172): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.-85-2785T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3003683 | ||||||
chr6:3003736
|
A | G | 85 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0018others(82): Show | 132 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.-85-2732A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3003736 | ||||||
chr6:3003817
|
A | AGCCCTTA others(1): Show |
24 | a0001c0001t0001g0098a0001c0001t0001g0123a0001c0001t0001g0124others(21): Show | 34 | HG00099.hp1 HG00323.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.-85-2649_-85-2648i others(10): Show |
NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 3003817 | |||||
chr6:3003820
|
A | C | 1 | a0001c0003t0002g0211 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-85-2648A>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3003820 | ||||||
chr6:3003861
|
T | A | 3 | a0001c0003t0001g0118a0003c0004t0001g0113a0003c0004t0001g0128 | 3 | HG02109.hp2 HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-85-2607T>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3003861 | ||||||
chr6:3004018
|
G | A | 1 | a0002c0002t0001g0256 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-85-2450G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3004018 | ||||||
chr6:3004025
|
A | G | 8 | a0001c0001t0001g0125a0001c0001t0001g0212a0001c0001t0004g0115others(5): Show | 8 | HG02109.hp1 HG02486.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-85-2443A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3004025 | ||||||
chr6:3004050
|
C | T | 1 | a0001c0003t0001g0137 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-85-2418C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3004050 | ||||||
chr6:3004055
|
G | T | 6 | a0001c0001t0004g0021a0001c0001t0004g0060a0001c0001t0004g0115others(3): Show | 11 | HG02451.hp2 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-85-2413G>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3004055 | ||||||
chr6:3004077
|
C | T | 2 | a0003c0004t0001g0129a0003c0004t0001g0130 | 2 | HG01109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-85-2391C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3004077 | ||||||
chr6:3004153
|
G | T | 1 | a0001c0003t0002g0195 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-85-2315G>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3004153 | ||||||
chr6:3004220
|
G | A | 8 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(5): Show | 8 | HG01884.hp1 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-85-2248G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3004220 | ||||||
chr6:3004299
|
T | C | 197 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(194): Show | 270 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.-85-2169T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3004299 | ||||||
chr6:3004336
|
C | T | 6 | a0004c0006t0001g0067a0004c0006t0001g0087a0004c0006t0001g0101others(3): Show | 6 | HG00140.hp1 HG01081.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.-85-2132C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3004336 | ||||||
chr6:3004352
|
T | C | 1 | a0002c0002t0001g0281 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-85-2116T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3004352 | ||||||
chr6:3004393
|
C | CCT | 18 | a0001c0001t0003g0202a0001c0001t0004g0015a0001c0001t0004g0044others(15): Show | 26 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.-85-2074_-85-2073i others(4): Show |
NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 3004393 | |||||
chr6:3004440
|
C | T | 1 | a0004c0006t0001g0101 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-85-2028C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3004440 | ||||||
chr6:3004485
|
C | A | 1 | a0001c0003t0002g0217 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-85-1983C>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3004485 | ||||||
chr6:3004486
|
C | T | 2 | a0001c0001t0001g0212a0001c0003t0002g0217 | 2 | HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-85-1982C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3004486 | ||||||
chr6:3004487
|
A | G | 1 | a0001c0003t0002g0217 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-85-1981A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3004487 | ||||||
chr6:3004491
|
A | G | 1 | a0001c0003t0002g0217 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-85-1977A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3004491 | ||||||
chr6:3004496
|
G | A | 1 | a0001c0003t0002g0217 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-85-1972G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3004496 | ||||||
chr6:3004748
|
C | T | 6 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(3): Show | 6 | HG01884.hp1 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-85-1720C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3004748 | ||||||
chr6:3004871
|
G | A | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | NA18981.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.-85-1597G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3004871 | ||||||
chr6:3004902
|
G | A | 2 | a0001c0001t0001g0110a0001c0001t0001g0111 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-85-1566G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3004902 | ||||||
chr6:3004920
|
G | A | 1 | a0001c0003t0001g0118 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-85-1548G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3004920 | ||||||
chr6:3004941
|
C | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0235 | 3 | HG02630.hp2 HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-85-1527C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3004941 | ||||||
chr6:3005015
|
G | A | 1 | a0004c0006t0001g0067 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-85-1453G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3005015 | ||||||
chr6:3005325
|
G | A | 176 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(173): Show | 242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-85-1143G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3005325 | ||||||
chr6:3005343
|
C | T | 1 | a0001c0001t0001g0035 | 2 | NA18982.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-85-1125C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3005343 | ||||||
chr6:3005351
|
G | A | 3 | a0001c0001t0001g0031a0001c0001t0001g0073a0001c0001t0001g0074 | 4 | NA18962.hp1 NA18972.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.-85-1117G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3005351 | ||||||
chr6:3005393
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-85-1075C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3005393 | ||||||
chr6:3005402
|
C | T | 9 | a0001c0001t0001g0016a0001c0001t0001g0049a0001c0001t0001g0231others(6): Show | 13 | HG00639.hp2 HG02055.hp1 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.-85-1066C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3005402 | ||||||
chr6:3005445
|
T | C | 10 | a0001c0001t0001g0014a0001c0001t0001g0088a0001c0001t0002g0014others(7): Show | 12 | HG00621.hp2 HG01099.hp1 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.-85-1023T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3005445 | ||||||
chr6:3005502
|
A | G | 1 | a0001c0001t0002g0170 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-85-966A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3005502 | ||||||
chr6:3005620
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-85-848G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3005620 | ||||||
chr6:3005697
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-85-771G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3005697 | ||||||
chr6:3005723
|
C | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0235 | 3 | HG02630.hp2 HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-85-745C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3005723 | ||||||
chr6:3005864
|
G | A | 2 | a0001c0003t0001g0116a0001c0003t0002g0204 | 2 | HG02572.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-85-604G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3005864 | ||||||
chr6:3005882
|
A | G | 1 | a0001c0003t0001g0250 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-85-586A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3005882 | ||||||
chr6:3005902
|
T | C | 3 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0002g0222 | 3 | HG03041.hp1 HG03130.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-85-566T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3005902 | ||||||
chr6:3005952
|
G | A | 10 | a0001c0003t0001g0012a0001c0003t0001g0039a0001c0003t0001g0061others(7): Show | 14 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.-85-516G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3005952 | ||||||
chr6:3006121
|
C | T | 45 | a0001c0003t0001g0012a0001c0003t0001g0024a0001c0003t0001g0039others(42): Show | 73 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-85-347C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3006121 | ||||||
chr6:3006138
|
G | C | 7 | a0001c0001t0004g0021a0001c0001t0004g0060a0001c0001t0004g0115others(4): Show | 13 | HG02451.hp2 HG02559.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-85-330G>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3006138 | ||||||
chr6:3006145
|
G | A | 1 | a0001c0003t0001g0118 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-85-323G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3006145 | ||||||
chr6:3006278
|
A | G | 1 | a0001c0009t0002g0038 | 2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-85-190A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3006278 | ||||||
chr6:3006296
|
C | T | 1 | a0002c0002t0001g0275 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-85-172C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3006296 | ||||||
chr6:3006340
|
C | G | 1 | a0002c0002t0001g0256 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-85-128C>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3006340 | ||||||
chr6:3006443
|
C | A | 1 | a0001c0001t0001g0077 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-85-25C>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3006443 | ||||||
chr6:3006453
|
C | T | 22 | a0001c0003t0001g0069a0001c0003t0001g0245a0001c0003t0001g0276others(19): Show | 43 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.-85-15C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 1/6 | chr6 | 3006453 | ||||||
chr6:3006573
|
A | G | 39 | a0001c0001t0003g0009a0001c0001t0003g0013a0001c0001t0003g0025others(36): Show | 53 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.7+14A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3006573 | ||||||
chr6:3006581
|
G | A | 6 | a0004c0006t0001g0067a0004c0006t0001g0087a0004c0006t0001g0101others(3): Show | 6 | HG00140.hp1 HG01081.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.7+22G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3006581 | ||||||
chr6:3006607
|
G | A | 1 | a0001c0003t0002g0187 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.7+48G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3006607 | ||||||
chr6:3006625
|
A | G | 2 | a0001c0005t0001g0022a0002c0002t0002g0147 | 4 | HG00323.hp2 HG01515.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.7+66A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3006625 | ||||||
chr6:3006650
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.7+91A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3006650 | ||||||
chr6:3006751
|
C | T | 175 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(172): Show | 241 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.7+192C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3006751 | ||||||
chr6:3007038
|
A | G | 1 | a0001c0003t0002g0169 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.7+479A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3007038 | ||||||
chr6:3007039
|
A | G | 1 | a0001c0003t0002g0205 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.7+480A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3007039 | ||||||
chr6:3007104
|
C | T | 2 | a0003c0004t0001g0113a0003c0004t0001g0128 | 2 | HG02109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.7+545C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3007104 | ||||||
chr6:3007130
|
C | T | 1 | a0002c0002t0001g0274 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.7+571C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3007130 | ||||||
chr6:3007138
|
G | A | 2 | a0001c0003t0002g0169a0002c0002t0001g0260 | 2 | HG01891.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.7+579G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3007138 | ||||||
chr6:3007171
|
G | T | 1 | a0001c0009t0002g0038 | 2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.7+612G>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3007171 | ||||||
chr6:3007194
|
A | C | 78 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(75): Show | 108 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.7+635A>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3007194 | ||||||
chr6:3007224
|
A | G | 1 | a0005c0007t0001g0086 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.7+665A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3007224 | ||||||
chr6:3007244
|
G | A | 41 | a0001c0001t0003g0009a0001c0001t0003g0013a0001c0001t0003g0025others(38): Show | 56 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.7+685G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3007244 | ||||||
chr6:3007457
|
C | T | 7 | a0003c0004t0001g0113a0003c0004t0001g0128a0003c0004t0001g0129others(4): Show | 7 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.7+898C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3007457 | ||||||
chr6:3007463
|
C | G | 7 | a0003c0004t0001g0113a0003c0004t0001g0128a0003c0004t0001g0129others(4): Show | 7 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.7+904C>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3007463 | ||||||
chr6:3007581
|
T | C | 2 | a0001c0001t0001g0136a0001c0001t0002g0224 | 2 | HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.7+1022T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3007581 | ||||||
chr6:3007610
|
C | G | 7 | a0003c0004t0001g0113a0003c0004t0001g0128a0003c0004t0001g0129others(4): Show | 7 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.7+1051C>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3007610 | ||||||
chr6:3007916
|
C | T | 7 | a0003c0004t0001g0113a0003c0004t0001g0128a0003c0004t0001g0129others(4): Show | 7 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.7+1357C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3007916 | ||||||
chr6:3007970
|
C | T | 7 | a0003c0004t0001g0113a0003c0004t0001g0128a0003c0004t0001g0129others(4): Show | 7 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.7+1411C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3007970 | ||||||
chr6:3008018
|
A | G | 1 | a0001c0003t0002g0194 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.7+1459A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3008018 | ||||||
chr6:3008116
|
A | G | 3 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0002g0222 | 3 | HG03041.hp1 HG03130.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.7+1557A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3008116 | ||||||
chr6:3008161
|
T | C | 22 | a0001c0003t0001g0069a0001c0003t0001g0245a0001c0003t0001g0276others(19): Show | 43 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.7+1602T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3008161 | ||||||
chr6:3008199
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.7+1640C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3008199 | ||||||
chr6:3008203
|
A | G | 1 | a0001c0001t0003g0180 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.7+1644A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3008203 | ||||||
chr6:3008288
|
G | T | 2 | a0001c0003t0002g0217a0001c0003t0002g0221 | 2 | HG02257.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.7+1729G>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3008288 | ||||||
chr6:3008343
|
C | T | 3 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0002g0222 | 3 | HG03041.hp1 HG03130.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.8-1682C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3008343 | ||||||
chr6:3008344
|
G | A | 1 | a0001c0001t0002g0171 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.8-1681G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3008344 | ||||||
chr6:3008369
|
G | A | 7 | a0003c0004t0001g0113a0003c0004t0001g0128a0003c0004t0001g0129others(4): Show | 7 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-1656G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3008369 | ||||||
chr6:3008369
|
G | T | 5 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(2): Show | 5 | HG01884.hp1 HG02109.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.8-1656G>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3008369 | ||||||
chr6:3008374
|
G | A | 1 | a0005c0007t0001g0086 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.8-1651G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3008374 | ||||||
chr6:3008393
|
C | T | 45 | a0001c0003t0001g0012a0001c0003t0001g0024a0001c0003t0001g0039others(42): Show | 73 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.8-1632C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3008393 | ||||||
chr6:3008412
|
C | CA | 12 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0003g0156others(9): Show | 17 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.8-1598dupA | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 3008412 | |||||
chr6:3008412
|
CA | C | 12 | a0001c0001t0001g0121a0001c0001t0003g0163a0001c0003t0001g0024others(9): Show | 15 | HG01255.hp1 HG01891.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.8-1598delA | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 3008412 | |||||
chr6:3008412
|
CAAAA | C | 7 | a0003c0004t0001g0113a0003c0004t0001g0128a0003c0004t0001g0129others(4): Show | 7 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-1601_8-1598delAA others(2): Show |
NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 3008412 | |||||
chr6:3008431
|
A | G | 2 | a0001c0003t0001g0069a0001c0003t0002g0192 | 2 | HG01070.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.8-1594A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3008431 | ||||||
chr6:3008431
|
AAAG | A | 20 | a0001c0003t0001g0245a0001c0003t0001g0276a0001c0003t0002g0002others(17): Show | 41 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.8-1591_8-1589delGA others(1): Show |
NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 3008431 | |||||
chr6:3008434
|
G | A | 2 | a0001c0003t0001g0069a0001c0003t0002g0192 | 2 | HG01070.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.8-1591G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3008434 | ||||||
chr6:3008446
|
G | A | 7 | a0003c0004t0001g0113a0003c0004t0001g0128a0003c0004t0001g0129others(4): Show | 7 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-1579G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3008446 | ||||||
chr6:3008478
|
G | A | 2 | a0002c0002t0001g0246a0002c0002t0001g0249 | 2 | NA18963.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.8-1547G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3008478 | ||||||
chr6:3008594
|
A | G | 7 | a0003c0004t0001g0113a0003c0004t0001g0128a0003c0004t0001g0129others(4): Show | 7 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-1431A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3008594 | ||||||
chr6:3008595
|
C | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0235 | 3 | HG02630.hp2 HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.8-1430C>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3008595 | ||||||
chr6:3008660
|
A | G | 1 | a0001c0003t0001g0250 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.8-1365A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3008660 | ||||||
chr6:3008671
|
A | G | 1 | a0001c0001t0001g0230 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.8-1354A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3008671 | ||||||
chr6:3008708
|
T | C | 1 | a0001c0003t0002g0211 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.8-1317T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3008708 | ||||||
chr6:3008729
|
C | T | 7 | a0003c0004t0001g0113a0003c0004t0001g0128a0003c0004t0001g0129others(4): Show | 7 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-1296C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3008729 | ||||||
chr6:3008755
|
T | C | 7 | a0003c0004t0001g0113a0003c0004t0001g0128a0003c0004t0001g0129others(4): Show | 7 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-1270T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3008755 | ||||||
chr6:3008799
|
C | T | 1 | a0001c0009t0002g0038 | 2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.8-1226C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3008799 | ||||||
chr6:3008810
|
C | T | 7 | a0003c0004t0001g0113a0003c0004t0001g0128a0003c0004t0001g0129others(4): Show | 7 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-1215C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3008810 | ||||||
chr6:3008811
|
A | G | 7 | a0003c0004t0001g0113a0003c0004t0001g0128a0003c0004t0001g0129others(4): Show | 7 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-1214A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3008811 | ||||||
chr6:3008816
|
G | A | 17 | a0002c0002t0001g0007a0002c0002t0001g0052a0002c0002t0001g0243others(14): Show | 23 | HG00099.hp1 HG00733.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.8-1209G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3008816 | ||||||
chr6:3008903
|
A | C | 1 | a0001c0003t0002g0205 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.8-1122A>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3008903 | ||||||
chr6:3008956
|
C | T | 1 | a0002c0002t0001g0263 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.8-1069C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3008956 | ||||||
chr6:3008957
|
G | A | 7 | a0003c0004t0001g0113a0003c0004t0001g0128a0003c0004t0001g0129others(4): Show | 7 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-1068G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3008957 | ||||||
chr6:3008960
|
A | AC | 7 | a0003c0004t0001g0113a0003c0004t0001g0128a0003c0004t0001g0129others(4): Show | 7 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-1064dupC | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 3008960 | |||||
chr6:3008966
|
C | T | 1 | a0003c0004t0001g0128 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.8-1059C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3008966 | ||||||
chr6:3008992
|
T | C | 7 | a0003c0004t0001g0113a0003c0004t0001g0128a0003c0004t0001g0129others(4): Show | 7 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-1033T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3008992 | ||||||
chr6:3008998
|
C | CA | 7 | a0003c0004t0001g0113a0003c0004t0001g0128a0003c0004t0001g0129others(4): Show | 7 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-1027_8-1026insA | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3008998 | ||||||
chr6:3009001
|
T | C | 7 | a0003c0004t0001g0113a0003c0004t0001g0128a0003c0004t0001g0129others(4): Show | 7 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-1024T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3009001 | ||||||
chr6:3009105
|
C | T | 1 | a0001c0001t0003g0202 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.8-920C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3009105 | ||||||
chr6:3009122
|
G | A | 1 | a0004c0006t0001g0101 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.8-903G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3009122 | ||||||
chr6:3009128
|
T | C | 7 | a0003c0004t0001g0113a0003c0004t0001g0128a0003c0004t0001g0129others(4): Show | 7 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-897T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3009128 | ||||||
chr6:3009310
|
C | T | 11 | a0001c0003t0001g0012a0001c0003t0001g0039a0001c0003t0001g0061others(8): Show | 15 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.8-715C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3009310 | ||||||
chr6:3009365
|
G | A | 7 | a0003c0004t0001g0113a0003c0004t0001g0128a0003c0004t0001g0129others(4): Show | 7 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-660G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3009365 | ||||||
chr6:3009381
|
G | T | 1 | a0001c0003t0002g0211 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.8-644G>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3009381 | ||||||
chr6:3009440
|
A | G | 3 | a0001c0001t0003g0141a0001c0001t0003g0157a0001c0001t0003g0162 | 3 | NA18949.hp2 NA18953.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.8-585A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3009440 | ||||||
chr6:3009452
|
G | A | 4 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0002g0222others(1): Show | 4 | HG03041.hp1 HG03130.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-573G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3009452 | ||||||
chr6:3009480
|
C | T | 1 | a0001c0003t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.8-545C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3009480 | ||||||
chr6:3009484
|
T | C | 7 | a0003c0004t0001g0113a0003c0004t0001g0128a0003c0004t0001g0129others(4): Show | 7 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-541T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3009484 | ||||||
chr6:3009518
|
C | T | 18 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0002g0222others(15): Show | 22 | HG00140.hp1 HG01081.hp2 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.8-507C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3009518 | ||||||
chr6:3009710
|
A | G | 226 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(223): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.8-315A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3009710 | ||||||
chr6:3009733
|
G | A | 7 | a0003c0004t0001g0113a0003c0004t0001g0128a0003c0004t0001g0129others(4): Show | 7 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-292G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3009733 | ||||||
chr6:3009746
|
A | G | 3 | a0001c0001t0004g0015a0001c0001t0004g0127a0001c0001t0004g0134 | 6 | HG02280.hp1 HG02922.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.8-279A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3009746 | ||||||
chr6:3009839
|
C | A | 14 | a0001c0003t0001g0011a0001c0003t0001g0114a0001c0003t0001g0133others(11): Show | 17 | HG00140.hp1 HG01081.hp2 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.8-186C>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3009839 | ||||||
chr6:3009869
|
G | A | 233 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(230): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.8-156G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3009869 | ||||||
chr6:3009880
|
A | G | 7 | a0003c0004t0001g0113a0003c0004t0001g0128a0003c0004t0001g0129others(4): Show | 7 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-145A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3009880 | ||||||
chr6:3009944
|
T | C | 1 | a0001c0009t0002g0038 | 2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.8-81T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3009944 | ||||||
chr6:3009948
|
A | G | 6 | a0004c0006t0001g0067a0004c0006t0001g0087a0004c0006t0001g0101others(3): Show | 6 | HG00140.hp1 HG01081.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.8-77A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3009948 | ||||||
chr6:3010001
|
G | C | 1 | a0001c0001t0003g0202 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.8-24G>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 2/6 | chr6 | 3010001 | ||||||
chr6:3010216
|
T | TATAAAAA others(319): Show |
1 | a0001c0001t0001g0234 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.172+35_172+36insTA others(324): Show |
NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 3010216 | |||||
chr6:3010216
|
T | TATAAAAA others(343): Show |
1 | a0001c0001t0001g0233 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.172+35_172+36insTA others(348): Show |
NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 3010216 | |||||
chr6:3010225
|
C | T | 161 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(158): Show | 235 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.172+36C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 3/6 | chr6 | 3010225 | ||||||
chr6:3010231
|
T | A | 6 | a0004c0006t0001g0067a0004c0006t0001g0087a0004c0006t0001g0101others(3): Show | 6 | HG00140.hp1 HG01081.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.172+42T>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 3/6 | chr6 | 3010231 | ||||||
chr6:3010248
|
A | G | 7 | a0003c0004t0001g0113a0003c0004t0001g0128a0003c0004t0001g0129others(4): Show | 7 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.172+59A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 3/6 | chr6 | 3010248 | ||||||
chr6:3010363
|
A | G | 1 | a0001c0009t0002g0038 | 2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.172+174A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 3/6 | chr6 | 3010363 | ||||||
chr6:3010464
|
C | G | 1 | a0002c0002t0001g0272 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.172+275C>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 3/6 | chr6 | 3010464 | ||||||
chr6:3010513
|
T | C | 1 | a0001c0005t0001g0022 | 3 | HG00323.hp2 HG01515.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.172+324T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 3/6 | chr6 | 3010513 | ||||||
chr6:3010649
|
AG | A | 7 | a0003c0004t0001g0113a0003c0004t0001g0128a0003c0004t0001g0129others(4): Show | 7 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.172+461delG | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 3/6 | chr6 | 3010649 | ||||||
chr6:3010676
|
A | G | 7 | a0003c0004t0001g0113a0003c0004t0001g0128a0003c0004t0001g0129others(4): Show | 7 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.172+487A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 3/6 | chr6 | 3010676 | ||||||
chr6:3010770
|
T | A | 8 | a0001c0001t0003g0164a0003c0004t0001g0113a0003c0004t0001g0128others(5): Show | 8 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.172+581T>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 3/6 | chr6 | 3010770 | ||||||
chr6:3010829
|
A | G | 7 | a0003c0004t0001g0113a0003c0004t0001g0128a0003c0004t0001g0129others(4): Show | 7 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.172+640A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 3/6 | chr6 | 3010829 | ||||||
chr6:3010842
|
C | T | 1 | a0001c0003t0002g0047 | 2 | HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.172+653C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 3/6 | chr6 | 3010842 | ||||||
chr6:3010900
|
G | A | 7 | a0003c0004t0001g0113a0003c0004t0001g0128a0003c0004t0001g0129others(4): Show | 7 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.172+711G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 3/6 | chr6 | 3010900 | ||||||
chr6:3010915
|
C | T | 159 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(156): Show | 221 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(218): Show |
intron_variant | MODIFIER | c.172+726C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 3/6 | chr6 | 3010915 | ||||||
chr6:3010941
|
G | A | 229 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(226): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.172+752G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 3/6 | chr6 | 3010941 | ||||||
chr6:3010952
|
G | GA | 174 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(171): Show | 239 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(236): Show |
intron_variant | MODIFIER | c.172+775dupA | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 3010952 | |||||
chr6:3010952
|
G | GAA | 8 | a0001c0009t0002g0038a0003c0004t0001g0128a0004c0006t0001g0067others(5): Show | 9 | HG00140.hp1 HG01081.hp2 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.172+774_172+775dup others(2): Show |
NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 3010952 | |||||
chr6:3011106
|
C | T | 1 | a0001c0001t0004g0020 | 3 | HG01255.hp2 HG01358.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.172+917C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 3/6 | chr6 | 3011106 | ||||||
chr6:3011136
|
G | A | 1 | a0002c0002t0001g0264 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.172+947G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 3/6 | chr6 | 3011136 | ||||||
chr6:3011225
|
G | T | 7 | a0003c0004t0001g0113a0003c0004t0001g0128a0003c0004t0001g0129others(4): Show | 7 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.172+1036G>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 3/6 | chr6 | 3011225 | ||||||
chr6:3011308
|
C | T | 47 | a0001c0001t0003g0009a0001c0001t0003g0013a0001c0001t0003g0025others(44): Show | 67 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.172+1119C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 3/6 | chr6 | 3011308 | ||||||
chr6:3011388
|
G | A | 1 | a0002c0002t0001g0262 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.173-1156G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 3/6 | chr6 | 3011388 | ||||||
chr6:3011517
|
G | A | 2 | a0003c0004t0001g0253a0003c0004t0001g0273 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.173-1027G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 3/6 | chr6 | 3011517 | ||||||
chr6:3011537
|
G | T | 13 | a0001c0003t0001g0011a0001c0003t0001g0114a0001c0003t0001g0133others(10): Show | 16 | HG00140.hp1 HG01081.hp2 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.173-1007G>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 3/6 | chr6 | 3011537 | ||||||
chr6:3011654
|
TA | T | 3 | a0001c0005t0002g0203a0001c0005t0002g0207a0001c0005t0002g0214 | 3 | HG02258.hp2 HG02486.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.173-887delA | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 3011654 | |||||
chr6:3011714
|
C | T | 3 | a0001c0003t0001g0137a0001c0003t0001g0210a0001c0003t0002g0220 | 3 | HG02809.hp2 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.173-830C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 3/6 | chr6 | 3011714 | ||||||
chr6:3011855
|
A | G | 3 | a0001c0005t0002g0203a0001c0005t0002g0207a0001c0005t0002g0214 | 3 | HG02258.hp2 HG02486.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.173-689A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 3/6 | chr6 | 3011855 | ||||||
chr6:3012098
|
C | T | 1 | a0001c0003t0002g0149 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.173-446C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 3/6 | chr6 | 3012098 | ||||||
chr6:3012099
|
T | C | 3 | a0001c0003t0001g0144a0001c0003t0002g0218a0001c0003t0002g0219 | 3 | HG01243.hp1 HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.173-445T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 3/6 | chr6 | 3012099 | ||||||
chr6:3012194
|
G | A | 1 | a0004c0006t0001g0067 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.173-350G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 3/6 | chr6 | 3012194 | ||||||
chr6:3012491
|
TG | T | 159 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(156): Show | 221 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(218): Show |
intron_variant | MODIFIER | c.173-50delG | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 3012491 | |||||
chr6:3012503
|
G | A | 1 | a0002c0002t0001g0244 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.173-41G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 3/6 | chr6 | 3012503 | ||||||
chr6:3012538
|
C | G | 1 | a0001c0003t0002g0205 | 1 | HG01192.hp2 | splice_region_variant&intron_variant | LOW | c.173-6C>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 3/6 | chr6 | 3012538 | ||||||
chr6:3012539
|
G | A | 3 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0002g0153 | 6 | HG01934.hp2 HG01943.hp1 HG01952.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.173-5G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 3/6 | chr6 | 3012539 | ||||||
chr6:3012714
|
C | T | 1 | a0001c0001t0001g0238 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.303+40C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3012714 | ||||||
chr6:3012856
|
CCACTTCA others(11): Show |
C | 1 | a0001c0001t0002g0222 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.303+208_303+225del others(18): Show |
NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr6 | 3012856 | |||||
chr6:3012874
|
A | C | 10 | a0001c0001t0002g0042a0001c0001t0002g0155a0002c0002t0001g0053others(7): Show | 12 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(9): Show |
intron_variant | MODIFIER | c.303+200A>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3012874 | ||||||
chr6:3012878
|
T | C | 7 | a0003c0004t0001g0113a0003c0004t0001g0128a0003c0004t0001g0129others(4): Show | 7 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.303+204T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3012878 | ||||||
chr6:3012946
|
C | CT | 25 | a0001c0003t0001g0069a0001c0003t0002g0063a0001c0003t0002g0182others(22): Show | 38 | HG00408.hp2 HG00597.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.303+299dupT | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr6 | 3012946 | |||||
chr6:3012946
|
C | CTTTT | 18 | a0001c0001t0003g0025a0001c0001t0003g0026a0001c0001t0003g0065others(15): Show | 27 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.303+296_303+299dup others(4): Show |
NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr6 | 3012946 | |||||
chr6:3012946
|
C | CTTTTT | 24 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0002g0222others(21): Show | 32 | HG00673.hp1 HG01106.hp1 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.303+295_303+299dup others(5): Show |
NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr6 | 3012946 | |||||
chr6:3012946
|
C | CTTTTTT | 6 | a0001c0001t0003g0013a0001c0001t0003g0157a0001c0001t0003g0162others(3): Show | 9 | HG01081.hp1 HG01169.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.303+294_303+299dup others(6): Show |
NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr6 | 3012946 | |||||
chr6:3012946
|
C | CTTTTTTT others(3): Show |
6 | a0001c0001t0001g0125a0001c0001t0001g0131a0001c0001t0001g0212others(3): Show | 6 | HG02109.hp1 HG02258.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.303+290_303+299dup others(10): Show |
NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr6 | 3012946 | |||||
chr6:3012946
|
C | CTTTTTTT others(4): Show |
7 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0080others(4): Show | 9 | HG00733.hp1 HG02630.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.303+289_303+299dup others(11): Show |
NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr6 | 3012946 | |||||
chr6:3012946
|
C | CTTTTTTT others(5): Show |
41 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0016others(38): Show | 60 | HG00544.hp2 HG00609.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.303+288_303+299dup others(12): Show |
NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr6 | 3012946 | |||||
chr6:3012946
|
C | CTTTTTTT others(6): Show |
38 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(35): Show | 52 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.303+287_303+299dup others(13): Show |
NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr6 | 3012946 | |||||
chr6:3012946
|
C | CTTTTTTT others(7): Show |
10 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0001g0036others(7): Show | 13 | HG00280.hp1 HG00642.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.303+286_303+299dup others(14): Show |
NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr6 | 3012946 | |||||
chr6:3012946
|
C | CTTTTTTT others(9): Show |
2 | a0001c0001t0001g0084a0001c0001t0001g0242 | 2 | HG00597.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.303+284_303+299dup others(16): Show |
NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr6 | 3012946 | |||||
chr6:3012946
|
C | CTTTTTTT others(10): Show |
1 | a0001c0001t0001g0034 | 2 | HG01433.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.303+283_303+299dup others(17): Show |
NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr6 | 3012946 | |||||
chr6:3012946
|
C | CTTTTTTT others(11): Show |
1 | a0001c0001t0001g0095 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.303+282_303+299dup others(18): Show |
NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr6 | 3012946 | |||||
chr6:3012946
|
C | CTTTTTTT others(12): Show |
1 | a0003c0004t0001g0128 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.303+281_303+299dup others(19): Show |
NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr6 | 3012946 | |||||
chr6:3012946
|
CT | C | 20 | a0001c0003t0001g0012a0001c0003t0001g0024a0001c0003t0001g0039others(17): Show | 29 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.303+299delT | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr6 | 3012946 | |||||
chr6:3012946
|
CTTTTTTT others(1): Show |
C | 4 | a0001c0001t0001g0106a0001c0003t0001g0011a0001c0003t0001g0133others(1): Show | 7 | HG01192.hp2 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.303+292_303+299del others(8): Show |
NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr6 | 3012946 | |||||
chr6:3013008
|
T | G | 2 | a0001c0001t0003g0161a0001c0001t0003g0168 | 2 | HG02056.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.303+334T>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3013008 | ||||||
chr6:3013025
|
G | T | 5 | a0001c0003t0002g0004a0001c0003t0002g0063a0001c0003t0002g0190others(2): Show | 12 | NA18940.hp1 NA18942.hp2 NA18953.hp1 others(9): Show |
intron_variant | MODIFIER | c.303+351G>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3013025 | ||||||
chr6:3013057
|
G | A | 1 | a0001c0001t0004g0093 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.303+383G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3013057 | ||||||
chr6:3013067
|
C | T | 1 | a0001c0005t0001g0022 | 3 | HG00323.hp2 HG01515.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.303+393C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3013067 | ||||||
chr6:3013080
|
C | T | 159 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(156): Show | 221 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(218): Show |
intron_variant | MODIFIER | c.303+406C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3013080 | ||||||
chr6:3013081
|
G | T | 5 | a0002c0002t0001g0261a0002c0002t0001g0270a0002c0002t0001g0271others(2): Show | 5 | HG00597.hp1 HG02015.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.303+407G>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3013081 | ||||||
chr6:3013146
|
C | T | 2 | a0002c0002t0001g0017a0002c0002t0001g0264 | 5 | HG02027.hp1 NA18981.hp1 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.303+472C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3013146 | ||||||
chr6:3013167
|
G | T | 1 | a0001c0001t0002g0145 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.303+493G>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3013167 | ||||||
chr6:3013176
|
C | T | 1 | a0002c0002t0001g0268 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.303+502C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3013176 | ||||||
chr6:3013177
|
G | A | 9 | a0001c0001t0001g0082a0001c0001t0001g0110a0001c0001t0001g0111others(6): Show | 9 | HG00140.hp1 HG00642.hp2 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.303+503G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3013177 | ||||||
chr6:3013201
|
C | A | 1 | a0001c0001t0001g0229 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.303+527C>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3013201 | ||||||
chr6:3013209
|
C | CT | 10 | a0001c0003t0001g0012a0001c0003t0001g0039a0001c0003t0001g0061others(7): Show | 14 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.303+535_303+536ins others(1): Show |
NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3013209 | ||||||
chr6:3013210
|
C | T | 10 | a0001c0003t0001g0012a0001c0003t0001g0039a0001c0003t0001g0061others(7): Show | 14 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.303+536C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3013210 | ||||||
chr6:3013235
|
G | A | 1 | a0001c0009t0002g0038 | 2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.303+561G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3013235 | ||||||
chr6:3013245
|
G | A | 3 | a0001c0003t0001g0137a0001c0003t0001g0210a0001c0003t0002g0220 | 3 | HG02809.hp2 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.303+571G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3013245 | ||||||
chr6:3013250
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.303+576C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3013250 | ||||||
chr6:3013254
|
C | T | 47 | a0001c0001t0003g0009a0001c0001t0003g0013a0001c0001t0003g0025others(44): Show | 67 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.303+580C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3013254 | ||||||
chr6:3013332
|
G | A | 59 | a0001c0003t0001g0011a0001c0003t0001g0012a0001c0003t0001g0024others(56): Show | 90 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.303+658G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3013332 | ||||||
chr6:3013360
|
A | C | 59 | a0001c0003t0001g0011a0001c0003t0001g0012a0001c0003t0001g0024others(56): Show | 90 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.303+686A>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3013360 | ||||||
chr6:3013370
|
T | G | 59 | a0001c0003t0001g0011a0001c0003t0001g0012a0001c0003t0001g0024others(56): Show | 90 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.303+696T>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3013370 | ||||||
chr6:3013371
|
T | C | 59 | a0001c0003t0001g0011a0001c0003t0001g0012a0001c0003t0001g0024others(56): Show | 90 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.303+697T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3013371 | ||||||
chr6:3013382
|
A | G | 59 | a0001c0003t0001g0011a0001c0003t0001g0012a0001c0003t0001g0024others(56): Show | 90 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.303+708A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3013382 | ||||||
chr6:3013488
|
T | A | 4 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0002g0222others(1): Show | 5 | HG02615.hp1 HG03041.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.303+814T>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3013488 | ||||||
chr6:3013624
|
T | C | 1 | a0006c0012t0002g0188 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.303+950T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3013624 | ||||||
chr6:3013662
|
A | C | 70 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0002g0222others(67): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.303+988A>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3013662 | ||||||
chr6:3013900
|
A | T | 233 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(230): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.303+1226A>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3013900 | ||||||
chr6:3014086
|
G | A | 1 | a0001c0001t0001g0085 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.303+1412G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3014086 | ||||||
chr6:3014197
|
G | A | 1 | a0001c0003t0002g0169 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.304-1333G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3014197 | ||||||
chr6:3014249
|
C | T | 112 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(109): Show | 154 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.304-1281C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3014249 | ||||||
chr6:3014376
|
C | A | 1 | a0001c0001t0003g0202 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.304-1154C>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3014376 | ||||||
chr6:3014393
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.304-1137C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3014393 | ||||||
chr6:3014504
|
C | T | 22 | a0001c0003t0001g0069a0001c0003t0001g0245a0001c0003t0001g0276others(19): Show | 43 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.304-1026C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3014504 | ||||||
chr6:3014553
|
G | T | 6 | a0004c0006t0001g0067a0004c0006t0001g0087a0004c0006t0001g0101others(3): Show | 6 | HG00140.hp1 HG01081.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.304-977G>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3014553 | ||||||
chr6:3014575
|
A | G | 1 | a0001c0003t0001g0137 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.304-955A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3014575 | ||||||
chr6:3014597
|
T | A | 6 | a0004c0006t0001g0067a0004c0006t0001g0087a0004c0006t0001g0101others(3): Show | 6 | HG00140.hp1 HG01081.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.304-933T>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3014597 | ||||||
chr6:3014798
|
TGTGAGCT others(11): Show |
T | 1 | a0001c0003t0002g0169 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.304-729_304-712del others(18): Show |
NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr6 | 3014798 | |||||
chr6:3014858
|
G | C | 1 | a0001c0003t0002g0045 | 2 | HG02165.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.304-672G>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3014858 | ||||||
chr6:3015202
|
G | A | 1 | a0001c0001t0004g0021 | 3 | HG02451.hp2 HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.304-328G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3015202 | ||||||
chr6:3015242
|
A | G | 11 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0002g0222others(8): Show | 12 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.304-288A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3015242 | ||||||
chr6:3015243
|
C | T | 11 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0002g0222others(8): Show | 12 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.304-287C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3015243 | ||||||
chr6:3015255
|
C | T | 58 | a0001c0003t0001g0011a0001c0003t0001g0012a0001c0003t0001g0024others(55): Show | 89 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.304-275C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 4/6 | chr6 | 3015255 | ||||||
chr6:3015664
|
A | T | 59 | a0001c0003t0001g0011a0001c0003t0001g0012a0001c0003t0001g0024others(56): Show | 90 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.417+21A>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 5/6 | chr6 | 3015664 | ||||||
chr6:3015823
|
A | G | 11 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0002g0222others(8): Show | 12 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.417+180A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 5/6 | chr6 | 3015823 | ||||||
chr6:3015842
|
G | C | 3 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0002g0222 | 3 | HG03041.hp1 HG03130.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.417+199G>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 5/6 | chr6 | 3015842 | ||||||
chr6:3015873
|
C | T | 43 | a0001c0001t0003g0009a0001c0001t0003g0013a0001c0001t0003g0025others(40): Show | 59 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.417+230C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 5/6 | chr6 | 3015873 | ||||||
chr6:3015896
|
T | C | 229 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(226): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.417+253T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 5/6 | chr6 | 3015896 | ||||||
chr6:3016015
|
C | T | 12 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0036others(9): Show | 20 | HG01978.hp1 HG01981.hp1 HG02015.hp1 others(17): Show |
intron_variant | MODIFIER | c.417+372C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 5/6 | chr6 | 3016015 | ||||||
chr6:3016037
|
G | A | 1 | a0001c0003t0002g0169 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.417+394G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 5/6 | chr6 | 3016037 | ||||||
chr6:3016066
|
G | A | 2 | a0001c0001t0001g0123a0001c0001t0001g0125 | 2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.417+423G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 5/6 | chr6 | 3016066 | ||||||
chr6:3016152
|
T | C | 229 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(226): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.417+509T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 5/6 | chr6 | 3016152 | ||||||
chr6:3016206
|
G | A | 1 | a0001c0001t0001g0083 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.417+563G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 5/6 | chr6 | 3016206 | ||||||
chr6:3016260
|
A | G | 229 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(226): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.417+617A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 5/6 | chr6 | 3016260 | ||||||
chr6:3016304
|
G | A | 1 | a0001c0001t0002g0154 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.418-580G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 5/6 | chr6 | 3016304 | ||||||
chr6:3016331
|
C | T | 1 | a0001c0003t0002g0205 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.418-553C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 5/6 | chr6 | 3016331 | ||||||
chr6:3016377
|
G | A | 11 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0002g0222others(8): Show | 12 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.418-507G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 5/6 | chr6 | 3016377 | ||||||
chr6:3016430
|
C | CA | 10 | a0001c0005t0002g0207a0002c0002t0001g0053a0002c0002t0001g0097others(7): Show | 11 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(8): Show |
intron_variant | MODIFIER | c.418-434dupA | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr6 | 3016430 | |||||
chr6:3016430
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0002g0206 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.418-445_418-434dup others(12): Show |
NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr6 | 3016430 | |||||
chr6:3016430
|
C | CAAAAAAA others(15): Show |
1 | a0001c0009t0002g0038 | 2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.418-434_418-433ins others(22): Show |
NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr6 | 3016430 | |||||
chr6:3016430
|
C | CAAAAAAA others(24): Show |
1 | a0001c0001t0002g0222 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.418-434_418-433ins others(31): Show |
NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr6 | 3016430 | |||||
chr6:3016430
|
CA | C | 158 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(155): Show | 224 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(221): Show |
intron_variant | MODIFIER | c.418-434delA | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr6 | 3016430 | |||||
chr6:3016430
|
CAA | C | 54 | a0001c0001t0001g0121a0001c0001t0001g0240a0001c0001t0003g0160others(51): Show | 82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.418-435_418-434del others(2): Show |
NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr6 | 3016430 | |||||
chr6:3016456
|
G | A | 1 | a0001c0001t0001g0041 | 2 | HG01358.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.418-428G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 5/6 | chr6 | 3016456 | ||||||
chr6:3016494
|
G | A | 11 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0002g0222others(8): Show | 12 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.418-390G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 5/6 | chr6 | 3016494 | ||||||
chr6:3016498
|
G | A | 113 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(110): Show | 155 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.418-386G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 5/6 | chr6 | 3016498 | ||||||
chr6:3016510
|
G | A | 1 | a0001c0005t0001g0022 | 3 | HG00323.hp2 HG01515.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.418-374G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 5/6 | chr6 | 3016510 | ||||||
chr6:3016560
|
C | T | 11 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0002g0222others(8): Show | 12 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.418-324C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 5/6 | chr6 | 3016560 | ||||||
chr6:3016561
|
A | G | 11 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0002g0222others(8): Show | 12 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.418-323A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 5/6 | chr6 | 3016561 | ||||||
chr6:3016601
|
C | T | 2 | a0002c0002t0002g0165a0002c0002t0002g0166 | 2 | NA19070.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.418-283C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 5/6 | chr6 | 3016601 | ||||||
chr6:3016602
|
G | A | 11 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0002g0222others(8): Show | 12 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.418-282G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 5/6 | chr6 | 3016602 | ||||||
chr6:3016777
|
A | G | 13 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0049others(10): Show | 20 | HG00639.hp2 HG02027.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.418-107A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 5/6 | chr6 | 3016777 | ||||||
chr6:3016780
|
C | T | 3 | a0001c0003t0001g0011a0001c0003t0001g0114a0001c0003t0001g0133 | 6 | HG02559.hp2 HG02615.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.418-104C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 5/6 | chr6 | 3016780 | ||||||
chr6:3016809
|
C | T | 1 | a0002c0002t0001g0262 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.418-75C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 5/6 | chr6 | 3016809 | ||||||
chr6:3016832
|
T | C | 2 | a0001c0003t0002g0063a0001c0003t0002g0192 | 2 | NA18940.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.418-52T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 5/6 | chr6 | 3016832 | ||||||
chr6:3017066
|
ACACG | A | 4 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0002g0222others(1): Show | 5 | HG02615.hp1 HG03041.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.519+85_519+88delGC others(2): Show |
NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 3017066 | |||||
chr6:3017068
|
A | G | 6 | a0001c0001t0004g0015a0001c0001t0004g0127a0001c0001t0004g0134others(3): Show | 9 | HG02280.hp1 HG02809.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.519+83A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3017068 | ||||||
chr6:3017068
|
ACG | A | 7 | a0003c0004t0001g0113a0003c0004t0001g0128a0003c0004t0001g0129others(4): Show | 7 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.519+85_519+86delGC | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 3017068 | |||||
chr6:3017070
|
G | A | 3 | a0001c0003t0001g0137a0001c0003t0001g0210a0001c0003t0002g0220 | 3 | HG02809.hp2 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.519+85G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3017070 | ||||||
chr6:3017076
|
A | G | 57 | a0001c0001t0003g0009a0001c0001t0003g0013a0001c0001t0003g0025others(54): Show | 80 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.519+91A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3017076 | ||||||
chr6:3017097
|
C | T | 1 | a0001c0001t0002g0176 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.519+112C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3017097 | ||||||
chr6:3017164
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.519+179A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3017164 | ||||||
chr6:3017185
|
T | C | 3 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0002g0222 | 3 | HG03041.hp1 HG03130.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.519+200T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3017185 | ||||||
chr6:3017261
|
G | A | 42 | a0001c0001t0003g0009a0001c0001t0003g0013a0001c0001t0003g0025others(39): Show | 58 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.519+276G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3017261 | ||||||
chr6:3017283
|
A | C | 1 | a0001c0001t0003g0159 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.519+298A>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3017283 | ||||||
chr6:3017346
|
G | T | 47 | a0001c0001t0003g0009a0001c0001t0003g0013a0001c0001t0003g0025others(44): Show | 67 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.519+361G>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3017346 | ||||||
chr6:3017573
|
C | T | 2 | a0001c0003t0001g0210a0001c0003t0002g0220 | 2 | HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.519+588C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3017573 | ||||||
chr6:3017597
|
G | T | 11 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0002g0222others(8): Show | 12 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.519+612G>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3017597 | ||||||
chr6:3017627
|
A | C | 48 | a0001c0001t0003g0009a0001c0001t0003g0013a0001c0001t0003g0025others(45): Show | 68 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.519+642A>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3017627 | ||||||
chr6:3017669
|
C | T | 11 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0002g0222others(8): Show | 12 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.519+684C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3017669 | ||||||
chr6:3017695
|
A | G | 170 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(167): Show | 243 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.519+710A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3017695 | ||||||
chr6:3017726
|
C | A | 1 | a0002c0002t0002g0147 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.519+741C>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3017726 | ||||||
chr6:3017740
|
A | G | 11 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0002g0222others(8): Show | 12 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.519+755A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3017740 | ||||||
chr6:3017812
|
C | T | 2 | a0001c0003t0001g0118a0001c0005t0001g0022 | 4 | HG00323.hp2 HG01515.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.519+827C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3017812 | ||||||
chr6:3017855
|
A | G | 1 | a0001c0003t0002g0169 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.519+870A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3017855 | ||||||
chr6:3017878
|
T | C | 12 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0002g0222others(9): Show | 13 | HG00099.hp1 HG01109.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.519+893T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3017878 | ||||||
chr6:3017910
|
T | G | 12 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0002g0222others(9): Show | 13 | HG00099.hp1 HG01109.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.519+925T>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3017910 | ||||||
chr6:3017940
|
T | C | 217 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(214): Show | 310 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.519+955T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3017940 | ||||||
chr6:3017950
|
A | G | 1 | a0001c0003t0001g0210 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.519+965A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3017950 | ||||||
chr6:3017992
|
T | A | 12 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0002g0222others(9): Show | 13 | HG00099.hp1 HG01109.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.519+1007T>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3017992 | ||||||
chr6:3018003
|
T | C | 12 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0002g0222others(9): Show | 13 | HG00099.hp1 HG01109.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.519+1018T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3018003 | ||||||
chr6:3018012
|
AGTGCACA others(31): Show |
A | 1 | a0002c0002t0002g0199 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.519+1030_519+1067d others(40): Show |
NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 3018012 | |||||
chr6:3018150
|
G | A | 12 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0002g0222others(9): Show | 13 | HG00099.hp1 HG01109.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.519+1165G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3018150 | ||||||
chr6:3018163
|
T | G | 45 | a0001c0003t0001g0012a0001c0003t0001g0024a0001c0003t0001g0039others(42): Show | 73 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.519+1178T>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3018163 | ||||||
chr6:3018209
|
A | G | 3 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0091 | 3 | HG01074.hp1 HG02698.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.519+1224A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3018209 | ||||||
chr6:3018221
|
C | T | 12 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0002g0222others(9): Show | 13 | HG00099.hp1 HG01109.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.519+1236C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3018221 | ||||||
chr6:3018225
|
A | G | 229 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(226): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.519+1240A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3018225 | ||||||
chr6:3018228
|
T | C | 12 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0002g0222others(9): Show | 13 | HG00099.hp1 HG01109.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.519+1243T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3018228 | ||||||
chr6:3018235
|
G | A | 2 | a0001c0005t0002g0207a0001c0005t0002g0214 | 2 | HG02486.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.520-1244G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3018235 | ||||||
chr6:3018244
|
C | T | 12 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0002g0222others(9): Show | 13 | HG00099.hp1 HG01109.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.520-1235C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3018244 | ||||||
chr6:3018254
|
T | C | 12 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0002g0222others(9): Show | 13 | HG00099.hp1 HG01109.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.520-1225T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3018254 | ||||||
chr6:3018285
|
C | T | 12 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0002g0222others(9): Show | 13 | HG00099.hp1 HG01109.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.520-1194C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3018285 | ||||||
chr6:3018361
|
C | T | 9 | a0001c0003t0001g0024a0001c0003t0001g0070a0001c0003t0001g0143others(6): Show | 12 | HG01891.hp2 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.520-1118C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3018361 | ||||||
chr6:3018420
|
G | A | 1 | a0001c0001t0003g0164 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.520-1059G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3018420 | ||||||
chr6:3018434
|
G | A | 1 | a0002c0002t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.520-1045G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3018434 | ||||||
chr6:3018470
|
A | G | 169 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(166): Show | 242 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.520-1009A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3018470 | ||||||
chr6:3018500
|
A | C | 12 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0002g0222others(9): Show | 13 | HG00099.hp1 HG01109.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.520-979A>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3018500 | ||||||
chr6:3018540
|
G | C | 230 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(227): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.520-939G>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3018540 | ||||||
chr6:3018577
|
T | A | 47 | a0001c0001t0003g0009a0001c0001t0003g0013a0001c0001t0003g0025others(44): Show | 67 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.520-902T>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3018577 | ||||||
chr6:3018600
|
C | A | 1 | a0001c0003t0002g0189 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.520-879C>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3018600 | ||||||
chr6:3018661
|
C | T | 13 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0049others(10): Show | 20 | HG00639.hp2 HG02027.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.520-818C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3018661 | ||||||
chr6:3018703
|
C | T | 12 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0002g0222others(9): Show | 13 | HG00099.hp1 HG01109.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.520-776C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3018703 | ||||||
chr6:3018748
|
T | G | 170 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(167): Show | 243 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.520-731T>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3018748 | ||||||
chr6:3018796
|
T | C | 51 | a0001c0003t0001g0011a0001c0003t0001g0012a0001c0003t0001g0024others(48): Show | 82 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.520-683T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3018796 | ||||||
chr6:3018833
|
C | CT | 15 | a0001c0003t0001g0012a0001c0003t0001g0039a0001c0003t0001g0061others(12): Show | 19 | HG01243.hp1 HG01884.hp2 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.520-635dupT | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 3018833 | |||||
chr6:3018833
|
CT | C | 12 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0002g0222others(9): Show | 13 | HG00099.hp1 HG01109.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.520-635delT | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 3018833 | |||||
chr6:3018858
|
T | C | 47 | a0001c0001t0003g0009a0001c0001t0003g0013a0001c0001t0003g0025others(44): Show | 67 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.520-621T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3018858 | ||||||
chr6:3018870
|
C | CAA | 4 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0002g0222others(1): Show | 4 | HG01192.hp2 HG03041.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-609_520-608ins others(2): Show |
NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3018870 | ||||||
chr6:3018870
|
C | CAAA | 8 | a0001c0009t0002g0038a0003c0004t0001g0113a0003c0004t0001g0128others(5): Show | 9 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.520-609_520-608ins others(3): Show |
NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3018870 | ||||||
chr6:3018871
|
C | A | 12 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0002g0222others(9): Show | 13 | HG00099.hp1 HG01109.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.520-608C>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3018871 | ||||||
chr6:3018881
|
A | G | 46 | a0001c0001t0003g0009a0001c0001t0003g0013a0001c0001t0003g0025others(43): Show | 66 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.520-598A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3018881 | ||||||
chr6:3018910
|
A | G | 12 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0002g0222others(9): Show | 13 | HG00099.hp1 HG01109.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.520-569A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3018910 | ||||||
chr6:3018923
|
CT | C | 12 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0002g0222others(9): Show | 13 | HG00099.hp1 HG01109.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.520-555delT | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3018923 | ||||||
chr6:3018975
|
C | CT | 12 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0002g0222others(9): Show | 13 | HG00099.hp1 HG01109.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.520-503dupT | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 3018975 | |||||
chr6:3019059
|
G | A | 7 | a0003c0004t0001g0113a0003c0004t0001g0128a0003c0004t0001g0129others(4): Show | 7 | HG00099.hp1 HG01109.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.520-420G>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3019059 | ||||||
chr6:3019190
|
C | T | 1 | a0002c0002t0001g0265 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.520-289C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3019190 | ||||||
chr6:3019283
|
G | T | 1 | a0002c0002t0001g0097 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.520-196G>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3019283 | ||||||
chr6:3019334
|
A | G | 1 | a0001c0001t0001g0068 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.520-145A>G | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3019334 | ||||||
chr6:3019400
|
C | T | 12 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0002g0222others(9): Show | 13 | HG00099.hp1 HG01109.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.520-79C>T | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3019400 | ||||||
chr6:3019420
|
T | C | 229 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(226): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.520-59T>C | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3019420 | ||||||
chr6:3019456
|
C | A | 3 | a0001c0003t0001g0011a0001c0003t0001g0114a0001c0003t0001g0133 | 6 | HG02559.hp2 HG02615.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.520-23C>A | NQO2 | ENSG00000124588.22 | transcript | ENST00000380455.11 | protein_coding | 6/6 | chr6 | 3019456 |