geneid | 4780 |
---|---|
ensemblid | ENSG00000116044.17 |
hgncid | 7782 |
symbol | NFE2L2 |
name | NFE2 like bZIP transcription factor 2 |
refseq_nuc | NM_006164.5 |
refseq_prot | NP_006155.2 |
ensembl_nuc | ENST00000397062.8 |
ensembl_prot | ENSP00000380252.3 |
mane_status | MANE Select |
chr | chr2 |
start | 177230308 |
end | 177264727 |
strand | - |
ver | v1.2 |
region | chr2:177230308-177264727 |
region5000 | chr2:177225308-177269727 |
regionname0 | NFE2L2_chr2_177230308_177264727 |
regionname5000 | NFE2L2_chr2_177225308_177269727 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 605 | 320 | 90 | 70 | 120 | 14 | 24 | 86 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
a0002 | 0/0 | 605 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
a0003 | 0/0 | 605 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
a0004 | 0/0 | 605 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
a0005 | 0/0 | 605 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1818 | 319 | 90 | 69 | 120 | 14 | 24 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
c0002 | 0/0 | 1818 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
c0003 | 0/0 | 1818 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
c0004 | 0/0 | 1818 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
c0005 | 0/0 | 1818 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
c0006 | 0/0 | 1818 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 629 | 187 | 56 | 44 | 66 | 7 | 12 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
t0002 | 0/0 | 626 | 103 | 13 | 21 | 50 | 7 | 12 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
t0003 | 0/0 | 620 | 8 | 8 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
t0004 | 0/0 | 628 | 6 | 1 | 4 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
t0005 | 0/0 | 629 | 6 | 6 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
t0006 | 0/0 | 625 | 4 | 0 | 0 | 4 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
t0007 | 0/0 | 629 | 4 | 4 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
t0008 | 0/0 | 626 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
t0009 | 0/0 | 629 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
t0010 | 0/0 | 629 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
t0011 | 0/0 | 620 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
t0012 | 0/0 | 626 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
t0013 | 0/0 | 629 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 30 | 0 | 5 | 20 | 1 | 4 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0002 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0005 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0006 | 0/0 | 5 | 0 | 2 | 1 | 0 | 2 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0008 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0009 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0010 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0013 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0016 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0029 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0146 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0167 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1818 | 319 | 90 | 69 | 120 | 14 | 24 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
a0001c0005 | 0/0 | 1818 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
a0002c0002 | 0/0 | 1818 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
a0003c0003 | 0/0 | 1818 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
a0004c0004 | 0/0 | 1818 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
a0005c0006 | 0/0 | 1818 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2446 | 182 | 53 | 43 | 65 | 7 | 12 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
a0001c0001t0002 | 0/0 | 2443 | 102 | 13 | 21 | 49 | 7 | 12 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
a0001c0001t0003 | 0/0 | 2437 | 8 | 8 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
a0001c0001t0004 | 0/0 | 2445 | 5 | 0 | 4 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
a0001c0001t0005 | 0/0 | 2446 | 6 | 6 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
a0001c0001t0006 | 0/0 | 2442 | 4 | 0 | 0 | 4 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
a0001c0001t0007 | 0/0 | 2446 | 4 | 4 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
a0001c0001t0008 | 0/0 | 2443 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
a0001c0001t0009 | 0/0 | 2446 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
a0001c0001t0010 | 0/0 | 2446 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
a0001c0001t0011 | 0/0 | 2437 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
a0001c0001t0012 | 0/0 | 2443 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
a0001c0001t0013 | 0/0 | 2446 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
a0001c0005t0001 | 0/0 | 2446 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
a0002c0002t0001 | 0/0 | 2446 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
a0003c0003t0001 | 0/0 | 2446 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
a0003c0003t0004 | 0/0 | 2445 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
a0004c0004t0002 | 0/0 | 2443 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
a0005c0006t0001 | 0/0 | 2446 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | copy fasta | chr2 | 177225308 | 177269727 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0005 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0146 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0167 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0001 | 0/0 | 30 | 0 | 5 | 20 | 1 | 4 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0006 | 0/0 | 5 | 0 | 2 | 1 | 0 | 2 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0009 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0013 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0004g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0004g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0004g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0005g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0005g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0006g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0006g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0006g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0007g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0007g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0008g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0009g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0010g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0011g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0012g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0001t0013g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0001c0005t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0002c0002t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0003c0003t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0003c0003t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0004c0004t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
a0005c0006t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0009 | EUR | GBR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | GBR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | GBR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0120 | EUR | GBR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | FIN | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0065 | EUR | FIN | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0022 | EUR | FIN | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | CHS | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | CHS | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | CHS | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0056 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG00735 | hp1 | a0001 | c0001 | t0010 | g0038 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG00738 | hp1 | a0001 | c0005 | t0001 | g0126 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01257 | hp2 | a0001 | c0001 | t0004 | g0149 | AMR | CLM | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01258 | hp2 | a0001 | c0001 | t0004 | g0028 | AMR | CLM | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | CLM | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | CLM | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0013 | EUR | IBS | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0013 | EUR | IBS | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0132 | EUR | IBS | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | ACB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | ACB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01928 | hp1 | a0001 | c0001 | t0004 | g0150 | AMR | PEL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01952 | hp2 | a0001 | c0001 | t0004 | g0028 | AMR | PEL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | KHV | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | KHV | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | KHV | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | ACB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02055 | hp2 | a0001 | c0001 | t0003 | g0041 | AFR | ACB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | KHV | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | KHV | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02129 | hp2 | a0001 | c0001 | t0006 | g0024 | EAS | KHV | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0042 | AFR | ACB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | ACB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | CDX | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | CDX | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02257 | hp1 | a0002 | c0002 | t0001 | g0033 | AFR | ACB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02280 | hp1 | a0001 | c0001 | t0009 | g0032 | AFR | ACB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02280 | hp2 | a0001 | c0001 | t0007 | g0020 | AFR | ACB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PEL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0075 | AMR | PEL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | KHV | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02615 | hp1 | a0001 | c0001 | t0008 | g0021 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02630 | hp1 | a0001 | c0001 | t0008 | g0021 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02647 | hp2 | a0001 | c0001 | t0009 | g0032 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02717 | hp1 | a0001 | c0001 | t0005 | g0200 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02723 | hp1 | a0001 | c0001 | t0005 | g0019 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0086 | SAS | PJL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02895 | hp1 | a0003 | c0003 | t0001 | g0170 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02896 | hp1 | a0001 | c0001 | t0007 | g0020 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02897 | hp1 | a0003 | c0003 | t0004 | g0171 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02897 | hp2 | a0001 | c0001 | t0007 | g0204 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02922 | hp1 | a0001 | c0001 | t0005 | g0019 | AFR | ESN | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | ESN | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG03098 | hp1 | a0001 | c0001 | t0013 | g0207 | AFR | MSL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | ESN | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG03195 | hp1 | a0001 | c0001 | t0005 | g0019 | AFR | ESN | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG03195 | hp2 | a0001 | c0001 | t0007 | g0020 | AFR | ESN | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | MSL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG03225 | hp2 | a0001 | c0001 | t0005 | g0135 | AFR | MSL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | MSL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0040 | AFR | MSL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | ESN | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG03540 | hp1 | a0001 | c0001 | t0005 | g0202 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | MSL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | STU | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | STU | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0087 | SAS | BEB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0083 | SAS | BEB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0081 | SAS | BEB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0048 | SAS | STU | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | STU | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0102 | SAS | BEB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | BEB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | STU | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | STU | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | YRI | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | YRI | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18747 | hp2 | a0001 | c0001 | t0004 | g0161 | EAS | CHB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | YRI | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | YRI | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18951 | hp2 | a0004 | c0004 | t0002 | g0072 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18968 | hp2 | a0001 | c0001 | t0012 | g0076 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18987 | hp2 | a0001 | c0001 | t0006 | g0103 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18990 | hp2 | a0001 | c0001 | t0006 | g0024 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA18999 | hp2 | a0001 | c0001 | t0006 | g0104 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA19000 | hp1 | a0005 | c0006 | t0001 | g0158 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | LWK | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0039 | AFR | LWK | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA19043 | hp1 | a0002 | c0002 | t0001 | g0033 | AFR | LWK | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | LWK | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | YRI | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA19240 | hp2 | a0001 | c0001 | t0011 | g0046 | AFR | YRI | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | ASW | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0047 | AFR | ASW | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0013 | EUR | TSI | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | TSI | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | MSL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | USA | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | USA | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | USA | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0073 | AFR | USA | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | LWK | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | LWK | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0167 | REF | REF | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0146 | REF | REF | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:177231257
|
C | T | 1 | a0004 | 1 | NA18951.hp2 | missense_variant | MODERATE | c.1346G>A | p.Arg449His | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 5/5 | 1497/2446 | 1346/1818 | 449/605 | chr2 | 177231257 | ||
chr2:177231906
|
G | A | 1 | a0005 | 1 | NA19000.hp1 | missense_variant | MODERATE | c.697C>T | p.Pro233Ser | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 5/5 | 848/2446 | 697/1818 | 233/605 | chr2 | 177231906 | ||
chr2:177231947
|
T | C | 1 | a0003 | 2 | HG02895.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.656A>G | p.Lys219Arg | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 5/5 | 807/2446 | 656/1818 | 219/605 | chr2 | 177231947 | ||
chr2:177234189
|
C | T | 1 | a0002 | 2 | HG02257.hp1 NA19043.hp1 |
missense_variant | MODERATE | c.128G>A | p.Arg43Gln | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 2/5 | 279/2446 | 128/1818 | 43/605 | chr2 | 177234189 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:177231559
|
T | C | 1 | a0001c0005 | 1 | HG00738.hp1 | synonymous_variant | LOW | c.1044A>G | p.Leu348Leu | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 5/5 | 1195/2446 | 1044/1818 | 348/605 | chr2 | 177231559 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:177230317
|
C | T | 1 | a0001c0001t0007 | 4 | HG02280.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*468G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 5/5 | 468 | chr2 | 177230317 | |||||
chr2:177230350
|
AT | A | 3 | a0001c0001t0004a0001c0001t0006a0003c0003t0004 | 10 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*434delA | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 5/5 | 434 | chr2 | 177230350 | |||||
chr2:177230374
|
A | C | 1 | a0001c0001t0012 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*411T>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 5/5 | 411 | chr2 | 177230374 | |||||
chr2:177230431
|
T | C | 1 | a0001c0001t0013 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*354A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 5/5 | 354 | chr2 | 177230431 | |||||
chr2:177230617
|
T | C | 2 | a0001c0001t0008a0001c0001t0009 | 4 | HG02280.hp1 HG02615.hp1 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*168A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 5/5 | 168 | chr2 | 177230617 | |||||
chr2:177230697
|
T | C | 1 | a0001c0001t0011 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*88A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 5/5 | 88 | chr2 | 177230697 | |||||
chr2:177230767
|
G | C | 2 | a0001c0001t0005a0001c0001t0010 | 7 | HG00735.hp1 HG02717.hp1 HG02723.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*18C>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 5/5 | 18 | chr2 | 177230767 | |||||
chr2:177264662
|
TGGC | T | 5 | a0001c0001t0002a0001c0001t0006a0001c0001t0008others(2): Show | 110 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(107): Show |
5_prime_UTR_variant | MODIFIER | c.-89_-87delGCC | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/5 | 87 | chr2 | 177264662 | |||||
chr2:177264662
|
TGGCGGCG others(2): Show |
T | 2 | a0001c0001t0003a0001c0001t0011 | 9 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-95_-87delGCCGCCGC others(1): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/5 | 87 | chr2 | 177264662 | |||||
chr2:177264684
|
G | T | 1 | a0001c0001t0010 | 1 | HG00735.hp1 | 5_prime_UTR_variant | MODIFIER | c.-108C>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/5 | 108 | chr2 | 177264684 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:177232109
|
T | A | 2 | a0001c0001t0002g0077a0001c0001t0002g0082 | 2 | HG00609.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.595-101A>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 4/4 | chr2 | 177232109 | ||||||
chr2:177232111
|
T | G | 5 | a0001c0001t0005g0019a0001c0001t0005g0135a0001c0001t0005g0200others(2): Show | 7 | HG00735.hp1 HG02717.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.595-103A>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 4/4 | chr2 | 177232111 | ||||||
chr2:177232688
|
C | G | 1 | a0001c0001t0001g0153 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.403-105G>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 3/4 | chr2 | 177232688 | ||||||
chr2:177232704
|
C | T | 1 | a0001c0001t0002g0075 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.403-121G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 3/4 | chr2 | 177232704 | ||||||
chr2:177232740
|
T | G | 1 | a0001c0001t0001g0174 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.403-157A>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 3/4 | chr2 | 177232740 | ||||||
chr2:177232764
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.403-181T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 3/4 | chr2 | 177232764 | ||||||
chr2:177232817
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.403-234C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 3/4 | chr2 | 177232817 | ||||||
chr2:177232859
|
C | G | 2 | a0001c0001t0002g0013a0001c0001t0002g0099 | 4 | HG01167.hp2 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.403-276G>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 3/4 | chr2 | 177232859 | ||||||
chr2:177232936
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.402+314G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 3/4 | chr2 | 177232936 | ||||||
chr2:177232938
|
C | T | 51 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(48): Show | 68 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.402+312G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 3/4 | chr2 | 177232938 | ||||||
chr2:177233064
|
T | C | 2 | a0001c0001t0001g0201a0001c0001t0002g0057 | 2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.402+186A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 3/4 | chr2 | 177233064 | ||||||
chr2:177233359
|
CA | C | 6 | a0001c0001t0001g0016a0001c0001t0001g0025a0001c0001t0001g0110others(3): Show | 9 | HG00140.hp2 HG00733.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.313-21delT | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 2/4 | chr2 | 177233359 | ||||||
chr2:177233364
|
G | A | 2 | a0001c0001t0001g0174a0001c0001t0013g0207 | 2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.313-25C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 2/4 | chr2 | 177233364 | ||||||
chr2:177233582
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.313-243G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 2/4 | chr2 | 177233582 | ||||||
chr2:177233774
|
G | T | 7 | a0001c0001t0004g0028a0001c0001t0004g0149a0001c0001t0004g0150others(4): Show | 9 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.312+231C>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 2/4 | chr2 | 177233774 | ||||||
chr2:177233932
|
C | T | 7 | a0001c0001t0004g0028a0001c0001t0004g0149a0001c0001t0004g0150others(4): Show | 9 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.312+73G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 2/4 | chr2 | 177233932 | ||||||
chr2:177233951
|
C | T | 10 | a0001c0001t0001g0216a0001c0001t0002g0059a0001c0001t0002g0060others(7): Show | 10 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.312+54G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 2/4 | chr2 | 177233951 | ||||||
chr2:177233994
|
G | A | 3 | a0001c0001t0003g0040a0001c0001t0003g0042a0001c0001t0003g0044 | 3 | HG02145.hp1 HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.312+11C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 2/4 | chr2 | 177233994 | ||||||
chr2:177234345
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.46-74G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177234345 | ||||||
chr2:177234532
|
G | A | 2 | a0001c0001t0001g0172a0001c0001t0001g0210 | 2 | HG03704.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.46-261C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177234532 | ||||||
chr2:177234605
|
T | C | 1 | a0001c0001t0001g0217 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.46-334A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177234605 | ||||||
chr2:177234735
|
T | C | 7 | a0001c0001t0004g0028a0001c0001t0004g0149a0001c0001t0004g0150others(4): Show | 9 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-464A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177234735 | ||||||
chr2:177234794
|
C | T | 1 | a0001c0001t0002g0093 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.46-523G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177234794 | ||||||
chr2:177234802
|
T | A | 1 | a0001c0001t0002g0074 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.46-531A>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177234802 | ||||||
chr2:177234884
|
G | C | 95 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(92): Show | 163 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.46-613C>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177234884 | ||||||
chr2:177234925
|
G | C | 1 | a0001c0001t0001g0121 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.46-654C>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177234925 | ||||||
chr2:177234987
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.46-716C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177234987 | ||||||
chr2:177235040
|
C | T | 1 | a0001c0001t0013g0207 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.46-769G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177235040 | ||||||
chr2:177235047
|
G | A | 4 | a0001c0001t0002g0050a0001c0001t0002g0051a0001c0001t0002g0052others(1): Show | 4 | HG02145.hp2 HG02572.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-776C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177235047 | ||||||
chr2:177235070
|
T | G | 1 | a0001c0001t0001g0134 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.46-799A>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177235070 | ||||||
chr2:177235164
|
G | A | 2 | a0001c0001t0001g0172a0001c0001t0001g0210 | 2 | HG03704.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.46-893C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177235164 | ||||||
chr2:177235169
|
C | T | 7 | a0001c0001t0001g0216a0001c0001t0002g0059a0001c0001t0002g0060others(4): Show | 7 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.46-898G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177235169 | ||||||
chr2:177235187
|
A | G | 7 | a0001c0001t0004g0028a0001c0001t0004g0149a0001c0001t0004g0150others(4): Show | 9 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-916T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177235187 | ||||||
chr2:177235275
|
AAAC | A | 3 | a0001c0001t0001g0109a0001c0001t0001g0174a0001c0001t0013g0207 | 3 | HG02976.hp2 HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.46-1007_46-1005del others(3): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177235275 | ||||||
chr2:177235342
|
T | TA | 7 | a0001c0001t0004g0028a0001c0001t0004g0149a0001c0001t0004g0150others(4): Show | 9 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-1072dupT | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177235342 | ||||||
chr2:177235362
|
A | G | 5 | a0001c0001t0005g0019a0001c0001t0005g0135a0001c0001t0005g0200others(2): Show | 7 | HG00735.hp1 HG02717.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.46-1091T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177235362 | ||||||
chr2:177235694
|
A | G | 1 | a0001c0001t0001g0142 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.46-1423T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177235694 | ||||||
chr2:177235697
|
C | T | 173 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0008others(170): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.46-1426G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177235697 | ||||||
chr2:177235740
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.46-1469A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177235740 | ||||||
chr2:177236007
|
G | A | 2 | a0001c0001t0002g0050a0001c0001t0002g0051 | 2 | HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.46-1736C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177236007 | ||||||
chr2:177236080
|
A | G | 8 | a0001c0001t0001g0137a0001c0001t0001g0220a0001c0001t0003g0040others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.46-1809T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177236080 | ||||||
chr2:177236464
|
A | G | 2 | a0003c0003t0001g0170a0003c0003t0004g0171 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.46-2193T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177236464 | ||||||
chr2:177236486
|
T | C | 14 | a0001c0001t0001g0216a0001c0001t0002g0059a0001c0001t0002g0060others(11): Show | 16 | HG01081.hp1 HG01109.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.46-2215A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177236486 | ||||||
chr2:177236507
|
C | T | 90 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0008others(87): Show | 153 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.46-2236G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177236507 | ||||||
chr2:177236598
|
A | G | 7 | a0001c0001t0001g0216a0001c0001t0002g0059a0001c0001t0002g0060others(4): Show | 7 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.46-2327T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177236598 | ||||||
chr2:177236599
|
C | A | 1 | a0001c0001t0001g0192 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.46-2328G>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177236599 | ||||||
chr2:177236833
|
G | T | 14 | a0001c0001t0001g0216a0001c0001t0002g0059a0001c0001t0002g0060others(11): Show | 16 | HG01081.hp1 HG01109.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.46-2562C>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177236833 | ||||||
chr2:177237035
|
C | A | 7 | a0001c0001t0004g0028a0001c0001t0004g0149a0001c0001t0004g0150others(4): Show | 9 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-2764G>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177237035 | ||||||
chr2:177237048
|
T | C | 6 | a0001c0001t0002g0050a0001c0001t0002g0051a0001c0001t0002g0052others(3): Show | 6 | HG02145.hp2 HG02572.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.46-2777A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177237048 | ||||||
chr2:177237222
|
G | A | 21 | a0001c0001t0001g0172a0001c0001t0001g0210a0001c0001t0001g0216others(18): Show | 25 | HG00735.hp1 HG01081.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.46-2951C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177237222 | ||||||
chr2:177237527
|
AT | A | 19 | a0001c0001t0001g0216a0001c0001t0002g0059a0001c0001t0002g0060others(16): Show | 23 | HG00735.hp1 HG01081.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.46-3257delA | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177237527 | ||||||
chr2:177237557
|
C | T | 7 | a0001c0001t0001g0216a0001c0001t0002g0059a0001c0001t0002g0060others(4): Show | 7 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.46-3286G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177237557 | ||||||
chr2:177237879
|
C | T | 219 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(216): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.46-3608G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177237879 | ||||||
chr2:177237950
|
A | G | 1 | a0001c0001t0001g0205 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.46-3679T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177237950 | ||||||
chr2:177237969
|
G | T | 7 | a0001c0001t0001g0216a0001c0001t0002g0059a0001c0001t0002g0060others(4): Show | 7 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.46-3698C>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177237969 | ||||||
chr2:177238275
|
ATCT | A | 7 | a0001c0001t0004g0028a0001c0001t0004g0149a0001c0001t0004g0150others(4): Show | 9 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-4007_46-4005del others(3): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177238275 | ||||||
chr2:177238501
|
A | G | 91 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0008others(88): Show | 154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.46-4230T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177238501 | ||||||
chr2:177238600
|
C | T | 7 | a0001c0001t0004g0028a0001c0001t0004g0149a0001c0001t0004g0150others(4): Show | 9 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-4329G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177238600 | ||||||
chr2:177238609
|
T | G | 2 | a0001c0001t0001g0172a0001c0001t0001g0210 | 2 | HG03704.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.46-4338A>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177238609 | ||||||
chr2:177238664
|
G | A | 2 | a0001c0001t0001g0172a0001c0001t0001g0210 | 2 | HG03704.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.46-4393C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177238664 | ||||||
chr2:177238786
|
C | T | 1 | a0001c0001t0001g0199 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.46-4515G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177238786 | ||||||
chr2:177239175
|
T | C | 1 | a0001c0001t0002g0078 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.46-4904A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177239175 | ||||||
chr2:177239366
|
C | G | 1 | a0001c0001t0002g0052 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.46-5095G>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177239366 | ||||||
chr2:177239378
|
T | G | 1 | a0001c0001t0001g0118 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.46-5107A>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177239378 | ||||||
chr2:177239513
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.46-5242G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177239513 | ||||||
chr2:177239681
|
AAAAGTTT others(37): Show |
A | 1 | a0001c0001t0001g0172 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.46-5454_46-5411del others(44): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177239681 | ||||||
chr2:177239717
|
T | G | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG00735.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.46-5446A>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177239717 | ||||||
chr2:177239949
|
T | TA | 18 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0143others(15): Show | 31 | HG00544.hp2 HG00642.hp2 HG01168.hp2 others(28): Show |
intron_variant | MODIFIER | c.46-5679dupT | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177239949 | ||||||
chr2:177239949
|
TA | T | 162 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(159): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.46-5679delT | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177239949 | ||||||
chr2:177239949
|
TAA | T | 6 | a0001c0001t0001g0121a0001c0001t0001g0185a0001c0001t0002g0061others(3): Show | 6 | HG01106.hp2 HG01167.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.46-5680_46-5679del others(2): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177239949 | ||||||
chr2:177240032
|
A | G | 2 | a0001c0001t0002g0067a0001c0001t0002g0068 | 2 | HG02523.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.46-5761T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177240032 | ||||||
chr2:177240270
|
C | G | 1 | a0001c0001t0001g0113 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.46-5999G>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177240270 | ||||||
chr2:177240311
|
G | T | 2 | a0001c0001t0001g0196a0001c0001t0001g0197 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.46-6040C>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177240311 | ||||||
chr2:177240416
|
A | G | 167 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(164): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.46-6145T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177240416 | ||||||
chr2:177240644
|
G | C | 1 | a0001c0001t0002g0079 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.46-6373C>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177240644 | ||||||
chr2:177240803
|
G | A | 2 | a0001c0001t0002g0087a0001c0001t0002g0102 | 2 | HG03831.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.46-6532C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177240803 | ||||||
chr2:177240948
|
A | G | 7 | a0001c0001t0004g0028a0001c0001t0004g0149a0001c0001t0004g0150others(4): Show | 9 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-6677T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177240948 | ||||||
chr2:177240994
|
C | T | 7 | a0001c0001t0004g0028a0001c0001t0004g0149a0001c0001t0004g0150others(4): Show | 9 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-6723G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177240994 | ||||||
chr2:177241043
|
G | C | 7 | a0001c0001t0004g0028a0001c0001t0004g0149a0001c0001t0004g0150others(4): Show | 9 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-6772C>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177241043 | ||||||
chr2:177241118
|
T | C | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.46-6847A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177241118 | ||||||
chr2:177241268
|
C | G | 87 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0018others(84): Show | 146 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.46-6997G>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177241268 | ||||||
chr2:177241607
|
C | T | 2 | a0001c0001t0001g0172a0001c0001t0001g0210 | 2 | HG03704.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.46-7336G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177241607 | ||||||
chr2:177241998
|
G | A | 1 | a0001c0001t0013g0207 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.46-7727C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177241998 | ||||||
chr2:177242030
|
A | C | 7 | a0001c0001t0005g0019a0001c0001t0005g0135a0001c0001t0005g0200others(4): Show | 9 | HG00735.hp1 HG02717.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-7759T>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177242030 | ||||||
chr2:177242163
|
T | A | 1 | a0001c0001t0001g0175 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.46-7892A>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177242163 | ||||||
chr2:177242234
|
G | A | 3 | a0001c0001t0001g0134a0001c0001t0001g0174a0001c0001t0013g0207 | 3 | HG02818.hp1 HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.46-7963C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177242234 | ||||||
chr2:177242374
|
T | A | 1 | a0001c0001t0001g0206 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.46-8103A>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177242374 | ||||||
chr2:177242433
|
A | G | 2 | a0001c0001t0002g0063a0001c0001t0002g0064 | 2 | HG01109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.46-8162T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177242433 | ||||||
chr2:177242899
|
G | T | 7 | a0001c0001t0005g0019a0001c0001t0005g0135a0001c0001t0005g0200others(4): Show | 9 | HG00735.hp1 HG02717.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-8628C>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177242899 | ||||||
chr2:177242900
|
T | TG | 6 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.46-8630_46-8629ins others(1): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177242900 | ||||||
chr2:177242908
|
T | G | 2 | a0001c0001t0005g0135a0001c0001t0010g0038 | 2 | HG00735.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.46-8637A>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177242908 | ||||||
chr2:177242910
|
G | GT | 14 | a0001c0001t0001g0152a0001c0001t0003g0040a0001c0001t0003g0041others(11): Show | 16 | HG01257.hp2 HG01258.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.46-8640dupA | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177242910 | ||||||
chr2:177242910
|
G | T | 7 | a0001c0001t0005g0019a0001c0001t0005g0135a0001c0001t0005g0200others(4): Show | 9 | HG00735.hp1 HG02717.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-8639C>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177242910 | ||||||
chr2:177242990
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.46-8719C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177242990 | ||||||
chr2:177243150
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.46-8879A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177243150 | ||||||
chr2:177243214
|
T | G | 1 | a0001c0001t0001g0026 | 2 | HG00099.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.46-8943A>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177243214 | ||||||
chr2:177243227
|
C | T | 1 | a0001c0001t0002g0071 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.46-8956G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177243227 | ||||||
chr2:177243333
|
T | A | 1 | a0001c0001t0001g0029 | 2 | HG00140.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.46-9062A>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177243333 | ||||||
chr2:177243421
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.46-9150G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177243421 | ||||||
chr2:177243474
|
G | A | 2 | a0001c0001t0002g0050a0001c0001t0002g0051 | 2 | HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.46-9203C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177243474 | ||||||
chr2:177243522
|
A | AT | 7 | a0001c0001t0004g0028a0001c0001t0004g0149a0001c0001t0004g0150others(4): Show | 9 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-9252dupA | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177243522 | ||||||
chr2:177243765
|
A | C | 7 | a0001c0001t0004g0028a0001c0001t0004g0149a0001c0001t0004g0150others(4): Show | 9 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-9494T>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177243765 | ||||||
chr2:177243824
|
C | T | 5 | a0001c0001t0001g0005a0001c0001t0001g0203a0001c0001t0001g0205others(2): Show | 10 | HG01243.hp2 HG02559.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.46-9553G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177243824 | ||||||
chr2:177243837
|
A | G | 1 | a0001c0001t0002g0022 | 2 | HG00323.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.46-9566T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177243837 | ||||||
chr2:177243997
|
T | TA | 19 | a0001c0001t0001g0105a0001c0001t0001g0183a0001c0001t0003g0040others(16): Show | 23 | HG00735.hp1 HG01258.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.46-9727dupT | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177243997 | ||||||
chr2:177243997
|
TA | T | 6 | a0001c0001t0001g0112a0001c0001t0001g0140a0001c0001t0001g0153others(3): Show | 6 | HG01168.hp2 HG01256.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.46-9727delT | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177243997 | ||||||
chr2:177244038
|
C | T | 1 | a0001c0001t0002g0065 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.46-9767G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177244038 | ||||||
chr2:177244110
|
C | A | 3 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0219 | 3 | HG00438.hp1 NA18747.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.46-9839G>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177244110 | ||||||
chr2:177244187
|
G | A | 1 | a0001c0001t0003g0044 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.46-9916C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177244187 | ||||||
chr2:177244188
|
C | G | 1 | a0001c0001t0002g0101 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.46-9917G>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177244188 | ||||||
chr2:177244194
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.46-9923C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177244194 | ||||||
chr2:177244303
|
A | C | 7 | a0001c0001t0004g0028a0001c0001t0004g0149a0001c0001t0004g0150others(4): Show | 9 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-10032T>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177244303 | ||||||
chr2:177244367
|
C | T | 7 | a0001c0001t0004g0028a0001c0001t0004g0149a0001c0001t0004g0150others(4): Show | 9 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-10096G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177244367 | ||||||
chr2:177244644
|
C | T | 1 | a0001c0001t0002g0070 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.46-10373G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177244644 | ||||||
chr2:177244700
|
G | T | 1 | a0001c0001t0001g0117 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.46-10429C>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177244700 | ||||||
chr2:177244706
|
A | C | 3 | a0001c0001t0001g0037a0001c0001t0001g0199a0001c0001t0001g0209 | 4 | HG02818.hp2 HG03471.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-10435T>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177244706 | ||||||
chr2:177244777
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.46-10506G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177244777 | ||||||
chr2:177244781
|
C | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0213a0001c0001t0001g0214others(1): Show | 8 | HG03831.hp2 NA18939.hp1 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.46-10510G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177244781 | ||||||
chr2:177244873
|
G | A | 1 | a0001c0001t0002g0099 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.46-10602C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177244873 | ||||||
chr2:177244940
|
T | C | 1 | a0001c0001t0001g0177 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.46-10669A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177244940 | ||||||
chr2:177245002
|
CA | C | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.46-10732delT | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177245002 | ||||||
chr2:177245233
|
A | G | 15 | a0001c0001t0001g0034a0001c0001t0001g0134a0001c0001t0001g0137others(12): Show | 17 | HG01361.hp1 HG01884.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.46-10962T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177245233 | ||||||
chr2:177245241
|
G | T | 1 | a0001c0001t0001g0198 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.46-10970C>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177245241 | ||||||
chr2:177245396
|
C | T | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.46-11125G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177245396 | ||||||
chr2:177245555
|
G | T | 9 | a0001c0001t0001g0014a0001c0001t0001g0105a0001c0001t0001g0112others(6): Show | 11 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(8): Show |
intron_variant | MODIFIER | c.46-11284C>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177245555 | ||||||
chr2:177245615
|
CT | C | 7 | a0001c0001t0001g0216a0001c0001t0002g0059a0001c0001t0002g0060others(4): Show | 7 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.46-11345delA | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177245615 | ||||||
chr2:177245902
|
G | C | 1 | a0001c0001t0001g0111 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.46-11631C>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177245902 | ||||||
chr2:177245923
|
T | G | 1 | a0001c0001t0001g0191 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.46-11652A>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177245923 | ||||||
chr2:177246144
|
T | A | 1 | a0001c0001t0001g0173 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.46-11873A>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177246144 | ||||||
chr2:177246174
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.46-11903C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177246174 | ||||||
chr2:177246239
|
A | T | 7 | a0001c0001t0001g0216a0001c0001t0002g0059a0001c0001t0002g0060others(4): Show | 7 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.46-11968T>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177246239 | ||||||
chr2:177246403
|
A | G | 1 | a0001c0001t0001g0175 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.46-12132T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177246403 | ||||||
chr2:177246484
|
C | A | 6 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.46-12213G>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177246484 | ||||||
chr2:177246599
|
C | CT | 4 | a0001c0001t0001g0196a0001c0001t0002g0069a0001c0001t0007g0020others(1): Show | 6 | HG01071.hp2 HG02280.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.46-12329dupA | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177246599 | ||||||
chr2:177246599
|
C | CTT | 7 | a0001c0001t0004g0028a0001c0001t0004g0149a0001c0001t0004g0150others(4): Show | 9 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-12330_46-12329d others(4): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177246599 | ||||||
chr2:177246608
|
C | T | 172 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(169): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.46-12337G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177246608 | ||||||
chr2:177246774
|
C | CT | 161 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(158): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.46-12504dupA | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177246774 | ||||||
chr2:177246774
|
C | CTT | 7 | a0001c0001t0001g0105a0001c0001t0001g0111a0001c0001t0001g0174others(4): Show | 7 | HG01109.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-12505_46-12504d others(4): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177246774 | ||||||
chr2:177246774
|
CTTTTTT | C | 13 | a0001c0001t0001g0034a0001c0001t0001g0137a0001c0001t0001g0178others(10): Show | 14 | HG01361.hp1 HG01884.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.46-12509_46-12504d others(8): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177246774 | ||||||
chr2:177247365
|
A | G | 2 | a0001c0001t0002g0067a0001c0001t0002g0068 | 2 | HG02523.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.46-13094T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177247365 | ||||||
chr2:177247521
|
C | T | 1 | a0001c0001t0001g0168 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.46-13250G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177247521 | ||||||
chr2:177247576
|
G | A | 1 | a0001c0001t0001g0036 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.46-13305C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177247576 | ||||||
chr2:177247633
|
T | C | 3 | a0001c0001t0005g0019a0001c0001t0005g0200a0001c0001t0005g0202 | 5 | HG02717.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-13362A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177247633 | ||||||
chr2:177247684
|
C | CA | 17 | a0001c0001t0001g0105a0001c0001t0001g0117a0001c0001t0001g0147others(14): Show | 17 | HG01081.hp1 HG01109.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.46-13414dupT | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177247684 | ||||||
chr2:177247727
|
A | G | 7 | a0001c0001t0001g0216a0001c0001t0002g0059a0001c0001t0002g0060others(4): Show | 7 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.46-13456T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177247727 | ||||||
chr2:177247867
|
G | A | 1 | a0001c0001t0005g0200 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.46-13596C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177247867 | ||||||
chr2:177247883
|
C | T | 6 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.46-13612G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177247883 | ||||||
chr2:177247911
|
G | C | 1 | a0001c0001t0001g0118 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.46-13640C>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177247911 | ||||||
chr2:177247982
|
G | A | 7 | a0001c0001t0004g0028a0001c0001t0004g0149a0001c0001t0004g0150others(4): Show | 9 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-13711C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177247982 | ||||||
chr2:177247994
|
A | G | 6 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.46-13723T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177247994 | ||||||
chr2:177247997
|
G | A | 7 | a0001c0001t0001g0216a0001c0001t0002g0059a0001c0001t0002g0060others(4): Show | 7 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.46-13726C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177247997 | ||||||
chr2:177248471
|
G | A | 3 | a0001c0001t0005g0019a0001c0001t0005g0200a0001c0001t0005g0202 | 5 | HG02717.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-14200C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177248471 | ||||||
chr2:177248476
|
C | G | 2 | a0001c0001t0001g0174a0001c0001t0013g0207 | 2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.46-14205G>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177248476 | ||||||
chr2:177248519
|
C | G | 1 | a0001c0001t0001g0176 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.46-14248G>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177248519 | ||||||
chr2:177248538
|
T | C | 1 | a0001c0001t0001g0134 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.46-14267A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177248538 | ||||||
chr2:177248556
|
T | C | 13 | a0001c0001t0001g0034a0001c0001t0001g0137a0001c0001t0001g0178others(10): Show | 14 | HG01361.hp1 HG01884.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.46-14285A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177248556 | ||||||
chr2:177248687
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.46-14416C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177248687 | ||||||
chr2:177248756
|
A | G | 187 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(184): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.46-14485T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177248756 | ||||||
chr2:177248816
|
A | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0152 | 6 | HG00408.hp2 HG02015.hp1 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.46-14545T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177248816 | ||||||
chr2:177248897
|
C | A | 1 | a0001c0001t0001g0134 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.46-14626G>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177248897 | ||||||
chr2:177248922
|
C | T | 2 | a0001c0001t0001g0201a0001c0001t0002g0057 | 2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.46-14651G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177248922 | ||||||
chr2:177249090
|
C | T | 2 | a0001c0001t0008g0021a0001c0001t0009g0032 | 4 | HG02280.hp1 HG02615.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-14819G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177249090 | ||||||
chr2:177249179
|
A | G | 1 | a0001c0001t0002g0066 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.46-14908T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177249179 | ||||||
chr2:177249217
|
C | CATAA | 134 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(131): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.46-14950_46-14947d others(6): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177249217 | ||||||
chr2:177249217
|
C | CATAAATA others(1): Show |
6 | a0001c0001t0001g0132a0001c0001t0001g0172a0001c0001t0001g0174others(3): Show | 6 | HG00609.hp1 HG01517.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.46-14954_46-14947d others(10): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177249217 | ||||||
chr2:177249217
|
C | CATAAATA others(5): Show |
8 | a0001c0001t0001g0175a0001c0001t0004g0028a0001c0001t0004g0149others(5): Show | 10 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.46-14958_46-14947d others(14): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177249217 | ||||||
chr2:177249217
|
CATAAATA others(1): Show |
C | 3 | a0001c0001t0001g0151a0001c0001t0001g0179a0001c0001t0001g0180 | 3 | HG01361.hp1 HG01884.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.46-14954_46-14947d others(10): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177249217 | ||||||
chr2:177249217
|
CATAAATA others(5): Show |
C | 2 | a0001c0001t0001g0016a0001c0001t0001g0121 | 4 | HG00733.hp2 HG01175.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-14958_46-14947d others(14): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177249217 | ||||||
chr2:177249376
|
G | A | 1 | a0001c0001t0002g0083 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.46-15105C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177249376 | ||||||
chr2:177249494
|
A | C | 1 | a0001c0001t0001g0216 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.45+15038T>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177249494 | ||||||
chr2:177249642
|
T | C | 2 | a0001c0001t0001g0172a0001c0001t0001g0210 | 2 | HG03704.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.45+14890A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177249642 | ||||||
chr2:177249800
|
A | G | 7 | a0001c0001t0004g0028a0001c0001t0004g0149a0001c0001t0004g0150others(4): Show | 9 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.45+14732T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177249800 | ||||||
chr2:177249904
|
A | G | 182 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(179): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.45+14628T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177249904 | ||||||
chr2:177250012
|
C | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0213a0001c0001t0001g0214others(1): Show | 8 | HG03831.hp2 NA18939.hp1 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.45+14520G>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177250012 | ||||||
chr2:177250082
|
T | C | 1 | a0001c0001t0001g0192 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.45+14450A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177250082 | ||||||
chr2:177250244
|
G | A | 2 | a0001c0001t0001g0174a0001c0001t0013g0207 | 2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.45+14288C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177250244 | ||||||
chr2:177250623
|
G | A | 7 | a0001c0001t0001g0216a0001c0001t0002g0059a0001c0001t0002g0060others(4): Show | 7 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.45+13909C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177250623 | ||||||
chr2:177250748
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.45+13784G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177250748 | ||||||
chr2:177250825
|
G | T | 6 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.45+13707C>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177250825 | ||||||
chr2:177251430
|
A | G | 4 | a0001c0001t0005g0019a0001c0001t0005g0200a0001c0001t0005g0202others(1): Show | 7 | HG02257.hp1 HG02717.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.45+13102T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177251430 | ||||||
chr2:177251534
|
A | G | 1 | a0001c0001t0001g0025 | 2 | HG01106.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.45+12998T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177251534 | ||||||
chr2:177251600
|
G | A | 1 | a0001c0001t0002g0092 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.45+12932C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177251600 | ||||||
chr2:177251718
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.45+12814C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177251718 | ||||||
chr2:177251731
|
C | T | 5 | a0001c0001t0001g0003a0001c0001t0001g0031a0001c0001t0001g0148others(2): Show | 11 | HG00558.hp1 HG02523.hp1 NA18949.hp1 others(8): Show |
intron_variant | MODIFIER | c.45+12801G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177251731 | ||||||
chr2:177251787
|
C | T | 1 | a0001c0001t0003g0040 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.45+12745G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177251787 | ||||||
chr2:177251863
|
A | G | 2 | a0001c0001t0001g0110a0001c0001t0001g0120 | 2 | HG00140.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.45+12669T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177251863 | ||||||
chr2:177251900
|
G | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0203a0001c0001t0001g0205others(2): Show | 10 | HG01243.hp2 HG02559.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.45+12632C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177251900 | ||||||
chr2:177252000
|
C | CA | 39 | a0001c0001t0001g0034a0001c0001t0001g0134a0001c0001t0001g0162others(36): Show | 45 | HG01081.hp1 HG01361.hp1 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.45+12531dupT | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177252000 | ||||||
chr2:177252000
|
C | CAA | 132 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(129): Show | 201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.45+12530_45+12531d others(4): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177252000 | ||||||
chr2:177252000
|
C | CAAA | 10 | a0001c0001t0001g0016a0001c0001t0001g0106a0001c0001t0001g0108others(7): Show | 13 | HG00140.hp2 HG00733.hp2 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.45+12529_45+12531d others(5): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177252000 | ||||||
chr2:177252021
|
AT | A | 7 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0090others(4): Show | 7 | HG00423.hp1 HG02027.hp2 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+12510delA | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177252021 | ||||||
chr2:177252209
|
T | C | 1 | a0001c0001t0001g0212 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.45+12323A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177252209 | ||||||
chr2:177252249
|
C | T | 1 | a0001c0001t0001g0213 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.45+12283G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177252249 | ||||||
chr2:177252660
|
T | TC | 216 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(213): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.45+11871_45+11872i others(3): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177252660 | ||||||
chr2:177252662
|
T | G | 216 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(213): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.45+11870A>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177252662 | ||||||
chr2:177252680
|
C | T | 3 | a0001c0001t0006g0024a0001c0001t0006g0103a0001c0001t0006g0104 | 4 | HG02129.hp2 NA18987.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+11852G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177252680 | ||||||
chr2:177252887
|
A | G | 1 | a0001c0001t0002g0060 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.45+11645T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177252887 | ||||||
chr2:177252917
|
G | A | 6 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.45+11615C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177252917 | ||||||
chr2:177252941
|
T | G | 1 | a0001c0001t0001g0199 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.45+11591A>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177252941 | ||||||
chr2:177252999
|
T | C | 1 | a0001c0001t0001g0174 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.45+11533A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177252999 | ||||||
chr2:177253037
|
C | T | 130 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0014others(127): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.45+11495G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177253037 | ||||||
chr2:177253174
|
A | T | 1 | a0001c0001t0002g0065 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.45+11358T>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177253174 | ||||||
chr2:177253277
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.45+11255T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177253277 | ||||||
chr2:177253424
|
C | T | 32 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(29): Show | 42 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(39): Show |
intron_variant | MODIFIER | c.45+11108G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177253424 | ||||||
chr2:177253570
|
C | A | 2 | a0001c0001t0001g0172a0001c0001t0002g0057 | 2 | HG03704.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.45+10962G>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177253570 | ||||||
chr2:177253613
|
A | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0142a0001c0001t0001g0143 | 9 | HG00642.hp2 HG01257.hp1 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.45+10919T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177253613 | ||||||
chr2:177253671
|
A | G | 3 | a0001c0001t0001g0005a0001c0001t0001g0205a0001c0001t0001g0206 | 8 | HG01243.hp2 HG02559.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.45+10861T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177253671 | ||||||
chr2:177253772
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.45+10760T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177253772 | ||||||
chr2:177253822
|
C | A | 161 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(158): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.45+10710G>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177253822 | ||||||
chr2:177254262
|
A | G | 69 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(66): Show | 86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.45+10270T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177254262 | ||||||
chr2:177254293
|
T | G | 3 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177 | 3 | HG02486.hp2 HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.45+10239A>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177254293 | ||||||
chr2:177254312
|
G | C | 2 | a0001c0001t0001g0172a0001c0001t0002g0057 | 2 | HG03704.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.45+10220C>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177254312 | ||||||
chr2:177254476
|
A | C | 49 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(46): Show | 63 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.45+10056T>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177254476 | ||||||
chr2:177254568
|
G | A | 179 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(176): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.45+9964C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177254568 | ||||||
chr2:177254570
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.45+9962C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177254570 | ||||||
chr2:177254585
|
A | T | 1 | a0001c0001t0001g0209 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.45+9947T>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177254585 | ||||||
chr2:177254612
|
C | T | 2 | a0001c0001t0001g0175a0002c0002t0001g0033 | 3 | HG02257.hp1 HG02486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.45+9920G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177254612 | ||||||
chr2:177254638
|
C | T | 3 | a0001c0001t0006g0024a0001c0001t0006g0103a0001c0001t0006g0104 | 4 | HG02129.hp2 NA18987.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+9894G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177254638 | ||||||
chr2:177254787
|
T | C | 12 | a0001c0001t0001g0134a0001c0001t0001g0172a0001c0001t0001g0175others(9): Show | 15 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.45+9745A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177254787 | ||||||
chr2:177254839
|
T | C | 3 | a0001c0001t0001g0134a0001c0001t0001g0198a0001c0001t0005g0135 | 3 | HG02818.hp1 HG03225.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.45+9693A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177254839 | ||||||
chr2:177254985
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.45+9547A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177254985 | ||||||
chr2:177255005
|
A | G | 1 | a0001c0001t0002g0057 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.45+9527T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177255005 | ||||||
chr2:177255047
|
T | C | 1 | a0001c0001t0002g0093 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.45+9485A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177255047 | ||||||
chr2:177255090
|
C | T | 3 | a0001c0001t0006g0024a0001c0001t0006g0103a0001c0001t0006g0104 | 4 | HG02129.hp2 NA18987.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+9442G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177255090 | ||||||
chr2:177255097
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.45+9435G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177255097 | ||||||
chr2:177255108
|
G | A | 1 | a0001c0001t0001g0128 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.45+9424C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177255108 | ||||||
chr2:177255155
|
T | C | 1 | a0001c0001t0002g0057 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.45+9377A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177255155 | ||||||
chr2:177255225
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.45+9307C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177255225 | ||||||
chr2:177255296
|
C | T | 2 | a0001c0001t0001g0140a0001c0001t0001g0141 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.45+9236G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177255296 | ||||||
chr2:177255309
|
C | A | 1 | a0001c0001t0002g0057 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.45+9223G>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177255309 | ||||||
chr2:177255521
|
C | A | 1 | a0001c0001t0003g0045 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.45+9011G>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177255521 | ||||||
chr2:177255531
|
ACCAG | A | 2 | a0001c0001t0001g0030a0001c0001t0001g0163 | 3 | NA18983.hp2 NA18992.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.45+8997_45+9000del others(4): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177255531 | ||||||
chr2:177255584
|
T | G | 179 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(176): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.45+8948A>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177255584 | ||||||
chr2:177255591
|
A | T | 1 | a0001c0001t0001g0178 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.45+8941T>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177255591 | ||||||
chr2:177255663
|
T | C | 178 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(175): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.45+8869A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177255663 | ||||||
chr2:177255697
|
T | C | 3 | a0001c0001t0006g0024a0001c0001t0006g0103a0001c0001t0006g0104 | 4 | HG02129.hp2 NA18987.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+8835A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177255697 | ||||||
chr2:177255859
|
C | T | 5 | a0001c0001t0001g0201a0001c0001t0005g0019a0001c0001t0005g0200others(2): Show | 7 | HG00735.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.45+8673G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177255859 | ||||||
chr2:177255938
|
G | T | 6 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.45+8594C>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177255938 | ||||||
chr2:177255953
|
G | T | 1 | a0001c0001t0002g0057 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.45+8579C>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177255953 | ||||||
chr2:177256148
|
G | A | 1 | a0001c0001t0002g0094 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.45+8384C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177256148 | ||||||
chr2:177256244
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.45+8288T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177256244 | ||||||
chr2:177256277
|
C | T | 49 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(46): Show | 63 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.45+8255G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177256277 | ||||||
chr2:177256384
|
T | C | 68 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(65): Show | 87 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.45+8148A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177256384 | ||||||
chr2:177256499
|
C | CA | 20 | a0001c0001t0001g0109a0001c0001t0001g0166a0001c0001t0001g0190others(17): Show | 27 | HG00099.hp1 HG00735.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.45+8032dupT | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177256499 | ||||||
chr2:177256499
|
C | CAA | 44 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(41): Show | 58 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.45+8031_45+8032dup others(2): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177256499 | ||||||
chr2:177256499
|
CA | C | 22 | a0001c0001t0001g0034a0001c0001t0001g0139a0001c0001t0001g0172others(19): Show | 24 | HG01168.hp1 HG01361.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.45+8032delT | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177256499 | ||||||
chr2:177256649
|
A | T | 1 | a0001c0001t0001g0174 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.45+7883T>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177256649 | ||||||
chr2:177256796
|
C | A | 48 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(45): Show | 62 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.45+7736G>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177256796 | ||||||
chr2:177256925
|
C | T | 36 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0018others(33): Show | 52 | HG00642.hp1 HG00738.hp2 HG01070.hp2 others(49): Show |
intron_variant | MODIFIER | c.45+7607G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177256925 | ||||||
chr2:177256979
|
G | A | 3 | a0001c0001t0006g0024a0001c0001t0006g0103a0001c0001t0006g0104 | 4 | HG02129.hp2 NA18987.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+7553C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177256979 | ||||||
chr2:177257010
|
G | A | 2 | a0001c0001t0001g0134a0001c0001t0005g0135 | 2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.45+7522C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177257010 | ||||||
chr2:177257074
|
C | T | 2 | a0001c0001t0001g0134a0001c0001t0005g0135 | 2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.45+7458G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177257074 | ||||||
chr2:177257153
|
T | G | 1 | a0001c0001t0002g0053 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.45+7379A>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177257153 | ||||||
chr2:177257175
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.45+7357C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177257175 | ||||||
chr2:177257194
|
A | G | 2 | a0001c0001t0001g0134a0001c0001t0005g0135 | 2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.45+7338T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177257194 | ||||||
chr2:177257465
|
C | T | 1 | a0001c0001t0002g0059 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.45+7067G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177257465 | ||||||
chr2:177257476
|
T | G | 1 | a0001c0001t0001g0193 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.45+7056A>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177257476 | ||||||
chr2:177257509
|
G | C | 1 | a0001c0001t0002g0096 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.45+7023C>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177257509 | ||||||
chr2:177257573
|
C | G | 2 | a0001c0001t0002g0012a0001c0001t0002g0049 | 4 | HG00733.hp1 HG01928.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+6959G>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177257573 | ||||||
chr2:177257600
|
T | C | 2 | a0001c0001t0001g0134a0001c0001t0005g0135 | 2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.45+6932A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177257600 | ||||||
chr2:177257602
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.45+6930G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177257602 | ||||||
chr2:177257637
|
A | C | 58 | a0001c0001t0001g0216a0001c0001t0002g0001a0001c0001t0002g0006others(55): Show | 101 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.45+6895T>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177257637 | ||||||
chr2:177257676
|
T | C | 1 | a0001c0001t0006g0104 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.45+6856A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177257676 | ||||||
chr2:177257731
|
C | T | 1 | a0001c0001t0002g0058 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.45+6801G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177257731 | ||||||
chr2:177257868
|
G | A | 1 | a0001c0001t0002g0098 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.45+6664C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177257868 | ||||||
chr2:177257907
|
A | G | 2 | a0001c0001t0001g0134a0001c0001t0005g0135 | 2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.45+6625T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177257907 | ||||||
chr2:177257939
|
T | C | 9 | a0001c0001t0003g0039a0001c0001t0003g0040a0001c0001t0003g0041others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.45+6593A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177257939 | ||||||
chr2:177257999
|
G | A | 44 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(41): Show | 57 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.45+6533C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177257999 | ||||||
chr2:177258177
|
ACAACT | A | 2 | a0001c0001t0002g0013a0001c0001t0002g0099 | 4 | HG01167.hp2 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+6350_45+6354del others(5): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177258177 | ||||||
chr2:177258274
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.45+6258C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177258274 | ||||||
chr2:177258345
|
T | TGATTCCA others(9): Show |
3 | a0001c0001t0006g0024a0001c0001t0006g0103a0001c0001t0006g0104 | 4 | HG02129.hp2 NA18987.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+6171_45+6186dup others(16): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177258345 | ||||||
chr2:177258401
|
T | C | 4 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(1): Show | 4 | HG00735.hp2 HG01070.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+6131A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177258401 | ||||||
chr2:177258455
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.45+6077A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177258455 | ||||||
chr2:177258633
|
A | G | 2 | a0001c0001t0001g0134a0001c0001t0005g0135 | 2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.45+5899T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177258633 | ||||||
chr2:177258656
|
T | C | 2 | a0001c0001t0001g0175a0002c0002t0001g0033 | 3 | HG02257.hp1 HG02486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.45+5876A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177258656 | ||||||
chr2:177258726
|
T | A | 1 | a0001c0001t0002g0100 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.45+5806A>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177258726 | ||||||
chr2:177258964
|
T | C | 7 | a0001c0001t0001g0034a0001c0001t0001g0178a0001c0001t0001g0179others(4): Show | 8 | HG01361.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.45+5568A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177258964 | ||||||
chr2:177259139
|
T | C | 5 | a0001c0001t0001g0201a0001c0001t0005g0019a0001c0001t0005g0200others(2): Show | 7 | HG00735.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.45+5393A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177259139 | ||||||
chr2:177259168
|
G | A | 3 | a0001c0001t0001g0031a0001c0001t0001g0168a0001c0001t0001g0169 | 4 | NA18949.hp1 NA18989.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+5364C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177259168 | ||||||
chr2:177259227
|
G | A | 1 | a0001c0001t0001g0133 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.45+5305C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177259227 | ||||||
chr2:177259301
|
C | A | 9 | a0001c0001t0003g0039a0001c0001t0003g0040a0001c0001t0003g0041others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.45+5231G>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177259301 | ||||||
chr2:177259346
|
TG | T | 3 | a0001c0001t0009g0032a0003c0003t0001g0170a0003c0003t0004g0171 | 4 | HG02280.hp1 HG02647.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+5185delC | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177259346 | ||||||
chr2:177259471
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.45+5061C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177259471 | ||||||
chr2:177259609
|
TTTTCATG others(26): Show |
T | 3 | a0001c0001t0006g0024a0001c0001t0006g0103a0001c0001t0006g0104 | 4 | HG02129.hp2 NA18987.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+4890_45+4922del others(33): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177259609 | ||||||
chr2:177259658
|
C | T | 59 | a0001c0001t0001g0216a0001c0001t0002g0001a0001c0001t0002g0006others(56): Show | 102 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.45+4874G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177259658 | ||||||
chr2:177259780
|
A | G | 2 | a0001c0001t0002g0057a0001c0001t0008g0021 | 3 | HG02615.hp1 HG02630.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.45+4752T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177259780 | ||||||
chr2:177259910
|
C | T | 1 | a0001c0001t0002g0056 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.45+4622G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177259910 | ||||||
chr2:177259911
|
G | A | 3 | a0001c0001t0006g0024a0001c0001t0006g0103a0001c0001t0006g0104 | 4 | HG02129.hp2 NA18987.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+4621C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177259911 | ||||||
chr2:177260059
|
A | G | 59 | a0001c0001t0001g0216a0001c0001t0002g0001a0001c0001t0002g0006others(56): Show | 102 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.45+4473T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177260059 | ||||||
chr2:177260140
|
T | C | 1 | a0001c0001t0001g0010 | 4 | HG00280.hp1 HG01261.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+4392A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177260140 | ||||||
chr2:177260375
|
A | G | 3 | a0001c0001t0006g0024a0001c0001t0006g0103a0001c0001t0006g0104 | 4 | HG02129.hp2 NA18987.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+4157T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177260375 | ||||||
chr2:177260414
|
A | G | 43 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(40): Show | 56 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.45+4118T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177260414 | ||||||
chr2:177260800
|
A | G | 43 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(40): Show | 56 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.45+3732T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177260800 | ||||||
chr2:177260807
|
G | GCAAA | 105 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(102): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.45+3724_45+3725ins others(4): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177260807 | ||||||
chr2:177260835
|
C | A | 2 | a0001c0001t0001g0134a0001c0001t0005g0135 | 2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.45+3697G>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177260835 | ||||||
chr2:177260895
|
G | A | 9 | a0001c0001t0001g0172a0001c0001t0001g0175a0001c0001t0001g0176others(6): Show | 11 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.45+3637C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177260895 | ||||||
chr2:177260994
|
G | A | 37 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0018others(34): Show | 53 | HG00642.hp1 HG00738.hp2 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.45+3538C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177260994 | ||||||
chr2:177261170
|
C | CA | 12 | a0001c0001t0001g0107a0001c0001t0001g0173a0001c0001t0001g0174others(9): Show | 12 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.45+3361dupT | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177261170 | ||||||
chr2:177261170
|
C | CAA | 45 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(42): Show | 59 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.45+3360_45+3361dup others(2): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177261170 | ||||||
chr2:177261170
|
C | CAAA | 42 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0018others(39): Show | 60 | HG00423.hp2 HG00642.hp1 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.45+3359_45+3361dup others(3): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177261170 | ||||||
chr2:177261170
|
C | CAAAA | 8 | a0001c0001t0001g0037a0001c0001t0001g0194a0001c0001t0001g0195others(5): Show | 9 | HG01099.hp2 HG02818.hp2 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.45+3358_45+3361dup others(4): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177261170 | ||||||
chr2:177261179
|
A | C | 1 | a0001c0001t0002g0055 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.45+3353T>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177261179 | ||||||
chr2:177261186
|
C | A | 4 | a0001c0001t0001g0175a0001c0001t0002g0054a0001c0001t0002g0101others(1): Show | 5 | HG02257.hp1 HG02486.hp2 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+3346G>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177261186 | ||||||
chr2:177261187
|
A | C | 1 | a0001c0001t0002g0054 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.45+3345T>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177261187 | ||||||
chr2:177261224
|
C | A | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.45+3308G>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177261224 | ||||||
chr2:177261265
|
G | A | 7 | a0001c0001t0001g0034a0001c0001t0001g0178a0001c0001t0001g0179others(4): Show | 8 | HG01361.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.45+3267C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177261265 | ||||||
chr2:177261366
|
G | C | 2 | a0001c0001t0001g0196a0001c0001t0001g0197 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.45+3166C>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177261366 | ||||||
chr2:177261399
|
C | T | 23 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0035others(20): Show | 31 | HG00642.hp1 HG00738.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.45+3133G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177261399 | ||||||
chr2:177261588
|
C | A | 4 | a0001c0001t0001g0008a0001c0001t0001g0213a0001c0001t0001g0214others(1): Show | 8 | HG03831.hp2 NA18939.hp1 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.45+2944G>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177261588 | ||||||
chr2:177261818
|
G | C | 59 | a0001c0001t0001g0216a0001c0001t0002g0001a0001c0001t0002g0006others(56): Show | 102 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.45+2714C>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177261818 | ||||||
chr2:177262312
|
A | C | 41 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(38): Show | 54 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.45+2220T>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177262312 | ||||||
chr2:177262361
|
A | G | 58 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0009others(55): Show | 101 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.45+2171T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177262361 | ||||||
chr2:177262444
|
A | G | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.45+2088T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177262444 | ||||||
chr2:177262739
|
AAAT | A | 8 | a0001c0001t0001g0034a0001c0001t0001g0178a0001c0001t0001g0179others(5): Show | 9 | HG01361.hp1 HG01884.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.45+1790_45+1792del others(3): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177262739 | ||||||
chr2:177263018
|
T | A | 1 | a0001c0001t0002g0102 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.45+1514A>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177263018 | ||||||
chr2:177263098
|
C | T | 8 | a0001c0001t0001g0034a0001c0001t0001g0178a0001c0001t0001g0179others(5): Show | 9 | HG01361.hp1 HG01884.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.45+1434G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177263098 | ||||||
chr2:177263111
|
T | C | 58 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0009others(55): Show | 101 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.45+1421A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177263111 | ||||||
chr2:177263275
|
T | C | 52 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0018others(49): Show | 71 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(68): Show |
intron_variant | MODIFIER | c.45+1257A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177263275 | ||||||
chr2:177263405
|
T | C | 1 | a0001c0001t0001g0217 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.45+1127A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177263405 | ||||||
chr2:177263634
|
C | G | 3 | a0001c0001t0006g0024a0001c0001t0006g0103a0001c0001t0006g0104 | 4 | HG02129.hp2 NA18987.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+898G>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177263634 | ||||||
chr2:177263720
|
C | A | 3 | a0001c0001t0006g0024a0001c0001t0006g0103a0001c0001t0006g0104 | 4 | HG02129.hp2 NA18987.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+812G>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177263720 | ||||||
chr2:177263763
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.45+769C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177263763 | ||||||
chr2:177263965
|
A | C | 41 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(38): Show | 54 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.45+567T>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177263965 | ||||||
chr2:177264103
|
C | T | 1 | a0001c0001t0002g0049 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.45+429G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264103 | ||||||
chr2:177264249
|
C | A | 1 | a0001c0001t0001g0219 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.45+283G>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264249 | ||||||
chr2:177264273
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+259C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264273 | ||||||
chr2:177264276
|
C | G | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+256G>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264276 | ||||||
chr2:177264284
|
AGACCTTC others(7): Show |
A | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+234_45+247delGT others(12): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264284 | ||||||
chr2:177264299
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+233A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264299 | ||||||
chr2:177264304
|
A | G | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+228T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264304 | ||||||
chr2:177264306
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+226G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264306 | ||||||
chr2:177264328
|
T | G | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+204A>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264328 | ||||||
chr2:177264332
|
T | A | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+200A>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264332 | ||||||
chr2:177264335
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+197C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264335 | ||||||
chr2:177264357
|
T | G | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+175A>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264357 | ||||||
chr2:177264363
|
T | G | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+169A>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264363 | ||||||
chr2:177264367
|
C | A | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+165G>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264367 | ||||||
chr2:177264375
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+157G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264375 | ||||||
chr2:177264380
|
C | A | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+152G>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264380 | ||||||
chr2:177264386
|
C | A | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+146G>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264386 | ||||||
chr2:177264392
|
G | C | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+140C>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264392 | ||||||
chr2:177264394
|
C | G | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+138G>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264394 | ||||||
chr2:177264401
|
C | G | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+131G>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264401 | ||||||
chr2:177264402
|
A | G | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+130T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264402 | ||||||
chr2:177264407
|
C | G | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+125G>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264407 | ||||||
chr2:177264412
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+120A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264412 | ||||||
chr2:177264414
|
C | G | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+118G>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264414 | ||||||
chr2:177264415
|
T | A | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+117A>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264415 | ||||||
chr2:177264419
|
T | G | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+113A>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264419 | ||||||
chr2:177264426
|
A | G | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+106T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264426 | ||||||
chr2:177264434
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.45+98C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264434 | ||||||
chr2:177264434
|
G | C | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+98C>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264434 | ||||||
chr2:177264435
|
G | C | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+97C>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264435 | ||||||
chr2:177264437
|
A | G | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+95T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264437 | ||||||
chr2:177264445
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+87A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264445 | ||||||
chr2:177264453
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+79A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264453 | ||||||
chr2:177264456
|
C | T | 3 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0002g0048 | 3 | HG01175.hp1 HG04115.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.45+76G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264456 | ||||||
chr2:177264460
|
C | G | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+72G>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264460 | ||||||
chr2:177264465
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+67G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264465 | ||||||
chr2:177264470
|
T | G | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+62A>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264470 | ||||||
chr2:177264475
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+57A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264475 | ||||||
chr2:177264476
|
A | C | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+56T>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264476 |