geneid | 9603 |
---|---|
ensemblid | ENSG00000050344.9 |
hgncid | 7783 |
symbol | NFE2L3 |
name | NFE2 like bZIP transcription factor 3 |
refseq_nuc | NM_004289.7 |
refseq_prot | NP_004280.5 |
ensembl_nuc | ENST00000056233.4 |
ensembl_prot | ENSP00000056233.3 |
mane_status | MANE Select |
chr | chr7 |
start | 26152198 |
end | 26187137 |
strand | + |
ver | v1.2 |
region | chr7:26152198-26187137 |
region5000 | chr7:26147198-26192137 |
regionname0 | NFE2L3_chr7_26152198_26187137 |
regionname5000 | NFE2L3_chr7_26147198_26192137 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 694 | 359 | 75 | 66 | 161 | 14 | 41 | 126 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0002 | 0/0 | 695 | 11 | 6 | 4 | 0 | 0 | 1 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0003 | 0/0 | 694 | 10 | 0 | 0 | 10 | 0 | 0 | 10 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0004 | 0/0 | 694 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0005 | 0/0 | 694 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0006 | 0/0 | 694 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0007 | 0/0 | 694 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0008 | 0/0 | 694 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0009 | 0/0 | 694 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0010 | 0/0 | 694 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0011 | 0/0 | 694 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0012 | 0/0 | 694 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0013 | 0/0 | 694 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0014 | 0/0 | 694 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0015 | 0/0 | 694 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0016 | 0/0 | 694 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2085 | 209 | 28 | 49 | 83 | 13 | 34 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
c0002 | 0/0 | 2085 | 147 | 47 | 17 | 75 | 1 | 7 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
c0003 | 0/0 | 2085 | 10 | 0 | 0 | 10 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
c0004 | 0/0 | 2088 | 8 | 5 | 3 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
c0005 | 0/0 | 2085 | 3 | 0 | 0 | 3 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
c0006 | 0/0 | 2085 | 3 | 3 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
c0007 | 0/0 | 2088 | 3 | 1 | 1 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
c0008 | 0/0 | 2085 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
c0009 | 0/0 | 2085 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
c0010 | 0/0 | 2085 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
c0011 | 0/0 | 2085 | 2 | 0 | 0 | 0 | 0 | 2 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
c0012 | 0/0 | 2085 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
c0013 | 0/0 | 2085 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
c0014 | 0/0 | 2085 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
c0015 | 0/0 | 2085 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
c0016 | 0/0 | 2085 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
c0017 | 0/0 | 2085 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
c0018 | 0/0 | 2085 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
c0019 | 0/0 | 2085 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1656 | 239 | 54 | 50 | 87 | 13 | 33 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
t0002 | 0/0 | 1661 | 69 | 5 | 9 | 50 | 0 | 5 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
t0003 | 0/0 | 1654 | 26 | 1 | 5 | 19 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
t0004 | 0/0 | 1656 | 10 | 0 | 0 | 9 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
t0005 | 0/0 | 1656 | 8 | 5 | 3 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
t0006 | 0/0 | 1656 | 7 | 6 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
t0007 | 0/0 | 1652 | 7 | 0 | 0 | 7 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
t0008 | 0/0 | 1656 | 5 | 2 | 1 | 0 | 1 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
t0009 | 0/0 | 1656 | 4 | 4 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
t0010 | 0/0 | 1656 | 3 | 0 | 0 | 3 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
t0011 | 0/0 | 1651 | 3 | 3 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
t0012 | 0/0 | 1656 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
t0013 | 0/0 | 1656 | 2 | 1 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
t0014 | 0/0 | 1656 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
t0015 | 0/0 | 1656 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
t0016 | 0/0 | 1654 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
t0017 | 0/0 | 1661 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
t0018 | 0/0 | 1656 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
t0019 | 0/0 | 1656 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
t0020 | 0/0 | 1656 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
t0021 | 0/0 | 1656 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
t0022 | 0/0 | 1656 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
t0023 | 0/0 | 1656 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
t0024 | 0/0 | 1656 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
t0025 | 0/0 | 1656 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
t0026 | 0/0 | 1656 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/1 | 12 | 0 | 1 | 6 | 2 | 2 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0002 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0003 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0004 | 0/0 | 9 | 1 | 4 | 2 | 1 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0005 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0006 | 0/0 | 7 | 0 | 2 | 4 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0007 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0008 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0009 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0010 | 0/0 | 4 | 1 | 2 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0013 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0014 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0016 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0021 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0023 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0024 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0025 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0038 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0045 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0047 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0196 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2085 | 209 | 28 | 49 | 83 | 13 | 34 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0001c0002 | 0/0 | 2085 | 147 | 47 | 17 | 75 | 1 | 7 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0001c0005 | 0/0 | 2085 | 3 | 0 | 0 | 3 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0002c0004 | 0/0 | 2088 | 8 | 5 | 3 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0002c0007 | 0/0 | 2088 | 3 | 1 | 1 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0003c0003 | 0/0 | 2085 | 10 | 0 | 0 | 10 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0004c0006 | 0/0 | 2085 | 3 | 3 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0005c0012 | 0/0 | 2085 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0006c0008 | 0/0 | 2085 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0007c0009 | 0/0 | 2085 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0008c0010 | 0/0 | 2085 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0009c0011 | 0/0 | 2085 | 2 | 0 | 0 | 0 | 0 | 2 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0010c0019 | 0/0 | 2085 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0011c0013 | 0/0 | 2085 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0012c0015 | 0/0 | 2085 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0013c0016 | 0/0 | 2085 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0014c0014 | 0/0 | 2085 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0015c0017 | 0/0 | 2085 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0016c0018 | 0/0 | 2085 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 3740 | 198 | 25 | 46 | 81 | 13 | 31 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0001c0001t0005 | 0/0 | 3740 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0001c0001t0013 | 0/0 | 3740 | 2 | 1 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0001c0001t0018 | 0/0 | 3740 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0001c0001t0019 | 0/0 | 3740 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0001c0001t0020 | 0/0 | 3740 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0001c0001t0021 | 0/0 | 3740 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0001c0001t0022 | 0/0 | 3740 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0001c0001t0025 | 0/0 | 3740 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0001c0001t0026 | 0/0 | 3740 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0001c0002t0001 | 0/0 | 3740 | 29 | 27 | 2 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0001c0002t0002 | 0/0 | 3745 | 67 | 5 | 9 | 48 | 0 | 5 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0001c0002t0003 | 0/0 | 3738 | 11 | 0 | 4 | 7 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0001c0002t0004 | 0/0 | 3740 | 9 | 0 | 0 | 8 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0001c0002t0006 | 0/0 | 3740 | 7 | 6 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0001c0002t0007 | 0/0 | 3736 | 7 | 0 | 0 | 7 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0001c0002t0008 | 0/0 | 3740 | 5 | 2 | 1 | 0 | 1 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0001c0002t0010 | 0/0 | 3740 | 3 | 0 | 0 | 3 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0001c0002t0011 | 0/0 | 3735 | 3 | 3 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0001c0002t0014 | 0/0 | 3740 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0001c0002t0015 | 0/0 | 3740 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0001c0002t0017 | 0/0 | 3745 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0001c0002t0023 | 0/0 | 3740 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0001c0002t0024 | 0/0 | 3740 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0001c0005t0001 | 0/0 | 3740 | 3 | 0 | 0 | 3 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0002c0004t0005 | 0/0 | 3743 | 6 | 3 | 3 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0002c0004t0009 | 0/0 | 3743 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0002c0007t0003 | 0/0 | 3741 | 3 | 1 | 1 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0003c0003t0003 | 0/0 | 3738 | 9 | 0 | 0 | 9 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0003c0003t0016 | 0/0 | 3738 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0004c0006t0001 | 0/0 | 3740 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0004c0006t0012 | 0/0 | 3740 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0005c0012t0009 | 0/0 | 3740 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0006c0008t0001 | 0/0 | 3740 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0007c0009t0003 | 0/0 | 3738 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0008c0010t0002 | 0/0 | 3745 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0009c0011t0001 | 0/0 | 3740 | 2 | 0 | 0 | 0 | 0 | 2 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0010c0019t0001 | 0/0 | 3740 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0011c0013t0001 | 0/0 | 3740 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0012c0015t0003 | 0/0 | 3738 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0013c0016t0004 | 0/0 | 3740 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0014c0014t0001 | 0/0 | 3740 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0015c0017t0001 | 0/0 | 3740 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
a0016c0018t0014 | 0/0 | 3740 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | copy fasta | chr7 | 26147198 | 26192137 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/1 | 11 | 0 | 1 | 5 | 2 | 2 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0004 | 0/0 | 8 | 0 | 4 | 2 | 1 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0006 | 0/0 | 7 | 0 | 2 | 4 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0013 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0014 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0024 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0196 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0005g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0013g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0013g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0018g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0019g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0020g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0021g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0022g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0025g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0001t0026g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0001g0009 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0002g0003 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0002g0007 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0002g0016 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0002g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0002g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0002g0045 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0002g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0003g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0004g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0004g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0006g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0006g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0006g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0006g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0007g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0007g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0007g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0008g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0008g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0008g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0008g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0010g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0010g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0011g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0014g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0015g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0015g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0017g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0023g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0002t0024g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0005t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0005t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0001c0005t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0002c0004t0005g0047 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0002c0004t0005g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0002c0004t0005g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0002c0004t0005g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0002c0004t0009g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0002c0007t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0002c0007t0003g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0002c0007t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0003c0003t0003g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0003c0003t0003g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0003c0003t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0003c0003t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0003c0003t0016g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0004c0006t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0004c0006t0012g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0004c0006t0012g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0005c0012t0009g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0005c0012t0009g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0006c0008t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0006c0008t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0007c0009t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0007c0009t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0008c0010t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0009c0011t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0009c0011t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0010c0019t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0011c0013t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0012c0015t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0013c0016t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0014c0014t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0015c0017t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
a0016c0018t0014g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0176 | EUR | GBR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0175 | EUR | GBR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0030 | EUR | FIN | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0101 | EUR | FIN | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0100 | EUR | FIN | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG00423 | hp2 | a0001 | c0002 | t0007 | g0002 | EAS | CHS | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG00438 | hp1 | a0013 | c0016 | t0004 | g0118 | EAS | CHS | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG00438 | hp2 | a0001 | c0002 | t0003 | g0221 | EAS | CHS | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG00544 | hp2 | a0008 | c0010 | t0002 | g0042 | EAS | CHS | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG00597 | hp2 | a0001 | c0002 | t0003 | g0005 | EAS | CHS | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG00609 | hp1 | a0001 | c0002 | t0004 | g0093 | EAS | CHS | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG00642 | hp1 | a0001 | c0001 | t0019 | g0148 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG00733 | hp1 | a0001 | c0002 | t0003 | g0241 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG00741 | hp1 | a0001 | c0002 | t0003 | g0041 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG00741 | hp2 | a0002 | c0004 | t0005 | g0048 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01069 | hp2 | a0001 | c0002 | t0001 | g0050 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01081 | hp2 | a0001 | c0001 | t0013 | g0077 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01099 | hp2 | a0001 | c0002 | t0008 | g0028 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01106 | hp1 | a0001 | c0002 | t0003 | g0041 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01106 | hp2 | a0002 | c0007 | t0003 | g0232 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01109 | hp1 | a0001 | c0002 | t0006 | g0071 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01167 | hp2 | a0002 | c0004 | t0005 | g0047 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01169 | hp2 | a0002 | c0004 | t0005 | g0048 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01255 | hp2 | a0001 | c0002 | t0002 | g0007 | AMR | CLM | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01346 | hp2 | a0001 | c0002 | t0002 | g0007 | AMR | CLM | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01358 | hp1 | a0001 | c0001 | t0021 | g0010 | AMR | CLM | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01361 | hp1 | a0010 | c0019 | t0001 | g0268 | AMR | CLM | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01496 | hp2 | a0001 | c0002 | t0002 | g0187 | AMR | CLM | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0087 | EUR | IBS | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01517 | hp2 | a0001 | c0002 | t0008 | g0064 | EUR | IBS | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01884 | hp1 | a0001 | c0002 | t0001 | g0133 | AFR | ACB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01891 | hp2 | a0001 | c0002 | t0001 | g0079 | AFR | ACB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01928 | hp2 | a0001 | c0002 | t0002 | g0007 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01975 | hp1 | a0001 | c0002 | t0003 | g0230 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01978 | hp1 | a0001 | c0002 | t0002 | g0233 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02004 | hp2 | a0001 | c0002 | t0002 | g0007 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02015 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02015 | hp2 | a0001 | c0001 | t0026 | g0081 | EAS | KHV | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02027 | hp1 | a0001 | c0002 | t0003 | g0265 | EAS | KHV | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02027 | hp2 | a0007 | c0009 | t0003 | g0229 | EAS | KHV | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02055 | hp1 | a0001 | c0002 | t0006 | g0157 | AFR | ACB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02055 | hp2 | a0002 | c0004 | t0005 | g0264 | AFR | ACB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02056 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02071 | hp2 | a0001 | c0002 | t0002 | g0255 | EAS | KHV | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02080 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02129 | hp1 | a0001 | c0002 | t0007 | g0033 | EAS | KHV | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02135 | hp1 | a0001 | c0002 | t0002 | g0016 | EAS | KHV | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02145 | hp1 | a0001 | c0002 | t0001 | g0139 | AFR | ACB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02145 | hp2 | a0005 | c0012 | t0009 | g0025 | AFR | ACB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CDX | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02155 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | CDX | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02165 | hp2 | a0001 | c0002 | t0007 | g0002 | EAS | CDX | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02258 | hp1 | a0004 | c0006 | t0012 | g0054 | AFR | ACB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02258 | hp2 | a0001 | c0002 | t0006 | g0069 | AFR | ACB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02273 | hp1 | a0014 | c0014 | t0001 | g0036 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02273 | hp2 | a0001 | c0002 | t0002 | g0007 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02280 | hp2 | a0015 | c0017 | t0001 | g0088 | AFR | ACB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02293 | hp1 | a0001 | c0002 | t0002 | g0007 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02300 | hp2 | a0001 | c0002 | t0002 | g0007 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02451 | hp1 | a0001 | c0002 | t0011 | g0026 | AFR | ACB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02451 | hp2 | a0001 | c0002 | t0008 | g0066 | AFR | ACB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02572 | hp2 | a0002 | c0004 | t0005 | g0263 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02615 | hp1 | a0001 | c0002 | t0001 | g0156 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02615 | hp2 | a0001 | c0002 | t0001 | g0124 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0068 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02647 | hp1 | a0002 | c0004 | t0009 | g0039 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02647 | hp2 | a0001 | c0002 | t0001 | g0134 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02683 | hp1 | a0001 | c0002 | t0004 | g0129 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02683 | hp2 | a0009 | c0011 | t0001 | g0114 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02717 | hp1 | a0001 | c0002 | t0001 | g0112 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02723 | hp1 | a0001 | c0002 | t0001 | g0049 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02735 | hp1 | a0002 | c0007 | t0003 | g0231 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02818 | hp1 | a0001 | c0002 | t0001 | g0056 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02886 | hp1 | a0001 | c0001 | t0013 | g0168 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02886 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02895 | hp1 | a0001 | c0002 | t0001 | g0090 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02895 | hp2 | a0001 | c0002 | t0006 | g0070 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02896 | hp1 | a0001 | c0002 | t0001 | g0052 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02896 | hp2 | a0001 | c0002 | t0001 | g0091 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02922 | hp2 | a0001 | c0002 | t0011 | g0026 | AFR | ESN | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | ESN | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02965 | hp2 | a0001 | c0002 | t0001 | g0089 | AFR | ESN | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02970 | hp1 | a0001 | c0002 | t0001 | g0067 | AFR | ESN | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02970 | hp2 | a0002 | c0004 | t0009 | g0039 | AFR | ESN | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02976 | hp1 | a0001 | c0002 | t0002 | g0266 | AFR | ESN | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03017 | hp1 | a0001 | c0002 | t0008 | g0065 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03041 | hp1 | a0001 | c0002 | t0024 | g0051 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03041 | hp2 | a0001 | c0002 | t0001 | g0078 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03139 | hp2 | a0001 | c0002 | t0011 | g0026 | AFR | ESN | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03195 | hp1 | a0005 | c0012 | t0009 | g0004 | AFR | ESN | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03195 | hp2 | a0016 | c0018 | t0014 | g0141 | AFR | ESN | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03209 | hp2 | a0001 | c0002 | t0014 | g0076 | AFR | MSL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03225 | hp1 | a0001 | c0001 | t0005 | g0128 | AFR | MSL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03225 | hp2 | a0002 | c0004 | t0005 | g0047 | AFR | MSL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03239 | hp1 | a0001 | c0002 | t0002 | g0016 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03453 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | MSL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03486 | hp1 | a0002 | c0007 | t0003 | g0224 | AFR | MSL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03486 | hp2 | a0001 | c0002 | t0001 | g0138 | AFR | MSL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03491 | hp2 | a0001 | c0001 | t0020 | g0021 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0173 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03579 | hp1 | a0001 | c0002 | t0002 | g0218 | AFR | MSL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03579 | hp2 | a0001 | c0002 | t0006 | g0018 | AFR | MSL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03669 | hp1 | a0001 | c0002 | t0002 | g0045 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | STU | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03688 | hp2 | a0001 | c0002 | t0002 | g0045 | SAS | STU | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | BEB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03927 | hp1 | a0001 | c0002 | t0002 | g0259 | SAS | BEB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03942 | hp1 | a0009 | c0011 | t0001 | g0115 | SAS | BEB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03942 | hp2 | a0001 | c0001 | t0018 | g0225 | SAS | BEB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | BEB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG04184 | hp2 | a0001 | c0002 | t0002 | g0016 | SAS | BEB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | STU | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | STU | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | STU | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | STU | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | STU | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | STU | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | YRI | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18522 | hp2 | a0001 | c0002 | t0006 | g0018 | AFR | YRI | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18612 | hp1 | a0001 | c0002 | t0004 | g0172 | EAS | CHB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18612 | hp2 | a0001 | c0002 | t0002 | g0027 | EAS | CHB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18747 | hp1 | a0001 | c0002 | t0002 | g0044 | EAS | CHB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18747 | hp2 | a0001 | c0002 | t0002 | g0236 | EAS | CHB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | YRI | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18906 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | YRI | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18940 | hp1 | a0001 | c0002 | t0010 | g0137 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18940 | hp2 | a0001 | c0002 | t0002 | g0046 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18941 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18944 | hp1 | a0001 | c0002 | t0003 | g0222 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18947 | hp1 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18947 | hp2 | a0001 | c0002 | t0010 | g0002 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18949 | hp2 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18950 | hp2 | a0001 | c0002 | t0007 | g0002 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18951 | hp1 | a0001 | c0002 | t0002 | g0250 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18952 | hp1 | a0001 | c0002 | t0002 | g0132 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18952 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18953 | hp1 | a0001 | c0002 | t0003 | g0165 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18953 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18954 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18957 | hp2 | a0001 | c0002 | t0002 | g0248 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18959 | hp1 | a0011 | c0013 | t0001 | g0110 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18959 | hp2 | a0008 | c0010 | t0002 | g0042 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18964 | hp1 | a0001 | c0002 | t0002 | g0251 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18967 | hp1 | a0001 | c0002 | t0017 | g0254 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18968 | hp1 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18968 | hp2 | a0001 | c0002 | t0004 | g0237 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18969 | hp2 | a0001 | c0002 | t0002 | g0256 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18970 | hp2 | a0001 | c0002 | t0002 | g0258 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18971 | hp1 | a0003 | c0003 | t0016 | g0005 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18971 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18972 | hp2 | a0001 | c0002 | t0002 | g0244 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18973 | hp1 | a0001 | c0002 | t0007 | g0002 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18973 | hp2 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18974 | hp1 | a0001 | c0002 | t0007 | g0033 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18974 | hp2 | a0003 | c0003 | t0003 | g0226 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18975 | hp2 | a0001 | c0001 | t0022 | g0010 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18979 | hp2 | a0001 | c0002 | t0002 | g0239 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18980 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18981 | hp1 | a0001 | c0002 | t0002 | g0249 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18982 | hp1 | a0001 | c0005 | t0001 | g0215 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18982 | hp2 | a0001 | c0002 | t0002 | g0261 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18983 | hp1 | a0001 | c0002 | t0003 | g0220 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18983 | hp2 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18984 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18985 | hp1 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18990 | hp1 | a0006 | c0008 | t0001 | g0202 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18990 | hp2 | a0001 | c0002 | t0004 | g0080 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18991 | hp1 | a0001 | c0002 | t0002 | g0252 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18995 | hp1 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18995 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18997 | hp2 | a0003 | c0003 | t0003 | g0223 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18999 | hp1 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA18999 | hp2 | a0001 | c0002 | t0023 | g0002 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19002 | hp2 | a0003 | c0003 | t0003 | g0040 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19004 | hp1 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19004 | hp2 | a0001 | c0002 | t0002 | g0046 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19009 | hp1 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19009 | hp2 | a0006 | c0008 | t0001 | g0199 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19011 | hp1 | a0001 | c0002 | t0002 | g0245 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19012 | hp1 | a0012 | c0015 | t0003 | g0228 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | LWK | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19030 | hp2 | a0001 | c0002 | t0001 | g0117 | AFR | LWK | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | LWK | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19043 | hp2 | a0001 | c0002 | t0015 | g0269 | AFR | LWK | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19057 | hp1 | a0003 | c0003 | t0003 | g0040 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19057 | hp2 | a0001 | c0002 | t0002 | g0234 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19062 | hp2 | a0001 | c0002 | t0002 | g0257 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19065 | hp1 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19065 | hp2 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19067 | hp1 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19067 | hp2 | a0001 | c0002 | t0002 | g0260 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19068 | hp1 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19070 | hp1 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19076 | hp1 | a0001 | c0002 | t0002 | g0253 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19076 | hp2 | a0001 | c0002 | t0002 | g0057 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19078 | hp2 | a0001 | c0002 | t0010 | g0002 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19079 | hp1 | a0001 | c0005 | t0001 | g0001 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19079 | hp2 | a0001 | c0002 | t0007 | g0227 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19081 | hp1 | a0001 | c0002 | t0002 | g0240 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19082 | hp2 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19083 | hp1 | a0007 | c0009 | t0003 | g0005 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19083 | hp2 | a0001 | c0002 | t0002 | g0217 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19084 | hp2 | a0001 | c0002 | t0002 | g0243 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19085 | hp2 | a0001 | c0005 | t0001 | g0178 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19086 | hp1 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19086 | hp2 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19091 | hp1 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19240 | hp1 | a0001 | c0002 | t0008 | g0028 | AFR | YRI | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | YRI | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0019 | AFR | ASW | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA20129 | hp2 | a0001 | c0001 | t0005 | g0085 | AFR | ASW | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | TSI | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0103 | EUR | TSI | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA20905 | hp1 | a0001 | c0001 | t0025 | g0095 | SAS | GIH | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | GIH | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02109 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | ACB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02486 | hp1 | a0001 | c0002 | t0002 | g0262 | AFR | ACB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02486 | hp2 | a0001 | c0002 | t0015 | g0102 | AFR | ACB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02559 | hp1 | a0001 | c0002 | t0001 | g0074 | AFR | ACB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG02559 | hp2 | a0004 | c0006 | t0012 | g0053 | AFR | ACB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03471 | hp1 | a0001 | c0002 | t0002 | g0242 | AFR | MSL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG06807 | hp1 | a0001 | c0002 | t0006 | g0018 | AFR | USA | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | USA | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA20300 | hp1 | a0001 | c0002 | t0002 | g0247 | AFR | USA | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | USA | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA21309 | hp1 | a0004 | c0006 | t0001 | g0055 | AFR | LWK | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
NA21309 | hp2 | a0001 | c0002 | t0001 | g0246 | AFR | LWK | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0196 | REF | REF | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:26152564
|
C | G | 1 | a0010 | 1 | HG01361.hp1 | missense_variant | MODERATE | c.66C>G | p.Ser22Arg | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/4 | 367/3740 | 66/2085 | 22/694 | chr7 | 26152564 | ||
chr7:26152597
|
C | CCTG | 1 | a0002 | 11 | HG00741.hp2 HG01106.hp2 HG01167.hp2 others(8): Show |
disruptive_inframe_insertion | MODERATE | c.107_109dupTGC | p.Leu36dup | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/4 | 411/3740 | 110/2085 | 37/694 | INFO_REALIGN_3_PRIME | chr7 | 26152597 | |
chr7:26152772
|
C | T | 1 | a0005 | 2 | HG02145.hp2 HG03195.hp1 |
missense_variant | MODERATE | c.274C>T | p.Leu92Phe | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/4 | 575/3740 | 274/2085 | 92/694 | chr7 | 26152772 | ||
chr7:26152980
|
G | A | 1 | a0011 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.482G>A | p.Arg161Gln | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/4 | 783/3740 | 482/2085 | 161/694 | chr7 | 26152980 | ||
chr7:26153047
|
C | G | 1 | a0009 | 2 | HG02683.hp2 HG03942.hp1 |
missense_variant | MODERATE | c.549C>G | p.Asp183Glu | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/4 | 850/3740 | 549/2085 | 183/694 | chr7 | 26153047 | ||
chr7:26178049
|
A | G | 1 | a0016 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.677A>G | p.Asn226Ser | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/4 | 978/3740 | 677/2085 | 226/694 | chr7 | 26178049 | ||
chr7:26178061
|
A | G | 1 | a0004 | 3 | HG02258.hp1 HG02559.hp2 NA21309.hp1 |
missense_variant | MODERATE | c.689A>G | p.Glu230Gly | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/4 | 990/3740 | 689/2085 | 230/694 | chr7 | 26178061 | ||
chr7:26184623
|
A | G | 1 | a0015 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.925A>G | p.Ile309Val | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 1226/3740 | 925/2085 | 309/694 | chr7 | 26184623 | ||
chr7:26184819
|
A | G | 1 | a0008 | 2 | HG00544.hp2 NA18959.hp2 |
missense_variant | MODERATE | c.1121A>G | p.Asn374Ser | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 1422/3740 | 1121/2085 | 374/694 | chr7 | 26184819 | ||
chr7:26185020
|
T | A | 1 | a0006 | 2 | NA18990.hp1 NA19009.hp2 |
missense_variant | MODERATE | c.1322T>A | p.Val441Glu | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 1623/3740 | 1322/2085 | 441/694 | chr7 | 26185020 | ||
chr7:26185116
|
G | A | 1 | a0012 | 1 | NA19012.hp1 | missense_variant | MODERATE | c.1418G>A | p.Ser473Asn | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 1719/3740 | 1418/2085 | 473/694 | chr7 | 26185116 | ||
chr7:26185161
|
A | G | 1 | a0014 | 1 | HG02273.hp1 | missense_variant | MODERATE | c.1463A>G | p.Asp488Gly | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 1764/3740 | 1463/2085 | 488/694 | chr7 | 26185161 | ||
chr7:26185402
|
A | C | 1 | a0013 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.1704A>C | p.Arg568Ser | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 2005/3740 | 1704/2085 | 568/694 | chr7 | 26185402 | ||
chr7:26185548
|
A | C | 2 | a0007a0012 | 3 | HG02027.hp2 NA19012.hp1 NA19083.hp1 |
missense_variant | MODERATE | c.1850A>C | p.Lys617Thr | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 2151/3740 | 1850/2085 | 617/694 | chr7 | 26185548 | ||
chr7:26185559
|
A | G | 1 | a0003 | 10 | NA18971.hp1 NA18974.hp2 NA18983.hp2 others(7): Show |
missense_variant | MODERATE | c.1861A>G | p.Lys621Glu | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 2162/3740 | 1861/2085 | 621/694 | chr7 | 26185559 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:26185048
|
C | T | 9 | a0001c0002a0002c0007a0003c0003others(6): Show | 168 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(165): Show |
synonymous_variant | LOW | c.1350C>T | p.Cys450Cys | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 1651/3740 | 1350/2085 | 450/694 | chr7 | 26185048 | ||
chr7:26185519
|
A | G | 1 | a0001c0005 | 3 | NA18982.hp1 NA19079.hp1 NA19085.hp2 |
synonymous_variant | LOW | c.1821A>G | p.Glu607Glu | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 2122/3740 | 1821/2085 | 607/694 | chr7 | 26185519 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:26152240
|
G | C | 1 | a0003c0003t0016 | 1 | NA18971.hp1 | 5_prime_UTR_variant | MODIFIER | c.-259G>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/4 | 259 | chr7 | 26152240 | |||||
chr7:26152419
|
G | A | 1 | a0001c0002t0017 | 1 | NA18967.hp1 | 5_prime_UTR_variant | MODIFIER | c.-80G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/4 | 80 | chr7 | 26152419 | |||||
chr7:26185800
|
G | T | 1 | a0001c0002t0015 | 2 | HG02486.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*17G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 17 | chr7 | 26185800 | |||||
chr7:26185836
|
A | G | 1 | a0001c0001t0026 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*53A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 53 | chr7 | 26185836 | |||||
chr7:26185913
|
C | A | 1 | a0001c0002t0006 | 7 | HG01109.hp1 HG02055.hp1 HG02258.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*130C>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 130 | chr7 | 26185913 | |||||
chr7:26186029
|
T | C | 1 | a0001c0001t0018 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*246T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 246 | chr7 | 26186029 | |||||
chr7:26186149
|
G | A | 1 | a0001c0002t0010 | 3 | NA18940.hp1 NA18947.hp2 NA19078.hp2 |
3_prime_UTR_variant | MODIFIER | c.*366G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 366 | chr7 | 26186149 | |||||
chr7:26186152
|
T | A | 2 | a0002c0004t0009a0005c0012t0009 | 4 | HG02145.hp2 HG02647.hp1 HG02970.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*369T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 369 | chr7 | 26186152 | |||||
chr7:26186244
|
CTT | C | 7 | a0001c0002t0003a0001c0002t0011a0002c0007t0003others(4): Show | 30 | HG00438.hp2 HG00597.hp2 HG00733.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*462_*463delTT | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 462 | chr7 | 26186244 | |||||
chr7:26186265
|
G | A | 1 | a0004c0006t0012 | 2 | HG02258.hp1 HG02559.hp2 |
3_prime_UTR_variant | MODIFIER | c.*482G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 482 | chr7 | 26186265 | |||||
chr7:26186298
|
C | T | 1 | a0001c0001t0025 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*515C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 515 | chr7 | 26186298 | |||||
chr7:26186333
|
CCTTA | C | 1 | a0001c0002t0007 | 7 | HG00423.hp2 HG02129.hp1 HG02165.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*554_*557delACTT | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 554 | INFO_REALIGN_3_PRIME | chr7 | 26186333 | ||||
chr7:26186402
|
C | T | 2 | a0001c0001t0005a0002c0004t0005 | 8 | HG00741.hp2 HG01167.hp2 HG01169.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*619C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 619 | chr7 | 26186402 | |||||
chr7:26186479
|
A | ATACTT | 3 | a0001c0002t0002a0001c0002t0017a0008c0010t0002 | 70 | HG00544.hp2 HG01255.hp2 HG01346.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*697_*701dupTACTT | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 702 | INFO_REALIGN_3_PRIME | chr7 | 26186479 | ||||
chr7:26186517
|
C | T | 1 | a0001c0002t0008 | 5 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*734C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 734 | chr7 | 26186517 | |||||
chr7:26186569
|
C | T | 6 | a0001c0002t0003a0002c0007t0003a0003c0003t0003others(3): Show | 27 | HG00438.hp2 HG00597.hp2 HG00733.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*786C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 786 | chr7 | 26186569 | |||||
chr7:26186723
|
G | T | 1 | a0001c0002t0024 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*940G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 940 | chr7 | 26186723 | |||||
chr7:26186808
|
C | A | 1 | a0001c0001t0019 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1025C>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 1025 | chr7 | 26186808 | |||||
chr7:26186808
|
C | T | 5 | a0001c0002t0004a0001c0002t0007a0001c0002t0010others(2): Show | 21 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1025C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 1025 | chr7 | 26186808 | |||||
chr7:26186830
|
A | G | 1 | a0001c0001t0022 | 1 | NA18975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1047A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 1047 | chr7 | 26186830 | |||||
chr7:26186834
|
T | G | 1 | a0001c0001t0013 | 2 | HG01081.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1051T>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 1051 | chr7 | 26186834 | |||||
chr7:26186959
|
G | A | 1 | a0001c0002t0023 | 1 | NA18999.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1176G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 1176 | chr7 | 26186959 | |||||
chr7:26187009
|
ATAT | A | 1 | a0001c0002t0011 | 3 | HG02451.hp1 HG02922.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1231_*1233delATT | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 1231 | INFO_REALIGN_3_PRIME | chr7 | 26187009 | ||||
chr7:26187034
|
A | G | 2 | a0001c0002t0014a0016c0018t0014 | 2 | HG03195.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1251A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 1251 | chr7 | 26187034 | |||||
chr7:26187086
|
A | G | 1 | a0001c0001t0021 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1303A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 1303 | chr7 | 26187086 | |||||
chr7:26187126
|
T | G | 1 | a0001c0001t0020 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1343T>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 1343 | chr7 | 26187126 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:26153193
|
G | A | 5 | a0001c0002t0001g0009a0001c0002t0001g0049a0001c0002t0001g0050others(2): Show | 8 | HG01069.hp2 HG01071.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.570+125G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26153193 | ||||||
chr7:26153216
|
C | G | 1 | a0001c0002t0015g0269 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.570+148C>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26153216 | ||||||
chr7:26153312
|
C | T | 1 | a0010c0019t0001g0268 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.570+244C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26153312 | ||||||
chr7:26153536
|
A | G | 1 | a0001c0002t0015g0269 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.570+468A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26153536 | ||||||
chr7:26153539
|
G | T | 1 | a0001c0001t0001g0267 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.570+471G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26153539 | ||||||
chr7:26153540
|
C | A | 1 | a0001c0001t0001g0267 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.570+472C>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26153540 | ||||||
chr7:26153556
|
C | T | 72 | a0001c0001t0001g0216a0001c0001t0001g0219a0001c0001t0001g0235others(69): Show | 113 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.570+488C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26153556 | ||||||
chr7:26153618
|
C | T | 1 | a0001c0002t0002g0266 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.570+550C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26153618 | ||||||
chr7:26153689
|
C | A | 190 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0020others(187): Show | 264 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.570+621C>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26153689 | ||||||
chr7:26153740
|
T | G | 1 | a0001c0005t0001g0215 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.570+672T>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26153740 | ||||||
chr7:26153838
|
A | G | 1 | a0001c0002t0001g0052 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.570+770A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26153838 | ||||||
chr7:26153853
|
C | T | 1 | a0001c0002t0003g0265 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.570+785C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26153853 | ||||||
chr7:26153886
|
C | T | 1 | a0001c0002t0002g0266 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.570+818C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26153886 | ||||||
chr7:26153898
|
T | A | 3 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144 | 3 | HG03669.hp2 HG03710.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.570+830T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26153898 | ||||||
chr7:26153899
|
C | A | 3 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144 | 3 | HG03669.hp2 HG03710.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.570+831C>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26153899 | ||||||
chr7:26154017
|
T | C | 2 | a0004c0006t0012g0053a0004c0006t0012g0054 | 2 | HG02258.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.570+949T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26154017 | ||||||
chr7:26154114
|
A | AG | 4 | a0001c0002t0001g0056a0004c0006t0001g0055a0004c0006t0012g0053others(1): Show | 4 | HG02258.hp1 HG02559.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+1050dupG | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26154114 | |||||
chr7:26154153
|
T | G | 1 | a0001c0001t0001g0145 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.570+1085T>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26154153 | ||||||
chr7:26154185
|
C | T | 1 | a0016c0018t0014g0141 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.570+1117C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26154185 | ||||||
chr7:26154535
|
T | C | 6 | a0001c0001t0001g0035a0001c0001t0001g0146a0001c0001t0001g0147others(3): Show | 7 | HG00642.hp1 HG01192.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.570+1467T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26154535 | ||||||
chr7:26154582
|
G | C | 1 | a0001c0001t0001g0216 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.570+1514G>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26154582 | ||||||
chr7:26154590
|
G | A | 1 | a0001c0002t0002g0217 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.570+1522G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26154590 | ||||||
chr7:26154644
|
C | T | 1 | a0001c0001t0001g0214 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.570+1576C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26154644 | ||||||
chr7:26154657
|
C | G | 4 | a0002c0004t0005g0047a0002c0004t0005g0048a0002c0004t0005g0263others(1): Show | 6 | HG00741.hp2 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.570+1589C>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26154657 | ||||||
chr7:26154928
|
A | C | 1 | a0001c0002t0002g0262 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.570+1860A>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26154928 | ||||||
chr7:26154933
|
G | A | 1 | a0001c0002t0002g0218 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.570+1865G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26154933 | ||||||
chr7:26155240
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.570+2172C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26155240 | ||||||
chr7:26155319
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.570+2251G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26155319 | ||||||
chr7:26155373
|
C | T | 3 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213 | 3 | NA18944.hp2 NA18950.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.570+2305C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26155373 | ||||||
chr7:26155396
|
T | A | 1 | a0001c0002t0002g0057 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.570+2328T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26155396 | ||||||
chr7:26155438
|
T | A | 1 | a0001c0002t0003g0265 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.570+2370T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26155438 | ||||||
chr7:26155564
|
CATTA | C | 4 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(1): Show | 4 | HG00738.hp2 HG02717.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+2502_570+2505d others(6): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26155564 | |||||
chr7:26155974
|
C | T | 141 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0020others(138): Show | 197 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.570+2906C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26155974 | ||||||
chr7:26156058
|
G | A | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG00733.hp2 HG01175.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.570+2990G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26156058 | ||||||
chr7:26156199
|
G | T | 1 | a0001c0002t0001g0074 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.570+3131G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26156199 | ||||||
chr7:26156209
|
A | C | 2 | a0001c0002t0001g0138a0001c0002t0001g0139 | 2 | HG02145.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.570+3141A>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26156209 | ||||||
chr7:26156239
|
C | T | 1 | a0002c0007t0003g0232 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.570+3171C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26156239 | ||||||
chr7:26156520
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.570+3452T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26156520 | ||||||
chr7:26156810
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.570+3742C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26156810 | ||||||
chr7:26156835
|
G | A | 1 | a0001c0002t0014g0076 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.570+3767G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26156835 | ||||||
chr7:26156969
|
G | A | 1 | a0001c0002t0002g0233 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.570+3901G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26156969 | ||||||
chr7:26157044
|
G | A | 1 | a0001c0002t0002g0234 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.570+3976G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26157044 | ||||||
chr7:26157064
|
A | C | 1 | a0001c0002t0010g0137 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.570+3996A>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26157064 | ||||||
chr7:26157077
|
A | G | 5 | a0001c0002t0001g0009a0001c0002t0001g0049a0001c0002t0001g0050others(2): Show | 8 | HG01069.hp2 HG01071.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.570+4009A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26157077 | ||||||
chr7:26157199
|
G | A | 187 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0020others(184): Show | 260 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.570+4131G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26157199 | ||||||
chr7:26157282
|
A | G | 18 | a0001c0001t0001g0075a0001c0002t0001g0009a0001c0002t0001g0049others(15): Show | 24 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.570+4214A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26157282 | ||||||
chr7:26157343
|
G | A | 182 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0020others(179): Show | 255 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.570+4275G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26157343 | ||||||
chr7:26157345
|
T | A | 1 | a0001c0002t0002g0057 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.570+4277T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26157345 | ||||||
chr7:26157418
|
C | T | 1 | a0001c0001t0001g0207 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.570+4350C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26157418 | ||||||
chr7:26157524
|
A | G | 1 | a0001c0002t0001g0134 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.570+4456A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26157524 | ||||||
chr7:26157779
|
T | G | 1 | a0001c0001t0001g0072 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.570+4711T>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26157779 | ||||||
chr7:26158059
|
T | G | 140 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0020others(137): Show | 197 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.570+4991T>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26158059 | ||||||
chr7:26158060
|
TA | T | 140 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0020others(137): Show | 197 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.570+4993delA | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26158060 | ||||||
chr7:26158206
|
G | A | 10 | a0001c0001t0001g0011a0001c0001t0001g0158a0001c0001t0001g0159others(7): Show | 15 | HG00741.hp2 HG01081.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.570+5138G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26158206 | ||||||
chr7:26158420
|
T | C | 95 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0020others(92): Show | 121 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.570+5352T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26158420 | ||||||
chr7:26158518
|
C | T | 2 | a0001c0002t0001g0133a0001c0002t0001g0156 | 2 | HG01884.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.570+5450C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26158518 | ||||||
chr7:26158587
|
A | G | 186 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0020others(183): Show | 259 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.570+5519A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26158587 | ||||||
chr7:26158883
|
A | G | 1 | a0001c0001t0001g0206 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.570+5815A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26158883 | ||||||
chr7:26159043
|
G | C | 1 | a0001c0002t0001g0049 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.570+5975G>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26159043 | ||||||
chr7:26159065
|
C | T | 1 | a0001c0002t0002g0261 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.570+5997C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26159065 | ||||||
chr7:26159105
|
A | G | 12 | a0001c0002t0001g0009a0001c0002t0001g0049a0001c0002t0001g0050others(9): Show | 17 | HG01069.hp2 HG01071.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.570+6037A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26159105 | ||||||
chr7:26159490
|
A | T | 1 | a0001c0001t0001g0162 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.570+6422A>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26159490 | ||||||
chr7:26159587
|
A | G | 185 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0020others(182): Show | 256 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.570+6519A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26159587 | ||||||
chr7:26159900
|
G | A | 21 | a0001c0001t0018g0225a0001c0002t0003g0005a0001c0002t0003g0041others(18): Show | 29 | HG00438.hp2 HG00597.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.570+6832G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26159900 | ||||||
chr7:26159949
|
C | CT | 41 | a0001c0001t0001g0022a0001c0001t0001g0060a0001c0001t0001g0073others(38): Show | 50 | HG00544.hp1 HG00735.hp2 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.570+6901dupT | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26159949 | |||||
chr7:26159949
|
C | CTT | 11 | a0001c0001t0001g0061a0001c0001t0001g0072a0001c0001t0001g0075others(8): Show | 12 | HG00639.hp1 HG00738.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.570+6900_570+6901d others(4): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26159949 | |||||
chr7:26160247
|
G | A | 1 | a0001c0002t0011g0026 | 3 | HG02451.hp1 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.570+7179G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26160247 | ||||||
chr7:26160493
|
C | G | 1 | a0001c0002t0007g0033 | 2 | HG02129.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.570+7425C>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26160493 | ||||||
chr7:26160593
|
A | G | 187 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0020others(184): Show | 260 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.570+7525A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26160593 | ||||||
chr7:26160595
|
T | C | 46 | a0001c0001t0001g0216a0001c0001t0001g0235a0001c0002t0001g0133others(43): Show | 75 | HG00544.hp2 HG00733.hp1 HG01255.hp2 others(72): Show |
intron_variant | MODIFIER | c.570+7527T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26160595 | ||||||
chr7:26160735
|
A | G | 4 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0131others(1): Show | 4 | NA18946.hp1 NA18960.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.570+7667A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26160735 | ||||||
chr7:26160797
|
C | T | 93 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0020others(90): Show | 119 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.570+7729C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26160797 | ||||||
chr7:26160836
|
A | G | 2 | a0001c0001t0001g0022a0001c0001t0001g0130 | 4 | NA18957.hp1 NA18977.hp2 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.570+7768A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26160836 | ||||||
chr7:26161333
|
CTCT | C | 3 | a0001c0002t0002g0017a0001c0002t0002g0236a0001c0002t0002g0257 | 6 | NA18747.hp2 NA18947.hp1 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.570+8267_570+8269d others(5): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26161333 | |||||
chr7:26161335
|
CT | C | 64 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(61): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.570+8296delT | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26161335 | |||||
chr7:26161335
|
CTT | C | 8 | a0001c0001t0001g0012a0001c0001t0001g0036a0001c0001t0001g0164others(5): Show | 11 | HG02132.hp1 HG02273.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.570+8295_570+8296d others(4): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26161335 | |||||
chr7:26161337
|
T | C | 5 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0131others(2): Show | 5 | HG01081.hp2 NA18946.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.570+8269T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26161337 | ||||||
chr7:26161339
|
T | C | 1 | a0001c0002t0002g0262 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.570+8271T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26161339 | ||||||
chr7:26161348
|
TTTTTTTT others(10): Show |
T | 1 | a0001c0002t0015g0269 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.570+8281_570+8297d others(19): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26161348 | ||||||
chr7:26161350
|
TTTTTTTT others(8): Show |
T | 2 | a0001c0002t0001g0078a0001c0002t0002g0239 | 2 | HG03041.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.570+8283_570+8297d others(17): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26161350 | ||||||
chr7:26161352
|
TTTTTTTT others(6): Show |
T | 1 | a0001c0001t0001g0130 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.570+8285_570+8297d others(15): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26161352 | ||||||
chr7:26161353
|
TTTTTTTT others(5): Show |
T | 2 | a0001c0001t0001g0238a0001c0002t0001g0133 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.570+8286_570+8297d others(14): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26161353 | ||||||
chr7:26161354
|
TTTTTTTT others(4): Show |
T | 1 | a0001c0002t0014g0076 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.570+8287_570+8297d others(13): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26161354 | ||||||
chr7:26161355
|
TTTTTTTT others(3): Show |
T | 1 | a0001c0002t0001g0079 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.570+8288_570+8297d others(12): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26161355 | ||||||
chr7:26161360
|
TTTTTG | T | 27 | a0001c0001t0001g0082a0001c0001t0001g0121a0001c0001t0001g0122others(24): Show | 35 | HG00741.hp2 HG01071.hp1 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.570+8293_570+8297d others(7): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26161360 | ||||||
chr7:26161361
|
TTTTG | T | 88 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0020others(85): Show | 120 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.570+8294_570+8297d others(6): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26161361 | ||||||
chr7:26161362
|
TTTG | T | 17 | a0001c0001t0001g0021a0001c0001t0001g0063a0001c0001t0001g0119others(14): Show | 19 | HG00438.hp1 HG00741.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.570+8295_570+8297d others(5): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26161362 | ||||||
chr7:26161363
|
TTG | T | 31 | a0001c0001t0001g0216a0001c0001t0001g0235a0001c0002t0001g0246others(28): Show | 57 | HG00544.hp2 HG00733.hp1 HG01255.hp2 others(54): Show |
intron_variant | MODIFIER | c.570+8296_570+8297d others(4): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26161363 | ||||||
chr7:26161364
|
T | G | 1 | a0001c0001t0001g0163 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.570+8296T>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26161364 | ||||||
chr7:26161364
|
TG | T | 7 | a0001c0002t0002g0251a0001c0002t0002g0252a0001c0002t0002g0253others(4): Show | 7 | HG02071.hp2 NA18964.hp1 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.570+8299delG | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26161364 | |||||
chr7:26161365
|
G | T | 5 | a0001c0002t0002g0017a0001c0002t0002g0057a0001c0002t0002g0236others(2): Show | 10 | HG02451.hp1 HG02922.hp2 HG03139.hp2 others(7): Show |
intron_variant | MODIFIER | c.570+8297G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26161365 | ||||||
chr7:26161412
|
A | G | 1 | a0003c0003t0003g0040 | 2 | NA19002.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.570+8344A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26161412 | ||||||
chr7:26161486
|
G | A | 4 | a0002c0004t0005g0047a0002c0004t0005g0048a0002c0004t0005g0263others(1): Show | 6 | HG00741.hp2 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.570+8418G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26161486 | ||||||
chr7:26161572
|
C | G | 2 | a0001c0001t0001g0020a0001c0001t0001g0116 | 4 | HG00639.hp2 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.570+8504C>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26161572 | ||||||
chr7:26161590
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.570+8522C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26161590 | ||||||
chr7:26161778
|
G | A | 1 | a0002c0004t0009g0039 | 2 | HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.570+8710G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26161778 | ||||||
chr7:26162051
|
G | A | 1 | a0001c0001t0013g0168 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.570+8983G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26162051 | ||||||
chr7:26162142
|
C | CA | 29 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0001g0083others(26): Show | 35 | HG00738.hp2 HG01069.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.570+9091dupA | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26162142 | |||||
chr7:26162202
|
A | G | 2 | a0009c0011t0001g0114a0009c0011t0001g0115 | 2 | HG02683.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.570+9134A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26162202 | ||||||
chr7:26162309
|
G | A | 1 | a0001c0002t0001g0124 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.570+9241G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26162309 | ||||||
chr7:26162470
|
GAA | G | 1 | a0001c0001t0001g0020 | 3 | HG00639.hp2 HG01071.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.570+9404_570+9405d others(4): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26162470 | |||||
chr7:26162693
|
T | C | 3 | a0001c0001t0005g0085a0001c0001t0005g0128a0010c0019t0001g0268 | 3 | HG01361.hp1 HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.570+9625T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26162693 | ||||||
chr7:26162788
|
C | G | 132 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0020others(129): Show | 173 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.570+9720C>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26162788 | ||||||
chr7:26162870
|
G | A | 180 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0020others(177): Show | 251 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.570+9802G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26162870 | ||||||
chr7:26163197
|
A | G | 1 | a0001c0002t0006g0070 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.570+10129A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26163197 | ||||||
chr7:26163251
|
C | T | 1 | a0001c0002t0011g0026 | 3 | HG02451.hp1 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.570+10183C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26163251 | ||||||
chr7:26163375
|
T | C | 1 | a0001c0001t0013g0168 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.570+10307T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26163375 | ||||||
chr7:26163391
|
G | A | 44 | a0001c0001t0001g0216a0001c0002t0001g0133a0001c0002t0001g0156others(41): Show | 73 | HG00544.hp2 HG00733.hp1 HG01255.hp2 others(70): Show |
intron_variant | MODIFIER | c.570+10323G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26163391 | ||||||
chr7:26163590
|
G | T | 2 | a0001c0001t0005g0085a0001c0001t0005g0128 | 2 | HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.570+10522G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26163590 | ||||||
chr7:26163619
|
T | A | 1 | a0008c0010t0002g0042 | 2 | HG00544.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.570+10551T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26163619 | ||||||
chr7:26163621
|
A | C | 1 | a0008c0010t0002g0042 | 2 | HG00544.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.570+10553A>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26163621 | ||||||
chr7:26163815
|
C | T | 2 | a0001c0001t0005g0085a0001c0001t0005g0128 | 2 | HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.570+10747C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26163815 | ||||||
chr7:26163911
|
G | A | 2 | a0001c0001t0001g0086a0001c0001t0001g0125 | 2 | NA18962.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.570+10843G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26163911 | ||||||
chr7:26163971
|
G | A | 45 | a0001c0001t0001g0216a0001c0002t0001g0133a0001c0002t0001g0156others(42): Show | 74 | HG00544.hp2 HG00733.hp1 HG01255.hp2 others(71): Show |
intron_variant | MODIFIER | c.570+10903G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26163971 | ||||||
chr7:26163982
|
A | G | 45 | a0001c0001t0001g0216a0001c0002t0001g0133a0001c0002t0001g0156others(42): Show | 74 | HG00544.hp2 HG00733.hp1 HG01255.hp2 others(71): Show |
intron_variant | MODIFIER | c.570+10914A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26163982 | ||||||
chr7:26164364
|
T | C | 5 | a0001c0002t0001g0009a0001c0002t0001g0049a0001c0002t0001g0050others(2): Show | 8 | HG01069.hp2 HG01071.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.570+11296T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26164364 | ||||||
chr7:26164387
|
C | T | 1 | a0007c0009t0003g0229 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.570+11319C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26164387 | ||||||
chr7:26164884
|
A | G | 1 | a0001c0002t0011g0026 | 3 | HG02451.hp1 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.570+11816A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26164884 | ||||||
chr7:26165031
|
A | G | 44 | a0001c0001t0001g0216a0001c0002t0001g0133a0001c0002t0001g0156others(41): Show | 73 | HG00544.hp2 HG00733.hp1 HG01255.hp2 others(70): Show |
intron_variant | MODIFIER | c.570+11963A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26165031 | ||||||
chr7:26165052
|
C | A | 1 | a0001c0001t0001g0087 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.570+11984C>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26165052 | ||||||
chr7:26165057
|
T | C | 1 | a0001c0002t0011g0026 | 3 | HG02451.hp1 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.570+11989T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26165057 | ||||||
chr7:26165187
|
C | A | 1 | a0001c0002t0004g0129 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.570+12119C>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26165187 | ||||||
chr7:26165224
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.570+12156A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26165224 | ||||||
chr7:26165257
|
G | A | 1 | a0002c0007t0003g0232 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.570+12189G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26165257 | ||||||
chr7:26165323
|
G | A | 1 | a0001c0002t0014g0076 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.570+12255G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26165323 | ||||||
chr7:26165419
|
T | C | 1 | a0001c0001t0001g0214 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.570+12351T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26165419 | ||||||
chr7:26165708
|
G | A | 44 | a0001c0001t0001g0216a0001c0002t0001g0133a0001c0002t0001g0156others(41): Show | 73 | HG00544.hp2 HG00733.hp1 HG01255.hp2 others(70): Show |
intron_variant | MODIFIER | c.571-12235G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26165708 | ||||||
chr7:26165816
|
C | T | 1 | a0002c0007t0003g0231 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.571-12127C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26165816 | ||||||
chr7:26165900
|
A | G | 2 | a0001c0001t0001g0084a0001c0001t0001g0113 | 2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.571-12043A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26165900 | ||||||
chr7:26165982
|
C | T | 1 | a0001c0002t0001g0112 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.571-11961C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26165982 | ||||||
chr7:26166029
|
A | C | 1 | a0001c0001t0001g0189 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.571-11914A>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26166029 | ||||||
chr7:26166136
|
CG | C | 180 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0020others(177): Show | 251 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.571-11800delG | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26166136 | |||||
chr7:26166230
|
G | C | 12 | a0001c0002t0001g0019a0001c0002t0001g0078a0001c0002t0001g0089others(9): Show | 14 | HG02145.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.571-11713G>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26166230 | ||||||
chr7:26166249
|
G | A | 2 | a0001c0001t0001g0022a0001c0001t0001g0130 | 4 | NA18957.hp1 NA18977.hp2 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-11694G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26166249 | ||||||
chr7:26166360
|
C | T | 42 | a0001c0001t0001g0216a0001c0002t0001g0246a0001c0002t0002g0003others(39): Show | 71 | HG00544.hp2 HG00733.hp1 HG01255.hp2 others(68): Show |
intron_variant | MODIFIER | c.571-11583C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26166360 | ||||||
chr7:26166400
|
G | A | 1 | a0001c0002t0008g0064 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.571-11543G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26166400 | ||||||
chr7:26166589
|
T | A | 1 | a0001c0001t0001g0092 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.571-11354T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26166589 | ||||||
chr7:26166678
|
A | C | 1 | a0012c0015t0003g0228 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.571-11265A>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26166678 | ||||||
chr7:26166854
|
C | T | 1 | a0001c0002t0011g0026 | 3 | HG02451.hp1 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.571-11089C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26166854 | ||||||
chr7:26167033
|
G | A | 1 | a0009c0011t0001g0114 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.571-10910G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26167033 | ||||||
chr7:26167058
|
T | C | 5 | a0001c0002t0002g0043a0001c0002t0002g0057a0001c0002t0002g0132others(2): Show | 6 | NA18949.hp2 NA18952.hp1 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.571-10885T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26167058 | ||||||
chr7:26167101
|
C | A | 2 | a0001c0002t0003g0220a0001c0002t0003g0221 | 2 | HG00438.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.571-10842C>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26167101 | ||||||
chr7:26167175
|
G | A | 2 | a0001c0001t0001g0170a0001c0001t0001g0191 | 2 | NA18981.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.571-10768G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26167175 | ||||||
chr7:26167494
|
A | T | 44 | a0001c0001t0001g0216a0001c0002t0001g0133a0001c0002t0001g0156others(41): Show | 73 | HG00544.hp2 HG00733.hp1 HG01255.hp2 others(70): Show |
intron_variant | MODIFIER | c.571-10449A>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26167494 | ||||||
chr7:26167529
|
C | CT | 44 | a0001c0001t0001g0216a0001c0002t0001g0133a0001c0002t0001g0156others(41): Show | 73 | HG00544.hp2 HG00733.hp1 HG01255.hp2 others(70): Show |
intron_variant | MODIFIER | c.571-10403dupT | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26167529 | |||||
chr7:26167736
|
C | A | 1 | a0001c0001t0001g0238 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.571-10207C>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26167736 | ||||||
chr7:26167864
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.571-10079C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26167864 | ||||||
chr7:26167970
|
G | A | 44 | a0001c0001t0001g0216a0001c0002t0001g0133a0001c0002t0001g0156others(41): Show | 73 | HG00544.hp2 HG00733.hp1 HG01255.hp2 others(70): Show |
intron_variant | MODIFIER | c.571-9973G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26167970 | ||||||
chr7:26168103
|
C | T | 20 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0032others(17): Show | 28 | HG00609.hp2 HG00642.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.571-9840C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26168103 | ||||||
chr7:26168135
|
C | A | 134 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0020others(131): Show | 175 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.571-9808C>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26168135 | ||||||
chr7:26168163
|
G | T | 1 | a0001c0002t0011g0026 | 3 | HG02451.hp1 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.571-9780G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26168163 | ||||||
chr7:26168405
|
A | G | 178 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0020others(175): Show | 248 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.571-9538A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26168405 | ||||||
chr7:26168426
|
G | GTGCCCAG others(113): Show |
179 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0020others(176): Show | 249 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.571-9516_571-9515i others(122): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26168426 | |||||
chr7:26168470
|
G | A | 1 | a0001c0002t0011g0026 | 3 | HG02451.hp1 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.571-9473G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26168470 | ||||||
chr7:26168516
|
G | T | 20 | a0001c0001t0018g0225a0001c0002t0003g0005a0001c0002t0003g0041others(17): Show | 27 | HG00438.hp2 HG00597.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.571-9427G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26168516 | ||||||
chr7:26168517
|
A | G | 20 | a0001c0001t0018g0225a0001c0002t0003g0005a0001c0002t0003g0041others(17): Show | 27 | HG00438.hp2 HG00597.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.571-9426A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26168517 | ||||||
chr7:26168524
|
G | A | 44 | a0001c0001t0001g0216a0001c0002t0001g0133a0001c0002t0001g0156others(41): Show | 73 | HG00544.hp2 HG00733.hp1 HG01255.hp2 others(70): Show |
intron_variant | MODIFIER | c.571-9419G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26168524 | ||||||
chr7:26168530
|
AAT | A | 44 | a0001c0001t0001g0216a0001c0002t0001g0133a0001c0002t0001g0156others(41): Show | 73 | HG00544.hp2 HG00733.hp1 HG01255.hp2 others(70): Show |
intron_variant | MODIFIER | c.571-9403_571-9402d others(4): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26168530 | |||||
chr7:26168567
|
T | G | 4 | a0002c0004t0005g0047a0002c0004t0005g0048a0002c0004t0005g0263others(1): Show | 6 | HG00741.hp2 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.571-9376T>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26168567 | ||||||
chr7:26168569
|
G | T | 45 | a0001c0001t0001g0216a0001c0002t0001g0056a0001c0002t0001g0133others(42): Show | 74 | HG00544.hp2 HG00733.hp1 HG01255.hp2 others(71): Show |
intron_variant | MODIFIER | c.571-9374G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26168569 | ||||||
chr7:26168772
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.571-9171C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26168772 | ||||||
chr7:26168796
|
G | A | 44 | a0001c0001t0001g0216a0001c0002t0001g0133a0001c0002t0001g0156others(41): Show | 73 | HG00544.hp2 HG00733.hp1 HG01255.hp2 others(70): Show |
intron_variant | MODIFIER | c.571-9147G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26168796 | ||||||
chr7:26168868
|
A | G | 44 | a0001c0001t0001g0216a0001c0002t0001g0133a0001c0002t0001g0156others(41): Show | 73 | HG00544.hp2 HG00733.hp1 HG01255.hp2 others(70): Show |
intron_variant | MODIFIER | c.571-9075A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26168868 | ||||||
chr7:26169116
|
G | A | 180 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0020others(177): Show | 250 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.571-8827G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26169116 | ||||||
chr7:26169128
|
T | C | 2 | a0001c0002t0006g0018a0001c0002t0006g0071 | 4 | HG01109.hp1 HG03579.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-8815T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26169128 | ||||||
chr7:26169185
|
C | T | 180 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0020others(177): Show | 250 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.571-8758C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26169185 | ||||||
chr7:26169369
|
A | G | 1 | a0001c0001t0001g0206 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.571-8574A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26169369 | ||||||
chr7:26169374
|
C | T | 2 | a0001c0002t0007g0227a0012c0015t0003g0228 | 2 | NA19012.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.571-8569C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26169374 | ||||||
chr7:26169441
|
G | A | 134 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0020others(131): Show | 174 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.571-8502G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26169441 | ||||||
chr7:26169497
|
G | A | 1 | a0001c0001t0001g0038 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.571-8446G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26169497 | ||||||
chr7:26169586
|
C | A | 179 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0020others(176): Show | 248 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(245): Show |
intron_variant | MODIFIER | c.571-8357C>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26169586 | ||||||
chr7:26169811
|
A | G | 4 | a0001c0001t0001g0015a0001c0001t0001g0164a0001c0001t0001g0167others(1): Show | 7 | HG00597.hp1 NA18946.hp2 NA18988.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-8132A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26169811 | ||||||
chr7:26169835
|
C | T | 45 | a0001c0001t0001g0216a0001c0002t0001g0056a0001c0002t0001g0133others(42): Show | 74 | HG00544.hp2 HG00733.hp1 HG01255.hp2 others(71): Show |
intron_variant | MODIFIER | c.571-8108C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26169835 | ||||||
chr7:26169935
|
CA | C | 42 | a0001c0001t0001g0216a0001c0002t0001g0246a0001c0002t0002g0003others(39): Show | 73 | HG00544.hp2 HG00733.hp1 HG01255.hp2 others(70): Show |
intron_variant | MODIFIER | c.571-7997delA | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26169935 | |||||
chr7:26170126
|
A | G | 13 | a0001c0002t0001g0009a0001c0002t0001g0049a0001c0002t0001g0050others(10): Show | 18 | HG01069.hp2 HG01071.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.571-7817A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26170126 | ||||||
chr7:26170686
|
C | A | 73 | a0001c0001t0001g0209a0001c0001t0001g0238a0001c0001t0018g0225others(70): Show | 100 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.571-7257C>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26170686 | ||||||
chr7:26170908
|
C | T | 1 | a0001c0002t0006g0069 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.571-7035C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26170908 | ||||||
chr7:26170926
|
G | A | 1 | a0001c0001t0001g0171 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.571-7017G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26170926 | ||||||
chr7:26171030
|
A | G | 1 | a0001c0001t0001g0198 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.571-6913A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26171030 | ||||||
chr7:26171089
|
A | G | 1 | a0001c0001t0001g0104 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.571-6854A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26171089 | ||||||
chr7:26171140
|
C | G | 10 | a0001c0002t0001g0019a0001c0002t0001g0078a0001c0002t0001g0089others(7): Show | 12 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.571-6803C>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26171140 | ||||||
chr7:26171183
|
A | G | 34 | a0001c0001t0001g0209a0001c0001t0026g0081a0001c0002t0001g0019others(31): Show | 46 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.571-6760A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26171183 | ||||||
chr7:26171267
|
T | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG00738.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.571-6676T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26171267 | ||||||
chr7:26171268
|
G | C | 1 | a0001c0002t0001g0079 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.571-6675G>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26171268 | ||||||
chr7:26171286
|
C | T | 4 | a0001c0001t0001g0015a0001c0001t0001g0164a0001c0001t0001g0167others(1): Show | 7 | HG00597.hp1 NA18946.hp2 NA18988.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-6657C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26171286 | ||||||
chr7:26171379
|
A | G | 1 | a0001c0001t0001g0103 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.571-6564A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26171379 | ||||||
chr7:26171392
|
A | G | 1 | a0001c0001t0001g0111 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.571-6551A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26171392 | ||||||
chr7:26171436
|
C | T | 1 | a0001c0002t0002g0250 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.571-6507C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26171436 | ||||||
chr7:26171709
|
T | A | 8 | a0001c0002t0001g0078a0001c0002t0001g0089a0001c0002t0001g0090others(5): Show | 8 | HG02145.hp1 HG02717.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.571-6234T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26171709 | ||||||
chr7:26171770
|
C | G | 1 | a0003c0003t0003g0226 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.571-6173C>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26171770 | ||||||
chr7:26171773
|
A | G | 2 | a0001c0002t0015g0102a0001c0002t0015g0269 | 2 | HG02486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.571-6170A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26171773 | ||||||
chr7:26171851
|
C | CA | 5 | a0001c0001t0001g0192a0001c0001t0001g0200a0001c0002t0002g0044others(2): Show | 6 | HG02572.hp1 NA18747.hp1 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.571-6084dupA | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26171851 | |||||
chr7:26171922
|
C | T | 1 | a0001c0001t0005g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.571-6021C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26171922 | ||||||
chr7:26172003
|
T | C | 5 | a0001c0001t0001g0075a0001c0002t0008g0028a0001c0002t0008g0064others(2): Show | 6 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.571-5940T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26172003 | ||||||
chr7:26172083
|
T | A | 5 | a0001c0001t0001g0075a0001c0002t0008g0028a0001c0002t0008g0064others(2): Show | 6 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.571-5860T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26172083 | ||||||
chr7:26172154
|
C | T | 42 | a0001c0002t0001g0246a0001c0002t0002g0003a0001c0002t0002g0007others(39): Show | 71 | HG00544.hp2 HG01255.hp2 HG01346.hp2 others(68): Show |
intron_variant | MODIFIER | c.571-5789C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26172154 | ||||||
chr7:26172162
|
G | T | 5 | a0001c0001t0001g0075a0001c0002t0008g0028a0001c0002t0008g0064others(2): Show | 6 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.571-5781G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26172162 | ||||||
chr7:26172163
|
C | A | 1 | a0001c0001t0001g0011 | 4 | HG03209.hp1 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-5780C>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26172163 | ||||||
chr7:26172195
|
G | T | 1 | a0001c0001t0001g0205 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.571-5748G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26172195 | ||||||
chr7:26172261
|
G | A | 1 | a0001c0002t0002g0242 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.571-5682G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26172261 | ||||||
chr7:26172431
|
T | C | 1 | a0001c0002t0004g0172 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.571-5512T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26172431 | ||||||
chr7:26172433
|
A | C | 1 | a0001c0002t0001g0049 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.571-5510A>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26172433 | ||||||
chr7:26172562
|
G | A | 72 | a0001c0001t0001g0075a0001c0001t0001g0209a0001c0002t0001g0009others(69): Show | 97 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.571-5381G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26172562 | ||||||
chr7:26172709
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.571-5234T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26172709 | ||||||
chr7:26172771
|
G | T | 2 | a0001c0001t0013g0077a0001c0001t0013g0168 | 2 | HG01081.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.571-5172G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26172771 | ||||||
chr7:26172842
|
C | T | 5 | a0001c0002t0001g0009a0001c0002t0001g0049a0001c0002t0001g0050others(2): Show | 8 | HG01069.hp2 HG01071.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.571-5101C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26172842 | ||||||
chr7:26172851
|
T | G | 56 | a0001c0001t0001g0075a0001c0001t0001g0209a0001c0002t0001g0019others(53): Show | 76 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.571-5092T>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26172851 | ||||||
chr7:26173234
|
C | T | 1 | a0001c0002t0001g0078 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.571-4709C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26173234 | ||||||
chr7:26173286
|
A | C | 1 | a0001c0001t0001g0060 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.571-4657A>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26173286 | ||||||
chr7:26173388
|
TTGTGTGT others(5): Show |
T | 1 | a0001c0001t0001g0101 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.571-4547_571-4536d others(14): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26173388 | |||||
chr7:26173544
|
A | C | 1 | a0001c0002t0001g0074 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.571-4399A>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26173544 | ||||||
chr7:26173776
|
G | A | 42 | a0001c0002t0001g0246a0001c0002t0002g0003a0001c0002t0002g0007others(39): Show | 71 | HG00544.hp2 HG01255.hp2 HG01346.hp2 others(68): Show |
intron_variant | MODIFIER | c.571-4167G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26173776 | ||||||
chr7:26173914
|
T | G | 1 | a0001c0001t0005g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.571-4029T>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26173914 | ||||||
chr7:26174160
|
A | G | 7 | a0001c0001t0005g0085a0001c0001t0005g0128a0002c0004t0005g0047others(4): Show | 9 | HG00741.hp2 HG01167.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.571-3783A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26174160 | ||||||
chr7:26174162
|
C | G | 14 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0023others(11): Show | 24 | HG00423.hp1 HG01256.hp1 HG01515.hp1 others(21): Show |
intron_variant | MODIFIER | c.571-3781C>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26174162 | ||||||
chr7:26174210
|
G | T | 2 | a0001c0002t0015g0102a0001c0002t0015g0269 | 2 | HG02486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.571-3733G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26174210 | ||||||
chr7:26174285
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.571-3658A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26174285 | ||||||
chr7:26174477
|
A | T | 1 | a0001c0001t0001g0150 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.571-3466A>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26174477 | ||||||
chr7:26174568
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.571-3375G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26174568 | ||||||
chr7:26174611
|
A | G | 1 | a0001c0002t0004g0129 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.571-3332A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26174611 | ||||||
chr7:26174707
|
G | T | 115 | a0001c0001t0001g0209a0001c0002t0001g0009a0001c0002t0001g0019others(112): Show | 169 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.571-3236G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26174707 | ||||||
chr7:26174799
|
G | T | 6 | a0001c0002t0008g0028a0001c0002t0008g0064a0001c0002t0008g0065others(3): Show | 7 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-3144G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26174799 | ||||||
chr7:26174800
|
A | T | 6 | a0001c0002t0008g0028a0001c0002t0008g0064a0001c0002t0008g0065others(3): Show | 7 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-3143A>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26174800 | ||||||
chr7:26174869
|
T | A | 1 | a0001c0002t0001g0124 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.571-3074T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26174869 | ||||||
chr7:26174894
|
A | C | 1 | a0001c0002t0015g0269 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.571-3049A>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26174894 | ||||||
chr7:26175121
|
C | G | 6 | a0001c0002t0008g0028a0001c0002t0008g0064a0001c0002t0008g0065others(3): Show | 7 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-2822C>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175121 | ||||||
chr7:26175174
|
G | A | 30 | a0001c0001t0001g0209a0001c0002t0001g0019a0001c0002t0001g0056others(27): Show | 40 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.571-2769G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175174 | ||||||
chr7:26175192
|
C | A | 1 | a0001c0001t0001g0189 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.571-2751C>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175192 | ||||||
chr7:26175192
|
C | CA | 113 | a0001c0001t0001g0072a0001c0001t0001g0143a0001c0001t0001g0146others(110): Show | 167 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(164): Show |
intron_variant | MODIFIER | c.571-2732dupA | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26175192 | |||||
chr7:26175192
|
CA | C | 10 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0063others(7): Show | 13 | HG00323.hp1 HG00639.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.571-2732delA | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26175192 | |||||
chr7:26175217
|
G | A | 2 | a0001c0002t0002g0027a0001c0002t0002g0253 | 4 | NA18612.hp2 NA19070.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-2726G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175217 | ||||||
chr7:26175233
|
A | G | 115 | a0001c0001t0001g0209a0001c0002t0001g0009a0001c0002t0001g0019others(112): Show | 169 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.571-2710A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175233 | ||||||
chr7:26175252
|
T | C | 6 | a0001c0002t0008g0028a0001c0002t0008g0064a0001c0002t0008g0065others(3): Show | 7 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-2691T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175252 | ||||||
chr7:26175268
|
G | A | 6 | a0001c0002t0008g0028a0001c0002t0008g0064a0001c0002t0008g0065others(3): Show | 7 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-2675G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175268 | ||||||
chr7:26175407
|
T | C | 1 | a0001c0002t0002g0243 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.571-2536T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175407 | ||||||
chr7:26175486
|
T | A | 51 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0020others(48): Show | 67 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.571-2457T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175486 | ||||||
chr7:26175495
|
C | T | 2 | a0001c0002t0003g0220a0001c0002t0003g0221 | 2 | HG00438.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.571-2448C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175495 | ||||||
chr7:26175496
|
C | T | 2 | a0001c0002t0003g0220a0001c0002t0003g0221 | 2 | HG00438.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.571-2447C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175496 | ||||||
chr7:26175515
|
C | T | 15 | a0001c0002t0002g0016a0001c0002t0002g0027a0001c0002t0002g0043others(12): Show | 23 | HG02135.hp1 HG03239.hp1 HG04184.hp2 others(20): Show |
intron_variant | MODIFIER | c.571-2428C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175515 | ||||||
chr7:26175543
|
C | T | 6 | a0001c0002t0008g0028a0001c0002t0008g0064a0001c0002t0008g0065others(3): Show | 7 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-2400C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175543 | ||||||
chr7:26175687
|
G | A | 2 | a0001c0002t0002g0244a0001c0002t0017g0254 | 2 | NA18967.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.571-2256G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175687 | ||||||
chr7:26175728
|
A | T | 1 | a0001c0002t0014g0076 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.571-2215A>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175728 | ||||||
chr7:26175750
|
G | T | 1 | a0001c0002t0014g0076 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.571-2193G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175750 | ||||||
chr7:26175751
|
C | T | 1 | a0001c0002t0014g0076 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.571-2192C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175751 | ||||||
chr7:26175778
|
C | CA | 53 | a0001c0001t0001g0059a0001c0001t0001g0072a0001c0001t0001g0105others(50): Show | 83 | HG00544.hp2 HG00639.hp1 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.571-2149dupA | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26175778 | |||||
chr7:26175794
|
A | T | 1 | a0016c0018t0014g0141 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-2149A>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175794 | ||||||
chr7:26175795
|
T | A | 1 | a0001c0001t0001g0147 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.571-2148T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175795 | ||||||
chr7:26175822
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.571-2121T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175822 | ||||||
chr7:26175848
|
C | A | 5 | a0001c0002t0001g0009a0001c0002t0001g0049a0001c0002t0001g0050others(2): Show | 8 | HG01069.hp2 HG01071.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.571-2095C>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175848 | ||||||
chr7:26175853
|
C | CT | 32 | a0001c0001t0001g0029a0001c0001t0001g0094a0001c0001t0001g0097others(29): Show | 42 | HG00438.hp2 HG00597.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.571-2071dupT | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26175853 | |||||
chr7:26175853
|
CT | C | 85 | a0001c0001t0001g0159a0001c0001t0001g0188a0001c0001t0001g0209others(82): Show | 129 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.571-2071delT | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26175853 | |||||
chr7:26175928
|
T | C | 8 | a0001c0001t0001g0084a0001c0001t0001g0098a0001c0001t0001g0113others(5): Show | 8 | HG01081.hp2 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.571-2015T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175928 | ||||||
chr7:26175964
|
C | T | 1 | a0002c0007t0003g0224 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.571-1979C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175964 | ||||||
chr7:26175999
|
T | A | 3 | a0001c0002t0002g0017a0001c0002t0002g0236a0001c0002t0002g0257 | 6 | NA18747.hp2 NA18947.hp1 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.571-1944T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175999 | ||||||
chr7:26176005
|
T | C | 3 | a0001c0002t0002g0017a0001c0002t0002g0236a0001c0002t0002g0257 | 6 | NA18747.hp2 NA18947.hp1 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.571-1938T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176005 | ||||||
chr7:26176027
|
C | A | 1 | a0001c0002t0002g0057 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.571-1916C>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176027 | ||||||
chr7:26176036
|
C | G | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG00738.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.571-1907C>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176036 | ||||||
chr7:26176053
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.571-1890G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176053 | ||||||
chr7:26176067
|
T | C | 1 | a0001c0001t0001g0106 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.571-1876T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176067 | ||||||
chr7:26176354
|
A | G | 7 | a0001c0001t0001g0075a0001c0002t0008g0028a0001c0002t0008g0064others(4): Show | 8 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.571-1589A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176354 | ||||||
chr7:26176474
|
G | GGCCGGGC others(32): Show |
1 | a0001c0001t0001g0198 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.571-1436_571-1398d others(41): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176474 | |||||
chr7:26176474
|
GGCCGGGC others(32): Show |
G | 70 | a0001c0001t0001g0209a0001c0002t0001g0019a0001c0002t0001g0056others(67): Show | 109 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.571-1436_571-1398d others(41): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176474 | |||||
chr7:26176474
|
GGCCGGGC others(145): Show |
G | 1 | a0001c0002t0002g0248 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.571-1436_571-1285d others(2): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176474 | |||||
chr7:26176478
|
G | GGGCAGAG others(106): Show |
27 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0024others(24): Show | 43 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(40): Show |
intron_variant | MODIFIER | c.571-1294_571-1182d others(115): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176478 | |||||
chr7:26176512
|
C | T | 1 | a0001c0002t0001g0079 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.571-1431C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176512 | ||||||
chr7:26176513
|
A | G | 1 | a0001c0002t0001g0079 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.571-1430A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176513 | ||||||
chr7:26176517
|
G | A | 1 | a0001c0002t0001g0079 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.571-1426G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176517 | ||||||
chr7:26176517
|
G | GGGCAGAG others(30): Show |
6 | a0001c0002t0003g0041a0001c0002t0003g0220a0001c0002t0003g0221others(3): Show | 7 | HG00438.hp2 HG00733.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.571-1407_571-1371d others(39): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176517 | |||||
chr7:26176536
|
A | T | 51 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0020others(48): Show | 67 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.571-1407A>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176536 | ||||||
chr7:26176545
|
G | A | 1 | a0001c0002t0014g0076 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.571-1398G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176545 | ||||||
chr7:26176549
|
T | C | 1 | a0001c0002t0001g0079 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.571-1394T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176549 | ||||||
chr7:26176550
|
G | A | 1 | a0001c0002t0001g0079 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.571-1393G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176550 | ||||||
chr7:26176554
|
A | G | 1 | a0001c0002t0001g0079 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.571-1389A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176554 | ||||||
chr7:26176573
|
T | A | 1 | a0001c0002t0001g0079 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.571-1370T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176573 | ||||||
chr7:26176573
|
TTCCCAGA others(69): Show |
T | 1 | a0001c0001t0001g0111 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.571-1333_571-1258d others(78): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176573 | |||||
chr7:26176586
|
T | C | 1 | a0002c0004t0009g0039 | 2 | HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.571-1357T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176586 | ||||||
chr7:26176591
|
A | G | 2 | a0001c0001t0001g0037a0002c0004t0009g0039 | 4 | HG01255.hp1 HG02647.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-1352A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176591 | ||||||
chr7:26176601
|
G | A | 1 | a0001c0002t0001g0156 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.571-1342G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176601 | ||||||
chr7:26176610
|
A | T | 1 | a0001c0002t0001g0079 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.571-1333A>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176610 | ||||||
chr7:26176619
|
G | C | 1 | a0015c0017t0001g0088 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.571-1324G>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176619 | ||||||
chr7:26176625
|
C | T | 1 | a0001c0002t0001g0079 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.571-1318C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176625 | ||||||
chr7:26176626
|
A | G | 4 | a0001c0002t0001g0079a0001c0002t0002g0007a0001c0002t0002g0187others(1): Show | 10 | HG01255.hp2 HG01346.hp2 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.571-1317A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176626 | ||||||
chr7:26176630
|
G | A | 1 | a0001c0002t0001g0079 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.571-1313G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176630 | ||||||
chr7:26176630
|
GGGCAGAG others(67): Show |
G | 1 | a0001c0002t0002g0245 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.571-1284_571-1211d others(76): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176630 | |||||
chr7:26176640
|
G | A | 2 | a0001c0001t0001g0107a0011c0013t0001g0110 | 2 | HG00609.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.571-1303G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176640 | ||||||
chr7:26176649
|
A | ATCCCAGA others(106): Show |
1 | a0004c0006t0012g0054 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.571-1220_571-1108d others(115): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176649 | |||||
chr7:26176649
|
A | T | 3 | a0001c0001t0001g0198a0001c0001t0001g0206a0001c0002t0001g0079 | 3 | HG01243.hp1 HG01891.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.571-1294A>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176649 | ||||||
chr7:26176649
|
ATCCCAGA others(30): Show |
A | 2 | a0001c0001t0001g0100a0001c0001t0025g0095 | 2 | HG00323.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.571-1257_571-1221d others(39): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176649 | |||||
chr7:26176675
|
GCGCTCCT others(490): Show |
G | 2 | a0001c0001t0001g0186a0001c0001t0001g0208 | 2 | HG02738.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.571-1253_571-757de others(1): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176675 | |||||
chr7:26176686
|
T | A | 2 | a0001c0002t0001g0079a0001c0002t0003g0230 | 2 | HG01891.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.571-1257T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176686 | ||||||
chr7:26176694
|
C | CAA | 4 | a0001c0002t0008g0028a0001c0002t0008g0064a0001c0002t0008g0065others(1): Show | 5 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.571-1249_571-1248i others(4): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176694 | ||||||
chr7:26176695
|
G | T | 4 | a0001c0002t0008g0028a0001c0002t0008g0064a0001c0002t0008g0065others(1): Show | 5 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.571-1248G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176695 | ||||||
chr7:26176699
|
T | C | 2 | a0001c0001t0001g0119a0001c0002t0001g0079 | 2 | HG01891.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.571-1244T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176699 | ||||||
chr7:26176700
|
G | A | 1 | a0001c0002t0001g0079 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.571-1243G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176700 | ||||||
chr7:26176704
|
A | AGGCAGAG others(69): Show |
1 | a0001c0001t0001g0198 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.571-1221_571-1220i others(78): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176704 | |||||
chr7:26176704
|
A | G | 5 | a0001c0002t0001g0079a0001c0002t0008g0028a0001c0002t0008g0064others(2): Show | 6 | HG01099.hp2 HG01517.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.571-1239A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176704 | ||||||
chr7:26176704
|
AGGCAGAG others(32): Show |
A | 1 | a0015c0017t0001g0088 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.571-1220_571-1182d others(41): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176704 | |||||
chr7:26176720
|
C | T | 4 | a0001c0002t0008g0028a0001c0002t0008g0064a0001c0002t0008g0065others(1): Show | 5 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.571-1223C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176720 | ||||||
chr7:26176723
|
A | T | 4 | a0001c0002t0001g0067a0001c0002t0014g0076a0001c0002t0015g0102others(1): Show | 4 | HG02486.hp2 HG02970.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-1220A>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176723 | ||||||
chr7:26176732
|
G | A | 2 | a0001c0002t0001g0067a0001c0002t0014g0076 | 2 | HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.571-1211G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176732 | ||||||
chr7:26176735
|
G | GGGCAGCC others(183): Show |
1 | a0001c0002t0011g0026 | 3 | HG02451.hp1 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.571-1182_571-1181i others(192): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176735 | |||||
chr7:26176735
|
GGGCAGCC others(222): Show |
G | 4 | a0001c0002t0008g0028a0001c0002t0008g0064a0001c0002t0008g0065others(1): Show | 5 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.571-1181_571-953de others(1): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176735 | |||||
chr7:26176738
|
C | T | 2 | a0001c0002t0001g0067a0001c0002t0001g0079 | 2 | HG01891.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.571-1205C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176738 | ||||||
chr7:26176739
|
A | G | 2 | a0001c0002t0001g0067a0001c0002t0001g0079 | 2 | HG01891.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.571-1204A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176739 | ||||||
chr7:26176743
|
G | A | 1 | a0001c0002t0001g0079 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.571-1200G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176743 | ||||||
chr7:26176752
|
C | T | 19 | a0001c0002t0003g0005a0001c0002t0003g0041a0001c0002t0003g0165others(16): Show | 26 | HG00438.hp2 HG00597.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.571-1191C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176752 | ||||||
chr7:26176753
|
G | A | 1 | a0001c0002t0001g0074 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.571-1190G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176753 | ||||||
chr7:26176759
|
C | T | 1 | a0001c0002t0001g0067 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.571-1184C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176759 | ||||||
chr7:26176762
|
T | A | 188 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0011others(185): Show | 273 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(270): Show |
intron_variant | MODIFIER | c.571-1181T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176762 | ||||||
chr7:26176772
|
G | A | 1 | a0001c0002t0001g0067 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.571-1171G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176772 | ||||||
chr7:26176773
|
G | T | 1 | a0001c0002t0001g0067 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.571-1170G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176773 | ||||||
chr7:26176774
|
GTGGCCAG others(183): Show |
G | 1 | a0001c0002t0001g0067 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.571-1168_571-979de others(1): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176774 | ||||||
chr7:26176780
|
AGGCAGAG others(106): Show |
A | 2 | a0001c0001t0001g0013a0001c0001t0001g0201 | 5 | HG00738.hp1 HG01069.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-1144_571-1032d others(2): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176780 | |||||
chr7:26176788
|
GCGCTCCT others(377): Show |
G | 17 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0014others(14): Show | 30 | HG00423.hp1 HG01081.hp1 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.571-1140_571-757de others(1): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176788 | |||||
chr7:26176799
|
T | A | 1 | a0001c0002t0001g0079 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.571-1144T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176799 | ||||||
chr7:26176808
|
G | T | 1 | a0015c0017t0001g0088 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.571-1135G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176808 | ||||||
chr7:26176812
|
T | C | 1 | a0001c0002t0001g0079 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.571-1131T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176812 | ||||||
chr7:26176817
|
A | AGGCAGAG others(32): Show |
4 | a0001c0001t0001g0086a0001c0001t0001g0125a0001c0001t0001g0135others(1): Show | 4 | NA18941.hp1 NA18962.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-1108_571-1107i others(41): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176817 | |||||
chr7:26176817
|
A | C | 5 | a0001c0002t0001g0009a0001c0002t0001g0049a0001c0002t0001g0050others(2): Show | 8 | HG01069.hp2 HG01071.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.571-1126A>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176817 | ||||||
chr7:26176817
|
A | G | 2 | a0001c0002t0001g0079a0015c0017t0001g0088 | 2 | HG01891.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.571-1126A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176817 | ||||||
chr7:26176833
|
C | T | 1 | a0015c0017t0001g0088 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.571-1110C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176833 | ||||||
chr7:26176836
|
T | A | 92 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0025others(89): Show | 120 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.571-1107T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176836 | ||||||
chr7:26176845
|
G | A | 73 | a0001c0001t0001g0209a0001c0002t0001g0019a0001c0002t0001g0056others(70): Show | 114 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.571-1098G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176845 | ||||||
chr7:26176845
|
GAT | G | 3 | a0001c0001t0001g0096a0001c0001t0001g0184a0001c0002t0001g0079 | 3 | HG01261.hp1 HG01891.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.571-1097_571-1096d others(4): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176845 | ||||||
chr7:26176847
|
T | TGGGCAGC others(30): Show |
5 | a0001c0001t0001g0012a0001c0001t0001g0166a0001c0001t0001g0177others(2): Show | 8 | HG02080.hp2 HG02132.hp1 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.571-1093_571-1092i others(39): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176847 | |||||
chr7:26176850
|
G | T | 1 | a0015c0017t0001g0088 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.571-1093G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176850 | ||||||
chr7:26176851
|
T | C | 87 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0035others(84): Show | 112 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.571-1092T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176851 | ||||||
chr7:26176852
|
G | A | 87 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0035others(84): Show | 112 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.571-1091G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176852 | ||||||
chr7:26176856
|
G | A | 8 | a0001c0001t0001g0012a0001c0001t0001g0096a0001c0001t0001g0166others(5): Show | 11 | HG01261.hp1 HG01891.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.571-1087G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176856 | ||||||
chr7:26176866
|
A | G | 169 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0025others(166): Show | 239 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(236): Show |
intron_variant | MODIFIER | c.571-1077A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176866 | ||||||
chr7:26176872
|
C | T | 73 | a0001c0001t0001g0209a0001c0002t0001g0019a0001c0002t0001g0056others(70): Show | 114 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.571-1071C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176872 | ||||||
chr7:26176875
|
C | A | 110 | a0001c0001t0001g0096a0001c0001t0001g0184a0001c0001t0001g0209others(107): Show | 163 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.571-1068C>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176875 | ||||||
chr7:26176875
|
C | T | 57 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0025others(54): Show | 73 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.571-1068C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176875 | ||||||
chr7:26176884
|
G | GAT | 4 | a0001c0001t0001g0096a0001c0001t0001g0184a0001c0002t0003g0220others(1): Show | 6 | HG01261.hp1 HG02148.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.571-1059_571-1058i others(4): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176884 | ||||||
chr7:26176884
|
G | GGGGTGGC others(69): Show |
1 | a0002c0007t0003g0232 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.571-1056_571-1055i others(78): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176884 | |||||
chr7:26176885
|
G | A | 71 | a0001c0001t0001g0209a0001c0002t0001g0019a0001c0002t0001g0056others(68): Show | 110 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.571-1058G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176885 | ||||||
chr7:26176886
|
G | T | 71 | a0001c0001t0001g0209a0001c0002t0001g0019a0001c0002t0001g0056others(68): Show | 110 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.571-1057G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176886 | ||||||
chr7:26176887
|
GCGGCCGG others(70): Show |
G | 71 | a0001c0001t0001g0209a0001c0002t0001g0019a0001c0002t0001g0056others(68): Show | 110 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.571-1055_571-979de others(78): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176887 | ||||||
chr7:26176888
|
C | T | 92 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0025others(89): Show | 120 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.571-1055C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176888 | ||||||
chr7:26176888
|
CGGCCGGG others(109): Show |
C | 55 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0020others(52): Show | 71 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.571-918_571-803del | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176888 | |||||
chr7:26176889
|
G | A | 4 | a0001c0001t0001g0096a0001c0001t0001g0184a0001c0002t0003g0220others(1): Show | 6 | HG01261.hp1 HG02148.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.571-1054G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176889 | ||||||
chr7:26176893
|
G | A | 91 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0025others(88): Show | 119 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.571-1050G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176893 | ||||||
chr7:26176909
|
C | T | 1 | a0002c0007t0003g0232 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.571-1034C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176909 | ||||||
chr7:26176911
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.571-1032C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176911 | ||||||
chr7:26176912
|
A | T | 87 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0035others(84): Show | 112 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.571-1031A>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176912 | ||||||
chr7:26176921
|
G | A | 3 | a0001c0002t0001g0079a0001c0002t0015g0102a0001c0002t0015g0269 | 3 | HG01891.hp2 HG02486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.571-1022G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176921 | ||||||
chr7:26176921
|
GAT | G | 87 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0035others(84): Show | 114 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.571-1021_571-1020d others(4): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176921 | ||||||
chr7:26176927
|
C | T | 90 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0035others(87): Show | 117 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.571-1016C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176927 | ||||||
chr7:26176928
|
G | A | 1 | a0002c0007t0003g0232 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.571-1015G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176928 | ||||||
chr7:26176932
|
A | G | 4 | a0001c0002t0001g0079a0001c0002t0015g0102a0001c0002t0015g0269others(1): Show | 4 | HG01106.hp2 HG01891.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-1011A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176932 | ||||||
chr7:26176940
|
A | G | 91 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0035others(88): Show | 118 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.571-1003A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176940 | ||||||
chr7:26176941
|
T | C | 91 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0035others(88): Show | 118 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.571-1002T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176941 | ||||||
chr7:26176948
|
C | T | 3 | a0001c0002t0001g0079a0001c0002t0015g0102a0001c0002t0015g0269 | 3 | HG01891.hp2 HG02486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.571-995C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176948 | ||||||
chr7:26176951
|
T | A | 6 | a0001c0002t0001g0079a0001c0002t0001g0173a0001c0002t0015g0102others(3): Show | 7 | HG01106.hp2 HG01891.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-992T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176951 | ||||||
chr7:26176955
|
T | C | 91 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0035others(88): Show | 118 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.571-988T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176955 | ||||||
chr7:26176959
|
C | CAA | 31 | a0001c0002t0001g0009a0001c0002t0001g0049a0001c0002t0001g0050others(28): Show | 43 | HG00438.hp2 HG00597.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.571-984_571-983ins others(2): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176959 | ||||||
chr7:26176960
|
G | GAT | 51 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0035others(48): Show | 63 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.571-983_571-982ins others(2): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176960 | ||||||
chr7:26176960
|
G | T | 31 | a0001c0002t0001g0009a0001c0002t0001g0049a0001c0002t0001g0050others(28): Show | 43 | HG00438.hp2 HG00597.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.571-983G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176960 | ||||||
chr7:26176961
|
G | A | 5 | a0001c0002t0001g0079a0001c0002t0001g0173a0001c0002t0015g0102others(2): Show | 6 | HG01891.hp2 HG02486.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.571-982G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176961 | ||||||
chr7:26176962
|
G | T | 5 | a0001c0002t0001g0079a0001c0002t0001g0173a0001c0002t0015g0102others(2): Show | 6 | HG01891.hp2 HG02486.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.571-981G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176962 | ||||||
chr7:26176963
|
GT | G | 5 | a0001c0002t0001g0079a0001c0002t0001g0173a0001c0002t0015g0102others(2): Show | 6 | HG01891.hp2 HG02486.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.571-979delT | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176963 | ||||||
chr7:26176964
|
T | TGGCCAGG others(68): Show |
2 | a0001c0002t0011g0026a0002c0007t0003g0232 | 4 | HG01106.hp2 HG02451.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-976_571-975ins others(75): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176964 | |||||
chr7:26176964
|
T | TGGCCGGG others(29): Show |
13 | a0001c0002t0001g0009a0001c0002t0001g0049a0001c0002t0001g0050others(10): Show | 18 | HG01069.hp2 HG01071.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.571-976_571-975ins others(36): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176964 | |||||
chr7:26176964
|
T | TGGCCGGG others(144): Show |
18 | a0001c0002t0003g0005a0001c0002t0003g0041a0001c0002t0003g0165others(15): Show | 25 | HG00438.hp2 HG00597.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.571-976_571-975ins others(151): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176964 | |||||
chr7:26176965
|
GGCA | G | 51 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0035others(48): Show | 63 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.571-975_571-973del others(3): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176965 | |||||
chr7:26176966
|
G | T | 70 | a0001c0001t0001g0209a0001c0002t0001g0019a0001c0002t0001g0056others(67): Show | 109 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.571-977G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176966 | ||||||
chr7:26176967
|
C | CCAGGCAG others(142): Show |
1 | a0001c0001t0001g0184 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.571-976_571-975ins others(149): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176967 | ||||||
chr7:26176967
|
C | CCAGGCAG others(29): Show |
1 | a0001c0001t0001g0096 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.571-976_571-975ins others(36): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176967 | ||||||
chr7:26176968
|
A | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0184 | 2 | HG01261.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.571-975A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176968 | ||||||
chr7:26176971
|
C | T | 1 | a0001c0002t0011g0026 | 3 | HG02451.hp1 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.571-972C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176971 | ||||||
chr7:26176982
|
G | A | 164 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0035others(161): Show | 230 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(227): Show |
intron_variant | MODIFIER | c.571-961G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176982 | ||||||
chr7:26176988
|
C | T | 1 | a0016c0018t0014g0141 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-955C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176988 | ||||||
chr7:26176991
|
A | C | 164 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0035others(161): Show | 230 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(227): Show |
intron_variant | MODIFIER | c.571-952A>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176991 | ||||||
chr7:26176991
|
A | T | 1 | a0004c0006t0012g0054 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.571-952A>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176991 | ||||||
chr7:26177004
|
T | C | 165 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0035others(162): Show | 231 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(228): Show |
intron_variant | MODIFIER | c.571-939T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177004 | ||||||
chr7:26177004
|
T | TGGCCAGG others(258): Show |
1 | a0001c0002t0001g0173 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.571-935_571-934ins others(265): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26177004 | |||||
chr7:26177004
|
T | TGGCCAGG others(219): Show |
1 | a0002c0004t0009g0039 | 2 | HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.571-935_571-934ins others(226): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26177004 | |||||
chr7:26177004
|
T | TGGCCAGG others(106): Show |
1 | a0004c0006t0012g0054 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.571-935_571-934ins others(113): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26177004 | |||||
chr7:26177005
|
G | A | 1 | a0016c0018t0014g0141 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-938G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177005 | ||||||
chr7:26177019
|
G | A | 1 | a0016c0018t0014g0141 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-924G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177019 | ||||||
chr7:26177028
|
A | C | 1 | a0016c0018t0014g0141 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-915A>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177028 | ||||||
chr7:26177037
|
G | A | 1 | a0001c0002t0001g0067 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.571-906G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177037 | ||||||
chr7:26177043
|
C | T | 2 | a0001c0001t0001g0143a0001c0001t0001g0181 | 2 | HG03831.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.571-900C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177043 | ||||||
chr7:26177048
|
A | G | 1 | a0016c0018t0014g0141 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-895A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177048 | ||||||
chr7:26177056
|
A | G | 1 | a0016c0018t0014g0141 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-887A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177056 | ||||||
chr7:26177057
|
T | C | 1 | a0016c0018t0014g0141 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-886T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177057 | ||||||
chr7:26177067
|
T | A | 1 | a0016c0018t0014g0141 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-876T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177067 | ||||||
chr7:26177071
|
T | C | 1 | a0016c0018t0014g0141 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-872T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177071 | ||||||
chr7:26177077
|
G | A | 1 | a0016c0018t0014g0141 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-866G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177077 | ||||||
chr7:26177078
|
G | T | 1 | a0016c0018t0014g0141 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-865G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177078 | ||||||
chr7:26177084
|
A | G | 1 | a0016c0018t0014g0141 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-859A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177084 | ||||||
chr7:26177084
|
AGCCGGGC others(30): Show |
A | 3 | a0001c0002t0002g0046a0001c0002t0002g0239a0001c0002t0004g0129 | 4 | HG02683.hp1 NA18940.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-839_571-803del others(37): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26177084 | |||||
chr7:26177088
|
G | A | 13 | a0001c0002t0001g0019a0001c0002t0001g0078a0001c0002t0001g0089others(10): Show | 15 | HG02145.hp1 HG02280.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.571-855G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177088 | ||||||
chr7:26177096
|
G | A | 1 | a0016c0018t0014g0141 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-847G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177096 | ||||||
chr7:26177097
|
C | T | 1 | a0016c0018t0014g0141 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-846C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177097 | ||||||
chr7:26177107
|
A | T | 1 | a0016c0018t0014g0141 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-836A>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177107 | ||||||
chr7:26177111
|
C | T | 1 | a0016c0018t0014g0141 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-832C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177111 | ||||||
chr7:26177134
|
C | G | 6 | a0001c0002t0008g0028a0001c0002t0008g0064a0001c0002t0008g0065others(3): Show | 7 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-809C>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177134 | ||||||
chr7:26177141
|
T | C | 1 | a0016c0018t0014g0141 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-802T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177141 | ||||||
chr7:26177156
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.571-787G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177156 | ||||||
chr7:26177173
|
C | T | 6 | a0001c0002t0008g0028a0001c0002t0008g0064a0001c0002t0008g0065others(3): Show | 7 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-770C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177173 | ||||||
chr7:26177270
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.571-673C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177270 | ||||||
chr7:26177410
|
A | G | 1 | a0016c0018t0014g0141 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-533A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177410 | ||||||
chr7:26177415
|
G | A | 2 | a0001c0001t0001g0163a0001c0001t0001g0180 | 2 | HG01346.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.571-528G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177415 | ||||||
chr7:26177426
|
A | G | 4 | a0001c0002t0008g0028a0001c0002t0008g0064a0001c0002t0008g0065others(1): Show | 5 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.571-517A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177426 | ||||||
chr7:26177463
|
G | A | 5 | a0001c0001t0001g0122a0001c0001t0001g0131a0004c0006t0001g0055others(2): Show | 5 | HG02258.hp1 HG02559.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-480G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177463 | ||||||
chr7:26177495
|
G | GCCGAGGC others(17): Show |
1 | a0001c0001t0001g0176 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.571-437_571-414dup others(24): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26177495 | |||||
chr7:26177590
|
G | T | 1 | a0001c0001t0001g0201 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.571-353G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177590 | ||||||
chr7:26177682
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.571-261A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177682 | ||||||
chr7:26177830
|
T | A | 6 | a0001c0002t0008g0028a0001c0002t0008g0064a0001c0002t0008g0065others(3): Show | 7 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-113T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177830 | ||||||
chr7:26177931
|
G | T | 1 | a0001c0002t0006g0070 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.571-12G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177931 | ||||||
chr7:26178153
|
G | A | 1 | a0001c0005t0001g0178 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.750+31G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26178153 | ||||||
chr7:26178517
|
A | G | 1 | a0001c0001t0001g0179 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.750+395A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26178517 | ||||||
chr7:26178543
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.750+421G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26178543 | ||||||
chr7:26178692
|
GCTGAAGG others(28): Show |
G | 1 | a0001c0002t0002g0250 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.750+573_750+607del others(35): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 26178692 | |||||
chr7:26178767
|
G | C | 1 | a0001c0001t0001g0097 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.750+645G>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26178767 | ||||||
chr7:26178852
|
A | G | 1 | a0001c0002t0001g0246 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.750+730A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26178852 | ||||||
chr7:26178899
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.750+777T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26178899 | ||||||
chr7:26179038
|
C | CTTGA | 4 | a0001c0002t0008g0028a0001c0002t0008g0064a0001c0002t0008g0065others(1): Show | 5 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.750+918_750+919ins others(4): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 26179038 | |||||
chr7:26179148
|
ATAAATTC others(7): Show |
A | 21 | a0001c0002t0003g0005a0001c0002t0003g0041a0001c0002t0003g0165others(18): Show | 30 | HG00438.hp2 HG00597.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.750+1030_750+1043d others(16): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 26179148 | |||||
chr7:26179433
|
G | A | 1 | a0001c0001t0005g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.750+1311G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26179433 | ||||||
chr7:26179654
|
C | T | 4 | a0001c0002t0008g0028a0001c0002t0008g0064a0001c0002t0008g0065others(1): Show | 5 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.750+1532C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26179654 | ||||||
chr7:26179657
|
C | G | 1 | a0001c0001t0001g0155 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.750+1535C>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26179657 | ||||||
chr7:26179691
|
G | GC | 25 | a0001c0002t0001g0019a0001c0002t0001g0078a0001c0002t0001g0089others(22): Show | 35 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.750+1570dupC | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 26179691 | |||||
chr7:26179776
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.750+1654G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26179776 | ||||||
chr7:26179796
|
G | C | 1 | a0001c0001t0019g0148 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.750+1674G>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26179796 | ||||||
chr7:26179856
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.750+1734T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26179856 | ||||||
chr7:26179939
|
T | C | 29 | a0001c0002t0001g0019a0001c0002t0001g0056a0001c0002t0001g0078others(26): Show | 39 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.750+1817T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26179939 | ||||||
chr7:26179995
|
C | T | 4 | a0002c0004t0005g0047a0002c0004t0005g0048a0002c0004t0005g0263others(1): Show | 6 | HG00741.hp2 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.750+1873C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26179995 | ||||||
chr7:26180067
|
C | T | 29 | a0001c0002t0001g0019a0001c0002t0001g0056a0001c0002t0001g0078others(26): Show | 39 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.750+1945C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26180067 | ||||||
chr7:26180157
|
A | C | 2 | a0001c0002t0008g0028a0001c0002t0008g0066 | 3 | HG01099.hp2 HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.750+2035A>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26180157 | ||||||
chr7:26180157
|
A | G | 2 | a0001c0002t0008g0064a0001c0002t0008g0065 | 2 | HG01517.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.750+2035A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26180157 | ||||||
chr7:26180690
|
A | T | 1 | a0001c0001t0001g0073 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.750+2568A>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26180690 | ||||||
chr7:26180936
|
A | G | 1 | a0001c0001t0001g0206 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.751-2765A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26180936 | ||||||
chr7:26180952
|
C | T | 1 | a0001c0002t0001g0090 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.751-2749C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26180952 | ||||||
chr7:26180965
|
C | CT | 24 | a0001c0001t0001g0109a0001c0001t0001g0188a0001c0001t0018g0225others(21): Show | 31 | HG00438.hp2 HG00597.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.751-2723dupT | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 26180965 | |||||
chr7:26181062
|
A | C | 2 | a0001c0002t0015g0102a0001c0002t0015g0269 | 2 | HG02486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.751-2639A>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26181062 | ||||||
chr7:26181216
|
A | G | 1 | a0001c0002t0015g0102 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.751-2485A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26181216 | ||||||
chr7:26181252
|
C | T | 2 | a0001c0002t0002g0027a0001c0002t0002g0253 | 4 | NA18612.hp2 NA19070.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.751-2449C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26181252 | ||||||
chr7:26181560
|
A | G | 1 | a0001c0001t0001g0106 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.751-2141A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26181560 | ||||||
chr7:26181580
|
ATATAAAC others(50): Show |
A | 1 | a0001c0001t0001g0144 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.751-2119_751-2063d others(59): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 26181580 | |||||
chr7:26181612
|
A | G | 1 | a0001c0002t0008g0065 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.751-2089A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26181612 | ||||||
chr7:26181683
|
A | T | 4 | a0001c0002t0008g0028a0001c0002t0008g0064a0001c0002t0008g0065others(1): Show | 5 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.751-2018A>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26181683 | ||||||
chr7:26181819
|
T | C | 3 | a0001c0002t0002g0242a0001c0002t0002g0247a0001c0002t0002g0262 | 3 | HG02486.hp1 HG03471.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.751-1882T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26181819 | ||||||
chr7:26181913
|
T | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0207 | 2 | HG01081.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.751-1788T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26181913 | ||||||
chr7:26181989
|
A | T | 1 | a0001c0002t0002g0250 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.751-1712A>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26181989 | ||||||
chr7:26182022
|
A | C | 1 | a0001c0001t0001g0075 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.751-1679A>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26182022 | ||||||
chr7:26182111
|
C | T | 41 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0016others(38): Show | 70 | HG00544.hp2 HG01255.hp2 HG01346.hp2 others(67): Show |
intron_variant | MODIFIER | c.751-1590C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26182111 | ||||||
chr7:26182144
|
G | GAAACAGA others(12): Show |
1 | a0001c0001t0005g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.751-1554_751-1536d others(21): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 26182144 | |||||
chr7:26182214
|
T | G | 1 | a0001c0002t0001g0090 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.751-1487T>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26182214 | ||||||
chr7:26182287
|
A | G | 1 | a0001c0002t0002g0257 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.751-1414A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26182287 | ||||||
chr7:26182308
|
T | C | 1 | a0001c0002t0011g0026 | 3 | HG02451.hp1 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.751-1393T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26182308 | ||||||
chr7:26182311
|
T | TGAAGCA | 27 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0017others(24): Show | 49 | HG01255.hp2 HG01346.hp2 HG01496.hp2 others(46): Show |
intron_variant | MODIFIER | c.751-1390_751-1389i others(8): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26182311 | ||||||
chr7:26182311
|
T | TGAAGCAT others(6): Show |
59 | a0001c0002t0001g0009a0001c0002t0001g0019a0001c0002t0001g0049others(56): Show | 81 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.751-1390_751-1389i others(15): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26182311 | ||||||
chr7:26182313
|
T | G | 86 | a0001c0002t0001g0009a0001c0002t0001g0019a0001c0002t0001g0049others(83): Show | 130 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.751-1388T>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26182313 | ||||||
chr7:26182366
|
GTAATCCC others(766): Show |
G | 1 | a0001c0001t0001g0179 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.751-1331_751-559de others(1): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 26182366 | |||||
chr7:26182368
|
A | AATCCCAA others(25): Show |
6 | a0001c0002t0001g0009a0001c0002t0001g0049a0001c0002t0001g0050others(3): Show | 9 | HG01069.hp2 HG01071.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.751-1329_751-1298d others(34): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 26182368 | |||||
chr7:26182382
|
G | A | 1 | a0001c0002t0001g0078 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.751-1319G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26182382 | ||||||
chr7:26182392
|
G | A | 3 | a0001c0002t0003g0041a0001c0002t0003g0222a0001c0002t0003g0230 | 4 | HG00741.hp1 HG01106.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.751-1309G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26182392 | ||||||
chr7:26182449
|
C | T | 2 | a0001c0002t0002g0244a0001c0002t0017g0254 | 2 | NA18967.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.751-1252C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26182449 | ||||||
chr7:26182454
|
G | A | 1 | a0001c0002t0002g0250 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.751-1247G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26182454 | ||||||
chr7:26182470
|
A | G | 1 | a0001c0002t0008g0064 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.751-1231A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26182470 | ||||||
chr7:26182475
|
T | TTGGCCAG others(57): Show |
7 | a0001c0002t0001g0067a0001c0002t0001g0068a0001c0002t0001g0074others(4): Show | 9 | HG01109.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.751-1225_751-1162d others(66): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 26182475 | |||||
chr7:26182606
|
C | T | 4 | a0001c0001t0001g0022a0001c0001t0001g0121a0001c0001t0001g0130others(1): Show | 6 | NA18957.hp1 NA18977.hp2 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.751-1095C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26182606 | ||||||
chr7:26182618
|
A | ACTGTCTC others(62): Show |
2 | a0001c0002t0003g0041a0001c0002t0003g0230 | 3 | HG00741.hp1 HG01106.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.751-1082_751-1014d others(71): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 26182618 | |||||
chr7:26182648
|
ACTGGGTT others(397): Show |
A | 1 | a0016c0018t0014g0141 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.751-1047_751-644de others(1): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 26182648 | |||||
chr7:26182652
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G | A | 4 | a0001c0002t0008g0028a0001c0002t0008g0064a0001c0002t0008g0065others(1): Show | 5 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.751-1049G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26182652 | ||||||
chr7:26182730
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G | A | 4 | a0001c0002t0008g0028a0001c0002t0008g0064a0001c0002t0008g0065others(1): Show | 5 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.751-971G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26182730 | ||||||
chr7:26183252
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T | C | 1 | a0001c0001t0001g0159 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.751-449T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26183252 | ||||||
chr7:26183353
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A | G | 41 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0016others(38): Show | 70 | HG00544.hp2 HG01255.hp2 HG01346.hp2 others(67): Show |
intron_variant | MODIFIER | c.751-348A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26183353 | ||||||
chr7:26183355
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T | C | 41 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0016others(38): Show | 70 | HG00544.hp2 HG01255.hp2 HG01346.hp2 others(67): Show |
intron_variant | MODIFIER | c.751-346T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26183355 | ||||||
chr7:26183363
|
C | A | 41 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0016others(38): Show | 70 | HG00544.hp2 HG01255.hp2 HG01346.hp2 others(67): Show |
intron_variant | MODIFIER | c.751-338C>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26183363 | ||||||
chr7:26183368
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T | G | 41 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0016others(38): Show | 70 | HG00544.hp2 HG01255.hp2 HG01346.hp2 others(67): Show |
intron_variant | MODIFIER | c.751-333T>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26183368 | ||||||
chr7:26183369
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G | GCA | 41 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0016others(38): Show | 70 | HG00544.hp2 HG01255.hp2 HG01346.hp2 others(67): Show |
intron_variant | MODIFIER | c.751-332_751-331ins others(2): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26183369 | ||||||
chr7:26183379
|
C | G | 4 | a0001c0002t0008g0028a0001c0002t0008g0064a0001c0002t0008g0065others(1): Show | 5 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.751-322C>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26183379 | ||||||
chr7:26183381
|
C | G | 41 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0016others(38): Show | 70 | HG00544.hp2 HG01255.hp2 HG01346.hp2 others(67): Show |
intron_variant | MODIFIER | c.751-320C>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26183381 | ||||||
chr7:26183384
|
C | G | 41 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0016others(38): Show | 70 | HG00544.hp2 HG01255.hp2 HG01346.hp2 others(67): Show |
intron_variant | MODIFIER | c.751-317C>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26183384 | ||||||
chr7:26183391
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.751-310T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26183391 | ||||||
chr7:26183434
|
G | C | 1 | a0001c0001t0001g0092 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.751-267G>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26183434 | ||||||
chr7:26183440
|
CCGGAGGC others(110): Show |
C | 4 | a0001c0002t0008g0028a0001c0002t0008g0064a0001c0002t0008g0065others(1): Show | 5 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.751-260_751-144del | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26183440 | ||||||
chr7:26183529
|
G | C | 2 | a0001c0001t0001g0023a0001c0001t0001g0038 | 5 | HG01515.hp1 HG01517.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.751-172G>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26183529 | ||||||
chr7:26183540
|
G | A | 4 | a0001c0001t0001g0031a0001c0001t0001g0083a0001c0001t0001g0105others(1): Show | 5 | HG03831.hp2 NA18966.hp1 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.751-161G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26183540 | ||||||
chr7:26183620
|
T | TGATCCTT others(4): Show |
1 | a0003c0003t0003g0223 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.751-77_751-67dupCC others(9): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 26183620 | |||||
chr7:26183674
|
A | G | 111 | a0001c0002t0001g0009a0001c0002t0001g0019a0001c0002t0001g0049others(108): Show | 165 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.751-27A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26183674 | ||||||
chr7:26183698
|
C | G | 1 | a0001c0002t0001g0173 | 1 | HG03540.hp1 | splice_region_variant&intron_variant | LOW | c.751-3C>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26183698 | ||||||
chr7:26183811
|
C | T | 4 | a0001c0002t0008g0028a0001c0002t0008g0064a0001c0002t0008g0065others(1): Show | 5 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.834+27C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 3/3 | chr7 | 26183811 | ||||||
chr7:26183986
|
A | G | 4 | a0001c0002t0008g0028a0001c0002t0008g0064a0001c0002t0008g0065others(1): Show | 5 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.834+202A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 3/3 | chr7 | 26183986 | ||||||
chr7:26183999
|
A | T | 5 | a0001c0002t0001g0009a0001c0002t0001g0049a0001c0002t0001g0050others(2): Show | 8 | HG01069.hp2 HG01071.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.834+215A>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 3/3 | chr7 | 26183999 | ||||||
chr7:26184097
|
T | C | 16 | a0001c0002t0001g0009a0001c0002t0001g0049a0001c0002t0001g0050others(13): Show | 21 | HG01069.hp2 HG01071.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.834+313T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 3/3 | chr7 | 26184097 | ||||||
chr7:26184386
|
A | AT | 113 | a0001c0002t0001g0009a0001c0002t0001g0019a0001c0002t0001g0049others(110): Show | 167 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.835-144dupT | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 26184386 | |||||
chr7:26184395
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.835-138G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 3/3 | chr7 | 26184395 | ||||||
chr7:26184454
|
G | C | 1 | a0001c0001t0001g0208 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.835-79G>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 3/3 | chr7 | 26184454 | ||||||
chr7:26184478
|
A | G | 12 | a0001c0002t0001g0019a0001c0002t0001g0078a0001c0002t0001g0089others(9): Show | 14 | HG02145.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.835-55A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 3/3 | chr7 | 26184478 | ||||||
chr7:26184508
|
G | A | 4 | a0001c0002t0008g0028a0001c0002t0008g0064a0001c0002t0008g0065others(1): Show | 5 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.835-25G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 3/3 | chr7 | 26184508 |