Item | Value |
---|---|
geneid | 4688 |
ensemblid | ENSG00000116701.16 |
hgncid | 7661 |
symbol | NCF2 |
name | neutrophil cytosolic factor 2 |
refseq_nuc | NM_000433.4 |
refseq_prot | NP_000424.2 |
ensembl_nuc | ENST00000367535.8 |
ensembl_prot | ENSP00000356505.4 |
mane_status | MANE Select |
chr | chr1 |
start | 183555562 |
end | 183590459 |
strand | - |
ver | v1.2 |
region | chr1:183555562-183590459 |
region5000 | chr1:183550562-183595459 |
regionname0 | NCF2_chr1_183555562_183590459 |
regionname5000 | NCF2_chr1_183550562_183595459 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 526 | 187 | 64 | 26 | 63 | 11 | 21 | 45 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
a0002 | 0/0 | 526 | 184 | 24 | 46 | 91 | 4 | 19 | 74 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
a0003 | 0/0 | 526 | 10 | 1 | 2 | 7 | 0 | 0 | 4 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
a0004 | 0/0 | 526 | 9 | 0 | 0 | 9 | 0 | 0 | 5 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
a0005 | 0/0 | 526 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
a0006 | 0/0 | 526 | 3 | 0 | 1 | 0 | 2 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
a0007 | 0/0 | 526 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
a0008 | 0/0 | 526 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
a0009 | 0/0 | 526 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
a0010 | 0/0 | 526 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
a0011 | 0/0 | 526 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1581 | 186 | 63 | 26 | 63 | 11 | 21 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
c0002 | 0/0 | 1581 | 181 | 24 | 46 | 91 | 4 | 16 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
c0003 | 0/0 | 1581 | 10 | 1 | 2 | 7 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
c0004 | 0/0 | 1581 | 9 | 0 | 0 | 9 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
c0005 | 0/0 | 1581 | 7 | 7 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
c0006 | 0/0 | 1581 | 3 | 0 | 1 | 0 | 2 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
c0007 | 0/0 | 1581 | 3 | 0 | 0 | 0 | 0 | 3 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
c0008 | 0/0 | 1581 | 2 | 0 | 1 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
c0009 | 0/0 | 1581 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
c0010 | 0/0 | 1581 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
c0011 | 0/0 | 1581 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
c0012 | 0/0 | 1581 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
c0013 | 0/0 | 1581 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 687 | 314 | 86 | 59 | 139 | 6 | 23 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
t0002 | 0/0 | 690 | 63 | 2 | 11 | 26 | 8 | 16 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
t0003 | 1/0 | 687 | 18 | 4 | 6 | 0 | 4 | 3 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
t0004 | 0/0 | 687 | 6 | 6 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
t0005 | 0/0 | 684 | 4 | 0 | 0 | 4 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
t0006 | 0/0 | 687 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0005 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0008 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0021 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0203 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0213 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0344 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0348 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0349 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1581 | 186 | 63 | 26 | 63 | 11 | 21 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
a0001c0010 | 0/0 | 1581 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
a0002c0002 | 0/0 | 1581 | 181 | 24 | 46 | 91 | 4 | 16 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
a0002c0007 | 0/0 | 1581 | 3 | 0 | 0 | 0 | 0 | 3 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
a0003c0003 | 0/0 | 1581 | 10 | 1 | 2 | 7 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
a0004c0004 | 0/0 | 1581 | 9 | 0 | 0 | 9 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
a0005c0005 | 0/0 | 1581 | 7 | 7 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
a0006c0006 | 0/0 | 1581 | 3 | 0 | 1 | 0 | 2 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
a0007c0008 | 0/0 | 1581 | 2 | 0 | 1 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
a0008c0009 | 0/0 | 1581 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
a0009c0013 | 0/0 | 1581 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
a0010c0012 | 0/0 | 1581 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
a0011c0011 | 0/0 | 1581 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2267 | 109 | 58 | 10 | 35 | 0 | 5 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
a0001c0001t0002 | 0/0 | 2270 | 55 | 2 | 10 | 23 | 7 | 13 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
a0001c0001t0003 | 1/0 | 2267 | 17 | 3 | 6 | 0 | 4 | 3 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
a0001c0001t0005 | 0/0 | 2264 | 4 | 0 | 0 | 4 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
a0001c0001t0006 | 0/0 | 2267 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
a0001c0010t0001 | 0/0 | 2267 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
a0002c0002t0001 | 0/0 | 2267 | 177 | 23 | 46 | 88 | 4 | 16 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
a0002c0002t0002 | 0/0 | 2270 | 3 | 0 | 0 | 3 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
a0002c0002t0003 | 0/0 | 2267 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
a0002c0007t0002 | 0/0 | 2270 | 3 | 0 | 0 | 0 | 0 | 3 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
a0003c0003t0001 | 0/0 | 2267 | 10 | 1 | 2 | 7 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
a0004c0004t0001 | 0/0 | 2267 | 9 | 0 | 0 | 9 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
a0005c0005t0001 | 0/0 | 2267 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
a0005c0005t0004 | 0/0 | 2267 | 6 | 6 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
a0006c0006t0001 | 0/0 | 2267 | 3 | 0 | 1 | 0 | 2 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
a0007c0008t0002 | 0/0 | 2270 | 2 | 0 | 1 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
a0008c0009t0001 | 0/0 | 2267 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
a0009c0013t0001 | 0/0 | 2267 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
a0010c0012t0001 | 0/0 | 2267 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
a0011c0011t0001 | 0/0 | 2267 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | copy fasta | chr1 | 183550562 | 183595459 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0213 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0003g0021 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0003g0203 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0003g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0003g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0003g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0003g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0005g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0005g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0005g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0006g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0010t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0001 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0008 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0348 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0003g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0007t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0007t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0007t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0003c0003t0001g0005 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0003c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0003c0003t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0003c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0003c0003t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0003c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0003c0003t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0003c0003t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0004c0004t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0004c0004t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0004c0004t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0004c0004t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0004c0004t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0004c0004t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0004c0004t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0004c0004t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0004c0004t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0005c0005t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0005c0005t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0005c0005t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0005c0005t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0005c0005t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0005c0005t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0005c0005t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0006c0006t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0006c0006t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0006c0006t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0007c0008t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0007c0008t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0008c0009t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0009c0013t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0010c0012t0001g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0011c0011t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0021 | EUR | GBR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0170 | EUR | GBR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00140 | hp1 | a0006 | c0006 | t0001 | g0109 | EUR | GBR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0204 | EUR | GBR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0243 | EUR | FIN | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0073 | EUR | FIN | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0344 | EUR | FIN | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0264 | EUR | FIN | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00408 | hp1 | a0002 | c0002 | t0002 | g0101 | EAS | CHS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0155 | EAS | CHS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0153 | EAS | CHS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | CHS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | CHS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00544 | hp2 | a0002 | c0002 | t0001 | g0102 | EAS | CHS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | CHS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0283 | EAS | CHS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00597 | hp2 | a0004 | c0004 | t0001 | g0239 | EAS | CHS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00609 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | CHS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00609 | hp2 | a0002 | c0002 | t0001 | g0352 | EAS | CHS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00621 | hp1 | a0003 | c0003 | t0001 | g0154 | EAS | CHS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0221 | EAS | CHS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0093 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00639 | hp2 | a0002 | c0002 | t0001 | g0201 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0244 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00642 | hp2 | a0002 | c0002 | t0001 | g0017 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00673 | hp1 | a0002 | c0002 | t0002 | g0100 | EAS | CHS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00673 | hp2 | a0002 | c0002 | t0002 | g0107 | EAS | CHS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00735 | hp1 | a0003 | c0003 | t0001 | g0225 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00735 | hp2 | a0002 | c0002 | t0001 | g0010 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0282 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0079 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0364 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0186 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0158 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0312 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01074 | hp2 | a0006 | c0006 | t0001 | g0295 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0262 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0323 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01109 | hp1 | a0002 | c0002 | t0001 | g0358 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0276 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0098 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0360 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01169 | hp1 | a0002 | c0002 | t0001 | g0097 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0255 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0290 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0293 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0231 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0359 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01243 | hp2 | a0002 | c0002 | t0001 | g0338 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01255 | hp1 | a0003 | c0003 | t0001 | g0005 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01255 | hp2 | a0002 | c0002 | t0001 | g0169 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0055 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01256 | hp2 | a0002 | c0002 | t0001 | g0022 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0116 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01257 | hp2 | a0002 | c0002 | t0001 | g0013 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0117 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0022 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0138 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0291 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0015 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0273 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01358 | hp2 | a0002 | c0002 | t0001 | g0354 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0353 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0168 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0263 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0015 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0270 | EUR | IBS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0206 | EUR | IBS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01516 | hp1 | a0002 | c0002 | t0001 | g0348 | EUR | IBS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0021 | EUR | IBS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0269 | EUR | IBS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01517 | hp2 | a0002 | c0002 | t0001 | g0349 | EUR | IBS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01884 | hp1 | a0002 | c0002 | t0001 | g0296 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01884 | hp2 | a0001 | c0001 | t0003 | g0306 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0356 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01891 | hp2 | a0002 | c0002 | t0001 | g0307 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0017 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01934 | hp2 | a0002 | c0002 | t0001 | g0345 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0330 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01943 | hp2 | a0002 | c0002 | t0001 | g0268 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01952 | hp1 | a0002 | c0002 | t0001 | g0205 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01952 | hp2 | a0002 | c0002 | t0001 | g0067 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0077 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01975 | hp2 | a0002 | c0002 | t0001 | g0341 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0010 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0119 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01993 | hp2 | a0002 | c0002 | t0001 | g0347 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0357 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02015 | hp1 | a0001 | c0001 | t0005 | g0025 | EAS | KHV | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02027 | hp1 | a0003 | c0003 | t0001 | g0046 | EAS | KHV | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02027 | hp2 | a0001 | c0001 | t0005 | g0171 | EAS | KHV | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02055 | hp1 | a0002 | c0002 | t0001 | g0207 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02056 | hp2 | a0001 | c0001 | t0005 | g0025 | EAS | KHV | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02074 | hp2 | a0002 | c0002 | t0001 | g0217 | EAS | KHV | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02083 | hp1 | a0003 | c0003 | t0001 | g0096 | EAS | KHV | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02129 | hp1 | a0002 | c0002 | t0001 | g0139 | EAS | KHV | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | KHV | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02132 | hp2 | a0004 | c0004 | t0001 | g0163 | EAS | KHV | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02135 | hp1 | a0002 | c0002 | t0001 | g0232 | EAS | KHV | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02135 | hp2 | a0004 | c0004 | t0001 | g0234 | EAS | KHV | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0288 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02148 | hp2 | a0002 | c0002 | t0001 | g0118 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | CDX | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CDX | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CDX | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0265 | EAS | CDX | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02257 | hp2 | a0002 | c0002 | t0001 | g0242 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0342 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02273 | hp1 | a0002 | c0002 | t0001 | g0144 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02273 | hp2 | a0002 | c0002 | t0001 | g0331 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0053 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0278 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0285 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02300 | hp2 | a0002 | c0002 | t0001 | g0346 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02451 | hp1 | a0002 | c0002 | t0001 | g0125 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0279 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0089 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0316 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0304 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0337 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0335 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0202 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0106 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0361 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02723 | hp2 | a0002 | c0002 | t0001 | g0267 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0058 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02735 | hp2 | a0009 | c0013 | t0001 | g0056 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0084 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0227 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02809 | hp1 | a0005 | c0005 | t0004 | g0031 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0329 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02896 | hp2 | a0005 | c0005 | t0004 | g0029 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02897 | hp2 | a0005 | c0005 | t0004 | g0030 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0322 | AFR | ESN | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ESN | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0315 | AFR | ESN | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0250 | AFR | ESN | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02976 | hp2 | a0002 | c0002 | t0001 | g0248 | AFR | ESN | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | MSL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03130 | hp2 | a0005 | c0005 | t0004 | g0032 | AFR | ESN | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0362 | AFR | ESN | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03209 | hp1 | a0002 | c0002 | t0001 | g0314 | AFR | MSL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03209 | hp2 | a0008 | c0009 | t0001 | g0122 | AFR | MSL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | MSL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03453 | hp2 | a0002 | c0002 | t0001 | g0319 | AFR | MSL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03486 | hp1 | a0002 | c0002 | t0001 | g0249 | AFR | MSL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03486 | hp2 | a0005 | c0005 | t0004 | g0034 | AFR | MSL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0173 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0274 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0256 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0080 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0172 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0277 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0094 | AFR | ESN | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03540 | hp1 | a0002 | c0002 | t0003 | g0305 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03540 | hp2 | a0011 | c0011 | t0001 | g0336 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03579 | hp1 | a0002 | c0002 | t0001 | g0309 | AFR | MSL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03579 | hp2 | a0002 | c0002 | t0001 | g0303 | AFR | MSL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0294 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0182 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0286 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03688 | hp1 | a0002 | c0002 | t0001 | g0166 | SAS | STU | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0287 | SAS | STU | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0059 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0131 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03710 | hp1 | a0010 | c0012 | t0001 | g0351 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0252 | SAS | BEB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | BEB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03834 | hp2 | a0002 | c0002 | t0001 | g0135 | SAS | BEB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03927 | hp1 | a0002 | c0002 | t0001 | g0237 | SAS | BEB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0187 | SAS | BEB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03942 | hp1 | a0002 | c0002 | t0001 | g0229 | SAS | BEB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0024 | SAS | BEB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0226 | SAS | STU | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0142 | SAS | STU | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0099 | SAS | BEB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG04184 | hp2 | a0002 | c0007 | t0002 | g0247 | SAS | BEB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | STU | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG04228 | hp2 | a0002 | c0007 | t0002 | g0063 | SAS | STU | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18522 | hp1 | a0002 | c0002 | t0001 | g0339 | AFR | YRI | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | YRI | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | CHB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18612 | hp2 | a0004 | c0004 | t0001 | g0156 | EAS | CHB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18906 | hp1 | a0002 | c0002 | t0001 | g0036 | AFR | YRI | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18943 | hp1 | a0003 | c0003 | t0001 | g0005 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18944 | hp1 | a0002 | c0002 | t0001 | g0332 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18946 | hp1 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18947 | hp1 | a0002 | c0002 | t0001 | g0350 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18948 | hp1 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18949 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18950 | hp2 | a0002 | c0002 | t0001 | g0301 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18951 | hp2 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18952 | hp1 | a0004 | c0004 | t0001 | g0162 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0300 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18953 | hp2 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18954 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18959 | hp1 | a0002 | c0002 | t0001 | g0165 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18959 | hp2 | a0003 | c0003 | t0001 | g0091 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18961 | hp1 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18963 | hp2 | a0002 | c0002 | t0001 | g0066 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18966 | hp1 | a0003 | c0003 | t0001 | g0005 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18967 | hp1 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18967 | hp2 | a0002 | c0002 | t0001 | g0245 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18968 | hp1 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18969 | hp1 | a0004 | c0004 | t0001 | g0060 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18969 | hp2 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18971 | hp2 | a0003 | c0003 | t0001 | g0233 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18972 | hp1 | a0002 | c0002 | t0001 | g0224 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18973 | hp1 | a0002 | c0002 | t0001 | g0238 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18974 | hp2 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18975 | hp1 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18983 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18988 | hp2 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18990 | hp1 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18990 | hp2 | a0004 | c0004 | t0001 | g0157 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0104 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18992 | hp1 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18993 | hp2 | a0002 | c0002 | t0001 | g0132 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18998 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18999 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18999 | hp2 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19000 | hp1 | a0002 | c0002 | t0001 | g0253 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19001 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19002 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19003 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19004 | hp1 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19004 | hp2 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19006 | hp1 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19006 | hp2 | a0001 | c0001 | t0005 | g0298 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0223 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19009 | hp1 | a0001 | c0001 | t0006 | g0129 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19009 | hp2 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19011 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19012 | hp2 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0340 | AFR | LWK | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19030 | hp2 | a0005 | c0005 | t0004 | g0033 | AFR | LWK | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | LWK | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19043 | hp2 | a0002 | c0002 | t0001 | g0261 | AFR | LWK | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19057 | hp2 | a0002 | c0002 | t0001 | g0092 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19062 | hp1 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19062 | hp2 | a0002 | c0002 | t0001 | g0167 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19063 | hp1 | a0004 | c0004 | t0001 | g0159 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19063 | hp2 | a0002 | c0002 | t0001 | g0246 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0333 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19067 | hp1 | a0002 | c0002 | t0001 | g0209 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19067 | hp2 | a0002 | c0002 | t0001 | g0241 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19068 | hp1 | a0002 | c0002 | t0001 | g0087 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0103 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19074 | hp1 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19078 | hp2 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19079 | hp1 | a0002 | c0002 | t0001 | g0222 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19081 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19081 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19082 | hp2 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19084 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19085 | hp1 | a0004 | c0004 | t0001 | g0105 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0208 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19090 | hp2 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19240 | hp1 | a0002 | c0002 | t0001 | g0313 | AFR | YRI | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | YRI | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA20129 | hp1 | a0002 | c0002 | t0001 | g0284 | AFR | ASW | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ASW | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0292 | EUR | TSI | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA20752 | hp2 | a0007 | c0008 | t0002 | g0136 | EUR | TSI | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0184 | EUR | TSI | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA20805 | hp2 | a0006 | c0006 | t0001 | g0220 | EUR | TSI | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA20905 | hp1 | a0002 | c0007 | t0002 | g0160 | SAS | GIH | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0275 | SAS | GIH | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01123 | hp1 | a0007 | c0008 | t0002 | g0071 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0334 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0363 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03471 | hp1 | a0001 | c0010 | t0001 | g0052 | AFR | MSL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03471 | hp2 | a0002 | c0002 | t0001 | g0054 | AFR | MSL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0074 | AFR | USA | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG06807 | hp2 | a0005 | c0005 | t0001 | g0355 | AFR | USA | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0289 | AFR | USA | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA20300 | hp2 | a0003 | c0003 | t0001 | g0076 | AFR | USA | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | LWK | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA21309 | hp2 | a0002 | c0002 | t0001 | g0343 | AFR | LWK | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0213 | REF | REF | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0203 | REF | REF | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:183556147
|
C | G | 1 | a0011 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.1552G>C | p.Asp518His | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 15/15 | 1682/2267 | 1552/1581 | 518/526 | chr1 | 183556147 | ||
chr1:183560222
|
T | C | 1 | a0010 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.1342A>G | p.Asn448Asp | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/15 | 1472/2267 | 1342/1581 | 448/526 | chr1 | 183560222 | ||
chr1:183563229
|
T | A | 1 | a0009 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.1256A>T | p.Asn419Ile | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/15 | 1386/2267 | 1256/1581 | 419/526 | chr1 | 183563229 | ||
chr1:183563301
|
C | T | 1 | a0007 | 2 | HG01123.hp1 NA20752.hp2 |
missense_variant | MODERATE | c.1184G>A | p.Arg395Gln | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/15 | 1314/2267 | 1184/1581 | 395/526 | chr1 | 183563301 | ||
chr1:183563302
|
G | A | 1 | a0003 | 10 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(7): Show |
missense_variant | MODERATE | c.1183C>T | p.Arg395Trp | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/15 | 1313/2267 | 1183/1581 | 395/526 | chr1 | 183563302 | ||
chr1:183563445
|
G | T | 1 | a0006 | 3 | HG00140.hp1 HG01074.hp2 NA20805.hp2 |
missense_variant | MODERATE | c.1167C>A | p.His389Gln | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 12/15 | 1297/2267 | 1167/1581 | 389/526 | chr1 | 183563445 | ||
chr1:183566954
|
A | G | 1 | a0005 | 7 | HG02809.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
missense_variant | MODERATE | c.890T>C | p.Val297Ala | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 9/15 | 1020/2267 | 890/1581 | 297/526 | chr1 | 183566954 | ||
chr1:183567223
|
G | A | 1 | a0004 | 9 | HG00597.hp2 HG02132.hp2 HG02135.hp2 others(6): Show |
missense_variant | MODERATE | c.836C>T | p.Thr279Met | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 8/15 | 966/2267 | 836/1581 | 279/526 | chr1 | 183567223 | ||
chr1:183573231
|
C | T | 1 | a0008 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.563G>A | p.Arg188Lys | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/15 | 693/2267 | 563/1581 | 188/526 | chr1 | 183573231 | ||
chr1:183573252
|
T | C | 8 | a0002a0003a0004others(5): Show | 216 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(213): Show |
missense_variant | MODERATE | c.542A>G | p.Lys181Arg | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/15 | 672/2267 | 542/1581 | 181/526 | chr1 | 183573252 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:183556196
|
C | T | 1 | a0001c0010 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.1503G>A | p.Gly501Gly | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 15/15 | 1633/2267 | 1503/1581 | 501/526 | chr1 | 183556196 | ||
chr1:183566926
|
C | T | 1 | a0002c0007 | 3 | HG04184.hp2 HG04228.hp2 NA20905.hp1 |
synonymous_variant | LOW | c.918G>A | p.Gln306Gln | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 9/15 | 1048/2267 | 918/1581 | 306/526 | chr1 | 183566926 | ||
chr1:183573188
|
C | T | 1 | a0006c0006 | 3 | HG00140.hp1 HG01074.hp2 NA20805.hp2 |
synonymous_variant | LOW | c.606G>A | p.Ala202Ala | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/15 | 736/2267 | 606/1581 | 202/526 | chr1 | 183573188 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:183555571
|
AAAAC | A | 1 | a0001c0001t0005 | 4 | HG02015.hp1 HG02027.hp2 HG02056.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*543_*546delGTTT | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 15/15 | 543 | chr1 | 183555571 | |||||
chr1:183555600
|
T | TA | 1 | a0001c0001t0005 | 4 | HG02015.hp1 HG02027.hp2 HG02056.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*517dupT | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 15/15 | 517 | chr1 | 183555600 | |||||
chr1:183555715
|
A | AGAT | 4 | a0001c0001t0002a0002c0002t0002a0002c0007t0002others(1): Show | 63 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*400_*402dupATC | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 15/15 | 402 | chr1 | 183555715 | |||||
chr1:183555720
|
C | A | 18 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(15): Show | 388 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(385): Show |
3_prime_UTR_variant | MODIFIER | c.*398G>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 15/15 | 398 | chr1 | 183555720 | |||||
chr1:183555733
|
T | A | 1 | a0001c0001t0006 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*385A>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 15/15 | 385 | chr1 | 183555733 | |||||
chr1:183590458
|
A | G | 1 | a0005c0005t0004 | 6 | HG02809.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-129T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/15 | 129 | chr1 | 183590458 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:183556317
|
T | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0329 | 3 | HG02717.hp1 HG02896.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1469-87A>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183556317 | ||||||
chr1:183556317
|
T | G | 346 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0020others(343): Show | 386 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(383): Show |
intron_variant | MODIFIER | c.1469-87A>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183556317 | ||||||
chr1:183556485
|
A | T | 76 | a0001c0001t0001g0009a0001c0001t0001g0325a0001c0001t0001g0326others(73): Show | 85 | HG00140.hp2 HG00558.hp1 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.1469-255T>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183556485 | ||||||
chr1:183556669
|
C | G | 1 | a0004c0004t0001g0159 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1469-439G>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183556669 | ||||||
chr1:183556726
|
G | A | 1 | a0001c0001t0001g0340 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1469-496C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183556726 | ||||||
chr1:183556921
|
T | C | 1 | a0001c0001t0001g0364 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1469-691A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183556921 | ||||||
chr1:183557136
|
G | A | 1 | a0002c0002t0001g0187 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1469-906C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183557136 | ||||||
chr1:183557191
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1469-961G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183557191 | ||||||
chr1:183557203
|
G | A | 347 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0020others(344): Show | 388 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(385): Show |
intron_variant | MODIFIER | c.1469-973C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183557203 | ||||||
chr1:183557264
|
A | G | 2 | a0002c0002t0001g0168a0002c0002t0001g0207 | 2 | HG01361.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1469-1034T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183557264 | ||||||
chr1:183557365
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1469-1135A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183557365 | ||||||
chr1:183557586
|
G | A | 1 | a0006c0006t0001g0220 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1469-1356C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183557586 | ||||||
chr1:183557671
|
A | G | 2 | a0001c0001t0003g0255a0001c0001t0003g0276 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1469-1441T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183557671 | ||||||
chr1:183557812
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1469-1582G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183557812 | ||||||
chr1:183557881
|
A | AT | 9 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0124others(6): Show | 9 | HG02055.hp2 HG02145.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1469-1652dupA | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183557881 | ||||||
chr1:183557968
|
T | C | 79 | a0001c0001t0001g0009a0001c0001t0001g0325a0001c0001t0001g0326others(76): Show | 89 | HG00140.hp2 HG00558.hp1 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.1469-1738A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183557968 | ||||||
chr1:183558068
|
T | C | 1 | a0001c0010t0001g0052 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1469-1838A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183558068 | ||||||
chr1:183558123
|
C | T | 79 | a0001c0001t0001g0009a0001c0001t0001g0325a0001c0001t0001g0326others(76): Show | 89 | HG00140.hp2 HG00558.hp1 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.1469-1893G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183558123 | ||||||
chr1:183558221
|
C | T | 1 | a0002c0002t0001g0152 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1468+1875G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183558221 | ||||||
chr1:183558222
|
T | G | 2 | a0002c0002t0001g0097a0002c0002t0001g0098 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1468+1874A>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183558222 | ||||||
chr1:183558248
|
A | T | 2 | a0002c0002t0001g0015a0002c0002t0001g0138 | 3 | HG01261.hp1 HG01346.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1468+1848T>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183558248 | ||||||
chr1:183558330
|
C | G | 1 | a0001c0001t0001g0364 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1468+1766G>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183558330 | ||||||
chr1:183558355
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1468+1741G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183558355 | ||||||
chr1:183558597
|
G | A | 2 | a0002c0002t0001g0103a0002c0002t0001g0245 | 2 | NA18967.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1468+1499C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183558597 | ||||||
chr1:183558602
|
G | C | 6 | a0001c0001t0001g0011a0001c0001t0001g0047a0001c0001t0001g0048others(3): Show | 7 | HG02145.hp1 HG02809.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1468+1494C>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183558602 | ||||||
chr1:183558614
|
G | A | 1 | a0002c0002t0001g0198 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1468+1482C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183558614 | ||||||
chr1:183558695
|
G | T | 1 | a0001c0001t0001g0065 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1468+1401C>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183558695 | ||||||
chr1:183558855
|
G | C | 79 | a0001c0001t0001g0009a0001c0001t0001g0325a0001c0001t0001g0326others(76): Show | 89 | HG00140.hp2 HG00558.hp1 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.1468+1241C>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183558855 | ||||||
chr1:183559035
|
C | T | 4 | a0002c0002t0001g0067a0002c0002t0001g0235a0002c0002t0001g0301others(1): Show | 4 | HG01952.hp2 NA18944.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468+1061G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183559035 | ||||||
chr1:183559092
|
T | C | 2 | a0001c0001t0001g0121a0001c0010t0001g0052 | 2 | HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1468+1004A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183559092 | ||||||
chr1:183559118
|
C | G | 1 | a0001c0001t0003g0306 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1468+978G>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183559118 | ||||||
chr1:183559152
|
G | A | 4 | a0004c0004t0001g0156a0004c0004t0001g0157a0004c0004t0001g0159others(1): Show | 4 | HG02132.hp2 NA18612.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468+944C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183559152 | ||||||
chr1:183559308
|
A | C | 2 | a0002c0002t0001g0348a0002c0002t0001g0349 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1468+788T>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183559308 | ||||||
chr1:183559732
|
G | A | 3 | a0001c0001t0005g0025a0001c0001t0005g0171a0001c0001t0005g0298 | 4 | HG02015.hp1 HG02027.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468+364C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183559732 | ||||||
chr1:183559737
|
T | G | 1 | a0001c0001t0001g0364 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1468+359A>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183559737 | ||||||
chr1:183559920
|
T | C | 1 | a0001c0001t0002g0240 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1468+176A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183559920 | ||||||
chr1:183559977
|
G | A | 3 | a0001c0001t0005g0025a0001c0001t0005g0171a0001c0001t0005g0298 | 4 | HG02015.hp1 HG02027.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468+119C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183559977 | ||||||
chr1:183560379
|
C | T | 1 | a0002c0002t0001g0354 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1291-106G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183560379 | ||||||
chr1:183560519
|
G | A | 53 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0007others(50): Show | 60 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.1291-246C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183560519 | ||||||
chr1:183560569
|
G | A | 1 | a0004c0004t0001g0159 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1291-296C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183560569 | ||||||
chr1:183560592
|
G | C | 1 | a0001c0001t0001g0251 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1291-319C>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183560592 | ||||||
chr1:183560675
|
A | T | 1 | a0001c0001t0001g0364 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1291-402T>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183560675 | ||||||
chr1:183560831
|
A | G | 1 | a0001c0001t0002g0272 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1291-558T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183560831 | ||||||
chr1:183560927
|
G | T | 2 | a0002c0002t0001g0103a0002c0002t0001g0245 | 2 | NA18967.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1291-654C>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183560927 | ||||||
chr1:183561015
|
A | G | 1 | a0001c0001t0002g0161 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1291-742T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183561015 | ||||||
chr1:183561141
|
C | A | 8 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0127others(5): Show | 8 | HG02055.hp2 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1291-868G>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183561141 | ||||||
chr1:183561366
|
A | G | 7 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0302others(4): Show | 8 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1291-1093T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183561366 | ||||||
chr1:183561484
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1291-1211T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183561484 | ||||||
chr1:183561569
|
A | G | 1 | a0001c0001t0001g0266 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1291-1296T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183561569 | ||||||
chr1:183561576
|
G | C | 1 | a0003c0003t0001g0154 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1291-1303C>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183561576 | ||||||
chr1:183561641
|
C | CT | 75 | a0001c0001t0001g0009a0001c0001t0001g0325a0001c0001t0001g0326others(72): Show | 84 | HG00140.hp2 HG00558.hp1 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.1291-1369dupA | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183561641 | ||||||
chr1:183561695
|
GT | G | 3 | a0001c0001t0005g0025a0001c0001t0005g0171a0001c0001t0005g0298 | 4 | HG02015.hp1 HG02027.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1291-1423delA | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183561695 | ||||||
chr1:183561779
|
C | CT | 11 | a0001c0001t0001g0045a0001c0001t0001g0068a0001c0001t0001g0078others(8): Show | 11 | HG01109.hp2 HG01175.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.1290+1415dupA | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183561779 | ||||||
chr1:183561779
|
CT | C | 41 | a0001c0001t0001g0110a0001c0001t0001g0114a0001c0001t0001g0115others(38): Show | 45 | HG00423.hp1 HG00558.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1290+1415delA | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183561779 | ||||||
chr1:183561779
|
CTT | C | 27 | a0001c0001t0001g0020a0001c0001t0001g0041a0001c0001t0001g0064others(24): Show | 29 | HG00140.hp2 HG00609.hp2 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.1290+1414_1290+141 others(6): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183561779 | ||||||
chr1:183561779
|
CTTT | C | 26 | a0001c0001t0001g0023a0001c0001t0001g0039a0001c0001t0001g0042others(23): Show | 27 | HG00597.hp1 HG01891.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.1290+1413_1290+141 others(7): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183561779 | ||||||
chr1:183561779
|
CTTTT | C | 16 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0123others(13): Show | 16 | HG00408.hp2 HG01069.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.1290+1412_1290+141 others(8): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183561779 | ||||||
chr1:183561779
|
CTTTTTTT others(7): Show |
C | 15 | a0001c0001t0001g0192a0001c0001t0001g0335a0001c0001t0002g0038others(12): Show | 15 | HG00438.hp2 HG02293.hp1 HG02602.hp1 others(12): Show |
intron_variant | MODIFIER | c.1290+1402_1290+141 others(18): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183561779 | ||||||
chr1:183561779
|
CTTTTTTT others(8): Show |
C | 76 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0121others(73): Show | 87 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.1290+1401_1290+141 others(19): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183561779 | ||||||
chr1:183561779
|
CTTTTTTT others(9): Show |
C | 57 | a0001c0001t0001g0185a0001c0001t0002g0059a0001c0001t0002g0131others(54): Show | 70 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.1290+1400_1290+141 others(20): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183561779 | ||||||
chr1:183561779
|
CTTTTTTT others(10): Show |
C | 32 | a0002c0002t0001g0017a0002c0002t0001g0070a0002c0002t0001g0075others(29): Show | 35 | HG00438.hp1 HG00558.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.1290+1399_1290+141 others(21): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183561779 | ||||||
chr1:183561779
|
CTTTTTTT others(11): Show |
C | 9 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0047others(6): Show | 11 | HG01168.hp1 HG02145.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1290+1398_1290+141 others(22): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183561779 | ||||||
chr1:183561779
|
CTTTTTTT others(12): Show |
C | 2 | a0001c0001t0001g0280a0002c0002t0001g0253 | 2 | HG03831.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1290+1397_1290+141 others(23): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183561779 | ||||||
chr1:183562207
|
T | C | 2 | a0001c0001t0002g0227a0001c0001t0002g0279 | 2 | HG02602.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1290+988A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183562207 | ||||||
chr1:183562385
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1290+810T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183562385 | ||||||
chr1:183562481
|
G | C | 1 | a0002c0002t0001g0242 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1290+714C>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183562481 | ||||||
chr1:183562523
|
A | G | 1 | a0002c0002t0001g0195 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1290+672T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183562523 | ||||||
chr1:183562528
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1290+667G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183562528 | ||||||
chr1:183562662
|
G | A | 1 | a0001c0001t0001g0363 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1290+533C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183562662 | ||||||
chr1:183562803
|
G | A | 73 | a0002c0002t0001g0010a0002c0002t0001g0012a0002c0002t0001g0013others(70): Show | 80 | HG00140.hp2 HG00558.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.1290+392C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183562803 | ||||||
chr1:183562823
|
C | CA | 7 | a0001c0001t0001g0110a0001c0001t0001g0251a0001c0001t0002g0227others(4): Show | 7 | HG01175.hp2 HG01515.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1290+371dupT | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183562823 | ||||||
chr1:183562823
|
C | CAA | 74 | a0001c0001t0001g0009a0001c0001t0001g0325a0001c0001t0001g0326others(71): Show | 83 | HG00140.hp2 HG00558.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.1290+370_1290+371d others(4): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183562823 | ||||||
chr1:183562823
|
CA | C | 6 | a0001c0001t0001g0200a0001c0001t0001g0258a0001c0001t0005g0025others(3): Show | 7 | HG01975.hp1 HG02015.hp1 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.1290+371delT | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183562823 | ||||||
chr1:183562978
|
C | T | 3 | a0001c0001t0005g0025a0001c0001t0005g0171a0001c0001t0005g0298 | 4 | HG02015.hp1 HG02027.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1290+217G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183562978 | ||||||
chr1:183562994
|
G | A | 3 | a0001c0001t0005g0025a0001c0001t0005g0171a0001c0001t0005g0298 | 4 | HG02015.hp1 HG02027.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1290+201C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183562994 | ||||||
chr1:183563065
|
G | A | 40 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0039others(37): Show | 42 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.1290+130C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183563065 | ||||||
chr1:183563310
|
G | C | 3 | a0001c0001t0005g0025a0001c0001t0005g0171a0001c0001t0005g0298 | 4 | HG02015.hp1 HG02027.hp2 HG02056.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1179-4C>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 12/14 | chr1 | 183563310 | ||||||
chr1:183563337
|
C | A | 1 | a0001c0001t0001g0200 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1179-31G>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 12/14 | chr1 | 183563337 | ||||||
chr1:183563376
|
C | T | 1 | a0001c0001t0001g0364 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1178+58G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 12/14 | chr1 | 183563376 | ||||||
chr1:183563871
|
G | A | 1 | a0002c0002t0001g0231 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1026+134C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 11/14 | chr1 | 183563871 | ||||||
chr1:183563896
|
G | C | 1 | a0002c0002t0001g0287 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1026+109C>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 11/14 | chr1 | 183563896 | ||||||
chr1:183563925
|
C | A | 1 | a0001c0001t0001g0364 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1026+80G>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 11/14 | chr1 | 183563925 | ||||||
chr1:183564082
|
C | T | 2 | a0001c0001t0001g0146a0001c0001t0001g0340 | 2 | HG03225.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1001-52G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 10/14 | chr1 | 183564082 | ||||||
chr1:183564194
|
C | T | 2 | a0001c0001t0001g0322a0001c0001t0001g0364 | 2 | HG01069.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1001-164G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 10/14 | chr1 | 183564194 | ||||||
chr1:183564449
|
G | T | 3 | a0001c0001t0005g0025a0001c0001t0005g0171a0001c0001t0005g0298 | 4 | HG02015.hp1 HG02027.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1001-419C>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 10/14 | chr1 | 183564449 | ||||||
chr1:183564450
|
T | C | 1 | a0002c0002t0001g0287 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1001-420A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 10/14 | chr1 | 183564450 | ||||||
chr1:183564650
|
T | A | 3 | a0001c0001t0005g0025a0001c0001t0005g0171a0001c0001t0005g0298 | 4 | HG02015.hp1 HG02027.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1001-620A>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 10/14 | chr1 | 183564650 | ||||||
chr1:183564775
|
C | T | 188 | a0001c0001t0001g0185a0001c0001t0002g0181a0002c0002t0001g0001others(185): Show | 214 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.1001-745G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 10/14 | chr1 | 183564775 | ||||||
chr1:183564801
|
C | T | 1 | a0002c0002t0001g0139 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1001-771G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 10/14 | chr1 | 183564801 | ||||||
chr1:183564942
|
A | G | 1 | a0002c0002t0001g0118 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1000+762T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 10/14 | chr1 | 183564942 | ||||||
chr1:183564969
|
G | T | 1 | a0002c0002t0001g0249 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1000+735C>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 10/14 | chr1 | 183564969 | ||||||
chr1:183565007
|
T | C | 2 | a0001c0001t0002g0264a0001c0001t0002g0292 | 2 | HG00323.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1000+697A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 10/14 | chr1 | 183565007 | ||||||
chr1:183565104
|
G | C | 1 | a0002c0002t0001g0092 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1000+600C>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 10/14 | chr1 | 183565104 | ||||||
chr1:183565409
|
C | G | 335 | a0001c0001t0001g0011a0001c0001t0001g0020a0001c0001t0001g0023others(332): Show | 373 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(370): Show |
intron_variant | MODIFIER | c.1000+295G>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 10/14 | chr1 | 183565409 | ||||||
chr1:183565530
|
G | A | 4 | a0002c0002t0001g0067a0002c0002t0001g0235a0002c0002t0001g0301others(1): Show | 4 | HG01952.hp2 NA18944.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1000+174C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 10/14 | chr1 | 183565530 | ||||||
chr1:183565546
|
G | T | 2 | a0002c0002t0001g0022a0002c0002t0001g0244 | 3 | HG00642.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1000+158C>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 10/14 | chr1 | 183565546 | ||||||
chr1:183565559
|
A | G | 1 | a0002c0002t0001g0342 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1000+145T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 10/14 | chr1 | 183565559 | ||||||
chr1:183565800
|
C | T | 187 | a0001c0001t0001g0185a0001c0001t0002g0181a0002c0002t0001g0001others(184): Show | 213 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.925-21G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 9/14 | chr1 | 183565800 | ||||||
chr1:183565810
|
C | T | 3 | a0001c0001t0001g0045a0001c0001t0001g0257a0001c0001t0001g0281 | 3 | HG01109.hp2 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.925-31G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 9/14 | chr1 | 183565810 | ||||||
chr1:183565833
|
G | A | 1 | a0001c0001t0003g0055 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.925-54C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 9/14 | chr1 | 183565833 | ||||||
chr1:183566012
|
C | T | 1 | a0002c0002t0001g0207 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.925-233G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 9/14 | chr1 | 183566012 | ||||||
chr1:183566021
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.925-242C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 9/14 | chr1 | 183566021 | ||||||
chr1:183566177
|
G | A | 1 | a0001c0001t0001g0337 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.925-398C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 9/14 | chr1 | 183566177 | ||||||
chr1:183566251
|
T | C | 1 | a0001c0001t0001g0361 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.925-472A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 9/14 | chr1 | 183566251 | ||||||
chr1:183566417
|
T | G | 1 | a0001c0001t0001g0045 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.924+503A>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 9/14 | chr1 | 183566417 | ||||||
chr1:183566668
|
A | AC | 8 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0047others(5): Show | 10 | HG02145.hp1 HG02717.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.924+251dupG | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 9/14 | chr1 | 183566668 | ||||||
chr1:183566860
|
C | A | 1 | a0001c0010t0001g0052 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.924+60G>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 9/14 | chr1 | 183566860 | ||||||
chr1:183567126
|
G | A | 7 | a0001c0001t0001g0044a0001c0001t0001g0146a0001c0001t0001g0191others(4): Show | 7 | HG02257.hp1 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.855+78C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 8/14 | chr1 | 183567126 | ||||||
chr1:183567790
|
C | G | 3 | a0001c0001t0001g0045a0001c0001t0001g0257a0001c0001t0001g0281 | 3 | HG01109.hp2 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.714-445G>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 7/14 | chr1 | 183567790 | ||||||
chr1:183567905
|
G | A | 3 | a0001c0001t0005g0025a0001c0001t0005g0171a0001c0001t0005g0298 | 4 | HG02015.hp1 HG02027.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.714-560C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 7/14 | chr1 | 183567905 | ||||||
chr1:183568020
|
C | T | 1 | a0001c0001t0002g0059 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.714-675G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 7/14 | chr1 | 183568020 | ||||||
chr1:183568133
|
C | T | 3 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0197 | 3 | NA18948.hp2 NA18963.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.714-788G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 7/14 | chr1 | 183568133 | ||||||
chr1:183568138
|
A | G | 3 | a0001c0001t0005g0025a0001c0001t0005g0171a0001c0001t0005g0298 | 4 | HG02015.hp1 HG02027.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.714-793T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 7/14 | chr1 | 183568138 | ||||||
chr1:183568159
|
C | G | 2 | a0002c0002t0001g0097a0002c0002t0001g0098 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.714-814G>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 7/14 | chr1 | 183568159 | ||||||
chr1:183568339
|
T | G | 214 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0045others(211): Show | 243 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.713+803A>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 7/14 | chr1 | 183568339 | ||||||
chr1:183568343
|
G | T | 189 | a0001c0001t0001g0185a0001c0001t0002g0181a0002c0002t0001g0001others(186): Show | 215 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.713+799C>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 7/14 | chr1 | 183568343 | ||||||
chr1:183568467
|
A | G | 5 | a0001c0001t0001g0044a0001c0001t0001g0191a0001c0001t0001g0317others(2): Show | 5 | HG02257.hp1 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.713+675T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 7/14 | chr1 | 183568467 | ||||||
chr1:183568691
|
C | T | 16 | a0002c0002t0001g0010a0002c0002t0001g0013a0002c0002t0001g0014others(13): Show | 21 | HG00735.hp2 HG00738.hp1 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.713+451G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 7/14 | chr1 | 183568691 | ||||||
chr1:183568724
|
G | C | 189 | a0001c0001t0001g0185a0001c0001t0002g0181a0002c0002t0001g0001others(186): Show | 215 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.713+418C>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 7/14 | chr1 | 183568724 | ||||||
chr1:183568777
|
C | A | 1 | a0002c0002t0001g0089 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.713+365G>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 7/14 | chr1 | 183568777 | ||||||
chr1:183568799
|
A | G | 350 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0020others(347): Show | 391 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(388): Show |
intron_variant | MODIFIER | c.713+343T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 7/14 | chr1 | 183568799 | ||||||
chr1:183568890
|
A | G | 214 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0045others(211): Show | 243 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.713+252T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 7/14 | chr1 | 183568890 | ||||||
chr1:183568948
|
T | C | 2 | a0002c0002t0001g0248a0002c0002t0001g0249 | 2 | HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.713+194A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 7/14 | chr1 | 183568948 | ||||||
chr1:183568955
|
T | G | 1 | a0002c0002t0001g0268 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.713+187A>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 7/14 | chr1 | 183568955 | ||||||
chr1:183569299
|
A | C | 6 | a0001c0001t0001g0011a0001c0001t0001g0047a0001c0001t0001g0048others(3): Show | 7 | HG02145.hp1 HG02809.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.670-114T>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 6/14 | chr1 | 183569299 | ||||||
chr1:183569590
|
T | A | 189 | a0001c0001t0001g0185a0001c0001t0002g0181a0002c0002t0001g0001others(186): Show | 215 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.670-405A>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 6/14 | chr1 | 183569590 | ||||||
chr1:183569652
|
G | A | 1 | a0001c0001t0001g0115 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.670-467C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 6/14 | chr1 | 183569652 | ||||||
chr1:183569793
|
T | C | 3 | a0001c0001t0005g0025a0001c0001t0005g0171a0001c0001t0005g0298 | 4 | HG02015.hp1 HG02027.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.670-608A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 6/14 | chr1 | 183569793 | ||||||
chr1:183569990
|
A | G | 192 | a0001c0001t0001g0185a0001c0001t0002g0181a0001c0001t0005g0025others(189): Show | 219 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.669+790T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 6/14 | chr1 | 183569990 | ||||||
chr1:183570313
|
C | T | 2 | a0001c0001t0002g0256a0001c0001t0002g0277 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.669+467G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 6/14 | chr1 | 183570313 | ||||||
chr1:183570314
|
G | T | 188 | a0001c0001t0001g0185a0002c0002t0001g0001a0002c0002t0001g0002others(185): Show | 214 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.669+466C>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 6/14 | chr1 | 183570314 | ||||||
chr1:183570393
|
C | T | 1 | a0002c0002t0001g0142 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.669+387G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 6/14 | chr1 | 183570393 | ||||||
chr1:183570428
|
A | G | 1 | a0002c0002t0001g0093 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.669+352T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 6/14 | chr1 | 183570428 | ||||||
chr1:183570533
|
C | T | 1 | a0001c0001t0002g0286 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.669+247G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 6/14 | chr1 | 183570533 | ||||||
chr1:183570715
|
G | A | 2 | a0001c0001t0001g0047a0001c0001t0001g0049 | 2 | HG02970.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.669+65C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 6/14 | chr1 | 183570715 | ||||||
chr1:183570916
|
C | A | 1 | a0001c0001t0001g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.610-77G>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/14 | chr1 | 183570916 | ||||||
chr1:183571067
|
A | C | 2 | a0002c0002t0002g0100a0002c0002t0002g0101 | 2 | HG00408.hp1 HG00673.hp1 |
intron_variant | MODIFIER | c.610-228T>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/14 | chr1 | 183571067 | ||||||
chr1:183571080
|
TA | T | 191 | a0001c0001t0001g0185a0001c0001t0005g0025a0001c0001t0005g0171others(188): Show | 218 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.610-242delT | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/14 | chr1 | 183571080 | ||||||
chr1:183571110
|
T | G | 1 | a0001c0001t0001g0258 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.610-271A>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/14 | chr1 | 183571110 | ||||||
chr1:183571114
|
C | CT | 178 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0199others(175): Show | 204 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.610-276dupA | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/14 | chr1 | 183571114 | ||||||
chr1:183571114
|
CT | C | 14 | a0001c0001t0001g0042a0001c0001t0001g0123a0001c0001t0001g0124others(11): Show | 14 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.610-276delA | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/14 | chr1 | 183571114 | ||||||
chr1:183571114
|
CTTTTTTT others(4): Show |
C | 1 | a0007c0008t0002g0136 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.610-286_610-276del others(11): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/14 | chr1 | 183571114 | ||||||
chr1:183571279
|
G | A | 1 | a0002c0002t0001g0017 | 2 | HG00642.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.610-440C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/14 | chr1 | 183571279 | ||||||
chr1:183571280
|
G | A | 2 | a0002c0002t0001g0338a0002c0002t0001g0339 | 2 | HG01243.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.610-441C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/14 | chr1 | 183571280 | ||||||
chr1:183571376
|
C | T | 2 | a0001c0001t0003g0255a0001c0001t0003g0276 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.610-537G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/14 | chr1 | 183571376 | ||||||
chr1:183571641
|
G | T | 188 | a0001c0001t0001g0185a0002c0002t0001g0001a0002c0002t0001g0002others(185): Show | 214 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.610-802C>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/14 | chr1 | 183571641 | ||||||
chr1:183571963
|
C | T | 190 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0006others(187): Show | 216 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.610-1124G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/14 | chr1 | 183571963 | ||||||
chr1:183571964
|
A | ATGGATAT others(10): Show |
1 | a0001c0001t0005g0298 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.610-1142_610-1126d others(19): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/14 | chr1 | 183571964 | ||||||
chr1:183571991
|
T | C | 190 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0006others(187): Show | 216 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.610-1152A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/14 | chr1 | 183571991 | ||||||
chr1:183572337
|
G | A | 3 | a0001c0001t0001g0271a0001c0001t0001g0359a0001c0001t0001g0360 | 3 | HG01168.hp2 HG01243.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.609+848C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/14 | chr1 | 183572337 | ||||||
chr1:183572707
|
A | C | 190 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0006others(187): Show | 216 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.609+478T>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/14 | chr1 | 183572707 | ||||||
chr1:183572731
|
C | T | 190 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0006others(187): Show | 216 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.609+454G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/14 | chr1 | 183572731 | ||||||
chr1:183573012
|
T | C | 1 | a0001c0001t0002g0081 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.609+173A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/14 | chr1 | 183573012 | ||||||
chr1:183573143
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.609+42C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/14 | chr1 | 183573143 | ||||||
chr1:183573343
|
T | C | 1 | a0002c0002t0001g0125 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.502-51A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 4/14 | chr1 | 183573343 | ||||||
chr1:183573612
|
G | T | 189 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0006others(186): Show | 215 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.502-320C>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 4/14 | chr1 | 183573612 | ||||||
chr1:183573659
|
G | C | 1 | a0001c0001t0001g0192 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.502-367C>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 4/14 | chr1 | 183573659 | ||||||
chr1:183573732
|
A | G | 10 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0121others(7): Show | 11 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.502-440T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 4/14 | chr1 | 183573732 | ||||||
chr1:183573918
|
C | T | 190 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0006others(187): Show | 216 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.501+569G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 4/14 | chr1 | 183573918 | ||||||
chr1:183574076
|
C | T | 1 | a0002c0002t0001g0099 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.501+411G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 4/14 | chr1 | 183574076 | ||||||
chr1:183574445
|
C | A | 1 | a0002c0002t0001g0054 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.501+42G>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 4/14 | chr1 | 183574445 | ||||||
chr1:183574637
|
C | T | 2 | a0002c0002t0001g0097a0002c0002t0001g0098 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.367-16G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183574637 | ||||||
chr1:183574639
|
G | A | 1 | a0001c0001t0001g0340 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.367-18C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183574639 | ||||||
chr1:183575123
|
C | T | 8 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0127others(5): Show | 8 | HG02055.hp2 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.367-502G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183575123 | ||||||
chr1:183575207
|
T | C | 1 | a0004c0004t0001g0162 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.367-586A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183575207 | ||||||
chr1:183575208
|
G | A | 1 | a0004c0004t0001g0162 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.367-587C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183575208 | ||||||
chr1:183575252
|
T | C | 1 | a0001c0001t0003g0306 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.367-631A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183575252 | ||||||
chr1:183575339
|
A | G | 1 | a0002c0002t0001g0054 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.367-718T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183575339 | ||||||
chr1:183575353
|
T | C | 1 | a0001c0001t0001g0193 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.367-732A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183575353 | ||||||
chr1:183575357
|
C | A | 1 | a0001c0001t0002g0134 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.367-736G>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183575357 | ||||||
chr1:183575443
|
G | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0041 | 2 | NA18993.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.367-822C>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183575443 | ||||||
chr1:183575508
|
G | A | 1 | a0001c0001t0001g0325 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.367-887C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183575508 | ||||||
chr1:183575542
|
C | T | 12 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0047others(9): Show | 15 | HG02015.hp1 HG02027.hp2 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.367-921G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183575542 | ||||||
chr1:183575559
|
G | A | 57 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0042others(54): Show | 59 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.367-938C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183575559 | ||||||
chr1:183575593
|
C | T | 8 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0047others(5): Show | 10 | HG02145.hp1 HG02717.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.367-972G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183575593 | ||||||
chr1:183575815
|
A | C | 1 | a0001c0001t0001g0364 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.367-1194T>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183575815 | ||||||
chr1:183576103
|
C | T | 6 | a0005c0005t0004g0029a0005c0005t0004g0030a0005c0005t0004g0031others(3): Show | 6 | HG02809.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.367-1482G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183576103 | ||||||
chr1:183576131
|
G | A | 2 | a0001c0001t0001g0183a0002c0002t0001g0182 | 2 | HG01433.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.366+1468C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183576131 | ||||||
chr1:183576143
|
A | G | 1 | a0002c0002t0001g0093 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.366+1456T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183576143 | ||||||
chr1:183576190
|
G | A | 1 | a0004c0004t0001g0163 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.366+1409C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183576190 | ||||||
chr1:183576297
|
A | G | 1 | a0001c0001t0003g0323 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.366+1302T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183576297 | ||||||
chr1:183576462
|
G | A | 1 | a0001c0001t0002g0164 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.366+1137C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183576462 | ||||||
chr1:183576468
|
G | A | 13 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0183others(10): Show | 13 | HG01123.hp2 HG01192.hp1 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.366+1131C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183576468 | ||||||
chr1:183576504
|
C | T | 2 | a0001c0001t0001g0322a0001c0001t0001g0364 | 2 | HG01069.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.366+1095G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183576504 | ||||||
chr1:183576505
|
G | A | 1 | a0001c0001t0001g0266 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.366+1094C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183576505 | ||||||
chr1:183576522
|
G | C | 1 | a0001c0001t0001g0340 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.366+1077C>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183576522 | ||||||
chr1:183576530
|
C | T | 147 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0127others(144): Show | 166 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.366+1069G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183576530 | ||||||
chr1:183576533
|
A | G | 1 | a0001c0001t0001g0110 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.366+1066T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183576533 | ||||||
chr1:183576535
|
C | A | 2 | a0002c0002t0001g0106a0002c0002t0001g0284 | 2 | HG02698.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.366+1064G>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183576535 | ||||||
chr1:183576549
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.366+1050G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183576549 | ||||||
chr1:183576550
|
G | A | 9 | a0001c0001t0001g0110a0001c0001t0001g0114a0001c0001t0001g0115others(6): Show | 9 | HG00423.hp1 HG01168.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.366+1049C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183576550 | ||||||
chr1:183576681
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.366+918C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183576681 | ||||||
chr1:183576926
|
G | A | 146 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0127others(143): Show | 165 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.366+673C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183576926 | ||||||
chr1:183576990
|
T | C | 1 | a0001c0001t0003g0250 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.366+609A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183576990 | ||||||
chr1:183577062
|
G | T | 6 | a0002c0002t0001g0012a0002c0002t0001g0051a0002c0002t0001g0061others(3): Show | 7 | NA18960.hp1 NA18969.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.366+537C>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183577062 | ||||||
chr1:183577181
|
C | T | 1 | a0001c0001t0002g0170 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.366+418G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183577181 | ||||||
chr1:183577192
|
C | T | 1 | a0001c0010t0001g0052 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.366+407G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183577192 | ||||||
chr1:183577338
|
G | A | 276 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0026others(273): Show | 315 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.366+261C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183577338 | ||||||
chr1:183577367
|
G | A | 17 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0035others(14): Show | 20 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.366+232C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183577367 | ||||||
chr1:183577385
|
G | T | 3 | a0002c0002t0001g0097a0002c0002t0001g0098a0002c0002t0001g0242 | 3 | HG01168.hp1 HG01169.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.366+214C>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183577385 | ||||||
chr1:183577779
|
G | T | 1 | a0001c0001t0003g0323 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.258-72C>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183577779 | ||||||
chr1:183577787
|
C | T | 1 | a0002c0002t0001g0137 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.258-80G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183577787 | ||||||
chr1:183577795
|
T | C | 1 | a0001c0010t0001g0052 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.258-88A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183577795 | ||||||
chr1:183577838
|
G | C | 1 | a0001c0001t0001g0258 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.258-131C>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183577838 | ||||||
chr1:183577862
|
T | C | 7 | a0002c0002t0001g0006a0002c0002t0001g0095a0002c0002t0001g0126others(4): Show | 9 | HG00673.hp2 NA18959.hp1 NA19001.hp1 others(6): Show |
intron_variant | MODIFIER | c.258-155A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183577862 | ||||||
chr1:183577877
|
C | T | 1 | a0002c0002t0001g0168 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.258-170G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183577877 | ||||||
chr1:183577897
|
T | C | 46 | a0001c0001t0001g0143a0001c0001t0001g0214a0002c0002t0001g0010others(43): Show | 53 | HG00140.hp2 HG00558.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.258-190A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183577897 | ||||||
chr1:183577905
|
G | A | 1 | a0002c0002t0001g0168 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.258-198C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183577905 | ||||||
chr1:183578038
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.258-331G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183578038 | ||||||
chr1:183578120
|
A | G | 1 | a0001c0001t0003g0323 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.258-413T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183578120 | ||||||
chr1:183578216
|
G | C | 1 | a0002c0002t0001g0229 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.258-509C>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183578216 | ||||||
chr1:183578220
|
A | C | 1 | a0001c0010t0001g0052 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.258-513T>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183578220 | ||||||
chr1:183578355
|
C | CT | 72 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0042others(69): Show | 75 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.258-649dupA | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183578355 | ||||||
chr1:183578355
|
C | CTT | 6 | a0001c0001t0001g0044a0001c0001t0001g0191a0001c0001t0001g0317others(3): Show | 6 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.258-650_258-649dup others(2): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183578355 | ||||||
chr1:183578507
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.258-800C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183578507 | ||||||
chr1:183578547
|
G | A | 1 | a0002c0002t0001g0169 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.258-840C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183578547 | ||||||
chr1:183578554
|
C | T | 3 | a0001c0001t0005g0025a0001c0001t0005g0171a0001c0001t0005g0298 | 4 | HG02015.hp1 HG02027.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-847G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183578554 | ||||||
chr1:183578576
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.258-869C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183578576 | ||||||
chr1:183578693
|
C | T | 1 | a0002c0002t0001g0252 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.258-986G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183578693 | ||||||
chr1:183578737
|
T | G | 77 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0042others(74): Show | 80 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.258-1030A>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183578737 | ||||||
chr1:183578972
|
G | A | 3 | a0001c0001t0005g0025a0001c0001t0005g0171a0001c0001t0005g0298 | 4 | HG02015.hp1 HG02027.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-1265C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183578972 | ||||||
chr1:183578981
|
A | C | 1 | a0002c0002t0001g0253 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.258-1274T>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183578981 | ||||||
chr1:183579123
|
C | T | 1 | a0001c0010t0001g0052 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.258-1416G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183579123 | ||||||
chr1:183579361
|
C | T | 77 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0042others(74): Show | 80 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.258-1654G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183579361 | ||||||
chr1:183579464
|
C | T | 1 | a0002c0002t0001g0237 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.258-1757G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183579464 | ||||||
chr1:183579492
|
C | T | 1 | a0001c0010t0001g0052 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.258-1785G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183579492 | ||||||
chr1:183579497
|
C | T | 1 | a0003c0003t0001g0096 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.258-1790G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183579497 | ||||||
chr1:183579508
|
C | T | 49 | a0001c0001t0001g0045a0001c0001t0001g0143a0001c0001t0001g0214others(46): Show | 56 | HG00140.hp2 HG00558.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.258-1801G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183579508 | ||||||
chr1:183579520
|
A | G | 2 | a0002c0002t0001g0314a0002c0002t0001g0319 | 2 | HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.258-1813T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183579520 | ||||||
chr1:183579688
|
G | C | 8 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0047others(5): Show | 10 | HG02145.hp1 HG02717.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.258-1981C>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183579688 | ||||||
chr1:183579738
|
C | CA | 135 | a0001c0001t0001g0009a0001c0001t0001g0039a0001c0001t0001g0123others(132): Show | 156 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.258-2032dupT | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183579738 | ||||||
chr1:183579738
|
C | CAA | 33 | a0001c0001t0001g0041a0001c0001t0001g0045a0001c0001t0001g0124others(30): Show | 33 | HG00544.hp1 HG00597.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.258-2033_258-2032d others(4): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183579738 | ||||||
chr1:183579738
|
CA | C | 9 | a0001c0001t0001g0121a0001c0001t0001g0197a0001c0001t0002g0130others(6): Show | 9 | HG00323.hp2 HG01070.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.258-2032delT | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183579738 | ||||||
chr1:183579738
|
CAAAAAAA others(3): Show |
C | 25 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0001g0083others(22): Show | 25 | HG01123.hp2 HG01192.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.258-2041_258-2032d others(12): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183579738 | ||||||
chr1:183579766
|
A | G | 2 | a0002c0002t0001g0093a0002c0002t0001g0149 | 2 | HG00639.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.258-2059T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183579766 | ||||||
chr1:183579781
|
T | C | 1 | a0002c0002t0001g0207 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.258-2074A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183579781 | ||||||
chr1:183579857
|
A | G | 77 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0042others(74): Show | 80 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.258-2150T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183579857 | ||||||
chr1:183579970
|
A | C | 1 | a0001c0001t0001g0251 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.258-2263T>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183579970 | ||||||
chr1:183579991
|
A | G | 1 | a0002c0002t0001g0092 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.258-2284T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183579991 | ||||||
chr1:183580086
|
G | A | 1 | a0001c0001t0002g0264 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.258-2379C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183580086 | ||||||
chr1:183580348
|
G | A | 1 | a0001c0001t0001g0311 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.258-2641C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183580348 | ||||||
chr1:183580423
|
G | A | 1 | a0005c0005t0004g0032 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.258-2716C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183580423 | ||||||
chr1:183580468
|
C | G | 1 | a0002c0002t0001g0265 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.258-2761G>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183580468 | ||||||
chr1:183580469
|
AATTTCCA others(1721): Show |
A | 1 | a0002c0002t0001g0265 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.258-4490_258-2763d others(2): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183580469 | ||||||
chr1:183580498
|
G | A | 1 | a0001c0001t0003g0323 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.258-2791C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183580498 | ||||||
chr1:183580622
|
G | T | 137 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0127others(134): Show | 156 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.258-2915C>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183580622 | ||||||
chr1:183580672
|
T | C | 1 | a0002c0002t0001g0339 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.258-2965A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183580672 | ||||||
chr1:183580699
|
C | T | 2 | a0002c0002t0001g0312a0002c0002t0001g0313 | 2 | HG01074.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.258-2992G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183580699 | ||||||
chr1:183580717
|
C | G | 53 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0042others(50): Show | 56 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.258-3010G>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183580717 | ||||||
chr1:183580775
|
G | A | 1 | a0001c0001t0001g0337 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.258-3068C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183580775 | ||||||
chr1:183580839
|
C | T | 1 | a0001c0001t0003g0323 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.258-3132G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183580839 | ||||||
chr1:183580978
|
C | CA | 136 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0039others(133): Show | 146 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.258-3272dupT | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183580978 | ||||||
chr1:183580978
|
CA | C | 51 | a0001c0001t0001g0045a0001c0001t0001g0143a0001c0001t0001g0214others(48): Show | 58 | HG00140.hp2 HG00558.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.258-3272delT | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183580978 | ||||||
chr1:183581174
|
C | T | 3 | a0001c0001t0005g0025a0001c0001t0005g0171a0001c0001t0005g0298 | 4 | HG02015.hp1 HG02027.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-3467G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581174 | ||||||
chr1:183581231
|
A | G | 1 | a0001c0001t0001g0258 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.258-3524T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581231 | ||||||
chr1:183581281
|
C | CA | 117 | a0001c0001t0001g0011a0001c0001t0001g0047a0001c0001t0001g0048others(114): Show | 135 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.258-3575dupT | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581281 | ||||||
chr1:183581281
|
C | CAA | 22 | a0001c0001t0001g0320a0001c0001t0001g0337a0002c0002t0001g0053others(19): Show | 22 | HG01361.hp2 HG01891.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.258-3576_258-3575d others(4): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581281 | ||||||
chr1:183581281
|
C | CAAAAA | 13 | a0001c0001t0001g0044a0001c0001t0001g0111a0001c0001t0001g0190others(10): Show | 14 | HG01884.hp1 HG02015.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.258-3579_258-3575d others(7): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581281 | ||||||
chr1:183581281
|
C | CAAAAAA | 58 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0042others(55): Show | 60 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.258-3580_258-3575d others(8): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581281 | ||||||
chr1:183581281
|
C | CAAAAAAA | 8 | a0001c0001t0001g0057a0001c0001t0001g0120a0001c0001t0001g0188others(5): Show | 8 | HG01243.hp2 HG01884.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.258-3581_258-3575d others(9): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581281 | ||||||
chr1:183581297
|
AG | A | 54 | a0001c0001t0001g0035a0001c0001t0001g0039a0001c0001t0001g0041others(51): Show | 61 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.258-3591delC | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581297 | ||||||
chr1:183581298
|
G | A | 204 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0026others(201): Show | 235 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(232): Show |
intron_variant | MODIFIER | c.258-3591C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581298 | ||||||
chr1:183581308
|
A | C | 8 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0127others(5): Show | 8 | HG02055.hp2 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.258-3601T>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581308 | ||||||
chr1:183581314
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.258-3607C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581314 | ||||||
chr1:183581315
|
A | AAAAG | 83 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0042others(80): Show | 86 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.258-3612_258-3609d others(6): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581315 | ||||||
chr1:183581315
|
A | G | 1 | a0001c0001t0001g0258 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.258-3608T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581315 | ||||||
chr1:183581340
|
A | C | 134 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0127others(131): Show | 151 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.258-3633T>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581340 | ||||||
chr1:183581347
|
G | A | 1 | a0001c0001t0002g0294 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.258-3640C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581347 | ||||||
chr1:183581489
|
T | C | 1 | a0001c0001t0003g0080 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.258-3782A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581489 | ||||||
chr1:183581516
|
C | T | 1 | a0001c0001t0001g0361 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.258-3809G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581516 | ||||||
chr1:183581595
|
C | G | 1 | a0001c0001t0001g0047 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.258-3888G>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581595 | ||||||
chr1:183581674
|
GT | G | 131 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0127others(128): Show | 148 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.258-3968delA | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581674 | ||||||
chr1:183581678
|
T | G | 1 | a0001c0001t0001g0340 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.258-3971A>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581678 | ||||||
chr1:183581707
|
T | C | 1 | a0002c0002t0001g0169 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.258-4000A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581707 | ||||||
chr1:183581708
|
G | A | 1 | a0002c0002t0001g0169 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.258-4001C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581708 | ||||||
chr1:183581747
|
G | C | 1 | a0001c0001t0001g0190 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.258-4040C>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581747 | ||||||
chr1:183581754
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.258-4047G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581754 | ||||||
chr1:183581869
|
G | A | 1 | a0002c0002t0001g0054 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.258-4162C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581869 | ||||||
chr1:183581910
|
G | A | 83 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0042others(80): Show | 86 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.258-4203C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581910 | ||||||
chr1:183581911
|
C | A | 1 | a0001c0001t0003g0306 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.258-4204G>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581911 | ||||||
chr1:183581957
|
T | G | 3 | a0001c0001t0002g0059a0001c0001t0002g0170a0001c0001t0002g0202 | 3 | HG00099.hp2 HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.258-4250A>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581957 | ||||||
chr1:183582027
|
T | C | 80 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0042others(77): Show | 83 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.258-4320A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183582027 | ||||||
chr1:183582198
|
C | T | 1 | a0002c0002t0001g0265 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.258-4491G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183582198 | ||||||
chr1:183582625
|
G | A | 87 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0042others(84): Show | 90 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.257+4270C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183582625 | ||||||
chr1:183582904
|
C | T | 3 | a0001c0001t0001g0258a0001c0001t0001g0322a0001c0001t0001g0364 | 3 | HG01069.hp1 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.257+3991G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183582904 | ||||||
chr1:183582958
|
T | TA | 83 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0042others(80): Show | 86 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.257+3936dupT | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183582958 | ||||||
chr1:183583012
|
C | T | 1 | a0002c0002t0001g0345 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.257+3883G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183583012 | ||||||
chr1:183583371
|
G | A | 1 | a0001c0001t0003g0323 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.257+3524C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183583371 | ||||||
chr1:183583391
|
A | G | 27 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0001g0083others(24): Show | 27 | HG01123.hp2 HG01192.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.257+3504T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183583391 | ||||||
chr1:183583520
|
A | G | 1 | a0002c0002t0001g0036 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.257+3375T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183583520 | ||||||
chr1:183583621
|
C | T | 2 | a0002c0002t0001g0087a0002c0002t0001g0215 | 2 | NA18961.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.257+3274G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183583621 | ||||||
chr1:183583763
|
G | A | 1 | a0005c0005t0001g0355 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.257+3132C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183583763 | ||||||
chr1:183583909
|
A | G | 1 | a0002c0002t0001g0054 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.257+2986T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183583909 | ||||||
chr1:183583989
|
C | T | 2 | a0001c0001t0002g0316a0001c0001t0002g0344 | 2 | HG00323.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.257+2906G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183583989 | ||||||
chr1:183584191
|
A | G | 8 | a0001c0001t0001g0023a0001c0001t0001g0064a0001c0001t0001g0065others(5): Show | 9 | HG00597.hp1 HG02155.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.257+2704T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183584191 | ||||||
chr1:183584348
|
C | T | 1 | a0002c0002t0001g0126 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.257+2547G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183584348 | ||||||
chr1:183584349
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.257+2546C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183584349 | ||||||
chr1:183584425
|
C | T | 292 | a0001c0001t0001g0011a0001c0001t0001g0020a0001c0001t0001g0023others(289): Show | 330 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(327): Show |
intron_variant | MODIFIER | c.257+2470G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183584425 | ||||||
chr1:183584433
|
T | C | 7 | a0001c0001t0001g0324a0005c0005t0004g0029a0005c0005t0004g0030others(4): Show | 7 | HG02809.hp1 HG02809.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.257+2462A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183584433 | ||||||
chr1:183584502
|
A | C | 12 | a0001c0001t0001g0191a0001c0001t0001g0254a0001c0001t0001g0258others(9): Show | 12 | HG01099.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.257+2393T>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183584502 | ||||||
chr1:183584533
|
C | T | 4 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0361others(1): Show | 4 | HG02559.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.257+2362G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183584533 | ||||||
chr1:183584559
|
C | T | 1 | a0001c0001t0001g0334 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.257+2336G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183584559 | ||||||
chr1:183584735
|
C | T | 100 | a0001c0001t0001g0023a0001c0001t0001g0035a0001c0001t0001g0042others(97): Show | 114 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.257+2160G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183584735 | ||||||
chr1:183584915
|
A | C | 15 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0086others(12): Show | 16 | HG01081.hp1 HG01978.hp1 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.257+1980T>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183584915 | ||||||
chr1:183584916
|
TA | T | 15 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0086others(12): Show | 16 | HG01081.hp1 HG01978.hp1 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.257+1978delT | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183584916 | ||||||
chr1:183585038
|
T | G | 1 | a0001c0001t0001g0326 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.257+1857A>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585038 | ||||||
chr1:183585146
|
A | G | 113 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0023others(110): Show | 123 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.257+1749T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585146 | ||||||
chr1:183585314
|
T | C | 122 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0026others(119): Show | 134 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.257+1581A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585314 | ||||||
chr1:183585398
|
G | A | 32 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0302others(29): Show | 35 | HG01069.hp1 HG01074.hp1 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.257+1497C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585398 | ||||||
chr1:183585410
|
G | A | 1 | a0001c0001t0001g0257 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.257+1485C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585410 | ||||||
chr1:183585574
|
G | A | 2 | a0002c0002t0001g0206a0002c0002t0001g0245 | 2 | HG01515.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.257+1321C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585574 | ||||||
chr1:183585579
|
C | T | 37 | a0001c0001t0001g0028a0001c0001t0001g0189a0001c0001t0001g0190others(34): Show | 40 | HG00323.hp1 HG00609.hp2 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.257+1316G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585579 | ||||||
chr1:183585612
|
G | A | 5 | a0001c0001t0001g0315a0001c0001t0001g0317a0001c0001t0001g0318others(2): Show | 5 | HG02257.hp1 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.257+1283C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585612 | ||||||
chr1:183585624
|
C | CAAAAAAA others(3): Show |
47 | a0001c0001t0001g0028a0001c0001t0001g0189a0001c0001t0001g0190others(44): Show | 51 | HG00323.hp1 HG00323.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.257+1261_257+1270d others(12): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585624 | ||||||
chr1:183585624
|
C | CAAAAAAA others(4): Show |
50 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0042others(47): Show | 55 | HG00558.hp2 HG00738.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.257+1260_257+1270d others(13): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585624 | ||||||
chr1:183585624
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0197 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.257+1259_257+1270d others(14): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585624 | ||||||
chr1:183585624
|
C | CAAAAAAA others(9): Show |
2 | a0001c0001t0001g0302a0001c0001t0001g0329 | 2 | HG02896.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.257+1270_257+1271i others(18): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585624 | ||||||
chr1:183585624
|
C | CAAAAAAA others(10): Show |
14 | a0001c0001t0001g0308a0001c0001t0001g0310a0001c0001t0001g0311others(11): Show | 14 | HG01074.hp1 HG01099.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.257+1270_257+1271i others(19): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585624 | ||||||
chr1:183585624
|
C | CAAAAAAA others(11): Show |
9 | a0001c0001t0001g0026a0001c0001t0001g0257a0001c0001t0001g0258others(6): Show | 10 | HG01433.hp1 HG01884.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.257+1270_257+1271i others(20): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585624 | ||||||
chr1:183585624
|
C | CAAAAAAA others(12): Show |
1 | a0001c0001t0001g0320 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.257+1270_257+1271i others(21): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585624 | ||||||
chr1:183585624
|
C | CAAAAAAA others(14): Show |
5 | a0001c0001t0001g0009a0001c0001t0001g0324a0001c0001t0001g0325others(2): Show | 7 | HG02647.hp2 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.257+1270_257+1271i others(23): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585624 | ||||||
chr1:183585624
|
C | CAAAAAAA others(15): Show |
1 | a0001c0001t0001g0328 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.257+1270_257+1271i others(24): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585624 | ||||||
chr1:183585624
|
C | CAAAAAAA others(17): Show |
2 | a0001c0010t0001g0052a0002c0002t0001g0054 | 2 | HG03471.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.257+1270_257+1271i others(26): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585624 | ||||||
chr1:183585624
|
C | CAAAAAAA others(18): Show |
2 | a0001c0001t0001g0251a0001c0001t0003g0250 | 2 | HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.257+1270_257+1271i others(27): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585624 | ||||||
chr1:183585624
|
C | CAAAAAAA others(21): Show |
5 | a0005c0005t0004g0029a0005c0005t0004g0030a0005c0005t0004g0031others(2): Show | 5 | HG02809.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.257+1270_257+1271i others(30): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585624 | ||||||
chr1:183585624
|
C | CAAAAAAA others(22): Show |
1 | a0005c0005t0004g0034 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.257+1270_257+1271i others(31): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585624 | ||||||
chr1:183585642
|
T | C | 1 | a0001c0001t0001g0257 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.257+1253A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585642 | ||||||
chr1:183585699
|
T | C | 1 | a0002c0002t0001g0198 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.257+1196A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585699 | ||||||
chr1:183586032
|
C | G | 1 | a0001c0001t0001g0258 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.257+863G>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586032 | ||||||
chr1:183586035
|
T | C | 1 | a0001c0001t0001g0258 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.257+860A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586035 | ||||||
chr1:183586035
|
T | G | 10 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0322others(7): Show | 13 | HG01099.hp2 HG02109.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.257+860A>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586035 | ||||||
chr1:183586060
|
C | A | 1 | a0002c0007t0002g0247 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.257+835G>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586060 | ||||||
chr1:183586063
|
G | A | 1 | a0002c0002t0001g0358 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.257+832C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586063 | ||||||
chr1:183586094
|
G | T | 31 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0302others(28): Show | 34 | HG01074.hp1 HG01099.hp2 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.257+801C>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586094 | ||||||
chr1:183586211
|
G | A | 1 | a0001c0001t0002g0294 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.257+684C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586211 | ||||||
chr1:183586226
|
C | T | 1 | a0002c0007t0002g0063 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.257+669G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586226 | ||||||
chr1:183586227
|
G | A | 4 | a0001c0001t0001g0254a0001c0001t0001g0259a0001c0001t0001g0260others(1): Show | 4 | HG02145.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.257+668C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586227 | ||||||
chr1:183586235
|
A | G | 94 | a0001c0001t0001g0028a0001c0001t0001g0039a0001c0001t0001g0041others(91): Show | 104 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.257+660T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586235 | ||||||
chr1:183586238
|
C | G | 94 | a0001c0001t0001g0028a0001c0001t0001g0039a0001c0001t0001g0041others(91): Show | 104 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.257+657G>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586238 | ||||||
chr1:183586271
|
C | T | 356 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0020others(353): Show | 398 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(395): Show |
intron_variant | MODIFIER | c.257+624G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586271 | ||||||
chr1:183586319
|
A | C | 44 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0042others(41): Show | 49 | HG00323.hp2 HG00558.hp2 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.257+576T>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586319 | ||||||
chr1:183586379
|
T | C | 6 | a0005c0005t0004g0029a0005c0005t0004g0030a0005c0005t0004g0031others(3): Show | 6 | HG02809.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.257+516A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586379 | ||||||
chr1:183586411
|
A | G | 1 | a0002c0002t0001g0252 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.257+484T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586411 | ||||||
chr1:183586504
|
A | G | 3 | a0001c0001t0002g0269a0001c0001t0002g0270a0001c0001t0002g0288 | 3 | HG01515.hp1 HG01517.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.257+391T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586504 | ||||||
chr1:183586575
|
C | T | 1 | a0002c0002t0001g0062 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.257+320G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586575 | ||||||
chr1:183586622
|
T | C | 356 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0020others(353): Show | 398 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(395): Show |
intron_variant | MODIFIER | c.257+273A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586622 | ||||||
chr1:183586644
|
C | T | 94 | a0001c0001t0001g0028a0001c0001t0001g0039a0001c0001t0001g0041others(91): Show | 104 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.257+251G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586644 | ||||||
chr1:183586744
|
G | A | 31 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0302others(28): Show | 34 | HG01074.hp1 HG01099.hp2 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.257+151C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586744 | ||||||
chr1:183586828
|
C | T | 6 | a0001c0001t0001g0297a0001c0001t0001g0299a0001c0001t0005g0025others(3): Show | 7 | HG02015.hp1 HG02056.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.257+67G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586828 | ||||||
chr1:183586990
|
G | A | 1 | a0002c0002t0001g0054 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.175-13C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183586990 | ||||||
chr1:183587075
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.175-98T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587075 | ||||||
chr1:183587126
|
C | T | 2 | a0001c0001t0001g0257a0001c0001t0001g0258 | 2 | HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.175-149G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587126 | ||||||
chr1:183587156
|
A | G | 137 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0028others(134): Show | 150 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(147): Show |
intron_variant | MODIFIER | c.175-179T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587156 | ||||||
chr1:183587186
|
C | T | 2 | a0001c0001t0001g0308a0002c0002t0001g0309 | 2 | HG01192.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.175-209G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587186 | ||||||
chr1:183587260
|
T | C | 44 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0042others(41): Show | 49 | HG00323.hp2 HG00558.hp2 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.175-283A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587260 | ||||||
chr1:183587261
|
G | A | 2 | a0001c0001t0002g0286a0002c0002t0001g0287 | 2 | HG03669.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.175-284C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587261 | ||||||
chr1:183587295
|
C | T | 1 | a0002c0002t0001g0053 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.175-318G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587295 | ||||||
chr1:183587485
|
T | C | 94 | a0001c0001t0001g0028a0001c0001t0001g0039a0001c0001t0001g0041others(91): Show | 104 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.175-508A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587485 | ||||||
chr1:183587509
|
G | C | 2 | a0001c0001t0001g0359a0001c0001t0001g0360 | 2 | HG01168.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.175-532C>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587509 | ||||||
chr1:183587524
|
G | A | 1 | a0001c0001t0001g0199 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.175-547C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587524 | ||||||
chr1:183587536
|
G | A | 6 | a0001c0001t0001g0297a0001c0001t0001g0299a0001c0001t0005g0025others(3): Show | 7 | HG02015.hp1 HG02056.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.175-559C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587536 | ||||||
chr1:183587595
|
C | CAAA | 24 | a0001c0001t0001g0045a0001c0001t0001g0271a0001c0001t0001g0280others(21): Show | 25 | HG00558.hp2 HG00738.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.175-621_175-619dup others(3): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587595 | ||||||
chr1:183587595
|
C | CAAAA | 14 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0042others(11): Show | 16 | HG01175.hp1 HG01175.hp2 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.175-622_175-619dup others(4): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587595 | ||||||
chr1:183587595
|
C | CAAAAAAA others(4): Show |
1 | a0006c0006t0001g0295 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.175-629_175-619dup others(11): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587595 | ||||||
chr1:183587595
|
CA | C | 161 | a0001c0001t0001g0020a0001c0001t0001g0035a0001c0001t0001g0064others(158): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.175-619delT | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587595 | ||||||
chr1:183587595
|
CAA | C | 37 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0026others(34): Show | 41 | HG01256.hp1 HG01891.hp2 HG02109.hp1 others(38): Show |
intron_variant | MODIFIER | c.175-620_175-619del others(2): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587595 | ||||||
chr1:183587595
|
CAAA | C | 18 | a0001c0001t0001g0302a0001c0001t0001g0308a0001c0001t0001g0310others(15): Show | 18 | HG01074.hp1 HG01099.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.175-621_175-619del others(3): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587595 | ||||||
chr1:183587595
|
CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0001g0361a0001c0001t0001g0362 | 2 | HG02717.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.175-628_175-619del others(10): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587595 | ||||||
chr1:183587595
|
CAAAAAAA others(4): Show |
C | 38 | a0001c0001t0001g0028a0001c0001t0001g0334a0001c0001t0001g0335others(35): Show | 42 | HG00323.hp1 HG00609.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.175-629_175-619del others(11): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587595 | ||||||
chr1:183587595
|
CAAAAAAA others(7): Show |
C | 1 | a0002c0002t0001g0053 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.175-632_175-619del others(14): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587595 | ||||||
chr1:183587635
|
A | G | 1 | a0001c0001t0002g0262 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.175-658T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587635 | ||||||
chr1:183587661
|
G | C | 2 | a0001c0001t0001g0026a0001c0001t0001g0329 | 3 | HG02717.hp1 HG02896.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.175-684C>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587661 | ||||||
chr1:183587772
|
C | T | 1 | a0001c0010t0001g0052 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.175-795G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587772 | ||||||
chr1:183587773
|
G | A | 1 | a0001c0001t0001g0363 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.175-796C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587773 | ||||||
chr1:183587821
|
T | C | 2 | a0002c0002t0001g0248a0002c0002t0001g0249 | 2 | HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.175-844A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587821 | ||||||
chr1:183588184
|
A | G | 4 | a0001c0001t0001g0254a0001c0001t0001g0259a0001c0001t0001g0260others(1): Show | 4 | HG02145.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.175-1207T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183588184 | ||||||
chr1:183588206
|
A | T | 6 | a0001c0001t0001g0320a0001c0001t0003g0306a0002c0002t0001g0303others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.175-1229T>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183588206 | ||||||
chr1:183588224
|
C | G | 1 | a0002c0002t0001g0051 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.175-1247G>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183588224 | ||||||
chr1:183588420
|
A | C | 1 | a0002c0002t0001g0050 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.175-1443T>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183588420 | ||||||
chr1:183588427
|
A | C | 1 | a0001c0001t0001g0302 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.175-1450T>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183588427 | ||||||
chr1:183588458
|
G | A | 2 | a0001c0001t0001g0257a0001c0001t0001g0258 | 2 | HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.175-1481C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183588458 | ||||||
chr1:183588474
|
C | CA | 88 | a0001c0001t0001g0028a0001c0001t0001g0039a0001c0001t0001g0041others(85): Show | 97 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.175-1498dupT | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183588474 | ||||||
chr1:183588611
|
TA | T | 4 | a0001c0001t0001g0011a0001c0001t0001g0047a0001c0001t0001g0048others(1): Show | 5 | HG02145.hp1 HG02970.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.174+1544delT | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183588611 | ||||||
chr1:183588650
|
T | C | 1 | a0001c0001t0001g0364 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.174+1506A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183588650 | ||||||
chr1:183588664
|
T | C | 6 | a0001c0001t0001g0297a0001c0001t0001g0299a0001c0001t0005g0025others(3): Show | 7 | HG02015.hp1 HG02056.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.174+1492A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183588664 | ||||||
chr1:183588808
|
C | T | 1 | a0003c0003t0001g0046 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.174+1348G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183588808 | ||||||
chr1:183589032
|
A | T | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG01109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.174+1124T>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183589032 | ||||||
chr1:183589039
|
T | C | 76 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0028others(73): Show | 84 | HG00323.hp1 HG00609.hp2 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.174+1117A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183589039 | ||||||
chr1:183589141
|
G | A | 1 | a0002c0002t0001g0252 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.174+1015C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183589141 | ||||||
chr1:183589143
|
C | T | 30 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0302others(27): Show | 33 | HG01074.hp1 HG01099.hp2 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.174+1013G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183589143 | ||||||
chr1:183589212
|
T | C | 1 | a0002c0002t0001g0253 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.174+944A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183589212 | ||||||
chr1:183589222
|
A | G | 76 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0028others(73): Show | 84 | HG00323.hp1 HG00609.hp2 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.174+934T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183589222 | ||||||
chr1:183589288
|
G | A | 76 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0028others(73): Show | 84 | HG00323.hp1 HG00609.hp2 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.174+868C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183589288 | ||||||
chr1:183589302
|
G | A | 127 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0028others(124): Show | 140 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.174+854C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183589302 | ||||||
chr1:183589303
|
A | G | 76 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0028others(73): Show | 84 | HG00323.hp1 HG00609.hp2 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.174+853T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183589303 | ||||||
chr1:183589646
|
TAA | T | 8 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0042others(5): Show | 12 | HG02523.hp2 NA18945.hp2 NA18951.hp1 others(9): Show |
intron_variant | MODIFIER | c.174+508_174+509del others(2): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183589646 | ||||||
chr1:183589668
|
G | T | 30 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0302others(27): Show | 33 | HG01074.hp1 HG01099.hp2 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.174+488C>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183589668 | ||||||
chr1:183589748
|
CATGAAAG others(13): Show |
C | 20 | a0001c0001t0001g0302a0001c0001t0001g0308a0001c0001t0001g0310others(17): Show | 20 | HG01074.hp1 HG01192.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.174+388_174+407del others(20): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183589748 | ||||||
chr1:183589806
|
G | A | 30 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0302others(27): Show | 33 | HG01074.hp1 HG01099.hp2 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.174+350C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183589806 | ||||||
chr1:183589861
|
G | A | 38 | a0001c0001t0001g0028a0001c0001t0001g0334a0001c0001t0001g0335others(35): Show | 42 | HG00323.hp1 HG00609.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.174+295C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183589861 | ||||||
chr1:183589970
|
G | A | 75 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0028others(72): Show | 83 | HG00323.hp1 HG00609.hp2 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.174+186C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183589970 | ||||||
chr1:183590148
|
C | G | 2 | a0001c0001t0001g0035a0002c0002t0001g0036 | 2 | HG02976.hp1 NA18906.hp1 |
splice_region_variant&intron_variant | LOW | c.174+8G>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183590148 |