geneid | 653361 |
---|---|
ensemblid | ENSG00000158517.16 |
hgncid | 7660 |
symbol | NCF1 |
name | neutrophil cytosolic factor 1 |
refseq_nuc | NM_000265.7 |
refseq_prot | NP_000256.4 |
ensembl_nuc | ENST00000289473.11 |
ensembl_prot | ENSP00000289473.4 |
mane_status | MANE Select |
chr | chr7 |
start | 74774011 |
end | 74789315 |
strand | + |
ver | v1.2 |
region | chr7:74774011-74789315 |
region5000 | chr7:74769011-74794315 |
regionname0 | NCF1_chr7_74774011_74789315 |
regionname5000 | NCF1_chr7_74769011_74794315 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 390 | 203 | 45 | 39 | 79 | 10 | 28 | 52 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0002 | 0/0 | 390 | 65 | 29 | 17 | 16 | 0 | 3 | 12 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0003 | 0/0 | 390 | 32 | 1 | 0 | 28 | 2 | 1 | 24 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0004 | 0/0 | 390 | 13 | 3 | 3 | 7 | 0 | 0 | 7 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0005 | 0/0 | 390 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0006 | 0/0 | 390 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0007 | 0/0 | 390 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0008 | 0/0 | 390 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0009 | 0/0 | 390 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0010 | 0/0 | 390 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0011 | 0/0 | 390 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0012 | 0/0 | 390 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1173 | 158 | 27 | 31 | 64 | 7 | 27 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
c0002 | 0/0 | 1173 | 44 | 12 | 14 | 16 | 0 | 2 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
c0003 | 0/0 | 1173 | 40 | 17 | 7 | 12 | 3 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
c0004 | 0/0 | 1173 | 32 | 1 | 0 | 28 | 2 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
c0005 | 0/0 | 1173 | 21 | 17 | 3 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
c0006 | 0/0 | 1173 | 12 | 3 | 2 | 7 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
c0007 | 0/0 | 1173 | 3 | 0 | 0 | 3 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
c0008 | 0/0 | 1173 | 3 | 0 | 0 | 3 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
c0009 | 0/0 | 1173 | 3 | 3 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
c0010 | 0/0 | 1173 | 2 | 2 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
c0011 | 0/0 | 1173 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
c0012 | 0/0 | 1173 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
c0013 | 0/0 | 1173 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
c0014 | 0/0 | 1173 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
c0015 | 0/0 | 1173 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
c0016 | 0/0 | 1173 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
c0017 | 0/0 | 1173 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
c0018 | 0/0 | 1173 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
c0019 | 0/0 | 1173 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
c0020 | 0/0 | 1173 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
c0021 | 0/0 | 1173 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
c0022 | 0/0 | 1173 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 80 | 9 | 14 | 45 | 5 | 7 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0002 | 0/0 | 14 | 12 | 2 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0003 | 0/0 | 11 | 0 | 8 | 3 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0004 | 0/0 | 10 | 0 | 0 | 7 | 2 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0005 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0007 | 0/0 | 7 | 0 | 4 | 0 | 2 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0008 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0009 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0014 | 0/0 | 4 | 1 | 1 | 0 | 0 | 2 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0015 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0017 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0019 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0035 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0136 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1173 | 158 | 27 | 31 | 64 | 7 | 27 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0001c0003 | 0/0 | 1173 | 40 | 17 | 7 | 12 | 3 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0001c0013 | 0/0 | 1173 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0001c0014 | 0/0 | 1173 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0001c0015 | 0/0 | 1173 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0001c0016 | 0/0 | 1173 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0001c0017 | 0/0 | 1173 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0002c0002 | 0/0 | 1173 | 44 | 12 | 14 | 16 | 0 | 2 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0002c0005 | 0/0 | 1173 | 21 | 17 | 3 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0003c0004 | 0/0 | 1173 | 32 | 1 | 0 | 28 | 2 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0004c0006 | 0/0 | 1173 | 12 | 3 | 2 | 7 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0004c0012 | 0/0 | 1173 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0005c0009 | 0/0 | 1173 | 3 | 3 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0006c0010 | 0/0 | 1173 | 2 | 2 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0006c0019 | 0/0 | 1173 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0007c0008 | 0/0 | 1173 | 3 | 0 | 0 | 3 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0008c0007 | 0/0 | 1173 | 3 | 0 | 0 | 3 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0009c0021 | 0/0 | 1173 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0009c0022 | 0/0 | 1173 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0010c0020 | 0/0 | 1173 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0011c0018 | 0/0 | 1173 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0012c0011 | 0/0 | 1173 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1349 | 136 | 24 | 22 | 63 | 6 | 21 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0001c0001t0002 | 1/1 | 1349 | 22 | 3 | 9 | 1 | 1 | 6 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0001c0003t0001 | 0/0 | 1349 | 40 | 17 | 7 | 12 | 3 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0001c0013t0001 | 0/0 | 1349 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0001c0014t0001 | 0/0 | 1349 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0001c0015t0001 | 0/0 | 1349 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0001c0016t0001 | 0/0 | 1349 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0001c0017t0001 | 0/0 | 1349 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0002c0002t0001 | 0/0 | 1349 | 30 | 7 | 10 | 12 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0002c0002t0002 | 0/0 | 1349 | 14 | 5 | 4 | 4 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0002c0005t0001 | 0/0 | 1349 | 21 | 17 | 3 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0003c0004t0001 | 0/0 | 1349 | 32 | 1 | 0 | 28 | 2 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0004c0006t0001 | 0/0 | 1349 | 11 | 3 | 2 | 6 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0004c0006t0002 | 0/0 | 1349 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0004c0012t0001 | 0/0 | 1349 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0005c0009t0001 | 0/0 | 1349 | 3 | 3 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0006c0010t0001 | 0/0 | 1349 | 2 | 2 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0006c0019t0001 | 0/0 | 1349 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0007c0008t0001 | 0/0 | 1349 | 3 | 0 | 0 | 3 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0008c0007t0001 | 0/0 | 1349 | 3 | 0 | 0 | 3 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0009c0021t0001 | 0/0 | 1349 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0009c0022t0001 | 0/0 | 1349 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0010c0020t0001 | 0/0 | 1349 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0011c0018t0001 | 0/0 | 1349 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
a0012c0011t0001 | 0/0 | 1349 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | copy fasta | chr7 | 74769011 | 74794315 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 54 | 5 | 8 | 30 | 5 | 6 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0003 | 0/0 | 8 | 0 | 6 | 2 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0002g0014 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0002g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0002g0035 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0002g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0002g0136 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0003t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0003t0001g0002 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0003t0001g0007 | 0/0 | 7 | 0 | 4 | 0 | 2 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0003t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0003t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0003t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0003t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0003t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0003t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0003t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0003t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0003t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0003t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0003t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0003t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0013t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0014t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0015t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0016t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0001c0017t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0002c0002t0001g0001 | 0/0 | 10 | 1 | 5 | 3 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0002c0002t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0002c0002t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0002c0002t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0002c0002t0001g0009 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0002c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0002c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0002c0002t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0002c0002t0002g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0002c0002t0002g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0002c0002t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0002c0002t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0002c0002t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0002c0002t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0002c0002t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0002c0002t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0002c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0002c0005t0001g0002 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0002c0005t0001g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0002c0005t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0002c0005t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0002c0005t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0002c0005t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0002c0005t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0002c0005t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0002c0005t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0002c0005t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0002c0005t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0002c0005t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0002c0005t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0002c0005t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0003c0004t0001g0001 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0003c0004t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0003c0004t0001g0004 | 0/0 | 10 | 0 | 0 | 7 | 2 | 1 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0003c0004t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0003c0004t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0003c0004t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0003c0004t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0003c0004t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0003c0004t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0003c0004t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0003c0004t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0003c0004t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0003c0004t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0003c0004t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0004c0006t0001g0001 | 0/0 | 4 | 2 | 0 | 2 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0004c0006t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0004c0006t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0004c0006t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0004c0006t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0004c0006t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0004c0006t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0004c0006t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0004c0006t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0004c0012t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0005c0009t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0005c0009t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0006c0010t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0006c0010t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0006c0019t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0007c0008t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0008c0007t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0009c0021t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0009c0022t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0010c0020t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0011c0018t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
a0012c0011t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0003 | t0001 | g0007 | EUR | GBR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG00280 | hp2 | a0003 | c0004 | t0001 | g0004 | EUR | FIN | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG00323 | hp2 | a0003 | c0004 | t0001 | g0004 | EUR | FIN | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG00408 | hp1 | a0003 | c0004 | t0001 | g0054 | EAS | CHS | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG00408 | hp2 | a0003 | c0004 | t0001 | g0004 | EAS | CHS | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG00423 | hp2 | a0003 | c0004 | t0001 | g0004 | EAS | CHS | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG00438 | hp2 | a0003 | c0004 | t0001 | g0023 | EAS | CHS | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG00544 | hp1 | a0001 | c0003 | t0001 | g0109 | EAS | CHS | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG00597 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG00639 | hp1 | a0001 | c0003 | t0001 | g0122 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG00673 | hp1 | a0008 | c0007 | t0001 | g0012 | EAS | CHS | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG00673 | hp2 | a0001 | c0003 | t0001 | g0031 | EAS | CHS | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG00733 | hp2 | a0002 | c0005 | t0001 | g0022 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG00735 | hp1 | a0001 | c0003 | t0001 | g0007 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01070 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01070 | hp2 | a0002 | c0002 | t0002 | g0116 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01071 | hp2 | a0002 | c0002 | t0002 | g0032 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01074 | hp2 | a0002 | c0002 | t0001 | g0009 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0141 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01109 | hp2 | a0001 | c0003 | t0001 | g0002 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01167 | hp1 | a0002 | c0002 | t0001 | g0078 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01167 | hp2 | a0001 | c0003 | t0001 | g0007 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01169 | hp2 | a0001 | c0003 | t0001 | g0007 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01192 | hp2 | a0009 | c0021 | t0001 | g0021 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01243 | hp1 | a0002 | c0005 | t0001 | g0002 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01243 | hp2 | a0002 | c0002 | t0001 | g0009 | AMR | PUR | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01255 | hp1 | a0002 | c0002 | t0002 | g0032 | AMR | CLM | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0134 | AMR | CLM | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01258 | hp1 | a0001 | c0003 | t0001 | g0029 | AMR | CLM | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | CLM | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01346 | hp1 | a0001 | c0014 | t0001 | g0001 | AMR | CLM | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | CLM | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01433 | hp2 | a0002 | c0005 | t0001 | g0127 | AMR | CLM | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | CLM | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0035 | EUR | IBS | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0085 | EUR | IBS | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01884 | hp1 | a0001 | c0003 | t0001 | g0002 | AFR | ACB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01884 | hp2 | a0002 | c0005 | t0001 | g0097 | AFR | ACB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01891 | hp1 | a0006 | c0019 | t0001 | g0021 | AFR | ACB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01934 | hp1 | a0002 | c0002 | t0002 | g0019 | AMR | PEL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01934 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0147 | AMR | PEL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01978 | hp2 | a0001 | c0003 | t0001 | g0007 | AMR | PEL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | PEL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02004 | hp1 | a0004 | c0006 | t0001 | g0062 | AMR | PEL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02004 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0056 | EAS | KHV | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02055 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | ACB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02055 | hp2 | a0001 | c0003 | t0001 | g0033 | AFR | ACB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02056 | hp2 | a0001 | c0003 | t0001 | g0110 | EAS | KHV | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02071 | hp1 | a0001 | c0013 | t0001 | g0073 | EAS | KHV | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02071 | hp2 | a0002 | c0002 | t0002 | g0037 | EAS | KHV | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02083 | hp1 | a0002 | c0002 | t0001 | g0071 | EAS | KHV | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02132 | hp2 | a0007 | c0008 | t0001 | g0016 | EAS | KHV | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02145 | hp1 | a0002 | c0002 | t0001 | g0042 | AFR | ACB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02145 | hp2 | a0002 | c0002 | t0001 | g0104 | AFR | ACB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02165 | hp1 | a0012 | c0011 | t0001 | g0012 | EAS | CDX | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02257 | hp1 | a0002 | c0005 | t0001 | g0124 | AFR | ACB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02257 | hp2 | a0001 | c0003 | t0001 | g0098 | AFR | ACB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02258 | hp2 | a0002 | c0005 | t0001 | g0002 | AFR | ACB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02280 | hp1 | a0002 | c0005 | t0001 | g0033 | AFR | ACB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02293 | hp1 | a0004 | c0006 | t0001 | g0081 | AMR | PEL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02300 | hp2 | a0004 | c0012 | t0001 | g0049 | AMR | PEL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02451 | hp1 | a0001 | c0003 | t0001 | g0018 | AFR | ACB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02451 | hp2 | a0002 | c0005 | t0001 | g0011 | AFR | ACB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02572 | hp2 | a0010 | c0020 | t0001 | g0002 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02615 | hp2 | a0002 | c0005 | t0001 | g0008 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02622 | hp1 | a0002 | c0005 | t0001 | g0008 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02622 | hp2 | a0005 | c0009 | t0001 | g0117 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02630 | hp1 | a0004 | c0006 | t0001 | g0001 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02630 | hp2 | a0001 | c0003 | t0001 | g0119 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02698 | hp1 | a0002 | c0002 | t0002 | g0115 | SAS | PJL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02809 | hp1 | a0001 | c0003 | t0001 | g0018 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02818 | hp2 | a0006 | c0010 | t0001 | g0046 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02886 | hp1 | a0002 | c0005 | t0001 | g0008 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02895 | hp1 | a0005 | c0009 | t0001 | g0038 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02896 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02897 | hp2 | a0005 | c0009 | t0001 | g0038 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02922 | hp2 | a0003 | c0004 | t0001 | g0121 | AFR | ESN | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02965 | hp1 | a0002 | c0002 | t0002 | g0130 | AFR | ESN | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02970 | hp2 | a0001 | c0003 | t0001 | g0011 | AFR | ESN | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0135 | SAS | PJL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG03041 | hp2 | a0002 | c0005 | t0001 | g0008 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG03098 | hp1 | a0001 | c0017 | t0001 | g0002 | AFR | MSL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG03130 | hp1 | a0002 | c0005 | t0001 | g0002 | AFR | ESN | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG03139 | hp1 | a0002 | c0002 | t0002 | g0129 | AFR | ESN | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG03139 | hp2 | a0001 | c0003 | t0001 | g0002 | AFR | ESN | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG03195 | hp1 | a0001 | c0003 | t0001 | g0011 | AFR | ESN | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG03195 | hp2 | a0002 | c0005 | t0001 | g0123 | AFR | ESN | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG03209 | hp2 | a0002 | c0005 | t0001 | g0008 | AFR | MSL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG03225 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | MSL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG03225 | hp2 | a0006 | c0010 | t0001 | g0090 | AFR | MSL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG03453 | hp1 | a0001 | c0003 | t0001 | g0087 | AFR | MSL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG03453 | hp2 | a0002 | c0005 | t0001 | g0125 | AFR | MSL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG03486 | hp1 | a0001 | c0003 | t0001 | g0001 | AFR | MSL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0146 | SAS | PJL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG03540 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG03579 | hp1 | a0002 | c0005 | t0001 | g0126 | AFR | MSL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG03579 | hp2 | a0001 | c0003 | t0001 | g0002 | AFR | MSL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | STU | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG03704 | hp1 | a0001 | c0003 | t0001 | g0007 | SAS | PJL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG03704 | hp2 | a0003 | c0004 | t0001 | g0004 | SAS | PJL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | BEB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | BEB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0145 | SAS | BEB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | STU | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | STU | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | STU | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG04199 | hp2 | a0002 | c0005 | t0001 | g0075 | SAS | STU | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | STU | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0092 | SAS | STU | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | STU | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | STU | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18522 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | YRI | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | YRI | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | CHB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18939 | hp2 | a0002 | c0002 | t0002 | g0142 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18944 | hp1 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18945 | hp1 | a0003 | c0004 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18948 | hp2 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18949 | hp2 | a0004 | c0006 | t0002 | g0140 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18959 | hp2 | a0004 | c0006 | t0001 | g0030 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18960 | hp2 | a0011 | c0018 | t0001 | g0111 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18962 | hp2 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18964 | hp1 | a0001 | c0016 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18966 | hp1 | a0003 | c0004 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18966 | hp2 | a0003 | c0004 | t0001 | g0096 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18968 | hp2 | a0004 | c0006 | t0001 | g0138 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18970 | hp2 | a0003 | c0004 | t0001 | g0086 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18971 | hp1 | a0003 | c0004 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18973 | hp1 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18973 | hp2 | a0001 | c0003 | t0001 | g0112 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18974 | hp1 | a0003 | c0004 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18974 | hp2 | a0003 | c0004 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18979 | hp1 | a0002 | c0002 | t0002 | g0037 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18981 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18983 | hp1 | a0004 | c0006 | t0001 | g0059 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18984 | hp2 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18989 | hp1 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18993 | hp1 | a0003 | c0004 | t0001 | g0053 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18993 | hp2 | a0004 | c0006 | t0001 | g0101 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18995 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18995 | hp2 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18998 | hp1 | a0007 | c0008 | t0001 | g0016 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19001 | hp1 | a0004 | c0006 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19001 | hp2 | a0008 | c0007 | t0001 | g0012 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19002 | hp1 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19003 | hp1 | a0003 | c0004 | t0001 | g0005 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19004 | hp1 | a0003 | c0004 | t0001 | g0079 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19004 | hp2 | a0001 | c0003 | t0001 | g0108 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19007 | hp2 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19009 | hp1 | a0003 | c0004 | t0001 | g0050 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19009 | hp2 | a0001 | c0015 | t0001 | g0005 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19012 | hp2 | a0001 | c0003 | t0001 | g0031 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19030 | hp1 | a0002 | c0005 | t0001 | g0040 | AFR | LWK | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19030 | hp2 | a0002 | c0005 | t0001 | g0002 | AFR | LWK | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19043 | hp1 | a0002 | c0002 | t0002 | g0118 | AFR | LWK | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19043 | hp2 | a0002 | c0005 | t0001 | g0128 | AFR | LWK | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19054 | hp1 | a0003 | c0004 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19056 | hp1 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19057 | hp1 | a0008 | c0007 | t0001 | g0012 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19058 | hp1 | a0003 | c0004 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19058 | hp2 | a0007 | c0008 | t0001 | g0016 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19060 | hp1 | a0004 | c0006 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19060 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19062 | hp1 | a0003 | c0004 | t0001 | g0052 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19064 | hp1 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19065 | hp1 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19065 | hp2 | a0003 | c0004 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19066 | hp1 | a0001 | c0003 | t0001 | g0106 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19082 | hp2 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19085 | hp2 | a0003 | c0004 | t0001 | g0023 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19088 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19088 | hp2 | a0003 | c0004 | t0001 | g0051 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19090 | hp2 | a0001 | c0003 | t0001 | g0107 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19240 | hp1 | a0001 | c0003 | t0001 | g0002 | AFR | YRI | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA19240 | hp2 | a0009 | c0022 | t0001 | g0008 | AFR | YRI | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA20129 | hp1 | a0001 | c0003 | t0001 | g0018 | AFR | ASW | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA20129 | hp2 | a0001 | c0003 | t0001 | g0105 | AFR | ASW | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA20752 | hp2 | a0001 | c0003 | t0001 | g0113 | EUR | TSI | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA20805 | hp2 | a0001 | c0003 | t0001 | g0007 | EUR | TSI | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | CLM | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02486 | hp1 | a0001 | c0003 | t0001 | g0002 | AFR | ACB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | ACB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | ACB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG03471 | hp1 | a0002 | c0002 | t0002 | g0014 | AFR | MSL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG06807 | hp1 | a0004 | c0006 | t0001 | g0074 | AFR | USA | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18955 | hp1 | a0003 | c0004 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | USA | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA20300 | hp2 | a0004 | c0006 | t0001 | g0001 | AFR | USA | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA21309 | hp1 | a0001 | c0003 | t0001 | g0114 | AFR | LWK | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
NA21309 | hp2 | a0002 | c0002 | t0002 | g0132 | AFR | LWK | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0035 | REF | REF | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0136 | REF | REF | NCF1_chr7_74769011_74794315 | NCF1 | chr7 | 74769011 | 74794315 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:74779138
|
G | C | 2 | a0008a0012 | 4 | HG00673.hp1 HG02165.hp1 NA19001.hp2 others(1): Show |
missense_variant | MODERATE | c.210G>C | p.Arg70Ser | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 3/11 | 231/1349 | 210/1173 | 70/390 | chr7 | 74779138 | ||
chr7:74779296
|
G | A | 2 | a0003a0004 | 45 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(42): Show |
missense_variant | MODERATE | c.269G>A | p.Arg90His | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 4/11 | 290/1349 | 269/1173 | 90/390 | chr7 | 74779296 | ||
chr7:74779322
|
A | G | 5 | a0002a0003a0005others(2): Show | 103 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(100): Show |
missense_variant | MODERATE | c.295A>G | p.Ser99Gly | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 4/11 | 316/1349 | 295/1173 | 99/390 | chr7 | 74779322 | ||
chr7:74779326
|
C | T | 1 | a0010 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.299C>T | p.Thr100Met | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 4/11 | 320/1349 | 299/1173 | 100/390 | chr7 | 74779326 | ||
chr7:74782983
|
A | G | 3 | a0005a0006a0009 | 8 | HG01192.hp2 HG01891.hp1 HG02622.hp2 others(5): Show |
missense_variant | MODERATE | c.496A>G | p.Asn166Asp | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 6/11 | 517/1349 | 496/1173 | 166/390 | chr7 | 74782983 | ||
chr7:74788576
|
C | T | 1 | a0007 | 3 | HG02132.hp2 NA18998.hp1 NA19058.hp2 |
missense_variant | MODERATE | c.923C>T | p.Ala308Val | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 10/11 | 944/1349 | 923/1173 | 308/390 | chr7 | 74788576 | ||
chr7:74788604
|
G | C | 1 | a0005 | 3 | HG02622.hp2 HG02895.hp1 HG02897.hp2 |
missense_variant | MODERATE | c.951G>C | p.Lys317Asn | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 10/11 | 972/1349 | 951/1173 | 317/390 | chr7 | 74788604 | ||
chr7:74789048
|
G | T | 1 | a0011 | 1 | NA18960.hp2 | missense_variant | MODERATE | c.1061G>T | p.Arg354Leu | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 11/11 | 1082/1349 | 1061/1173 | 354/390 | chr7 | 74789048 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:74779372
|
C | T | 9 | a0001c0003a0001c0016a0001c0017others(6): Show | 68 | HG00140.hp1 HG00544.hp1 HG00639.hp1 others(65): Show |
synonymous_variant | LOW | c.345C>T | p.Leu115Leu | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 4/11 | 366/1349 | 345/1173 | 115/390 | chr7 | 74779372 | ||
chr7:74779414
|
G | A | 2 | a0001c0013a0001c0016 | 2 | HG02071.hp1 NA18964.hp1 |
synonymous_variant | LOW | c.387G>A | p.Thr129Thr | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 4/11 | 408/1349 | 387/1173 | 129/390 | chr7 | 74779414 | ||
chr7:74783045
|
A | G | 4 | a0001c0015a0006c0010a0006c0019others(1): Show | 5 | HG01192.hp2 HG01891.hp1 HG02818.hp2 others(2): Show |
synonymous_variant | LOW | c.558A>G | p.Val186Val | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 6/11 | 579/1349 | 558/1173 | 186/390 | chr7 | 74783045 | ||
chr7:74783571
|
G | A | 1 | a0001c0017 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.621G>A | p.Ala207Ala | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 7/11 | 642/1349 | 621/1173 | 207/390 | chr7 | 74783571 | ||
chr7:74785285
|
C | T | 1 | a0001c0014 | 1 | HG01346.hp1 | synonymous_variant | LOW | c.786C>T | p.Gly262Gly | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/11 | 807/1349 | 786/1173 | 262/390 | chr7 | 74785285 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:74789215
|
T | C | 22 | a0001c0001t0001a0001c0003t0001a0001c0013t0001others(19): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
3_prime_UTR_variant | MODIFIER | c.*55T>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 11/11 | 55 | chr7 | 74789215 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:74774463
|
C | T | 1 | a0005c0009t0001g0038 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.72+360C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74774463 | ||||||
chr7:74774752
|
T | G | 111 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(108): Show | 238 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.72+649T>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74774752 | ||||||
chr7:74774819
|
A | G | 2 | a0001c0001t0001g0103a0002c0002t0001g0104 | 2 | HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.72+716A>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74774819 | ||||||
chr7:74774884
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.72+781G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74774884 | ||||||
chr7:74774887
|
C | T | 2 | a0008c0007t0001g0012a0012c0011t0001g0012 | 4 | HG00673.hp1 HG02165.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.72+784C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74774887 | ||||||
chr7:74775097
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.72+994G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74775097 | ||||||
chr7:74775104
|
C | A | 10 | a0001c0003t0001g0007a0001c0003t0001g0013a0001c0003t0001g0031others(7): Show | 20 | HG00140.hp1 HG00544.hp1 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.72+1001C>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74775104 | ||||||
chr7:74775131
|
C | T | 3 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0147 | 3 | HG01975.hp1 HG03490.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.72+1028C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74775131 | ||||||
chr7:74775134
|
C | G | 1 | a0001c0001t0001g0102 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.72+1031C>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74775134 | ||||||
chr7:74775218
|
T | C | 2 | a0002c0002t0001g0009a0002c0005t0001g0040 | 5 | HG01074.hp2 HG01243.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.72+1115T>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74775218 | ||||||
chr7:74775318
|
C | A | 1 | a0001c0001t0001g0041 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.72+1215C>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74775318 | ||||||
chr7:74775471
|
T | C | 2 | a0001c0003t0001g0007a0001c0003t0001g0105 | 8 | HG00140.hp1 HG00735.hp1 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.72+1368T>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74775471 | ||||||
chr7:74775607
|
C | T | 3 | a0001c0001t0001g0020a0001c0001t0001g0143a0001c0001t0001g0144 | 5 | HG01891.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.72+1504C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74775607 | ||||||
chr7:74775881
|
G | A | 3 | a0001c0003t0001g0112a0001c0003t0001g0113a0001c0003t0001g0114 | 3 | NA18973.hp2 NA20752.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.73-1386G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74775881 | ||||||
chr7:74775882
|
C | T | 7 | a0001c0001t0001g0020a0001c0001t0001g0143a0001c0001t0001g0144others(4): Show | 11 | HG01346.hp2 HG01891.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.73-1385C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74775882 | ||||||
chr7:74775890
|
T | C | 5 | a0001c0001t0001g0039a0002c0002t0002g0032a0002c0002t0002g0115others(2): Show | 7 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.73-1377T>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74775890 | ||||||
chr7:74775900
|
GCAT | G | 5 | a0001c0001t0001g0039a0002c0002t0002g0032a0002c0002t0002g0115others(2): Show | 7 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.73-1366_73-1364del others(3): Show |
NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74775900 | ||||||
chr7:74775948
|
C | CT | 6 | a0001c0001t0002g0019a0002c0002t0002g0019a0002c0002t0002g0032others(3): Show | 9 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.73-1305dupT | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 74775948 | |||||
chr7:74775948
|
C | CTT | 4 | a0001c0001t0001g0020a0001c0001t0001g0143a0001c0001t0001g0144others(1): Show | 7 | HG01891.hp2 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.73-1306_73-1305dup others(2): Show |
NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 74775948 | |||||
chr7:74775948
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.73-1319C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74775948 | ||||||
chr7:74775948
|
CT | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(134): Show | 282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.73-1305delT | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 74775948 | |||||
chr7:74776003
|
A | G | 1 | a0002c0002t0001g0099 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.73-1264A>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74776003 | ||||||
chr7:74776011
|
A | G | 1 | a0001c0001t0002g0141 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.73-1256A>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74776011 | ||||||
chr7:74776039
|
C | T | 28 | a0001c0001t0001g0120a0001c0003t0001g0002a0001c0003t0001g0007others(25): Show | 52 | HG00140.hp1 HG00544.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.73-1228C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74776039 | ||||||
chr7:74776132
|
A | T | 1 | a0001c0001t0001g0102 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.73-1135A>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74776132 | ||||||
chr7:74776509
|
A | C | 145 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(142): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.73-758A>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74776509 | ||||||
chr7:74776619
|
C | T | 1 | a0003c0004t0001g0096 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.73-648C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74776619 | ||||||
chr7:74776701
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.73-566C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74776701 | ||||||
chr7:74776707
|
G | GCCCCTCC others(23): Show |
1 | a0002c0002t0001g0042 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.73-551_73-522dupGT others(28): Show |
NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 74776707 | |||||
chr7:74776711
|
C | T | 2 | a0002c0002t0002g0032a0002c0002t0002g0116 | 3 | HG01070.hp2 HG01071.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.73-556C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74776711 | ||||||
chr7:74776716
|
G | GTCCCCTC others(23): Show |
89 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(86): Show | 206 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.73-538_73-509dupTC others(28): Show |
NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 74776716 | |||||
chr7:74776716
|
G | GTCCCCTC others(53): Show |
1 | a0001c0001t0001g0094 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.73-509_73-508insTC others(58): Show |
NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 74776716 | |||||
chr7:74776716
|
G | T | 7 | a0001c0001t0002g0019a0002c0002t0002g0019a0002c0002t0002g0032others(4): Show | 10 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.73-551G>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74776716 | ||||||
chr7:74776717
|
T | C | 7 | a0001c0001t0002g0019a0002c0002t0002g0019a0002c0002t0002g0032others(4): Show | 10 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.73-550T>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74776717 | ||||||
chr7:74777114
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.73-153C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | chr7 | 74777114 | ||||||
chr7:74777361
|
T | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(140): Show | 289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.153+14T>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 2/10 | chr7 | 74777361 | ||||||
chr7:74777502
|
A | ACAGGGTC others(13): Show |
5 | a0001c0001t0002g0035a0001c0001t0002g0036a0002c0005t0001g0126others(2): Show | 7 | HG01169.hp1 HG01433.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.153+156_153+175dup others(20): Show |
NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 74777502 | |||||
chr7:74777567
|
C | T | 1 | a0002c0002t0001g0091 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.153+220C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 2/10 | chr7 | 74777567 | ||||||
chr7:74777569
|
C | G | 1 | a0001c0001t0002g0036 | 2 | HG01169.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.153+222C>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 2/10 | chr7 | 74777569 | ||||||
chr7:74777616
|
G | A | 1 | a0001c0001t0002g0036 | 2 | HG01169.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.153+269G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 2/10 | chr7 | 74777616 | ||||||
chr7:74777927
|
AAAAC | A | 2 | a0005c0009t0001g0038a0005c0009t0001g0117 | 3 | HG02622.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.153+582_153+585del others(4): Show |
NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 74777927 | |||||
chr7:74778106
|
G | A | 1 | a0002c0002t0002g0130 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.153+759G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 2/10 | chr7 | 74778106 | ||||||
chr7:74778319
|
G | A | 3 | a0001c0001t0001g0020a0001c0001t0001g0143a0001c0001t0001g0144 | 5 | HG01891.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.154-763G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 2/10 | chr7 | 74778319 | ||||||
chr7:74778377
|
C | T | 8 | a0001c0001t0001g0022a0001c0001t0001g0047a0001c0001t0001g0048others(5): Show | 9 | HG00733.hp2 HG01169.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.154-705C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 2/10 | chr7 | 74778377 | ||||||
chr7:74778595
|
G | A | 5 | a0001c0001t0001g0120a0001c0001t0002g0036a0001c0003t0001g0119others(2): Show | 6 | HG01169.hp1 HG02486.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.154-487G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 2/10 | chr7 | 74778595 | ||||||
chr7:74778644
|
C | T | 10 | a0001c0001t0001g0022a0001c0001t0001g0047a0001c0001t0001g0048others(7): Show | 11 | HG00733.hp2 HG01169.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.154-438C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 2/10 | chr7 | 74778644 | ||||||
chr7:74778736
|
A | G | 145 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(142): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.154-346A>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 2/10 | chr7 | 74778736 | ||||||
chr7:74778776
|
G | A | 10 | a0001c0001t0001g0022a0001c0001t0001g0047a0001c0001t0001g0048others(7): Show | 11 | HG00733.hp2 HG01169.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.154-306G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 2/10 | chr7 | 74778776 | ||||||
chr7:74779020
|
C | A | 37 | a0001c0003t0001g0002a0001c0003t0001g0007a0001c0003t0001g0013others(34): Show | 66 | HG00140.hp1 HG00544.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.154-62C>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 2/10 | chr7 | 74779020 | ||||||
chr7:74779221
|
C | A | 2 | a0003c0004t0001g0121a0004c0012t0001g0049 | 2 | HG02300.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.230-36C>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 3/10 | chr7 | 74779221 | ||||||
chr7:74779228
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0143 | 4 | HG01891.hp2 HG02280.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.230-29G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 3/10 | chr7 | 74779228 | ||||||
chr7:74779594
|
C | T | 2 | a0001c0001t0001g0047a0001c0001t0001g0048 | 2 | HG02738.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.395+172C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 4/10 | chr7 | 74779594 | ||||||
chr7:74779691
|
C | T | 2 | a0001c0001t0002g0137a0002c0005t0001g0125 | 2 | HG03453.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.395+269C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 4/10 | chr7 | 74779691 | ||||||
chr7:74779878
|
C | G | 1 | a0006c0010t0001g0090 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.395+456C>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 4/10 | chr7 | 74779878 | ||||||
chr7:74779935
|
C | T | 2 | a0001c0001t0001g0088a0001c0001t0001g0089 | 2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.395+513C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 4/10 | chr7 | 74779935 | ||||||
chr7:74780048
|
C | T | 17 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0047others(14): Show | 21 | HG00733.hp2 HG01074.hp2 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.395+626C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 4/10 | chr7 | 74780048 | ||||||
chr7:74780073
|
G | C | 5 | a0003c0004t0001g0004a0003c0004t0001g0050a0003c0004t0001g0051others(2): Show | 14 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(11): Show |
intron_variant | MODIFIER | c.395+651G>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 4/10 | chr7 | 74780073 | ||||||
chr7:74780103
|
G | A | 5 | a0001c0001t0001g0022a0001c0001t0001g0047a0001c0001t0001g0048others(2): Show | 5 | HG00733.hp2 HG02735.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.396-677G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 4/10 | chr7 | 74780103 | ||||||
chr7:74780132
|
C | T | 5 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0002g0036others(2): Show | 6 | HG01169.hp1 HG01975.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.396-648C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 4/10 | chr7 | 74780132 | ||||||
chr7:74780137
|
C | T | 4 | a0001c0001t0001g0029a0001c0001t0001g0085a0001c0001t0001g0102others(1): Show | 4 | HG00642.hp2 HG00735.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.396-643C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 4/10 | chr7 | 74780137 | ||||||
chr7:74780198
|
G | C | 172 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(169): Show | 327 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.396-582G>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 4/10 | chr7 | 74780198 | ||||||
chr7:74780234
|
G | A | 4 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 7 | HG02559.hp2 HG02809.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.396-546G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 4/10 | chr7 | 74780234 | ||||||
chr7:74780384
|
G | C | 2 | a0005c0009t0001g0038a0005c0009t0001g0117 | 3 | HG02622.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.396-396G>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 4/10 | chr7 | 74780384 | ||||||
chr7:74780405
|
G | C | 2 | a0002c0002t0001g0009a0002c0005t0001g0040 | 5 | HG01074.hp2 HG01243.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.396-375G>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 4/10 | chr7 | 74780405 | ||||||
chr7:74780556
|
G | T | 1 | a0001c0001t0001g0084 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.396-224G>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 4/10 | chr7 | 74780556 | ||||||
chr7:74780639
|
C | G | 3 | a0001c0001t0001g0011a0001c0003t0001g0011a0002c0005t0001g0011 | 4 | HG02451.hp2 HG02970.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.396-141C>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 4/10 | chr7 | 74780639 | ||||||
chr7:74780859
|
C | CG | 30 | a0001c0001t0001g0017a0001c0001t0001g0083a0001c0001t0001g0095others(27): Show | 57 | HG00140.hp1 HG00544.hp2 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.451+32dupG | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 74780859 | |||||
chr7:74780989
|
G | A | 1 | a0004c0006t0001g0081 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.451+154G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74780989 | ||||||
chr7:74781244
|
CA | C | 131 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(128): Show | 265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.451+430delA | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 74781244 | |||||
chr7:74781244
|
CAA | C | 13 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0044others(10): Show | 20 | HG00558.hp2 HG01167.hp1 HG01515.hp2 others(17): Show |
intron_variant | MODIFIER | c.451+429_451+430del others(2): Show |
NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 74781244 | |||||
chr7:74781342
|
A | T | 1 | a0001c0001t0001g0080 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.451+507A>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74781342 | ||||||
chr7:74781375
|
G | A | 1 | a0004c0006t0001g0081 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.451+540G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74781375 | ||||||
chr7:74781407
|
T | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(140): Show | 289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.451+572T>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74781407 | ||||||
chr7:74781422
|
C | T | 1 | a0002c0005t0001g0128 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.451+587C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74781422 | ||||||
chr7:74781492
|
C | T | 110 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(107): Show | 230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.451+657C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74781492 | ||||||
chr7:74781555
|
C | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0144 | 4 | HG01891.hp2 HG02280.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.451+720C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74781555 | ||||||
chr7:74781580
|
T | C | 2 | a0005c0009t0001g0038a0005c0009t0001g0117 | 3 | HG02622.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.451+745T>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74781580 | ||||||
chr7:74781617
|
C | T | 1 | a0002c0005t0001g0040 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.451+782C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74781617 | ||||||
chr7:74781642
|
C | T | 1 | a0001c0003t0001g0114 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.451+807C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74781642 | ||||||
chr7:74781743
|
A | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(133): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.451+908A>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74781743 | ||||||
chr7:74781745
|
CT | C | 26 | a0001c0001t0001g0120a0001c0003t0001g0002a0001c0003t0001g0007others(23): Show | 45 | HG00140.hp1 HG00544.hp1 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.451+911delT | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74781745 | ||||||
chr7:74781755
|
G | A | 102 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(99): Show | 219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.451+920G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74781755 | ||||||
chr7:74781786
|
G | C | 11 | a0001c0001t0001g0022a0001c0001t0001g0047a0001c0001t0001g0048others(8): Show | 14 | HG00733.hp2 HG01074.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.451+951G>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74781786 | ||||||
chr7:74781840
|
C | A | 8 | a0003c0004t0001g0004a0003c0004t0001g0023a0003c0004t0001g0050others(5): Show | 18 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(15): Show |
intron_variant | MODIFIER | c.451+1005C>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74781840 | ||||||
chr7:74781899
|
T | C | 153 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(150): Show | 304 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.452-1040T>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74781899 | ||||||
chr7:74781928
|
G | C | 1 | a0002c0002t0001g0082 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.452-1011G>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74781928 | ||||||
chr7:74782011
|
G | A | 2 | a0001c0001t0001g0088a0001c0001t0001g0089 | 2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.452-928G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74782011 | ||||||
chr7:74782019
|
T | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(140): Show | 289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.452-920T>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74782019 | ||||||
chr7:74782181
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.452-758G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74782181 | ||||||
chr7:74782209
|
C | T | 1 | a0002c0005t0001g0075 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.452-730C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74782209 | ||||||
chr7:74782432
|
CAA | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(135): Show | 282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.452-490_452-489del others(2): Show |
NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 74782432 | |||||
chr7:74782482
|
A | G | 150 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(147): Show | 300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.452-457A>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74782482 | ||||||
chr7:74782501
|
T | C | 1 | a0001c0003t0001g0114 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.452-438T>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74782501 | ||||||
chr7:74782613
|
A | G | 2 | a0005c0009t0001g0038a0005c0009t0001g0117 | 3 | HG02622.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.452-326A>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74782613 | ||||||
chr7:74782668
|
C | T | 2 | a0005c0009t0001g0038a0005c0009t0001g0117 | 3 | HG02622.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.452-271C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74782668 | ||||||
chr7:74782846
|
C | A | 1 | a0005c0009t0001g0038 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.452-93C>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 5/10 | chr7 | 74782846 | ||||||
chr7:74783128
|
G | A | 1 | a0002c0005t0001g0040 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.574+67G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 6/10 | chr7 | 74783128 | ||||||
chr7:74783215
|
G | C | 4 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 7 | HG02559.hp2 HG02809.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.574+154G>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 6/10 | chr7 | 74783215 | ||||||
chr7:74783255
|
A | T | 31 | a0001c0001t0001g0120a0001c0003t0001g0002a0001c0003t0001g0007others(28): Show | 56 | HG00140.hp1 HG00544.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.574+194A>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 6/10 | chr7 | 74783255 | ||||||
chr7:74783387
|
A | G | 31 | a0001c0001t0001g0120a0001c0003t0001g0002a0001c0003t0001g0007others(28): Show | 56 | HG00140.hp1 HG00544.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.575-138A>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 6/10 | chr7 | 74783387 | ||||||
chr7:74783439
|
G | C | 5 | a0001c0001t0001g0022a0001c0001t0001g0047a0001c0001t0001g0048others(2): Show | 5 | HG00733.hp2 HG02735.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.575-86G>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 6/10 | chr7 | 74783439 | ||||||
chr7:74783476
|
G | A | 1 | a0002c0002t0001g0009 | 4 | HG01074.hp2 HG01243.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.575-49G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 6/10 | chr7 | 74783476 | ||||||
chr7:74783481
|
G | A | 1 | a0002c0005t0001g0128 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.575-44G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 6/10 | chr7 | 74783481 | ||||||
chr7:74783649
|
G | A | 3 | a0001c0001t0001g0020a0001c0001t0001g0143a0001c0001t0001g0144 | 5 | HG01891.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.682+17G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 7/10 | chr7 | 74783649 | ||||||
chr7:74784054
|
T | A | 1 | a0002c0002t0001g0056 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.682+422T>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 7/10 | chr7 | 74784054 | ||||||
chr7:74784109
|
C | T | 143 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(140): Show | 289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.682+477C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 7/10 | chr7 | 74784109 | ||||||
chr7:74784210
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.682+578T>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 7/10 | chr7 | 74784210 | ||||||
chr7:74784315
|
T | C | 172 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(169): Show | 328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.682+683T>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 7/10 | chr7 | 74784315 | ||||||
chr7:74784418
|
C | CTTG | 162 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(159): Show | 313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.683-762_683-761ins others(3): Show |
NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr7 | 74784418 | |||||
chr7:74784418
|
C | CTTGT | 8 | a0001c0001t0001g0083a0001c0003t0001g0098a0001c0013t0001g0073others(5): Show | 13 | HG02056.hp1 HG02071.hp1 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.683-762_683-761ins others(4): Show |
NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr7 | 74784418 | |||||
chr7:74784553
|
A | G | 170 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(167): Show | 325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.683-629A>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 7/10 | chr7 | 74784553 | ||||||
chr7:74784667
|
C | G | 170 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(167): Show | 325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.683-515C>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 7/10 | chr7 | 74784667 | ||||||
chr7:74784709
|
T | C | 170 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(167): Show | 325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.683-473T>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 7/10 | chr7 | 74784709 | ||||||
chr7:74784815
|
C | G | 170 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(167): Show | 325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.683-367C>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 7/10 | chr7 | 74784815 | ||||||
chr7:74784878
|
G | A | 29 | a0001c0001t0002g0014a0001c0001t0002g0019a0001c0001t0002g0034others(26): Show | 38 | HG01070.hp2 HG01071.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.683-304G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 7/10 | chr7 | 74784878 | ||||||
chr7:74784945
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.683-237A>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 7/10 | chr7 | 74784945 | ||||||
chr7:74784972
|
C | T | 5 | a0001c0001t0001g0027a0001c0001t0001g0072a0001c0001t0001g0088others(2): Show | 6 | HG02886.hp2 HG02895.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.683-210C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 7/10 | chr7 | 74784972 | ||||||
chr7:74785049
|
G | C | 8 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0058others(5): Show | 15 | HG00558.hp2 HG02135.hp2 NA18944.hp2 others(12): Show |
intron_variant | MODIFIER | c.683-133G>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 7/10 | chr7 | 74785049 | ||||||
chr7:74785092
|
C | G | 30 | a0001c0001t0001g0120a0001c0003t0001g0002a0001c0003t0001g0007others(27): Show | 55 | HG00140.hp1 HG00544.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.683-90C>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 7/10 | chr7 | 74785092 | ||||||
chr7:74785099
|
G | A | 2 | a0005c0009t0001g0038a0005c0009t0001g0117 | 3 | HG02622.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.683-83G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 7/10 | chr7 | 74785099 | ||||||
chr7:74785106
|
G | A | 1 | a0001c0001t0002g0092 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.683-76G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 7/10 | chr7 | 74785106 | ||||||
chr7:74785126
|
C | T | 1 | a0005c0009t0001g0117 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.683-56C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 7/10 | chr7 | 74785126 | ||||||
chr7:74785354
|
C | T | 3 | a0001c0003t0001g0018a0001c0003t0001g0098a0002c0005t0001g0097 | 5 | HG01884.hp2 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.800+55C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74785354 | ||||||
chr7:74785449
|
A | G | 3 | a0001c0001t0001g0011a0001c0003t0001g0011a0002c0005t0001g0011 | 4 | HG02451.hp2 HG02970.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.800+150A>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74785449 | ||||||
chr7:74785602
|
G | A | 1 | a0004c0006t0001g0059 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.800+303G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74785602 | ||||||
chr7:74785617
|
T | C | 3 | a0001c0001t0001g0011a0001c0003t0001g0011a0002c0005t0001g0011 | 4 | HG02451.hp2 HG02970.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.800+318T>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74785617 | ||||||
chr7:74785652
|
A | G | 3 | a0001c0001t0001g0011a0001c0003t0001g0011a0002c0005t0001g0011 | 4 | HG02451.hp2 HG02970.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.800+353A>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74785652 | ||||||
chr7:74785664
|
T | C | 3 | a0001c0001t0001g0011a0001c0003t0001g0011a0002c0005t0001g0011 | 4 | HG02451.hp2 HG02970.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.800+365T>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74785664 | ||||||
chr7:74785708
|
C | A | 1 | a0001c0001t0001g0060 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.800+409C>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74785708 | ||||||
chr7:74785746
|
G | T | 1 | a0002c0002t0001g0071 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.800+447G>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74785746 | ||||||
chr7:74785883
|
CA | C | 25 | a0001c0001t0001g0003a0001c0001t0001g0028a0001c0001t0001g0047others(22): Show | 38 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.800+605delA | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 74785883 | |||||
chr7:74785883
|
CAA | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(118): Show | 259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.800+604_800+605del others(2): Show |
NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 74785883 | |||||
chr7:74785883
|
CAAA | C | 7 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0077others(4): Show | 7 | HG02083.hp2 HG02965.hp2 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.800+603_800+605del others(3): Show |
NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 74785883 | |||||
chr7:74785914
|
C | A | 1 | a0006c0010t0001g0046 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.800+615C>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74785914 | ||||||
chr7:74786081
|
A | T | 1 | a0001c0001t0001g0063 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.800+782A>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74786081 | ||||||
chr7:74786173
|
T | A | 144 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(141): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.800+874T>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74786173 | ||||||
chr7:74786191
|
C | T | 1 | a0003c0004t0001g0054 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.800+892C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74786191 | ||||||
chr7:74786227
|
C | G | 1 | a0002c0002t0001g0070 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.800+928C>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74786227 | ||||||
chr7:74786234
|
C | CA | 9 | a0001c0001t0001g0064a0001c0001t0002g0131a0001c0001t0002g0141others(6): Show | 13 | HG01074.hp2 HG01109.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.800+956dupA | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 74786234 | |||||
chr7:74786234
|
CA | C | 88 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(85): Show | 192 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.800+956delA | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 74786234 | |||||
chr7:74786234
|
CAA | C | 5 | a0001c0001t0001g0027a0001c0001t0001g0067a0001c0001t0001g0076others(2): Show | 6 | HG00558.hp2 HG01993.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.800+955_800+956del others(2): Show |
NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 74786234 | |||||
chr7:74786349
|
G | A | 1 | a0002c0002t0001g0104 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.800+1050G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74786349 | ||||||
chr7:74786576
|
G | A | 1 | a0002c0002t0002g0132 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.800+1277G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74786576 | ||||||
chr7:74786809
|
T | A | 2 | a0001c0001t0002g0133a0001c0001t0002g0134 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.801-1175T>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74786809 | ||||||
chr7:74786994
|
T | G | 31 | a0001c0001t0001g0120a0001c0003t0001g0002a0001c0003t0001g0007others(28): Show | 56 | HG00140.hp1 HG00544.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.801-990T>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74786994 | ||||||
chr7:74787035
|
G | GA | 12 | a0001c0001t0002g0139a0001c0003t0001g0007a0001c0003t0001g0013others(9): Show | 22 | HG00140.hp1 HG00544.hp1 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.801-935dupA | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 74787035 | |||||
chr7:74787035
|
G | GAA | 7 | a0001c0001t0002g0019a0002c0002t0002g0019a0002c0002t0002g0032others(4): Show | 10 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.801-936_801-935dup others(2): Show |
NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 74787035 | |||||
chr7:74787135
|
C | A | 2 | a0005c0009t0001g0038a0005c0009t0001g0117 | 3 | HG02622.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.801-849C>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74787135 | ||||||
chr7:74787238
|
G | A | 1 | a0001c0001t0001g0041 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.801-746G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74787238 | ||||||
chr7:74787254
|
C | T | 144 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(141): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.801-730C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74787254 | ||||||
chr7:74787400
|
A | G | 1 | a0004c0006t0001g0062 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.801-584A>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74787400 | ||||||
chr7:74787450
|
C | T | 1 | a0001c0001t0001g0061 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.801-534C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74787450 | ||||||
chr7:74787698
|
G | A | 1 | a0005c0009t0001g0117 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.801-286G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74787698 | ||||||
chr7:74787871
|
T | A | 1 | a0001c0001t0001g0057 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.801-113T>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74787871 | ||||||
chr7:74787889
|
G | C | 1 | a0001c0003t0001g0114 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.801-95G>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 8/10 | chr7 | 74787889 | ||||||
chr7:74788133
|
C | T | 1 | a0005c0009t0001g0038 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.905+45C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 9/10 | chr7 | 74788133 | ||||||
chr7:74788173
|
G | A | 31 | a0001c0001t0001g0120a0001c0003t0001g0002a0001c0003t0001g0007others(28): Show | 56 | HG00140.hp1 HG00544.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.905+85G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 9/10 | chr7 | 74788173 | ||||||
chr7:74788213
|
C | T | 1 | a0003c0004t0001g0051 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.905+125C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 9/10 | chr7 | 74788213 | ||||||
chr7:74788262
|
G | C | 1 | a0002c0002t0002g0129 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.905+174G>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 9/10 | chr7 | 74788262 | ||||||
chr7:74788320
|
G | C | 146 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(143): Show | 294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.905+232G>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 9/10 | chr7 | 74788320 | ||||||
chr7:74788340
|
C | T | 1 | a0001c0001t0001g0026 | 2 | HG03017.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.906-219C>T | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 9/10 | chr7 | 74788340 | ||||||
chr7:74788363
|
G | A | 4 | a0001c0001t0001g0027a0001c0001t0001g0072a0001c0001t0001g0088others(1): Show | 5 | HG02895.hp2 HG02922.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.906-196G>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 9/10 | chr7 | 74788363 | ||||||
chr7:74788441
|
T | C | 1 | a0001c0001t0001g0065 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.906-118T>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 9/10 | chr7 | 74788441 | ||||||
chr7:74788740
|
C | G | 134 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(131): Show | 277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.1051+36C>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 10/10 | chr7 | 74788740 | ||||||
chr7:74788744
|
A | G | 10 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0047others(7): Show | 14 | HG00733.hp2 HG01891.hp2 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.1051+40A>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 10/10 | chr7 | 74788744 | ||||||
chr7:74788777
|
T | C | 1 | a0002c0002t0002g0118 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1051+73T>C | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 10/10 | chr7 | 74788777 | ||||||
chr7:74788845
|
T | G | 2 | a0002c0002t0002g0118a0002c0005t0001g0126 | 2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1051+141T>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 10/10 | chr7 | 74788845 | ||||||
chr7:74788952
|
C | A | 144 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(141): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.1052-87C>A | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 10/10 | chr7 | 74788952 | ||||||
chr7:74788979
|
T | TGTGGGCG others(6): Show |
4 | a0001c0001t0001g0025a0002c0002t0001g0025a0002c0002t0001g0091others(1): Show | 4 | NA18948.hp1 NA18948.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.1052-56_1052-44dup others(13): Show |
NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 74788979 | |||||
chr7:74788996
|
T | G | 144 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(141): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.1052-43T>G | NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 10/10 | chr7 | 74788996 |