Item | Value |
---|---|
geneid | 4846 |
ensemblid | ENSG00000164867.11 |
hgncid | 7876 |
symbol | NOS3 |
name | nitric oxide synthase 3 |
refseq_nuc | NM_000603.5 |
refseq_prot | NP_000594.2 |
ensembl_nuc | ENST00000297494.8 |
ensembl_prot | ENSP00000297494.3 |
mane_status | MANE Select |
chr | chr7 |
start | 150991017 |
end | 151014588 |
strand | + |
ver | v1.2 |
region | chr7:150991017-151014588 |
region5000 | chr7:150986017-151019588 |
regionname0 | NOS3_chr7_150991017_151014588 |
regionname5000 | NOS3_chr7_150986017_151019588 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 1203 | 308 | 77 | 50 | 139 | 8 | 33 | 102 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0002 | 1/0 | 1203 | 47 | 3 | 18 | 17 | 3 | 5 | 9 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0003 | 0/0 | 1203 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0004 | 0/0 | 1203 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0005 | 0/0 | 1203 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0006 | 0/0 | 1203 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0007 | 0/0 | 1203 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0008 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0009 | 0/0 | 241 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0010 | 0/0 | 1203 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0011 | 0/0 | 1203 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0012 | 0/0 | 1203 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0013 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0014 | 0/0 | 1203 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0015 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0016 | 0/0 | 1203 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0017 | 0/0 | 1203 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 3612 | 144 | 35 | 22 | 61 | 7 | 18 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
c0002 | 0/0 | 3612 | 138 | 29 | 25 | 68 | 1 | 15 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
c0003 | 1/0 | 3612 | 41 | 3 | 17 | 14 | 3 | 3 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
c0004 | 0/0 | 3612 | 8 | 0 | 0 | 8 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
c0005 | 0/0 | 3612 | 6 | 6 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
c0006 | 0/0 | 3612 | 5 | 4 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
c0007 | 0/0 | 3612 | 3 | 1 | 2 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
c0008 | 0/0 | 3612 | 3 | 0 | 0 | 2 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
c0009 | 0/0 | 3612 | 2 | 0 | 0 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
c0010 | 0/0 | 3612 | 2 | 2 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
c0011 | 0/0 | 3612 | 2 | 0 | 2 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
c0012 | 0/0 | 3612 | 2 | 0 | 0 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
c0013 | 0/0 | 3612 | 2 | 2 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
c0014 | 0/0 | 3612 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
c0015 | 0/0 | 3612 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
c0016 | 0/0 | 3612 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
c0017 | 0/0 | 3612 | 1 | 0 | 0 | 0 | 1 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
c0018 | 0/0 | 3612 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
c0019 | 0/0 | 3612 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
c0020 | 0/0 | 3612 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
c0021 | 0/0 | 3612 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
c0022 | 0/0 | 3612 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
c0023 | 0/0 | 3612 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
c0024 | 0/0 | 3612 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
c0025 | 0/0 | 3612 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
c0026 | 0/0 | 3612 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
c0027 | 0/0 | 3612 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
c0028 | 0/0 | 3612 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
c0029 | 0/0 | 3612 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
c0030 | 0/0 | 3612 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
c0031 | 0/0 | 3612 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
c0032 | 0/0 | 3612 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
c0033 | 0/0 | 3612 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
c0034 | 0/0 | 3612 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
c0035 | 0/0 | 3612 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
c0036 | 0/0 | 3612 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
c0037 | 0/0 | 3612 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 755 | 373 | 90 | 69 | 161 | 12 | 39 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
t0002 | 0/0 | 755 | 3 | 0 | 2 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
t0003 | 0/0 | 755 | 2 | 2 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
t0004 | 0/0 | 779 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
t0005 | 0/0 | 755 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
t0006 | 0/0 | 755 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
t0007 | 0/0 | 755 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0002 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0003 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0004 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0005 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0006 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0007 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0009 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0020 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0022 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0321 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 3612 | 144 | 35 | 22 | 61 | 7 | 18 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0001c0002 | 0/0 | 3612 | 138 | 29 | 25 | 68 | 1 | 15 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0001c0004 | 0/0 | 3612 | 8 | 0 | 0 | 8 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0001c0005 | 0/0 | 3612 | 6 | 6 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0001c0010 | 0/0 | 3612 | 2 | 2 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0001c0011 | 0/0 | 3612 | 2 | 0 | 2 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0001c0021 | 0/0 | 3612 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0001c0022 | 0/0 | 3612 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0001c0023 | 0/0 | 3612 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0001c0024 | 0/0 | 3612 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0001c0027 | 0/0 | 3612 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0001c0029 | 0/0 | 3612 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0001c0032 | 0/0 | 3612 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0001c0033 | 0/0 | 3612 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0002c0003 | 1/0 | 3612 | 41 | 3 | 17 | 14 | 3 | 3 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0002c0008 | 0/0 | 3612 | 3 | 0 | 0 | 2 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0002c0018 | 0/0 | 3612 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0002c0030 | 0/0 | 3612 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0002c0034 | 0/0 | 3612 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0003c0006 | 0/0 | 3612 | 5 | 4 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0003c0014 | 0/0 | 3612 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0003c0037 | 0/0 | 3612 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0004c0013 | 0/0 | 3612 | 2 | 2 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0004c0031 | 0/0 | 3612 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0005c0007 | 0/0 | 3612 | 3 | 1 | 2 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0006c0012 | 0/0 | 3612 | 2 | 0 | 0 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0007c0009 | 0/0 | 3612 | 2 | 0 | 0 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0008c0036 | 0/0 | 3612 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0009c0035 | 0/0 | 3612 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0010c0016 | 0/0 | 3612 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0011c0028 | 0/0 | 3612 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0012c0025 | 0/0 | 3612 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0013c0026 | 0/0 | 3612 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0014c0020 | 0/0 | 3612 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0015c0019 | 0/0 | 3612 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0016c0017 | 0/0 | 3612 | 1 | 0 | 0 | 0 | 1 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0017c0015 | 0/0 | 3612 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 4366 | 140 | 35 | 19 | 61 | 7 | 17 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0001c0001t0002 | 0/0 | 4366 | 3 | 0 | 2 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0001c0001t0006 | 0/0 | 4366 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0001c0002t0001 | 0/0 | 4366 | 134 | 26 | 25 | 67 | 1 | 15 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0001c0002t0003 | 0/0 | 4366 | 2 | 2 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0001c0002t0004 | 0/0 | 4390 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0001c0002t0007 | 0/0 | 4366 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0001c0004t0001 | 0/0 | 4366 | 8 | 0 | 0 | 8 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0001c0005t0001 | 0/0 | 4366 | 6 | 6 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0001c0010t0001 | 0/0 | 4366 | 2 | 2 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0001c0011t0001 | 0/0 | 4366 | 2 | 0 | 2 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0001c0021t0001 | 0/0 | 4366 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0001c0022t0001 | 0/0 | 4366 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0001c0023t0001 | 0/0 | 4366 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0001c0024t0001 | 0/0 | 4366 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0001c0027t0001 | 0/0 | 4366 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0001c0029t0001 | 0/0 | 4366 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0001c0032t0001 | 0/0 | 4366 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0001c0033t0001 | 0/0 | 4366 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0002c0003t0001 | 1/0 | 4366 | 41 | 3 | 17 | 14 | 3 | 3 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0002c0008t0001 | 0/0 | 4366 | 3 | 0 | 0 | 2 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0002c0018t0001 | 0/0 | 4366 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0002c0030t0001 | 0/0 | 4366 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0002c0034t0001 | 0/0 | 4366 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0003c0006t0001 | 0/0 | 4366 | 5 | 4 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0003c0014t0005 | 0/0 | 4366 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0003c0037t0001 | 0/0 | 4366 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0004c0013t0001 | 0/0 | 4366 | 2 | 2 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0004c0031t0001 | 0/0 | 4366 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0005c0007t0001 | 0/0 | 4366 | 3 | 1 | 2 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0006c0012t0001 | 0/0 | 4366 | 2 | 0 | 0 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0007c0009t0001 | 0/0 | 4366 | 2 | 0 | 0 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0008c0036t0001 | 0/0 | 4366 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0009c0035t0001 | 0/0 | 4366 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0010c0016t0001 | 0/0 | 4366 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0011c0028t0001 | 0/0 | 4366 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0012c0025t0001 | 0/0 | 4366 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0013c0026t0001 | 0/0 | 4366 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0014c0020t0001 | 0/0 | 4366 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0015c0019t0001 | 0/0 | 4366 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0016c0017t0001 | 0/0 | 4366 | 1 | 0 | 0 | 0 | 1 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
a0017c0015t0001 | 0/0 | 4366 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | copy fasta | chr7 | 150986017 | 151019588 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0020 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0006g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0001 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0002 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0004 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0005 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0007g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0004t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0004t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0004t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0004t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0004t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0005t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0005t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0005t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0005t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0005t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0010t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0010t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0011t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0011t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0021t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0022t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0023t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0024t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0027t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0029t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0032t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0033t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0321 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0008t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0008t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0008t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0018t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0030t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0034t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0003c0006t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0003c0006t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0003c0006t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0003c0006t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0003c0006t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0003c0014t0005g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0003c0037t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0004c0013t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0004c0031t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0005c0007t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0005c0007t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0005c0007t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0006c0012t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0006c0012t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0007c0009t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0007c0009t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0008c0036t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0009c0035t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0010c0016t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0011c0028t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0012c0025t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0013c0026t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0014c0020t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0015c0019t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0016c0017t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0017c0015t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0003 | t0001 | g0310 | EUR | GBR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0331 | EUR | GBR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0234 | EUR | GBR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0265 | EUR | GBR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00280 | hp1 | a0016 | c0017 | t0001 | g0022 | EUR | FIN | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0144 | EUR | FIN | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0218 | EUR | FIN | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0330 | EUR | FIN | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00423 | hp2 | a0002 | c0003 | t0001 | g0109 | EAS | CHS | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00438 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | CHS | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0296 | EAS | CHS | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0134 | EAS | CHS | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | CHS | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0167 | EAS | CHS | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00597 | hp1 | a0001 | c0004 | t0001 | g0149 | EAS | CHS | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | CHS | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | CHS | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00621 | hp1 | a0002 | c0003 | t0001 | g0102 | EAS | CHS | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | CHS | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0306 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00639 | hp2 | a0002 | c0003 | t0001 | g0308 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00642 | hp1 | a0002 | c0034 | t0001 | g0113 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0018 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00673 | hp1 | a0011 | c0028 | t0001 | g0164 | EAS | CHS | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00733 | hp1 | a0002 | c0003 | t0001 | g0316 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00735 | hp2 | a0001 | c0001 | t0006 | g0183 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0293 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00741 | hp1 | a0002 | c0003 | t0001 | g0064 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0249 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01070 | hp1 | a0002 | c0003 | t0001 | g0314 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0158 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0248 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01071 | hp2 | a0002 | c0003 | t0001 | g0312 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01074 | hp1 | a0002 | c0003 | t0001 | g0047 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0299 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0291 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01081 | hp2 | a0001 | c0011 | t0001 | g0018 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0305 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01106 | hp1 | a0002 | c0003 | t0001 | g0013 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01106 | hp2 | a0002 | c0003 | t0001 | g0309 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01109 | hp1 | a0005 | c0007 | t0001 | g0087 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01109 | hp2 | a0001 | c0011 | t0001 | g0002 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01167 | hp1 | a0002 | c0003 | t0001 | g0116 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01167 | hp2 | a0003 | c0006 | t0001 | g0336 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01169 | hp2 | a0002 | c0003 | t0001 | g0115 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01175 | hp2 | a0002 | c0003 | t0001 | g0315 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01192 | hp1 | a0002 | c0003 | t0001 | g0033 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0160 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01243 | hp1 | a0002 | c0003 | t0001 | g0065 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0300 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01256 | hp1 | a0001 | c0002 | t0001 | g0302 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01256 | hp2 | a0002 | c0003 | t0001 | g0320 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01257 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01258 | hp1 | a0002 | c0003 | t0001 | g0319 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0032 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01346 | hp1 | a0002 | c0003 | t0001 | g0317 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01358 | hp2 | a0001 | c0002 | t0001 | g0267 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01361 | hp2 | a0002 | c0003 | t0001 | g0311 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0069 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0070 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01517 | hp1 | a0002 | c0003 | t0001 | g0313 | EUR | IBS | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0080 | EUR | IBS | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01884 | hp1 | a0001 | c0002 | t0001 | g0060 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01891 | hp1 | a0001 | c0005 | t0001 | g0046 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01943 | hp1 | a0001 | c0002 | t0001 | g0301 | AMR | PEL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0177 | AMR | PEL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01952 | hp1 | a0005 | c0007 | t0001 | g0088 | AMR | PEL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0138 | AMR | PEL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01993 | hp1 | a0001 | c0029 | t0001 | g0003 | AMR | PEL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01993 | hp2 | a0012 | c0025 | t0001 | g0175 | AMR | PEL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02015 | hp1 | a0002 | c0008 | t0001 | g0108 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0168 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0141 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02071 | hp1 | a0002 | c0003 | t0001 | g0105 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0285 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02074 | hp1 | a0001 | c0004 | t0001 | g0021 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02074 | hp2 | a0002 | c0003 | t0001 | g0122 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02080 | hp1 | a0001 | c0004 | t0001 | g0187 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02080 | hp2 | a0001 | c0002 | t0001 | g0270 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02129 | hp1 | a0002 | c0003 | t0001 | g0103 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02129 | hp2 | a0006 | c0012 | t0001 | g0292 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02145 | hp2 | a0001 | c0002 | t0001 | g0032 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02155 | hp1 | a0006 | c0012 | t0001 | g0294 | EAS | CDX | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0275 | EAS | CDX | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02165 | hp1 | a0002 | c0003 | t0001 | g0104 | EAS | CDX | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CDX | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02257 | hp1 | a0001 | c0002 | t0001 | g0061 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02258 | hp2 | a0001 | c0002 | t0001 | g0059 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02280 | hp1 | a0001 | c0005 | t0001 | g0011 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02451 | hp1 | a0001 | c0002 | t0001 | g0089 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0169 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02572 | hp2 | a0001 | c0032 | t0001 | g0042 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02615 | hp1 | a0001 | c0002 | t0001 | g0038 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02615 | hp2 | a0001 | c0002 | t0001 | g0255 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02622 | hp1 | a0001 | c0002 | t0001 | g0090 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0254 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02630 | hp1 | a0003 | c0006 | t0001 | g0335 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02647 | hp1 | a0001 | c0002 | t0001 | g0257 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02647 | hp2 | a0001 | c0002 | t0001 | g0048 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0071 | SAS | PJL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02683 | hp2 | a0017 | c0015 | t0001 | g0114 | SAS | PJL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02698 | hp1 | a0002 | c0030 | t0001 | g0107 | SAS | PJL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02723 | hp1 | a0001 | c0002 | t0001 | g0039 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02723 | hp2 | a0001 | c0033 | t0001 | g0082 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02735 | hp1 | a0001 | c0002 | t0001 | g0097 | SAS | PJL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0322 | SAS | PJL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02809 | hp1 | a0001 | c0021 | t0001 | g0226 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02809 | hp2 | a0001 | c0002 | t0001 | g0091 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02818 | hp1 | a0003 | c0006 | t0001 | g0334 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02818 | hp2 | a0001 | c0002 | t0001 | g0054 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02886 | hp1 | a0001 | c0002 | t0001 | g0328 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02886 | hp2 | a0001 | c0005 | t0001 | g0011 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02896 | hp2 | a0001 | c0005 | t0001 | g0044 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02970 | hp1 | a0001 | c0002 | t0001 | g0041 | AFR | ESN | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02970 | hp2 | a0001 | c0005 | t0001 | g0043 | AFR | ESN | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02976 | hp2 | a0001 | c0010 | t0001 | g0326 | AFR | ESN | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0063 | SAS | PJL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0225 | SAS | PJL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03041 | hp1 | a0001 | c0002 | t0001 | g0281 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03041 | hp2 | a0001 | c0010 | t0001 | g0083 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03098 | hp1 | a0002 | c0003 | t0001 | g0239 | AFR | MSL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0049 | AFR | MSL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03130 | hp2 | a0004 | c0013 | t0001 | g0012 | AFR | ESN | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03139 | hp1 | a0003 | c0006 | t0001 | g0337 | AFR | ESN | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | ESN | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | MSL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03239 | hp2 | a0002 | c0003 | t0001 | g0106 | SAS | PJL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03453 | hp1 | a0003 | c0037 | t0001 | g0332 | AFR | MSL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | MSL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03490 | hp2 | a0002 | c0003 | t0001 | g0119 | SAS | PJL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03516 | hp2 | a0003 | c0006 | t0001 | g0093 | AFR | ESN | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0325 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03540 | hp2 | a0001 | c0005 | t0001 | g0045 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03579 | hp1 | a0001 | c0023 | t0001 | g0086 | AFR | MSL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03579 | hp2 | a0005 | c0007 | t0001 | g0050 | AFR | MSL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03669 | hp1 | a0001 | c0002 | t0001 | g0145 | SAS | PJL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03669 | hp2 | a0001 | c0002 | t0001 | g0133 | SAS | PJL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0170 | SAS | STU | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0096 | SAS | STU | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0208 | SAS | PJL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0323 | SAS | PJL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03831 | hp1 | a0002 | c0008 | t0001 | g0117 | SAS | BEB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03831 | hp2 | a0001 | c0002 | t0001 | g0092 | SAS | BEB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0264 | SAS | BEB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | BEB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0282 | SAS | BEB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | BEB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | BEB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | BEB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0213 | SAS | STU | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0031 | SAS | STU | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0156 | SAS | BEB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG04184 | hp2 | a0002 | c0003 | t0001 | g0033 | SAS | BEB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | STU | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | STU | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG04204 | hp1 | a0014 | c0020 | t0001 | g0182 | SAS | STU | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0247 | SAS | STU | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | YRI | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18522 | hp2 | a0001 | c0002 | t0001 | g0127 | AFR | YRI | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18612 | hp1 | a0002 | c0003 | t0001 | g0013 | EAS | CHB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | CHB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CHB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0140 | EAS | CHB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18906 | hp1 | a0001 | c0002 | t0007 | g0327 | AFR | YRI | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18906 | hp2 | a0001 | c0002 | t0001 | g0256 | AFR | YRI | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18943 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18943 | hp2 | a0002 | c0008 | t0001 | g0266 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0159 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18945 | hp1 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0231 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18946 | hp2 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0297 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18952 | hp1 | a0001 | c0002 | t0001 | g0304 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18953 | hp2 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18956 | hp2 | a0001 | c0002 | t0001 | g0277 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18957 | hp2 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18959 | hp2 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18960 | hp2 | a0002 | c0003 | t0001 | g0099 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18963 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18964 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18964 | hp2 | a0001 | c0027 | t0001 | g0006 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18968 | hp2 | a0001 | c0002 | t0001 | g0298 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18970 | hp1 | a0001 | c0022 | t0001 | g0278 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18970 | hp2 | a0007 | c0009 | t0001 | g0077 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18973 | hp2 | a0001 | c0004 | t0001 | g0199 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18980 | hp2 | a0002 | c0003 | t0001 | g0100 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0289 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18984 | hp2 | a0001 | c0002 | t0004 | g0286 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18985 | hp2 | a0001 | c0002 | t0001 | g0276 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18991 | hp1 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18994 | hp2 | a0001 | c0002 | t0001 | g0274 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0243 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18999 | hp2 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19000 | hp1 | a0002 | c0018 | t0001 | g0073 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0287 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19003 | hp1 | a0001 | c0004 | t0001 | g0008 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19007 | hp2 | a0002 | c0003 | t0001 | g0110 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19009 | hp1 | a0001 | c0004 | t0001 | g0008 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19011 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19012 | hp1 | a0001 | c0002 | t0001 | g0295 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19012 | hp2 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19030 | hp1 | a0001 | c0002 | t0003 | g0057 | AFR | LWK | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19030 | hp2 | a0001 | c0002 | t0001 | g0084 | AFR | LWK | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | LWK | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19043 | hp2 | a0013 | c0026 | t0001 | g0269 | AFR | LWK | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19055 | hp1 | a0002 | c0003 | t0001 | g0094 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19055 | hp2 | a0001 | c0002 | t0001 | g0271 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19062 | hp1 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19062 | hp2 | a0002 | c0003 | t0001 | g0280 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19064 | hp1 | a0002 | c0003 | t0001 | g0279 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19065 | hp1 | a0002 | c0003 | t0001 | g0101 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0290 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19070 | hp2 | a0001 | c0004 | t0001 | g0008 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19079 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19079 | hp2 | a0001 | c0002 | t0001 | g0273 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19080 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19084 | hp2 | a0010 | c0016 | t0001 | g0283 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19085 | hp1 | a0007 | c0009 | t0001 | g0214 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19085 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19088 | hp1 | a0001 | c0004 | t0001 | g0021 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19089 | hp1 | a0001 | c0002 | t0001 | g0307 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19240 | hp1 | a0001 | c0002 | t0001 | g0040 | AFR | YRI | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19240 | hp2 | a0004 | c0013 | t0001 | g0012 | AFR | YRI | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA20129 | hp1 | a0008 | c0036 | t0001 | g0223 | AFR | ASW | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA20129 | hp2 | a0001 | c0002 | t0003 | g0058 | AFR | ASW | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA20752 | hp1 | a0002 | c0003 | t0001 | g0318 | EUR | TSI | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | TSI | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | GIH | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | GIH | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0288 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02109 | hp1 | a0004 | c0031 | t0001 | g0051 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02486 | hp1 | a0002 | c0003 | t0001 | g0052 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02559 | hp1 | a0009 | c0035 | t0001 | g0068 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | MSL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03471 | hp2 | a0003 | c0014 | t0005 | g0333 | AFR | MSL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG06807 | hp1 | a0002 | c0003 | t0001 | g0112 | AFR | USA | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG06807 | hp2 | a0001 | c0002 | t0001 | g0258 | AFR | USA | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18955 | hp1 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA20300 | hp1 | a0001 | c0002 | t0001 | g0132 | AFR | USA | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0006 | AFR | USA | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA21309 | hp1 | a0015 | c0019 | t0001 | g0204 | AFR | LWK | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA21309 | hp2 | a0001 | c0024 | t0001 | g0085 | AFR | LWK | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0020 | REF | REF | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
homoSapiens_grch38 | hp1 | a0002 | c0003 | t0001 | g0321 | REF | REF | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:150996468 | G | A | 1 | a0003 | 7 | HG01167.hp2 HG02630.hp1 HG02818.hp1 others(4): Show |
missense_variant | MODERATE | c.335G>A | p.Arg112Gln | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 4/27 | 670/4366 | 335/3612 | 112/1203 | chr7 | 150996468 | ||
chr7:150996479 | G | A | 1 | a0007 | 2 | NA18970.hp2 NA19085.hp1 |
missense_variant | MODERATE | c.346G>A | p.Gly116Ser | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 4/27 | 681/4366 | 346/3612 | 116/1203 | chr7 | 150996479 | ||
chr7:150996497 | C | G | 1 | a0008 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.364C>G | p.Gln122Glu | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 4/27 | 699/4366 | 364/3612 | 122/1203 | chr7 | 150996497 | ||
chr7:150996809 | G | A | 1 | a0017 | 1 | HG02683.hp2 | missense_variant | MODERATE | c.466G>A | p.Glu156Lys | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/27 | 801/4366 | 466/3612 | 156/1203 | chr7 | 150996809 | ||
chr7:150998588 | C | T | 1 | a0009 | 1 | HG02559.hp1 | stop_gained | HIGH | c.724C>T | p.Arg242* | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 7/27 | 1059/4366 | 724/3612 | 242/1203 | chr7 | 150998588 | ||
chr7:150998676 | C | A | 1 | a0010 | 1 | NA19084.hp2 | missense_variant | MODERATE | c.812C>A | p.Thr271Asn | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 7/27 | 1147/4366 | 812/3612 | 271/1203 | chr7 | 150998676 | ||
chr7:150998988 | G | A | 1 | a0016 | 1 | HG00280.hp1 | missense_variant | MODERATE | c.859G>A | p.Asp287Asn | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 8/27 | 1194/4366 | 859/3612 | 287/1203 | chr7 | 150998988 | ||
chr7:150999023 | T | G | 14 | a0001a0003a0004others(11): Show | 333 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(330): Show |
missense_variant | MODERATE | c.894T>G | p.Asp298Glu | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 8/27 | 1229/4366 | 894/3612 | 298/1203 | chr7 | 150999023 | ||
chr7:151001261 | G | A | 1 | a0015 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.1264G>A | p.Ala422Thr | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 11/27 | 1599/4366 | 1264/3612 | 422/1203 | chr7 | 151001261 | ||
chr7:151001264 | G | A | 1 | a0014 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.1267G>A | p.Ala423Thr | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 11/27 | 1602/4366 | 1267/3612 | 423/1203 | chr7 | 151001264 | ||
chr7:151001835 | C | T | 1 | a0011 | 1 | HG00673.hp1 | missense_variant | MODERATE | c.1517C>T | p.Ser506Phe | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 13/27 | 1852/4366 | 1517/3612 | 506/1203 | chr7 | 151001835 | ||
chr7:151007158 | G | A | 1 | a0004 | 3 | HG02109.hp1 HG03130.hp2 NA19240.hp2 |
missense_variant | MODERATE | c.1994G>A | p.Arg665His | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 17/27 | 2329/4366 | 1994/3612 | 665/1203 | chr7 | 151007158 | ||
chr7:151009457 | C | T | 1 | a0006 | 2 | HG02129.hp2 HG02155.hp1 |
missense_variant | MODERATE | c.2384C>T | p.Pro795Leu | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 20/27 | 2719/4366 | 2384/3612 | 795/1203 | chr7 | 151009457 | ||
chr7:151010256 | G | T | 1 | a0005 | 3 | HG01109.hp1 HG01952.hp1 HG03579.hp2 |
missense_variant | MODERATE | c.2654G>T | p.Arg885Met | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 21/27 | 2989/4366 | 2654/3612 | 885/1203 | chr7 | 151010256 | ||
chr7:151013799 | A | G | 1 | a0013 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.3331A>G | p.Met1111Val | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 26/27 | 3666/4366 | 3331/3612 | 1111/1203 | chr7 | 151013799 | ||
chr7:151014140 | C | T | 1 | a0012 | 1 | HG01993.hp2 | missense_variant | MODERATE | c.3583C>T | p.Pro1195Ser | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 27/27 | 3918/4366 | 3583/3612 | 1195/1203 | chr7 | 151014140 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:150993938 | A | G | 1 | a0003c0037 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.135A>G | p.Leu45Leu | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 2/27 | 470/4366 | 135/3612 | 45/1203 | chr7 | 150993938 | ||
chr7:150998638 | T | C | 31 | a0001c0001a0001c0002a0001c0005others(28): Show | 329 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(326): Show |
synonymous_variant | LOW | c.774T>C | p.Asp258Asp | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 7/27 | 1109/4366 | 774/3612 | 258/1203 | chr7 | 150998638 | ||
chr7:150998978 | C | T | 4 | a0001c0005a0001c0032a0004c0013others(1): Show | 10 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(7): Show |
synonymous_variant | LOW | c.849C>T | p.Asn283Asn | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 8/27 | 1184/4366 | 849/3612 | 283/1203 | chr7 | 150998978 | ||
chr7:150998990 | C | T | 2 | a0003c0006a0003c0037 | 6 | HG01167.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
synonymous_variant | LOW | c.861C>T | p.Asp287Asp | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 8/27 | 1196/4366 | 861/3612 | 287/1203 | chr7 | 150998990 | ||
chr7:150999023 | T | C | 1 | a0002c0018 | 1 | NA19000.hp1 | synonymous_variant | LOW | c.894T>C | p.Asp298Asp | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 8/27 | 1229/4366 | 894/3612 | 298/1203 | chr7 | 150999023 | ||
chr7:150999286 | C | T | 1 | a0001c0029 | 1 | HG01993.hp1 | synonymous_variant | LOW | c.1053C>T | p.Ala351Ala | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/27 | 1388/4366 | 1053/3612 | 351/1203 | chr7 | 150999286 | ||
chr7:151002235 | C | T | 1 | a0001c0027 | 1 | NA18964.hp2 | synonymous_variant | LOW | c.1683C>T | p.Leu561Leu | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/27 | 2018/4366 | 1683/3612 | 561/1203 | chr7 | 151002235 | ||
chr7:151007162 | C | G | 22 | a0001c0002a0001c0005a0001c0010others(19): Show | 174 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(171): Show |
synonymous_variant | LOW | c.1998C>G | p.Ala666Ala | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 17/27 | 2333/4366 | 1998/3612 | 666/1203 | chr7 | 151007162 | ||
chr7:151009425 | C | T | 1 | a0002c0030 | 1 | HG02698.hp1 | synonymous_variant | LOW | c.2352C>T | p.Asp784Asp | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 20/27 | 2687/4366 | 2352/3612 | 784/1203 | chr7 | 151009425 | ||
chr7:151009533 | G | A | 1 | a0001c0023 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.2460G>A | p.Pro820Pro | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 20/27 | 2795/4366 | 2460/3612 | 820/1203 | chr7 | 151009533 | ||
chr7:151010224 | G | A | 1 | a0001c0024 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.2622G>A | p.Leu874Leu | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 21/27 | 2957/4366 | 2622/3612 | 874/1203 | chr7 | 151010224 | ||
chr7:151012396 | C | T | 1 | a0001c0022 | 1 | NA18970.hp1 | synonymous_variant | LOW | c.3030C>T | p.Ile1010Ile | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 24/27 | 3365/4366 | 3030/3612 | 1010/1203 | chr7 | 151012396 | ||
chr7:151013819 | T | C | 5 | a0001c0005a0001c0010a0001c0021others(2): Show | 14 | HG01109.hp1 HG01891.hp1 HG01952.hp1 others(11): Show |
synonymous_variant | LOW | c.3351T>C | p.Val1117Val | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 26/27 | 3686/4366 | 3351/3612 | 1117/1203 | chr7 | 151013819 | ||
chr7:151013882 | G | A | 1 | a0001c0011 | 2 | HG01081.hp2 HG01109.hp2 |
synonymous_variant | LOW | c.3414G>A | p.Glu1138Glu | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 26/27 | 3749/4366 | 3414/3612 | 1138/1203 | chr7 | 151013882 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:150991021 | C | T | 1 | a0001c0001t0002 | 3 | HG01069.hp2 HG01071.hp1 HG04204.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-331C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/27 | chr7 | 150991021 | ||||||
chr7:150991038 | G | A | 1 | a0001c0002t0003 | 2 | NA19030.hp1 NA20129.hp2 |
5_prime_UTR_variant | MODIFIER | c.-314G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/27 | 2766 | chr7 | 150991038 | |||||
chr7:150991088 | A | C | 1 | a0001c0002t0007 | 1 | NA18906.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-264A>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/27 | chr7 | 150991088 | ||||||
chr7:150991148 | G | GAGAGGAT others(17): Show |
1 | a0001c0002t0004 | 1 | NA18984.hp2 | 5_prime_UTR_variant | MODIFIER | c.-203_-180dupAGAGGA others(18): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/27 | 2631 | INFO_REALIGN_3_PRIME | chr7 | 150991148 | ||||
chr7:151014198 | G | A | 1 | a0003c0014t0005 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*29G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 27/27 | 29 | chr7 | 151014198 | |||||
chr7:151014417 | C | G | 1 | a0001c0001t0006 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*248C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 27/27 | 248 | chr7 | 151014417 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:150991391 | G | A | 6 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-52+91G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150991391 | ||||||
chr7:150991428 | C | T | 6 | a0003c0006t0001g0334a0003c0006t0001g0335a0003c0006t0001g0336others(3): Show | 6 | HG01167.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-52+128C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150991428 | ||||||
chr7:150991587 | G | A | 2 | a0001c0002t0001g0040a0001c0002t0001g0041 | 2 | HG02970.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-52+287G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150991587 | ||||||
chr7:150991679 | C | T | 1 | a0001c0001t0001g0331 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-52+379C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150991679 | ||||||
chr7:150991857 | G | A | 6 | a0001c0005t0001g0011a0001c0005t0001g0043a0001c0005t0001g0044others(3): Show | 7 | HG01891.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-52+557G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150991857 | ||||||
chr7:150991928 | G | A | 1 | a0002c0003t0001g0047 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-52+628G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150991928 | ||||||
chr7:150991996 | C | CA | 14 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0066others(11): Show | 14 | HG00741.hp1 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.-52+711dupA | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr7 | 150991996 | |||||
chr7:150991996 | CA | C | 9 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(6): Show | 9 | HG00323.hp2 HG01243.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-52+711delA | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr7 | 150991996 | |||||
chr7:150992012 | T | A | 7 | a0001c0001t0001g0053a0001c0002t0001g0048a0001c0002t0001g0049others(4): Show | 7 | HG02109.hp1 HG02486.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-52+712T>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150992012 | ||||||
chr7:150992038 | G | T | 3 | a0001c0002t0001g0325a0001c0002t0007g0327a0001c0010t0001g0326 | 3 | HG02976.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-52+738G>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150992038 | ||||||
chr7:150992147 | T | A | 2 | a0001c0002t0001g0069a0001c0002t0001g0070 | 2 | HG01433.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.-52+847T>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150992147 | ||||||
chr7:150992147 | T | TA | 275 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0014others(272): Show | 309 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.-52+861dupA | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr7 | 150992147 | |||||
chr7:150992147 | T | TAA | 15 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0072others(12): Show | 16 | HG00735.hp1 HG01517.hp2 HG01978.hp2 others(13): Show |
intron_variant | MODIFIER | c.-52+860_-52+861dup others(2): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr7 | 150992147 | |||||
chr7:150992309 | A | T | 254 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0014others(251): Show | 288 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.-52+1009A>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150992309 | ||||||
chr7:150992338 | A | T | 2 | a0001c0002t0001g0328a0003c0006t0001g0093 | 2 | HG02886.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-52+1038A>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150992338 | ||||||
chr7:150992402 | T | G | 341 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0014others(338): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.-52+1102T>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150992402 | ||||||
chr7:150992405 | T | G | 1 | a0002c0003t0001g0094 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-52+1105T>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150992405 | ||||||
chr7:150992612 | C | T | 1 | a0001c0002t0001g0281 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-51-1141C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150992612 | ||||||
chr7:150992682 | C | T | 6 | a0001c0005t0001g0011a0001c0005t0001g0043a0001c0005t0001g0044others(3): Show | 7 | HG01891.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-51-1071C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150992682 | ||||||
chr7:150992694 | T | C | 6 | a0001c0005t0001g0011a0001c0005t0001g0043a0001c0005t0001g0044others(3): Show | 7 | HG01891.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-51-1059T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150992694 | ||||||
chr7:150992772 | G | C | 1 | a0001c0002t0001g0282 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-51-981G>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150992772 | ||||||
chr7:150992802 | G | A | 1 | a0002c0003t0001g0047 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-51-951G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150992802 | ||||||
chr7:150992844 | C | G | 2 | a0001c0002t0001g0040a0001c0002t0001g0041 | 2 | HG02970.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-51-909C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150992844 | ||||||
chr7:150992855 | G | A | 280 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0014others(277): Show | 315 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.-51-898G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150992855 | ||||||
chr7:150992882 | C | T | 7 | a0001c0001t0001g0053a0001c0002t0001g0048a0001c0002t0001g0049others(4): Show | 7 | HG02109.hp1 HG02486.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-51-871C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150992882 | ||||||
chr7:150992991 | C | T | 279 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0014others(276): Show | 314 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.-51-762C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150992991 | ||||||
chr7:150993037 | C | T | 2 | a0002c0003t0001g0279a0002c0003t0001g0280 | 2 | NA19062.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-51-716C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150993037 | ||||||
chr7:150993045 | G | A | 4 | a0001c0002t0001g0063a0001c0002t0001g0071a0001c0002t0001g0096others(1): Show | 4 | HG02683.hp1 HG02735.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51-708G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150993045 | ||||||
chr7:150993088 | C | T | 5 | a0002c0003t0001g0047a0002c0003t0001g0318a0002c0003t0001g0319others(2): Show | 5 | HG01074.hp1 HG01256.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-665C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150993088 | ||||||
chr7:150993135 | GGGTTCCA others(23): Show |
G | 1 | a0010c0016t0001g0283 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-51-615_-51-586del others(30): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr7 | 150993135 | |||||
chr7:150993141 | C | T | 1 | a0003c0006t0001g0093 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-51-612C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150993141 | ||||||
chr7:150993198 | A | G | 3 | a0001c0023t0001g0086a0005c0007t0001g0087a0005c0007t0001g0088 | 3 | HG01109.hp1 HG01952.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-51-555A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150993198 | ||||||
chr7:150993204 | T | A | 3 | a0001c0023t0001g0086a0005c0007t0001g0087a0005c0007t0001g0088 | 3 | HG01109.hp1 HG01952.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-51-549T>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150993204 | ||||||
chr7:150993431 | G | A | 2 | a0001c0002t0003g0057a0001c0002t0003g0058 | 2 | NA19030.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-51-322G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150993431 | ||||||
chr7:150993562 | A | C | 10 | a0001c0002t0001g0030a0001c0002t0001g0270a0001c0002t0001g0271others(7): Show | 11 | HG02080.hp2 HG02155.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.-51-191A>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150993562 | ||||||
chr7:150993597 | A | C | 1 | a0001c0001t0001g0081 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-51-156A>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150993597 | ||||||
chr7:150993666 | G | A | 1 | a0001c0002t0001g0062 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-51-87G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150993666 | ||||||
chr7:150993751 | A | G | 1 | a0001c0002t0001g0062 | 1 | NA18991.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.-51-2A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150993751 | ||||||
chr7:150993752 | G | T | 1 | a0001c0002t0001g0062 | 1 | NA18991.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.-51-1G>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150993752 | ||||||
chr7:150994085 | C | T | 9 | a0001c0001t0001g0053a0001c0002t0001g0048a0001c0002t0001g0049others(6): Show | 9 | HG02109.hp1 HG02486.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.158+124C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 2/26 | chr7 | 150994085 | ||||||
chr7:150994330 | G | A | 1 | a0001c0001t0001g0284 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.158+369G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 2/26 | chr7 | 150994330 | ||||||
chr7:150994344 | C | T | 1 | a0001c0001t0001g0268 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.158+383C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 2/26 | chr7 | 150994344 | ||||||
chr7:150994386 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.158+425G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 2/26 | chr7 | 150994386 | ||||||
chr7:150994547 | A | G | 1 | a0001c0002t0001g0267 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.158+586A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 2/26 | chr7 | 150994547 | ||||||
chr7:150994571 | G | C | 4 | a0001c0002t0001g0063a0001c0002t0001g0071a0001c0002t0001g0096others(1): Show | 4 | HG02683.hp1 HG02735.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.158+610G>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 2/26 | chr7 | 150994571 | ||||||
chr7:150994810 | C | T | 1 | a0002c0008t0001g0266 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.159-393C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 2/26 | chr7 | 150994810 | ||||||
chr7:150995049 | C | T | 3 | a0001c0023t0001g0086a0005c0007t0001g0087a0005c0007t0001g0088 | 3 | HG01109.hp1 HG01952.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.159-154C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 2/26 | chr7 | 150995049 | ||||||
chr7:150995098 | G | T | 7 | a0001c0005t0001g0011a0001c0005t0001g0043a0001c0005t0001g0044others(4): Show | 8 | HG01891.hp1 HG02280.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.159-105G>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 2/26 | chr7 | 150995098 | ||||||
chr7:150995135 | G | A | 1 | a0002c0003t0001g0318 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.159-68G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 2/26 | chr7 | 150995135 | ||||||
chr7:150995356 | G | A | 33 | a0001c0001t0001g0284a0001c0001t0001g0303a0001c0002t0001g0010others(30): Show | 37 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.270+42G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995356 | ||||||
chr7:150995451 | A | G | 1 | a0001c0001t0001g0265 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.270+137A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995451 | ||||||
chr7:150995535 | C | T | 2 | a0001c0002t0001g0038a0001c0002t0001g0039 | 2 | HG02615.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.270+221C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995535 | ||||||
chr7:150995583 | T | C | 1 | a0001c0002t0001g0062 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.270+269T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995583 | ||||||
chr7:150995584 | C | T | 1 | a0001c0002t0001g0062 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.270+270C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995584 | ||||||
chr7:150995593 | C | CCCCATCC others(190): Show |
1 | a0002c0003t0001g0094 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.270+282_270+283ins others(197): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(330): Show |
2 | a0001c0001t0001g0055a0001c0001t0001g0072 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.270+283_270+284ins others(337): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(305): Show |
1 | a0002c0003t0001g0099 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(312): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(304): Show |
20 | a0001c0001t0001g0111a0002c0003t0001g0013a0002c0003t0001g0064others(17): Show | 21 | HG00423.hp2 HG00621.hp1 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.270+283_270+284ins others(311): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(597): Show |
1 | a0002c0003t0001g0065 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.270+283_270+284ins others(604): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(565): Show |
1 | a0002c0003t0001g0115 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(572): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(362): Show |
1 | a0002c0008t0001g0117 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.270+283_270+284ins others(369): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(329): Show |
3 | a0001c0001t0001g0120a0001c0002t0001g0118a0002c0003t0001g0119 | 3 | HG03490.hp2 NA18959.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.270+283_270+284ins others(336): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(329): Show |
1 | a0001c0001t0001g0121 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(336): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(329): Show |
14 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(11): Show | 14 | HG01243.hp2 HG02055.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.270+283_270+284ins others(336): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(329): Show |
5 | a0003c0006t0001g0093a0003c0006t0001g0334a0003c0006t0001g0335others(2): Show | 5 | HG02630.hp1 HG02818.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.270+283_270+284ins others(336): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(393): Show |
1 | a0001c0002t0001g0059 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(400): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(329): Show |
23 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0123others(20): Show | 26 | HG01109.hp1 HG01167.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.270+283_270+284ins others(336): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(329): Show |
2 | a0001c0002t0001g0040a0001c0002t0001g0041 | 2 | HG02970.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.270+283_270+284ins others(336): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(329): Show |
3 | a0001c0002t0001g0089a0001c0002t0001g0090a0001c0002t0001g0091 | 3 | HG02451.hp1 HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.270+283_270+284ins others(336): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(329): Show |
1 | a0001c0002t0001g0328 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.270+283_270+284ins others(336): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(329): Show |
9 | a0001c0001t0001g0053a0001c0002t0001g0048a0001c0002t0001g0054others(6): Show | 9 | HG02109.hp1 HG02486.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.270+283_270+284ins others(336): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(879): Show |
1 | a0001c0024t0001g0085 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(886): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(230): Show |
1 | a0001c0002t0001g0127 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(237): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(164): Show |
1 | a0013c0026t0001g0269 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(171): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(389): Show |
1 | a0001c0001t0001g0056 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(396): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(462): Show |
1 | a0001c0001t0001g0128 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(469): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(332): Show |
1 | a0001c0002t0001g0129 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.270+283_270+284ins others(339): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(331): Show |
1 | a0001c0002t0001g0270 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(338): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(331): Show |
1 | a0001c0001t0001g0130 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(338): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(457): Show |
1 | a0002c0018t0001g0073 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.270+283_270+284ins others(464): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(329): Show |
1 | a0001c0002t0001g0131 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.270+283_270+284ins others(336): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(305): Show |
2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG03669.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.270+283_270+284ins others(312): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(355): Show |
2 | a0002c0003t0001g0308a0002c0003t0001g0309 | 2 | HG00639.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.270+283_270+284ins others(362): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(305): Show |
1 | a0001c0001t0001g0074 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(312): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(305): Show |
4 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(1): Show | 4 | HG00544.hp2 HG02717.hp1 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.270+283_270+284ins others(312): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(305): Show |
1 | a0001c0002t0001g0271 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(312): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(362): Show |
4 | a0001c0001t0001g0329a0001c0002t0001g0138a0001c0002t0001g0139others(1): Show | 4 | HG01978.hp1 HG03195.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.270+283_270+284ins others(369): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(330): Show |
134 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0019others(131): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.270+283_270+284ins others(337): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(821): Show |
1 | a0001c0002t0001g0141 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(828): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(263): Show |
1 | a0001c0001t0001g0222 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(270): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(331): Show |
1 | a0008c0036t0001g0223 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.270+283_270+284ins others(338): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(331): Show |
2 | a0001c0001t0001g0224a0001c0001t0001g0323 | 2 | HG02300.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.270+283_270+284ins others(338): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(542): Show |
1 | a0001c0002t0001g0225 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(549): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(354): Show |
4 | a0002c0003t0001g0318a0002c0003t0001g0319a0002c0003t0001g0320others(1): Show | 4 | HG01256.hp2 HG01258.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.270+283_270+284ins others(361): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(330): Show |
4 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0229others(1): Show | 4 | HG02258.hp1 HG02280.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.270+283_270+284ins others(337): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(328): Show |
1 | a0001c0002t0001g0277 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(335): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(329): Show |
1 | a0001c0002t0001g0230 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(336): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(429): Show |
3 | a0001c0001t0001g0232a0001c0002t0001g0231a0001c0002t0001g0233 | 3 | NA18945.hp2 NA18971.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.270+283_270+284ins others(436): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(330): Show |
1 | a0001c0001t0001g0234 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.270+283_270+284ins others(337): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(394): Show |
1 | a0001c0001t0001g0235 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.270+283_270+284ins others(401): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(362): Show |
1 | a0001c0001t0001g0236 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.270+283_270+284ins others(369): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(428): Show |
1 | a0001c0002t0001g0237 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.270+283_270+284ins others(435): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(297): Show |
1 | a0001c0001t0001g0259 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(304): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(330): Show |
25 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(22): Show | 28 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.270+283_270+284ins others(337): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(355): Show |
1 | a0001c0022t0001g0278 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.270+283_270+284ins others(362): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(329): Show |
1 | a0001c0001t0001g0324 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(336): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCATC others(330): Show |
3 | a0001c0001t0001g0080a0001c0001t0001g0260a0001c0001t0001g0261 | 3 | HG01257.hp1 HG01258.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.270+283_270+284ins others(337): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCCAT others(598): Show |
1 | a0001c0001t0001g0262 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.270+284_270+285ins others(605): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCCAT others(331): Show |
2 | a0001c0001t0001g0081a0001c0001t0001g0095 | 2 | HG00738.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.270+284_270+285ins others(338): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | CCCCCCAT others(298): Show |
1 | a0001c0001t0001g0263 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.270+284_270+285ins others(305): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995593 | C | T | 1 | a0001c0002t0001g0062 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.270+279C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995593 | ||||||
chr7:150995593 | CCCCCCGT others(26): Show |
C | 32 | a0001c0001t0001g0284a0001c0001t0001g0303a0001c0002t0001g0010others(29): Show | 36 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.270+284_270+316del others(33): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | |||||
chr7:150995594 | C | CCCCATCC others(564): Show |
1 | a0002c0003t0001g0116 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.270+283_270+284ins others(571): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995594 | |||||
chr7:150995594 | C | CCCCATCC others(329): Show |
1 | a0001c0001t0001g0221 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(336): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995594 | |||||
chr7:150995594 | CCCCCGTC others(25): Show |
C | 1 | a0001c0002t0001g0062 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.270+285_270+316del others(32): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995594 | |||||
chr7:150995599 | G | C | 1 | a0001c0002t0001g0264 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+285G>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995599 | ||||||
chr7:150995600 | T | A | 1 | a0001c0002t0001g0264 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+286T>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995600 | ||||||
chr7:150995607 | C | CCCCCCCT others(12): Show |
1 | a0001c0002t0001g0264 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+294_270+295ins others(19): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995607 | |||||
chr7:150995610 | G | A | 1 | a0001c0002t0001g0264 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+296G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995610 | ||||||
chr7:150995611 | C | A | 1 | a0001c0002t0001g0264 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+297C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995611 | ||||||
chr7:150995613 | T | C | 1 | a0001c0002t0001g0264 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+299T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995613 | ||||||
chr7:150995614 | T | C | 1 | a0001c0002t0001g0264 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+300T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995614 | ||||||
chr7:150995630 | C | T | 1 | a0001c0002t0001g0233 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.270+316C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995630 | ||||||
chr7:150995631 | A | G | 1 | a0001c0002t0001g0264 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+317A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995631 | ||||||
chr7:150995634 | T | C | 34 | a0001c0001t0001g0284a0001c0001t0001g0303a0001c0002t0001g0010others(31): Show | 38 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+320T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995634 | ||||||
chr7:150995642 | G | A | 1 | a0001c0002t0001g0264 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+328G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995642 | ||||||
chr7:150995643 | C | A | 1 | a0001c0002t0001g0264 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+329C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995643 | ||||||
chr7:150995647 | CCT | C | 44 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(41): Show | 44 | HG01109.hp1 HG01167.hp2 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.270+336_270+337del others(2): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995647 | |||||
chr7:150995649 | T | A | 1 | a0001c0002t0001g0264 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+335T>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995649 | ||||||
chr7:150995649 | TCTTC | T | 32 | a0001c0001t0001g0284a0001c0001t0001g0303a0001c0002t0001g0010others(29): Show | 36 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.270+337_270+340del others(4): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995649 | |||||
chr7:150995651 | T | C | 1 | a0001c0002t0001g0264 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+337T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995651 | ||||||
chr7:150995656 | T | C | 33 | a0001c0001t0001g0284a0001c0001t0001g0303a0001c0002t0001g0010others(30): Show | 37 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.270+342T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995656 | ||||||
chr7:150995657 | C | A | 33 | a0001c0001t0001g0284a0001c0001t0001g0303a0001c0002t0001g0010others(30): Show | 37 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.270+343C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995657 | ||||||
chr7:150995657 | C | G | 1 | a0001c0002t0001g0264 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+343C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995657 | ||||||
chr7:150995658 | T | TCCCACCC others(122): Show |
1 | a0002c0034t0001g0113 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.270+375_270+503dup others(129): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995658 | |||||
chr7:150995665 | C | T | 34 | a0001c0001t0001g0284a0001c0001t0001g0303a0001c0002t0001g0010others(31): Show | 38 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+351C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995665 | ||||||
chr7:150995668 | G | A | 34 | a0001c0001t0001g0284a0001c0001t0001g0303a0001c0002t0001g0010others(31): Show | 38 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+354G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995668 | ||||||
chr7:150995669 | C | A | 34 | a0001c0001t0001g0284a0001c0001t0001g0303a0001c0002t0001g0010others(31): Show | 38 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+355C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995669 | ||||||
chr7:150995673 | C | T | 1 | a0003c0006t0001g0337 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.270+359C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995673 | ||||||
chr7:150995683 | C | G | 1 | a0001c0002t0001g0264 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+369C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995683 | ||||||
chr7:150995684 | T | TC | 31 | a0001c0001t0001g0284a0001c0001t0001g0303a0001c0002t0001g0010others(28): Show | 35 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.270+374dupC | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995684 | |||||
chr7:150995688 | CGTCCCAC others(22): Show |
C | 2 | a0001c0002t0001g0305a0001c0002t0001g0306 | 2 | HG00639.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.270+375_270+403del others(29): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995688 | ||||||
chr7:150995689 | G | C | 1 | a0001c0002t0001g0264 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+375G>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995689 | ||||||
chr7:150995692 | C | T | 1 | a0001c0002t0001g0264 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+378C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995692 | ||||||
chr7:150995693 | C | A | 1 | a0001c0002t0001g0264 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+379C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995693 | ||||||
chr7:150995695 | C | A | 1 | a0001c0002t0001g0264 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+381C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995695 | ||||||
chr7:150995698 | T | C | 31 | a0001c0001t0001g0284a0001c0001t0001g0303a0001c0002t0001g0010others(28): Show | 35 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.270+384T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995698 | ||||||
chr7:150995699 | G | T | 31 | a0001c0001t0001g0284a0001c0001t0001g0303a0001c0002t0001g0010others(28): Show | 35 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.270+385G>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995699 | ||||||
chr7:150995700 | C | A | 31 | a0001c0001t0001g0284a0001c0001t0001g0303a0001c0002t0001g0010others(28): Show | 35 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.270+386C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995700 | ||||||
chr7:150995701 | A | C | 1 | a0001c0001t0001g0253 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.270+387A>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995701 | ||||||
chr7:150995702 | C | A | 31 | a0001c0001t0001g0284a0001c0001t0001g0303a0001c0002t0001g0010others(28): Show | 35 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.270+388C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995702 | ||||||
chr7:150995703 | T | C | 32 | a0001c0001t0001g0284a0001c0001t0001g0303a0001c0002t0001g0010others(29): Show | 36 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.270+389T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995703 | ||||||
chr7:150995704 | C | A | 1 | a0001c0002t0001g0264 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+390C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995704 | ||||||
chr7:150995707 | G | A | 30 | a0001c0001t0001g0284a0001c0001t0001g0303a0001c0002t0001g0010others(27): Show | 34 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.270+393G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995707 | ||||||
chr7:150995707 | G | C | 1 | a0001c0002t0001g0062 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.270+393G>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995707 | ||||||
chr7:150995707 | G | T | 1 | a0001c0002t0001g0264 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+393G>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995707 | ||||||
chr7:150995708 | C | A | 1 | a0001c0002t0001g0062 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.270+394C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995708 | ||||||
chr7:150995708 | CCCT | C | 29 | a0001c0001t0001g0284a0001c0001t0001g0303a0001c0002t0001g0010others(26): Show | 33 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.270+396_270+398del others(3): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995708 | |||||
chr7:150995709 | C | T | 1 | a0001c0002t0001g0307 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.270+395C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995709 | ||||||
chr7:150995711 | T | C | 1 | a0001c0002t0001g0307 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.270+397T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995711 | ||||||
chr7:150995713 | T | C | 1 | a0001c0002t0001g0062 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.270+399T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995713 | ||||||
chr7:150995715 | CA | C | 30 | a0001c0001t0001g0284a0001c0001t0001g0303a0001c0002t0001g0010others(27): Show | 34 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.270+402delA | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995715 | ||||||
chr7:150995717 | G | C | 30 | a0001c0001t0001g0284a0001c0001t0001g0303a0001c0002t0001g0010others(27): Show | 34 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.270+403G>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995717 | ||||||
chr7:150995718 | C | T | 30 | a0001c0001t0001g0284a0001c0001t0001g0303a0001c0002t0001g0010others(27): Show | 34 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.270+404C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995718 | ||||||
chr7:150995719 | G | A | 19 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(16): Show | 19 | HG01243.hp2 HG02055.hp1 HG02615.hp1 others(16): Show |
intron_variant | MODIFIER | c.270+405G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995719 | ||||||
chr7:150995723 | CA | C | 31 | a0001c0001t0001g0284a0001c0001t0001g0303a0001c0002t0001g0010others(28): Show | 35 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.270+410delA | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995723 | ||||||
chr7:150995727 | C | T | 31 | a0001c0001t0001g0284a0001c0001t0001g0303a0001c0002t0001g0010others(28): Show | 35 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.270+413C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995727 | ||||||
chr7:150995730 | A | G | 1 | a0001c0002t0001g0264 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+416A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995730 | ||||||
chr7:150995731 | C | A | 33 | a0001c0001t0001g0284a0001c0001t0001g0303a0001c0002t0001g0010others(30): Show | 37 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.270+417C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995731 | ||||||
chr7:150995732 | A | ACCCCTCC others(27): Show |
1 | a0001c0002t0001g0145 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.270+438_270+471dup others(34): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995732 | |||||
chr7:150995736 | C | T | 1 | a0001c0002t0001g0264 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+422C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995736 | ||||||
chr7:150995737 | T | A | 2 | a0001c0002t0001g0305a0001c0002t0001g0306 | 2 | HG00639.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.270+423T>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995737 | ||||||
chr7:150995745 | C | G | 32 | a0001c0001t0001g0284a0001c0001t0001g0303a0001c0002t0001g0010others(29): Show | 36 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.270+431C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995745 | ||||||
chr7:150995747 | G | C | 32 | a0001c0001t0001g0284a0001c0001t0001g0303a0001c0002t0001g0010others(29): Show | 36 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.270+433G>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995747 | ||||||
chr7:150995749 | C | T | 12 | a0001c0001t0001g0053a0001c0002t0001g0040a0001c0002t0001g0041others(9): Show | 12 | HG02109.hp1 HG02486.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.270+435C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995749 | ||||||
chr7:150995751 | CAT | C | 32 | a0001c0001t0001g0284a0001c0001t0001g0303a0001c0002t0001g0010others(29): Show | 36 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.270+438_270+439del others(2): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995751 | ||||||
chr7:150995752 | A | G | 1 | a0001c0002t0001g0264 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+438A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995752 | ||||||
chr7:150995753 | T | G | 1 | a0001c0002t0001g0307 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.270+439T>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995753 | ||||||
chr7:150995754 | T | C | 1 | a0001c0002t0001g0264 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+440T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995754 | ||||||
chr7:150995756 | C | T | 32 | a0001c0001t0001g0284a0001c0001t0001g0303a0001c0002t0001g0010others(29): Show | 36 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.270+442C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995756 | ||||||
chr7:150995757 | A | C | 1 | a0001c0002t0001g0307 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.270+443A>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995757 | ||||||
chr7:150995757 | ACCCCTGC | A | 32 | a0001c0001t0001g0284a0001c0001t0001g0303a0001c0002t0001g0010others(29): Show | 36 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.270+444_270+450del others(7): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995757 | ||||||
chr7:150995759 | C | G | 1 | a0001c0002t0001g0264 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+445C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995759 | ||||||
chr7:150995760 | C | T | 1 | a0001c0002t0001g0307 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.270+446C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995760 | ||||||
chr7:150995763 | G | A | 1 | a0001c0002t0001g0307 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.270+449G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995763 | ||||||
chr7:150995764 | C | A | 1 | a0001c0002t0001g0307 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.270+450C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995764 | ||||||
chr7:150995764 | C | T | 1 | a0001c0002t0001g0264 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+450C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995764 | ||||||
chr7:150995766 | C | A | 32 | a0001c0001t0001g0284a0001c0001t0001g0303a0001c0002t0001g0010others(29): Show | 36 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.270+452C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995766 | ||||||
chr7:150995766 | CCCCCTCC others(26): Show |
C | 1 | a0001c0001t0001g0144 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.270+467_270+499del others(33): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995766 | |||||
chr7:150995768 | C | T | 1 | a0001c0002t0001g0264 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+454C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995768 | ||||||
chr7:150995770 | C | T | 1 | a0001c0002t0001g0307 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.270+456C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995770 | ||||||
chr7:150995771 | T | C | 1 | a0001c0002t0001g0307 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.270+457T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995771 | ||||||
chr7:150995779 | C | G | 2 | a0001c0002t0001g0305a0001c0002t0001g0306 | 2 | HG00639.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.270+465C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995779 | ||||||
chr7:150995780 | TG | T | 30 | a0001c0001t0001g0284a0001c0001t0001g0303a0001c0002t0001g0010others(27): Show | 34 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.270+467delG | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995780 | ||||||
chr7:150995781 | G | C | 4 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0002t0001g0264others(1): Show | 4 | HG02015.hp2 HG03834.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.270+467G>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995781 | ||||||
chr7:150995786 | G | A | 33 | a0001c0001t0001g0284a0001c0001t0001g0303a0001c0002t0001g0010others(30): Show | 37 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.270+472G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995786 | ||||||
chr7:150995787 | A | ACCCACCC others(794): Show |
3 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0229 | 3 | HG02258.hp1 HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.270+534_270+535ins others(801): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995787 | |||||
chr7:150995787 | A | ACCCACCC others(126): Show |
8 | a0001c0002t0001g0127a0001c0002t0001g0254a0001c0002t0001g0255others(5): Show | 8 | HG02615.hp2 HG02622.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.270+485_270+486ins others(133): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995787 | |||||
chr7:150995787 | A | ACCCACCC others(125): Show |
7 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(4): Show | 7 | HG01243.hp2 HG02683.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.270+485_270+486ins others(132): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995787 | |||||
chr7:150995787 | A | T | 37 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0284others(34): Show | 41 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.270+473A>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995787 | ||||||
chr7:150995787 | ACCCACCC others(26): Show |
A | 2 | a0001c0001t0001g0252a0001c0002t0001g0257 | 2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.270+486_270+518del others(33): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995787 | |||||
chr7:150995789 | C | A | 1 | a0001c0002t0001g0264 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+475C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995789 | ||||||
chr7:150995791 | A | C | 2 | a0001c0002t0001g0305a0001c0002t0001g0306 | 2 | HG00639.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.270+477A>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995791 | ||||||
chr7:150995794 | C | T | 2 | a0001c0002t0001g0305a0001c0002t0001g0306 | 2 | HG00639.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.270+480C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995794 | ||||||
chr7:150995797 | G | A | 4 | a0001c0002t0001g0219a0001c0002t0001g0220a0001c0002t0001g0305others(1): Show | 4 | HG00639.hp1 HG01099.hp2 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.270+483G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995797 | ||||||
chr7:150995798 | C | A | 2 | a0001c0002t0001g0305a0001c0002t0001g0306 | 2 | HG00639.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.270+484C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995798 | ||||||
chr7:150995800 | C | T | 3 | a0001c0001t0001g0037a0001c0002t0001g0038a0001c0002t0001g0039 | 3 | HG02055.hp1 HG02615.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.270+486C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995800 | ||||||
chr7:150995814 | C | G | 3 | a0001c0001t0001g0037a0001c0002t0001g0038a0001c0002t0001g0039 | 3 | HG02055.hp1 HG02615.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.270+500C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995814 | ||||||
chr7:150995818 | C | T | 1 | a0001c0002t0001g0059 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.270+504C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995818 | ||||||
chr7:150995819 | G | A | 5 | a0001c0002t0001g0219a0001c0002t0001g0220a0001c0002t0001g0264others(2): Show | 5 | HG00639.hp1 HG01099.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.270+505G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995819 | ||||||
chr7:150995819 | G | GTCCCACC others(92): Show |
3 | a0001c0001t0001g0037a0001c0002t0001g0038a0001c0002t0001g0039 | 3 | HG02055.hp1 HG02615.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.270+515_270+516ins others(99): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995819 | |||||
chr7:150995822 | C | T | 4 | a0001c0002t0001g0089a0001c0002t0001g0090a0001c0002t0001g0091others(1): Show | 4 | HG02451.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.270+508C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995822 | ||||||
chr7:150995825 | C | T | 1 | a0001c0002t0001g0264 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+511C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995825 | ||||||
chr7:150995833 | T | C | 6 | a0001c0001t0001g0037a0001c0002t0001g0038a0001c0002t0001g0039others(3): Show | 6 | HG00639.hp1 HG01099.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.270+519T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995833 | ||||||
chr7:150995847 | G | C | 5 | a0001c0001t0001g0037a0001c0002t0001g0038a0001c0002t0001g0039others(2): Show | 5 | HG00639.hp1 HG01099.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.270+533G>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995847 | ||||||
chr7:150995852 | G | A | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | HG02132.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.270+538G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995852 | ||||||
chr7:150995863 | A | ACACCCCT others(472): Show |
1 | a0003c0037t0001g0332 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.271-488_271-487ins others(479): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995863 | |||||
chr7:150995863 | A | ACACCCCT others(25): Show |
4 | a0003c0006t0001g0093a0003c0006t0001g0334a0003c0006t0001g0335others(1): Show | 4 | HG02630.hp1 HG02818.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-521_271-520ins others(32): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995863 | |||||
chr7:150995863 | A | G | 5 | a0001c0001t0001g0037a0001c0002t0001g0038a0001c0002t0001g0039others(2): Show | 5 | HG00639.hp1 HG01099.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.271-541A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995863 | ||||||
chr7:150995866 | C | T | 5 | a0001c0001t0001g0037a0001c0002t0001g0038a0001c0002t0001g0039others(2): Show | 5 | HG00639.hp1 HG01099.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.271-538C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995866 | ||||||
chr7:150995880 | C | G | 3 | a0001c0001t0001g0037a0001c0002t0001g0038a0001c0002t0001g0039 | 3 | HG02055.hp1 HG02615.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.271-524C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995880 | ||||||
chr7:150995885 | A | G | 3 | a0001c0001t0001g0037a0001c0002t0001g0038a0001c0002t0001g0039 | 3 | HG02055.hp1 HG02615.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.271-519A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995885 | ||||||
chr7:150995891 | C | T | 1 | a0001c0001t0001g0284 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.271-513C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995891 | ||||||
chr7:150995896 | A | G | 1 | a0001c0001t0001g0284 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.271-508A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995896 | ||||||
chr7:150995897 | A | C | 4 | a0001c0001t0001g0037a0001c0001t0001g0284a0001c0002t0001g0038others(1): Show | 4 | HG02055.hp1 HG02615.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-507A>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995897 | ||||||
chr7:150995903 | T | C | 1 | a0010c0016t0001g0283 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.271-501T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995903 | ||||||
chr7:150995904 | C | T | 1 | a0010c0016t0001g0283 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.271-500C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995904 | ||||||
chr7:150995913 | C | CCCCGTCC others(89): Show |
4 | a0001c0002t0001g0089a0001c0002t0001g0090a0001c0002t0001g0091others(1): Show | 4 | HG02451.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-488_271-487ins others(96): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995913 | |||||
chr7:150995916 | CT | C | 7 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(4): Show | 7 | HG01243.hp2 HG02683.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.271-487delT | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995916 | ||||||
chr7:150995917 | T | C | 8 | a0001c0001t0001g0037a0001c0001t0001g0284a0001c0002t0001g0038others(5): Show | 8 | HG02055.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.271-487T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995917 | ||||||
chr7:150995917 | T | TGTCCCAT others(25): Show |
1 | a0001c0001t0001g0251 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.271-437_271-406dup others(32): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995917 | |||||
chr7:150995917 | TGTCCCAT others(25): Show |
T | 2 | a0001c0001t0001g0148a0001c0001t0001g0265 | 2 | HG00140.hp2 HG00733.hp2 |
intron_variant | MODIFIER | c.271-437_271-406del others(32): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995917 | |||||
chr7:150995918 | G | A | 3 | a0001c0001t0001g0037a0001c0002t0001g0038a0001c0002t0001g0039 | 3 | HG02055.hp1 HG02615.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.271-486G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995918 | ||||||
chr7:150995919 | T | A | 4 | a0001c0002t0001g0089a0001c0002t0001g0090a0001c0002t0001g0091others(1): Show | 4 | HG02451.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-485T>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995919 | ||||||
chr7:150995924 | T | C | 8 | a0001c0001t0001g0037a0001c0001t0001g0284a0001c0002t0001g0038others(5): Show | 8 | HG02055.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.271-480T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995924 | ||||||
chr7:150995929 | G | A | 4 | a0001c0001t0001g0037a0001c0001t0001g0284a0001c0002t0001g0038others(1): Show | 4 | HG02055.hp1 HG02615.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-475G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995929 | ||||||
chr7:150995930 | C | A | 4 | a0001c0001t0001g0037a0001c0001t0001g0284a0001c0002t0001g0038others(1): Show | 4 | HG02055.hp1 HG02615.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-474C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995930 | ||||||
chr7:150995930 | C | CACCCCTC others(126): Show |
7 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(4): Show | 7 | HG01243.hp2 HG02683.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.271-470_271-469ins others(133): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995930 | |||||
chr7:150995930 | C | T | 1 | a0001c0002t0001g0127 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.271-474C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995930 | ||||||
chr7:150995935 | T | C | 15 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(12): Show | 15 | HG01243.hp2 HG02055.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.271-469T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995935 | ||||||
chr7:150995956 | T | C | 4 | a0001c0002t0001g0089a0001c0002t0001g0090a0001c0002t0001g0091others(1): Show | 4 | HG02451.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-448T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995956 | ||||||
chr7:150995964 | C | T | 4 | a0001c0002t0001g0089a0001c0002t0001g0090a0001c0002t0001g0091others(1): Show | 4 | HG02451.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-440C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995964 | ||||||
chr7:150995965 | C | T | 81 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(78): Show | 86 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.271-439C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995965 | ||||||
chr7:150995967 | T | C | 85 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(82): Show | 90 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.271-437T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995967 | ||||||
chr7:150995969 | C | A | 81 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(78): Show | 86 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.271-435C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995969 | ||||||
chr7:150995972 | C | A | 38 | a0001c0001t0001g0303a0001c0002t0001g0010a0001c0002t0001g0031others(35): Show | 43 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.271-432C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995972 | ||||||
chr7:150995977 | T | TC | 82 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(79): Show | 87 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.271-423dupC | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995977 | |||||
chr7:150995977 | T | TG | 4 | a0001c0002t0001g0089a0001c0002t0001g0090a0001c0002t0001g0091others(1): Show | 4 | HG02451.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-427_271-426ins others(1): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995977 | ||||||
chr7:150995978 | CCCCGTCC others(92): Show |
C | 1 | a0001c0002t0001g0285 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.271-422_271-324del others(99): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995978 | |||||
chr7:150995981 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.271-423C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995981 | ||||||
chr7:150995982 | G | C | 1 | a0001c0001t0001g0221 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.271-422G>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995982 | ||||||
chr7:150995988 | T | C | 5 | a0001c0001t0001g0221a0001c0002t0001g0089a0001c0002t0001g0090others(2): Show | 5 | HG02451.hp1 HG02622.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.271-416T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995988 | ||||||
chr7:150995988 | T | TCCCTGCA others(27): Show |
1 | a0002c0034t0001g0113 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.271-392_271-359dup others(34): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995988 | |||||
chr7:150995993 | G | A | 4 | a0001c0002t0001g0089a0001c0002t0001g0090a0001c0002t0001g0091others(1): Show | 4 | HG02451.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-411G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995993 | ||||||
chr7:150995997 | C | T | 4 | a0001c0001t0001g0284a0001c0002t0001g0059a0001c0002t0001g0060others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-407C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995997 | ||||||
chr7:150996001 | C | A | 4 | a0001c0001t0001g0284a0001c0002t0001g0059a0001c0002t0001g0060others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-403C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996001 | ||||||
chr7:150996004 | C | A | 4 | a0001c0001t0001g0284a0001c0002t0001g0059a0001c0002t0001g0060others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-400C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996004 | ||||||
chr7:150996009 | TG | T | 4 | a0001c0001t0001g0284a0001c0002t0001g0059a0001c0002t0001g0060others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-394delG | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996009 | ||||||
chr7:150996009 | TGC | T | 4 | a0001c0002t0001g0089a0001c0002t0001g0090a0001c0002t0001g0091others(1): Show | 4 | HG02451.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-394_271-393del others(2): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996009 | ||||||
chr7:150996012 | T | C | 8 | a0001c0001t0001g0284a0001c0002t0001g0059a0001c0002t0001g0060others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.271-392T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996012 | ||||||
chr7:150996012 | TCCCATCC others(59): Show |
T | 39 | a0001c0001t0001g0142a0001c0001t0001g0303a0001c0002t0001g0010others(36): Show | 44 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.271-346_271-281del others(66): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150996012 | |||||
chr7:150996016 | A | G | 4 | a0001c0001t0001g0284a0001c0002t0001g0059a0001c0002t0001g0060others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-388A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996016 | ||||||
chr7:150996022 | C | T | 4 | a0001c0001t0001g0284a0001c0002t0001g0059a0001c0002t0001g0060others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-382C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996022 | ||||||
chr7:150996033 | C | T | 4 | a0001c0002t0001g0089a0001c0002t0001g0090a0001c0002t0001g0091others(1): Show | 4 | HG02451.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-371C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996033 | ||||||
chr7:150996045 | CCCCTACC others(25): Show |
C | 4 | a0001c0001t0001g0284a0001c0002t0001g0059a0001c0002t0001g0060others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-355_271-324del others(32): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150996045 | |||||
chr7:150996049 | T | C | 4 | a0001c0002t0001g0089a0001c0002t0001g0090a0001c0002t0001g0091others(1): Show | 4 | HG02451.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-355T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996049 | ||||||
chr7:150996050 | A | G | 4 | a0001c0002t0001g0089a0001c0002t0001g0090a0001c0002t0001g0091others(1): Show | 4 | HG02451.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-354A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996050 | ||||||
chr7:150996051 | C | T | 4 | a0001c0002t0001g0089a0001c0002t0001g0090a0001c0002t0001g0091others(1): Show | 4 | HG02451.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-353C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996051 | ||||||
chr7:150996056 | C | CGCCTGTA others(91): Show |
4 | a0001c0002t0001g0089a0001c0002t0001g0090a0001c0002t0001g0091others(1): Show | 4 | HG02451.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-348_271-347ins others(98): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996056 | ||||||
chr7:150996058 | T | C | 4 | a0001c0002t0001g0089a0001c0002t0001g0090a0001c0002t0001g0091others(1): Show | 4 | HG02451.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-346T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996058 | ||||||
chr7:150996074 | T | C | 4 | a0001c0002t0001g0089a0001c0002t0001g0090a0001c0002t0001g0091others(1): Show | 4 | HG02451.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-330T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996074 | ||||||
chr7:150996077 | T | TGC | 4 | a0001c0002t0001g0089a0001c0002t0001g0090a0001c0002t0001g0091others(1): Show | 4 | HG02451.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-327_271-326ins others(2): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996077 | ||||||
chr7:150996078 | C | T | 8 | a0001c0001t0001g0284a0001c0002t0001g0059a0001c0002t0001g0060others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.271-326C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996078 | ||||||
chr7:150996082 | A | G | 1 | a0001c0002t0001g0285 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.271-322A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996082 | ||||||
chr7:150996088 | C | T | 1 | a0001c0002t0001g0285 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.271-316C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996088 | ||||||
chr7:150996124 | C | CCTGCACC others(188): Show |
1 | a0002c0003t0001g0094 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.271-265_271-264ins others(195): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150996124 | |||||
chr7:150996124 | C | CCTGCACC others(191): Show |
4 | a0002c0003t0001g0100a0002c0003t0001g0101a0002c0003t0001g0102others(1): Show | 4 | HG00621.hp1 HG02074.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-265_271-264ins others(198): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150996124 | |||||
chr7:150996195 | C | T | 1 | a0002c0003t0001g0112 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.271-209C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996195 | ||||||
chr7:150996197 | C | T | 1 | a0001c0002t0001g0304 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.271-207C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996197 | ||||||
chr7:150996242 | ACCCATCC others(26): Show |
A | 1 | a0001c0004t0001g0149 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.271-150_271-118del others(33): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150996242 | |||||
chr7:150996248 | C | G | 2 | a0002c0003t0001g0319a0002c0003t0001g0320 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.271-156C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996248 | ||||||
chr7:150996267 | TC | T | 3 | a0001c0002t0001g0145a0002c0003t0001g0094a0010c0016t0001g0283 | 3 | HG03669.hp1 NA19055.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.271-134delC | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150996267 | |||||
chr7:150996342 | C | G | 12 | a0001c0001t0001g0053a0001c0002t0001g0048a0001c0002t0001g0049others(9): Show | 12 | HG02486.hp1 HG02647.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.271-62C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996342 | ||||||
chr7:150996595 | G | C | 1 | a0001c0001t0001g0150 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.419+43G>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 4/26 | chr7 | 150996595 | ||||||
chr7:150996597 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.419+45C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 4/26 | chr7 | 150996597 | ||||||
chr7:150996614 | C | T | 1 | a0001c0002t0001g0061 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.419+62C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 4/26 | chr7 | 150996614 | ||||||
chr7:150996746 | A | G | 3 | a0001c0002t0001g0325a0001c0002t0007g0327a0001c0010t0001g0326 | 3 | HG02976.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.420-17A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 4/26 | chr7 | 150996746 | ||||||
chr7:150997141 | T | G | 1 | a0001c0002t0001g0307 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.582+216T>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/26 | chr7 | 150997141 | ||||||
chr7:150997169 | A | AGAAGTCT others(20): Show |
6 | a0001c0002t0001g0127a0001c0002t0001g0254a0001c0002t0001g0255others(3): Show | 6 | HG02615.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.582+317_582+343dup others(27): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr7 | 150997169 | |||||
chr7:150997169 | AGAAGTCT others(20): Show |
A | 63 | a0001c0001t0001g0053a0001c0001t0001g0284a0001c0001t0001g0303others(60): Show | 67 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.582+317_582+343del others(27): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr7 | 150997169 | |||||
chr7:150997242 | A | G | 2 | a0001c0001t0001g0253a0010c0016t0001g0283 | 2 | HG00408.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.582+317A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/26 | chr7 | 150997242 | ||||||
chr7:150997269 | GGGGGTGA others(19): Show |
G | 1 | a0010c0016t0001g0283 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.582+349_582+374del others(26): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr7 | 150997269 | |||||
chr7:150997334 | G | A | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | NA18952.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.582+409G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/26 | chr7 | 150997334 | ||||||
chr7:150997351 | C | G | 1 | a0001c0002t0001g0218 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.582+426C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/26 | chr7 | 150997351 | ||||||
chr7:150997450 | A | AC | 15 | a0001c0001t0001g0078a0001c0001t0001g0095a0001c0001t0001g0121others(12): Show | 15 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.582+529dupC | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr7 | 150997450 | |||||
chr7:150997474 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.582+549G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/26 | chr7 | 150997474 | ||||||
chr7:150997502 | A | C | 1 | a0001c0001t0001g0215 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.582+577A>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/26 | chr7 | 150997502 | ||||||
chr7:150997518 | A | G | 92 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(89): Show | 98 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.582+593A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/26 | chr7 | 150997518 | ||||||
chr7:150997583 | C | G | 1 | a0001c0002t0001g0225 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.582+658C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/26 | chr7 | 150997583 | ||||||
chr7:150997807 | C | T | 2 | a0001c0002t0001g0040a0001c0002t0001g0041 | 2 | HG02970.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.583-550C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/26 | chr7 | 150997807 | ||||||
chr7:150997820 | G | A | 1 | a0001c0002t0004g0286 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.583-537G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/26 | chr7 | 150997820 | ||||||
chr7:150997975 | A | T | 1 | a0001c0002t0001g0307 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.583-382A>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/26 | chr7 | 150997975 | ||||||
chr7:150997976 | T | A | 1 | a0001c0002t0001g0307 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.583-381T>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/26 | chr7 | 150997976 | ||||||
chr7:150997992 | G | A | 1 | a0003c0006t0001g0334 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.583-365G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/26 | chr7 | 150997992 | ||||||
chr7:150998096 | T | C | 3 | a0001c0002t0001g0325a0001c0002t0007g0327a0001c0010t0001g0326 | 3 | HG02976.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.583-261T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/26 | chr7 | 150998096 | ||||||
chr7:150998107 | G | A | 40 | a0001c0001t0001g0284a0001c0001t0001g0303a0001c0002t0001g0010others(37): Show | 44 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.583-250G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/26 | chr7 | 150998107 | ||||||
chr7:150998126 | A | G | 92 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(89): Show | 98 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.583-231A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/26 | chr7 | 150998126 | ||||||
chr7:150998504 | G | A | 3 | a0001c0001t0001g0066a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG02602.hp1 HG03492.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.675-35G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 6/26 | chr7 | 150998504 | ||||||
chr7:150998714 | C | A | 1 | a0010c0016t0001g0283 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.816+34C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 7/26 | chr7 | 150998714 | ||||||
chr7:150998717 | G | A | 1 | a0001c0002t0001g0155 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.816+37G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 7/26 | chr7 | 150998717 | ||||||
chr7:150998811 | A | C | 1 | a0002c0003t0001g0112 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.816+131A>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 7/26 | chr7 | 150998811 | ||||||
chr7:150998871 | A | G | 1 | a0001c0001t0001g0253 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.817-75A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 7/26 | chr7 | 150998871 | ||||||
chr7:150998920 | A | G | 167 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0014others(164): Show | 185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.817-26A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 7/26 | chr7 | 150998920 | ||||||
chr7:150999385 | C | G | 2 | a0001c0002t0001g0040a0001c0002t0001g0041 | 2 | HG02970.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1131+21C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | chr7 | 150999385 | ||||||
chr7:150999542 | AGGGGTGT others(5): Show |
A | 1 | a0001c0023t0001g0086 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1131+187_1131+198d others(14): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr7 | 150999542 | |||||
chr7:150999839 | G | T | 2 | a0007c0009t0001g0077a0007c0009t0001g0214 | 2 | NA18970.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1131+475G>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | chr7 | 150999839 | ||||||
chr7:150999896 | GTGA | G | 19 | a0001c0001t0001g0176a0002c0003t0001g0013a0002c0003t0001g0064others(16): Show | 20 | HG00621.hp1 HG00642.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.1131+533_1131+535d others(5): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | chr7 | 150999896 | ||||||
chr7:150999899 | A | G | 1 | a0002c0003t0001g0094 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1131+535A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | chr7 | 150999899 | ||||||
chr7:150999909 | A | G | 20 | a0001c0001t0001g0176a0002c0003t0001g0013a0002c0003t0001g0064others(17): Show | 21 | HG00621.hp1 HG00642.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.1131+545A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | chr7 | 150999909 | ||||||
chr7:150999911 | T | C | 20 | a0001c0001t0001g0176a0002c0003t0001g0013a0002c0003t0001g0064others(17): Show | 21 | HG00621.hp1 HG00642.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.1131+547T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | chr7 | 150999911 | ||||||
chr7:150999925 | T | C | 20 | a0001c0001t0001g0176a0002c0003t0001g0013a0002c0003t0001g0064others(17): Show | 21 | HG00621.hp1 HG00642.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.1131+561T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | chr7 | 150999925 | ||||||
chr7:150999956 | G | C | 1 | a0005c0007t0001g0087 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1132-542G>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | chr7 | 150999956 | ||||||
chr7:151000007 | G | A | 17 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(14): Show | 17 | HG01243.hp2 HG02055.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1132-491G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | chr7 | 151000007 | ||||||
chr7:151000008 | C | T | 1 | a0001c0002t0007g0327 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1132-490C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | chr7 | 151000008 | ||||||
chr7:151000058 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1132-440G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | chr7 | 151000058 | ||||||
chr7:151000099 | A | T | 1 | a0010c0016t0001g0283 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1132-399A>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | chr7 | 151000099 | ||||||
chr7:151000101 | T | A | 1 | a0010c0016t0001g0283 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1132-397T>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | chr7 | 151000101 | ||||||
chr7:151000118 | G | A | 5 | a0001c0002t0001g0059a0001c0002t0001g0060a0001c0002t0001g0061others(2): Show | 5 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1132-380G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | chr7 | 151000118 | ||||||
chr7:151000120 | G | T | 1 | a0001c0002t0001g0062 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1132-378G>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | chr7 | 151000120 | ||||||
chr7:151000206 | A | G | 42 | a0001c0002t0001g0010a0001c0002t0001g0031a0001c0002t0001g0032others(39): Show | 46 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.1132-292A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | chr7 | 151000206 | ||||||
chr7:151000245 | C | A | 267 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0014others(264): Show | 302 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.1132-253C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | chr7 | 151000245 | ||||||
chr7:151000293 | A | G | 1 | a0001c0002t0001g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1132-205A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | chr7 | 151000293 | ||||||
chr7:151000299 | G | A | 8 | a0001c0005t0001g0011a0001c0005t0001g0043a0001c0005t0001g0044others(5): Show | 10 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1132-199G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | chr7 | 151000299 | ||||||
chr7:151000451 | C | G | 1 | a0001c0002t0001g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1132-47C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | chr7 | 151000451 | ||||||
chr7:151000712 | A | G | 1 | a0001c0001t0001g0152 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1233+113A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 10/26 | chr7 | 151000712 | ||||||
chr7:151000723 | C | T | 1 | a0001c0002t0001g0208 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1233+124C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 10/26 | chr7 | 151000723 | ||||||
chr7:151000743 | G | A | 1 | a0001c0002t0001g0267 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1233+144G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 10/26 | chr7 | 151000743 | ||||||
chr7:151000872 | G | A | 1 | a0001c0002t0001g0304 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1233+273G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 10/26 | chr7 | 151000872 | ||||||
chr7:151000986 | T | G | 1 | a0001c0002t0001g0062 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1234-245T>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 10/26 | chr7 | 151000986 | ||||||
chr7:151000988 | G | T | 1 | a0001c0002t0001g0062 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1234-243G>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 10/26 | chr7 | 151000988 | ||||||
chr7:151000991 | T | G | 1 | a0001c0002t0001g0062 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1234-240T>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 10/26 | chr7 | 151000991 | ||||||
chr7:151000992 | G | T | 1 | a0002c0003t0001g0094 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1234-239G>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 10/26 | chr7 | 151000992 | ||||||
chr7:151001008 | G | A | 2 | a0001c0002t0001g0040a0001c0002t0001g0041 | 2 | HG02970.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1234-223G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 10/26 | chr7 | 151001008 | ||||||
chr7:151001181 | C | T | 2 | a0001c0001t0001g0076a0001c0001t0001g0081 | 2 | HG00735.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1234-50C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 10/26 | chr7 | 151001181 | ||||||
chr7:151001690 | A | C | 1 | a0001c0001t0001g0207 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1502+73A>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 12/26 | chr7 | 151001690 | ||||||
chr7:151001740 | G | A | 1 | a0001c0002t0001g0325 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1503-81G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 12/26 | chr7 | 151001740 | ||||||
chr7:151001791 | A | G | 209 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0014others(206): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1503-30A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 12/26 | chr7 | 151001791 | ||||||
chr7:151002157 | C | A | 1 | a0001c0002t0001g0287 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1648-43C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 13/26 | chr7 | 151002157 | ||||||
chr7:151002162 | G | T | 41 | a0001c0002t0001g0010a0001c0002t0001g0031a0001c0002t0001g0048others(38): Show | 44 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.1648-38G>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 13/26 | chr7 | 151002162 | ||||||
chr7:151002383 | A | AAC | 21 | a0001c0001t0001g0079a0001c0001t0001g0123a0001c0001t0001g0146others(18): Show | 26 | HG00140.hp1 HG01074.hp2 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.1752+148_1752+149d others(4): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | |||||
chr7:151002383 | A | AACAC | 22 | a0001c0001t0001g0029a0001c0001t0001g0144a0001c0001t0001g0162others(19): Show | 24 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(21): Show |
intron_variant | MODIFIER | c.1752+146_1752+149d others(6): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | |||||
chr7:151002383 | A | AACACAC | 21 | a0001c0001t0001g0034a0001c0001t0001g0176a0001c0001t0001g0221others(18): Show | 24 | HG00423.hp2 HG00639.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.1752+144_1752+149d others(8): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | |||||
chr7:151002383 | A | AACACACA others(1): Show |
15 | a0001c0001t0001g0028a0001c0001t0001g0055a0001c0001t0001g0072others(12): Show | 17 | HG00621.hp2 HG01099.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1752+142_1752+149d others(10): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | |||||
chr7:151002383 | A | AACACACA others(3): Show |
5 | a0001c0002t0001g0038a0001c0002t0001g0159a0001c0002t0001g0160others(2): Show | 5 | HG00621.hp1 HG01192.hp2 HG02015.hp1 others(2): Show |
intron_variant | MODIFIER | c.1752+140_1752+149d others(12): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | |||||
chr7:151002383 | A | AACACACA others(5): Show |
2 | a0001c0002t0001g0158a0001c0002t0001g0288 | 2 | HG01070.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.1752+138_1752+149d others(14): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | |||||
chr7:151002383 | A | AACACACA others(9): Show |
1 | a0001c0002t0001g0243 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1752+134_1752+149d others(18): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | |||||
chr7:151002383 | A | AACACACA others(11): Show |
1 | a0001c0002t0001g0157 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1752+132_1752+149d others(20): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | |||||
chr7:151002383 | AAC | A | 27 | a0001c0001t0001g0037a0001c0001t0001g0076a0001c0001t0001g0128others(24): Show | 30 | HG00408.hp2 HG00735.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.1752+148_1752+149d others(4): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | |||||
chr7:151002383 | AACAC | A | 30 | a0001c0001t0001g0053a0001c0001t0001g0124a0001c0001t0001g0130others(27): Show | 30 | HG00099.hp2 HG00558.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.1752+146_1752+149d others(6): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | |||||
chr7:151002383 | AACACAC | A | 20 | a0001c0001t0001g0036a0001c0001t0001g0078a0001c0001t0001g0125others(17): Show | 21 | HG00733.hp1 HG01243.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.1752+144_1752+149d others(8): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | |||||
chr7:151002383 | AACACACA others(1): Show |
A | 22 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0095others(19): Show | 26 | HG00544.hp1 HG00609.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.1752+142_1752+149d others(10): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | |||||
chr7:151002383 | AACACACA others(3): Show |
A | 25 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0098others(22): Show | 29 | HG00438.hp1 HG00558.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1752+140_1752+149d others(12): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | |||||
chr7:151002383 | AACACACA others(5): Show |
A | 17 | a0001c0001t0001g0080a0001c0001t0001g0121a0001c0001t0001g0142others(14): Show | 17 | HG00323.hp1 HG00597.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.1752+138_1752+149d others(14): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | |||||
chr7:151002383 | AACACACA others(7): Show |
A | 10 | a0001c0001t0001g0007a0001c0001t0001g0154a0001c0001t0001g0190others(7): Show | 14 | HG01069.hp2 HG02602.hp2 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.1752+136_1752+149d others(16): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | |||||
chr7:151002383 | AACACACA others(9): Show |
A | 16 | a0001c0001t0001g0009a0001c0001t0001g0135a0001c0001t0001g0151others(13): Show | 19 | HG00423.hp1 HG00597.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.1752+134_1752+149d others(18): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | |||||
chr7:151002383 | AACACACA others(11): Show |
A | 17 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0066others(14): Show | 18 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.1752+132_1752+149d others(20): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | |||||
chr7:151002383 | AACACACA others(13): Show |
A | 12 | a0001c0001t0001g0024a0001c0001t0001g0056a0001c0001t0001g0202others(9): Show | 13 | HG00323.hp2 HG00438.hp2 HG02735.hp2 others(10): Show |
intron_variant | MODIFIER | c.1752+130_1752+149d others(22): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | |||||
chr7:151002383 | AACACACA others(15): Show |
A | 10 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0074others(7): Show | 12 | HG01978.hp2 HG02027.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.1752+128_1752+149d others(24): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | |||||
chr7:151002383 | AACACACA others(17): Show |
A | 2 | a0001c0001t0001g0206a0001c0002t0001g0060 | 2 | HG01884.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1752+126_1752+149d others(26): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | |||||
chr7:151002383 | AACACACA others(19): Show |
A | 4 | a0001c0002t0001g0059a0001c0002t0001g0131a0001c0002t0001g0172others(1): Show | 4 | HG02258.hp2 HG02886.hp1 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.1752+124_1752+149d others(28): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | |||||
chr7:151002383 | AACACACA others(23): Show |
A | 2 | a0001c0002t0001g0054a0001c0002t0001g0281 | 2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1752+120_1752+149d others(32): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | |||||
chr7:151002383 | AACACACA others(25): Show |
A | 2 | a0001c0002t0001g0048a0001c0002t0001g0049 | 2 | HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1752+118_1752+149d others(34): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | |||||
chr7:151002383 | AACACACA others(29): Show |
A | 2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | NA18963.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.1752+114_1752+149d others(38): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | |||||
chr7:151002383 | AACACACA others(33): Show |
A | 1 | a0001c0002t0001g0061 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1752+110_1752+149d others(42): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | |||||
chr7:151002384 | A | C | 1 | a0012c0025t0001g0175 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1752+80A>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151002384 | ||||||
chr7:151002385 | C | A | 1 | a0012c0025t0001g0175 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1752+81C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151002385 | ||||||
chr7:151002444 | ACACACAC others(3): Show |
A | 1 | a0002c0003t0001g0112 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1752+142_1752+151d others(12): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002444 | |||||
chr7:151002523 | C | G | 44 | a0001c0002t0001g0010a0001c0002t0001g0031a0001c0002t0001g0048others(41): Show | 47 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.1752+219C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151002523 | ||||||
chr7:151002568 | C | T | 2 | a0002c0003t0001g0115a0002c0003t0001g0116 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1752+264C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151002568 | ||||||
chr7:151002696 | T | C | 1 | a0002c0003t0001g0094 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1752+392T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151002696 | ||||||
chr7:151002710 | A | G | 8 | a0001c0002t0001g0127a0001c0002t0001g0254a0001c0002t0001g0255others(5): Show | 8 | HG02615.hp2 HG02622.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1752+406A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151002710 | ||||||
chr7:151002789 | G | A | 260 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0014others(257): Show | 293 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.1752+485G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151002789 | ||||||
chr7:151002804 | C | CATTTT | 18 | a0001c0002t0001g0040a0001c0002t0001g0041a0001c0002t0001g0089others(15): Show | 18 | HG01109.hp1 HG01952.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.1752+510_1752+514d others(7): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002804 | |||||
chr7:151002806 | TTTTATTT others(2): Show |
T | 154 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0014others(151): Show | 172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.1752+506_1752+514d others(11): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002806 | |||||
chr7:151002846 | C | T | 112 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0014others(109): Show | 127 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.1752+542C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151002846 | ||||||
chr7:151002847 | G | A | 1 | a0001c0002t0007g0327 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1752+543G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151002847 | ||||||
chr7:151002864 | T | TG | 4 | a0001c0002t0001g0040a0001c0002t0001g0041a0001c0002t0001g0089others(1): Show | 4 | HG02451.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1752+561dupG | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002864 | |||||
chr7:151002869 | T | C | 1 | a0001c0023t0001g0086 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1752+565T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151002869 | ||||||
chr7:151002893 | C | T | 17 | a0001c0002t0001g0040a0001c0002t0001g0041a0001c0002t0001g0089others(14): Show | 17 | HG01109.hp1 HG01952.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1752+589C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151002893 | ||||||
chr7:151003203 | G | A | 39 | a0001c0002t0001g0010a0001c0002t0001g0031a0001c0002t0001g0048others(36): Show | 42 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1752+899G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151003203 | ||||||
chr7:151003395 | C | G | 4 | a0001c0002t0001g0090a0001c0002t0001g0325a0001c0010t0001g0326others(1): Show | 4 | HG02622.hp1 HG02976.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1752+1091C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151003395 | ||||||
chr7:151003427 | T | G | 88 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(85): Show | 103 | HG00323.hp1 HG00544.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.1752+1123T>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151003427 | ||||||
chr7:151003549 | A | G | 39 | a0001c0002t0001g0010a0001c0002t0001g0031a0001c0002t0001g0048others(36): Show | 42 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1752+1245A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151003549 | ||||||
chr7:151003858 | C | A | 19 | a0001c0001t0001g0176a0002c0003t0001g0013a0002c0003t0001g0064others(16): Show | 20 | HG00621.hp1 HG00741.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.1752+1554C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151003858 | ||||||
chr7:151004004 | T | C | 1 | a0002c0003t0001g0279 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1752+1700T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151004004 | ||||||
chr7:151004153 | A | G | 8 | a0001c0005t0001g0011a0001c0005t0001g0043a0001c0005t0001g0044others(5): Show | 10 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1752+1849A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151004153 | ||||||
chr7:151004210 | G | A | 4 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0054others(1): Show | 4 | HG02647.hp2 HG02818.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1752+1906G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151004210 | ||||||
chr7:151004636 | T | C | 1 | a0001c0001t0001g0210 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1753-1791T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151004636 | ||||||
chr7:151004667 | G | A | 4 | a0001c0002t0001g0040a0001c0002t0001g0041a0001c0002t0001g0089others(1): Show | 4 | HG02451.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1753-1760G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151004667 | ||||||
chr7:151004695 | G | A | 114 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0014others(111): Show | 129 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1753-1732G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151004695 | ||||||
chr7:151004748 | G | C | 4 | a0001c0002t0001g0040a0001c0002t0001g0041a0001c0002t0001g0089others(1): Show | 4 | HG02451.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1753-1679G>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151004748 | ||||||
chr7:151004838 | A | ATGTT | 5 | a0001c0002t0001g0090a0001c0002t0007g0327a0002c0003t0001g0103others(2): Show | 5 | HG02071.hp1 HG02129.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1753-1563_1753-156 others(8): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151004838 | |||||
chr7:151004838 | ATGTT | A | 136 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0014others(133): Show | 151 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.1753-1563_1753-156 others(8): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151004838 | |||||
chr7:151004838 | ATGTTTGT others(5): Show |
A | 4 | a0001c0002t0001g0059a0001c0002t0001g0060a0001c0002t0001g0061others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1753-1571_1753-156 others(16): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151004838 | |||||
chr7:151004951 | C | A | 1 | a0001c0001t0001g0215 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1753-1476C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151004951 | ||||||
chr7:151004983 | G | A | 114 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0014others(111): Show | 129 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1753-1444G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151004983 | ||||||
chr7:151005131 | C | T | 114 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0014others(111): Show | 129 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1753-1296C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151005131 | ||||||
chr7:151005243 | G | A | 4 | a0001c0002t0001g0040a0001c0002t0001g0041a0001c0002t0001g0089others(1): Show | 4 | HG02451.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1753-1184G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151005243 | ||||||
chr7:151005344 | A | T | 48 | a0001c0002t0001g0010a0001c0002t0001g0031a0001c0002t0001g0048others(45): Show | 51 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.1753-1083A>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151005344 | ||||||
chr7:151005503 | A | G | 4 | a0001c0002t0001g0040a0001c0002t0001g0041a0001c0002t0001g0089others(1): Show | 4 | HG02451.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1753-924A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151005503 | ||||||
chr7:151005536 | T | C | 1 | a0004c0031t0001g0051 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1753-891T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151005536 | ||||||
chr7:151005693 | C | A | 113 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0014others(110): Show | 128 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.1753-734C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151005693 | ||||||
chr7:151005693 | C | T | 1 | a0003c0006t0001g0337 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1753-734C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151005693 | ||||||
chr7:151005769 | GACTGAGG others(4): Show |
G | 1 | a0001c0001t0001g0196 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1753-657_1753-647d others(13): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151005769 | ||||||
chr7:151005933 | A | C | 1 | a0001c0002t0001g0254 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1753-494A>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151005933 | ||||||
chr7:151005953 | C | T | 133 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(130): Show | 151 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(148): Show |
intron_variant | MODIFIER | c.1753-474C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151005953 | ||||||
chr7:151006000 | C | T | 1 | a0001c0023t0001g0086 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1753-427C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151006000 | ||||||
chr7:151006042 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1753-385C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151006042 | ||||||
chr7:151006043 | G | A | 2 | a0001c0002t0001g0089a0001c0002t0001g0091 | 2 | HG02451.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1753-384G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151006043 | ||||||
chr7:151006130 | T | TA | 7 | a0001c0001t0001g0193a0001c0001t0001g0211a0001c0002t0007g0327others(4): Show | 7 | HG01109.hp1 HG01952.hp1 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.1753-288dupA | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151006130 | |||||
chr7:151006154 | A | G | 82 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(79): Show | 97 | HG00323.hp1 HG00544.hp2 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.1753-273A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151006154 | ||||||
chr7:151006604 | C | T | 11 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0029others(8): Show | 14 | HG00408.hp1 HG01069.hp1 HG02040.hp1 others(11): Show |
intron_variant | MODIFIER | c.1820+110C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 15/26 | chr7 | 151006604 | ||||||
chr7:151006654 | C | CT | 40 | a0001c0002t0001g0010a0001c0002t0001g0031a0001c0002t0001g0048others(37): Show | 43 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.1820+160_1820+161i others(3): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 15/26 | chr7 | 151006654 | ||||||
chr7:151006799 | A | T | 1 | a0001c0002t0001g0169 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1821-90A>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 15/26 | chr7 | 151006799 | ||||||
chr7:151006827 | G | T | 192 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0014others(189): Show | 222 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.1821-62G>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 15/26 | chr7 | 151006827 | ||||||
chr7:151007054 | C | G | 1 | a0001c0002t0001g0281 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1938-48C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 16/26 | chr7 | 151007054 | ||||||
chr7:151007285 | A | G | 1 | a0001c0001t0001g0111 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2112+9A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 17/26 | chr7 | 151007285 | ||||||
chr7:151007312 | C | A | 53 | a0001c0002t0001g0010a0001c0002t0001g0031a0001c0002t0001g0048others(50): Show | 58 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.2112+36C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 17/26 | chr7 | 151007312 | ||||||
chr7:151007391 | A | G | 5 | a0001c0001t0001g0121a0001c0001t0001g0189a0001c0001t0001g0227others(2): Show | 5 | HG01891.hp2 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2112+115A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 17/26 | chr7 | 151007391 | ||||||
chr7:151007563 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2112+287C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 17/26 | chr7 | 151007563 | ||||||
chr7:151007599 | C | A | 1 | a0001c0002t0001g0161 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2112+323C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 17/26 | chr7 | 151007599 | ||||||
chr7:151007750 | G | T | 1 | a0001c0001t0001g0211 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2112+474G>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 17/26 | chr7 | 151007750 | ||||||
chr7:151007755 | G | A | 194 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0019others(191): Show | 223 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.2112+479G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 17/26 | chr7 | 151007755 | ||||||
chr7:151007888 | C | T | 3 | a0001c0002t0001g0295a0006c0012t0001g0292a0006c0012t0001g0294 | 3 | HG02129.hp2 HG02155.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.2112+612C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 17/26 | chr7 | 151007888 | ||||||
chr7:151007890 | GTTC | G | 8 | a0001c0005t0001g0011a0001c0005t0001g0043a0001c0005t0001g0044others(5): Show | 10 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.2112+615_2112+617d others(5): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 17/26 | chr7 | 151007890 | ||||||
chr7:151008111 | TC | T | 5 | a0001c0002t0001g0254a0001c0002t0001g0255a0001c0002t0001g0256others(2): Show | 5 | HG02615.hp2 HG02622.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.2113-818delC | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 17/26 | chr7 | 151008111 | ||||||
chr7:151008136 | T | C | 1 | a0001c0010t0001g0326 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2113-794T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 17/26 | chr7 | 151008136 | ||||||
chr7:151008237 | C | T | 2 | a0004c0013t0001g0012a0004c0031t0001g0051 | 3 | HG02109.hp1 HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2113-693C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 17/26 | chr7 | 151008237 | ||||||
chr7:151008522 | T | C | 36 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0025others(33): Show | 40 | HG00735.hp1 HG02027.hp1 HG02027.hp2 others(37): Show |
intron_variant | MODIFIER | c.2113-408T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 17/26 | chr7 | 151008522 | ||||||
chr7:151008680 | G | A | 1 | a0001c0002t0001g0297 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2113-250G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 17/26 | chr7 | 151008680 | ||||||
chr7:151008754 | G | A | 35 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0029others(32): Show | 38 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.2113-176G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 17/26 | chr7 | 151008754 | ||||||
chr7:151008880 | G | T | 1 | a0001c0002t0001g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2113-50G>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 17/26 | chr7 | 151008880 | ||||||
chr7:151008894 | C | CG | 4 | a0001c0001t0001g0189a0001c0001t0001g0227a0001c0001t0001g0228others(1): Show | 4 | HG02258.hp1 HG02280.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2113-33dupG | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr7 | 151008894 | |||||
chr7:151009089 | G | A | 4 | a0001c0002t0001g0038a0001c0002t0001g0039a0001c0002t0001g0069others(1): Show | 4 | HG01433.hp1 HG01496.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.2245+27G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 18/26 | chr7 | 151009089 | ||||||
chr7:151009102 | G | T | 1 | a0001c0001t0001g0179 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2245+40G>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 18/26 | chr7 | 151009102 | ||||||
chr7:151009289 | C | A | 6 | a0001c0005t0001g0011a0001c0005t0001g0043a0001c0005t0001g0044others(3): Show | 7 | HG01891.hp1 HG02280.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2324+22C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 19/26 | chr7 | 151009289 | ||||||
chr7:151009295 | C | A | 292 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0014others(289): Show | 329 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(326): Show |
intron_variant | MODIFIER | c.2324+28C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 19/26 | chr7 | 151009295 | ||||||
chr7:151009348 | G | GC | 158 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0024others(155): Show | 180 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.2325-45dupC | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr7 | 151009348 | |||||
chr7:151009648 | C | T | 1 | a0001c0023t0001g0086 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2512+63C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 20/26 | chr7 | 151009648 | ||||||
chr7:151009653 | C | A | 2 | a0001c0001t0001g0197a0003c0006t0001g0337 | 2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2512+68C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 20/26 | chr7 | 151009653 | ||||||
chr7:151009827 | G | A | 253 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0019others(250): Show | 284 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.2512+242G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 20/26 | chr7 | 151009827 | ||||||
chr7:151009994 | G | A | 1 | a0001c0001t0001g0203 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2513-121G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 20/26 | chr7 | 151009994 | ||||||
chr7:151010029 | T | C | 22 | a0001c0001t0001g0023a0001c0001t0001g0074a0001c0001t0001g0075others(19): Show | 23 | HG01884.hp2 HG01978.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.2513-86T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 20/26 | chr7 | 151010029 | ||||||
chr7:151010093 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2513-22G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 20/26 | chr7 | 151010093 | ||||||
chr7:151010104 | A | G | 1 | a0002c0003t0001g0104 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2513-11A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 20/26 | chr7 | 151010104 | ||||||
chr7:151010400 | C | T | 275 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0019others(272): Show | 307 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.2685+113C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 21/26 | chr7 | 151010400 | ||||||
chr7:151010427 | G | A | 1 | a0001c0024t0001g0085 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2685+140G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 21/26 | chr7 | 151010427 | ||||||
chr7:151010437 | G | T | 2 | a0001c0001t0001g0197a0003c0006t0001g0337 | 2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2685+150G>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 21/26 | chr7 | 151010437 | ||||||
chr7:151010855 | G | A | 15 | a0001c0001t0001g0023a0001c0001t0001g0074a0001c0001t0001g0075others(12): Show | 16 | HG01884.hp2 HG01978.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.2897-44G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 22/26 | chr7 | 151010855 | ||||||
chr7:151010860 | C | T | 1 | a0001c0002t0001g0049 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2897-39C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 22/26 | chr7 | 151010860 | ||||||
chr7:151011001 | A | G | 316 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0014others(313): Show | 355 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(352): Show |
intron_variant | MODIFIER | c.2984+15A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 23/26 | chr7 | 151011001 | ||||||
chr7:151011114 | G | A | 4 | a0001c0001t0001g0056a0002c0003t0001g0052a0002c0003t0001g0112others(1): Show | 4 | HG02486.hp1 HG02897.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2984+128G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 23/26 | chr7 | 151011114 | ||||||
chr7:151011127 | T | C | 2 | a0001c0001t0001g0162a0001c0001t0001g0232 | 2 | NA18946.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.2984+141T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 23/26 | chr7 | 151011127 | ||||||
chr7:151011210 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2984+224C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 23/26 | chr7 | 151011210 | ||||||
chr7:151011214 | G | T | 275 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0019others(272): Show | 307 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.2984+228G>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 23/26 | chr7 | 151011214 | ||||||
chr7:151011369 | C | CT | 241 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0019others(238): Show | 272 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.2984+385dupT | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr7 | 151011369 | |||||
chr7:151011553 | A | G | 3 | a0005c0007t0001g0050a0005c0007t0001g0087a0005c0007t0001g0088 | 3 | HG01109.hp1 HG01952.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2984+567A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 23/26 | chr7 | 151011553 | ||||||
chr7:151011580 | C | G | 1 | a0001c0010t0001g0326 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2984+594C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 23/26 | chr7 | 151011580 | ||||||
chr7:151011611 | CA | C | 236 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0019others(233): Show | 265 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.2984+642delA | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr7 | 151011611 | |||||
chr7:151011611 | CAA | C | 10 | a0001c0001t0001g0162a0001c0001t0001g0197a0001c0002t0001g0017others(7): Show | 11 | HG00323.hp1 HG00558.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.2984+641_2984+642d others(4): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr7 | 151011611 | |||||
chr7:151011628 | A | G | 4 | a0001c0001t0001g0197a0001c0002t0001g0089a0001c0002t0001g0091others(1): Show | 4 | HG02451.hp1 HG02809.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2984+642A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 23/26 | chr7 | 151011628 | ||||||
chr7:151011762 | G | A | 267 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0019others(264): Show | 297 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.2985-589G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 23/26 | chr7 | 151011762 | ||||||
chr7:151011984 | C | T | 1 | a0004c0031t0001g0051 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2985-367C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 23/26 | chr7 | 151011984 | ||||||
chr7:151012008 | A | T | 1 | a0002c0003t0001g0110 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2985-343A>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 23/26 | chr7 | 151012008 | ||||||
chr7:151012059 | G | A | 1 | a0001c0024t0001g0085 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2985-292G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 23/26 | chr7 | 151012059 | ||||||
chr7:151012235 | T | A | 1 | a0001c0010t0001g0326 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2985-116T>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 23/26 | chr7 | 151012235 | ||||||
chr7:151012247 | G | T | 1 | a0001c0002t0001g0129 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2985-104G>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 23/26 | chr7 | 151012247 | ||||||
chr7:151012483 | G | T | 134 | a0001c0001t0001g0019a0001c0001t0001g0034a0001c0001t0001g0035others(131): Show | 152 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(149): Show |
intron_variant | MODIFIER | c.3106+11G>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 24/26 | chr7 | 151012483 | ||||||
chr7:151012596 | C | T | 5 | a0001c0001t0001g0023a0001c0001t0001g0075a0001c0001t0001g0126others(2): Show | 6 | HG01884.hp2 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.3106+124C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 24/26 | chr7 | 151012596 | ||||||
chr7:151012763 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3106+291G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 24/26 | chr7 | 151012763 | ||||||
chr7:151012816 | T | C | 1 | a0003c0014t0005g0333 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3106+344T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 24/26 | chr7 | 151012816 | ||||||
chr7:151012892 | G | C | 7 | a0001c0005t0001g0011a0001c0005t0001g0043a0001c0005t0001g0044others(4): Show | 9 | HG01891.hp1 HG02280.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.3107-339G>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 24/26 | chr7 | 151012892 | ||||||
chr7:151013116 | G | A | 4 | a0001c0010t0001g0083a0005c0007t0001g0050a0005c0007t0001g0087others(1): Show | 4 | HG01109.hp1 HG01952.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.3107-115G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 24/26 | chr7 | 151013116 | ||||||
chr7:151013540 | A | C | 22 | a0001c0001t0001g0023a0001c0001t0001g0074a0001c0001t0001g0075others(19): Show | 23 | HG01884.hp2 HG01978.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.3255+161A>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 25/26 | chr7 | 151013540 | ||||||
chr7:151013596 | G | A | 2 | a0001c0001t0001g0066a0001c0001t0001g0153 | 2 | HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.3256-128G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 25/26 | chr7 | 151013596 | ||||||
chr7:151013597 | C | A | 2 | a0001c0001t0001g0066a0001c0001t0001g0153 | 2 | HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.3256-127C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 25/26 | chr7 | 151013597 | ||||||
chr7:151013652 | C | T | 1 | a0001c0010t0001g0326 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3256-72C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 25/26 | chr7 | 151013652 | ||||||
chr7:151013676 | C | G | 1 | a0002c0003t0001g0317 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3256-48C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 25/26 | chr7 | 151013676 | ||||||
chr7:151013712 | G | A | 20 | a0001c0001t0001g0023a0001c0001t0001g0074a0001c0001t0001g0075others(17): Show | 21 | HG01884.hp2 HG01978.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.3256-12G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 25/26 | chr7 | 151013712 | ||||||
chr7:151013945 | C | G | 1 | a0001c0002t0001g0165 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.3450+27C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 26/26 | chr7 | 151013945 |