Item | Value |
---|---|
geneid | 25920 |
ensemblid | ENSG00000188986.9 |
hgncid | 24324 |
symbol | NELFB |
name | negative elongation factor complex member B |
refseq_nuc | NM_015456.5 |
refseq_prot | NP_056271.3 |
ensembl_nuc | ENST00000343053.6 |
ensembl_prot | ENSP00000339495.6 |
mane_status | MANE Select |
chr | chr9 |
start | 137255327 |
end | 137273542 |
strand | + |
ver | v1.2 |
region | chr9:137255327-137273542 |
region5000 | chr9:137250327-137278542 |
regionname0 | NELFB_chr9_137255327_137273542 |
regionname5000 | NELFB_chr9_137250327_137278542 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 28 | 364 | 94 | 70 | 146 | 14 | 38 | 106 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1887 | 196 | 50 | 35 | 76 | 8 | 26 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
c0002 | 1/0 | 1887 | 141 | 40 | 23 | 63 | 4 | 10 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
c0003 | 0/0 | 1887 | 7 | 0 | 7 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
c0004 | 0/0 | 1887 | 3 | 0 | 2 | 0 | 1 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
c0005 | 0/0 | 1887 | 2 | 0 | 0 | 2 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
c0006 | 0/0 | 1887 | 2 | 2 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
c0007 | 0/0 | 1887 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
c0008 | 0/0 | 1887 | 1 | 0 | 0 | 0 | 1 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
c0009 | 0/0 | 1887 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
c0010 | 0/0 | 1887 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
c0011 | 0/0 | 1887 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
c0012 | 0/0 | 1887 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
c0013 | 0/0 | 1887 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
c0014 | 0/0 | 1887 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
c0015 | 0/0 | 1887 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
c0016 | 0/0 | 1887 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
c0017 | 0/0 | 1887 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
c0018 | 0/0 | 1887 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
c0019 | 0/0 | 1887 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 654 | 209 | 49 | 45 | 79 | 10 | 25 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
t0002 | 1/0 | 654 | 133 | 30 | 22 | 65 | 4 | 11 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
t0003 | 0/0 | 654 | 5 | 4 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
t0004 | 0/0 | 654 | 2 | 1 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
t0005 | 0/0 | 654 | 2 | 2 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
t0006 | 0/0 | 654 | 2 | 2 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
t0007 | 0/0 | 654 | 2 | 2 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
t0008 | 0/0 | 654 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
t0009 | 0/0 | 654 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
t0010 | 0/0 | 654 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
t0011 | 0/0 | 654 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
t0012 | 0/0 | 654 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
t0013 | 0/0 | 654 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
t0014 | 0/0 | 654 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
t0015 | 0/0 | 654 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
t0016 | 0/0 | 654 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 32 | 7 | 7 | 13 | 1 | 4 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0002 | 0/0 | 15 | 1 | 7 | 7 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0003 | 0/0 | 10 | 7 | 1 | 1 | 1 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0004 | 0/0 | 8 | 2 | 1 | 5 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0005 | 0/0 | 8 | 0 | 6 | 0 | 1 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0006 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0007 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0008 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0009 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0010 | 1/0 | 5 | 4 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0012 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0015 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0017 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0021 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0025 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0035 | 0/1 | 2 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0036 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1887 | 196 | 50 | 35 | 76 | 8 | 26 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0002 | 1/0 | 1887 | 141 | 40 | 23 | 63 | 4 | 10 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0003 | 0/0 | 1887 | 7 | 0 | 7 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0004 | 0/0 | 1887 | 3 | 0 | 2 | 0 | 1 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0005 | 0/0 | 1887 | 2 | 0 | 0 | 2 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0006 | 0/0 | 1887 | 2 | 2 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0007 | 0/0 | 1887 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0008 | 0/0 | 1887 | 1 | 0 | 0 | 0 | 1 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0009 | 0/0 | 1887 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0010 | 0/0 | 1887 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0011 | 0/0 | 1887 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0012 | 0/0 | 1887 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0013 | 0/0 | 1887 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0014 | 0/0 | 1887 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0015 | 0/0 | 1887 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0016 | 0/0 | 1887 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0017 | 0/0 | 1887 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0018 | 0/0 | 1887 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0019 | 0/0 | 1887 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2540 | 190 | 47 | 34 | 76 | 8 | 24 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0001t0009 | 0/0 | 2540 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0001t0010 | 0/0 | 2540 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0001t0013 | 0/0 | 2540 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0001t0014 | 0/0 | 2540 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0001t0015 | 0/0 | 2540 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0001t0016 | 0/0 | 2540 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0002t0002 | 1/0 | 2540 | 128 | 30 | 21 | 62 | 4 | 10 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0002t0003 | 0/0 | 2540 | 5 | 4 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0002t0004 | 0/0 | 2540 | 2 | 1 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0002t0006 | 0/0 | 2540 | 2 | 2 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0002t0007 | 0/0 | 2540 | 2 | 2 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0002t0011 | 0/0 | 2540 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0002t0012 | 0/0 | 2540 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0003t0001 | 0/0 | 2540 | 7 | 0 | 7 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0004t0001 | 0/0 | 2540 | 3 | 0 | 2 | 0 | 1 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0005t0001 | 0/0 | 2540 | 2 | 0 | 0 | 2 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0006t0005 | 0/0 | 2540 | 2 | 2 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0007t0002 | 0/0 | 2540 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0008t0001 | 0/0 | 2540 | 1 | 0 | 0 | 0 | 1 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0009t0001 | 0/0 | 2540 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0010t0001 | 0/0 | 2540 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0011t0002 | 0/0 | 2540 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0012t0002 | 0/0 | 2540 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0013t0001 | 0/0 | 2540 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0014t0002 | 0/0 | 2540 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0015t0002 | 0/0 | 2540 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0016t0001 | 0/0 | 2540 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0017t0001 | 0/0 | 2540 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0018t0001 | 0/0 | 2540 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
a0001c0019t0008 | 0/0 | 2540 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | copy fasta | chr9 | 137250327 | 137278542 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 29 | 7 | 6 | 12 | 1 | 3 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0003 | 0/0 | 10 | 7 | 1 | 1 | 1 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0004 | 0/0 | 8 | 2 | 1 | 5 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0006 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0007 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0009 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0035 | 0/1 | 2 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0009g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0010g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0013g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0014g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0015g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0001t0016g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0002 | 0/0 | 13 | 1 | 6 | 6 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0008 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0010 | 1/0 | 5 | 4 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0012 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0017 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0021 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0003g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0004g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0006g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0006g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0007g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0011g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0002t0012g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0003t0001g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0003t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0003t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0003t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0003t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0004t0001g0005 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0005t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0006t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0006t0005g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0007t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0008t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0009t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0010t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0011t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0012t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0013t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0014t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0015t0002g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0016t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0017t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0018t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
a0001c0019t0008g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0231 | EUR | GBR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | GBR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | FIN | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0170 | EUR | FIN | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG00423 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | CHS | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG00544 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | CHS | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG00597 | hp2 | a0001 | c0002 | t0002 | g0023 | EAS | CHS | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG00621 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | CHS | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG00673 | hp1 | a0001 | c0002 | t0002 | g0049 | EAS | CHS | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG00733 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG00738 | hp2 | a0001 | c0003 | t0001 | g0005 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG00741 | hp1 | a0001 | c0004 | t0001 | g0005 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG00741 | hp2 | a0001 | c0002 | t0002 | g0215 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01070 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01071 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01074 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01081 | hp1 | a0001 | c0009 | t0001 | g0009 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01081 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01109 | hp1 | a0001 | c0002 | t0004 | g0081 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01167 | hp1 | a0001 | c0002 | t0002 | g0206 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01167 | hp2 | a0001 | c0002 | t0002 | g0056 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01168 | hp2 | a0001 | c0001 | t0015 | g0001 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01169 | hp1 | a0001 | c0002 | t0002 | g0038 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01243 | hp1 | a0001 | c0002 | t0002 | g0213 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01243 | hp2 | a0001 | c0002 | t0002 | g0022 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01255 | hp1 | a0001 | c0002 | t0002 | g0064 | AMR | CLM | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01346 | hp2 | a0001 | c0003 | t0001 | g0171 | AMR | CLM | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01361 | hp1 | a0001 | c0017 | t0001 | g0186 | AMR | CLM | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01361 | hp2 | a0001 | c0002 | t0002 | g0202 | AMR | CLM | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01496 | hp1 | a0001 | c0002 | t0002 | g0044 | AMR | CLM | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0111 | EUR | IBS | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01516 | hp1 | a0001 | c0002 | t0002 | g0017 | EUR | IBS | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01516 | hp2 | a0001 | c0008 | t0001 | g0145 | EUR | IBS | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01517 | hp1 | a0001 | c0002 | t0002 | g0017 | EUR | IBS | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01884 | hp2 | a0001 | c0002 | t0011 | g0216 | AFR | ACB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01891 | hp2 | a0001 | c0002 | t0002 | g0226 | AFR | ACB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01928 | hp1 | a0001 | c0002 | t0002 | g0205 | AMR | PEL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01928 | hp2 | a0001 | c0003 | t0001 | g0189 | AMR | PEL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01934 | hp2 | a0001 | c0002 | t0002 | g0022 | AMR | PEL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01952 | hp2 | a0001 | c0004 | t0001 | g0005 | AMR | PEL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01975 | hp2 | a0001 | c0002 | t0003 | g0227 | AMR | PEL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01978 | hp1 | a0001 | c0002 | t0002 | g0012 | AMR | PEL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02004 | hp1 | a0001 | c0002 | t0002 | g0038 | AMR | PEL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02004 | hp2 | a0001 | c0003 | t0001 | g0005 | AMR | PEL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02015 | hp1 | a0001 | c0002 | t0002 | g0093 | EAS | KHV | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02015 | hp2 | a0001 | c0016 | t0001 | g0001 | EAS | KHV | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02027 | hp1 | a0001 | c0002 | t0002 | g0018 | EAS | KHV | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02027 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | KHV | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02040 | hp2 | a0001 | c0011 | t0002 | g0002 | EAS | KHV | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02055 | hp1 | a0001 | c0002 | t0002 | g0212 | AFR | ACB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02055 | hp2 | a0001 | c0002 | t0002 | g0219 | AFR | ACB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02056 | hp2 | a0001 | c0002 | t0002 | g0018 | EAS | KHV | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02080 | hp1 | a0001 | c0002 | t0002 | g0023 | EAS | KHV | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02083 | hp1 | a0001 | c0002 | t0002 | g0053 | EAS | KHV | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02083 | hp2 | a0001 | c0002 | t0002 | g0047 | EAS | KHV | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02132 | hp2 | a0001 | c0002 | t0002 | g0089 | EAS | KHV | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02145 | hp1 | a0001 | c0002 | t0002 | g0224 | AFR | ACB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02148 | hp1 | a0001 | c0002 | t0002 | g0225 | AMR | PEL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02148 | hp2 | a0001 | c0003 | t0001 | g0188 | AMR | PEL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02155 | hp1 | a0001 | c0005 | t0001 | g0040 | EAS | CDX | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CDX | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02165 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | CDX | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02258 | hp1 | a0001 | c0002 | t0002 | g0008 | AFR | ACB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02258 | hp2 | a0001 | c0002 | t0002 | g0228 | AFR | ACB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02273 | hp2 | a0001 | c0003 | t0001 | g0005 | AMR | PEL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02293 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02293 | hp2 | a0001 | c0002 | t0002 | g0060 | AMR | PEL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02300 | hp1 | a0001 | c0015 | t0002 | g0002 | AMR | PEL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02300 | hp2 | a0001 | c0003 | t0001 | g0193 | AMR | PEL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02451 | hp1 | a0001 | c0002 | t0007 | g0037 | AFR | ACB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02615 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02622 | hp1 | a0001 | c0001 | t0013 | g0128 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02630 | hp1 | a0001 | c0002 | t0003 | g0011 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02630 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02698 | hp1 | a0001 | c0002 | t0002 | g0045 | SAS | PJL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02698 | hp2 | a0001 | c0014 | t0002 | g0025 | SAS | PJL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02717 | hp2 | a0001 | c0002 | t0002 | g0008 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02723 | hp1 | a0001 | c0002 | t0002 | g0214 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02735 | hp1 | a0001 | c0001 | t0009 | g0232 | SAS | PJL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02809 | hp1 | a0001 | c0002 | t0003 | g0011 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02809 | hp2 | a0001 | c0002 | t0002 | g0008 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02818 | hp1 | a0001 | c0001 | t0014 | g0143 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02818 | hp2 | a0001 | c0001 | t0010 | g0116 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02896 | hp1 | a0001 | c0002 | t0002 | g0199 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02896 | hp2 | a0001 | c0002 | t0002 | g0223 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02897 | hp1 | a0001 | c0002 | t0002 | g0201 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02922 | hp1 | a0001 | c0002 | t0002 | g0210 | AFR | ESN | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02922 | hp2 | a0001 | c0002 | t0006 | g0211 | AFR | ESN | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02970 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | ESN | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03017 | hp1 | a0001 | c0002 | t0002 | g0055 | SAS | PJL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03017 | hp2 | a0001 | c0002 | t0002 | g0041 | SAS | PJL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03041 | hp2 | a0001 | c0002 | t0003 | g0011 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03130 | hp2 | a0001 | c0002 | t0006 | g0039 | AFR | ESN | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03139 | hp1 | a0001 | c0006 | t0005 | g0077 | AFR | ESN | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03209 | hp1 | a0001 | c0002 | t0002 | g0008 | AFR | MSL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03225 | hp1 | a0001 | c0002 | t0007 | g0037 | AFR | MSL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03239 | hp2 | a0001 | c0010 | t0001 | g0001 | SAS | PJL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03453 | hp2 | a0001 | c0002 | t0002 | g0222 | AFR | MSL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03486 | hp1 | a0001 | c0002 | t0002 | g0008 | AFR | MSL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03491 | hp1 | a0001 | c0001 | t0016 | g0112 | SAS | PJL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03516 | hp1 | a0001 | c0006 | t0005 | g0078 | AFR | ESN | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03516 | hp2 | a0001 | c0002 | t0002 | g0218 | AFR | ESN | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03540 | hp2 | a0001 | c0002 | t0002 | g0208 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03579 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | MSL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03654 | hp1 | a0001 | c0002 | t0002 | g0050 | SAS | PJL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03669 | hp1 | a0001 | c0002 | t0002 | g0065 | SAS | PJL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03688 | hp1 | a0001 | c0002 | t0002 | g0021 | SAS | STU | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | STU | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03831 | hp1 | a0001 | c0002 | t0002 | g0066 | SAS | BEB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03834 | hp1 | a0001 | c0002 | t0002 | g0092 | SAS | BEB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03834 | hp2 | a0001 | c0002 | t0002 | g0236 | SAS | BEB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | BEB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | STU | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG04115 | hp2 | a0001 | c0002 | t0002 | g0067 | SAS | STU | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | BEB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | BEB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | STU | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | STU | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | STU | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | STU | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18522 | hp1 | a0001 | c0002 | t0002 | g0221 | AFR | YRI | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | YRI | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18612 | hp1 | a0001 | c0002 | t0002 | g0058 | EAS | CHB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18747 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | CHB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18906 | hp1 | a0001 | c0002 | t0002 | g0008 | AFR | YRI | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18941 | hp2 | a0001 | c0007 | t0002 | g0057 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18942 | hp1 | a0001 | c0019 | t0008 | g0100 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18943 | hp2 | a0001 | c0002 | t0002 | g0046 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18945 | hp2 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18953 | hp1 | a0001 | c0002 | t0002 | g0096 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18953 | hp2 | a0001 | c0002 | t0012 | g0068 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18954 | hp2 | a0001 | c0012 | t0002 | g0074 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18957 | hp1 | a0001 | c0002 | t0002 | g0070 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18961 | hp1 | a0001 | c0002 | t0002 | g0072 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18966 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18967 | hp1 | a0001 | c0002 | t0002 | g0061 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18968 | hp2 | a0001 | c0002 | t0002 | g0063 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18969 | hp2 | a0001 | c0002 | t0002 | g0207 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18971 | hp1 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18972 | hp1 | a0001 | c0002 | t0002 | g0204 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18972 | hp2 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18974 | hp1 | a0001 | c0002 | t0002 | g0019 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18977 | hp1 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18977 | hp2 | a0001 | c0002 | t0002 | g0091 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18979 | hp2 | a0001 | c0002 | t0002 | g0076 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18981 | hp1 | a0001 | c0002 | t0002 | g0075 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18984 | hp1 | a0001 | c0002 | t0002 | g0054 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18987 | hp2 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18993 | hp1 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18995 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18999 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18999 | hp2 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19004 | hp1 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19005 | hp2 | a0001 | c0002 | t0002 | g0069 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19010 | hp1 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19010 | hp2 | a0001 | c0002 | t0002 | g0098 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19011 | hp2 | a0001 | c0002 | t0002 | g0097 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19043 | hp1 | a0001 | c0002 | t0002 | g0220 | AFR | LWK | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19057 | hp1 | a0001 | c0002 | t0002 | g0094 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19064 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19065 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19067 | hp1 | a0001 | c0002 | t0002 | g0203 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19070 | hp1 | a0001 | c0002 | t0002 | g0079 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19076 | hp2 | a0001 | c0002 | t0002 | g0073 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19077 | hp1 | a0001 | c0002 | t0002 | g0019 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19080 | hp2 | a0001 | c0005 | t0001 | g0040 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19081 | hp2 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19084 | hp1 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19084 | hp2 | a0001 | c0002 | t0002 | g0095 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19085 | hp2 | a0001 | c0002 | t0002 | g0200 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19088 | hp1 | a0001 | c0002 | t0002 | g0090 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19088 | hp2 | a0001 | c0002 | t0002 | g0071 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19089 | hp1 | a0001 | c0002 | t0002 | g0099 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19089 | hp2 | a0001 | c0002 | t0002 | g0048 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19090 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19090 | hp2 | a0001 | c0002 | t0002 | g0051 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19240 | hp1 | a0001 | c0018 | t0001 | g0086 | AFR | YRI | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ASW | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA20752 | hp1 | a0001 | c0002 | t0002 | g0025 | EUR | TSI | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA20752 | hp2 | a0001 | c0004 | t0001 | g0005 | EUR | TSI | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA20805 | hp1 | a0001 | c0002 | t0002 | g0059 | EUR | TSI | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0036 | EUR | TSI | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | GIH | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02559 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | ACB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG02559 | hp2 | a0001 | c0002 | t0002 | g0217 | AFR | ACB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03471 | hp1 | a0001 | c0002 | t0004 | g0080 | AFR | MSL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG06807 | hp1 | a0001 | c0002 | t0002 | g0087 | AFR | USA | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
HG06807 | hp2 | a0001 | c0002 | t0002 | g0209 | AFR | USA | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18955 | hp1 | a0001 | c0002 | t0002 | g0088 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA20300 | hp1 | a0001 | c0002 | t0003 | g0011 | AFR | USA | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | USA | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA21309 | hp1 | a0001 | c0002 | t0002 | g0039 | AFR | LWK | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
NA21309 | hp2 | a0001 | c0013 | t0001 | g0164 | AFR | LWK | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0035 | REF | REF | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0002 | g0010 | REF | REF | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:137255457
|
G | A | 1 | a0001 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.92G>A | p.Gly31Glu | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 1/13 | 131/2540 | 92/1887 | 31/628 | chr9 | 137255457 | ||
chr9:137266340
|
G | A | 1 | a0001 | 1 | HG01081.hp1 | missense_variant | MODERATE | c.1153G>A | p.Asp385Asn | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 8/13 | 1192/2540 | 1153/1887 | 385/628 | chr9 | 137266340 | ||
chr9:137267074
|
A | G | 1 | a0001 | 2 | HG02155.hp1 NA19080.hp2 |
missense_variant | MODERATE | c.1370A>G | p.Glu457Gly | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 9/13 | 1409/2540 | 1370/1887 | 457/628 | chr9 | 137267074 | ||
chr9:137267319
|
G | T | 1 | a0001 | 1 | HG02300.hp1 | missense_variant | MODERATE | c.1462G>T | p.Ala488Ser | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/13 | 1501/2540 | 1462/1887 | 488/628 | chr9 | 137267319 | ||
chr9:137272530
|
C | T | 1 | a0001 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.1655C>T | p.Ala552Val | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 12/13 | 1694/2540 | 1655/1887 | 552/628 | chr9 | 137272530 | ||
chr9:137272851
|
C | A | 1 | a0001 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.1810C>A | p.Pro604Thr | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 13/13 | 1849/2540 | 1810/1887 | 604/628 | chr9 | 137272851 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:137255587
|
G | T | 1 | a0001c0006 | 2 | HG03139.hp1 HG03516.hp1 |
synonymous_variant | LOW | c.222G>T | p.Pro74Pro | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 1/13 | 261/2540 | 222/1887 | 74/628 | chr9 | 137255587 | ||
chr9:137255961
|
C | T | 1 | a0001c0004 | 3 | HG00741.hp1 HG01952.hp2 NA20752.hp2 |
synonymous_variant | LOW | c.301C>T | p.Leu101Leu | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 2/13 | 340/2540 | 301/1887 | 101/628 | chr9 | 137255961 | ||
chr9:137256024
|
C | T | 1 | a0001c0019 | 1 | NA18942.hp1 | synonymous_variant | LOW | c.364C>T | p.Leu122Leu | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 2/13 | 403/2540 | 364/1887 | 122/628 | chr9 | 137256024 | ||
chr9:137256386
|
C | G | 1 | a0001c0018 | 1 | NA19240.hp1 | synonymous_variant | LOW | c.468C>G | p.Ser156Ser | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 3/13 | 507/2540 | 468/1887 | 156/628 | chr9 | 137256386 | ||
chr9:137256928
|
C | T | 1 | a0001c0017 | 1 | HG01361.hp1 | synonymous_variant | LOW | c.615C>T | p.Phe205Phe | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/13 | 654/2540 | 615/1887 | 205/628 | chr9 | 137256928 | ||
chr9:137263126
|
G | A | 1 | a0001c0008 | 1 | HG01516.hp2 | synonymous_variant | LOW | c.831G>A | p.Thr277Thr | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/13 | 870/2540 | 831/1887 | 277/628 | chr9 | 137263126 | ||
chr9:137263127
|
C | A | 1 | a0001c0008 | 1 | HG01516.hp2 | synonymous_variant | LOW | c.832C>A | p.Arg278Arg | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/13 | 871/2540 | 832/1887 | 278/628 | chr9 | 137263127 | ||
chr9:137265946
|
G | T | 1 | a0001c0016 | 1 | HG02015.hp2 | synonymous_variant | LOW | c.1110G>T | p.Leu370Leu | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 7/13 | 1149/2540 | 1110/1887 | 370/628 | chr9 | 137265946 | ||
chr9:137272145
|
G | A | 1 | a0001c0003 | 7 | HG00738.hp2 HG01346.hp2 HG01928.hp2 others(4): Show |
synonymous_variant | LOW | c.1554G>A | p.Ala518Ala | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 11/13 | 1593/2540 | 1554/1887 | 518/628 | chr9 | 137272145 | ||
chr9:137272193
|
C | T | 1 | a0001c0014 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.1602C>T | p.Phe534Phe | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 11/13 | 1641/2540 | 1602/1887 | 534/628 | chr9 | 137272193 | ||
chr9:137272570
|
G | A | 11 | a0001c0001a0001c0003a0001c0004others(8): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
synonymous_variant | LOW | c.1695G>A | p.Pro565Pro | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 12/13 | 1734/2540 | 1695/1887 | 565/628 | chr9 | 137272570 | ||
chr9:137272871
|
G | A | 1 | a0001c0010 | 1 | HG03239.hp2 | synonymous_variant | LOW | c.1830G>A | p.Ala610Ala | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 13/13 | 1869/2540 | 1830/1887 | 610/628 | chr9 | 137272871 | ||
chr9:137272910
|
C | T | 1 | a0001c0012 | 1 | NA18954.hp2 | synonymous_variant | LOW | c.1869C>T | p.Pro623Pro | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 13/13 | 1908/2540 | 1869/1887 | 623/628 | chr9 | 137272910 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:137272932
|
C | A | 1 | a0001c0019t0008 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4C>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 13/13 | 4 | chr9 | 137272932 | |||||
chr9:137272933
|
C | A | 1 | a0001c0019t0008 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5C>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 13/13 | 5 | chr9 | 137272933 | |||||
chr9:137272947
|
C | T | 1 | a0001c0001t0016 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*19C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 13/13 | 19 | chr9 | 137272947 | |||||
chr9:137272953
|
C | T | 1 | a0001c0001t0015 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*25C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 13/13 | 25 | chr9 | 137272953 | |||||
chr9:137272965
|
C | T | 1 | a0001c0001t0014 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*37C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 13/13 | 37 | chr9 | 137272965 | |||||
chr9:137272966
|
G | A | 1 | a0001c0001t0009 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*38G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 13/13 | 38 | chr9 | 137272966 | |||||
chr9:137273013
|
C | T | 1 | a0001c0002t0007 | 2 | HG02451.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*85C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 13/13 | 85 | chr9 | 137273013 | |||||
chr9:137273065
|
C | T | 1 | a0001c0001t0013 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*137C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 13/13 | 137 | chr9 | 137273065 | |||||
chr9:137273098
|
G | A | 1 | a0001c0002t0004 | 2 | HG01109.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*170G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 13/13 | 170 | chr9 | 137273098 | |||||
chr9:137273252
|
G | T | 1 | a0001c0002t0012 | 1 | NA18953.hp2 | 3_prime_UTR_variant | MODIFIER | c.*324G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 13/13 | 324 | chr9 | 137273252 | |||||
chr9:137273278
|
G | A | 1 | a0001c0002t0003 | 5 | HG01975.hp2 HG02630.hp1 HG02809.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*350G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 13/13 | 350 | chr9 | 137273278 | |||||
chr9:137273386
|
G | A | 1 | a0001c0001t0010 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*458G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 13/13 | 458 | chr9 | 137273386 | |||||
chr9:137273395
|
C | T | 1 | a0001c0002t0006 | 2 | HG02922.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*467C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 13/13 | 467 | chr9 | 137273395 | |||||
chr9:137273425
|
T | G | 19 | a0001c0001t0001a0001c0001t0009a0001c0001t0010others(16): Show | 218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
3_prime_UTR_variant | MODIFIER | c.*497T>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 13/13 | 497 | chr9 | 137273425 | |||||
chr9:137273512
|
C | T | 1 | a0001c0002t0011 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*584C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 13/13 | 584 | chr9 | 137273512 | |||||
chr9:137273533
|
T | A | 17 | a0001c0001t0001a0001c0001t0009a0001c0001t0010others(14): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*605T>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 13/13 | 605 | chr9 | 137273533 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:137255731
|
C | T | 1 | a0001c0002t0002g0236 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.246+120C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 1/12 | chr9 | 137255731 | ||||||
chr9:137255829
|
G | A | 1 | a0001c0002t0002g0041 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.247-78G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 1/12 | chr9 | 137255829 | ||||||
chr9:137255836
|
C | T | 5 | a0001c0001t0001g0231a0001c0001t0001g0233a0001c0001t0001g0234others(2): Show | 5 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.247-71C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 1/12 | chr9 | 137255836 | ||||||
chr9:137255858
|
G | A | 47 | a0001c0002t0002g0002a0001c0002t0002g0012a0001c0002t0002g0017others(44): Show | 68 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.247-49G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 1/12 | chr9 | 137255858 | ||||||
chr9:137256147
|
T | C | 2 | a0001c0006t0005g0077a0001c0006t0005g0078 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.410+77T>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 2/12 | chr9 | 137256147 | ||||||
chr9:137256187
|
G | C | 1 | a0001c0002t0002g0079 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.410+117G>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 2/12 | chr9 | 137256187 | ||||||
chr9:137256601
|
G | A | 2 | a0001c0002t0004g0080a0001c0002t0004g0081 | 2 | HG01109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.510+173G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 3/12 | chr9 | 137256601 | ||||||
chr9:137256627
|
G | A | 4 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(1): Show | 4 | HG02572.hp1 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.511-197G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 3/12 | chr9 | 137256627 | ||||||
chr9:137256815
|
G | C | 1 | a0001c0018t0001g0086 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.511-9G>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 3/12 | chr9 | 137256815 | ||||||
chr9:137257172
|
C | T | 1 | a0001c0005t0001g0040 | 2 | HG02155.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.741+118C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137257172 | ||||||
chr9:137257316
|
C | T | 1 | a0001c0001t0001g0230 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.741+262C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137257316 | ||||||
chr9:137257338
|
T | A | 19 | a0001c0002t0002g0013a0001c0002t0002g0024a0001c0002t0002g0025others(16): Show | 22 | HG00544.hp1 HG02015.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.741+284T>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137257338 | ||||||
chr9:137257381
|
T | G | 1 | a0001c0019t0008g0100 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.741+327T>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137257381 | ||||||
chr9:137257403
|
A | G | 1 | a0001c0001t0001g0229 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.741+349A>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137257403 | ||||||
chr9:137257427
|
A | T | 1 | a0001c0002t0002g0228 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.741+373A>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137257427 | ||||||
chr9:137257504
|
CT | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(129): Show | 209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.741+465delT | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr9 | 137257504 | |||||
chr9:137257532
|
C | T | 1 | a0001c0002t0003g0227 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.741+478C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137257532 | ||||||
chr9:137257569
|
C | T | 47 | a0001c0002t0002g0002a0001c0002t0002g0012a0001c0002t0002g0017others(44): Show | 68 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.741+515C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137257569 | ||||||
chr9:137257571
|
C | T | 8 | a0001c0002t0002g0023a0001c0002t0002g0070a0001c0002t0002g0071others(5): Show | 9 | HG00597.hp2 HG02080.hp1 NA18954.hp2 others(6): Show |
intron_variant | MODIFIER | c.741+517C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137257571 | ||||||
chr9:137257582
|
G | A | 2 | a0001c0001t0001g0101a0001c0001t0001g0102 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.741+528G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137257582 | ||||||
chr9:137257650
|
G | A | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | HG01891.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.741+596G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137257650 | ||||||
chr9:137257660
|
G | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.741+606G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137257660 | ||||||
chr9:137257663
|
C | T | 2 | a0001c0002t0002g0226a0001c0002t0002g0228 | 2 | HG01891.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.741+609C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137257663 | ||||||
chr9:137257668
|
A | C | 47 | a0001c0002t0002g0002a0001c0002t0002g0012a0001c0002t0002g0017others(44): Show | 68 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.741+614A>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137257668 | ||||||
chr9:137257744
|
C | T | 2 | a0001c0002t0004g0080a0001c0002t0004g0081 | 2 | HG01109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.741+690C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137257744 | ||||||
chr9:137257782
|
G | A | 2 | a0001c0002t0002g0042a0001c0002t0002g0043 | 2 | NA18999.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.741+728G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137257782 | ||||||
chr9:137257791
|
C | T | 2 | a0001c0002t0004g0080a0001c0002t0004g0081 | 2 | HG01109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.741+737C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137257791 | ||||||
chr9:137257800
|
CTTTTTTT others(3): Show |
C | 139 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.741+761_741+770del others(10): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr9 | 137257800 | |||||
chr9:137257845
|
G | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.741+791G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137257845 | ||||||
chr9:137257974
|
A | G | 1 | a0001c0003t0001g0193 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.741+920A>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137257974 | ||||||
chr9:137258118
|
GT | G | 71 | a0001c0001t0001g0192a0001c0002t0002g0002a0001c0002t0002g0012others(68): Show | 100 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.741+1087delT | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr9 | 137258118 | |||||
chr9:137258118
|
GTT | G | 22 | a0001c0001t0001g0035a0001c0001t0001g0085a0001c0001t0001g0178others(19): Show | 23 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.741+1086_741+1087d others(4): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr9 | 137258118 | |||||
chr9:137258118
|
GTTT | G | 110 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(107): Show | 187 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.741+1085_741+1087d others(5): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr9 | 137258118 | |||||
chr9:137258118
|
GTTTT | G | 9 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(6): Show | 9 | HG00099.hp1 HG00639.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.741+1084_741+1087d others(6): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr9 | 137258118 | |||||
chr9:137258238
|
C | A | 3 | a0001c0002t0002g0008a0001c0002t0002g0199a0001c0002t0002g0208 | 8 | HG02258.hp1 HG02717.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.741+1184C>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137258238 | ||||||
chr9:137258385
|
C | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.741+1331C>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137258385 | ||||||
chr9:137258407
|
T | C | 1 | a0001c0002t0002g0209 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.741+1353T>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137258407 | ||||||
chr9:137258413
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.741+1359C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137258413 | ||||||
chr9:137258449
|
AT | A | 19 | a0001c0001t0001g0026a0001c0001t0001g0105a0001c0001t0001g0106others(16): Show | 20 | HG00099.hp1 HG01071.hp2 HG01515.hp2 others(17): Show |
intron_variant | MODIFIER | c.741+1412delT | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr9 | 137258449 | |||||
chr9:137258593
|
C | T | 19 | a0001c0002t0002g0013a0001c0002t0002g0024a0001c0002t0002g0025others(16): Show | 22 | HG00544.hp1 HG02015.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.741+1539C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137258593 | ||||||
chr9:137258597
|
C | T | 1 | a0001c0001t0001g0177 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.741+1543C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137258597 | ||||||
chr9:137258621
|
T | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.741+1567T>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137258621 | ||||||
chr9:137258653
|
C | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.741+1599C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137258653 | ||||||
chr9:137258693
|
A | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(137): Show | 218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.741+1639A>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137258693 | ||||||
chr9:137258764
|
T | A | 47 | a0001c0002t0002g0002a0001c0002t0002g0012a0001c0002t0002g0017others(44): Show | 68 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.741+1710T>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137258764 | ||||||
chr9:137258844
|
A | T | 2 | a0001c0001t0001g0175a0001c0001t0001g0176 | 2 | HG02602.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.741+1790A>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137258844 | ||||||
chr9:137258879
|
T | C | 1 | a0001c0019t0008g0100 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.741+1825T>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137258879 | ||||||
chr9:137259025
|
C | A | 19 | a0001c0002t0002g0013a0001c0002t0002g0024a0001c0002t0002g0025others(16): Show | 22 | HG00544.hp1 HG02015.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.741+1971C>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137259025 | ||||||
chr9:137259053
|
T | G | 1 | a0001c0001t0001g0107 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.741+1999T>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137259053 | ||||||
chr9:137259198
|
GA | G | 47 | a0001c0002t0002g0002a0001c0002t0002g0012a0001c0002t0002g0017others(44): Show | 68 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.741+2154delA | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr9 | 137259198 | |||||
chr9:137259329
|
G | T | 1 | a0001c0001t0001g0174 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.741+2275G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137259329 | ||||||
chr9:137259341
|
G | T | 2 | a0001c0002t0002g0025a0001c0014t0002g0025 | 2 | HG02698.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.741+2287G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137259341 | ||||||
chr9:137259343
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.741+2289C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137259343 | ||||||
chr9:137259344
|
G | A | 1 | a0001c0002t0002g0228 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.741+2290G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137259344 | ||||||
chr9:137259472
|
G | A | 1 | a0001c0001t0010g0116 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.741+2418G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137259472 | ||||||
chr9:137259649
|
T | C | 2 | a0001c0001t0001g0117a0001c0001t0001g0178 | 2 | HG01261.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.741+2595T>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137259649 | ||||||
chr9:137259728
|
T | G | 1 | a0001c0001t0001g0118 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.741+2674T>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137259728 | ||||||
chr9:137259787
|
C | T | 1 | a0001c0002t0002g0023 | 2 | HG00597.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.741+2733C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137259787 | ||||||
chr9:137259810
|
C | T | 1 | a0001c0018t0001g0086 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.741+2756C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137259810 | ||||||
chr9:137259811
|
G | A | 2 | a0001c0002t0004g0080a0001c0002t0004g0081 | 2 | HG01109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.741+2757G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137259811 | ||||||
chr9:137259818
|
G | A | 25 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0026others(22): Show | 37 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.741+2764G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137259818 | ||||||
chr9:137259841
|
C | T | 4 | a0001c0001t0001g0034a0001c0001t0001g0114a0001c0001t0001g0115others(1): Show | 5 | HG02109.hp1 HG02257.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.741+2787C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137259841 | ||||||
chr9:137259870
|
G | A | 1 | a0001c0002t0003g0011 | 4 | HG02630.hp1 HG02809.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.741+2816G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137259870 | ||||||
chr9:137259920
|
C | T | 2 | a0001c0006t0005g0077a0001c0006t0005g0078 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.741+2866C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137259920 | ||||||
chr9:137259931
|
A | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(217): Show | 325 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.741+2877A>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137259931 | ||||||
chr9:137259952
|
A | T | 1 | a0001c0018t0001g0086 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.741+2898A>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137259952 | ||||||
chr9:137260009
|
C | T | 48 | a0001c0001t0001g0172a0001c0002t0002g0002a0001c0002t0002g0012others(45): Show | 69 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.741+2955C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137260009 | ||||||
chr9:137260043
|
ATTTATTT others(3): Show |
A | 8 | a0001c0001t0001g0005a0001c0001t0001g0170a0001c0003t0001g0005others(5): Show | 13 | HG00280.hp2 HG00738.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.742-2980_742-2971d others(12): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr9 | 137260043 | |||||
chr9:137260106
|
G | T | 1 | a0001c0001t0001g0234 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.742-2931G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137260106 | ||||||
chr9:137260154
|
G | A | 1 | a0001c0019t0008g0100 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.742-2883G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137260154 | ||||||
chr9:137260157
|
C | T | 5 | a0001c0002t0002g0024a0001c0002t0002g0095a0001c0002t0002g0096others(2): Show | 6 | NA18945.hp2 NA18953.hp1 NA19010.hp1 others(3): Show |
intron_variant | MODIFIER | c.742-2880C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137260157 | ||||||
chr9:137260195
|
G | GCC | 18 | a0001c0002t0002g0013a0001c0002t0002g0024a0001c0002t0002g0025others(15): Show | 21 | HG00544.hp1 HG02015.hp1 HG02132.hp2 others(18): Show |
intron_variant | MODIFIER | c.742-2840_742-2839d others(4): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr9 | 137260195 | |||||
chr9:137260212
|
G | C | 1 | a0001c0001t0013g0128 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.742-2825G>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137260212 | ||||||
chr9:137260222
|
T | C | 1 | a0001c0001t0013g0128 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.742-2815T>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137260222 | ||||||
chr9:137260307
|
C | T | 140 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(137): Show | 218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.742-2730C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137260307 | ||||||
chr9:137260346
|
G | A | 3 | a0001c0002t0002g0212a0001c0002t0002g0213a0001c0002t0002g0214 | 3 | HG01243.hp1 HG02055.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.742-2691G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137260346 | ||||||
chr9:137260392
|
T | A | 1 | a0001c0002t0002g0202 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.742-2645T>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137260392 | ||||||
chr9:137260393
|
A | T | 186 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(183): Show | 285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.742-2644A>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137260393 | ||||||
chr9:137260396
|
A | T | 1 | a0001c0018t0001g0086 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.742-2641A>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137260396 | ||||||
chr9:137260401
|
T | A | 2 | a0001c0001t0001g0109a0001c0001t0010g0116 | 2 | HG02818.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.742-2636T>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137260401 | ||||||
chr9:137260405
|
A | ATTTAT | 138 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(135): Show | 216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.742-2622_742-2618d others(7): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr9 | 137260405 | |||||
chr9:137260457
|
ATT | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.742-2568_742-2567d others(4): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr9 | 137260457 | |||||
chr9:137260524
|
C | G | 1 | a0001c0002t0002g0209 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.742-2513C>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137260524 | ||||||
chr9:137260672
|
C | T | 2 | a0001c0002t0002g0236a0001c0019t0008g0100 | 2 | HG03834.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.742-2365C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137260672 | ||||||
chr9:137260680
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.742-2357T>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137260680 | ||||||
chr9:137260694
|
C | A | 19 | a0001c0002t0002g0013a0001c0002t0002g0024a0001c0002t0002g0025others(16): Show | 22 | HG00544.hp1 HG02015.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.742-2343C>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137260694 | ||||||
chr9:137260749
|
A | G | 5 | a0001c0002t0002g0020a0001c0002t0002g0061a0001c0002t0002g0062others(2): Show | 6 | NA18953.hp2 NA18967.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.742-2288A>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137260749 | ||||||
chr9:137260943
|
C | T | 1 | a0001c0002t0002g0214 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.742-2094C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137260943 | ||||||
chr9:137261015
|
C | T | 1 | a0001c0002t0002g0060 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.742-2022C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261015 | ||||||
chr9:137261031
|
G | A | 3 | a0001c0001t0001g0110a0001c0001t0001g0130a0001c0001t0001g0131 | 3 | NA18947.hp1 NA18970.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.742-2006G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261031 | ||||||
chr9:137261112
|
G | T | 2 | a0001c0006t0005g0077a0001c0006t0005g0078 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.742-1925G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261112 | ||||||
chr9:137261113
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.742-1924C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261113 | ||||||
chr9:137261123
|
A | T | 2 | a0001c0002t0002g0044a0001c0002t0002g0059 | 2 | HG01496.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.742-1914A>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261123 | ||||||
chr9:137261211
|
G | A | 1 | a0001c0002t0002g0095 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.742-1826G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261211 | ||||||
chr9:137261233
|
G | C | 1 | a0001c0001t0001g0198 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.742-1804G>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261233 | ||||||
chr9:137261241
|
G | A | 19 | a0001c0002t0002g0013a0001c0002t0002g0024a0001c0002t0002g0025others(16): Show | 22 | HG00544.hp1 HG02015.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.742-1796G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261241 | ||||||
chr9:137261266
|
G | C | 1 | a0001c0019t0008g0100 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.742-1771G>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261266 | ||||||
chr9:137261281
|
A | G | 1 | a0001c0003t0001g0171 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.742-1756A>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261281 | ||||||
chr9:137261297
|
G | A | 1 | a0001c0019t0008g0100 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.742-1740G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261297 | ||||||
chr9:137261321
|
C | A | 1 | a0001c0002t0002g0226 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.742-1716C>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261321 | ||||||
chr9:137261331
|
C | T | 11 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0033others(8): Show | 17 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.742-1706C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261331 | ||||||
chr9:137261332
|
T | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.742-1705T>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261332 | ||||||
chr9:137261339
|
CA | C | 18 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0033others(15): Show | 23 | HG00099.hp2 HG00642.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.742-1681delA | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr9 | 137261339 | |||||
chr9:137261339
|
CAAAAAA | C | 5 | a0001c0002t0002g0018a0001c0002t0002g0019a0001c0002t0002g0058others(2): Show | 7 | HG02027.hp1 HG02056.hp2 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.742-1686_742-1681d others(8): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr9 | 137261339 | |||||
chr9:137261358
|
T | TA | 9 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0234others(6): Show | 12 | HG00741.hp2 HG01175.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.742-1664dupA | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr9 | 137261358 | |||||
chr9:137261371
|
A | C | 2 | a0001c0002t0002g0019a0001c0002t0002g0058 | 3 | NA18612.hp1 NA18974.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.742-1666A>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261371 | ||||||
chr9:137261447
|
C | T | 1 | a0001c0002t0002g0208 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.742-1590C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261447 | ||||||
chr9:137261486
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.742-1551C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261486 | ||||||
chr9:137261502
|
C | G | 1 | a0001c0002t0002g0224 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.742-1535C>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261502 | ||||||
chr9:137261508
|
A | G | 1 | a0001c0002t0002g0236 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.742-1529A>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261508 | ||||||
chr9:137261588
|
G | A | 6 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0132others(3): Show | 8 | HG01261.hp2 HG02109.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.742-1449G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261588 | ||||||
chr9:137261612
|
C | T | 3 | a0001c0002t0003g0011a0001c0002t0003g0227a0001c0002t0007g0037 | 7 | HG01975.hp2 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.742-1425C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261612 | ||||||
chr9:137261652
|
C | T | 12 | a0001c0002t0002g0016a0001c0002t0002g0038a0001c0002t0002g0200others(9): Show | 15 | HG01167.hp1 HG01169.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.742-1385C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261652 | ||||||
chr9:137261653
|
G | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.742-1384G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261653 | ||||||
chr9:137261657
|
CA | C | 10 | a0001c0002t0002g0055a0001c0002t0002g0059a0001c0002t0002g0079others(7): Show | 10 | HG01975.hp2 HG02015.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.742-1360delA | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr9 | 137261657 | |||||
chr9:137261657
|
CAAAAAAA others(2): Show |
C | 137 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.742-1368_742-1360d others(11): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr9 | 137261657 | |||||
chr9:137261657
|
CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0001g0115a0001c0013t0001g0164 | 2 | HG02895.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.742-1369_742-1360d others(12): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr9 | 137261657 | |||||
chr9:137261702
|
C | T | 5 | a0001c0002t0002g0038a0001c0002t0002g0202a0001c0002t0002g0205others(2): Show | 6 | HG01167.hp1 HG01169.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.742-1335C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261702 | ||||||
chr9:137261720
|
T | C | 1 | a0001c0002t0003g0227 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.742-1317T>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261720 | ||||||
chr9:137261730
|
G | T | 1 | a0001c0002t0002g0054 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.742-1307G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261730 | ||||||
chr9:137261733
|
C | T | 1 | a0001c0002t0002g0066 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.742-1304C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261733 | ||||||
chr9:137261767
|
G | A | 140 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(137): Show | 218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.742-1270G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261767 | ||||||
chr9:137261816
|
C | A | 12 | a0001c0002t0002g0016a0001c0002t0002g0038a0001c0002t0002g0200others(9): Show | 15 | HG01167.hp1 HG01169.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.742-1221C>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261816 | ||||||
chr9:137261979
|
C | CAGAG | 133 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(130): Show | 211 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.742-1045_742-1042d others(6): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr9 | 137261979 | |||||
chr9:137261979
|
C | CAGAGAG | 7 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(4): Show | 7 | HG00673.hp2 HG03139.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.742-1047_742-1042d others(8): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr9 | 137261979 | |||||
chr9:137262030
|
G | T | 9 | a0001c0002t0002g0013a0001c0002t0002g0079a0001c0002t0002g0088others(6): Show | 11 | HG00544.hp1 HG02015.hp1 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.742-1007G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137262030 | ||||||
chr9:137262149
|
A | G | 47 | a0001c0002t0002g0002a0001c0002t0002g0012a0001c0002t0002g0017others(44): Show | 68 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.742-888A>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137262149 | ||||||
chr9:137262345
|
G | C | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0132others(2): Show | 7 | HG01261.hp2 HG02109.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.742-692G>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137262345 | ||||||
chr9:137262511
|
G | T | 1 | a0001c0002t0002g0043 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.742-526G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137262511 | ||||||
chr9:137262550
|
G | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.742-487G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137262550 | ||||||
chr9:137262611
|
G | A | 140 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(137): Show | 218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.742-426G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137262611 | ||||||
chr9:137262614
|
T | A | 1 | a0001c0002t0007g0037 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.742-423T>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137262614 | ||||||
chr9:137262798
|
C | T | 78 | a0001c0002t0002g0002a0001c0002t0002g0012a0001c0002t0002g0013others(75): Show | 105 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.742-239C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137262798 | ||||||
chr9:137262870
|
A | G | 2 | a0001c0006t0005g0077a0001c0006t0005g0078 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.742-167A>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137262870 | ||||||
chr9:137262977
|
G | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.742-60G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137262977 | ||||||
chr9:137263004
|
G | A | 6 | a0001c0002t0002g0038a0001c0002t0002g0202a0001c0002t0002g0203others(3): Show | 7 | HG01167.hp1 HG01169.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.742-33G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137263004 | ||||||
chr9:137263008
|
T | C | 159 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(156): Show | 240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.742-29T>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137263008 | ||||||
chr9:137263030
|
G | A | 10 | a0001c0002t0002g0016a0001c0002t0002g0038a0001c0002t0002g0200others(7): Show | 13 | HG01167.hp1 HG01169.hp1 HG01361.hp2 others(10): Show |
splice_region_variant&intron_variant | LOW | c.742-7G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137263030 | ||||||
chr9:137263249
|
C | T | 135 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.927+27C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | chr9 | 137263249 | ||||||
chr9:137263267
|
T | TGCTGCCC others(76): Show |
1 | a0001c0001t0001g0183 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.927+63_927+64insCT others(81): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr9 | 137263267 | |||||
chr9:137263295
|
ACTCCCCG others(77): Show |
A | 1 | a0001c0002t0002g0087 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.927+93_927+176delT others(83): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr9 | 137263295 | |||||
chr9:137263378
|
C | T | 5 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(2): Show | 5 | HG01106.hp2 HG01168.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.927+156C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | chr9 | 137263378 | ||||||
chr9:137263382
|
C | T | 18 | a0001c0002t0002g0013a0001c0002t0002g0024a0001c0002t0002g0025others(15): Show | 21 | HG00544.hp1 HG02015.hp1 HG02132.hp2 others(18): Show |
intron_variant | MODIFIER | c.927+160C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | chr9 | 137263382 | ||||||
chr9:137263385
|
C | T | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | HG02074.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.927+163C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | chr9 | 137263385 | ||||||
chr9:137263429
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.927+207C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | chr9 | 137263429 | ||||||
chr9:137263507
|
C | T | 2 | a0001c0006t0005g0077a0001c0006t0005g0078 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.927+285C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | chr9 | 137263507 | ||||||
chr9:137263508
|
C | T | 1 | a0001c0002t0002g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.927+286C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | chr9 | 137263508 | ||||||
chr9:137263518
|
CT | C | 1 | a0001c0002t0003g0011 | 4 | HG02630.hp1 HG02809.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+297delT | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | chr9 | 137263518 | ||||||
chr9:137263562
|
C | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(137): Show | 218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.927+340C>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | chr9 | 137263562 | ||||||
chr9:137263569
|
A | G | 1 | a0001c0001t0001g0177 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.927+347A>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | chr9 | 137263569 | ||||||
chr9:137263591
|
T | A | 140 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(137): Show | 218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.927+369T>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | chr9 | 137263591 | ||||||
chr9:137263600
|
C | T | 4 | a0001c0001t0001g0032a0001c0001t0001g0156a0001c0001t0001g0157others(1): Show | 5 | HG02602.hp2 HG02735.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.927+378C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | chr9 | 137263600 | ||||||
chr9:137263705
|
G | A | 13 | a0001c0002t0002g0016a0001c0002t0002g0038a0001c0002t0002g0200others(10): Show | 16 | HG01167.hp1 HG01169.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.927+483G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | chr9 | 137263705 | ||||||
chr9:137263749
|
C | T | 13 | a0001c0002t0002g0016a0001c0002t0002g0038a0001c0002t0002g0200others(10): Show | 16 | HG01167.hp1 HG01169.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.928-496C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | chr9 | 137263749 | ||||||
chr9:137263843
|
C | T | 2 | a0001c0002t0002g0091a0001c0002t0002g0094 | 2 | NA18977.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.928-402C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | chr9 | 137263843 | ||||||
chr9:137264017
|
C | T | 1 | a0001c0002t0002g0041 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.928-228C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | chr9 | 137264017 | ||||||
chr9:137264063
|
C | G | 1 | a0001c0002t0002g0099 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.928-182C>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | chr9 | 137264063 | ||||||
chr9:137264085
|
G | A | 1 | a0001c0002t0007g0037 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.928-160G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | chr9 | 137264085 | ||||||
chr9:137264198
|
C | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.928-47C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | chr9 | 137264198 | ||||||
chr9:137264419
|
T | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(137): Show | 218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.1040+62T>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137264419 | ||||||
chr9:137264475
|
G | T | 1 | a0001c0001t0001g0083 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1040+118G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137264475 | ||||||
chr9:137264497
|
G | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1040+140G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137264497 | ||||||
chr9:137264552
|
G | A | 1 | a0001c0002t0002g0047 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1040+195G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137264552 | ||||||
chr9:137264659
|
G | T | 2 | a0001c0002t0004g0080a0001c0002t0004g0081 | 2 | HG01109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1040+302G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137264659 | ||||||
chr9:137264772
|
G | A | 47 | a0001c0002t0002g0002a0001c0002t0002g0012a0001c0002t0002g0017others(44): Show | 68 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.1040+415G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137264772 | ||||||
chr9:137264787
|
C | G | 1 | a0001c0002t0002g0090 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1040+430C>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137264787 | ||||||
chr9:137264793
|
C | T | 2 | a0001c0002t0004g0080a0001c0002t0004g0081 | 2 | HG01109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1040+436C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137264793 | ||||||
chr9:137264799
|
C | T | 1 | a0001c0003t0001g0193 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1040+442C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137264799 | ||||||
chr9:137264869
|
T | A | 1 | a0001c0001t0001g0170 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1040+512T>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137264869 | ||||||
chr9:137264953
|
G | A | 1 | a0001c0019t0008g0100 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1040+596G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137264953 | ||||||
chr9:137265031
|
C | CT | 41 | a0001c0002t0002g0013a0001c0002t0002g0016a0001c0002t0002g0017others(38): Show | 48 | HG00544.hp1 HG01167.hp1 HG01169.hp1 others(45): Show |
intron_variant | MODIFIER | c.1040+697dupT | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr9 | 137265031 | |||||
chr9:137265031
|
C | CTT | 40 | a0001c0002t0002g0002a0001c0002t0002g0018a0001c0002t0002g0020others(37): Show | 57 | HG00597.hp2 HG00621.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.1040+696_1040+697d others(4): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr9 | 137265031 | |||||
chr9:137265031
|
C | CTTT | 5 | a0001c0002t0002g0012a0001c0002t0002g0019a0001c0002t0002g0061others(2): Show | 8 | HG00423.hp2 HG01978.hp1 HG03669.hp1 others(5): Show |
intron_variant | MODIFIER | c.1040+695_1040+697d others(5): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr9 | 137265031 | |||||
chr9:137265054
|
T | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(113): Show | 184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.1040+697T>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137265054 | ||||||
chr9:137265054
|
T | TC | 19 | a0001c0001t0001g0003a0001c0001t0001g0031a0001c0001t0001g0083others(16): Show | 29 | HG01106.hp1 HG01106.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.1040+698dupC | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr9 | 137265054 | |||||
chr9:137265109
|
A | G | 1 | a0001c0002t0002g0053 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1040+752A>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137265109 | ||||||
chr9:137265212
|
G | C | 10 | a0001c0002t0002g0016a0001c0002t0002g0038a0001c0002t0002g0200others(7): Show | 13 | HG01167.hp1 HG01169.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.1041-665G>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137265212 | ||||||
chr9:137265230
|
G | A | 140 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(137): Show | 218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.1041-647G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137265230 | ||||||
chr9:137265239
|
TCAAA | T | 5 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(2): Show | 5 | HG00673.hp2 NA18950.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1041-630_1041-627d others(6): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr9 | 137265239 | |||||
chr9:137265387
|
C | CTTTTTTT | 109 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(106): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1041-477_1041-471d others(9): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr9 | 137265387 | |||||
chr9:137265387
|
C | CTTTTTTT others(1): Show |
21 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0029others(18): Show | 34 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.1041-478_1041-471d others(10): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr9 | 137265387 | |||||
chr9:137265387
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0001g0153 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1041-484_1041-471d others(16): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr9 | 137265387 | |||||
chr9:137265387
|
CT | C | 70 | a0001c0002t0002g0002a0001c0002t0002g0012a0001c0002t0002g0013others(67): Show | 97 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.1041-471delT | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr9 | 137265387 | |||||
chr9:137265387
|
CTT | C | 6 | a0001c0002t0002g0048a0001c0002t0002g0054a0001c0002t0002g0066others(3): Show | 6 | HG01891.hp2 HG02258.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.1041-472_1041-471d others(4): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr9 | 137265387 | |||||
chr9:137265533
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1041-344C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137265533 | ||||||
chr9:137265580
|
G | C | 47 | a0001c0002t0002g0002a0001c0002t0002g0012a0001c0002t0002g0017others(44): Show | 68 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.1041-297G>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137265580 | ||||||
chr9:137265634
|
C | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1041-243C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137265634 | ||||||
chr9:137265638
|
TCGGCCTG others(36): Show |
T | 48 | a0001c0002t0002g0002a0001c0002t0002g0012a0001c0002t0002g0017others(45): Show | 69 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.1041-196_1041-154d others(45): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr9 | 137265638 | |||||
chr9:137265673
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1041-204C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137265673 | ||||||
chr9:137265674
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1041-203G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137265674 | ||||||
chr9:137265676
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1041-201C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137265676 | ||||||
chr9:137265721
|
C | T | 1 | a0001c0002t0002g0092 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1041-156C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137265721 | ||||||
chr9:137265726
|
G | T | 2 | a0001c0002t0002g0042a0001c0002t0002g0043 | 2 | NA18999.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1041-151G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137265726 | ||||||
chr9:137265803
|
C | T | 2 | a0001c0006t0005g0077a0001c0006t0005g0078 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1041-74C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137265803 | ||||||
chr9:137265821
|
C | A | 1 | a0001c0002t0012g0068 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1041-56C>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137265821 | ||||||
chr9:137266027
|
G | A | 1 | a0001c0006t0005g0078 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1143+48G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 7/12 | chr9 | 137266027 | ||||||
chr9:137266082
|
G | A | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG01261.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1143+103G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 7/12 | chr9 | 137266082 | ||||||
chr9:137266096
|
G | T | 1 | a0001c0018t0001g0086 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1143+117G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 7/12 | chr9 | 137266096 | ||||||
chr9:137266130
|
T | C | 1 | a0001c0002t0003g0227 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1143+151T>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 7/12 | chr9 | 137266130 | ||||||
chr9:137266185
|
C | T | 2 | a0001c0006t0005g0077a0001c0006t0005g0078 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1144-146C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 7/12 | chr9 | 137266185 | ||||||
chr9:137266191
|
G | A | 1 | a0001c0001t0001g0230 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1144-140G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 7/12 | chr9 | 137266191 | ||||||
chr9:137266205
|
T | A | 1 | a0001c0002t0002g0094 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1144-126T>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 7/12 | chr9 | 137266205 | ||||||
chr9:137266279
|
A | G | 1 | a0001c0003t0001g0193 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1144-52A>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 7/12 | chr9 | 137266279 | ||||||
chr9:137266529
|
T | G | 1 | a0001c0002t0002g0049 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1239+103T>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 8/12 | chr9 | 137266529 | ||||||
chr9:137266602
|
G | A | 1 | a0001c0019t0008g0100 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1239+176G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 8/12 | chr9 | 137266602 | ||||||
chr9:137266645
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1239+219G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 8/12 | chr9 | 137266645 | ||||||
chr9:137266662
|
G | A | 1 | a0001c0019t0008g0100 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1239+236G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 8/12 | chr9 | 137266662 | ||||||
chr9:137266668
|
G | A | 1 | a0001c0001t0014g0143 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1239+242G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 8/12 | chr9 | 137266668 | ||||||
chr9:137266732
|
C | T | 1 | a0001c0002t0002g0064 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1240-212C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 8/12 | chr9 | 137266732 | ||||||
chr9:137266749
|
T | C | 141 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(138): Show | 219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.1240-195T>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 8/12 | chr9 | 137266749 | ||||||
chr9:137266882
|
C | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1240-62C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 8/12 | chr9 | 137266882 | ||||||
chr9:137266900
|
C | T | 5 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(2): Show | 5 | HG00673.hp2 NA18950.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1240-44C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 8/12 | chr9 | 137266900 | ||||||
chr9:137266901
|
A | G | 5 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(2): Show | 5 | HG00673.hp2 NA18950.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1240-43A>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 8/12 | chr9 | 137266901 | ||||||
chr9:137267125
|
C | T | 1 | a0001c0002t0002g0075 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1382+39C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 9/12 | chr9 | 137267125 | ||||||
chr9:137267163
|
G | C | 1 | a0001c0002t0012g0068 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1382+77G>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 9/12 | chr9 | 137267163 | ||||||
chr9:137267176
|
CGGTGTGG others(4): Show |
C | 1 | a0001c0019t0008g0100 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1383-62_1383-52del others(11): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr9 | 137267176 | |||||
chr9:137267179
|
TGTGGGGC others(4): Show |
T | 137 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 213 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.1383-28_1383-18del others(11): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr9 | 137267179 | |||||
chr9:137267179
|
TGTGGGGC others(15): Show |
T | 2 | a0001c0001t0001g0015a0001c0001t0001g0168 | 4 | HG00099.hp2 HG00642.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1383-39_1383-18del others(22): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr9 | 137267179 | |||||
chr9:137267184
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1383-56G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 9/12 | chr9 | 137267184 | ||||||
chr9:137267190
|
G | T | 1 | a0001c0019t0008g0100 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1383-50G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 9/12 | chr9 | 137267190 | ||||||
chr9:137267195
|
G | A | 134 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(131): Show | 210 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.1383-45G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 9/12 | chr9 | 137267195 | ||||||
chr9:137267206
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0168 | 4 | HG00099.hp2 HG00642.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1383-34G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 9/12 | chr9 | 137267206 | ||||||
chr9:137267226
|
C | A | 1 | a0001c0002t0012g0068 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1383-14C>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 9/12 | chr9 | 137267226 | ||||||
chr9:137267397
|
G | A | 1 | a0001c0001t0001g0144 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1489+51G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137267397 | ||||||
chr9:137267419
|
C | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1489+73C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137267419 | ||||||
chr9:137267457
|
G | T | 140 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(137): Show | 218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.1489+111G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137267457 | ||||||
chr9:137267490
|
C | CT | 17 | a0001c0001t0001g0119a0001c0001t0001g0126a0001c0001t0001g0133others(14): Show | 17 | HG01106.hp2 HG01109.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.1489+164dupT | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr9 | 137267490 | |||||
chr9:137267490
|
CT | C | 23 | a0001c0001t0001g0230a0001c0002t0002g0013a0001c0002t0002g0024others(20): Show | 26 | HG00544.hp1 HG00741.hp2 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.1489+164delT | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr9 | 137267490 | |||||
chr9:137267492
|
T | C | 17 | a0001c0002t0002g0013a0001c0002t0002g0024a0001c0002t0002g0025others(14): Show | 20 | HG00544.hp1 HG02015.hp1 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.1489+146T>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137267492 | ||||||
chr9:137267493
|
T | C | 1 | a0001c0002t0002g0236 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1489+147T>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137267493 | ||||||
chr9:137267518
|
A | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(137): Show | 218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.1489+172A>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137267518 | ||||||
chr9:137267603
|
C | T | 1 | a0001c0012t0002g0074 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1489+257C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137267603 | ||||||
chr9:137267638
|
C | T | 1 | a0001c0002t0002g0221 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1489+292C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137267638 | ||||||
chr9:137267822
|
T | G | 1 | a0001c0018t0001g0086 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1489+476T>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137267822 | ||||||
chr9:137267889
|
G | C | 1 | a0001c0018t0001g0086 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1489+543G>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137267889 | ||||||
chr9:137268088
|
A | G | 85 | a0001c0001t0001g0123a0001c0002t0002g0002a0001c0002t0002g0012others(82): Show | 116 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.1489+742A>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137268088 | ||||||
chr9:137268181
|
C | T | 5 | a0001c0001t0001g0030a0001c0001t0001g0103a0001c0001t0001g0104others(2): Show | 6 | HG01891.hp1 HG02280.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.1489+835C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137268181 | ||||||
chr9:137268212
|
G | T | 19 | a0001c0002t0002g0013a0001c0002t0002g0024a0001c0002t0002g0025others(16): Show | 22 | HG00544.hp1 HG02015.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.1489+866G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137268212 | ||||||
chr9:137268227
|
T | G | 10 | a0001c0002t0002g0016a0001c0002t0002g0038a0001c0002t0002g0200others(7): Show | 13 | HG01167.hp1 HG01169.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.1489+881T>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137268227 | ||||||
chr9:137268243
|
A | C | 2 | a0001c0002t0002g0218a0001c0002t0002g0222 | 2 | HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1489+897A>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137268243 | ||||||
chr9:137268360
|
C | T | 1 | a0001c0006t0005g0078 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1489+1014C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137268360 | ||||||
chr9:137268381
|
C | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1489+1035C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137268381 | ||||||
chr9:137268443
|
G | A | 2 | a0001c0001t0001g0101a0001c0001t0001g0102 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1489+1097G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137268443 | ||||||
chr9:137268558
|
C | T | 1 | a0001c0002t0002g0228 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1489+1212C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137268558 | ||||||
chr9:137268573
|
G | A | 1 | a0001c0001t0001g0031 | 2 | HG02615.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1489+1227G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137268573 | ||||||
chr9:137268581
|
G | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1489+1235G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137268581 | ||||||
chr9:137268676
|
G | T | 2 | a0001c0002t0003g0011a0001c0002t0003g0227 | 5 | HG01975.hp2 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1489+1330G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137268676 | ||||||
chr9:137268717
|
C | T | 1 | a0001c0002t0002g0089 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1489+1371C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137268717 | ||||||
chr9:137268826
|
T | C | 1 | a0001c0003t0001g0189 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1489+1480T>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137268826 | ||||||
chr9:137268937
|
G | A | 1 | a0001c0019t0008g0100 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1489+1591G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137268937 | ||||||
chr9:137268998
|
A | G | 5 | a0001c0002t0002g0039a0001c0002t0002g0220a0001c0002t0002g0221others(2): Show | 5 | HG02922.hp2 HG03130.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.1489+1652A>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137268998 | ||||||
chr9:137269024
|
A | G | 47 | a0001c0002t0002g0002a0001c0002t0002g0012a0001c0002t0002g0017others(44): Show | 68 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.1489+1678A>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137269024 | ||||||
chr9:137269081
|
G | A | 1 | a0001c0002t0002g0226 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1489+1735G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137269081 | ||||||
chr9:137269139
|
C | T | 1 | a0001c0019t0008g0100 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1489+1793C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137269139 | ||||||
chr9:137269223
|
T | G | 3 | a0001c0002t0002g0212a0001c0002t0002g0213a0001c0002t0002g0214 | 3 | HG01243.hp1 HG02055.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1489+1877T>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137269223 | ||||||
chr9:137269261
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1489+1915C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137269261 | ||||||
chr9:137269292
|
G | A | 1 | a0001c0002t0002g0041 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1489+1946G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137269292 | ||||||
chr9:137269667
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1489+2321G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137269667 | ||||||
chr9:137269676
|
C | T | 1 | a0001c0002t0003g0227 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1489+2330C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137269676 | ||||||
chr9:137269803
|
G | A | 4 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0139others(1): Show | 4 | NA18950.hp1 NA18970.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.1490-2278G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137269803 | ||||||
chr9:137269924
|
C | T | 140 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(137): Show | 218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.1490-2157C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137269924 | ||||||
chr9:137269992
|
G | T | 1 | a0001c0002t0002g0048 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1490-2089G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137269992 | ||||||
chr9:137270031
|
G | A | 19 | a0001c0002t0002g0013a0001c0002t0002g0024a0001c0002t0002g0025others(16): Show | 22 | HG00544.hp1 HG02015.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.1490-2050G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137270031 | ||||||
chr9:137270158
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1490-1923G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137270158 | ||||||
chr9:137270195
|
C | T | 1 | a0001c0002t0011g0216 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1490-1886C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137270195 | ||||||
chr9:137270205
|
T | C | 1 | a0001c0002t0002g0079 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1490-1876T>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137270205 | ||||||
chr9:137270237
|
C | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1490-1844C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137270237 | ||||||
chr9:137270280
|
C | CA | 33 | a0001c0001t0001g0083a0001c0001t0001g0120a0001c0001t0001g0122others(30): Show | 37 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.1490-1781dupA | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr9 | 137270280 | |||||
chr9:137270280
|
CA | C | 8 | a0001c0001t0001g0150a0001c0001t0001g0173a0001c0002t0002g0073others(5): Show | 8 | HG01516.hp2 HG02897.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.1490-1781delA | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr9 | 137270280 | |||||
chr9:137270346
|
T | G | 1 | a0001c0002t0012g0068 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1490-1735T>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137270346 | ||||||
chr9:137270505
|
G | A | 2 | a0001c0006t0005g0077a0001c0006t0005g0078 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1490-1576G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137270505 | ||||||
chr9:137270571
|
C | G | 1 | a0001c0002t0002g0048 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1490-1510C>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137270571 | ||||||
chr9:137270651
|
G | A | 3 | a0001c0002t0002g0212a0001c0002t0002g0213a0001c0002t0002g0214 | 3 | HG01243.hp1 HG02055.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1490-1430G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137270651 | ||||||
chr9:137270713
|
G | A | 1 | a0001c0002t0012g0068 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1490-1368G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137270713 | ||||||
chr9:137270714
|
A | G | 1 | a0001c0002t0012g0068 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1490-1367A>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137270714 | ||||||
chr9:137270715
|
G | T | 1 | a0001c0002t0012g0068 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1490-1366G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137270715 | ||||||
chr9:137270795
|
C | T | 1 | a0001c0002t0002g0051 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1490-1286C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137270795 | ||||||
chr9:137271052
|
C | T | 3 | a0001c0002t0002g0008a0001c0002t0002g0199a0001c0002t0002g0208 | 8 | HG02258.hp1 HG02717.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1490-1029C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137271052 | ||||||
chr9:137271074
|
C | T | 1 | a0001c0019t0008g0100 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1490-1007C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137271074 | ||||||
chr9:137271115
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1490-966C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137271115 | ||||||
chr9:137271166
|
C | T | 1 | a0001c0002t0002g0048 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1490-915C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137271166 | ||||||
chr9:137271167
|
C | T | 1 | a0001c0002t0002g0048 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1490-914C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137271167 | ||||||
chr9:137271379
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1490-702C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137271379 | ||||||
chr9:137271459
|
G | A | 1 | a0001c0019t0008g0100 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1490-622G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137271459 | ||||||
chr9:137271533
|
C | T | 1 | a0001c0002t0002g0050 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1490-548C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137271533 | ||||||
chr9:137271545
|
C | T | 1 | a0001c0002t0002g0069 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1490-536C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137271545 | ||||||
chr9:137271606
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1490-475T>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137271606 | ||||||
chr9:137271647
|
ACT | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0167 | 3 | NA18951.hp2 NA19070.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1490-429_1490-428d others(4): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr9 | 137271647 | |||||
chr9:137271672
|
G | T | 1 | a0001c0002t0002g0087 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1490-409G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137271672 | ||||||
chr9:137271918
|
C | A | 2 | a0001c0002t0004g0080a0001c0002t0004g0081 | 2 | HG01109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1490-163C>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137271918 | ||||||
chr9:137272028
|
C | T | 1 | a0001c0002t0003g0011 | 4 | HG02630.hp1 HG02809.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1490-53C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137272028 |