geneid | 5340 |
---|---|
ensemblid | ENSG00000122194.20 |
hgncid | 9071 |
symbol | PLG |
name | plasminogen |
refseq_nuc | NM_000301.5 |
refseq_prot | NP_000292.1 |
ensembl_nuc | ENST00000308192.14 |
ensembl_prot | ENSP00000308938.9 |
mane_status | MANE Select |
chr | chr6 |
start | 160702244 |
end | 160754097 |
strand | + |
ver | v1.2 |
region | chr6:160702244-160754097 |
region5000 | chr6:160697244-160759097 |
regionname0 | PLG_chr6_160702244_160754097 |
regionname5000 | PLG_chr6_160697244_160759097 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 810 | 318 | 67 | 53 | 148 | 11 | 37 | 123 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0002 | 0/0 | 810 | 42 | 17 | 20 | 0 | 3 | 2 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0003 | 0/0 | 810 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0004 | 0/0 | 810 | 4 | 0 | 4 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0005 | 0/0 | 810 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0006 | 0/0 | 810 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0007 | 0/0 | 810 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0008 | 0/0 | 810 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0009 | 0/0 | 810 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0010 | 0/0 | 810 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0011 | 0/0 | 810 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0012 | 0/0 | 810 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 2433 | 119 | 11 | 15 | 71 | 6 | 15 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
c0002 | 0/0 | 2433 | 89 | 6 | 20 | 52 | 1 | 10 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
c0003 | 0/0 | 2433 | 37 | 3 | 7 | 21 | 1 | 5 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
c0004 | 0/0 | 2433 | 29 | 8 | 16 | 0 | 3 | 2 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
c0005 | 1/0 | 2433 | 21 | 5 | 6 | 1 | 2 | 6 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
c0006 | 0/0 | 2433 | 19 | 19 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
c0007 | 0/0 | 2433 | 12 | 9 | 3 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
c0008 | 0/0 | 2433 | 8 | 8 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
c0009 | 0/0 | 2433 | 7 | 2 | 4 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
c0010 | 0/0 | 2433 | 4 | 4 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
c0011 | 0/0 | 2433 | 4 | 1 | 0 | 3 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
c0012 | 0/0 | 2433 | 4 | 4 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
c0013 | 0/0 | 2433 | 4 | 4 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
c0014 | 0/0 | 2433 | 3 | 0 | 0 | 3 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
c0015 | 0/0 | 2433 | 3 | 2 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
c0016 | 0/0 | 2433 | 2 | 0 | 0 | 0 | 0 | 2 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
c0017 | 0/0 | 2433 | 2 | 0 | 0 | 2 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
c0018 | 0/0 | 2433 | 2 | 0 | 2 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
c0019 | 0/0 | 2433 | 2 | 0 | 0 | 2 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
c0020 | 0/0 | 2433 | 2 | 0 | 2 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
c0021 | 0/0 | 2433 | 2 | 2 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
c0022 | 0/0 | 2433 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
c0023 | 0/0 | 2433 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
c0024 | 0/0 | 2433 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
c0025 | 0/0 | 2433 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
c0026 | 0/0 | 2433 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
c0027 | 0/0 | 2433 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
c0028 | 0/0 | 2433 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
c0029 | 0/0 | 2433 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
c0030 | 0/0 | 2433 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1097 | 261 | 31 | 46 | 143 | 8 | 32 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
t0002 | 1/0 | 1098 | 27 | 7 | 10 | 1 | 2 | 6 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
t0003 | 0/0 | 1098 | 23 | 1 | 16 | 0 | 3 | 3 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
t0004 | 0/0 | 1098 | 13 | 10 | 3 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
t0005 | 0/0 | 1098 | 11 | 11 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
t0006 | 0/0 | 1097 | 10 | 0 | 0 | 10 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
t0007 | 0/0 | 1097 | 10 | 9 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
t0008 | 0/0 | 1098 | 6 | 6 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
t0009 | 0/0 | 1097 | 5 | 5 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
t0010 | 0/0 | 1098 | 3 | 3 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
t0011 | 0/0 | 1098 | 2 | 2 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
t0012 | 0/0 | 1098 | 2 | 0 | 1 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
t0013 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
t0014 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
t0015 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
t0016 | 0/0 | 1098 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
t0017 | 0/0 | 1097 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
t0018 | 0/0 | 1097 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
t0019 | 0/0 | 1097 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
t0020 | 0/0 | 1097 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
t0021 | 0/0 | 1097 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
t0022 | 0/0 | 1097 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
t0023 | 0/0 | 1097 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0002 | 1/0 | 3 | 0 | 0 | 0 | 0 | 2 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0004 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0027 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2433 | 119 | 11 | 15 | 71 | 6 | 15 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0002 | 0/0 | 2433 | 89 | 6 | 20 | 52 | 1 | 10 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0003 | 0/0 | 2433 | 37 | 3 | 7 | 21 | 1 | 5 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0005 | 1/0 | 2433 | 21 | 5 | 6 | 1 | 2 | 6 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0006 | 0/0 | 2433 | 19 | 19 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0008 | 0/0 | 2433 | 8 | 8 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0009 | 0/0 | 2433 | 7 | 2 | 4 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0011 | 0/0 | 2433 | 4 | 1 | 0 | 3 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0013 | 0/0 | 2433 | 4 | 4 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0015 | 0/0 | 2433 | 3 | 2 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0021 | 0/0 | 2433 | 2 | 2 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0024 | 0/0 | 2433 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0025 | 0/0 | 2433 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0027 | 0/0 | 2433 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0028 | 0/0 | 2433 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0029 | 0/0 | 2433 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0002c0004 | 0/0 | 2433 | 29 | 8 | 16 | 0 | 3 | 2 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0002c0007 | 0/0 | 2433 | 12 | 9 | 3 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0002c0022 | 0/0 | 2433 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0003c0012 | 0/0 | 2433 | 4 | 4 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0004c0018 | 0/0 | 2433 | 2 | 0 | 2 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0004c0020 | 0/0 | 2433 | 2 | 0 | 2 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0005c0010 | 0/0 | 2433 | 4 | 4 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0006c0014 | 0/0 | 2433 | 3 | 0 | 0 | 3 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0007c0016 | 0/0 | 2433 | 2 | 0 | 0 | 0 | 0 | 2 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0008c0017 | 0/0 | 2433 | 2 | 0 | 0 | 2 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0009c0019 | 0/0 | 2433 | 2 | 0 | 0 | 2 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0010c0030 | 0/0 | 2433 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0011c0026 | 0/0 | 2433 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0012c0023 | 0/0 | 2433 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3529 | 106 | 8 | 15 | 62 | 6 | 14 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0001t0006 | 0/0 | 3529 | 7 | 0 | 0 | 7 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0001t0007 | 0/0 | 3529 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0001t0017 | 0/0 | 3529 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0001t0018 | 0/0 | 3529 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0001t0019 | 0/0 | 3529 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0001t0020 | 0/0 | 3529 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0001t0022 | 0/0 | 3529 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0002t0001 | 0/0 | 3529 | 87 | 5 | 20 | 51 | 1 | 10 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0002t0006 | 0/0 | 3529 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0002t0009 | 0/0 | 3529 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0003t0001 | 0/0 | 3529 | 37 | 3 | 7 | 21 | 1 | 5 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0005t0002 | 1/0 | 3530 | 17 | 1 | 6 | 1 | 2 | 6 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0005t0005 | 0/0 | 3530 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0005t0010 | 0/0 | 3530 | 2 | 2 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0005t0011 | 0/0 | 3530 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0006t0002 | 0/0 | 3530 | 6 | 6 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0006t0004 | 0/0 | 3530 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0006t0005 | 0/0 | 3530 | 10 | 10 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0006t0013 | 0/0 | 3530 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0006t0014 | 0/0 | 3530 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0008t0001 | 0/0 | 3529 | 8 | 8 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0009t0002 | 0/0 | 3530 | 2 | 0 | 2 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0009t0004 | 0/0 | 3530 | 3 | 2 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0009t0012 | 0/0 | 3530 | 2 | 0 | 1 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0011t0001 | 0/0 | 3529 | 4 | 1 | 0 | 3 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0013t0001 | 0/0 | 3529 | 3 | 3 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0013t0009 | 0/0 | 3529 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0015t0001 | 0/0 | 3529 | 2 | 1 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0015t0009 | 0/0 | 3529 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0021t0004 | 0/0 | 3530 | 2 | 2 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0024t0009 | 0/0 | 3529 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0025t0001 | 0/0 | 3529 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0027t0010 | 0/0 | 3530 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0028t0004 | 0/0 | 3530 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0001c0029t0015 | 0/0 | 3530 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0002c0004t0003 | 0/0 | 3530 | 21 | 1 | 15 | 0 | 3 | 2 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0002c0004t0008 | 0/0 | 3530 | 6 | 6 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0002c0004t0011 | 0/0 | 3530 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0002c0004t0016 | 0/0 | 3530 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0002c0007t0001 | 0/0 | 3529 | 2 | 0 | 2 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0002c0007t0007 | 0/0 | 3529 | 9 | 8 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0002c0007t0023 | 0/0 | 3529 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0002c0022t0003 | 0/0 | 3530 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0003c0012t0001 | 0/0 | 3529 | 2 | 2 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0003c0012t0009 | 0/0 | 3529 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0003c0012t0021 | 0/0 | 3529 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0004c0018t0002 | 0/0 | 3530 | 2 | 0 | 2 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0004c0020t0004 | 0/0 | 3530 | 2 | 0 | 2 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0005c0010t0004 | 0/0 | 3530 | 4 | 4 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0006c0014t0001 | 0/0 | 3529 | 3 | 0 | 0 | 3 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0007c0016t0001 | 0/0 | 3529 | 2 | 0 | 0 | 0 | 0 | 2 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0008c0017t0006 | 0/0 | 3529 | 2 | 0 | 0 | 2 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0009c0019t0001 | 0/0 | 3529 | 2 | 0 | 0 | 2 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0010c0030t0003 | 0/0 | 3530 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0011c0026t0001 | 0/0 | 3529 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
a0012c0023t0001 | 0/0 | 3529 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | copy fasta | chr6 | 160697244 | 160759097 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0027 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0006g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0006g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0006g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0006g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0006g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0006g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0006g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0007g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0017g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0018g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0019g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0020g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0001t0022g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0006g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0002t0009g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0003t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0003t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0003t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0003t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0003t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0003t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0003t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0003t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0003t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0003t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0003t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0003t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0003t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0003t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0003t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0003t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0003t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0003t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0003t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0005t0002g0002 | 1/0 | 3 | 0 | 0 | 0 | 0 | 2 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0005t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0005t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0005t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0005t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0005t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0005t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0005t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0005t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0005t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0005t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0005t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0005t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0005t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0005t0002g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0005t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0005t0010g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0005t0010g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0005t0011g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0006t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0006t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0006t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0006t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0006t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0006t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0006t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0006t0005g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0006t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0006t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0006t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0006t0005g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0006t0005g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0006t0005g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0006t0005g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0006t0005g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0006t0013g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0006t0014g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0008t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0008t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0008t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0008t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0008t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0008t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0008t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0008t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0009t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0009t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0009t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0009t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0009t0004g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0009t0012g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0009t0012g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0011t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0011t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0011t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0011t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0013t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0013t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0013t0009g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0015t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0015t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0015t0009g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0021t0004g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0024t0009g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0025t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0027t0010g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0028t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0001c0029t0015g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0002c0004t0003g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0002c0004t0003g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0002c0004t0003g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0002c0004t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0002c0004t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0002c0004t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0002c0004t0003g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0002c0004t0003g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0002c0004t0003g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0002c0004t0003g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0002c0004t0003g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0002c0004t0003g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0002c0004t0003g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0002c0004t0003g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0002c0004t0003g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0002c0004t0003g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0002c0004t0003g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0002c0004t0003g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0002c0004t0003g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0002c0004t0008g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0002c0004t0008g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0002c0004t0008g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0002c0004t0008g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0002c0004t0008g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0002c0004t0011g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0002c0004t0016g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0002c0007t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0002c0007t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0002c0007t0007g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0002c0007t0007g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0002c0007t0007g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0002c0007t0007g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0002c0007t0007g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0002c0007t0007g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0002c0007t0007g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0002c0007t0007g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0002c0007t0007g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0002c0007t0023g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0002c0022t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0003c0012t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0003c0012t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0003c0012t0009g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0003c0012t0021g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0004c0018t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0004c0018t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0004c0020t0004g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0004c0020t0004g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0005c0010t0004g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0005c0010t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0005c0010t0004g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0006c0014t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0006c0014t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0006c0014t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0007c0016t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0008c0017t0006g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0009c0019t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0009c0019t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0010c0030t0003g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0011c0026t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
a0012c0023t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0002 | t0001 | g0145 | EUR | GBR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0275 | EUR | GBR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG00280 | hp1 | a0001 | c0005 | t0002 | g0107 | EUR | FIN | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0063 | EUR | FIN | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG00323 | hp1 | a0002 | c0004 | t0003 | g0284 | EUR | FIN | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG00323 | hp2 | a0001 | c0005 | t0002 | g0250 | EUR | FIN | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | CHS | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0158 | EAS | CHS | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | CHS | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0162 | EAS | CHS | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | CHS | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG00558 | hp2 | a0001 | c0003 | t0001 | g0235 | EAS | CHS | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0164 | EAS | CHS | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG00597 | hp2 | a0001 | c0002 | t0001 | g0129 | EAS | CHS | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | CHS | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0165 | EAS | CHS | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG00639 | hp1 | a0002 | c0004 | t0003 | g0279 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG00639 | hp2 | a0001 | c0003 | t0001 | g0153 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG00642 | hp1 | a0002 | c0004 | t0003 | g0077 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG00642 | hp2 | a0001 | c0005 | t0002 | g0304 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG00733 | hp2 | a0002 | c0004 | t0003 | g0020 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG00735 | hp1 | a0002 | c0004 | t0003 | g0020 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG00738 | hp1 | a0001 | c0005 | t0002 | g0111 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG00738 | hp2 | a0002 | c0004 | t0003 | g0023 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG00741 | hp1 | a0001 | c0003 | t0001 | g0289 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01069 | hp1 | a0001 | c0003 | t0001 | g0288 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01069 | hp2 | a0002 | c0004 | t0003 | g0079 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01070 | hp1 | a0001 | c0005 | t0002 | g0109 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01070 | hp2 | a0002 | c0004 | t0003 | g0283 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01071 | hp1 | a0002 | c0004 | t0003 | g0078 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01071 | hp2 | a0001 | c0005 | t0002 | g0106 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01074 | hp1 | a0001 | c0009 | t0002 | g0059 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01081 | hp1 | a0001 | c0003 | t0001 | g0266 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01081 | hp2 | a0002 | c0004 | t0003 | g0023 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0060 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01099 | hp2 | a0011 | c0026 | t0001 | g0068 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01106 | hp1 | a0001 | c0009 | t0004 | g0067 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01106 | hp2 | a0001 | c0003 | t0001 | g0112 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01109 | hp1 | a0002 | c0022 | t0003 | g0267 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01109 | hp2 | a0002 | c0004 | t0016 | g0080 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01168 | hp1 | a0002 | c0004 | t0003 | g0019 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01168 | hp2 | a0001 | c0002 | t0001 | g0133 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01169 | hp1 | a0002 | c0004 | t0003 | g0285 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01243 | hp1 | a0002 | c0007 | t0007 | g0042 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01243 | hp2 | a0001 | c0003 | t0001 | g0154 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0127 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01256 | hp1 | a0004 | c0020 | t0004 | g0342 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01257 | hp2 | a0001 | c0025 | t0001 | g0295 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01258 | hp1 | a0004 | c0020 | t0004 | g0336 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01258 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01261 | hp1 | a0002 | c0004 | t0003 | g0286 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01346 | hp1 | a0001 | c0009 | t0002 | g0058 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01346 | hp2 | a0002 | c0007 | t0001 | g0282 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01358 | hp2 | a0001 | c0005 | t0002 | g0345 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01361 | hp2 | a0001 | c0005 | t0002 | g0249 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01433 | hp1 | a0002 | c0007 | t0001 | g0278 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0062 | EUR | IBS | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0071 | EUR | IBS | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01884 | hp1 | a0001 | c0003 | t0001 | g0130 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01884 | hp2 | a0001 | c0006 | t0005 | g0352 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01891 | hp1 | a0001 | c0003 | t0001 | g0197 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01891 | hp2 | a0001 | c0006 | t0014 | g0037 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | PEL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PEL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0088 | AMR | PEL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01952 | hp2 | a0004 | c0018 | t0002 | g0269 | AMR | PEL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01975 | hp1 | a0002 | c0004 | t0003 | g0281 | AMR | PEL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01975 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01978 | hp1 | a0001 | c0009 | t0012 | g0070 | AMR | PEL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0128 | AMR | PEL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | PEL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02004 | hp2 | a0002 | c0004 | t0003 | g0287 | AMR | PEL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0135 | EAS | KHV | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02027 | hp1 | a0001 | c0003 | t0001 | g0132 | EAS | KHV | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0084 | EAS | KHV | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | KHV | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02055 | hp2 | a0002 | c0007 | t0007 | g0096 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0121 | EAS | KHV | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02080 | hp2 | a0001 | c0003 | t0001 | g0152 | EAS | KHV | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02132 | hp1 | a0009 | c0019 | t0001 | g0327 | EAS | KHV | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0155 | EAS | KHV | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02145 | hp1 | a0002 | c0004 | t0008 | g0033 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02145 | hp2 | a0001 | c0002 | t0001 | g0353 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02148 | hp1 | a0004 | c0018 | t0002 | g0268 | AMR | PEL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02148 | hp2 | a0001 | c0002 | t0001 | g0159 | AMR | PEL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02257 | hp2 | a0003 | c0012 | t0001 | g0239 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02258 | hp1 | a0001 | c0009 | t0004 | g0025 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02258 | hp2 | a0002 | c0007 | t0007 | g0097 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | PEL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02273 | hp2 | a0002 | c0004 | t0003 | g0271 | AMR | PEL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02280 | hp1 | a0002 | c0004 | t0008 | g0006 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02280 | hp2 | a0005 | c0010 | t0004 | g0017 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0126 | AMR | PEL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0207 | AMR | PEL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02300 | hp2 | a0001 | c0003 | t0001 | g0151 | AMR | PEL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02451 | hp1 | a0001 | c0006 | t0002 | g0276 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02451 | hp2 | a0001 | c0001 | t0022 | g0309 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02572 | hp1 | a0001 | c0008 | t0001 | g0300 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02572 | hp2 | a0001 | c0011 | t0001 | g0236 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02602 | hp1 | a0010 | c0030 | t0003 | g0019 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02602 | hp2 | a0001 | c0003 | t0001 | g0251 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02615 | hp1 | a0001 | c0001 | t0020 | g0299 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02615 | hp2 | a0002 | c0007 | t0007 | g0045 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02622 | hp1 | a0002 | c0004 | t0008 | g0030 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02622 | hp2 | a0001 | c0006 | t0005 | g0347 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02630 | hp1 | a0001 | c0008 | t0001 | g0301 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02647 | hp1 | a0001 | c0006 | t0005 | g0016 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02647 | hp2 | a0005 | c0010 | t0004 | g0017 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02683 | hp1 | a0001 | c0003 | t0001 | g0198 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02683 | hp2 | a0001 | c0001 | t0018 | g0262 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02698 | hp1 | a0002 | c0004 | t0003 | g0277 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02717 | hp1 | a0001 | c0006 | t0013 | g0243 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02717 | hp2 | a0002 | c0007 | t0007 | g0292 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02735 | hp2 | a0001 | c0002 | t0001 | g0144 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02809 | hp1 | a0001 | c0008 | t0001 | g0314 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02818 | hp1 | a0001 | c0006 | t0005 | g0354 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02818 | hp2 | a0005 | c0010 | t0004 | g0242 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02886 | hp1 | a0001 | c0013 | t0001 | g0024 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02886 | hp2 | a0001 | c0008 | t0001 | g0302 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02895 | hp1 | a0001 | c0013 | t0001 | g0024 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02896 | hp1 | a0001 | c0013 | t0001 | g0351 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02896 | hp2 | a0001 | c0006 | t0005 | g0238 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02922 | hp1 | a0001 | c0006 | t0002 | g0310 | AFR | ESN | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02922 | hp2 | a0001 | c0024 | t0009 | g0246 | AFR | ESN | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02965 | hp1 | a0002 | c0007 | t0007 | g0040 | AFR | ESN | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02965 | hp2 | a0003 | c0012 | t0001 | g0254 | AFR | ESN | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02970 | hp1 | a0005 | c0010 | t0004 | g0241 | AFR | ESN | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02970 | hp2 | a0001 | c0006 | t0004 | g0048 | AFR | ESN | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02976 | hp1 | a0001 | c0006 | t0005 | g0099 | AFR | ESN | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02976 | hp2 | a0001 | c0013 | t0009 | g0035 | AFR | ESN | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03041 | hp1 | a0001 | c0006 | t0002 | g0047 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03041 | hp2 | a0001 | c0002 | t0001 | g0199 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03098 | hp1 | a0001 | c0021 | t0004 | g0012 | AFR | MSL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03098 | hp2 | a0001 | c0029 | t0015 | g0032 | AFR | MSL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03130 | hp1 | a0001 | c0008 | t0001 | g0349 | AFR | ESN | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03130 | hp2 | a0001 | c0006 | t0005 | g0098 | AFR | ESN | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03139 | hp1 | a0001 | c0021 | t0004 | g0012 | AFR | ESN | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03139 | hp2 | a0001 | c0006 | t0002 | g0043 | AFR | ESN | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03195 | hp1 | a0002 | c0004 | t0008 | g0006 | AFR | ESN | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03195 | hp2 | a0001 | c0006 | t0005 | g0346 | AFR | ESN | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03209 | hp1 | a0002 | c0007 | t0007 | g0038 | AFR | MSL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03209 | hp2 | a0001 | c0005 | t0005 | g0240 | AFR | MSL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03225 | hp1 | a0002 | c0004 | t0011 | g0306 | AFR | MSL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03225 | hp2 | a0001 | c0005 | t0010 | g0026 | AFR | MSL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0125 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03239 | hp2 | a0001 | c0005 | t0002 | g0303 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03453 | hp1 | a0001 | c0002 | t0001 | g0208 | AFR | MSL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03453 | hp2 | a0001 | c0005 | t0010 | g0308 | AFR | MSL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03486 | hp1 | a0001 | c0002 | t0001 | g0124 | AFR | MSL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03486 | hp2 | a0001 | c0006 | t0005 | g0348 | AFR | MSL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03490 | hp1 | a0001 | c0015 | t0001 | g0316 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03490 | hp2 | a0007 | c0016 | t0001 | g0018 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03491 | hp1 | a0001 | c0002 | t0001 | g0339 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03491 | hp2 | a0001 | c0005 | t0002 | g0002 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03492 | hp1 | a0007 | c0016 | t0001 | g0018 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03492 | hp2 | a0001 | c0005 | t0002 | g0002 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03516 | hp1 | a0001 | c0006 | t0002 | g0114 | AFR | ESN | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03516 | hp2 | a0002 | c0004 | t0008 | g0034 | AFR | ESN | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03540 | hp1 | a0001 | c0006 | t0005 | g0016 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03540 | hp2 | a0001 | c0008 | t0001 | g0237 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03669 | hp1 | a0001 | c0005 | t0002 | g0270 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0073 | SAS | STU | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03688 | hp2 | a0001 | c0005 | t0002 | g0117 | SAS | STU | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0325 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0051 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0108 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03831 | hp1 | a0001 | c0002 | t0001 | g0007 | SAS | BEB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03831 | hp2 | a0001 | c0003 | t0001 | g0337 | SAS | BEB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0293 | SAS | BEB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03927 | hp2 | a0001 | c0005 | t0002 | g0252 | SAS | BEB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0166 | SAS | BEB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | BEB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | STU | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0138 | SAS | STU | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0338 | SAS | BEB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG04184 | hp2 | a0001 | c0003 | t0001 | g0156 | SAS | BEB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | STU | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG04199 | hp2 | a0001 | c0003 | t0001 | g0134 | SAS | STU | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | STU | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0334 | SAS | STU | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18522 | hp1 | a0001 | c0001 | t0007 | g0298 | AFR | YRI | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18522 | hp2 | a0002 | c0004 | t0008 | g0031 | AFR | YRI | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CHB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18612 | hp2 | a0001 | c0003 | t0001 | g0150 | EAS | CHB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18906 | hp1 | a0001 | c0027 | t0010 | g0120 | AFR | YRI | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18906 | hp2 | a0002 | c0007 | t0023 | g0050 | AFR | YRI | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18940 | hp1 | a0001 | c0011 | t0001 | g0231 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18940 | hp2 | a0001 | c0002 | t0001 | g0320 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18942 | hp2 | a0001 | c0003 | t0001 | g0261 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18945 | hp1 | a0001 | c0003 | t0001 | g0227 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0307 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18946 | hp2 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18952 | hp1 | a0001 | c0001 | t0006 | g0329 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18952 | hp2 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18953 | hp1 | a0001 | c0003 | t0001 | g0204 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18953 | hp2 | a0001 | c0001 | t0006 | g0186 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18956 | hp1 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18956 | hp2 | a0001 | c0001 | t0006 | g0187 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18960 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18962 | hp1 | a0001 | c0003 | t0001 | g0321 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18962 | hp2 | a0006 | c0014 | t0001 | g0148 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18963 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18963 | hp2 | a0001 | c0011 | t0001 | g0232 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18965 | hp1 | a0001 | c0002 | t0001 | g0319 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18965 | hp2 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18966 | hp1 | a0012 | c0023 | t0001 | g0100 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18969 | hp2 | a0001 | c0003 | t0001 | g0322 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18971 | hp2 | a0001 | c0003 | t0001 | g0203 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18974 | hp1 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18974 | hp2 | a0001 | c0001 | t0006 | g0253 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18975 | hp1 | a0001 | c0011 | t0001 | g0230 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18975 | hp2 | a0001 | c0001 | t0006 | g0188 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18978 | hp2 | a0006 | c0014 | t0001 | g0318 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0311 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18983 | hp1 | a0008 | c0017 | t0006 | g0014 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18983 | hp2 | a0001 | c0001 | t0017 | g0194 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18986 | hp1 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18987 | hp1 | a0001 | c0002 | t0006 | g0053 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18988 | hp2 | a0001 | c0003 | t0001 | g0228 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18990 | hp1 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18991 | hp1 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0257 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18995 | hp2 | a0001 | c0002 | t0001 | g0201 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18999 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19000 | hp1 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19002 | hp2 | a0001 | c0001 | t0019 | g0217 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19003 | hp2 | a0001 | c0002 | t0001 | g0290 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19004 | hp1 | a0001 | c0003 | t0001 | g0234 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19004 | hp2 | a0001 | c0001 | t0006 | g0189 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19006 | hp2 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19009 | hp2 | a0006 | c0014 | t0001 | g0146 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19030 | hp1 | a0001 | c0008 | t0001 | g0355 | AFR | LWK | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19030 | hp2 | a0003 | c0012 | t0009 | g0036 | AFR | LWK | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19043 | hp1 | a0001 | c0002 | t0009 | g0245 | AFR | LWK | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | LWK | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19056 | hp1 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19057 | hp1 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19060 | hp2 | a0001 | c0003 | t0001 | g0205 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19062 | hp2 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19063 | hp1 | a0008 | c0017 | t0006 | g0014 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19064 | hp1 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19065 | hp1 | a0001 | c0003 | t0001 | g0089 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19065 | hp2 | a0001 | c0001 | t0006 | g0190 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19066 | hp1 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19067 | hp1 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19068 | hp1 | a0009 | c0019 | t0001 | g0317 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19068 | hp2 | a0001 | c0003 | t0001 | g0229 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19070 | hp2 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19075 | hp2 | a0001 | c0003 | t0001 | g0323 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19078 | hp1 | a0001 | c0003 | t0001 | g0157 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19079 | hp1 | a0001 | c0003 | t0001 | g0206 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19079 | hp2 | a0001 | c0005 | t0002 | g0110 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19081 | hp2 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0265 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19088 | hp2 | a0001 | c0003 | t0001 | g0335 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19089 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA20129 | hp1 | a0001 | c0015 | t0009 | g0244 | AFR | ASW | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ASW | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA20752 | hp1 | a0002 | c0004 | t0003 | g0280 | EUR | TSI | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA20752 | hp2 | a0001 | c0009 | t0012 | g0064 | EUR | TSI | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA20805 | hp1 | a0002 | c0004 | t0003 | g0255 | EUR | TSI | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA20805 | hp2 | a0001 | c0003 | t0001 | g0057 | EUR | TSI | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA20905 | hp1 | a0002 | c0004 | t0003 | g0344 | SAS | GIH | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0007 | SAS | GIH | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0136 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02109 | hp1 | a0001 | c0005 | t0011 | g0115 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02109 | hp2 | a0002 | c0007 | t0007 | g0291 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02486 | hp1 | a0002 | c0007 | t0007 | g0039 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02486 | hp2 | a0001 | c0005 | t0002 | g0305 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02559 | hp1 | a0001 | c0015 | t0001 | g0350 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG02559 | hp2 | a0001 | c0008 | t0001 | g0224 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03471 | hp1 | a0001 | c0006 | t0002 | g0044 | AFR | MSL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG03471 | hp2 | a0002 | c0004 | t0003 | g0341 | AFR | MSL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG06807 | hp1 | a0001 | c0002 | t0001 | g0163 | AFR | USA | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
HG06807 | hp2 | a0003 | c0012 | t0021 | g0315 | AFR | USA | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA20300 | hp1 | a0001 | c0003 | t0001 | g0049 | AFR | USA | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | USA | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA21309 | hp1 | a0001 | c0028 | t0004 | g0233 | AFR | LWK | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
NA21309 | hp2 | a0001 | c0009 | t0004 | g0046 | AFR | LWK | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0027 | REF | REF | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
homoSapiens_grch38 | hp1 | a0001 | c0005 | t0002 | g0002 | REF | REF | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:160706469
|
A | G | 1 | a0010 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.112A>G | p.Lys38Glu | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 2/19 | 173/3530 | 112/2433 | 38/810 | chr6 | 160706469 | ||
chr6:160706526
|
G | A | 1 | a0005 | 4 | HG02280.hp2 HG02647.hp2 HG02818.hp2 others(1): Show |
missense_variant | MODERATE | c.169G>A | p.Glu57Lys | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 2/19 | 230/3530 | 169/2433 | 57/810 | chr6 | 160706526 | ||
chr6:160707780
|
G | A | 1 | a0007 | 2 | HG03490.hp2 HG03492.hp1 |
missense_variant | MODERATE | c.266G>A | p.Arg89Lys | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/19 | 327/3530 | 266/2433 | 89/810 | chr6 | 160707780 | ||
chr6:160714827
|
A | T | 1 | a0009 | 2 | HG02132.hp1 NA19068.hp1 |
missense_variant | MODERATE | c.581A>T | p.Asp194Val | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 6/19 | 642/3530 | 581/2433 | 194/810 | chr6 | 160714827 | ||
chr6:160714844
|
A | G | 1 | a0011 | 1 | HG01099.hp2 | missense_variant | MODERATE | c.598A>G | p.Thr200Ala | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 6/19 | 659/3530 | 598/2433 | 200/810 | chr6 | 160714844 | ||
chr6:160722431
|
G | T | 1 | a0008 | 2 | NA18983.hp1 NA19063.hp1 |
missense_variant | MODERATE | c.1120G>T | p.Val374Phe | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/19 | 1181/3530 | 1120/2433 | 374/810 | chr6 | 160722431 | ||
chr6:160722533
|
C | T | 1 | a0005 | 4 | HG02280.hp2 HG02647.hp2 HG02818.hp2 others(1): Show |
missense_variant | MODERATE | c.1222C>T | p.Arg408Trp | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/19 | 1283/3530 | 1222/2433 | 408/810 | chr6 | 160722533 | ||
chr6:160731174
|
T | A | 1 | a0003 | 4 | HG02257.hp2 HG02965.hp2 HG06807.hp2 others(1): Show |
missense_variant | MODERATE | c.1380T>A | p.Ser460Arg | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 11/19 | 1441/3530 | 1380/2433 | 460/810 | chr6 | 160731174 | ||
chr6:160731208
|
G | A | 2 | a0002a0010 | 43 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(40): Show |
missense_variant | MODERATE | c.1414G>A | p.Asp472Asn | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 11/19 | 1475/3530 | 1414/2433 | 472/810 | chr6 | 160731208 | ||
chr6:160731787
|
C | T | 1 | a0004 | 4 | HG01256.hp1 HG01258.hp1 HG01952.hp2 others(1): Show |
missense_variant | MODERATE | c.1481C>T | p.Ala494Val | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/19 | 1542/3530 | 1481/2433 | 494/810 | chr6 | 160731787 | ||
chr6:160738593
|
G | A | 1 | a0006 | 3 | NA18962.hp2 NA18978.hp2 NA19009.hp2 |
missense_variant | MODERATE | c.1858G>A | p.Ala620Thr | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 15/19 | 1919/3530 | 1858/2433 | 620/810 | chr6 | 160738593 | ||
chr6:160741375
|
G | A | 1 | a0012 | 1 | NA18966.hp1 | missense_variant | MODERATE | c.2083G>A | p.Asp695Asn | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/19 | 2144/3530 | 2083/2433 | 695/810 | chr6 | 160741375 | ||
chr6:160754097
|
A | G | 2 | a0001a0002 | 2 | HG02109.hp1 HG03225.hp1 |
splice_region_variant | LOW | c.*1036A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | chr6 | 160754097 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:160711114
|
C | T | 11 | a0001c0006a0001c0013a0001c0015others(8): Show | 78 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(75): Show |
synonymous_variant | LOW | c.330C>T | p.Asn110Asn | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/19 | 391/3530 | 330/2433 | 110/810 | chr6 | 160711114 | ||
chr6:160714828
|
C | T | 1 | a0001c0027 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.582C>T | p.Asp194Asp | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 6/19 | 643/3530 | 582/2433 | 194/810 | chr6 | 160714828 | ||
chr6:160716747
|
T | C | 16 | a0001c0001a0001c0006a0001c0009others(13): Show | 173 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(170): Show |
synonymous_variant | LOW | c.771T>C | p.Cys257Cys | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 7/19 | 832/3530 | 771/2433 | 257/810 | chr6 | 160716747 | ||
chr6:160718448
|
C | T | 11 | a0001c0001a0001c0009a0001c0011others(8): Show | 141 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(138): Show |
synonymous_variant | LOW | c.942C>T | p.Phe314Phe | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 8/19 | 1003/3530 | 942/2433 | 314/810 | chr6 | 160718448 | ||
chr6:160718825
|
A | G | 5 | a0001c0028a0001c0029a0002c0004others(2): Show | 44 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(41): Show |
synonymous_variant | LOW | c.1083A>G | p.Gln361Gln | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/19 | 1144/3530 | 1083/2433 | 361/810 | chr6 | 160718825 | ||
chr6:160731225
|
C | T | 2 | a0001c0025a0001c0027 | 2 | HG01257.hp2 NA18906.hp1 |
synonymous_variant | LOW | c.1431C>T | p.Ser477Ser | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 11/19 | 1492/3530 | 1431/2433 | 477/810 | chr6 | 160731225 | ||
chr6:160741374
|
T | C | 2 | a0001c0003a0001c0011 | 41 | HG00558.hp2 HG00639.hp2 HG00741.hp1 others(38): Show |
synonymous_variant | LOW | c.2082T>C | p.Ala694Ala | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/19 | 2143/3530 | 2082/2433 | 694/810 | chr6 | 160741374 | ||
chr6:160752248
|
T | C | 3 | a0001c0008a0001c0013a0001c0024 | 13 | HG02559.hp2 HG02572.hp1 HG02630.hp1 others(10): Show |
synonymous_variant | LOW | c.2259T>C | p.Thr753Thr | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 18/19 | 2320/3530 | 2259/2433 | 753/810 | chr6 | 160752248 | ||
chr6:160752914
|
T | G | 18 | a0001c0001a0001c0002a0001c0003others(15): Show | 294 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(291): Show |
synonymous_variant | LOW | c.2286T>G | p.Gly762Gly | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 2347/3530 | 2286/2433 | 762/810 | chr6 | 160752914 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:160702270
|
G | A | 9 | a0001c0002t0009a0001c0006t0013a0001c0006t0014others(6): Show | 14 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-35G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/19 | 35 | chr6 | 160702270 | |||||
chr6:160753106
|
A | G | 32 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(29): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(290): Show |
3_prime_UTR_variant | MODIFIER | c.*45A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 45 | chr6 | 160753106 | |||||
chr6:160753109
|
G | A | 3 | a0001c0001t0006a0001c0002t0006a0008c0017t0006 | 10 | NA18952.hp1 NA18953.hp2 NA18956.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*48G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 48 | chr6 | 160753109 | |||||
chr6:160753345
|
AT | A | 32 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(29): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(290): Show |
3_prime_UTR_variant | MODIFIER | c.*289delT | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 289 | INFO_REALIGN_3_PRIME | chr6 | 160753345 | ||||
chr6:160753415
|
G | C | 1 | a0002c0004t0016 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*354G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 354 | chr6 | 160753415 | |||||
chr6:160753434
|
G | A | 1 | a0001c0001t0017 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*373G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 373 | chr6 | 160753434 | |||||
chr6:160753488
|
T | G | 1 | a0001c0001t0018 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*427T>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 427 | chr6 | 160753488 | |||||
chr6:160753547
|
T | C | 29 | a0001c0001t0001a0001c0001t0006a0001c0001t0017others(26): Show | 282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
3_prime_UTR_variant | MODIFIER | c.*486T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 486 | chr6 | 160753547 | |||||
chr6:160753562
|
A | G | 32 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(29): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(290): Show |
3_prime_UTR_variant | MODIFIER | c.*501A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 501 | chr6 | 160753562 | |||||
chr6:160753577
|
T | C | 1 | a0001c0001t0019 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*516T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 516 | chr6 | 160753577 | |||||
chr6:160753598
|
G | A | 1 | a0002c0004t0008 | 6 | HG02145.hp1 HG02280.hp1 HG02622.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*537G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 537 | chr6 | 160753598 | |||||
chr6:160753626
|
G | A | 49 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(46): Show | 351 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(348): Show |
3_prime_UTR_variant | MODIFIER | c.*565G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 565 | chr6 | 160753626 | |||||
chr6:160753742
|
C | T | 1 | a0001c0001t0022 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*681C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 681 | chr6 | 160753742 | |||||
chr6:160753775
|
G | A | 1 | a0001c0001t0020 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*714G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 714 | chr6 | 160753775 | |||||
chr6:160753836
|
G | A | 3 | a0001c0005t0005a0001c0006t0005a0001c0006t0013 | 12 | HG01884.hp2 HG02622.hp2 HG02647.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*775G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 775 | chr6 | 160753836 | |||||
chr6:160753839
|
C | G | 30 | a0001c0001t0001a0001c0001t0006a0001c0001t0017others(27): Show | 283 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(280): Show |
3_prime_UTR_variant | MODIFIER | c.*778C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 778 | chr6 | 160753839 | |||||
chr6:160753842
|
A | G | 1 | a0001c0006t0014 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*781A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 781 | chr6 | 160753842 | |||||
chr6:160753844
|
G | A | 1 | a0003c0012t0021 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*783G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 783 | chr6 | 160753844 | |||||
chr6:160753901
|
C | T | 1 | a0001c0009t0012 | 2 | HG01978.hp1 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*840C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 840 | chr6 | 160753901 | |||||
chr6:160753972
|
C | T | 5 | a0002c0004t0003a0002c0004t0008a0002c0004t0016others(2): Show | 30 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*911C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 911 | chr6 | 160753972 | |||||
chr6:160754047
|
T | C | 2 | a0001c0005t0010a0001c0027t0010 | 3 | HG03225.hp2 HG03453.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*986T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 986 | chr6 | 160754047 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:160702381
|
G | T | 122 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0247others(119): Show | 130 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.49+28G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160702381 | ||||||
chr6:160702386
|
AT | A | 4 | a0001c0002t0009g0245a0001c0006t0013g0243a0001c0015t0009g0244others(1): Show | 4 | HG02717.hp1 HG02922.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+39delT | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr6 | 160702386 | |||||
chr6:160702419
|
T | C | 6 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0003t0001g0251others(3): Show | 6 | HG00323.hp2 HG01261.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+66T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160702419 | ||||||
chr6:160702509
|
A | G | 3 | a0005c0010t0004g0017a0005c0010t0004g0241a0005c0010t0004g0242 | 4 | HG02280.hp2 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+156A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160702509 | ||||||
chr6:160702555
|
G | A | 5 | a0001c0005t0010g0026a0001c0009t0004g0025a0005c0010t0004g0017others(2): Show | 6 | HG02258.hp1 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+202G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160702555 | ||||||
chr6:160702739
|
T | C | 129 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0022others(126): Show | 139 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.49+386T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160702739 | ||||||
chr6:160702829
|
T | C | 1 | a0001c0001t0006g0253 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.49+476T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160702829 | ||||||
chr6:160702862
|
G | A | 9 | a0001c0006t0014g0037a0001c0013t0009g0035a0001c0029t0015g0032others(6): Show | 10 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.49+509G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160702862 | ||||||
chr6:160702879
|
G | A | 11 | a0001c0001t0001g0041a0001c0006t0002g0043a0001c0006t0002g0044others(8): Show | 11 | HG01243.hp1 HG02486.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.49+526G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160702879 | ||||||
chr6:160702939
|
C | CACTT | 129 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0022others(126): Show | 139 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.49+587_49+588insCT others(2): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr6 | 160702939 | |||||
chr6:160702944
|
G | A | 1 | a0001c0003t0001g0049 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.49+591G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160702944 | ||||||
chr6:160703014
|
T | A | 4 | a0003c0012t0001g0254a0005c0010t0004g0017a0005c0010t0004g0241others(1): Show | 5 | HG02280.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+661T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160703014 | ||||||
chr6:160703033
|
TA | T | 15 | a0001c0002t0001g0353a0001c0002t0009g0245a0001c0006t0005g0346others(12): Show | 16 | HG01884.hp2 HG02145.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.49+681delA | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160703033 | ||||||
chr6:160703093
|
C | CT | 129 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0022others(126): Show | 139 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.49+740_49+741insT | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160703093 | ||||||
chr6:160703111
|
G | T | 4 | a0001c0001t0001g0004a0001c0005t0002g0345a0002c0004t0003g0023others(1): Show | 7 | HG00738.hp2 HG00741.hp2 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.49+758G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160703111 | ||||||
chr6:160703139
|
A | C | 15 | a0001c0002t0001g0353a0001c0002t0009g0245a0001c0006t0005g0346others(12): Show | 16 | HG01884.hp2 HG02145.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.49+786A>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160703139 | ||||||
chr6:160703268
|
T | TA | 16 | a0001c0001t0001g0041a0001c0001t0001g0054a0001c0002t0001g0051others(13): Show | 16 | HG01243.hp1 HG01256.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.49+927dupA | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr6 | 160703268 | |||||
chr6:160703268
|
T | TAA | 101 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0022others(98): Show | 110 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.49+926_49+927dupAA | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr6 | 160703268 | |||||
chr6:160703268
|
T | TAAA | 26 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0001g0260others(23): Show | 27 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.49+925_49+927dupAA others(1): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr6 | 160703268 | |||||
chr6:160703282
|
C | T | 6 | a0001c0005t0005g0240a0001c0006t0005g0016a0001c0006t0005g0238others(3): Show | 7 | HG02257.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+929C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160703282 | ||||||
chr6:160703309
|
A | G | 6 | a0001c0005t0005g0240a0001c0006t0005g0016a0001c0006t0005g0238others(3): Show | 7 | HG02257.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+956A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160703309 | ||||||
chr6:160703324
|
G | A | 4 | a0001c0006t0005g0016a0001c0006t0005g0238a0001c0008t0001g0237others(1): Show | 5 | HG02572.hp2 HG02647.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+971G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160703324 | ||||||
chr6:160703524
|
G | A | 1 | a0001c0006t0013g0243 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.49+1171G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160703524 | ||||||
chr6:160703842
|
C | G | 4 | a0001c0002t0009g0245a0001c0006t0013g0243a0001c0015t0009g0244others(1): Show | 4 | HG02717.hp1 HG02922.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+1489C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160703842 | ||||||
chr6:160703902
|
A | G | 4 | a0001c0002t0009g0245a0001c0006t0013g0243a0001c0015t0009g0244others(1): Show | 4 | HG02717.hp1 HG02922.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+1549A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160703902 | ||||||
chr6:160704168
|
C | T | 3 | a0005c0010t0004g0017a0005c0010t0004g0241a0005c0010t0004g0242 | 4 | HG02280.hp2 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+1815C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160704168 | ||||||
chr6:160704198
|
C | T | 1 | a0001c0003t0001g0235 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.49+1845C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160704198 | ||||||
chr6:160704251
|
C | A | 1 | a0001c0005t0002g0270 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.49+1898C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160704251 | ||||||
chr6:160704328
|
C | T | 1 | a0002c0004t0003g0341 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.49+1975C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160704328 | ||||||
chr6:160704387
|
T | C | 89 | a0001c0001t0001g0004a0001c0001t0001g0247a0001c0001t0001g0248others(86): Show | 96 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.50-2020T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160704387 | ||||||
chr6:160704422
|
T | C | 3 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0028 | 4 | HG01255.hp1 HG01256.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-1985T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160704422 | ||||||
chr6:160704434
|
C | T | 1 | a0001c0003t0001g0234 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.50-1973C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160704434 | ||||||
chr6:160704524
|
T | C | 9 | a0001c0006t0014g0037a0001c0013t0009g0035a0001c0029t0015g0032others(6): Show | 10 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.50-1883T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160704524 | ||||||
chr6:160704530
|
G | C | 1 | a0001c0001t0001g0055 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.50-1877G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160704530 | ||||||
chr6:160704599
|
T | C | 30 | a0001c0001t0001g0029a0001c0001t0001g0056a0001c0001t0001g0061others(27): Show | 31 | HG00280.hp2 HG00733.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.50-1808T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160704599 | ||||||
chr6:160704748
|
A | G | 1 | a0001c0028t0004g0233 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.50-1659A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160704748 | ||||||
chr6:160704808
|
A | G | 3 | a0001c0011t0001g0230a0001c0011t0001g0231a0001c0011t0001g0232 | 3 | NA18940.hp1 NA18963.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.50-1599A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160704808 | ||||||
chr6:160704816
|
A | T | 3 | a0001c0011t0001g0230a0001c0011t0001g0231a0001c0011t0001g0232 | 3 | NA18940.hp1 NA18963.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.50-1591A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160704816 | ||||||
chr6:160704956
|
T | C | 2 | a0001c0001t0001g0074a0001c0001t0001g0075 | 2 | NA19010.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.50-1451T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160704956 | ||||||
chr6:160705042
|
C | T | 152 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0001t0001g0055others(149): Show | 165 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.50-1365C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160705042 | ||||||
chr6:160705102
|
G | C | 5 | a0001c0001t0001g0056a0001c0001t0001g0076a0001c0001t0001g0274others(2): Show | 5 | HG01934.hp2 HG02809.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.50-1305G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160705102 | ||||||
chr6:160705138
|
C | T | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG03710.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.50-1269C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160705138 | ||||||
chr6:160705178
|
C | T | 1 | a0001c0006t0002g0310 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.50-1229C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160705178 | ||||||
chr6:160705213
|
C | T | 4 | a0001c0003t0001g0227a0001c0003t0001g0228a0001c0003t0001g0229others(1): Show | 4 | NA18945.hp1 NA18988.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-1194C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160705213 | ||||||
chr6:160705229
|
A | G | 1 | a0001c0005t0002g0345 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.50-1178A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160705229 | ||||||
chr6:160705239
|
T | C | 2 | a0001c0009t0004g0025a0002c0007t0023g0050 | 2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.50-1168T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160705239 | ||||||
chr6:160705267
|
T | C | 4 | a0001c0006t0002g0310a0001c0011t0001g0236a0001c0015t0009g0244others(1): Show | 4 | HG02572.hp2 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-1140T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160705267 | ||||||
chr6:160705291
|
C | T | 60 | a0001c0001t0001g0054a0001c0001t0001g0072a0001c0001t0001g0074others(57): Show | 61 | HG00408.hp2 HG01192.hp1 HG01256.hp1 others(58): Show |
intron_variant | MODIFIER | c.50-1116C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160705291 | ||||||
chr6:160705434
|
C | T | 5 | a0001c0005t0011g0115a0001c0006t0002g0114a0001c0013t0001g0024others(2): Show | 6 | HG02109.hp1 HG02559.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-973C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160705434 | ||||||
chr6:160705456
|
C | T | 2 | a0001c0002t0001g0113a0001c0002t0001g0199 | 2 | HG03041.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.50-951C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160705456 | ||||||
chr6:160705706
|
G | A | 1 | a0001c0006t0002g0114 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.50-701G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160705706 | ||||||
chr6:160705709
|
T | C | 1 | a0001c0015t0001g0316 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.50-698T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160705709 | ||||||
chr6:160705711
|
A | T | 5 | a0001c0015t0009g0244a0003c0012t0001g0239a0003c0012t0001g0254others(2): Show | 5 | HG02257.hp2 HG02965.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.50-696A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160705711 | ||||||
chr6:160705722
|
C | T | 1 | a0001c0009t0004g0025 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.50-685C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160705722 | ||||||
chr6:160705735
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.50-672G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160705735 | ||||||
chr6:160705889
|
T | A | 1 | a0001c0001t0001g0005 | 2 | HG01256.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.50-518T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160705889 | ||||||
chr6:160705950
|
G | A | 1 | a0001c0006t0002g0276 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.50-457G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160705950 | ||||||
chr6:160706093
|
G | A | 30 | a0001c0006t0014g0037a0001c0029t0015g0032a0002c0004t0003g0019others(27): Show | 33 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.50-314G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160706093 | ||||||
chr6:160706135
|
C | CT | 3 | a0001c0003t0001g0112a0001c0003t0001g0197a0001c0003t0001g0198 | 3 | HG01106.hp2 HG01891.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.50-271dupT | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr6 | 160706135 | |||||
chr6:160706203
|
T | C | 3 | a0001c0006t0005g0346a0001c0006t0005g0347a0001c0006t0005g0352 | 3 | HG01884.hp2 HG02622.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.50-204T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160706203 | ||||||
chr6:160706234
|
C | T | 6 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(3): Show | 6 | HG02451.hp1 HG02922.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-173C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160706234 | ||||||
chr6:160706268
|
T | C | 1 | a0009c0019t0001g0317 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.50-139T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160706268 | ||||||
chr6:160706294
|
CAG | C | 121 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0007others(118): Show | 132 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.50-111_50-110delGA | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr6 | 160706294 | |||||
chr6:160706546
|
T | C | 8 | a0001c0002t0001g0081a0001c0002t0001g0082a0001c0002t0001g0083others(5): Show | 8 | NA18954.hp2 NA18980.hp1 NA18991.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.185+4T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 2/18 | chr6 | 160706546 | ||||||
chr6:160706567
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.185+25C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 2/18 | chr6 | 160706567 | ||||||
chr6:160706643
|
T | C | 6 | a0001c0001t0001g0008a0001c0001t0001g0091a0001c0001t0001g0092others(3): Show | 7 | NA18977.hp2 NA18990.hp2 NA18999.hp2 others(4): Show |
intron_variant | MODIFIER | c.185+101T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 2/18 | chr6 | 160706643 | ||||||
chr6:160706689
|
T | C | 1 | a0001c0002t0001g0084 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.185+147T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 2/18 | chr6 | 160706689 | ||||||
chr6:160706951
|
T | TA | 29 | a0001c0002t0001g0007a0001c0002t0001g0121a0001c0002t0001g0122others(26): Show | 33 | HG01255.hp2 HG01256.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.185+423dupA | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr6 | 160706951 | |||||
chr6:160706951
|
T | TAA | 44 | a0001c0005t0010g0026a0001c0005t0010g0308a0001c0006t0002g0043others(41): Show | 47 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.185+422_185+423dup others(2): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr6 | 160706951 | |||||
chr6:160706951
|
T | TAAAAAA | 8 | a0002c0007t0007g0038a0002c0007t0007g0039a0002c0007t0007g0040others(5): Show | 8 | HG02055.hp2 HG02109.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.185+418_185+423dup others(6): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr6 | 160706951 | |||||
chr6:160707138
|
C | T | 16 | a0001c0001t0001g0008a0001c0001t0001g0091a0001c0001t0001g0092others(13): Show | 17 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(14): Show |
intron_variant | MODIFIER | c.186-562C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 2/18 | chr6 | 160707138 | ||||||
chr6:160707209
|
G | A | 6 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(3): Show | 6 | HG02451.hp1 HG02922.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.186-491G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 2/18 | chr6 | 160707209 | ||||||
chr6:160707232
|
A | T | 53 | a0001c0005t0010g0026a0001c0005t0010g0308a0001c0006t0014g0037others(50): Show | 57 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.186-468A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 2/18 | chr6 | 160707232 | ||||||
chr6:160707261
|
C | A | 4 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(1): Show | 4 | NA19003.hp1 NA19012.hp2 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.186-439C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 2/18 | chr6 | 160707261 | ||||||
chr6:160707261
|
C | T | 1 | a0001c0002t0001g0212 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.186-439C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 2/18 | chr6 | 160707261 | ||||||
chr6:160707499
|
G | A | 1 | a0001c0006t0004g0048 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.186-201G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 2/18 | chr6 | 160707499 | ||||||
chr6:160707585
|
G | A | 125 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0013others(122): Show | 132 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.186-115G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 2/18 | chr6 | 160707585 | ||||||
chr6:160707855
|
A | G | 7 | a0001c0002t0001g0007a0001c0002t0001g0073a0001c0002t0001g0125others(4): Show | 8 | HG01255.hp2 HG01978.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.292+49A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160707855 | ||||||
chr6:160707890
|
A | G | 51 | a0001c0006t0014g0037a0001c0013t0009g0035a0001c0015t0009g0244others(48): Show | 55 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.292+84A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160707890 | ||||||
chr6:160707913
|
T | C | 7 | a0001c0002t0001g0007a0001c0002t0001g0073a0001c0002t0001g0125others(4): Show | 8 | HG01255.hp2 HG01978.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.292+107T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160707913 | ||||||
chr6:160707915
|
G | A | 123 | a0001c0001t0001g0213a0001c0002t0001g0001a0001c0002t0001g0003others(120): Show | 134 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.292+109G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160707915 | ||||||
chr6:160707935
|
G | A | 13 | a0001c0006t0005g0016a0001c0006t0005g0098a0001c0006t0005g0099others(10): Show | 15 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.292+129G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160707935 | ||||||
chr6:160707954
|
T | C | 4 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173others(1): Show | 4 | HG00544.hp2 NA18944.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+148T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160707954 | ||||||
chr6:160707981
|
G | A | 64 | a0001c0006t0005g0016a0001c0006t0005g0098a0001c0006t0005g0099others(61): Show | 70 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.292+175G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160707981 | ||||||
chr6:160708199
|
T | TA | 48 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0074others(45): Show | 49 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.292+393_292+394ins others(1): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160708199 | ||||||
chr6:160708201
|
T | G | 48 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0074others(45): Show | 49 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.292+395T>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160708201 | ||||||
chr6:160708202
|
A | T | 48 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0074others(45): Show | 49 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.292+396A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160708202 | ||||||
chr6:160708204
|
A | C | 48 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0074others(45): Show | 49 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.292+398A>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160708204 | ||||||
chr6:160708362
|
CT | C | 10 | a0002c0004t0011g0306a0002c0007t0007g0038a0002c0007t0007g0039others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.292+560delT | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr6 | 160708362 | |||||
chr6:160708425
|
A | T | 1 | a0001c0002t0001g0166 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.292+619A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160708425 | ||||||
chr6:160708593
|
A | G | 10 | a0002c0004t0011g0306a0002c0007t0007g0038a0002c0007t0007g0039others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.292+787A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160708593 | ||||||
chr6:160708653
|
G | T | 10 | a0002c0004t0011g0306a0002c0007t0007g0038a0002c0007t0007g0039others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.292+847G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160708653 | ||||||
chr6:160708727
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.292+921G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160708727 | ||||||
chr6:160708969
|
T | TA | 39 | a0001c0013t0009g0035a0001c0015t0009g0244a0001c0021t0004g0012others(36): Show | 42 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.292+1163_292+1164i others(3): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160708969 | ||||||
chr6:160708970
|
T | A | 60 | a0001c0001t0001g0041a0001c0001t0001g0056a0001c0001t0001g0076others(57): Show | 64 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.292+1164T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160708970 | ||||||
chr6:160708970
|
T | TA | 8 | a0001c0002t0001g0129a0001c0006t0005g0346a0001c0006t0005g0348others(5): Show | 8 | HG00597.hp2 HG02572.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.292+1176dupA | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr6 | 160708970 | |||||
chr6:160708971
|
A | T | 1 | a0001c0003t0001g0323 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.292+1165A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160708971 | ||||||
chr6:160708980
|
A | C | 1 | a0001c0001t0001g0072 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.292+1174A>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160708980 | ||||||
chr6:160709135
|
G | C | 1 | a0001c0002t0001g0113 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.292+1329G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160709135 | ||||||
chr6:160709386
|
C | A | 1 | a0001c0003t0001g0057 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.292+1580C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160709386 | ||||||
chr6:160709784
|
C | T | 1 | a0002c0007t0023g0050 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.293-1293C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160709784 | ||||||
chr6:160709898
|
T | C | 72 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(69): Show | 78 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.293-1179T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160709898 | ||||||
chr6:160709985
|
G | A | 1 | a0002c0022t0003g0267 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.293-1092G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160709985 | ||||||
chr6:160710260
|
C | A | 1 | a0001c0001t0001g0258 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.293-817C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160710260 | ||||||
chr6:160710343
|
G | T | 3 | a0001c0021t0004g0012a0004c0020t0004g0336a0004c0020t0004g0342 | 4 | HG01256.hp1 HG01258.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-734G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160710343 | ||||||
chr6:160710430
|
G | A | 6 | a0001c0001t0001g0041a0001c0001t0001g0056a0001c0001t0001g0076others(3): Show | 6 | HG01934.hp2 HG02809.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.293-647G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160710430 | ||||||
chr6:160710451
|
G | T | 10 | a0002c0004t0011g0306a0002c0007t0007g0038a0002c0007t0007g0039others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.293-626G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160710451 | ||||||
chr6:160710455
|
C | T | 7 | a0001c0002t0001g0052a0001c0002t0001g0164a0001c0002t0001g0165others(4): Show | 7 | HG00597.hp1 HG00609.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.293-622C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160710455 | ||||||
chr6:160710480
|
G | C | 3 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169 | 3 | NA19012.hp2 NA19063.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.293-597G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160710480 | ||||||
chr6:160710484
|
G | A | 71 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(68): Show | 77 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.293-593G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160710484 | ||||||
chr6:160710512
|
G | T | 10 | a0002c0004t0011g0306a0002c0007t0007g0038a0002c0007t0007g0039others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.293-565G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160710512 | ||||||
chr6:160710548
|
A | G | 6 | a0001c0002t0001g0124a0001c0002t0001g0163a0001c0002t0001g0199others(3): Show | 6 | HG02145.hp2 HG03041.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.293-529A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160710548 | ||||||
chr6:160710559
|
A | G | 1 | a0001c0013t0009g0035 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.293-518A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160710559 | ||||||
chr6:160710649
|
G | C | 2 | a0001c0001t0001g0175a0012c0023t0001g0100 | 2 | NA18966.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.293-428G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160710649 | ||||||
chr6:160710786
|
C | T | 72 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(69): Show | 78 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.293-291C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160710786 | ||||||
chr6:160710843
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.293-234C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160710843 | ||||||
chr6:160710863
|
G | A | 1 | a0001c0003t0001g0261 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.293-214G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160710863 | ||||||
chr6:160710914
|
C | T | 3 | a0001c0005t0011g0115a0001c0008t0001g0224a0001c0008t0001g0349 | 3 | HG02109.hp1 HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.293-163C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160710914 | ||||||
chr6:160711005
|
G | A | 5 | a0002c0007t0007g0038a0002c0007t0007g0039a0002c0007t0007g0040others(2): Show | 5 | HG01243.hp1 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-72G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160711005 | ||||||
chr6:160711357
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.407+166A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160711357 | ||||||
chr6:160711385
|
T | G | 72 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(69): Show | 78 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.407+194T>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160711385 | ||||||
chr6:160711391
|
G | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0181a0001c0001t0001g0182others(1): Show | 5 | HG01192.hp2 NA18969.hp1 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.407+200G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160711391 | ||||||
chr6:160711453
|
A | C | 3 | a0001c0006t0004g0048a0001c0006t0014g0037a0001c0015t0001g0316 | 3 | HG01891.hp2 HG02970.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.407+262A>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160711453 | ||||||
chr6:160711685
|
C | T | 10 | a0002c0004t0011g0306a0002c0007t0007g0038a0002c0007t0007g0039others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.407+494C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160711685 | ||||||
chr6:160711693
|
T | C | 72 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(69): Show | 78 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.407+502T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160711693 | ||||||
chr6:160711772
|
T | C | 72 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(69): Show | 78 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.407+581T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160711772 | ||||||
chr6:160711798
|
G | A | 203 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(200): Show | 217 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.407+607G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160711798 | ||||||
chr6:160711806
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.407+615C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160711806 | ||||||
chr6:160712014
|
C | T | 72 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(69): Show | 78 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.407+823C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160712014 | ||||||
chr6:160712093
|
G | C | 72 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(69): Show | 78 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.408-893G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160712093 | ||||||
chr6:160712212
|
G | A | 72 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(69): Show | 78 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.408-774G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160712212 | ||||||
chr6:160712214
|
G | C | 1 | a0001c0001t0001g0193 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.408-772G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160712214 | ||||||
chr6:160712303
|
T | C | 130 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(127): Show | 138 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.408-683T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160712303 | ||||||
chr6:160712311
|
T | A | 5 | a0002c0007t0007g0038a0002c0007t0007g0039a0002c0007t0007g0040others(2): Show | 5 | HG01243.hp1 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.408-675T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160712311 | ||||||
chr6:160712512
|
A | T | 44 | a0001c0006t0005g0016a0001c0006t0005g0098a0001c0006t0005g0099others(41): Show | 49 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.408-474A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160712512 | ||||||
chr6:160712527
|
A | G | 28 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(25): Show | 29 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.408-459A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160712527 | ||||||
chr6:160712619
|
G | A | 129 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(126): Show | 137 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.408-367G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160712619 | ||||||
chr6:160712653
|
A | G | 44 | a0001c0006t0005g0016a0001c0006t0005g0098a0001c0006t0005g0099others(41): Show | 49 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.408-333A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160712653 | ||||||
chr6:160712677
|
G | C | 10 | a0002c0004t0011g0306a0002c0007t0007g0038a0002c0007t0007g0039others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.408-309G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160712677 | ||||||
chr6:160712906
|
G | A | 10 | a0002c0004t0011g0306a0002c0007t0007g0038a0002c0007t0007g0039others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.408-80G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160712906 | ||||||
chr6:160713241
|
C | G | 29 | a0001c0029t0015g0032a0002c0004t0003g0019a0002c0004t0003g0020others(26): Show | 32 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.547+116C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160713241 | ||||||
chr6:160713255
|
AC | A | 13 | a0001c0006t0005g0016a0001c0006t0005g0098a0001c0006t0005g0099others(10): Show | 15 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.547+134delC | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr6 | 160713255 | |||||
chr6:160713272
|
A | ATT | 4 | a0001c0006t0004g0048a0001c0006t0014g0037a0001c0013t0009g0035others(1): Show | 4 | HG01891.hp2 HG02970.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.547+147_547+148ins others(2): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160713272 | ||||||
chr6:160713273
|
A | AT | 29 | a0001c0029t0015g0032a0002c0004t0003g0019a0002c0004t0003g0020others(26): Show | 32 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.547+160dupT | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr6 | 160713273 | |||||
chr6:160713273
|
A | ATT | 23 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(20): Show | 25 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.547+159_547+160dup others(2): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr6 | 160713273 | |||||
chr6:160713273
|
A | ATTTT | 11 | a0001c0021t0004g0012a0002c0004t0011g0306a0002c0007t0007g0038others(8): Show | 12 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.547+157_547+160dup others(4): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr6 | 160713273 | |||||
chr6:160713273
|
A | T | 4 | a0001c0006t0004g0048a0001c0006t0014g0037a0001c0013t0009g0035others(1): Show | 4 | HG01891.hp2 HG02970.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.547+148A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160713273 | ||||||
chr6:160713342
|
C | T | 1 | a0002c0004t0003g0287 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.547+217C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160713342 | ||||||
chr6:160713389
|
C | A | 1 | a0001c0028t0004g0233 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.547+264C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160713389 | ||||||
chr6:160713492
|
C | A | 1 | a0001c0006t0004g0048 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.547+367C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160713492 | ||||||
chr6:160713505
|
G | A | 1 | a0001c0005t0011g0115 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.547+380G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160713505 | ||||||
chr6:160713535
|
C | T | 10 | a0002c0004t0011g0306a0002c0007t0007g0038a0002c0007t0007g0039others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.547+410C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160713535 | ||||||
chr6:160713540
|
A | C | 4 | a0002c0007t0007g0096a0002c0007t0007g0097a0002c0007t0007g0291others(1): Show | 4 | HG02055.hp2 HG02109.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.547+415A>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160713540 | ||||||
chr6:160713698
|
A | G | 1 | a0001c0002t0001g0162 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.547+573A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160713698 | ||||||
chr6:160713700
|
A | G | 72 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(69): Show | 78 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.547+575A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160713700 | ||||||
chr6:160713773
|
T | C | 29 | a0001c0029t0015g0032a0002c0004t0003g0019a0002c0004t0003g0020others(26): Show | 32 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.547+648T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160713773 | ||||||
chr6:160713788
|
G | T | 1 | a0001c0009t0012g0070 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.547+663G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160713788 | ||||||
chr6:160713879
|
A | T | 11 | a0001c0006t0004g0048a0002c0004t0011g0306a0002c0007t0007g0038others(8): Show | 11 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.547+754A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160713879 | ||||||
chr6:160713907
|
C | T | 1 | a0001c0002t0001g0161 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.547+782C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160713907 | ||||||
chr6:160713908
|
G | A | 72 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(69): Show | 78 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.547+783G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160713908 | ||||||
chr6:160714079
|
C | T | 130 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(127): Show | 138 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.548-715C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160714079 | ||||||
chr6:160714113
|
G | A | 1 | a0001c0011t0001g0236 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.548-681G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160714113 | ||||||
chr6:160714170
|
C | T | 13 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0069others(10): Show | 13 | HG01099.hp2 HG01106.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.548-624C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160714170 | ||||||
chr6:160714258
|
C | T | 2 | a0001c0002t0001g0290a0001c0002t0001g0311 | 2 | NA18979.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.548-536C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160714258 | ||||||
chr6:160714281
|
G | A | 30 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(27): Show | 32 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.548-513G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160714281 | ||||||
chr6:160714445
|
C | T | 6 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(3): Show | 6 | HG02451.hp1 HG02922.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.548-349C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160714445 | ||||||
chr6:160714474
|
G | GA | 40 | a0001c0029t0015g0032a0002c0004t0003g0019a0002c0004t0003g0020others(37): Show | 43 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.548-320_548-319ins others(1): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160714474 | ||||||
chr6:160714535
|
G | C | 1 | a0001c0028t0004g0233 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.548-259G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160714535 | ||||||
chr6:160714635
|
CTTATTGC others(5): Show |
C | 29 | a0001c0029t0015g0032a0002c0004t0003g0019a0002c0004t0003g0020others(26): Show | 32 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.548-148_548-137del others(12): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr6 | 160714635 | |||||
chr6:160714659
|
T | A | 1 | a0001c0021t0004g0012 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.548-135T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160714659 | ||||||
chr6:160714660
|
G | A | 1 | a0001c0021t0004g0012 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.548-134G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160714660 | ||||||
chr6:160714676
|
A | G | 10 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(7): Show | 10 | HG01891.hp2 HG02451.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.548-118A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160714676 | ||||||
chr6:160714722
|
T | C | 2 | a0001c0006t0014g0037a0001c0013t0009g0035 | 2 | HG01891.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.548-72T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160714722 | ||||||
chr6:160715026
|
T | A | 131 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(128): Show | 139 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.668+112T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 6/18 | chr6 | 160715026 | ||||||
chr6:160715262
|
G | A | 170 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(167): Show | 181 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.668+348G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 6/18 | chr6 | 160715262 | ||||||
chr6:160715453
|
G | A | 171 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(168): Show | 182 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.668+539G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 6/18 | chr6 | 160715453 | ||||||
chr6:160715485
|
G | A | 1 | a0001c0002t0001g0125 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.668+571G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 6/18 | chr6 | 160715485 | ||||||
chr6:160715549
|
G | A | 6 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(3): Show | 6 | HG02451.hp1 HG02922.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.668+635G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 6/18 | chr6 | 160715549 | ||||||
chr6:160715731
|
A | C | 2 | a0004c0020t0004g0336a0004c0020t0004g0342 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.668+817A>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 6/18 | chr6 | 160715731 | ||||||
chr6:160715746
|
C | T | 1 | a0001c0002t0001g0160 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.668+832C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 6/18 | chr6 | 160715746 | ||||||
chr6:160715821
|
G | A | 1 | a0002c0004t0011g0306 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.669-824G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 6/18 | chr6 | 160715821 | ||||||
chr6:160715864
|
G | A | 1 | a0001c0003t0001g0261 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.669-781G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 6/18 | chr6 | 160715864 | ||||||
chr6:160716123
|
T | C | 1 | a0002c0004t0003g0341 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.669-522T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 6/18 | chr6 | 160716123 | ||||||
chr6:160716131
|
C | G | 1 | a0001c0002t0001g0159 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.669-514C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 6/18 | chr6 | 160716131 | ||||||
chr6:160716226
|
A | G | 30 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(27): Show | 32 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.669-419A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 6/18 | chr6 | 160716226 | ||||||
chr6:160716341
|
T | C | 1 | a0001c0028t0004g0233 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.669-304T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 6/18 | chr6 | 160716341 | ||||||
chr6:160716481
|
C | T | 1 | a0001c0001t0001g0005 | 2 | HG01256.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.669-164C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 6/18 | chr6 | 160716481 | ||||||
chr6:160716486
|
T | C | 29 | a0001c0029t0015g0032a0002c0004t0003g0019a0002c0004t0003g0020others(26): Show | 32 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.669-159T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 6/18 | chr6 | 160716486 | ||||||
chr6:160716491
|
T | A | 203 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(200): Show | 216 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.669-154T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 6/18 | chr6 | 160716491 | ||||||
chr6:160716631
|
T | G | 40 | a0001c0029t0015g0032a0002c0004t0003g0019a0002c0004t0003g0020others(37): Show | 43 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.669-14T>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 6/18 | chr6 | 160716631 | ||||||
chr6:160716958
|
G | A | 147 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0007others(144): Show | 161 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.787+195G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 7/18 | chr6 | 160716958 | ||||||
chr6:160716990
|
T | G | 1 | a0001c0001t0001g0175 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.787+227T>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 7/18 | chr6 | 160716990 | ||||||
chr6:160717149
|
G | C | 129 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(126): Show | 137 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.787+386G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 7/18 | chr6 | 160717149 | ||||||
chr6:160717321
|
G | T | 1 | a0001c0021t0004g0012 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.787+558G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 7/18 | chr6 | 160717321 | ||||||
chr6:160717438
|
C | T | 1 | a0002c0007t0023g0050 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.787+675C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 7/18 | chr6 | 160717438 | ||||||
chr6:160717462
|
CT | C | 160 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(157): Show | 170 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.787+708delT | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr6 | 160717462 | |||||
chr6:160717570
|
T | A | 1 | a0001c0002t0009g0245 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.788-724T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 7/18 | chr6 | 160717570 | ||||||
chr6:160717724
|
A | G | 1 | a0001c0005t0002g0111 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.788-570A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 7/18 | chr6 | 160717724 | ||||||
chr6:160717816
|
C | G | 118 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0007others(115): Show | 129 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.788-478C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 7/18 | chr6 | 160717816 | ||||||
chr6:160717885
|
A | G | 205 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(202): Show | 218 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.788-409A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 7/18 | chr6 | 160717885 | ||||||
chr6:160717963
|
A | G | 1 | a0002c0007t0023g0050 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.788-331A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 7/18 | chr6 | 160717963 | ||||||
chr6:160717989
|
C | T | 4 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0207others(1): Show | 4 | HG02040.hp1 HG02300.hp1 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.788-305C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 7/18 | chr6 | 160717989 | ||||||
chr6:160718026
|
C | T | 163 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(160): Show | 173 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.788-268C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 7/18 | chr6 | 160718026 | ||||||
chr6:160718055
|
A | G | 1 | a0001c0002t0001g0158 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.788-239A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 7/18 | chr6 | 160718055 | ||||||
chr6:160718089
|
A | C | 1 | a0001c0002t0009g0245 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.788-205A>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 7/18 | chr6 | 160718089 | ||||||
chr6:160718118
|
G | A | 1 | a0001c0015t0001g0316 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.788-176G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 7/18 | chr6 | 160718118 | ||||||
chr6:160718246
|
G | A | 10 | a0002c0004t0011g0306a0002c0007t0007g0038a0002c0007t0007g0039others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.788-48G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 7/18 | chr6 | 160718246 | ||||||
chr6:160718255
|
A | AAT | 5 | a0001c0015t0009g0244a0003c0012t0001g0239a0003c0012t0001g0254others(2): Show | 5 | HG02257.hp2 HG02965.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.788-30_788-29dupAT | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr6 | 160718255 | |||||
chr6:160718470
|
G | A | 133 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(130): Show | 141 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.950+14G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 8/18 | chr6 | 160718470 | ||||||
chr6:160719104
|
G | A | 1 | a0001c0021t0004g0012 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1096+266G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160719104 | ||||||
chr6:160719136
|
C | G | 6 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(3): Show | 6 | HG02451.hp1 HG02922.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1096+298C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160719136 | ||||||
chr6:160719265
|
T | C | 1 | a0001c0015t0001g0316 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1096+427T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160719265 | ||||||
chr6:160719866
|
AT | A | 5 | a0001c0015t0009g0244a0003c0012t0001g0239a0003c0012t0001g0254others(2): Show | 5 | HG02257.hp2 HG02965.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1096+1033delT | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr6 | 160719866 | |||||
chr6:160719873
|
C | G | 5 | a0001c0015t0009g0244a0003c0012t0001g0239a0003c0012t0001g0254others(2): Show | 5 | HG02257.hp2 HG02965.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1096+1035C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160719873 | ||||||
chr6:160720126
|
T | C | 138 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(135): Show | 146 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.1096+1288T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160720126 | ||||||
chr6:160720152
|
C | T | 209 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(206): Show | 223 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.1096+1314C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160720152 | ||||||
chr6:160720292
|
C | T | 3 | a0001c0013t0001g0024a0001c0013t0001g0351a0001c0015t0001g0350 | 4 | HG02559.hp1 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1096+1454C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160720292 | ||||||
chr6:160720298
|
G | A | 1 | a0001c0002t0001g0131 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1096+1460G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160720298 | ||||||
chr6:160720395
|
TTTTTC | T | 4 | a0001c0015t0009g0244a0003c0012t0001g0239a0003c0012t0001g0254others(1): Show | 4 | HG02257.hp2 HG02965.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1096+1572_1096+157 others(9): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr6 | 160720395 | |||||
chr6:160720410
|
C | CT | 115 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0009others(112): Show | 126 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.1096+1599dupT | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr6 | 160720410 | |||||
chr6:160720410
|
C | CTT | 53 | a0001c0002t0001g0007a0001c0002t0001g0073a0001c0002t0001g0125others(50): Show | 59 | HG00323.hp1 HG00597.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.1096+1598_1096+159 others(6): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr6 | 160720410 | |||||
chr6:160720410
|
C | CTTT | 12 | a0001c0002t0001g0090a0001c0006t0005g0346a0001c0006t0005g0348others(9): Show | 12 | HG01109.hp2 HG01169.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1096+1597_1096+159 others(7): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr6 | 160720410 | |||||
chr6:160720410
|
CTTTTTT | C | 56 | a0001c0001t0001g0008a0001c0001t0001g0054a0001c0001t0001g0055others(53): Show | 58 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.1096+1594_1096+159 others(10): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr6 | 160720410 | |||||
chr6:160720410
|
CTTTTTTT | C | 76 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(73): Show | 82 | HG00280.hp2 HG00423.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.1096+1593_1096+159 others(11): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr6 | 160720410 | |||||
chr6:160720488
|
C | T | 1 | a0001c0028t0004g0233 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1096+1650C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160720488 | ||||||
chr6:160720568
|
T | C | 3 | a0001c0013t0001g0024a0001c0013t0001g0351a0001c0015t0001g0350 | 4 | HG02559.hp1 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1096+1730T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160720568 | ||||||
chr6:160720649
|
A | G | 1 | a0001c0028t0004g0233 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1097-1759A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160720649 | ||||||
chr6:160720779
|
T | C | 1 | a0001c0002t0001g0133 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1097-1629T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160720779 | ||||||
chr6:160720970
|
A | G | 13 | a0001c0006t0005g0016a0001c0006t0005g0098a0001c0006t0005g0099others(10): Show | 15 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.1097-1438A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160720970 | ||||||
chr6:160721094
|
A | C | 13 | a0001c0006t0005g0016a0001c0006t0005g0098a0001c0006t0005g0099others(10): Show | 15 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.1097-1314A>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160721094 | ||||||
chr6:160721792
|
C | A | 1 | a0001c0006t0014g0037 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1097-616C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160721792 | ||||||
chr6:160721803
|
T | A | 1 | a0001c0003t0001g0134 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1097-605T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160721803 | ||||||
chr6:160721957
|
C | G | 1 | a0001c0027t0010g0120 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1097-451C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160721957 | ||||||
chr6:160721996
|
T | C | 1 | a0001c0006t0014g0037 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1097-412T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160721996 | ||||||
chr6:160722112
|
G | A | 1 | a0001c0005t0002g0270 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1097-296G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160722112 | ||||||
chr6:160722158
|
T | C | 72 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(69): Show | 77 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.1097-250T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160722158 | ||||||
chr6:160722167
|
A | G | 5 | a0002c0004t0008g0006a0002c0004t0008g0030a0002c0004t0008g0031others(2): Show | 6 | HG02145.hp1 HG02280.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1097-241A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160722167 | ||||||
chr6:160722201
|
A | C | 30 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(27): Show | 32 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1097-207A>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160722201 | ||||||
chr6:160722326
|
C | T | 1 | a0001c0005t0002g0110 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1097-82C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160722326 | ||||||
chr6:160722344
|
A | G | 29 | a0002c0004t0003g0019a0002c0004t0003g0020a0002c0004t0003g0023others(26): Show | 32 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1097-64A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160722344 | ||||||
chr6:160722576
|
T | C | 40 | a0002c0004t0003g0019a0002c0004t0003g0020a0002c0004t0003g0023others(37): Show | 43 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1256+9T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160722576 | ||||||
chr6:160722602
|
A | G | 30 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(27): Show | 32 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1256+35A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160722602 | ||||||
chr6:160722808
|
G | T | 1 | a0001c0006t0004g0048 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1256+241G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160722808 | ||||||
chr6:160722919
|
T | G | 1 | a0001c0002t0001g0085 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1256+352T>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160722919 | ||||||
chr6:160722998
|
T | A | 1 | a0001c0001t0001g0324 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1256+431T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160722998 | ||||||
chr6:160723090
|
A | AGTGTGTA others(19): Show |
7 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(4): Show | 7 | HG02451.hp1 HG02922.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1256+560_1256+585d others(28): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr6 | 160723090 | |||||
chr6:160723090
|
A | AGTGTGTA others(45): Show |
4 | a0003c0012t0001g0239a0003c0012t0001g0254a0003c0012t0009g0036others(1): Show | 4 | HG02257.hp2 HG02965.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1256+534_1256+585d others(54): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr6 | 160723090 | |||||
chr6:160723097
|
A | ATATATAT others(45): Show |
1 | a0001c0006t0014g0037 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1256+581_1256+582i others(54): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr6 | 160723097 | |||||
chr6:160723143
|
G | A | 1 | a0001c0001t0001g0324 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1256+576G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160723143 | ||||||
chr6:160723176
|
G | GTA | 18 | a0001c0006t0005g0016a0001c0006t0005g0098a0001c0006t0005g0099others(15): Show | 20 | HG01884.hp2 HG02559.hp1 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.1256+621_1256+622d others(4): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr6 | 160723176 | |||||
chr6:160723242
|
T | A | 1 | a0001c0001t0001g0004 | 3 | HG00741.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1256+675T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160723242 | ||||||
chr6:160723304
|
A | G | 30 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(27): Show | 32 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1256+737A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160723304 | ||||||
chr6:160723329
|
A | T | 7 | a0001c0002t0001g0052a0001c0002t0001g0164a0001c0002t0001g0165others(4): Show | 7 | HG00597.hp1 HG00609.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.1256+762A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160723329 | ||||||
chr6:160723519
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1256+952C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160723519 | ||||||
chr6:160723538
|
A | C | 1 | a0001c0008t0001g0314 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1256+971A>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160723538 | ||||||
chr6:160723697
|
G | A | 30 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(27): Show | 32 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1256+1130G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160723697 | ||||||
chr6:160723747
|
T | C | 30 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(27): Show | 32 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1256+1180T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160723747 | ||||||
chr6:160723768
|
A | G | 29 | a0002c0004t0003g0019a0002c0004t0003g0020a0002c0004t0003g0023others(26): Show | 32 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1256+1201A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160723768 | ||||||
chr6:160723835
|
C | T | 1 | a0002c0004t0011g0306 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1256+1268C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160723835 | ||||||
chr6:160723906
|
A | G | 1 | a0001c0006t0014g0037 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1256+1339A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160723906 | ||||||
chr6:160723916
|
C | T | 30 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(27): Show | 32 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1256+1349C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160723916 | ||||||
chr6:160724055
|
C | T | 1 | a0001c0001t0001g0174 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1256+1488C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160724055 | ||||||
chr6:160724118
|
C | G | 1 | a0001c0009t0004g0025 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1256+1551C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160724118 | ||||||
chr6:160724144
|
A | T | 70 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(67): Show | 75 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.1256+1577A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160724144 | ||||||
chr6:160724202
|
T | C | 55 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0074others(52): Show | 56 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.1256+1635T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160724202 | ||||||
chr6:160724214
|
A | C | 28 | a0001c0001t0001g0013a0001c0001t0001g0103a0001c0001t0001g0181others(25): Show | 30 | HG00558.hp1 HG01192.hp2 HG02132.hp1 others(27): Show |
intron_variant | MODIFIER | c.1256+1647A>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160724214 | ||||||
chr6:160724265
|
A | G | 30 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(27): Show | 32 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1256+1698A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160724265 | ||||||
chr6:160724341
|
C | T | 1 | a0001c0028t0004g0233 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1256+1774C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160724341 | ||||||
chr6:160724361
|
A | G | 1 | a0001c0002t0001g0207 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1256+1794A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160724361 | ||||||
chr6:160724471
|
T | C | 2 | a0004c0020t0004g0336a0004c0020t0004g0342 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1256+1904T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160724471 | ||||||
chr6:160725009
|
G | A | 1 | a0001c0009t0012g0070 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1256+2442G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160725009 | ||||||
chr6:160725186
|
A | G | 210 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(207): Show | 224 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.1256+2619A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160725186 | ||||||
chr6:160725602
|
A | G | 30 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(27): Show | 32 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1256+3035A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160725602 | ||||||
chr6:160725672
|
A | G | 70 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(67): Show | 75 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.1256+3105A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160725672 | ||||||
chr6:160725739
|
A | G | 1 | a0001c0001t0022g0309 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1256+3172A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160725739 | ||||||
chr6:160725743
|
A | G | 1 | a0004c0018t0002g0269 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1256+3176A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160725743 | ||||||
chr6:160725771
|
A | G | 30 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(27): Show | 32 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1256+3204A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160725771 | ||||||
chr6:160725852
|
GA | G | 15 | a0001c0006t0005g0016a0001c0006t0005g0098a0001c0006t0005g0099others(12): Show | 17 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.1256+3290delA | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr6 | 160725852 | |||||
chr6:160726023
|
G | A | 1 | a0001c0002t0001g0135 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1256+3456G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160726023 | ||||||
chr6:160726070
|
A | C | 15 | a0001c0006t0005g0016a0001c0006t0005g0098a0001c0006t0005g0099others(12): Show | 17 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.1256+3503A>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160726070 | ||||||
chr6:160726336
|
A | T | 29 | a0002c0004t0003g0019a0002c0004t0003g0020a0002c0004t0003g0023others(26): Show | 32 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1256+3769A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160726336 | ||||||
chr6:160726348
|
T | C | 1 | a0001c0001t0001g0326 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1256+3781T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160726348 | ||||||
chr6:160726364
|
G | A | 1 | a0001c0001t0001g0312 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1256+3797G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160726364 | ||||||
chr6:160726378
|
T | G | 1 | a0001c0001t0001g0176 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1256+3811T>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160726378 | ||||||
chr6:160726408
|
G | C | 30 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(27): Show | 32 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1256+3841G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160726408 | ||||||
chr6:160726413
|
T | C | 1 | a0001c0006t0014g0037 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1256+3846T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160726413 | ||||||
chr6:160726587
|
T | TA | 28 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(25): Show | 30 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.1256+4020_1256+402 others(5): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160726587 | ||||||
chr6:160726588
|
T | A | 31 | a0001c0003t0001g0130a0001c0006t0002g0043a0001c0006t0002g0044others(28): Show | 33 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.1256+4021T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160726588 | ||||||
chr6:160726588
|
T | TA | 144 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(141): Show | 152 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.1256+4031dupA | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr6 | 160726588 | |||||
chr6:160726589
|
A | T | 1 | a0002c0004t0011g0306 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1256+4022A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160726589 | ||||||
chr6:160726687
|
C | G | 1 | a0001c0002t0001g0307 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1256+4120C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160726687 | ||||||
chr6:160726861
|
T | C | 1 | a0001c0001t0001g0177 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1257-4190T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160726861 | ||||||
chr6:160726939
|
A | G | 7 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(4): Show | 7 | HG02451.hp1 HG02922.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1257-4112A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160726939 | ||||||
chr6:160727064
|
C | T | 4 | a0003c0012t0001g0239a0003c0012t0001g0254a0003c0012t0009g0036others(1): Show | 4 | HG02257.hp2 HG02965.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1257-3987C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160727064 | ||||||
chr6:160727065
|
G | A | 1 | a0002c0004t0011g0306 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1257-3986G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160727065 | ||||||
chr6:160727115
|
T | C | 30 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(27): Show | 32 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1257-3936T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160727115 | ||||||
chr6:160727156
|
G | A | 4 | a0001c0006t0014g0037a0005c0010t0004g0017a0005c0010t0004g0241others(1): Show | 5 | HG01891.hp2 HG02280.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1257-3895G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160727156 | ||||||
chr6:160727189
|
T | A | 1 | a0001c0005t0002g0252 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1257-3862T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160727189 | ||||||
chr6:160727333
|
G | A | 1 | a0001c0002t0001g0136 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1257-3718G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160727333 | ||||||
chr6:160727367
|
G | T | 207 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(204): Show | 221 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.1257-3684G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160727367 | ||||||
chr6:160727376
|
T | TA | 30 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(27): Show | 32 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1257-3667dupA | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr6 | 160727376 | |||||
chr6:160727464
|
A | C | 35 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(32): Show | 37 | HG01243.hp1 HG01256.hp1 HG01258.hp1 others(34): Show |
intron_variant | MODIFIER | c.1257-3587A>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160727464 | ||||||
chr6:160727692
|
C | T | 1 | a0001c0027t0010g0120 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1257-3359C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160727692 | ||||||
chr6:160727730
|
T | C | 30 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(27): Show | 32 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1257-3321T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160727730 | ||||||
chr6:160727830
|
G | A | 1 | a0001c0001t0001g0027 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1257-3221G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160727830 | ||||||
chr6:160727905
|
T | G | 2 | a0002c0004t0003g0341a0002c0022t0003g0267 | 2 | HG01109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1257-3146T>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160727905 | ||||||
chr6:160728103
|
A | T | 1 | a0001c0002t0001g0307 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1257-2948A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160728103 | ||||||
chr6:160728290
|
G | T | 5 | a0001c0005t0002g0249a0001c0005t0002g0250a0001c0005t0002g0304others(2): Show | 5 | HG00323.hp2 HG00642.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1257-2761G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160728290 | ||||||
chr6:160728292
|
A | G | 35 | a0001c0003t0001g0011a0001c0003t0001g0049a0001c0003t0001g0057others(32): Show | 36 | HG00558.hp2 HG00639.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.1257-2759A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160728292 | ||||||
chr6:160728328
|
T | C | 1 | a0001c0001t0001g0258 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1257-2723T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160728328 | ||||||
chr6:160728335
|
T | TAAGAGTC others(103): Show |
15 | a0001c0006t0005g0016a0001c0006t0005g0098a0001c0006t0005g0099others(12): Show | 17 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.1257-2662_1257-266 others(114): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr6 | 160728335 | |||||
chr6:160728335
|
T | TAAGAGTC others(103): Show |
308 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(305): Show | 332 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(329): Show |
intron_variant | MODIFIER | c.1257-2662_1257-266 others(114): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr6 | 160728335 | |||||
chr6:160728560
|
C | T | 7 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(4): Show | 7 | HG02451.hp1 HG02922.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1257-2491C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160728560 | ||||||
chr6:160728657
|
T | C | 1 | a0001c0009t0004g0025 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1257-2394T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160728657 | ||||||
chr6:160728683
|
G | A | 1 | a0001c0001t0001g0325 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1257-2368G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160728683 | ||||||
chr6:160728886
|
A | G | 30 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(27): Show | 32 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1257-2165A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160728886 | ||||||
chr6:160729038
|
G | T | 1 | a0001c0001t0001g0063 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1257-2013G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160729038 | ||||||
chr6:160729145
|
G | GA | 29 | a0002c0004t0003g0019a0002c0004t0003g0020a0002c0004t0003g0023others(26): Show | 32 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1257-1900dupA | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr6 | 160729145 | |||||
chr6:160729219
|
G | T | 40 | a0002c0004t0003g0019a0002c0004t0003g0020a0002c0004t0003g0023others(37): Show | 43 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1257-1832G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160729219 | ||||||
chr6:160729291
|
G | A | 5 | a0002c0007t0007g0038a0002c0007t0007g0039a0002c0007t0007g0040others(2): Show | 5 | HG01243.hp1 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1257-1760G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160729291 | ||||||
chr6:160729296
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1257-1755C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160729296 | ||||||
chr6:160729500
|
T | C | 9 | a0002c0007t0007g0038a0002c0007t0007g0039a0002c0007t0007g0040others(6): Show | 9 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1257-1551T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160729500 | ||||||
chr6:160729518
|
T | C | 1 | a0001c0006t0005g0098 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1257-1533T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160729518 | ||||||
chr6:160729958
|
A | G | 1 | a0001c0028t0004g0233 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1257-1093A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160729958 | ||||||
chr6:160730116
|
A | G | 1 | a0001c0021t0004g0012 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1257-935A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160730116 | ||||||
chr6:160730133
|
G | T | 1 | a0001c0002t0001g0163 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1257-918G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160730133 | ||||||
chr6:160730168
|
G | A | 1 | a0001c0002t0001g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1257-883G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160730168 | ||||||
chr6:160730188
|
T | C | 1 | a0005c0010t0004g0242 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1257-863T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160730188 | ||||||
chr6:160730216
|
G | A | 1 | a0001c0003t0001g0266 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1257-835G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160730216 | ||||||
chr6:160730424
|
C | T | 15 | a0001c0006t0005g0016a0001c0006t0005g0098a0001c0006t0005g0099others(12): Show | 17 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.1257-627C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160730424 | ||||||
chr6:160730679
|
C | A | 1 | a0001c0009t0004g0046 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1257-372C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160730679 | ||||||
chr6:160730936
|
T | C | 6 | a0001c0006t0004g0048a0001c0015t0001g0316a0003c0012t0001g0239others(3): Show | 6 | HG02257.hp2 HG02965.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1257-115T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160730936 | ||||||
chr6:160730989
|
G | T | 4 | a0002c0007t0007g0096a0002c0007t0007g0097a0002c0007t0007g0291others(1): Show | 4 | HG02055.hp2 HG02109.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1257-62G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160730989 | ||||||
chr6:160731262
|
A | G | 30 | a0002c0004t0003g0019a0002c0004t0003g0020a0002c0004t0003g0023others(27): Show | 33 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.1438+30A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 11/18 | chr6 | 160731262 | ||||||
chr6:160731325
|
C | T | 1 | a0001c0003t0001g0049 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1438+93C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 11/18 | chr6 | 160731325 | ||||||
chr6:160731360
|
G | A | 1 | a0001c0021t0004g0012 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1438+128G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 11/18 | chr6 | 160731360 | ||||||
chr6:160731416
|
C | T | 4 | a0003c0012t0001g0239a0003c0012t0001g0254a0003c0012t0009g0036others(1): Show | 4 | HG02257.hp2 HG02965.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1438+184C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 11/18 | chr6 | 160731416 | ||||||
chr6:160731417
|
G | A | 292 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(289): Show | 315 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(312): Show |
intron_variant | MODIFIER | c.1438+185G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 11/18 | chr6 | 160731417 | ||||||
chr6:160731491
|
A | G | 1 | a0002c0004t0011g0306 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1439-254A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 11/18 | chr6 | 160731491 | ||||||
chr6:160732048
|
A | C | 30 | a0002c0004t0003g0019a0002c0004t0003g0020a0002c0004t0003g0023others(27): Show | 33 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.1587+155A>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160732048 | ||||||
chr6:160732151
|
C | A | 1 | a0001c0001t0001g0063 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1587+258C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160732151 | ||||||
chr6:160732168
|
T | C | 1 | a0002c0007t0023g0050 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1587+275T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160732168 | ||||||
chr6:160732256
|
GA | G | 15 | a0001c0006t0005g0016a0001c0006t0005g0098a0001c0006t0005g0099others(12): Show | 17 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.1587+369delA | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr6 | 160732256 | |||||
chr6:160732325
|
T | G | 3 | a0005c0010t0004g0017a0005c0010t0004g0241a0005c0010t0004g0242 | 4 | HG02280.hp2 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1587+432T>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160732325 | ||||||
chr6:160732495
|
T | C | 30 | a0002c0004t0003g0019a0002c0004t0003g0020a0002c0004t0003g0023others(27): Show | 33 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.1587+602T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160732495 | ||||||
chr6:160732529
|
T | C | 30 | a0002c0004t0003g0019a0002c0004t0003g0020a0002c0004t0003g0023others(27): Show | 33 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.1587+636T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160732529 | ||||||
chr6:160732626
|
G | A | 1 | a0002c0007t0023g0050 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1587+733G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160732626 | ||||||
chr6:160732663
|
G | C | 17 | a0001c0006t0005g0016a0001c0006t0005g0098a0001c0006t0005g0099others(14): Show | 19 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1587+770G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160732663 | ||||||
chr6:160732690
|
C | A | 6 | a0001c0008t0001g0237a0001c0008t0001g0300a0001c0008t0001g0301others(3): Show | 6 | HG02572.hp1 HG02630.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1587+797C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160732690 | ||||||
chr6:160732958
|
G | A | 109 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0007others(106): Show | 120 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.1588-1037G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160732958 | ||||||
chr6:160733075
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1588-920G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160733075 | ||||||
chr6:160733200
|
G | T | 29 | a0002c0004t0003g0019a0002c0004t0003g0020a0002c0004t0003g0023others(26): Show | 32 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1588-795G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160733200 | ||||||
chr6:160733205
|
G | A | 1 | a0001c0021t0004g0012 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1588-790G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160733205 | ||||||
chr6:160733385
|
G | C | 1 | a0001c0003t0001g0057 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1588-610G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160733385 | ||||||
chr6:160733401
|
G | C | 1 | a0002c0007t0007g0038 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1588-594G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160733401 | ||||||
chr6:160733418
|
G | A | 1 | a0001c0003t0001g0130 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1588-577G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160733418 | ||||||
chr6:160733492
|
C | T | 11 | a0001c0028t0004g0233a0002c0004t0011g0306a0002c0007t0007g0038others(8): Show | 11 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1588-503C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160733492 | ||||||
chr6:160733493
|
G | A | 1 | a0001c0005t0011g0115 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1588-502G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160733493 | ||||||
chr6:160733543
|
T | TAGAA | 77 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(74): Show | 84 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.1588-449_1588-446d others(6): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr6 | 160733543 | |||||
chr6:160733684
|
AG | A | 3 | a0001c0009t0004g0046a0004c0020t0004g0336a0004c0020t0004g0342 | 3 | HG01256.hp1 HG01258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1588-310delG | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160733684 | ||||||
chr6:160733685
|
G | C | 72 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(69): Show | 78 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.1588-310G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160733685 | ||||||
chr6:160733686
|
A | C | 3 | a0001c0009t0004g0046a0004c0020t0004g0336a0004c0020t0004g0342 | 3 | HG01256.hp1 HG01258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1588-309A>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160733686 | ||||||
chr6:160733705
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1588-290G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160733705 | ||||||
chr6:160733708
|
G | C | 1 | a0001c0011t0001g0236 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1588-287G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160733708 | ||||||
chr6:160733831
|
C | G | 1 | a0002c0004t0011g0306 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1588-164C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160733831 | ||||||
chr6:160733844
|
C | CAA | 4 | a0002c0004t0003g0079a0002c0004t0003g0283a0002c0004t0003g0284others(1): Show | 4 | HG00323.hp1 HG01069.hp2 HG01070.hp2 others(1): Show |
intron_variant | MODIFIER | c.1588-150_1588-149i others(4): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr6 | 160733844 | |||||
chr6:160733844
|
C | CAAA | 24 | a0002c0004t0003g0019a0002c0004t0003g0020a0002c0004t0003g0023others(21): Show | 27 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.1588-150_1588-149i others(5): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr6 | 160733844 | |||||
chr6:160733844
|
C | CAAAA | 3 | a0002c0004t0003g0277a0002c0004t0008g0033a0002c0004t0011g0306 | 3 | HG02145.hp1 HG02698.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1588-150_1588-149i others(6): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr6 | 160733844 | |||||
chr6:160733846
|
G | A | 31 | a0002c0004t0003g0019a0002c0004t0003g0020a0002c0004t0003g0023others(28): Show | 34 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.1588-149G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160733846 | ||||||
chr6:160733846
|
G | GA | 8 | a0001c0002t0001g0073a0001c0002t0001g0353a0001c0002t0009g0245others(5): Show | 8 | HG02027.hp1 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1588-127dupA | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr6 | 160733846 | |||||
chr6:160733846
|
GA | G | 10 | a0001c0008t0001g0237a0001c0008t0001g0300a0001c0008t0001g0301others(7): Show | 10 | HG01074.hp1 HG02572.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1588-127delA | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr6 | 160733846 | |||||
chr6:160733846
|
GAAA | G | 26 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(23): Show | 28 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.1588-129_1588-127d others(5): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr6 | 160733846 | |||||
chr6:160733846
|
GAAAA | G | 11 | a0001c0006t0005g0238a0001c0006t0005g0346a0001c0006t0005g0348others(8): Show | 13 | HG01891.hp2 HG02280.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.1588-130_1588-127d others(6): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr6 | 160733846 | |||||
chr6:160733846
|
GAAAAAA | G | 129 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(126): Show | 137 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.1588-132_1588-127d others(8): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr6 | 160733846 | |||||
chr6:160733869
|
G | A | 9 | a0002c0007t0007g0038a0002c0007t0007g0039a0002c0007t0007g0040others(6): Show | 9 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1588-126G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160733869 | ||||||
chr6:160733923
|
C | T | 38 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(35): Show | 42 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.1588-72C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160733923 | ||||||
chr6:160733992
|
C | T | 1 | a0001c0001t0001g0333 | 1 | NA18977.hp1 | splice_region_variant&intron_variant | LOW | c.1588-3C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160733992 | ||||||
chr6:160734143
|
A | C | 1 | a0001c0006t0014g0037 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1681+55A>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160734143 | ||||||
chr6:160734216
|
T | A | 1 | a0001c0001t0001g0214 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1681+128T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160734216 | ||||||
chr6:160734232
|
T | C | 1 | a0007c0016t0001g0018 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1681+144T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160734232 | ||||||
chr6:160734242
|
C | G | 1 | a0001c0003t0001g0323 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1681+154C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160734242 | ||||||
chr6:160734455
|
G | A | 1 | a0001c0002t0001g0137 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1681+367G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160734455 | ||||||
chr6:160734496
|
G | A | 1 | a0001c0003t0001g0321 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1681+408G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160734496 | ||||||
chr6:160734540
|
G | A | 1 | a0001c0006t0014g0037 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1681+452G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160734540 | ||||||
chr6:160734717
|
T | C | 1 | a0001c0001t0001g0296 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1681+629T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160734717 | ||||||
chr6:160734745
|
GA | G | 40 | a0001c0001t0001g0065a0001c0001t0001g0170a0001c0001t0001g0192others(37): Show | 43 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1681+676delA | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 160734745 | |||||
chr6:160734745
|
GAA | G | 35 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(32): Show | 39 | HG01069.hp2 HG01256.hp1 HG01258.hp1 others(36): Show |
intron_variant | MODIFIER | c.1681+675_1681+676d others(4): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 160734745 | |||||
chr6:160734745
|
GAAAAAAA | G | 13 | a0001c0001t0001g0013a0001c0001t0001g0066a0001c0001t0001g0072others(10): Show | 14 | HG00558.hp1 HG01192.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.1681+670_1681+676d others(9): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 160734745 | |||||
chr6:160734759
|
A | G | 113 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0007others(110): Show | 124 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.1681+671A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160734759 | ||||||
chr6:160734761
|
A | G | 5 | a0001c0001t0001g0054a0001c0001t0001g0101a0001c0001t0001g0221others(2): Show | 5 | HG02015.hp2 NA18955.hp1 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.1681+673A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160734761 | ||||||
chr6:160734790
|
C | T | 6 | a0001c0001t0007g0298a0002c0007t0007g0038a0002c0007t0007g0039others(3): Show | 6 | HG01243.hp1 HG02486.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1681+702C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160734790 | ||||||
chr6:160734994
|
T | A | 1 | a0001c0028t0004g0233 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1681+906T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160734994 | ||||||
chr6:160735008
|
C | CTGCCCAG others(8): Show |
18 | a0001c0006t0005g0016a0001c0006t0005g0098a0001c0006t0005g0099others(15): Show | 20 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1681+922_1681+936d others(17): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 160735008 | |||||
chr6:160735199
|
G | A | 7 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(4): Show | 7 | HG02451.hp1 HG02922.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1681+1111G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160735199 | ||||||
chr6:160735264
|
C | T | 29 | a0002c0004t0003g0019a0002c0004t0003g0020a0002c0004t0003g0023others(26): Show | 32 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1681+1176C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160735264 | ||||||
chr6:160735435
|
G | C | 3 | a0001c0009t0004g0046a0004c0020t0004g0336a0004c0020t0004g0342 | 3 | HG01256.hp1 HG01258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1681+1347G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160735435 | ||||||
chr6:160735635
|
G | A | 30 | a0001c0001t0001g0101a0002c0004t0003g0019a0002c0004t0003g0020others(27): Show | 33 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.1682-1252G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160735635 | ||||||
chr6:160735784
|
T | C | 1 | a0001c0001t0001g0275 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1682-1103T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160735784 | ||||||
chr6:160735897
|
T | A | 211 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(208): Show | 226 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.1682-990T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160735897 | ||||||
chr6:160736114
|
G | A | 1 | a0001c0002t0001g0160 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1682-773G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160736114 | ||||||
chr6:160736138
|
C | T | 3 | a0005c0010t0004g0017a0005c0010t0004g0241a0005c0010t0004g0242 | 4 | HG02280.hp2 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1682-749C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160736138 | ||||||
chr6:160736386
|
TAC | T | 10 | a0001c0001t0007g0298a0002c0007t0007g0038a0002c0007t0007g0039others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1682-486_1682-485d others(4): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 160736386 | |||||
chr6:160736775
|
T | C | 5 | a0001c0001t0001g0054a0001c0001t0001g0101a0001c0001t0001g0221others(2): Show | 5 | HG02015.hp2 NA18955.hp1 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.1682-112T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160736775 | ||||||
chr6:160737047
|
C | T | 1 | a0001c0005t0010g0308 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1802+40C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160737047 | ||||||
chr6:160737105
|
C | T | 1 | a0001c0021t0004g0012 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1802+98C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160737105 | ||||||
chr6:160737169
|
T | C | 4 | a0001c0008t0001g0237a0001c0008t0001g0300a0001c0008t0001g0302others(1): Show | 4 | HG02572.hp1 HG02886.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1802+162T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160737169 | ||||||
chr6:160737173
|
TA | T | 7 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(4): Show | 7 | HG02451.hp1 HG02922.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1802+167delA | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160737173 | ||||||
chr6:160737243
|
C | T | 1 | a0001c0001t0001g0313 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1802+236C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160737243 | ||||||
chr6:160737413
|
T | C | 4 | a0001c0001t0001g0178a0001c0001t0001g0180a0001c0001t0001g0215others(1): Show | 4 | HG00408.hp1 HG03654.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.1802+406T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160737413 | ||||||
chr6:160737465
|
T | C | 16 | a0001c0005t0005g0240a0001c0006t0005g0016a0001c0006t0005g0098others(13): Show | 18 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.1802+458T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160737465 | ||||||
chr6:160737630
|
T | C | 1 | a0002c0004t0011g0306 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1802+623T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160737630 | ||||||
chr6:160737697
|
G | A | 5 | a0001c0009t0004g0025a0003c0012t0001g0239a0003c0012t0001g0254others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1802+690G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160737697 | ||||||
chr6:160737702
|
T | C | 217 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(214): Show | 232 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.1802+695T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160737702 | ||||||
chr6:160737948
|
C | T | 4 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(1): Show | 4 | NA19003.hp1 NA19012.hp2 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.1803-590C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160737948 | ||||||
chr6:160737966
|
C | CA | 40 | a0001c0001t0007g0298a0002c0004t0003g0019a0002c0004t0003g0020others(37): Show | 43 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1803-572_1803-571i others(3): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160737966 | ||||||
chr6:160737967
|
T | A | 39 | a0001c0005t0005g0240a0001c0006t0002g0043a0001c0006t0002g0044others(36): Show | 43 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(40): Show |
intron_variant | MODIFIER | c.1803-571T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160737967 | ||||||
chr6:160737969
|
T | A | 40 | a0001c0001t0007g0298a0002c0004t0003g0019a0002c0004t0003g0020others(37): Show | 43 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1803-569T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160737969 | ||||||
chr6:160737970
|
A | AC | 39 | a0001c0005t0005g0240a0001c0006t0002g0043a0001c0006t0002g0044others(36): Show | 43 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(40): Show |
intron_variant | MODIFIER | c.1803-568_1803-567i others(3): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160737970 | ||||||
chr6:160737974
|
T | C | 79 | a0001c0001t0007g0298a0001c0005t0005g0240a0001c0006t0002g0043others(76): Show | 86 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.1803-564T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160737974 | ||||||
chr6:160737984
|
A | G | 79 | a0001c0001t0007g0298a0001c0005t0005g0240a0001c0006t0002g0043others(76): Show | 86 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.1803-554A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160737984 | ||||||
chr6:160738190
|
G | A | 1 | a0002c0007t0023g0050 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1803-348G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160738190 | ||||||
chr6:160738324
|
A | G | 1 | a0001c0005t0011g0115 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1803-214A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160738324 | ||||||
chr6:160738334
|
T | G | 39 | a0001c0005t0005g0240a0001c0006t0002g0043a0001c0006t0002g0044others(36): Show | 43 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(40): Show |
intron_variant | MODIFIER | c.1803-204T>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160738334 | ||||||
chr6:160738366
|
C | T | 1 | a0001c0005t0011g0115 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1803-172C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160738366 | ||||||
chr6:160738627
|
C | A | 2 | a0001c0021t0004g0012a0001c0028t0004g0233 | 3 | HG03098.hp1 HG03139.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1877+15C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 15/18 | chr6 | 160738627 | ||||||
chr6:160739051
|
G | A | 211 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(208): Show | 226 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.1878-17G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 15/18 | chr6 | 160739051 | ||||||
chr6:160739062
|
T | C | 1 | a0001c0005t0002g0304 | 1 | HG00642.hp2 | splice_region_variant&intron_variant | LOW | c.1878-6T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 15/18 | chr6 | 160739062 | ||||||
chr6:160739293
|
G | A | 1 | a0001c0002t0001g0138 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2018+85G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160739293 | ||||||
chr6:160739309
|
T | C | 4 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0001g0264others(1): Show | 4 | HG00408.hp2 HG00609.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.2018+101T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160739309 | ||||||
chr6:160739473
|
T | C | 33 | a0001c0005t0005g0240a0001c0006t0002g0043a0001c0006t0002g0044others(30): Show | 35 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.2018+265T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160739473 | ||||||
chr6:160739508
|
C | T | 3 | a0001c0009t0004g0025a0001c0021t0004g0012a0001c0028t0004g0233 | 4 | HG02258.hp1 HG03098.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2018+300C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160739508 | ||||||
chr6:160739509
|
G | A | 16 | a0001c0005t0005g0240a0001c0006t0005g0016a0001c0006t0005g0098others(13): Show | 18 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.2018+301G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160739509 | ||||||
chr6:160739608
|
G | C | 2 | a0001c0021t0004g0012a0001c0028t0004g0233 | 3 | HG03098.hp1 HG03139.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2018+400G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160739608 | ||||||
chr6:160739612
|
G | A | 35 | a0001c0003t0001g0011a0001c0003t0001g0049a0001c0003t0001g0057others(32): Show | 36 | HG00558.hp2 HG00639.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.2018+404G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160739612 | ||||||
chr6:160739727
|
TTC | T | 131 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(128): Show | 139 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.2018+520_2018+521d others(4): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160739727 | ||||||
chr6:160739760
|
C | CA | 24 | a0001c0002t0001g0138a0001c0003t0001g0132a0001c0003t0001g0156others(21): Show | 25 | HG01256.hp1 HG01258.hp1 HG02027.hp1 others(22): Show |
intron_variant | MODIFIER | c.2018+563dupA | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr6 | 160739760 | |||||
chr6:160739760
|
C | CAA | 16 | a0001c0005t0005g0240a0001c0006t0005g0016a0001c0006t0005g0098others(13): Show | 18 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.2018+562_2018+563d others(4): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr6 | 160739760 | |||||
chr6:160739794
|
CA | C | 35 | a0001c0005t0005g0240a0001c0006t0002g0043a0001c0006t0002g0044others(32): Show | 38 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.2018+596delA | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr6 | 160739794 | |||||
chr6:160740051
|
G | A | 1 | a0001c0006t0014g0037 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2018+843G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160740051 | ||||||
chr6:160740186
|
G | A | 1 | a0001c0021t0004g0012 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2018+978G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160740186 | ||||||
chr6:160740270
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2019-1041C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160740270 | ||||||
chr6:160740323
|
T | C | 7 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(4): Show | 7 | HG02451.hp1 HG02922.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.2019-988T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160740323 | ||||||
chr6:160740463
|
C | T | 7 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(4): Show | 7 | HG02451.hp1 HG02922.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.2019-848C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160740463 | ||||||
chr6:160740476
|
C | A | 1 | a0001c0027t0010g0120 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2019-835C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160740476 | ||||||
chr6:160740527
|
C | A | 34 | a0001c0006t0014g0037a0002c0004t0003g0019a0002c0004t0003g0020others(31): Show | 38 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.2019-784C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160740527 | ||||||
chr6:160740599
|
G | A | 2 | a0001c0001t0001g0102a0001c0001t0001g0176 | 2 | NA18971.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.2019-712G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160740599 | ||||||
chr6:160740640
|
A | G | 5 | a0001c0001t0006g0188a0001c0001t0006g0189a0001c0001t0006g0190others(2): Show | 5 | NA18952.hp1 NA18975.hp2 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.2019-671A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160740640 | ||||||
chr6:160740726
|
A | G | 1 | a0001c0006t0005g0099 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2019-585A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160740726 | ||||||
chr6:160740834
|
G | A | 1 | a0001c0002t0001g0136 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2019-477G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160740834 | ||||||
chr6:160740872
|
G | C | 10 | a0002c0004t0003g0023a0002c0004t0003g0077a0002c0004t0003g0255others(7): Show | 11 | HG00642.hp1 HG00738.hp2 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.2019-439G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160740872 | ||||||
chr6:160740945
|
TTCCATGC others(5): Show |
T | 7 | a0001c0006t0002g0043a0001c0006t0002g0044a0001c0006t0002g0047others(4): Show | 7 | HG02451.hp1 HG02922.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.2019-363_2019-352d others(14): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr6 | 160740945 | |||||
chr6:160741038
|
G | A | 1 | a0001c0021t0004g0012 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2019-273G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160741038 | ||||||
chr6:160741179
|
T | C | 4 | a0001c0006t0014g0037a0005c0010t0004g0017a0005c0010t0004g0241others(1): Show | 5 | HG01891.hp2 HG02280.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2019-132T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160741179 | ||||||
chr6:160741258
|
A | G | 2 | a0001c0009t0002g0058a0001c0009t0002g0059 | 2 | HG01074.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.2019-53A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160741258 | ||||||
chr6:160741295
|
G | A | 1 | a0002c0004t0011g0306 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2019-16G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160741295 | ||||||
chr6:160741446
|
G | A | 6 | a0001c0008t0001g0224a0001c0008t0001g0349a0001c0013t0001g0024others(3): Show | 7 | HG02559.hp2 HG02886.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.2125+29G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160741446 | ||||||
chr6:160741465
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2125+48G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160741465 | ||||||
chr6:160741587
|
A | T | 1 | a0001c0028t0004g0233 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2125+170A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160741587 | ||||||
chr6:160741739
|
G | A | 1 | a0001c0021t0004g0012 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2125+322G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160741739 | ||||||
chr6:160741851
|
T | A | 3 | a0001c0002t0001g0126a0001c0002t0001g0127a0001c0002t0001g0128 | 3 | HG01255.hp2 HG01978.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.2125+434T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160741851 | ||||||
chr6:160742022
|
A | G | 1 | a0001c0028t0004g0233 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2125+605A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160742022 | ||||||
chr6:160742042
|
A | T | 281 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(278): Show | 305 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(302): Show |
intron_variant | MODIFIER | c.2125+625A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160742042 | ||||||
chr6:160742069
|
T | G | 2 | a0001c0021t0004g0012a0001c0028t0004g0233 | 3 | HG03098.hp1 HG03139.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2125+652T>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160742069 | ||||||
chr6:160742217
|
G | T | 7 | a0001c0002t0001g0007a0001c0002t0001g0073a0001c0002t0001g0125others(4): Show | 8 | HG01255.hp2 HG01978.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.2125+800G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160742217 | ||||||
chr6:160742244
|
C | G | 3 | a0005c0010t0004g0017a0005c0010t0004g0241a0005c0010t0004g0242 | 4 | HG02280.hp2 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2125+827C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160742244 | ||||||
chr6:160742372
|
T | C | 3 | a0001c0009t0004g0046a0004c0020t0004g0336a0004c0020t0004g0342 | 3 | HG01256.hp1 HG01258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2125+955T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160742372 | ||||||
chr6:160742463
|
G | T | 1 | a0001c0003t0001g0049 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2125+1046G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160742463 | ||||||
chr6:160742497
|
G | T | 1 | a0001c0001t0001g0184 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2125+1080G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160742497 | ||||||
chr6:160742497
|
GT | G | 55 | a0001c0001t0001g0275a0001c0002t0001g0007a0001c0002t0001g0015others(52): Show | 58 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.2125+1090delT | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160742497 | |||||
chr6:160742498
|
T | G | 10 | a0001c0001t0007g0298a0002c0007t0007g0038a0002c0007t0007g0039others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2125+1081T>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160742498 | ||||||
chr6:160742566
|
T | C | 1 | a0001c0002t0001g0307 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2125+1149T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160742566 | ||||||
chr6:160742742
|
G | A | 12 | a0001c0008t0001g0224a0001c0008t0001g0237a0001c0008t0001g0300others(9): Show | 13 | HG02559.hp2 HG02572.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.2125+1325G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160742742 | ||||||
chr6:160742745
|
A | G | 231 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(228): Show | 250 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.2125+1328A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160742745 | ||||||
chr6:160742924
|
T | C | 4 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0001g0264others(1): Show | 4 | HG00408.hp2 HG00609.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.2125+1507T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160742924 | ||||||
chr6:160742957
|
T | C | 1 | a0001c0005t0010g0026 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2125+1540T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160742957 | ||||||
chr6:160742979
|
G | A | 1 | a0002c0004t0011g0306 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2125+1562G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160742979 | ||||||
chr6:160743011
|
CT | C | 61 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0003t0001g0011others(58): Show | 65 | HG00558.hp2 HG00639.hp2 HG00741.hp1 others(62): Show |
intron_variant | MODIFIER | c.2125+1613delT | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160743011 | |||||
chr6:160743011
|
CTT | C | 33 | a0001c0002t0001g0161a0001c0002t0001g0320a0001c0005t0011g0115others(30): Show | 36 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.2125+1612_2125+161 others(6): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160743011 | |||||
chr6:160743011
|
CTTT | C | 62 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0175others(59): Show | 67 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.2125+1611_2125+161 others(7): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160743011 | |||||
chr6:160743011
|
CTTTT | C | 167 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0013others(164): Show | 181 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.2125+1610_2125+161 others(8): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160743011 | |||||
chr6:160743068
|
G | C | 1 | a0001c0005t0010g0308 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2125+1651G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160743068 | ||||||
chr6:160743155
|
A | C | 12 | a0001c0001t0007g0298a0001c0021t0004g0012a0001c0028t0004g0233others(9): Show | 13 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2125+1738A>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160743155 | ||||||
chr6:160743158
|
T | C | 1 | a0001c0001t0001g0214 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2125+1741T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160743158 | ||||||
chr6:160743258
|
C | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0028 | 4 | HG01255.hp1 HG01256.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.2125+1841C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160743258 | ||||||
chr6:160743317
|
G | A | 1 | a0001c0021t0004g0012 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2125+1900G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160743317 | ||||||
chr6:160743587
|
G | C | 1 | a0001c0006t0014g0037 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2125+2170G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160743587 | ||||||
chr6:160743637
|
T | C | 2 | a0001c0005t0011g0115a0002c0004t0011g0306 | 2 | HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2125+2220T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160743637 | ||||||
chr6:160743643
|
C | T | 1 | a0001c0001t0018g0262 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2125+2226C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160743643 | ||||||
chr6:160743655
|
T | G | 1 | a0001c0002t0001g0162 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2125+2238T>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160743655 | ||||||
chr6:160743692
|
C | T | 4 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0071others(1): Show | 4 | HG01123.hp1 HG01192.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2125+2275C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160743692 | ||||||
chr6:160743768
|
C | G | 6 | a0001c0001t0001g0179a0001c0001t0001g0213a0001c0001t0001g0214others(3): Show | 6 | HG01167.hp2 HG02040.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.2125+2351C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160743768 | ||||||
chr6:160743780
|
G | A | 1 | a0001c0005t0011g0115 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2125+2363G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160743780 | ||||||
chr6:160743792
|
G | A | 1 | a0001c0021t0004g0012 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2125+2375G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160743792 | ||||||
chr6:160743945
|
AT | A | 3 | a0005c0010t0004g0017a0005c0010t0004g0241a0005c0010t0004g0242 | 4 | HG02280.hp2 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2125+2529delT | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160743945 | ||||||
chr6:160744029
|
G | A | 11 | a0001c0001t0007g0298a0001c0028t0004g0233a0002c0007t0007g0038others(8): Show | 11 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.2125+2612G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160744029 | ||||||
chr6:160744120
|
T | C | 1 | a0001c0011t0001g0236 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2125+2703T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160744120 | ||||||
chr6:160744267
|
C | A | 1 | a0002c0007t0023g0050 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2125+2850C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160744267 | ||||||
chr6:160744293
|
C | T | 10 | a0001c0001t0007g0298a0002c0007t0007g0038a0002c0007t0007g0039others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2125+2876C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160744293 | ||||||
chr6:160744399
|
T | C | 10 | a0001c0001t0007g0298a0002c0007t0007g0038a0002c0007t0007g0039others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2125+2982T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160744399 | ||||||
chr6:160744517
|
A | G | 4 | a0001c0006t0014g0037a0005c0010t0004g0017a0005c0010t0004g0241others(1): Show | 5 | HG01891.hp2 HG02280.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2125+3100A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160744517 | ||||||
chr6:160744612
|
A | C | 12 | a0001c0001t0007g0298a0001c0021t0004g0012a0001c0028t0004g0233others(9): Show | 13 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2125+3195A>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160744612 | ||||||
chr6:160745136
|
GGAAA | G | 4 | a0001c0001t0001g0013a0001c0001t0001g0181a0001c0001t0001g0182others(1): Show | 5 | HG01192.hp2 NA18969.hp1 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.2125+3722_2125+372 others(8): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160745136 | |||||
chr6:160745162
|
C | T | 1 | a0001c0001t0001g0055 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2125+3745C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160745162 | ||||||
chr6:160745222
|
C | T | 1 | a0001c0001t0006g0190 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2125+3805C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160745222 | ||||||
chr6:160745281
|
C | T | 1 | a0001c0003t0001g0057 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2125+3864C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160745281 | ||||||
chr6:160745382
|
A | ACCCTTTA others(1): Show |
28 | a0002c0004t0003g0019a0002c0004t0003g0020a0002c0004t0003g0023others(25): Show | 31 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.2125+3967_2125+397 others(12): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160745382 | |||||
chr6:160745392
|
A | G | 28 | a0002c0004t0003g0019a0002c0004t0003g0020a0002c0004t0003g0023others(25): Show | 31 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.2125+3975A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160745392 | ||||||
chr6:160745427
|
T | C | 1 | a0001c0005t0002g0345 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2125+4010T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160745427 | ||||||
chr6:160745468
|
C | T | 3 | a0001c0009t0004g0046a0004c0020t0004g0336a0004c0020t0004g0342 | 3 | HG01256.hp1 HG01258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2125+4051C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160745468 | ||||||
chr6:160745470
|
C | T | 149 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(146): Show | 163 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.2125+4053C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160745470 | ||||||
chr6:160745523
|
A | G | 10 | a0001c0001t0007g0298a0002c0007t0007g0038a0002c0007t0007g0039others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2125+4106A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160745523 | ||||||
chr6:160745534
|
A | G | 1 | a0002c0007t0023g0050 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2125+4117A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160745534 | ||||||
chr6:160745578
|
C | A | 7 | a0001c0001t0001g0185a0001c0002t0001g0052a0001c0002t0001g0164others(4): Show | 7 | HG00597.hp1 HG00609.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.2125+4161C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160745578 | ||||||
chr6:160745761
|
G | T | 3 | a0005c0010t0004g0017a0005c0010t0004g0241a0005c0010t0004g0242 | 4 | HG02280.hp2 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2125+4344G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160745761 | ||||||
chr6:160745983
|
G | T | 1 | a0001c0021t0004g0012 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2125+4566G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160745983 | ||||||
chr6:160746108
|
G | C | 1 | a0001c0002t0001g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2125+4691G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160746108 | ||||||
chr6:160746112
|
G | A | 1 | a0002c0007t0023g0050 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2125+4695G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160746112 | ||||||
chr6:160746184
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2125+4767T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160746184 | ||||||
chr6:160746198
|
A | T | 1 | a0001c0028t0004g0233 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2125+4781A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160746198 | ||||||
chr6:160746387
|
T | C | 1 | a0002c0004t0003g0271 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2125+4970T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160746387 | ||||||
chr6:160746420
|
A | G | 154 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(151): Show | 168 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.2125+5003A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160746420 | ||||||
chr6:160746624
|
C | G | 11 | a0001c0001t0007g0298a0001c0028t0004g0233a0002c0007t0007g0038others(8): Show | 11 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.2125+5207C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160746624 | ||||||
chr6:160746963
|
T | C | 1 | a0001c0003t0001g0134 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2126-5152T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160746963 | ||||||
chr6:160746983
|
G | A | 10 | a0001c0001t0007g0298a0002c0007t0007g0038a0002c0007t0007g0039others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2126-5132G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160746983 | ||||||
chr6:160747278
|
C | T | 11 | a0001c0001t0007g0298a0001c0028t0004g0233a0002c0007t0007g0038others(8): Show | 11 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.2126-4837C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160747278 | ||||||
chr6:160747365
|
A | T | 43 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0003t0001g0011others(40): Show | 45 | HG00558.hp2 HG00639.hp2 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.2126-4750A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160747365 | ||||||
chr6:160747420
|
G | C | 11 | a0001c0001t0007g0298a0001c0028t0004g0233a0002c0007t0007g0038others(8): Show | 11 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.2126-4695G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160747420 | ||||||
chr6:160747441
|
G | A | 1 | a0001c0001t0020g0299 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2126-4674G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160747441 | ||||||
chr6:160747446
|
C | A | 1 | a0001c0009t0004g0067 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2126-4669C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160747446 | ||||||
chr6:160747485
|
G | A | 11 | a0001c0001t0007g0298a0001c0028t0004g0233a0002c0007t0007g0038others(8): Show | 11 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.2126-4630G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160747485 | ||||||
chr6:160747516
|
G | A | 262 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(259): Show | 282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.2126-4599G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160747516 | ||||||
chr6:160747571
|
A | C | 2 | a0001c0006t0005g0347a0001c0006t0005g0352 | 2 | HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2126-4544A>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160747571 | ||||||
chr6:160747621
|
G | GTTTT | 323 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(320): Show | 349 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(346): Show |
intron_variant | MODIFIER | c.2126-4491_2126-449 others(8): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160747621 | |||||
chr6:160747662
|
G | A | 1 | a0005c0010t0004g0241 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2126-4453G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160747662 | ||||||
chr6:160747675
|
G | GATTTCAA others(32): Show |
1 | a0001c0002t0001g0202 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2126-4435_2126-439 others(43): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160747675 | |||||
chr6:160747727
|
T | C | 323 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(320): Show | 349 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(346): Show |
intron_variant | MODIFIER | c.2126-4388T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160747727 | ||||||
chr6:160747778
|
T | C | 2 | a0001c0006t0005g0347a0001c0006t0005g0352 | 2 | HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2126-4337T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160747778 | ||||||
chr6:160747894
|
A | G | 1 | a0001c0001t0001g0196 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2126-4221A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160747894 | ||||||
chr6:160747917
|
G | T | 29 | a0001c0028t0004g0233a0002c0004t0003g0019a0002c0004t0003g0020others(26): Show | 32 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.2126-4198G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160747917 | ||||||
chr6:160747929
|
G | T | 262 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(259): Show | 282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.2126-4186G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160747929 | ||||||
chr6:160747938
|
A | G | 12 | a0001c0008t0001g0224a0001c0008t0001g0237a0001c0008t0001g0300others(9): Show | 13 | HG02559.hp2 HG02572.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.2126-4177A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160747938 | ||||||
chr6:160748064
|
T | A | 12 | a0001c0001t0007g0298a0001c0021t0004g0012a0001c0028t0004g0233others(9): Show | 13 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2126-4051T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748064 | ||||||
chr6:160748076
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2126-4039G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748076 | ||||||
chr6:160748108
|
G | C | 12 | a0001c0001t0007g0298a0001c0021t0004g0012a0001c0028t0004g0233others(9): Show | 13 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2126-4007G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748108 | ||||||
chr6:160748162
|
G | A | 1 | a0001c0001t0001g0182 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2126-3953G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748162 | ||||||
chr6:160748237
|
G | A | 2 | a0001c0005t0010g0026a0001c0005t0010g0308 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2126-3878G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748237 | ||||||
chr6:160748313
|
AGAAAGAA others(1): Show |
A | 11 | a0001c0001t0007g0298a0001c0021t0004g0012a0001c0028t0004g0233others(8): Show | 13 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2126-3782_2126-377 others(12): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748313 | |||||
chr6:160748332
|
A | AG | 3 | a0002c0007t0007g0040a0002c0007t0007g0045a0005c0010t0004g0241 | 3 | HG02615.hp2 HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2126-3783_2126-378 others(5): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748332 | ||||||
chr6:160748334
|
G | A | 3 | a0002c0007t0007g0040a0002c0007t0007g0045a0005c0010t0004g0241 | 3 | HG02615.hp2 HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2126-3781G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748334 | ||||||
chr6:160748338
|
G | A | 3 | a0002c0007t0007g0040a0002c0007t0007g0045a0005c0010t0004g0241 | 3 | HG02615.hp2 HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2126-3777G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748338 | ||||||
chr6:160748348
|
A | AAGAGAAA others(35): Show |
1 | a0001c0002t0001g0339 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2126-3734_2126-373 others(46): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748348 | |||||
chr6:160748348
|
A | AAGAGAAA others(37): Show |
1 | a0001c0002t0001g0113 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2126-3734_2126-373 others(48): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748348 | |||||
chr6:160748348
|
A | AAGAGAAA others(25): Show |
1 | a0001c0001t0001g0219 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(36): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748348 | |||||
chr6:160748348
|
A | AAGAGAAA others(29): Show |
24 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0022others(21): Show | 30 | HG00423.hp1 HG00609.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(40): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748348 | |||||
chr6:160748348
|
A | AAGAGAAA others(31): Show |
1 | a0001c0002t0001g0265 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(42): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748348 | |||||
chr6:160748348
|
A | AAGAGAAA others(33): Show |
12 | a0001c0001t0001g0272a0001c0002t0001g0060a0001c0002t0001g0085others(9): Show | 14 | HG01081.hp1 HG01099.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(44): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748348 | |||||
chr6:160748348
|
A | AAGAGAAA others(35): Show |
1 | a0001c0003t0001g0337 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(46): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748348 | |||||
chr6:160748348
|
A | AAGAGAAA others(30): Show |
1 | a0001c0002t0001g0199 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2126-3741_2126-374 others(41): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748348 | |||||
chr6:160748348
|
A | AAGAGAAA others(25): Show |
1 | a0001c0002t0001g0129 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2126-3742_2126-374 others(36): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748348 | |||||
chr6:160748348
|
A | AAGAGAAA others(29): Show |
2 | a0001c0001t0001g0071a0001c0011t0001g0232 | 2 | HG01517.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.2126-3742_2126-374 others(40): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748348 | |||||
chr6:160748348
|
A | AAGAGAAA others(27): Show |
2 | a0001c0008t0001g0300a0001c0008t0001g0314 | 2 | HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2126-3746_2126-374 others(38): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748348 | |||||
chr6:160748348
|
A | G | 1 | a0002c0007t0007g0039 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2126-3767A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748348 | ||||||
chr6:160748350
|
G | A | 1 | a0002c0007t0007g0039 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2126-3765G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748350 | ||||||
chr6:160748350
|
G | GAA | 3 | a0002c0007t0007g0040a0002c0007t0007g0045a0005c0010t0004g0241 | 3 | HG02615.hp2 HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2126-3764_2126-376 others(6): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAA | 13 | a0001c0005t0002g0249a0001c0005t0002g0305a0001c0005t0005g0240others(10): Show | 14 | HG00323.hp1 HG01361.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.2126-3718_2126-371 others(8): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(1): Show |
7 | a0001c0005t0002g0304a0001c0006t0002g0043a0001c0006t0004g0048others(4): Show | 7 | HG00642.hp2 HG02148.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2126-3722_2126-371 others(12): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(5): Show |
2 | a0001c0005t0002g0107a0001c0005t0002g0270 | 2 | HG00280.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.2126-3726_2126-371 others(16): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(9): Show |
3 | a0001c0005t0010g0308a0001c0009t0002g0058a0001c0009t0012g0070 | 3 | HG01346.hp1 HG01978.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2126-3730_2126-371 others(20): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(45): Show |
1 | a0001c0001t0001g0072 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2126-3730_2126-372 others(56): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(37): Show |
1 | a0001c0001t0001g0061 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2126-3734_2126-373 others(48): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(41): Show |
1 | a0001c0001t0001g0062 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2126-3734_2126-373 others(52): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(47): Show |
1 | a0001c0002t0001g0139 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2126-3734_2126-373 others(58): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(45): Show |
1 | a0001c0002t0001g0140 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2126-3734_2126-373 others(56): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(45): Show |
1 | a0001c0002t0001g0082 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2126-3734_2126-373 others(56): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(33): Show |
1 | a0001c0001t0020g0299 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(44): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(33): Show |
38 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0041others(35): Show | 42 | HG00408.hp1 HG00558.hp1 HG01099.hp2 others(39): Show |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(44): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(37): Show |
18 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0169others(15): Show | 20 | HG00140.hp2 HG00597.hp1 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(48): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(41): Show |
3 | a0001c0001t0001g0213a0001c0001t0006g0329a0001c0002t0001g0136 | 3 | HG01123.hp2 NA18612.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(52): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(45): Show |
5 | a0001c0001t0001g0027a0001c0001t0001g0216a0001c0001t0006g0189others(2): Show | 5 | HG02148.hp2 NA19000.hp1 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(56): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(45): Show |
1 | a0001c0001t0001g0260 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(56): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(40): Show |
1 | a0003c0012t0021g0315 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(51): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(44): Show |
1 | a0001c0001t0001g0179 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(55): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(48): Show |
1 | a0003c0012t0009g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(59): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(35): Show |
2 | a0001c0002t0001g0127a0001c0002t0001g0131 | 2 | HG01255.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(46): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(39): Show |
3 | a0001c0002t0001g0126a0001c0002t0001g0141a0001c0002t0001g0257 | 3 | HG02293.hp1 NA18944.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(50): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(47): Show |
1 | a0001c0002t0001g0123 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(58): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(38): Show |
1 | a0001c0001t0001g0340 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(49): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(36): Show |
1 | a0001c0003t0001g0198 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(47): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(37): Show |
10 | a0001c0002t0001g0015a0001c0002t0001g0088a0001c0002t0001g0138others(7): Show | 11 | HG01952.hp1 HG02080.hp2 HG04115.hp2 others(8): Show |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(48): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(41): Show |
10 | a0001c0002t0001g0087a0001c0002t0001g0090a0001c0002t0001g0121others(7): Show | 10 | HG01069.hp1 HG01891.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(52): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(45): Show |
9 | a0001c0002t0001g0021a0001c0002t0001g0086a0001c0002t0001g0122others(6): Show | 10 | HG00558.hp2 HG02040.hp1 NA18945.hp2 others(7): Show |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(56): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(49): Show |
5 | a0001c0002t0001g0051a0001c0002t0001g0116a0001c0003t0001g0089others(2): Show | 5 | HG02300.hp2 HG03704.hp2 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(60): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(53): Show |
2 | a0001c0002t0001g0161a0001c0003t0001g0150 | 2 | NA18612.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(64): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(38): Show |
1 | a0001c0002t0001g0320 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(49): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(43): Show |
1 | a0001c0002t0001g0084 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(54): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(47): Show |
1 | a0001c0002t0001g0137 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(58): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(41): Show |
1 | a0001c0002t0001g0155 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(52): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(45): Show |
1 | a0001c0003t0001g0206 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(56): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(38): Show |
2 | a0001c0001t0001g0183a0002c0007t0001g0282 | 2 | HG01192.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.2126-3741_2126-374 others(49): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(40): Show |
1 | a0001c0002t0001g0128 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2126-3741_2126-374 others(51): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(39): Show |
1 | a0001c0002t0001g0311 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2126-3741_2126-374 others(50): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(33): Show |
1 | a0001c0001t0001g0095 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2126-3742_2126-374 others(44): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(37): Show |
1 | a0001c0002t0001g0165 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2126-3742_2126-374 others(48): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(35): Show |
1 | a0001c0003t0001g0130 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2126-3742_2126-374 others(46): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(33): Show |
3 | a0001c0008t0001g0224a0001c0011t0001g0230a0001c0011t0001g0231 | 3 | HG02559.hp2 NA18940.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.2126-3742_2126-374 others(44): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(37): Show |
2 | a0001c0002t0001g0201a0001c0008t0001g0349 | 2 | HG03130.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.2126-3742_2126-374 others(48): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(41): Show |
2 | a0001c0002t0001g0081a0001c0002t0001g0200 | 2 | NA18991.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.2126-3742_2126-374 others(52): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(36): Show |
1 | a0001c0003t0001g0321 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2126-3742_2126-374 others(47): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(41): Show |
1 | a0006c0014t0001g0318 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2126-3742_2126-374 others(52): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(31): Show |
1 | a0001c0024t0009g0246 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2126-3746_2126-374 others(42): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(28): Show |
1 | a0001c0008t0001g0302 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2126-3746_2126-374 others(39): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(29): Show |
1 | a0001c0013t0001g0024 | 2 | HG02886.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2126-3746_2126-374 others(40): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(33): Show |
1 | a0001c0013t0001g0351 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2126-3746_2126-374 others(44): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(39): Show |
1 | a0001c0008t0001g0301 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2126-3746_2126-374 others(50): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(33): Show |
1 | a0002c0007t0023g0050 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2126-3746_2126-374 others(44): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(30): Show |
1 | a0001c0008t0001g0355 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2126-3749_2126-374 others(41): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748350
|
G | GAGAAAGA others(32): Show |
1 | a0001c0008t0001g0237 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2126-3749_2126-374 others(43): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | |||||
chr6:160748354
|
A | AAGAAAGA others(31): Show |
1 | a0001c0002t0001g0073 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2126-3734_2126-373 others(42): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748354 | |||||
chr6:160748354
|
A | AAGAAAGA others(23): Show |
1 | a0001c0001t0001g0103 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(34): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748354 | |||||
chr6:160748354
|
A | AAGAAAGA others(25): Show |
22 | a0001c0001t0001g0029a0001c0001t0001g0054a0001c0001t0001g0055others(19): Show | 22 | HG00733.hp1 HG02071.hp1 HG02132.hp1 others(19): Show |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(36): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748354 | |||||
chr6:160748354
|
A | AAGAAAGA others(27): Show |
1 | a0001c0002t0001g0007 | 2 | HG03831.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(38): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748354 | |||||
chr6:160748354
|
A | AAGAAAGA others(29): Show |
7 | a0001c0001t0001g0247a0001c0001t0001g0273a0001c0002t0001g0144others(4): Show | 7 | HG00544.hp1 HG00639.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(40): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748354 | |||||
chr6:160748354
|
A | AAGAAAGA others(33): Show |
1 | a0001c0002t0001g0147 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(44): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748354 | |||||
chr6:160748354
|
A | AAGAAAGA others(26): Show |
1 | a0009c0019t0001g0317 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2126-3741_2126-374 others(37): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748354 | |||||
chr6:160748354
|
A | AAGAAAGA others(21): Show |
1 | a0001c0001t0001g0258 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.2126-3742_2126-374 others(32): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748354 | |||||
chr6:160748354
|
A | AAGAAAGA others(23): Show |
1 | a0001c0013t0009g0035 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2126-3742_2126-374 others(34): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748354 | |||||
chr6:160748357
|
A | AAAGAAAG others(26): Show |
1 | a0001c0002t0009g0245 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(37): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748357 | |||||
chr6:160748358
|
A | AAGAAAGA others(17): Show |
1 | a0001c0001t0001g0218 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(28): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748358 | |||||
chr6:160748358
|
A | AAGAAAGA others(21): Show |
8 | a0001c0001t0001g0056a0001c0001t0001g0066a0001c0001t0001g0264others(5): Show | 8 | HG00408.hp2 HG02451.hp2 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(32): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748358 | |||||
chr6:160748358
|
A | AAGAAAGA others(23): Show |
1 | a0001c0001t0017g0194 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(34): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748358 | |||||
chr6:160748358
|
A | AAGAAAGA others(25): Show |
3 | a0001c0002t0001g0083a0001c0003t0001g0154a0001c0003t0001g0205 | 3 | HG01243.hp2 NA18954.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(36): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748358 | |||||
chr6:160748358
|
A | AAGAAAGA others(22): Show |
1 | a0001c0001t0001g0180 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2126-3741_2126-374 others(33): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748358 | |||||
chr6:160748358
|
A | AAGAAAGA others(25): Show |
1 | a0006c0014t0001g0148 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2126-3742_2126-374 others(36): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748358 | |||||
chr6:160748361
|
A | AAAGAAAG others(23): Show |
1 | a0001c0003t0001g0134 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2126-3741_2126-374 others(34): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748361 | |||||
chr6:160748362
|
A | AAGAAAGA others(15): Show |
1 | a0001c0001t0001g0293 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(26): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748362 | |||||
chr6:160748362
|
A | AAGAAAGA others(17): Show |
2 | a0001c0001t0001g0312a0012c0023t0001g0100 | 2 | NA18966.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(28): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748362 | |||||
chr6:160748362
|
A | AAGAAAGA others(21): Show |
1 | a0001c0002t0001g0145 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(32): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748362 | |||||
chr6:160748365
|
A | AAAGAAAG others(20): Show |
1 | a0006c0014t0001g0146 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(31): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748365 | |||||
chr6:160748366
|
A | AAGAAAGA others(13): Show |
3 | a0001c0001t0001g0171a0001c0001t0001g0174a0001c0001t0001g0214 | 3 | HG00544.hp2 HG02293.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(24): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748366 | |||||
chr6:160748366
|
A | AAGAAAGA others(17): Show |
2 | a0001c0002t0001g0135a0001c0011t0001g0236 | 2 | HG02015.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(28): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748366 | |||||
chr6:160748370
|
A | AAGAAAGA others(9): Show |
1 | a0001c0001t0001g0173 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(20): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748370 | |||||
chr6:160748370
|
A | AAGAAAGA others(35): Show |
1 | a0001c0002t0001g0003 | 3 | HG00735.hp2 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(46): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748370 | |||||
chr6:160748374
|
A | AAGAAAGA others(13): Show |
1 | a0001c0002t0001g0202 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2126-3734_2126-373 others(24): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748374 | |||||
chr6:160748378
|
A | G | 1 | a0001c0001t0001g0063 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2126-3737A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748378 | ||||||
chr6:160748381
|
AAAGAAAG others(13): Show |
A | 1 | a0001c0009t0004g0067 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2126-3718_2126-369 others(24): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748381 | |||||
chr6:160748382
|
A | G | 1 | a0001c0001t0001g0063 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2126-3733A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748382 | ||||||
chr6:160748385
|
AAAGAAAG others(9): Show |
A | 3 | a0001c0005t0002g0110a0001c0006t0005g0348a0001c0029t0015g0032 | 3 | HG03098.hp2 HG03486.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.2126-3713_2126-369 others(20): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748385 | |||||
chr6:160748389
|
AAAGAAAG others(5): Show |
A | 6 | a0002c0004t0003g0020a0002c0004t0003g0023a0002c0004t0003g0281others(3): Show | 8 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.2126-3714_2126-370 others(16): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748389 | |||||
chr6:160748393
|
AAAGAAAG others(1): Show |
A | 13 | a0001c0005t0002g0250a0001c0005t0002g0345a0001c0006t0002g0114others(10): Show | 13 | HG00323.hp2 HG00642.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.2126-3714_2126-370 others(12): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748393 | |||||
chr6:160748397
|
AAAGG | A | 14 | a0001c0005t0002g0252a0001c0006t0002g0044a0001c0006t0005g0346others(11): Show | 15 | HG01070.hp2 HG01074.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.2126-3714_2126-371 others(8): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748397 | |||||
chr6:160748401
|
G | A | 314 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(311): Show | 336 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(333): Show |
intron_variant | MODIFIER | c.2126-3714G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748401 | ||||||
chr6:160748401
|
GAAGAAAG others(3): Show |
G | 1 | a0002c0007t0007g0096 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2126-3713_2126-370 others(14): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748401 | ||||||
chr6:160748403
|
AGAAAGAA others(6): Show |
A | 1 | a0001c0021t0004g0012 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2126-3710_2126-369 others(17): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748403 | |||||
chr6:160748404
|
G | GAA | 10 | a0001c0001t0001g0027a0001c0001t0018g0262a0001c0002t0001g0136others(7): Show | 10 | HG01123.hp2 HG01346.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.2126-3709_2126-370 others(6): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748404 | |||||
chr6:160748409
|
A | G | 1 | a0002c0004t0003g0286 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2126-3706A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748409 | ||||||
chr6:160748411
|
A | G | 2 | a0002c0007t0007g0038a0002c0007t0007g0292 | 2 | HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2126-3704A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748411 | ||||||
chr6:160748413
|
A | G | 2 | a0001c0001t0007g0298a0002c0007t0007g0042 | 2 | HG01243.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2126-3702A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748413 | ||||||
chr6:160748414
|
A | G | 3 | a0001c0001t0007g0298a0002c0007t0007g0042a0006c0014t0001g0318 | 3 | HG01243.hp1 NA18522.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.2126-3701A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748414 | ||||||
chr6:160748415
|
AGG | A | 5 | a0002c0004t0003g0285a0002c0007t0007g0038a0002c0007t0007g0096others(2): Show | 5 | HG01169.hp1 HG02055.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.2126-3698_2126-369 others(6): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748415 | |||||
chr6:160748416
|
G | A | 140 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(137): Show | 154 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.2126-3699G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748416 | ||||||
chr6:160748416
|
G | GAA | 3 | a0001c0002t0001g0135a0006c0014t0001g0146a0006c0014t0001g0148 | 3 | HG02015.hp1 NA18962.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.2126-3699_2126-369 others(6): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748416 | ||||||
chr6:160748417
|
G | A | 144 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(141): Show | 159 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.2126-3698G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748417 | ||||||
chr6:160748417
|
G | GGAAA | 123 | a0001c0001t0001g0027a0001c0001t0001g0172a0001c0001t0001g0272others(120): Show | 129 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.2126-3691_2126-368 others(8): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748417 | |||||
chr6:160748427
|
A | G | 138 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(135): Show | 152 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.2126-3688A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748427 | ||||||
chr6:160748428
|
G | A | 2 | a0001c0002t0001g0136a0001c0002t0001g0319 | 2 | HG01123.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.2126-3687G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748428 | ||||||
chr6:160748430
|
A | G | 2 | a0001c0002t0001g0136a0001c0002t0001g0319 | 2 | HG01123.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.2126-3685A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748430 | ||||||
chr6:160748431
|
C | A | 143 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(140): Show | 157 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.2126-3684C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748431 | ||||||
chr6:160748435
|
A | C | 2 | a0001c0002t0001g0136a0001c0002t0001g0319 | 2 | HG01123.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.2126-3680A>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748435 | ||||||
chr6:160748439
|
A | AGAGAAC | 140 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(137): Show | 154 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.2126-3674_2126-367 others(10): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748439 | |||||
chr6:160748441
|
A | AAGGG | 26 | a0001c0009t0004g0025a0002c0004t0003g0019a0002c0004t0003g0023others(23): Show | 28 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.2126-3642_2126-363 others(8): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748441 | |||||
chr6:160748441
|
AAGGG | A | 12 | a0001c0005t0002g0111a0001c0006t0005g0016a0001c0006t0005g0098others(9): Show | 13 | HG00738.hp1 HG01106.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.2126-3642_2126-363 others(8): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748441 | |||||
chr6:160748441
|
AAGGGAGG others(1): Show |
A | 120 | a0001c0001t0001g0027a0001c0001t0001g0172a0001c0001t0001g0272others(117): Show | 126 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.2126-3646_2126-363 others(12): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748441 | |||||
chr6:160748441
|
AAGGGAGG others(5): Show |
A | 16 | a0001c0001t0007g0298a0001c0005t0011g0115a0001c0021t0004g0012others(13): Show | 18 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.2126-3650_2126-363 others(16): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748441 | |||||
chr6:160748441
|
AAGGGAGG others(9): Show |
A | 1 | a0001c0005t0002g0110 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2126-3654_2126-363 others(20): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748441 | |||||
chr6:160748443
|
G | A | 142 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(139): Show | 156 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.2126-3672G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748443 | ||||||
chr6:160748443
|
G | C | 1 | a0002c0007t0007g0291 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2126-3672G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748443 | ||||||
chr6:160748445
|
G | A | 143 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(140): Show | 157 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.2126-3670G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748445 | ||||||
chr6:160748447
|
G | A | 141 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(138): Show | 155 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.2126-3668G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748447 | ||||||
chr6:160748449
|
G | A | 141 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(138): Show | 155 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.2126-3666G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748449 | ||||||
chr6:160748451
|
G | A | 2 | a0002c0007t0007g0291a0002c0007t0023g0050 | 2 | HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2126-3664G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748451 | ||||||
chr6:160748453
|
G | A | 2 | a0002c0007t0007g0291a0002c0007t0023g0050 | 2 | HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2126-3662G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748453 | ||||||
chr6:160748707
|
C | T | 274 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(271): Show | 295 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.2126-3408C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748707 | ||||||
chr6:160748783
|
C | T | 274 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(271): Show | 295 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.2126-3332C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748783 | ||||||
chr6:160748795
|
T | C | 12 | a0001c0001t0007g0298a0001c0021t0004g0012a0001c0028t0004g0233others(9): Show | 13 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2126-3320T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748795 | ||||||
chr6:160748803
|
C | T | 1 | a0001c0021t0004g0012 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2126-3312C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748803 | ||||||
chr6:160748891
|
C | T | 1 | a0001c0021t0004g0012 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2126-3224C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748891 | ||||||
chr6:160749093
|
C | T | 3 | a0005c0010t0004g0017a0005c0010t0004g0241a0005c0010t0004g0242 | 4 | HG02280.hp2 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2126-3022C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160749093 | ||||||
chr6:160749205
|
C | T | 3 | a0001c0009t0004g0046a0004c0020t0004g0336a0004c0020t0004g0342 | 3 | HG01256.hp1 HG01258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2126-2910C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160749205 | ||||||
chr6:160749238
|
A | G | 1 | a0001c0002t0001g0163 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2126-2877A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160749238 | ||||||
chr6:160749357
|
C | CCAT | 12 | a0001c0001t0007g0298a0001c0021t0004g0012a0001c0028t0004g0233others(9): Show | 13 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2126-2756_2126-275 others(7): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160749357 | |||||
chr6:160749369
|
C | A | 12 | a0001c0001t0007g0298a0001c0021t0004g0012a0001c0028t0004g0233others(9): Show | 13 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2126-2746C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160749369 | ||||||
chr6:160749396
|
C | T | 12 | a0001c0001t0007g0298a0001c0021t0004g0012a0001c0028t0004g0233others(9): Show | 13 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2126-2719C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160749396 | ||||||
chr6:160749482
|
TCAC | T | 275 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(272): Show | 295 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.2126-2613_2126-261 others(7): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160749482 | |||||
chr6:160749538
|
A | T | 2 | a0001c0005t0011g0115a0002c0004t0011g0306 | 2 | HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2126-2577A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160749538 | ||||||
chr6:160749553
|
A | G | 1 | a0001c0002t0001g0060 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2126-2562A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160749553 | ||||||
chr6:160749571
|
C | T | 10 | a0001c0001t0007g0298a0002c0007t0007g0038a0002c0007t0007g0039others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2126-2544C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160749571 | ||||||
chr6:160749588
|
C | T | 1 | a0001c0003t0001g0134 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2126-2527C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160749588 | ||||||
chr6:160749609
|
T | C | 12 | a0001c0001t0007g0298a0001c0021t0004g0012a0001c0028t0004g0233others(9): Show | 13 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2126-2506T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160749609 | ||||||
chr6:160749626
|
C | T | 2 | a0001c0006t0005g0347a0001c0006t0005g0352 | 2 | HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2126-2489C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160749626 | ||||||
chr6:160749633
|
CACCACCA others(5): Show |
C | 1 | a0001c0003t0001g0266 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2126-2471_2126-246 others(16): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160749633 | |||||
chr6:160749656
|
TCAC | T | 11 | a0001c0005t0005g0240a0001c0006t0005g0016a0001c0006t0005g0098others(8): Show | 12 | HG01884.hp2 HG02622.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.2126-2453_2126-245 others(7): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160749656 | |||||
chr6:160749660
|
CACCATCA others(8): Show |
C | 10 | a0001c0001t0007g0298a0002c0007t0007g0038a0002c0007t0007g0039others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2126-2441_2126-242 others(19): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160749660 | |||||
chr6:160749719
|
C | T | 1 | a0001c0002t0001g0052 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2126-2396C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160749719 | ||||||
chr6:160749776
|
C | A | 2 | a0001c0005t0010g0026a0001c0005t0010g0308 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2126-2339C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160749776 | ||||||
chr6:160749803
|
A | G | 100 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0002t0001g0007others(97): Show | 105 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.2126-2312A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160749803 | ||||||
chr6:160749823
|
A | G | 75 | a0001c0001t0001g0008a0001c0001t0001g0054a0001c0001t0001g0055others(72): Show | 76 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.2126-2292A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160749823 | ||||||
chr6:160749903
|
G | GCCACCAC others(8): Show |
275 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(272): Show | 296 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.2126-2203_2126-220 others(19): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160749903 | |||||
chr6:160749968
|
C | A | 1 | a0001c0028t0004g0233 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2126-2147C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160749968 | ||||||
chr6:160750059
|
T | G | 1 | a0001c0001t0020g0299 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2126-2056T>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160750059 | ||||||
chr6:160750081
|
T | C | 12 | a0001c0001t0007g0298a0001c0021t0004g0012a0001c0028t0004g0233others(9): Show | 13 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2126-2034T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160750081 | ||||||
chr6:160750238
|
C | T | 1 | a0001c0009t0004g0025 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2126-1877C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160750238 | ||||||
chr6:160750268
|
C | A | 1 | a0001c0001t0001g0103 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2126-1847C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160750268 | ||||||
chr6:160750282
|
C | G | 1 | a0001c0015t0001g0350 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2126-1833C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160750282 | ||||||
chr6:160750331
|
T | C | 12 | a0001c0001t0007g0298a0001c0021t0004g0012a0001c0028t0004g0233others(9): Show | 13 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2126-1784T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160750331 | ||||||
chr6:160750497
|
A | G | 1 | a0001c0002t0001g0073 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2126-1618A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160750497 | ||||||
chr6:160750534
|
A | G | 1 | a0001c0006t0014g0037 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2126-1581A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160750534 | ||||||
chr6:160750632
|
C | G | 308 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(305): Show | 333 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(330): Show |
intron_variant | MODIFIER | c.2126-1483C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160750632 | ||||||
chr6:160750650
|
T | A | 29 | a0001c0005t0011g0115a0002c0004t0003g0019a0002c0004t0003g0020others(26): Show | 32 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.2126-1465T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160750650 | ||||||
chr6:160750660
|
T | C | 1 | a0001c0028t0004g0233 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2126-1455T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160750660 | ||||||
chr6:160750754
|
G | A | 10 | a0001c0001t0007g0298a0002c0007t0007g0038a0002c0007t0007g0039others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2126-1361G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160750754 | ||||||
chr6:160750825
|
T | C | 13 | a0001c0005t0002g0106a0001c0005t0002g0109a0001c0005t0002g0110others(10): Show | 13 | HG00738.hp1 HG01070.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.2126-1290T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160750825 | ||||||
chr6:160750887
|
C | T | 263 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(260): Show | 283 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.2126-1228C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160750887 | ||||||
chr6:160750982
|
TCA | T | 15 | a0001c0005t0005g0240a0001c0006t0005g0016a0001c0006t0005g0098others(12): Show | 16 | HG01106.hp1 HG01256.hp1 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2126-1131_2126-113 others(6): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160750982 | |||||
chr6:160750985
|
C | G | 15 | a0001c0005t0005g0240a0001c0006t0005g0016a0001c0006t0005g0098others(12): Show | 16 | HG01106.hp1 HG01256.hp1 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2126-1130C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160750985 | ||||||
chr6:160750987
|
C | A | 15 | a0001c0005t0005g0240a0001c0006t0005g0016a0001c0006t0005g0098others(12): Show | 16 | HG01106.hp1 HG01256.hp1 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2126-1128C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160750987 | ||||||
chr6:160750989
|
C | T | 15 | a0001c0005t0005g0240a0001c0006t0005g0016a0001c0006t0005g0098others(12): Show | 16 | HG01106.hp1 HG01256.hp1 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2126-1126C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160750989 | ||||||
chr6:160751111
|
G | C | 1 | a0001c0028t0004g0233 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2126-1004G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160751111 | ||||||
chr6:160751239
|
C | A | 3 | a0001c0009t0004g0046a0004c0020t0004g0336a0004c0020t0004g0342 | 3 | HG01256.hp1 HG01258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2126-876C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160751239 | ||||||
chr6:160751240
|
A | G | 3 | a0001c0009t0004g0046a0004c0020t0004g0336a0004c0020t0004g0342 | 3 | HG01256.hp1 HG01258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2126-875A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160751240 | ||||||
chr6:160751241
|
A | T | 3 | a0001c0009t0004g0046a0004c0020t0004g0336a0004c0020t0004g0342 | 3 | HG01256.hp1 HG01258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2126-874A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160751241 | ||||||
chr6:160751242
|
A | T | 3 | a0001c0009t0004g0046a0004c0020t0004g0336a0004c0020t0004g0342 | 3 | HG01256.hp1 HG01258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2126-873A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160751242 | ||||||
chr6:160751243
|
G | T | 3 | a0001c0009t0004g0046a0004c0020t0004g0336a0004c0020t0004g0342 | 3 | HG01256.hp1 HG01258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2126-872G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160751243 | ||||||
chr6:160751265
|
A | G | 2 | a0001c0002t0001g0051a0001c0002t0001g0144 | 2 | HG02735.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.2126-850A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160751265 | ||||||
chr6:160751278
|
C | G | 5 | a0001c0001t0001g0041a0001c0001t0001g0056a0001c0001t0001g0076others(2): Show | 5 | HG01934.hp2 HG02559.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2126-837C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160751278 | ||||||
chr6:160751279
|
G | A | 1 | a0002c0022t0003g0267 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2126-836G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160751279 | ||||||
chr6:160751342
|
C | T | 3 | a0001c0001t0001g0065a0001c0001t0001g0191a0001c0002t0001g0166 | 3 | HG03942.hp1 NA18954.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.2126-773C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160751342 | ||||||
chr6:160751385
|
A | G | 1 | a0001c0006t0014g0037 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2126-730A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160751385 | ||||||
chr6:160751403
|
G | A | 1 | a0001c0001t0001g0331 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2126-712G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160751403 | ||||||
chr6:160751526
|
A | T | 3 | a0005c0010t0004g0017a0005c0010t0004g0241a0005c0010t0004g0242 | 4 | HG02280.hp2 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2126-589A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160751526 | ||||||
chr6:160751773
|
T | G | 1 | a0002c0022t0003g0267 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2126-342T>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160751773 | ||||||
chr6:160751910
|
C | G | 273 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(270): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(290): Show |
intron_variant | MODIFIER | c.2126-205C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160751910 | ||||||
chr6:160751961
|
A | T | 1 | a0001c0001t0001g0264 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2126-154A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160751961 | ||||||
chr6:160752040
|
G | A | 3 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0001g0174 | 3 | HG00544.hp2 NA18944.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.2126-75G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160752040 | ||||||
chr6:160752060
|
C | G | 12 | a0001c0008t0001g0224a0001c0008t0001g0237a0001c0008t0001g0300others(9): Show | 13 | HG02559.hp2 HG02572.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.2126-55C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160752060 | ||||||
chr6:160752069
|
T | A | 1 | a0001c0001t0001g0225 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2126-46T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160752069 | ||||||
chr6:160752317
|
C | T | 1 | a0001c0002t0001g0007 | 2 | HG03831.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2271+57C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 18/18 | chr6 | 160752317 | ||||||
chr6:160752578
|
A | G | 273 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(270): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(290): Show |
intron_variant | MODIFIER | c.2271+318A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 18/18 | chr6 | 160752578 | ||||||
chr6:160752696
|
C | G | 4 | a0001c0005t0002g0249a0001c0005t0002g0304a0001c0005t0002g0305others(1): Show | 4 | HG00642.hp2 HG01358.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.2272-204C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 18/18 | chr6 | 160752696 |