geneid | 145482 |
---|---|
ensemblid | ENSG00000140043.12 |
hgncid | 20149 |
symbol | PTGR2 |
name | prostaglandin reductase 2 |
refseq_nuc | NM_001146154.2 |
refseq_prot | NP_001139626.1 |
ensembl_nuc | ENST00000555661.6 |
ensembl_prot | ENSP00000452280.1 |
mane_status | MANE Select |
chr | chr14 |
start | 73851831 |
end | 73885726 |
strand | + |
ver | v1.2 |
region | chr14:73851831-73885726 |
region5000 | chr14:73846831-73890726 |
regionname0 | PTGR2_chr14_73851831_73885726 |
regionname5000 | PTGR2_chr14_73846831_73890726 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 351 | 418 | 93 | 78 | 183 | 18 | 44 | 139 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
a0002 | 0/0 | 351 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
a0003 | 0/0 | 351 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 1056 | 218 | 42 | 33 | 102 | 10 | 31 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
c0002 | 1/1 | 1056 | 200 | 51 | 45 | 81 | 8 | 13 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
c0003 | 0/0 | 1056 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
c0004 | 0/0 | 1056 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1710 | 136 | 41 | 17 | 64 | 6 | 6 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
t0002 | 0/0 | 1710 | 85 | 5 | 9 | 59 | 2 | 10 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
t0003 | 0/0 | 1710 | 71 | 18 | 19 | 17 | 7 | 10 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
t0004 | 0/0 | 1710 | 49 | 15 | 4 | 18 | 1 | 11 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
t0005 | 0/0 | 1710 | 41 | 0 | 22 | 11 | 2 | 6 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
t0006 | 0/0 | 1710 | 9 | 0 | 2 | 7 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
t0007 | 0/0 | 1711 | 8 | 6 | 2 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
t0008 | 0/0 | 1710 | 8 | 0 | 0 | 8 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
t0009 | 0/0 | 1710 | 2 | 2 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
t0010 | 0/0 | 1710 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
t0011 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
t0012 | 0/0 | 1710 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
t0013 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
t0014 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
t0015 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
t0016 | 0/0 | 1710 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
t0017 | 0/0 | 1710 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
t0018 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
t0019 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
t0020 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 9 | 0 | 0 | 8 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0002 | 0/0 | 5 | 0 | 1 | 1 | 0 | 3 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0003 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0015 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0018 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0139 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0265 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1056 | 218 | 42 | 33 | 102 | 10 | 31 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
a0001c0002 | 1/1 | 1056 | 200 | 51 | 45 | 81 | 8 | 13 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
a0002c0003 | 0/0 | 1056 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
a0003c0004 | 0/0 | 1056 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 2765 | 85 | 5 | 9 | 59 | 2 | 10 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
a0001c0001t0003 | 0/0 | 2765 | 71 | 18 | 19 | 17 | 7 | 10 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
a0001c0001t0004 | 0/0 | 2765 | 49 | 15 | 4 | 18 | 1 | 11 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
a0001c0001t0008 | 0/0 | 2765 | 8 | 0 | 0 | 8 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
a0001c0001t0011 | 0/0 | 2765 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
a0001c0001t0012 | 0/0 | 2765 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
a0001c0001t0013 | 0/0 | 2765 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
a0001c0001t0014 | 0/0 | 2765 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
a0001c0001t0015 | 0/0 | 2765 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
a0001c0002t0001 | 1/1 | 2765 | 134 | 40 | 17 | 63 | 6 | 6 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
a0001c0002t0005 | 0/0 | 2765 | 41 | 0 | 22 | 11 | 2 | 6 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
a0001c0002t0006 | 0/0 | 2765 | 9 | 0 | 2 | 7 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
a0001c0002t0007 | 0/0 | 2766 | 8 | 6 | 2 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
a0001c0002t0009 | 0/0 | 2765 | 2 | 2 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
a0001c0002t0010 | 0/0 | 2765 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
a0001c0002t0016 | 0/0 | 2765 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
a0001c0002t0017 | 0/0 | 2765 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
a0001c0002t0018 | 0/0 | 2765 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
a0001c0002t0019 | 0/0 | 2765 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
a0001c0002t0020 | 0/0 | 2765 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
a0002c0003t0001 | 0/0 | 2765 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
a0003c0004t0001 | 0/0 | 2765 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | copy fasta | chr14 | 73846831 | 73890726 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0001 | 0/0 | 9 | 0 | 0 | 8 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0002g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0002 | 0/0 | 5 | 0 | 1 | 1 | 0 | 3 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0003 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0008g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0008g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0008g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0008g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0008g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0008g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0008g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0008g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0011g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0012g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0013g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0014g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0001t0015g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0139 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0265 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0001g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0005g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0005g0015 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0005g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0005g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0005g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0005g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0005g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0005g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0005g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0005g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0005g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0005g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0005g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0005g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0005g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0005g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0005g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0005g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0005g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0005g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0005g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0005g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0005g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0005g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0005g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0005g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0005g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0005g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0005g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0005g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0005g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0005g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0005g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0005g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0005g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0005g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0005g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0006g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0006g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0006g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0006g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0006g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0006g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0006g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0006g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0007g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0007g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0007g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0007g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0007g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0007g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0009g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0009g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0010g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0016g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0017g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0018g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0019g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0001c0002t0020g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0002c0003t0001g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
a0003c0004t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0093 | EUR | GBR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG00099 | hp2 | a0001 | c0001 | t0004 | g0042 | EUR | GBR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0102 | EUR | GBR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0127 | EUR | GBR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG00280 | hp1 | a0001 | c0002 | t0005 | g0201 | EUR | FIN | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0011 | EUR | FIN | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG00323 | hp1 | a0001 | c0002 | t0005 | g0199 | EUR | FIN | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG00323 | hp2 | a0001 | c0002 | t0001 | g0018 | EUR | FIN | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG00408 | hp1 | a0001 | c0001 | t0008 | g0085 | EAS | CHS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG00408 | hp2 | a0001 | c0001 | t0004 | g0050 | EAS | CHS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0237 | EAS | CHS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0357 | EAS | CHS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0335 | EAS | CHS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG00438 | hp2 | a0001 | c0001 | t0004 | g0062 | EAS | CHS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | CHS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG00544 | hp2 | a0001 | c0001 | t0004 | g0029 | EAS | CHS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0095 | EAS | CHS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG00558 | hp2 | a0001 | c0002 | t0006 | g0007 | EAS | CHS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | CHS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG00597 | hp2 | a0001 | c0002 | t0001 | g0281 | EAS | CHS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG00621 | hp1 | a0001 | c0001 | t0008 | g0088 | EAS | CHS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0179 | EAS | CHS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0098 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG00639 | hp2 | a0001 | c0002 | t0005 | g0183 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0101 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0364 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0266 | EAS | CHS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0343 | EAS | CHS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0363 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG00735 | hp2 | a0001 | c0002 | t0010 | g0142 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0105 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG00738 | hp2 | a0001 | c0001 | t0004 | g0056 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG00741 | hp1 | a0001 | c0002 | t0005 | g0195 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG00741 | hp2 | a0001 | c0001 | t0004 | g0058 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0234 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0361 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01070 | hp1 | a0001 | c0002 | t0001 | g0171 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01070 | hp2 | a0001 | c0002 | t0005 | g0187 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01071 | hp1 | a0001 | c0002 | t0005 | g0014 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0235 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01074 | hp1 | a0001 | c0001 | t0004 | g0033 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0147 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0278 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0162 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01099 | hp1 | a0001 | c0002 | t0005 | g0207 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0148 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0144 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01106 | hp2 | a0001 | c0002 | t0005 | g0190 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0081 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01109 | hp2 | a0001 | c0002 | t0007 | g0178 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0317 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01167 | hp2 | a0001 | c0002 | t0005 | g0200 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0347 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01168 | hp2 | a0001 | c0002 | t0005 | g0016 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01169 | hp1 | a0001 | c0002 | t0005 | g0206 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0151 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01175 | hp2 | a0001 | c0001 | t0004 | g0057 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0236 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0172 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01243 | hp1 | a0001 | c0002 | t0016 | g0372 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01243 | hp2 | a0001 | c0001 | t0012 | g0369 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | CLM | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0135 | AMR | CLM | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01256 | hp1 | a0001 | c0002 | t0005 | g0188 | AMR | CLM | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01256 | hp2 | a0001 | c0002 | t0001 | g0257 | AMR | CLM | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01257 | hp1 | a0001 | c0002 | t0005 | g0186 | AMR | CLM | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0244 | AMR | CLM | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0025 | AMR | CLM | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01261 | hp2 | a0001 | c0002 | t0005 | g0204 | AMR | CLM | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0367 | AMR | CLM | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01346 | hp2 | a0001 | c0002 | t0005 | g0211 | AMR | CLM | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01358 | hp1 | a0001 | c0001 | t0003 | g0096 | AMR | CLM | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0366 | AMR | CLM | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0240 | AMR | CLM | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0110 | AMR | CLM | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01496 | hp1 | a0001 | c0002 | t0007 | g0175 | AMR | CLM | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0261 | AMR | CLM | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01515 | hp1 | a0001 | c0002 | t0001 | g0155 | EUR | IBS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01515 | hp2 | a0001 | c0002 | t0001 | g0138 | EUR | IBS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0024 | EUR | IBS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0009 | EUR | IBS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0009 | EUR | IBS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01517 | hp2 | a0001 | c0002 | t0001 | g0140 | EUR | IBS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0075 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01884 | hp2 | a0001 | c0002 | t0001 | g0159 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0229 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01891 | hp2 | a0001 | c0001 | t0004 | g0072 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01928 | hp1 | a0001 | c0002 | t0005 | g0017 | AMR | PEL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01928 | hp2 | a0001 | c0002 | t0006 | g0301 | AMR | PEL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0118 | AMR | PEL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01934 | hp2 | a0001 | c0002 | t0005 | g0185 | AMR | PEL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01943 | hp1 | a0001 | c0002 | t0005 | g0189 | AMR | PEL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01943 | hp2 | a0001 | c0002 | t0006 | g0302 | AMR | PEL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0119 | AMR | PEL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01952 | hp2 | a0001 | c0001 | t0003 | g0120 | AMR | PEL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0107 | AMR | PEL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0116 | AMR | PEL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0126 | AMR | PEL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01978 | hp2 | a0001 | c0002 | t0005 | g0197 | AMR | PEL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01981 | hp1 | a0001 | c0002 | t0005 | g0205 | AMR | PEL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0365 | AMR | PEL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01993 | hp1 | a0001 | c0002 | t0005 | g0184 | AMR | PEL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01993 | hp2 | a0001 | c0002 | t0005 | g0215 | AMR | PEL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0374 | EAS | KHV | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0268 | EAS | KHV | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0259 | EAS | KHV | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02040 | hp2 | a0001 | c0002 | t0005 | g0016 | EAS | KHV | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0356 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0243 | EAS | KHV | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0340 | EAS | KHV | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0368 | EAS | KHV | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02074 | hp2 | a0001 | c0002 | t0001 | g0233 | EAS | KHV | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0250 | EAS | KHV | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0324 | EAS | KHV | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02083 | hp1 | a0001 | c0001 | t0008 | g0086 | EAS | KHV | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0280 | EAS | KHV | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0267 | EAS | KHV | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02129 | hp2 | a0001 | c0002 | t0005 | g0015 | EAS | KHV | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02132 | hp1 | a0001 | c0001 | t0004 | g0048 | EAS | KHV | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | KHV | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0342 | EAS | KHV | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02135 | hp2 | a0001 | c0002 | t0001 | g0282 | EAS | KHV | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02145 | hp1 | a0001 | c0002 | t0001 | g0223 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02145 | hp2 | a0001 | c0002 | t0007 | g0006 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02148 | hp1 | a0001 | c0001 | t0003 | g0089 | AMR | PEL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02148 | hp2 | a0001 | c0002 | t0005 | g0014 | AMR | PEL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0165 | EAS | CDX | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02155 | hp2 | a0001 | c0001 | t0004 | g0047 | EAS | CDX | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | CDX | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02165 | hp2 | a0001 | c0002 | t0005 | g0203 | EAS | CDX | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0080 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0109 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0291 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0129 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02280 | hp1 | a0001 | c0002 | t0001 | g0297 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0121 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0112 | AMR | PEL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0108 | AMR | PEL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0113 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02451 | hp2 | a0001 | c0001 | t0004 | g0037 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02523 | hp2 | a0001 | c0002 | t0005 | g0209 | EAS | KHV | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02572 | hp1 | a0001 | c0002 | t0001 | g0146 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02572 | hp2 | a0001 | c0002 | t0001 | g0231 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02602 | hp1 | a0001 | c0001 | t0004 | g0054 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02602 | hp2 | a0001 | c0002 | t0005 | g0193 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02615 | hp1 | a0001 | c0001 | t0004 | g0066 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0070 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02622 | hp1 | a0001 | c0002 | t0001 | g0292 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0227 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0160 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02630 | hp2 | a0001 | c0002 | t0007 | g0006 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02647 | hp1 | a0001 | c0002 | t0001 | g0149 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02647 | hp2 | a0001 | c0002 | t0001 | g0228 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0251 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0263 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02698 | hp2 | a0001 | c0001 | t0004 | g0039 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02717 | hp1 | a0001 | c0002 | t0001 | g0226 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02717 | hp2 | a0001 | c0001 | t0004 | g0071 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02723 | hp1 | a0001 | c0002 | t0007 | g0174 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0079 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02735 | hp1 | a0001 | c0002 | t0005 | g0192 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02735 | hp2 | a0001 | c0001 | t0004 | g0027 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0371 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02738 | hp2 | a0001 | c0002 | t0017 | g0182 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02809 | hp1 | a0001 | c0002 | t0001 | g0298 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02809 | hp2 | a0001 | c0002 | t0018 | g0217 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02818 | hp1 | a0001 | c0002 | t0001 | g0163 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02818 | hp2 | a0001 | c0002 | t0001 | g0168 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0078 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0067 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02895 | hp1 | a0001 | c0002 | t0001 | g0220 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0092 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02897 | hp1 | a0001 | c0002 | t0001 | g0373 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0097 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02922 | hp1 | a0001 | c0002 | t0001 | g0295 | AFR | ESN | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02922 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | ESN | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0296 | AFR | ESN | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02965 | hp2 | a0001 | c0002 | t0020 | g0224 | AFR | ESN | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0077 | AFR | ESN | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02970 | hp2 | a0001 | c0001 | t0004 | g0046 | AFR | ESN | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02976 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | ESN | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02976 | hp2 | a0001 | c0002 | t0007 | g0006 | AFR | ESN | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03017 | hp1 | a0001 | c0002 | t0005 | g0210 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03041 | hp1 | a0001 | c0001 | t0013 | g0370 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03041 | hp2 | a0001 | c0002 | t0009 | g0180 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0305 | AFR | MSL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0150 | AFR | MSL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03130 | hp1 | a0001 | c0002 | t0009 | g0181 | AFR | ESN | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03130 | hp2 | a0001 | c0001 | t0011 | g0134 | AFR | ESN | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0073 | AFR | ESN | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03139 | hp2 | a0003 | c0004 | t0001 | g0164 | AFR | ESN | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | ESN | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0065 | AFR | ESN | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03209 | hp1 | a0001 | c0002 | t0007 | g0177 | AFR | MSL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03209 | hp2 | a0001 | c0001 | t0004 | g0038 | AFR | MSL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0348 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03453 | hp1 | a0001 | c0002 | t0001 | g0294 | AFR | MSL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | MSL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03486 | hp1 | a0001 | c0002 | t0001 | g0219 | AFR | MSL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0359 | AFR | MSL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0355 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0103 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03491 | hp1 | a0001 | c0002 | t0005 | g0191 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0331 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03492 | hp1 | a0001 | c0002 | t0005 | g0015 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0012 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0221 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0161 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03579 | hp1 | a0001 | c0002 | t0001 | g0293 | AFR | MSL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03579 | hp2 | a0001 | c0001 | t0015 | g0132 | AFR | MSL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03669 | hp1 | a0001 | c0001 | t0004 | g0064 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0012 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03688 | hp1 | a0001 | c0001 | t0004 | g0053 | SAS | STU | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0313 | SAS | STU | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0310 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0091 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03831 | hp1 | a0001 | c0001 | t0004 | g0045 | SAS | BEB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03831 | hp2 | a0001 | c0002 | t0001 | g0300 | SAS | BEB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | BEB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0352 | SAS | BEB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0114 | SAS | BEB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03942 | hp1 | a0001 | c0001 | t0004 | g0063 | SAS | BEB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03942 | hp2 | a0001 | c0002 | t0005 | g0212 | SAS | BEB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0351 | SAS | STU | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG04115 | hp2 | a0001 | c0001 | t0004 | g0049 | SAS | STU | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0225 | SAS | BEB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0145 | SAS | BEB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0117 | SAS | STU | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG04199 | hp2 | a0001 | c0001 | t0004 | g0069 | SAS | STU | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG04204 | hp1 | a0001 | c0001 | t0004 | g0061 | SAS | STU | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0353 | SAS | STU | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG04228 | hp1 | a0001 | c0002 | t0001 | g0141 | SAS | STU | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG04228 | hp2 | a0001 | c0001 | t0004 | g0060 | SAS | STU | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18522 | hp1 | a0001 | c0002 | t0001 | g0137 | AFR | YRI | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18522 | hp2 | a0001 | c0002 | t0001 | g0158 | AFR | YRI | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0166 | EAS | CHB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0258 | EAS | CHB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | CHB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0216 | AFR | YRI | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | YRI | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0277 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18940 | hp2 | a0001 | c0001 | t0004 | g0028 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18941 | hp1 | a0001 | c0002 | t0006 | g0284 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0337 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18944 | hp2 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0345 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18948 | hp1 | a0001 | c0001 | t0008 | g0087 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18949 | hp1 | a0001 | c0002 | t0006 | g0299 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18950 | hp1 | a0001 | c0002 | t0005 | g0214 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0341 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0334 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18951 | hp2 | a0001 | c0002 | t0001 | g0262 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18952 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18954 | hp1 | a0001 | c0001 | t0008 | g0082 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0260 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18956 | hp1 | a0001 | c0002 | t0001 | g0247 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0354 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18957 | hp1 | a0001 | c0002 | t0005 | g0202 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18957 | hp2 | a0001 | c0001 | t0008 | g0084 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18961 | hp1 | a0001 | c0002 | t0005 | g0194 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18962 | hp2 | a0001 | c0002 | t0005 | g0198 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18964 | hp1 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0270 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18966 | hp1 | a0001 | c0002 | t0001 | g0375 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0248 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18968 | hp2 | a0001 | c0002 | t0005 | g0213 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18969 | hp2 | a0001 | c0002 | t0001 | g0275 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18971 | hp1 | a0001 | c0001 | t0004 | g0036 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18972 | hp1 | a0001 | c0002 | t0005 | g0196 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18972 | hp2 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0346 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18974 | hp1 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18975 | hp1 | a0001 | c0002 | t0001 | g0274 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0376 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18980 | hp2 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18981 | hp1 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0360 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18982 | hp2 | a0001 | c0002 | t0006 | g0018 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0338 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0246 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0358 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18985 | hp2 | a0001 | c0002 | t0001 | g0289 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18986 | hp1 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18988 | hp1 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18988 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18991 | hp1 | a0001 | c0002 | t0001 | g0288 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0344 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18993 | hp2 | a0001 | c0002 | t0006 | g0007 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18994 | hp1 | a0001 | c0002 | t0005 | g0208 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18995 | hp2 | a0002 | c0003 | t0001 | g0377 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0269 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18999 | hp2 | a0001 | c0001 | t0004 | g0034 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19000 | hp1 | a0001 | c0002 | t0006 | g0290 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0327 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19001 | hp1 | a0001 | c0002 | t0001 | g0271 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19001 | hp2 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19005 | hp1 | a0001 | c0002 | t0001 | g0254 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19009 | hp1 | a0001 | c0001 | t0004 | g0051 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0264 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19012 | hp2 | a0001 | c0002 | t0001 | g0287 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19030 | hp1 | a0001 | c0002 | t0019 | g0157 | AFR | LWK | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19030 | hp2 | a0001 | c0001 | t0014 | g0133 | AFR | LWK | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0055 | AFR | LWK | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19043 | hp2 | a0001 | c0002 | t0001 | g0230 | AFR | LWK | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19054 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19055 | hp1 | a0001 | c0002 | t0006 | g0239 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19055 | hp2 | a0001 | c0001 | t0008 | g0130 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0332 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19058 | hp2 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19060 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0350 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19063 | hp2 | a0001 | c0001 | t0004 | g0068 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19066 | hp1 | a0001 | c0002 | t0001 | g0252 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0349 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19067 | hp1 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19067 | hp2 | a0001 | c0001 | t0004 | g0044 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19072 | hp1 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19072 | hp2 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19074 | hp2 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19077 | hp1 | a0001 | c0001 | t0004 | g0052 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19077 | hp2 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19079 | hp2 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19083 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19083 | hp2 | a0001 | c0002 | t0001 | g0249 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0285 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19086 | hp1 | a0001 | c0002 | t0001 | g0279 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0336 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0339 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19087 | hp2 | a0001 | c0002 | t0001 | g0276 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0286 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19089 | hp1 | a0001 | c0002 | t0001 | g0378 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19090 | hp1 | a0001 | c0001 | t0008 | g0083 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0283 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19240 | hp1 | a0001 | c0002 | t0007 | g0176 | AFR | YRI | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA19240 | hp2 | a0001 | c0002 | t0001 | g0136 | AFR | YRI | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | ASW | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | ASW | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0273 | EUR | TSI | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0156 | EUR | TSI | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0125 | EUR | TSI | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0024 | EUR | TSI | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0143 | AMR | CLM | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG01123 | hp2 | a0001 | c0002 | t0005 | g0017 | AMR | CLM | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02109 | hp1 | a0001 | c0001 | t0004 | g0043 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0306 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0076 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02486 | hp2 | a0001 | c0002 | t0001 | g0218 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02559 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG02559 | hp2 | a0001 | c0001 | t0004 | g0074 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03471 | hp1 | a0001 | c0002 | t0001 | g0238 | AFR | MSL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG03471 | hp2 | a0001 | c0002 | t0001 | g0173 | AFR | MSL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG06807 | hp1 | a0001 | c0002 | t0001 | g0232 | AFR | USA | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
HG06807 | hp2 | a0001 | c0001 | t0004 | g0059 | AFR | USA | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA20300 | hp1 | a0001 | c0002 | t0001 | g0152 | AFR | USA | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0124 | AFR | USA | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA21309 | hp1 | a0001 | c0002 | t0001 | g0222 | AFR | LWK | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0362 | AFR | LWK | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0265 | REF | REF | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0139 | REF | REF | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:73851942
|
G | C | 1 | a0001 | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
splice_region_variant | LOW | c.-49G>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/10 | chr14 | 73851942 | ||||||
chr14:73877114
|
T | A | 1 | a0002 | 1 | NA18995.hp2 | missense_variant | MODERATE | c.465T>A | p.Asn155Lys | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/10 | 625/2765 | 465/1056 | 155/351 | chr14 | 73877114 | ||
chr14:73880122
|
C | T | 1 | a0003 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.797C>T | p.Pro266Leu | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 7/10 | 957/2765 | 797/1056 | 266/351 | chr14 | 73880122 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:73874094
|
A | T | 1 | a0001c0001 | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
synonymous_variant | LOW | c.228A>T | p.Gly76Gly | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/10 | 388/2765 | 228/1056 | 76/351 | chr14 | 73874094 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:73851844
|
C | G | 2 | a0001c0001t0004a0001c0001t0008 | 57 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(54): Show |
5_prime_UTR_variant | MODIFIER | c.-147C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/10 | 7019 | chr14 | 73851844 | |||||
chr14:73851890
|
T | C | 1 | a0001c0002t0010 | 1 | HG00735.hp2 | 5_prime_UTR_variant | MODIFIER | c.-101T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/10 | 6973 | chr14 | 73851890 | |||||
chr14:73851896
|
C | T | 1 | a0001c0002t0020 | 1 | HG02965.hp2 | 5_prime_UTR_variant | MODIFIER | c.-95C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/10 | 6967 | chr14 | 73851896 | |||||
chr14:73851909
|
A | G | 1 | a0001c0002t0019 | 1 | NA19030.hp1 | 5_prime_UTR_variant | MODIFIER | c.-82A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/10 | 6954 | chr14 | 73851909 | |||||
chr14:73851911
|
C | T | 1 | a0001c0002t0018 | 1 | HG02809.hp2 | 5_prime_UTR_variant | MODIFIER | c.-80C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/10 | 6952 | chr14 | 73851911 | |||||
chr14:73884406
|
G | A | 9 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(6): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
3_prime_UTR_variant | MODIFIER | c.*229G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 10/10 | 229 | chr14 | 73884406 | |||||
chr14:73884446
|
G | A | 1 | a0001c0001t0011 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*269G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 10/10 | 269 | chr14 | 73884446 | |||||
chr14:73884566
|
G | A | 1 | a0001c0001t0012 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*389G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 10/10 | 389 | chr14 | 73884566 | |||||
chr14:73884610
|
C | T | 2 | a0001c0002t0005a0001c0002t0017 | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*433C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 10/10 | 433 | chr14 | 73884610 | |||||
chr14:73884785
|
G | A | 1 | a0001c0002t0016 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*608G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 10/10 | 608 | chr14 | 73884785 | |||||
chr14:73884785
|
G | C | 4 | a0001c0001t0003a0001c0001t0011a0001c0001t0012others(1): Show | 74 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*608G>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 10/10 | 608 | chr14 | 73884785 | |||||
chr14:73884843
|
A | AT | 1 | a0001c0002t0007 | 8 | HG01109.hp2 HG01496.hp1 HG02145.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*667dupT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 10/10 | 668 | INFO_REALIGN_3_PRIME | chr14 | 73884843 | ||||
chr14:73884849
|
T | G | 1 | a0001c0001t0014 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*672T>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 10/10 | 672 | chr14 | 73884849 | |||||
chr14:73884861
|
A | G | 3 | a0001c0001t0004a0001c0001t0014a0001c0001t0015 | 51 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*684A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 10/10 | 684 | chr14 | 73884861 | |||||
chr14:73884940
|
G | A | 1 | a0001c0002t0009 | 2 | HG03041.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*763G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 10/10 | 763 | chr14 | 73884940 | |||||
chr14:73885062
|
G | C | 5 | a0001c0001t0002a0001c0001t0004a0001c0001t0008others(2): Show | 144 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*885G>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 10/10 | 885 | chr14 | 73885062 | |||||
chr14:73885088
|
A | G | 6 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(3): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*911A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 10/10 | 911 | chr14 | 73885088 | |||||
chr14:73885126
|
T | C | 1 | a0001c0002t0006 | 9 | HG00558.hp2 HG01928.hp2 HG01943.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*949T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 10/10 | 949 | chr14 | 73885126 | |||||
chr14:73885257
|
C | G | 1 | a0001c0002t0017 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1080C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 10/10 | 1080 | chr14 | 73885257 | |||||
chr14:73885270
|
C | T | 5 | a0001c0001t0002a0001c0001t0004a0001c0001t0008others(2): Show | 144 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*1093C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 10/10 | 1093 | chr14 | 73885270 | |||||
chr14:73885285
|
A | G | 1 | a0001c0001t0014 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1108A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 10/10 | 1108 | chr14 | 73885285 | |||||
chr14:73885398
|
A | C | 4 | a0001c0001t0003a0001c0001t0011a0001c0001t0012others(1): Show | 74 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*1221A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 10/10 | 1221 | chr14 | 73885398 | |||||
chr14:73885611
|
G | T | 9 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(6): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
3_prime_UTR_variant | MODIFIER | c.*1434G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 10/10 | 1434 | chr14 | 73885611 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:73851961
|
G | T | 5 | a0001c0002t0001g0374a0001c0002t0001g0375a0001c0002t0001g0376others(2): Show | 5 | HG02015.hp1 NA18966.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+18G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73851961 | ||||||
chr14:73851970
|
G | A | 117 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(114): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.-48+27G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73851970 | ||||||
chr14:73851982
|
C | T | 2 | a0001c0002t0001g0373a0001c0002t0016g0372 | 2 | HG01243.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-48+39C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73851982 | ||||||
chr14:73851999
|
C | T | 3 | a0001c0001t0011g0134a0001c0001t0014g0133a0001c0001t0015g0132 | 3 | HG03130.hp2 HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-48+56C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73851999 | ||||||
chr14:73852011
|
A | G | 368 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(365): Show | 408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
intron_variant | MODIFIER | c.-48+68A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73852011 | ||||||
chr14:73852051
|
G | T | 191 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(188): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-48+108G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73852051 | ||||||
chr14:73852082
|
G | T | 2 | a0001c0002t0006g0301a0001c0002t0006g0302 | 2 | HG01928.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.-48+139G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73852082 | ||||||
chr14:73852083
|
C | G | 339 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(336): Show | 376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.-48+140C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73852083 | ||||||
chr14:73852129
|
G | GT | 5 | a0001c0001t0002g0371a0001c0001t0003g0131a0001c0001t0008g0130others(2): Show | 5 | HG02738.hp1 HG03831.hp2 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+194dupT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73852129 | |||||
chr14:73852154
|
G | A | 3 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026 | 4 | HG01261.hp1 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+211G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73852154 | ||||||
chr14:73852163
|
G | A | 6 | a0001c0002t0007g0006a0001c0002t0007g0174a0001c0002t0007g0175others(3): Show | 8 | HG01109.hp2 HG01496.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-48+220G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73852163 | ||||||
chr14:73852252
|
T | TTGGACTC others(319): Show |
1 | a0001c0001t0004g0129 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-48+326_-48+327ins others(326): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73852252 | |||||
chr14:73852281
|
G | A | 6 | a0001c0002t0001g0147a0001c0002t0001g0148a0001c0002t0001g0149others(3): Show | 6 | HG01074.hp2 HG01099.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48+338G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73852281 | ||||||
chr14:73852371
|
C | T | 1 | a0001c0002t0001g0298 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-48+428C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73852371 | ||||||
chr14:73852382
|
C | T | 7 | a0001c0002t0001g0291a0001c0002t0001g0292a0001c0002t0001g0293others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-48+439C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73852382 | ||||||
chr14:73852500
|
C | T | 191 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(188): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-48+557C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73852500 | ||||||
chr14:73852539
|
T | C | 192 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(189): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.-48+596T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73852539 | ||||||
chr14:73852616
|
T | G | 2 | a0001c0002t0009g0180a0001c0002t0009g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-48+673T>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73852616 | ||||||
chr14:73852752
|
G | A | 38 | a0001c0002t0005g0014a0001c0002t0005g0015a0001c0002t0005g0016others(35): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.-48+809G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73852752 | ||||||
chr14:73852752
|
G | C | 15 | a0001c0002t0001g0216a0001c0002t0001g0218a0001c0002t0001g0219others(12): Show | 15 | HG01243.hp1 HG02258.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.-48+809G>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73852752 | ||||||
chr14:73852785
|
G | A | 1 | a0001c0002t0001g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-48+842G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73852785 | ||||||
chr14:73852894
|
C | A | 1 | a0001c0001t0002g0303 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-48+951C>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73852894 | ||||||
chr14:73852922
|
T | C | 191 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(188): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-48+979T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73852922 | ||||||
chr14:73853018
|
C | G | 191 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(188): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-48+1075C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73853018 | ||||||
chr14:73853028
|
C | T | 48 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0009others(45): Show | 59 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(56): Show |
intron_variant | MODIFIER | c.-48+1085C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73853028 | ||||||
chr14:73853195
|
A | G | 1 | a0001c0002t0001g0005 | 3 | HG02559.hp1 HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-48+1252A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73853195 | ||||||
chr14:73853201
|
A | AG | 72 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(69): Show | 85 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.-48+1260dupG | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73853201 | |||||
chr14:73853205
|
A | G | 1 | a0001c0001t0002g0368 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-48+1262A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73853205 | ||||||
chr14:73853286
|
G | A | 188 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(185): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.-48+1343G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73853286 | ||||||
chr14:73853348
|
GT | G | 191 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(188): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-48+1408delT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73853348 | |||||
chr14:73853391
|
C | T | 188 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(185): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.-48+1448C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73853391 | ||||||
chr14:73853619
|
G | A | 1 | a0001c0001t0015g0132 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-48+1676G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73853619 | ||||||
chr14:73853677
|
T | G | 1 | a0001c0001t0012g0369 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-48+1734T>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73853677 | ||||||
chr14:73853689
|
G | T | 15 | a0001c0002t0001g0216a0001c0002t0001g0218a0001c0002t0001g0219others(12): Show | 15 | HG01243.hp1 HG02258.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.-48+1746G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73853689 | ||||||
chr14:73853783
|
T | TC | 70 | a0001c0002t0001g0007a0001c0002t0001g0018a0001c0002t0001g0019others(67): Show | 74 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.-48+1842dupC | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73853783 | |||||
chr14:73853845
|
T | A | 1 | a0001c0001t0004g0129 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-48+1902T>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73853845 | ||||||
chr14:73853896
|
C | G | 1 | a0001c0001t0003g0128 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-48+1953C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73853896 | ||||||
chr14:73853908
|
G | A | 49 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0029others(46): Show | 49 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.-48+1965G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73853908 | ||||||
chr14:73853945
|
A | G | 191 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(188): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-48+2002A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73853945 | ||||||
chr14:73854013
|
C | A | 108 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(105): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.-48+2070C>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73854013 | ||||||
chr14:73854013
|
C | G | 1 | a0001c0001t0011g0134 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-48+2070C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73854013 | ||||||
chr14:73854132
|
C | T | 1 | a0001c0002t0001g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-48+2189C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73854132 | ||||||
chr14:73854133
|
G | A | 108 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(105): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.-48+2190G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73854133 | ||||||
chr14:73854135
|
T | C | 38 | a0001c0002t0005g0014a0001c0002t0005g0015a0001c0002t0005g0016others(35): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.-48+2192T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73854135 | ||||||
chr14:73854138
|
T | C | 191 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(188): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-48+2195T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73854138 | ||||||
chr14:73854229
|
A | G | 1 | a0001c0002t0001g0146 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-48+2286A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73854229 | ||||||
chr14:73854535
|
T | A | 1 | a0001c0001t0011g0134 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-48+2592T>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73854535 | ||||||
chr14:73854619
|
G | A | 80 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(77): Show | 93 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.-48+2676G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73854619 | ||||||
chr14:73854633
|
A | G | 1 | a0001c0001t0004g0074 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-48+2690A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73854633 | ||||||
chr14:73855350
|
A | C | 190 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(187): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.-48+3407A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73855350 | ||||||
chr14:73855350
|
A | T | 1 | a0001c0001t0003g0127 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-48+3407A>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73855350 | ||||||
chr14:73855357
|
G | T | 2 | a0001c0001t0003g0004a0001c0001t0003g0081 | 4 | HG01109.hp1 HG03195.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+3414G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73855357 | ||||||
chr14:73855502
|
A | G | 191 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(188): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-47-3314A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73855502 | ||||||
chr14:73855524
|
G | A | 1 | a0001c0002t0001g0233 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-47-3292G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73855524 | ||||||
chr14:73855640
|
T | G | 1 | a0001c0001t0002g0304 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-47-3176T>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73855640 | ||||||
chr14:73855684
|
G | A | 1 | a0001c0001t0011g0134 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-47-3132G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73855684 | ||||||
chr14:73855970
|
C | T | 1 | a0001c0002t0005g0215 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-47-2846C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73855970 | ||||||
chr14:73856013
|
G | A | 190 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(187): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.-47-2803G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73856013 | ||||||
chr14:73856035
|
G | A | 1 | a0001c0002t0007g0174 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-47-2781G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73856035 | ||||||
chr14:73856056
|
A | G | 8 | a0001c0001t0002g0024a0001c0001t0002g0361a0001c0001t0002g0362others(5): Show | 9 | HG00642.hp2 HG00735.hp1 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.-47-2760A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73856056 | ||||||
chr14:73856389
|
G | A | 3 | a0001c0001t0011g0134a0001c0001t0012g0369a0001c0001t0013g0370 | 3 | HG01243.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-47-2427G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73856389 | ||||||
chr14:73856409
|
G | A | 1 | a0001c0002t0001g0223 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-47-2407G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73856409 | ||||||
chr14:73856413
|
A | AT | 108 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(105): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.-47-2394dupT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73856413 | |||||
chr14:73856677
|
G | C | 191 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(188): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-47-2139G>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73856677 | ||||||
chr14:73856679
|
A | G | 191 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(188): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-47-2137A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73856679 | ||||||
chr14:73856770
|
T | G | 191 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(188): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-47-2046T>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73856770 | ||||||
chr14:73856927
|
G | A | 2 | a0001c0001t0008g0082a0001c0001t0008g0083 | 2 | NA18954.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-47-1889G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73856927 | ||||||
chr14:73857039
|
A | T | 2 | a0001c0001t0012g0369a0001c0001t0013g0370 | 2 | HG01243.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-47-1777A>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73857039 | ||||||
chr14:73857092
|
C | T | 1 | a0001c0001t0002g0360 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-47-1724C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73857092 | ||||||
chr14:73857238
|
G | GT | 7 | a0001c0001t0002g0307a0001c0001t0002g0308a0001c0001t0003g0089others(4): Show | 7 | HG02074.hp2 HG02148.hp1 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.-47-1564dupT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73857238 | |||||
chr14:73857238
|
G | GTT | 165 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(162): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.-47-1565_-47-1564d others(4): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73857238 | |||||
chr14:73857238
|
G | GTTT | 21 | a0001c0001t0002g0359a0001c0001t0003g0010a0001c0001t0003g0076others(18): Show | 22 | HG00621.hp1 HG01891.hp2 HG01978.hp1 others(19): Show |
intron_variant | MODIFIER | c.-47-1566_-47-1564d others(5): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73857238 | |||||
chr14:73857281
|
A | G | 1 | a0001c0001t0015g0132 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-47-1535A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73857281 | ||||||
chr14:73857554
|
C | T | 108 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(105): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.-47-1262C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73857554 | ||||||
chr14:73857620
|
CA | C | 206 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(203): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.-47-1186delA | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73857620 | |||||
chr14:73857630
|
A | T | 6 | a0001c0001t0002g0358a0001c0002t0001g0153a0001c0002t0001g0154others(3): Show | 6 | HG01070.hp1 HG01192.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47-1186A>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73857630 | ||||||
chr14:73857664
|
G | GT | 19 | a0001c0002t0001g0013a0001c0002t0001g0143a0001c0002t0001g0144others(16): Show | 20 | HG01106.hp1 HG01109.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.-47-1130dupT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73857664 | |||||
chr14:73857664
|
G | GTGTTTTT others(6): Show |
1 | a0001c0001t0002g0309 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-47-1151_-47-1150i others(15): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73857664 | |||||
chr14:73857664
|
G | GTT | 13 | a0001c0001t0002g0311a0001c0002t0001g0169a0001c0002t0001g0170others(10): Show | 13 | HG02015.hp1 HG02145.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.-47-1131_-47-1130d others(4): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73857664 | |||||
chr14:73857664
|
G | GTTT | 16 | a0001c0002t0001g0218a0001c0002t0001g0219a0001c0002t0001g0220others(13): Show | 16 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47-1132_-47-1130d others(5): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73857664 | |||||
chr14:73857664
|
G | GTTTTTTT others(2): Show |
27 | a0001c0001t0003g0002a0001c0001t0003g0004a0001c0001t0003g0009others(24): Show | 37 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(34): Show |
intron_variant | MODIFIER | c.-47-1138_-47-1130d others(11): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73857664 | |||||
chr14:73857664
|
G | GTTTTTTT others(3): Show |
32 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0001t0002g0361others(29): Show | 36 | HG00099.hp2 HG01069.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.-47-1139_-47-1130d others(12): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73857664 | |||||
chr14:73857664
|
G | GTTTTTTT others(4): Show |
52 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(49): Show | 64 | HG00408.hp1 HG00408.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.-47-1140_-47-1130d others(13): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73857664 | |||||
chr14:73857664
|
G | GTTTTTTT others(5): Show |
38 | a0001c0001t0002g0023a0001c0001t0002g0303a0001c0001t0002g0304others(35): Show | 39 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.-47-1141_-47-1130d others(14): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73857664 | |||||
chr14:73857664
|
G | GTTTTTTT others(6): Show |
15 | a0001c0001t0002g0343a0001c0001t0002g0344a0001c0001t0002g0345others(12): Show | 15 | HG00673.hp2 HG01168.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.-47-1142_-47-1130d others(15): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73857664 | |||||
chr14:73857664
|
G | GTTTTTTT others(7): Show |
4 | a0001c0001t0002g0353a0001c0001t0004g0065a0001c0001t0004g0066others(1): Show | 4 | HG02615.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-1143_-47-1130d others(16): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73857664 | |||||
chr14:73857664
|
G | GTTTTTTT others(8): Show |
5 | a0001c0001t0002g0354a0001c0001t0002g0355a0001c0001t0002g0356others(2): Show | 5 | HG00423.hp2 HG02055.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-1144_-47-1130d others(17): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73857664 | |||||
chr14:73857664
|
GT | G | 46 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0029others(43): Show | 50 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.-47-1130delT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73857664 | |||||
chr14:73857666
|
T | TTTTTTTT others(4): Show |
1 | a0001c0001t0002g0310 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-47-1140_-47-1139i others(13): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73857666 | |||||
chr14:73857700
|
G | A | 80 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(77): Show | 93 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.-47-1116G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73857700 | ||||||
chr14:73857737
|
C | T | 191 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(188): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-47-1079C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73857737 | ||||||
chr14:73857804
|
G | A | 1 | a0001c0002t0017g0182 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-47-1012G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73857804 | ||||||
chr14:73857814
|
T | G | 249 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(246): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.-47-1002T>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73857814 | ||||||
chr14:73857829
|
T | C | 14 | a0001c0002t0001g0216a0001c0002t0001g0218a0001c0002t0001g0219others(11): Show | 14 | HG01243.hp1 HG02258.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.-47-987T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73857829 | ||||||
chr14:73857862
|
G | T | 4 | a0001c0002t0009g0180a0001c0002t0009g0181a0001c0002t0018g0217others(1): Show | 4 | HG02809.hp2 HG02965.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-954G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73857862 | ||||||
chr14:73857933
|
T | C | 1 | a0001c0001t0003g0093 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-47-883T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73857933 | ||||||
chr14:73857959
|
G | A | 108 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(105): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.-47-857G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73857959 | ||||||
chr14:73857960
|
C | T | 108 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(105): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.-47-856C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73857960 | ||||||
chr14:73857968
|
T | C | 191 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(188): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-47-848T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73857968 | ||||||
chr14:73857995
|
A | G | 1 | a0003c0004t0001g0164 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-47-821A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73857995 | ||||||
chr14:73858080
|
T | C | 3 | a0001c0001t0011g0134a0001c0001t0012g0369a0001c0001t0013g0370 | 3 | HG01243.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-47-736T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73858080 | ||||||
chr14:73858104
|
G | A | 70 | a0001c0002t0001g0007a0001c0002t0001g0018a0001c0002t0001g0019others(67): Show | 74 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.-47-712G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73858104 | ||||||
chr14:73858212
|
G | A | 3 | a0001c0001t0011g0134a0001c0001t0012g0369a0001c0001t0013g0370 | 3 | HG01243.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-47-604G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73858212 | ||||||
chr14:73858249
|
A | G | 1 | a0001c0001t0004g0072 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-47-567A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73858249 | ||||||
chr14:73858256
|
A | C | 1 | a0001c0001t0002g0367 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-47-560A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73858256 | ||||||
chr14:73858260
|
C | T | 335 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(332): Show | 372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.-47-556C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73858260 | ||||||
chr14:73858313
|
GA | G | 191 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(188): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-47-501delA | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73858313 | |||||
chr14:73858338
|
G | A | 1 | a0001c0002t0001g0135 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-47-478G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73858338 | ||||||
chr14:73858446
|
G | A | 2 | a0001c0001t0012g0369a0001c0001t0013g0370 | 2 | HG01243.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-47-370G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73858446 | ||||||
chr14:73858548
|
G | A | 108 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(105): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.-47-268G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73858548 | ||||||
chr14:73858550
|
C | A | 2 | a0001c0001t0003g0004a0001c0001t0003g0081 | 4 | HG01109.hp1 HG03195.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-266C>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73858550 | ||||||
chr14:73858743
|
A | G | 1 | a0001c0001t0003g0093 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-47-73A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73858743 | ||||||
chr14:73858948
|
T | G | 6 | a0001c0002t0007g0006a0001c0002t0007g0174a0001c0002t0007g0175others(3): Show | 8 | HG01109.hp2 HG01496.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.37+49T>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | chr14 | 73858948 | ||||||
chr14:73859089
|
A | G | 3 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0001t0002g0359 | 3 | HG02109.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.37+190A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | chr14 | 73859089 | ||||||
chr14:73859189
|
A | G | 15 | a0001c0002t0001g0216a0001c0002t0001g0218a0001c0002t0001g0219others(12): Show | 15 | HG01243.hp1 HG02258.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.37+290A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | chr14 | 73859189 | ||||||
chr14:73859190
|
T | C | 2 | a0001c0001t0012g0369a0001c0001t0013g0370 | 2 | HG01243.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.37+291T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | chr14 | 73859190 | ||||||
chr14:73859331
|
G | A | 2 | a0001c0001t0002g0312a0001c0001t0002g0327 | 2 | NA18993.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.37+432G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | chr14 | 73859331 | ||||||
chr14:73859713
|
T | A | 1 | a0001c0001t0003g0106 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.37+814T>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | chr14 | 73859713 | ||||||
chr14:73859748
|
C | T | 1 | a0001c0002t0001g0163 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.38-791C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | chr14 | 73859748 | ||||||
chr14:73859784
|
TA | T | 106 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(103): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.38-743delA | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 73859784 | |||||
chr14:73859805
|
T | C | 1 | a0001c0002t0020g0224 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.38-734T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | chr14 | 73859805 | ||||||
chr14:73859865
|
G | GT | 79 | a0001c0001t0003g0078a0001c0002t0001g0007a0001c0002t0001g0018others(76): Show | 83 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.38-661dupT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 73859865 | |||||
chr14:73859873
|
T | C | 1 | a0001c0001t0003g0094 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.38-666T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | chr14 | 73859873 | ||||||
chr14:73859906
|
T | G | 16 | a0001c0002t0001g0222a0001c0002t0001g0223a0001c0002t0001g0225others(13): Show | 16 | HG01891.hp1 HG02015.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.38-633T>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | chr14 | 73859906 | ||||||
chr14:73859918
|
G | A | 1 | a0001c0002t0005g0183 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.38-621G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | chr14 | 73859918 | ||||||
chr14:73859973
|
C | T | 2 | a0001c0001t0003g0004a0001c0001t0003g0081 | 4 | HG01109.hp1 HG03195.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-566C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | chr14 | 73859973 | ||||||
chr14:73860005
|
C | T | 2 | a0001c0002t0005g0213a0001c0002t0005g0214 | 2 | NA18950.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.38-534C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | chr14 | 73860005 | ||||||
chr14:73860021
|
G | A | 191 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(188): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.38-518G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | chr14 | 73860021 | ||||||
chr14:73860200
|
G | T | 131 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(128): Show | 144 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.38-339G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | chr14 | 73860200 | ||||||
chr14:73860263
|
T | C | 191 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(188): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.38-276T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | chr14 | 73860263 | ||||||
chr14:73860324
|
G | A | 8 | a0001c0002t0005g0014a0001c0002t0005g0183a0001c0002t0005g0184others(5): Show | 9 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.38-215G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | chr14 | 73860324 | ||||||
chr14:73860397
|
G | T | 188 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(185): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.38-142G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | chr14 | 73860397 | ||||||
chr14:73860495
|
C | A | 3 | a0001c0001t0011g0134a0001c0001t0012g0369a0001c0001t0013g0370 | 3 | HG01243.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.38-44C>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | chr14 | 73860495 | ||||||
chr14:73860790
|
A | G | 3 | a0001c0001t0011g0134a0001c0001t0012g0369a0001c0001t0013g0370 | 3 | HG01243.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.156+133A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73860790 | ||||||
chr14:73860913
|
A | G | 1 | a0001c0001t0004g0043 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.156+256A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73860913 | ||||||
chr14:73860918
|
A | C | 77 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(74): Show | 90 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.156+261A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73860918 | ||||||
chr14:73861047
|
G | C | 1 | a0001c0002t0001g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.156+390G>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73861047 | ||||||
chr14:73861053
|
C | A | 1 | a0001c0001t0002g0328 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.156+396C>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73861053 | ||||||
chr14:73861095
|
C | T | 1 | a0001c0001t0003g0075 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.156+438C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73861095 | ||||||
chr14:73861208
|
T | C | 1 | a0001c0002t0005g0190 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.156+551T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73861208 | ||||||
chr14:73861299
|
A | G | 3 | a0001c0002t0001g0233a0001c0002t0001g0280a0001c0002t0001g0281 | 3 | HG00597.hp2 HG02074.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.156+642A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73861299 | ||||||
chr14:73861410
|
C | T | 2 | a0001c0001t0003g0076a0001c0001t0003g0077 | 2 | HG02486.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.156+753C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73861410 | ||||||
chr14:73861424
|
T | C | 9 | a0001c0001t0003g0004a0001c0001t0003g0010a0001c0001t0003g0075others(6): Show | 12 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.156+767T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73861424 | ||||||
chr14:73861439
|
C | T | 2 | a0001c0001t0014g0133a0001c0001t0015g0132 | 2 | HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.156+782C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73861439 | ||||||
chr14:73861453
|
G | T | 191 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(188): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.156+796G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73861453 | ||||||
chr14:73861609
|
G | T | 1 | a0001c0001t0004g0043 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.156+952G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73861609 | ||||||
chr14:73861650
|
C | T | 6 | a0001c0002t0007g0006a0001c0002t0007g0174a0001c0002t0007g0175others(3): Show | 8 | HG01109.hp2 HG01496.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.156+993C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73861650 | ||||||
chr14:73861651
|
G | A | 1 | a0001c0001t0003g0075 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.156+994G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73861651 | ||||||
chr14:73861706
|
C | T | 3 | a0001c0001t0011g0134a0001c0001t0012g0369a0001c0001t0013g0370 | 3 | HG01243.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.156+1049C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73861706 | ||||||
chr14:73861883
|
C | CT | 7 | a0001c0001t0002g0328a0001c0002t0001g0170a0001c0002t0001g0223others(4): Show | 7 | HG02145.hp1 NA18991.hp1 NA18994.hp2 others(4): Show |
intron_variant | MODIFIER | c.156+1238dupT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73861883 | |||||
chr14:73861940
|
C | T | 191 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(188): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.156+1283C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73861940 | ||||||
chr14:73862002
|
C | T | 1 | a0001c0001t0002g0306 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.156+1345C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73862002 | ||||||
chr14:73862096
|
G | T | 77 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(74): Show | 90 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.156+1439G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73862096 | ||||||
chr14:73862199
|
G | T | 338 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(335): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.156+1542G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73862199 | ||||||
chr14:73862202
|
G | T | 316 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(313): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.156+1545G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73862202 | ||||||
chr14:73862300
|
C | T | 1 | a0001c0002t0007g0178 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.156+1643C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73862300 | ||||||
chr14:73862369
|
G | A | 60 | a0001c0001t0003g0004a0001c0001t0003g0010a0001c0001t0003g0075others(57): Show | 63 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.156+1712G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73862369 | ||||||
chr14:73862864
|
C | T | 191 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(188): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.156+2207C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73862864 | ||||||
chr14:73862869
|
G | A | 2 | a0001c0001t0012g0369a0001c0001t0013g0370 | 2 | HG01243.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.156+2212G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73862869 | ||||||
chr14:73862939
|
C | T | 1 | a0001c0002t0018g0217 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.156+2282C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73862939 | ||||||
chr14:73863078
|
A | G | 80 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(77): Show | 93 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.156+2421A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73863078 | ||||||
chr14:73863135
|
A | T | 1 | a0001c0001t0015g0132 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.156+2478A>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73863135 | ||||||
chr14:73863179
|
T | A | 1 | a0001c0001t0014g0133 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.156+2522T>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73863179 | ||||||
chr14:73863350
|
C | T | 1 | a0001c0002t0018g0217 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.156+2693C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73863350 | ||||||
chr14:73863355
|
C | G | 3 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0001t0002g0359 | 3 | HG02109.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.156+2698C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73863355 | ||||||
chr14:73863445
|
G | A | 1 | a0001c0001t0004g0027 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.156+2788G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73863445 | ||||||
chr14:73863475
|
C | T | 3 | a0001c0001t0011g0134a0001c0001t0012g0369a0001c0001t0013g0370 | 3 | HG01243.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.156+2818C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73863475 | ||||||
chr14:73863496
|
A | G | 2 | a0001c0001t0002g0325a0001c0001t0002g0326 | 2 | NA18955.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.156+2839A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73863496 | ||||||
chr14:73863682
|
T | G | 1 | a0001c0001t0014g0133 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.156+3025T>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73863682 | ||||||
chr14:73863760
|
C | T | 188 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(185): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.156+3103C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73863760 | ||||||
chr14:73863779
|
C | G | 3 | a0001c0002t0001g0161a0001c0002t0001g0162a0001c0002t0001g0173 | 3 | HG01081.hp2 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.156+3122C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73863779 | ||||||
chr14:73863903
|
A | G | 3 | a0001c0002t0009g0180a0001c0002t0009g0181a0001c0002t0018g0217 | 3 | HG02809.hp2 HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.156+3246A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73863903 | ||||||
chr14:73863907
|
C | T | 3 | a0001c0001t0004g0065a0001c0001t0004g0066a0001c0001t0004g0067 | 3 | HG02615.hp1 HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.156+3250C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73863907 | ||||||
chr14:73864272
|
G | A | 1 | a0001c0002t0005g0184 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.156+3615G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73864272 | ||||||
chr14:73864444
|
C | G | 1 | a0001c0001t0004g0071 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.156+3787C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73864444 | ||||||
chr14:73864854
|
C | T | 1 | a0003c0004t0001g0164 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.156+4197C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73864854 | ||||||
chr14:73864919
|
G | A | 3 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0001t0002g0359 | 3 | HG02109.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.156+4262G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73864919 | ||||||
chr14:73864984
|
G | A | 49 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0029others(46): Show | 49 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.156+4327G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73864984 | ||||||
chr14:73864984
|
G | T | 59 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(56): Show | 73 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.156+4327G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73864984 | ||||||
chr14:73865087
|
A | T | 3 | a0001c0002t0005g0211a0001c0002t0005g0212a0001c0002t0017g0182 | 3 | HG01346.hp2 HG02738.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.156+4430A>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73865087 | ||||||
chr14:73865209
|
C | T | 1 | a0001c0002t0005g0210 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.156+4552C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73865209 | ||||||
chr14:73865210
|
G | A | 7 | a0001c0002t0001g0216a0001c0002t0001g0218a0001c0002t0001g0219others(4): Show | 7 | HG01243.hp1 HG02486.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.156+4553G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73865210 | ||||||
chr14:73865212
|
C | T | 2 | a0001c0001t0012g0369a0001c0001t0013g0370 | 2 | HG01243.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.156+4555C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73865212 | ||||||
chr14:73865429
|
C | T | 108 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(105): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.156+4772C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73865429 | ||||||
chr14:73865559
|
T | C | 2 | a0001c0002t0001g0222a0001c0002t0001g0229 | 2 | HG01891.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.156+4902T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73865559 | ||||||
chr14:73865623
|
G | A | 4 | a0001c0002t0001g0155a0001c0002t0001g0156a0001c0002t0001g0163others(1): Show | 4 | HG01515.hp1 HG02818.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.156+4966G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73865623 | ||||||
chr14:73865631
|
T | A | 1 | a0001c0002t0001g0237 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.156+4974T>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73865631 | ||||||
chr14:73865725
|
T | C | 3 | a0001c0002t0009g0180a0001c0002t0009g0181a0001c0002t0018g0217 | 3 | HG02809.hp2 HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.156+5068T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73865725 | ||||||
chr14:73865753
|
A | G | 188 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(185): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.156+5096A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73865753 | ||||||
chr14:73865775
|
C | T | 69 | a0001c0002t0001g0007a0001c0002t0001g0018a0001c0002t0001g0019others(66): Show | 73 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.156+5118C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73865775 | ||||||
chr14:73866008
|
T | C | 1 | a0001c0001t0011g0134 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.156+5351T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73866008 | ||||||
chr14:73866106
|
G | A | 191 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(188): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.156+5449G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73866106 | ||||||
chr14:73866157
|
A | C | 3 | a0001c0001t0011g0134a0001c0001t0012g0369a0001c0001t0013g0370 | 3 | HG01243.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.156+5500A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73866157 | ||||||
chr14:73866292
|
C | A | 1 | a0001c0002t0001g0143 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.156+5635C>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73866292 | ||||||
chr14:73866348
|
A | C | 106 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(103): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.156+5691A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73866348 | ||||||
chr14:73866361
|
TCTC | T | 16 | a0001c0002t0001g0222a0001c0002t0001g0223a0001c0002t0001g0225others(13): Show | 16 | HG01891.hp1 HG02015.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.156+5707_156+5709d others(5): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73866361 | |||||
chr14:73866383
|
C | T | 1 | a0001c0002t0005g0193 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.156+5726C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73866383 | ||||||
chr14:73866395
|
C | T | 1 | a0001c0002t0001g0278 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.156+5738C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73866395 | ||||||
chr14:73866695
|
A | C | 48 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0009others(45): Show | 59 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(56): Show |
intron_variant | MODIFIER | c.156+6038A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73866695 | ||||||
chr14:73866725
|
A | T | 191 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(188): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.156+6068A>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73866725 | ||||||
chr14:73866816
|
C | T | 2 | a0001c0001t0003g0122a0001c0001t0003g0123 | 2 | NA19072.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.156+6159C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73866816 | ||||||
chr14:73866859
|
C | T | 1 | a0001c0002t0001g0143 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.156+6202C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73866859 | ||||||
chr14:73866904
|
C | T | 1 | a0001c0002t0005g0192 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.156+6247C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73866904 | ||||||
chr14:73866945
|
C | T | 13 | a0001c0002t0001g0216a0001c0002t0001g0218a0001c0002t0001g0219others(10): Show | 13 | HG01243.hp1 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.156+6288C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73866945 | ||||||
chr14:73866946
|
G | A | 5 | a0001c0002t0001g0226a0001c0002t0001g0227a0001c0002t0001g0230others(2): Show | 5 | HG02622.hp2 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.156+6289G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73866946 | ||||||
chr14:73867013
|
C | T | 70 | a0001c0002t0001g0007a0001c0002t0001g0018a0001c0002t0001g0019others(67): Show | 74 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.156+6356C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73867013 | ||||||
chr14:73867062
|
C | T | 1 | a0001c0001t0004g0064 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.156+6405C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73867062 | ||||||
chr14:73867088
|
C | CA | 39 | a0001c0002t0001g0005a0001c0002t0001g0135a0001c0002t0001g0136others(36): Show | 41 | HG00423.hp1 HG00621.hp2 HG01175.hp1 others(38): Show |
intron_variant | MODIFIER | c.156+6451dupA | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73867088 | |||||
chr14:73867088
|
CA | C | 6 | a0001c0002t0005g0185a0001c0002t0005g0191a0001c0002t0005g0194others(3): Show | 6 | HG00741.hp1 HG01934.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.156+6451delA | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73867088 | |||||
chr14:73867088
|
CAA | C | 46 | a0001c0001t0002g0304a0001c0001t0002g0311a0001c0001t0002g0313others(43): Show | 50 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.156+6450_156+6451d others(4): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73867088 | |||||
chr14:73867088
|
CAAA | C | 76 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(73): Show | 89 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.156+6449_156+6451d others(5): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73867088 | |||||
chr14:73867088
|
CAAAA | C | 98 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0001t0002g0359others(95): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.156+6448_156+6451d others(6): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73867088 | |||||
chr14:73867101
|
A | AAAC | 14 | a0001c0002t0001g0222a0001c0002t0001g0223a0001c0002t0001g0225others(11): Show | 14 | HG01891.hp1 HG02145.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.156+6446_156+6447i others(5): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73867101 | |||||
chr14:73867109
|
C | A | 69 | a0001c0002t0001g0007a0001c0002t0001g0018a0001c0002t0001g0019others(66): Show | 73 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.156+6452C>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73867109 | ||||||
chr14:73867117
|
C | A | 3 | a0001c0001t0003g0004a0001c0001t0003g0081a0001c0002t0001g0277 | 5 | HG01109.hp1 HG03195.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.156+6460C>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73867117 | ||||||
chr14:73867117
|
C | CA | 39 | a0001c0001t0004g0059a0001c0002t0005g0014a0001c0002t0005g0015others(36): Show | 43 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.156+6468dupA | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73867117 | |||||
chr14:73867190
|
C | T | 1 | a0001c0001t0011g0134 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.156+6533C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73867190 | ||||||
chr14:73867191
|
A | G | 191 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(188): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.156+6534A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73867191 | ||||||
chr14:73867324
|
T | C | 191 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(188): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.156+6667T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73867324 | ||||||
chr14:73867407
|
G | C | 1 | a0001c0001t0004g0036 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.157-6616G>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73867407 | ||||||
chr14:73867502
|
T | TA | 7 | a0001c0002t0001g0005a0001c0002t0001g0158a0001c0002t0001g0159others(4): Show | 9 | HG01081.hp2 HG01884.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.157-6511dupA | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73867502 | |||||
chr14:73867502
|
TA | T | 38 | a0001c0002t0005g0014a0001c0002t0005g0015a0001c0002t0005g0016others(35): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.157-6511delA | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73867502 | |||||
chr14:73867559
|
A | C | 1 | a0001c0001t0014g0133 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.157-6464A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73867559 | ||||||
chr14:73867689
|
T | C | 2 | a0001c0001t0002g0314a0001c0001t0002g0346 | 2 | NA18955.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.157-6334T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73867689 | ||||||
chr14:73868015
|
G | A | 43 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0119others(40): Show | 47 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.157-6008G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73868015 | ||||||
chr14:73868195
|
A | G | 1 | a0001c0001t0002g0353 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.157-5828A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73868195 | ||||||
chr14:73868246
|
G | A | 15 | a0001c0002t0001g0216a0001c0002t0001g0218a0001c0002t0001g0219others(12): Show | 15 | HG01243.hp1 HG02258.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.157-5777G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73868246 | ||||||
chr14:73868442
|
T | A | 3 | a0001c0001t0011g0134a0001c0001t0012g0369a0001c0001t0013g0370 | 3 | HG01243.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.157-5581T>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73868442 | ||||||
chr14:73868512
|
A | G | 191 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(188): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.157-5511A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73868512 | ||||||
chr14:73868619
|
C | A | 1 | a0001c0001t0011g0134 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.157-5404C>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73868619 | ||||||
chr14:73868787
|
TA | T | 191 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(188): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.157-5224delA | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73868787 | |||||
chr14:73868796
|
A | AG | 4 | a0001c0002t0001g0005a0001c0002t0001g0158a0001c0002t0001g0159others(1): Show | 6 | HG01884.hp2 HG02559.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.157-5227_157-5226i others(3): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73868796 | ||||||
chr14:73868936
|
C | G | 2 | a0001c0002t0001g0220a0001c0002t0001g0221 | 2 | HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.157-5087C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73868936 | ||||||
chr14:73868981
|
G | A | 1 | a0001c0001t0003g0109 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.157-5042G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73868981 | ||||||
chr14:73869132
|
G | A | 1 | a0001c0002t0001g0255 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.157-4891G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73869132 | ||||||
chr14:73869168
|
C | G | 1 | a0001c0002t0001g0223 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.157-4855C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73869168 | ||||||
chr14:73869427
|
C | T | 191 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(188): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.157-4596C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73869427 | ||||||
chr14:73869446
|
C | T | 2 | a0001c0002t0001g0220a0001c0002t0001g0221 | 2 | HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.157-4577C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73869446 | ||||||
chr14:73869451
|
GGTGGGAG others(19): Show |
G | 1 | a0001c0001t0008g0130 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.157-4550_157-4525d others(28): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73869451 | |||||
chr14:73869529
|
A | G | 6 | a0001c0002t0001g0253a0001c0002t0001g0254a0001c0002t0001g0274others(3): Show | 6 | NA18969.hp2 NA18975.hp1 NA18988.hp1 others(3): Show |
intron_variant | MODIFIER | c.157-4494A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73869529 | ||||||
chr14:73869554
|
A | G | 3 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0001t0002g0359 | 3 | HG02109.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.157-4469A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73869554 | ||||||
chr14:73869573
|
CA | C | 67 | a0001c0002t0001g0007a0001c0002t0001g0018a0001c0002t0001g0019others(64): Show | 71 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.157-4434delA | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73869573 | |||||
chr14:73869807
|
C | G | 1 | a0001c0002t0001g0152 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.157-4216C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73869807 | ||||||
chr14:73869851
|
C | G | 6 | a0001c0002t0007g0006a0001c0002t0007g0174a0001c0002t0007g0175others(3): Show | 8 | HG01109.hp2 HG01496.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.157-4172C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73869851 | ||||||
chr14:73870012
|
C | CAGAG | 191 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(188): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.157-4009_157-4006d others(6): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73870012 | |||||
chr14:73870015
|
A | G | 7 | a0001c0002t0001g0005a0001c0002t0001g0158a0001c0002t0001g0159others(4): Show | 9 | HG01081.hp2 HG01884.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.157-4008A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73870015 | ||||||
chr14:73870034
|
A | G | 38 | a0001c0002t0005g0014a0001c0002t0005g0015a0001c0002t0005g0016others(35): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.157-3989A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73870034 | ||||||
chr14:73870062
|
T | C | 1 | a0001c0001t0002g0330 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.157-3961T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73870062 | ||||||
chr14:73870114
|
C | T | 1 | a0001c0002t0018g0217 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.157-3909C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73870114 | ||||||
chr14:73870120
|
G | A | 80 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(77): Show | 93 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.157-3903G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73870120 | ||||||
chr14:73870167
|
T | C | 1 | a0001c0002t0001g0168 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.157-3856T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73870167 | ||||||
chr14:73870193
|
C | CT | 124 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(121): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.157-3812dupT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73870193 | |||||
chr14:73870193
|
C | CTT | 77 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(74): Show | 90 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.157-3813_157-3812d others(4): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73870193 | |||||
chr14:73870193
|
C | CTTT | 6 | a0001c0001t0002g0340a0001c0001t0002g0341a0001c0001t0002g0342others(3): Show | 6 | HG00423.hp2 HG00621.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.157-3814_157-3812d others(5): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73870193 | |||||
chr14:73870193
|
CT | C | 45 | a0001c0001t0011g0134a0001c0002t0001g0374a0001c0002t0005g0014others(42): Show | 51 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.157-3812delT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73870193 | |||||
chr14:73870247
|
T | C | 244 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(241): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.157-3776T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73870247 | ||||||
chr14:73870306
|
A | G | 191 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(188): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.157-3717A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73870306 | ||||||
chr14:73870325
|
C | G | 5 | a0001c0002t0001g0234a0001c0002t0001g0235a0001c0002t0001g0236others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.157-3698C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73870325 | ||||||
chr14:73870377
|
G | T | 188 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(185): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.157-3646G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73870377 | ||||||
chr14:73870435
|
C | T | 2 | a0001c0002t0001g0226a0001c0002t0001g0227 | 2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.157-3588C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73870435 | ||||||
chr14:73870440
|
A | G | 1 | a0001c0001t0004g0063 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.157-3583A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73870440 | ||||||
chr14:73870449
|
G | T | 1 | a0001c0001t0003g0117 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.157-3574G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73870449 | ||||||
chr14:73870562
|
AAATT | A | 3 | a0001c0001t0011g0134a0001c0001t0012g0369a0001c0001t0013g0370 | 3 | HG01243.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.157-3457_157-3454d others(6): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73870562 | |||||
chr14:73870801
|
T | C | 2 | a0001c0001t0012g0369a0001c0001t0013g0370 | 2 | HG01243.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.157-3222T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73870801 | ||||||
chr14:73870870
|
T | G | 1 | a0001c0001t0003g0108 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.157-3153T>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73870870 | ||||||
chr14:73871171
|
G | A | 1 | a0001c0002t0001g0144 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.157-2852G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73871171 | ||||||
chr14:73871289
|
C | T | 1 | a0001c0002t0001g0232 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.157-2734C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73871289 | ||||||
chr14:73871341
|
C | CT | 24 | a0001c0001t0002g0339a0001c0001t0002g0367a0001c0002t0001g0021others(21): Show | 25 | HG00597.hp1 HG01346.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.157-2656dupT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73871341 | |||||
chr14:73871341
|
C | CTT | 10 | a0001c0001t0002g0312a0001c0001t0002g0327a0001c0002t0005g0186others(7): Show | 10 | HG00323.hp1 HG01167.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.157-2657_157-2656d others(4): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73871341 | |||||
chr14:73871341
|
C | CTTT | 28 | a0001c0002t0005g0014a0001c0002t0005g0015a0001c0002t0005g0016others(25): Show | 32 | HG00280.hp1 HG00639.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.157-2658_157-2656d others(5): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73871341 | |||||
chr14:73871341
|
CT | C | 45 | a0001c0001t0002g0008a0001c0001t0002g0022a0001c0001t0002g0303others(42): Show | 48 | HG00323.hp2 HG01074.hp2 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.157-2656delT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73871341 | |||||
chr14:73871341
|
CTT | C | 7 | a0001c0001t0002g0354a0001c0001t0004g0042a0001c0001t0004g0056others(4): Show | 7 | HG00099.hp2 HG00738.hp2 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.157-2657_157-2656d others(4): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73871341 | |||||
chr14:73871341
|
CTTT | C | 41 | a0001c0001t0004g0028a0001c0001t0004g0029a0001c0001t0004g0031others(38): Show | 41 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.157-2658_157-2656d others(5): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73871341 | |||||
chr14:73871341
|
CTTTT | C | 11 | a0001c0001t0003g0012a0001c0001t0003g0076a0001c0001t0003g0077others(8): Show | 12 | HG02451.hp2 HG02486.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.157-2659_157-2656d others(6): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73871341 | |||||
chr14:73871341
|
CTTTTT | C | 48 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(45): Show | 61 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(58): Show |
intron_variant | MODIFIER | c.157-2660_157-2656d others(7): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73871341 | |||||
chr14:73871518
|
A | T | 188 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(185): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.157-2505A>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73871518 | ||||||
chr14:73871656
|
A | G | 2 | a0001c0001t0003g0011a0001c0001t0003g0089 | 3 | HG00280.hp2 HG01255.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.157-2367A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73871656 | ||||||
chr14:73871846
|
T | A | 48 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0009others(45): Show | 59 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(56): Show |
intron_variant | MODIFIER | c.157-2177T>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73871846 | ||||||
chr14:73872015
|
C | T | 7 | a0001c0002t0005g0196a0001c0002t0005g0198a0001c0002t0005g0208others(4): Show | 7 | HG02523.hp2 HG03017.hp1 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.157-2008C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73872015 | ||||||
chr14:73872079
|
C | G | 191 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(188): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.157-1944C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73872079 | ||||||
chr14:73872181
|
G | A | 191 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(188): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.157-1842G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73872181 | ||||||
chr14:73872188
|
A | G | 229 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(226): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.157-1835A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73872188 | ||||||
chr14:73872447
|
A | G | 1 | a0001c0001t0003g0079 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.157-1576A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73872447 | ||||||
chr14:73872508
|
C | T | 3 | a0001c0002t0001g0161a0001c0002t0001g0162a0001c0002t0001g0173 | 3 | HG01081.hp2 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.157-1515C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73872508 | ||||||
chr14:73872635
|
C | T | 38 | a0001c0002t0005g0014a0001c0002t0005g0015a0001c0002t0005g0016others(35): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.157-1388C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73872635 | ||||||
chr14:73872917
|
C | T | 1 | a0001c0001t0002g0324 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.157-1106C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73872917 | ||||||
chr14:73872972
|
CA | C | 14 | a0001c0001t0002g0326a0001c0001t0002g0354a0001c0001t0003g0081others(11): Show | 14 | HG01109.hp1 HG01243.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.157-1037delA | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73872972 | |||||
chr14:73872987
|
T | A | 3 | a0001c0001t0011g0134a0001c0001t0012g0369a0001c0001t0013g0370 | 3 | HG01243.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.157-1036T>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73872987 | ||||||
chr14:73873035
|
G | T | 3 | a0001c0001t0003g0004a0001c0001t0003g0075a0001c0001t0003g0081 | 5 | HG01109.hp1 HG01884.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.157-988G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73873035 | ||||||
chr14:73873056
|
A | C | 80 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(77): Show | 93 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.157-967A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73873056 | ||||||
chr14:73873182
|
C | G | 1 | a0001c0002t0006g0239 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.157-841C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73873182 | ||||||
chr14:73873318
|
AAAAG | A | 69 | a0001c0002t0001g0007a0001c0002t0001g0018a0001c0002t0001g0019others(66): Show | 73 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.157-701_157-698del others(4): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73873318 | |||||
chr14:73873381
|
A | G | 1 | a0001c0002t0005g0196 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.157-642A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73873381 | ||||||
chr14:73873438
|
G | A | 80 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(77): Show | 93 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.157-585G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73873438 | ||||||
chr14:73873465
|
CT | C | 39 | a0001c0002t0001g0169a0001c0002t0005g0014a0001c0002t0005g0015others(36): Show | 43 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.157-546delT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73873465 | |||||
chr14:73873473
|
T | C | 70 | a0001c0002t0001g0007a0001c0002t0001g0018a0001c0002t0001g0019others(67): Show | 74 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.157-550T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73873473 | ||||||
chr14:73873528
|
A | G | 6 | a0001c0002t0007g0006a0001c0002t0007g0174a0001c0002t0007g0175others(3): Show | 8 | HG01109.hp2 HG01496.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.157-495A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73873528 | ||||||
chr14:73873555
|
C | T | 1 | a0001c0002t0001g0168 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.157-468C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73873555 | ||||||
chr14:73873570
|
T | C | 1 | a0001c0002t0005g0193 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.157-453T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73873570 | ||||||
chr14:73873646
|
C | T | 191 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(188): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.157-377C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73873646 | ||||||
chr14:73873710
|
C | T | 3 | a0001c0002t0001g0248a0001c0002t0001g0249a0001c0002t0001g0287 | 3 | NA18966.hp2 NA19012.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.157-313C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73873710 | ||||||
chr14:73873852
|
A | G | 188 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(185): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.157-171A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73873852 | ||||||
chr14:73873902
|
G | A | 38 | a0001c0002t0005g0014a0001c0002t0005g0015a0001c0002t0005g0016others(35): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.157-121G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73873902 | ||||||
chr14:73874224
|
A | G | 4 | a0001c0001t0003g0093a0001c0001t0003g0101a0001c0001t0003g0102others(1): Show | 4 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+10A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73874224 | ||||||
chr14:73874252
|
G | C | 3 | a0001c0002t0005g0190a0001c0002t0005g0195a0001c0002t0005g0199 | 3 | HG00323.hp1 HG00741.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.348+38G>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73874252 | ||||||
chr14:73874254
|
A | G | 3 | a0001c0002t0005g0190a0001c0002t0005g0195a0001c0002t0005g0199 | 3 | HG00323.hp1 HG00741.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.348+40A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73874254 | ||||||
chr14:73874331
|
C | T | 1 | a0001c0001t0002g0365 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.348+117C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73874331 | ||||||
chr14:73874384
|
G | A | 1 | a0001c0001t0014g0133 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.348+170G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73874384 | ||||||
chr14:73874421
|
G | A | 132 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(129): Show | 145 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.348+207G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73874421 | ||||||
chr14:73874425
|
C | G | 38 | a0001c0002t0005g0014a0001c0002t0005g0015a0001c0002t0005g0016others(35): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.348+211C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73874425 | ||||||
chr14:73874608
|
C | T | 1 | a0001c0001t0002g0303 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.348+394C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73874608 | ||||||
chr14:73874735
|
G | A | 80 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(77): Show | 93 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.348+521G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73874735 | ||||||
chr14:73874901
|
C | T | 38 | a0001c0002t0005g0014a0001c0002t0005g0015a0001c0002t0005g0016others(35): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.348+687C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73874901 | ||||||
chr14:73874982
|
C | T | 4 | a0001c0002t0001g0155a0001c0002t0001g0156a0001c0002t0001g0163others(1): Show | 4 | HG01515.hp1 HG02818.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+768C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73874982 | ||||||
chr14:73874984
|
G | A | 1 | a0001c0001t0015g0132 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.348+770G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73874984 | ||||||
chr14:73874999
|
T | C | 191 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(188): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.348+785T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73874999 | ||||||
chr14:73875008
|
A | G | 1 | a0001c0002t0005g0215 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.348+794A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73875008 | ||||||
chr14:73875051
|
G | A | 38 | a0001c0002t0005g0014a0001c0002t0005g0015a0001c0002t0005g0016others(35): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.348+837G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73875051 | ||||||
chr14:73875090
|
C | G | 3 | a0001c0002t0001g0161a0001c0002t0001g0162a0001c0002t0001g0173 | 3 | HG01081.hp2 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.348+876C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73875090 | ||||||
chr14:73875235
|
C | G | 70 | a0001c0002t0001g0007a0001c0002t0001g0018a0001c0002t0001g0019others(67): Show | 74 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.348+1021C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73875235 | ||||||
chr14:73875293
|
C | T | 48 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0009others(45): Show | 59 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(56): Show |
intron_variant | MODIFIER | c.348+1079C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73875293 | ||||||
chr14:73875323
|
A | G | 1 | a0001c0001t0004g0055 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.348+1109A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73875323 | ||||||
chr14:73875408
|
C | T | 1 | a0001c0002t0007g0178 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.348+1194C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73875408 | ||||||
chr14:73875453
|
C | T | 74 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(71): Show | 88 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.348+1239C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73875453 | ||||||
chr14:73875462
|
C | A | 6 | a0001c0002t0007g0006a0001c0002t0007g0174a0001c0002t0007g0175others(3): Show | 8 | HG01109.hp2 HG01496.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.348+1248C>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73875462 | ||||||
chr14:73875538
|
A | G | 2 | a0001c0001t0012g0369a0001c0001t0013g0370 | 2 | HG01243.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.348+1324A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73875538 | ||||||
chr14:73875555
|
A | C | 1 | a0001c0001t0004g0063 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.348+1341A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73875555 | ||||||
chr14:73875639
|
C | T | 1 | a0001c0001t0002g0371 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.349-1359C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73875639 | ||||||
chr14:73875660
|
G | T | 1 | a0001c0001t0014g0133 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.349-1338G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73875660 | ||||||
chr14:73875710
|
T | C | 131 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(128): Show | 144 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.349-1288T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73875710 | ||||||
chr14:73875734
|
C | T | 191 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(188): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.349-1264C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73875734 | ||||||
chr14:73875738
|
C | CT | 11 | a0001c0001t0002g0323a0001c0002t0001g0291a0001c0002t0001g0292others(8): Show | 11 | HG00735.hp2 HG00741.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.349-1245dupT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73875738 | |||||
chr14:73875738
|
CT | C | 64 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(61): Show | 78 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.349-1245delT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73875738 | |||||
chr14:73875820
|
C | CT | 11 | a0001c0001t0002g0339a0001c0001t0003g0104a0001c0001t0003g0107others(8): Show | 11 | HG01975.hp1 HG02602.hp1 HG03098.hp2 others(8): Show |
intron_variant | MODIFIER | c.349-1159dupT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73875820 | |||||
chr14:73875820
|
C | CTT | 55 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(52): Show | 69 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(66): Show |
intron_variant | MODIFIER | c.349-1160_349-1159d others(4): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73875820 | |||||
chr14:73875820
|
CT | C | 13 | a0001c0002t0001g0230a0001c0002t0001g0234a0001c0002t0001g0256others(10): Show | 15 | HG00280.hp1 HG01069.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.349-1159delT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73875820 | |||||
chr14:73875935
|
C | T | 3 | a0001c0001t0004g0045a0001c0001t0004g0053a0001c0001t0004g0054 | 3 | HG02602.hp1 HG03688.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.349-1063C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73875935 | ||||||
chr14:73875939
|
G | T | 1 | a0001c0001t0003g0100 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.349-1059G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73875939 | ||||||
chr14:73876109
|
G | A | 80 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(77): Show | 93 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.349-889G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73876109 | ||||||
chr14:73876176
|
G | A | 7 | a0001c0002t0001g0216a0001c0002t0001g0218a0001c0002t0001g0219others(4): Show | 7 | HG01243.hp1 HG02486.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.349-822G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73876176 | ||||||
chr14:73876444
|
A | C | 1 | a0001c0001t0004g0129 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.349-554A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73876444 | ||||||
chr14:73876483
|
C | CTTTTTTT | 6 | a0001c0001t0003g0010a0001c0001t0003g0078a0001c0001t0003g0079others(3): Show | 7 | HG02055.hp1 HG02257.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.349-505_349-499dup others(7): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73876483 | |||||
chr14:73876483
|
C | CTTTTTTT others(1): Show |
47 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(44): Show | 59 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.349-506_349-499dup others(8): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73876483 | |||||
chr14:73876483
|
C | CTTTTTTT others(2): Show |
8 | a0001c0001t0003g0012a0001c0001t0003g0081a0001c0001t0003g0098others(5): Show | 9 | HG00140.hp1 HG00639.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.349-507_349-499dup others(9): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73876483 | |||||
chr14:73876483
|
C | CTTTTTTT others(5): Show |
5 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0001t0002g0331others(2): Show | 5 | HG02071.hp2 HG02109.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.349-510_349-499dup others(12): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73876483 | |||||
chr14:73876483
|
C | CTTTTTTT others(6): Show |
56 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(53): Show | 69 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.349-511_349-499dup others(13): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73876483 | |||||
chr14:73876483
|
C | CTTTTTTT others(7): Show |
18 | a0001c0001t0002g0307a0001c0001t0002g0308a0001c0001t0002g0311others(15): Show | 18 | HG02055.hp2 HG02074.hp1 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.349-512_349-499dup others(14): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73876483 | |||||
chr14:73876483
|
C | CTTTTTTT others(8): Show |
1 | a0001c0001t0002g0323 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.349-513_349-499dup others(15): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73876483 | |||||
chr14:73876483
|
C | CTTTTTTT others(19): Show |
8 | a0001c0001t0004g0028a0001c0001t0004g0030a0001c0001t0004g0034others(5): Show | 8 | HG00099.hp2 HG00738.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.349-499_349-498ins others(26): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73876483 | |||||
chr14:73876483
|
C | CTTTTTTT others(20): Show |
14 | a0001c0001t0004g0027a0001c0001t0004g0029a0001c0001t0004g0031others(11): Show | 14 | HG00408.hp2 HG00544.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.349-499_349-498ins others(27): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73876483 | |||||
chr14:73876483
|
C | CTTTTTTT others(21): Show |
15 | a0001c0001t0004g0032a0001c0001t0004g0033a0001c0001t0004g0051others(12): Show | 15 | HG01074.hp1 HG01891.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.349-499_349-498ins others(28): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73876483 | |||||
chr14:73876483
|
C | CTTTTTTT others(23): Show |
1 | a0001c0001t0004g0066 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.349-499_349-498ins others(30): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73876483 | |||||
chr14:73876483
|
C | CTTTTTTT others(24): Show |
1 | a0001c0001t0004g0069 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.349-499_349-498ins others(31): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73876483 | |||||
chr14:73876483
|
C | CTTTTTTT others(25): Show |
1 | a0001c0001t0004g0036 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.349-499_349-498ins others(32): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73876483 | |||||
chr14:73876483
|
C | CTTTTTTT others(29): Show |
2 | a0001c0001t0004g0052a0001c0001t0004g0068 | 2 | NA19063.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.349-499_349-498ins others(36): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73876483 | |||||
chr14:73876483
|
C | CTTTTTTT others(30): Show |
2 | a0001c0001t0004g0035a0001c0001t0004g0041 | 2 | NA18974.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.349-499_349-498ins others(37): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73876483 | |||||
chr14:73876483
|
C | CTTTTTTT others(31): Show |
1 | a0001c0001t0004g0062 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.349-499_349-498ins others(38): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73876483 | |||||
chr14:73876483
|
C | CTTTTTTT others(37): Show |
1 | a0001c0001t0004g0043 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.349-499_349-498ins others(44): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73876483 | |||||
chr14:73876558
|
T | G | 1 | a0001c0002t0001g0154 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.349-440T>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73876558 | ||||||
chr14:73876597
|
T | G | 1 | a0001c0001t0003g0095 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.349-401T>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73876597 | ||||||
chr14:73876674
|
G | A | 1 | a0001c0002t0005g0196 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.349-324G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73876674 | ||||||
chr14:73876717
|
T | C | 1 | a0001c0001t0003g0102 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.349-281T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73876717 | ||||||
chr14:73876758
|
T | A | 1 | a0001c0002t0005g0211 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.349-240T>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73876758 | ||||||
chr14:73876840
|
C | G | 1 | a0001c0001t0004g0043 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.349-158C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73876840 | ||||||
chr14:73876908
|
A | C | 1 | a0001c0001t0002g0321 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.349-90A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73876908 | ||||||
chr14:73876909
|
C | T | 38 | a0001c0002t0005g0014a0001c0002t0005g0015a0001c0002t0005g0016others(35): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.349-89C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73876909 | ||||||
chr14:73877275
|
A | C | 1 | a0001c0002t0001g0168 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.519+107A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | chr14 | 73877275 | ||||||
chr14:73877276
|
AT | A | 49 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0029others(46): Show | 49 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.519+118delT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 73877276 | |||||
chr14:73877278
|
T | A | 48 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0009others(45): Show | 59 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(56): Show |
intron_variant | MODIFIER | c.519+110T>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | chr14 | 73877278 | ||||||
chr14:73877350
|
C | T | 2 | a0001c0001t0014g0133a0001c0001t0015g0132 | 2 | HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.519+182C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | chr14 | 73877350 | ||||||
chr14:73877378
|
C | T | 6 | a0001c0001t0003g0010a0001c0001t0003g0076a0001c0001t0003g0077others(3): Show | 7 | HG02055.hp1 HG02257.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.519+210C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | chr14 | 73877378 | ||||||
chr14:73877409
|
T | C | 1 | a0001c0001t0015g0132 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.519+241T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | chr14 | 73877409 | ||||||
chr14:73877492
|
T | C | 1 | a0001c0001t0011g0134 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.519+324T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | chr14 | 73877492 | ||||||
chr14:73877573
|
C | A | 191 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(188): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.519+405C>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | chr14 | 73877573 | ||||||
chr14:73877587
|
A | G | 16 | a0001c0002t0001g0222a0001c0002t0001g0223a0001c0002t0001g0225others(13): Show | 16 | HG01891.hp1 HG02015.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.519+419A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | chr14 | 73877587 | ||||||
chr14:73877613
|
G | GT | 45 | a0001c0001t0003g0080a0001c0001t0011g0134a0001c0002t0001g0005others(42): Show | 51 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.519+457dupT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 73877613 | |||||
chr14:73877613
|
G | GTT | 50 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0029others(47): Show | 50 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.519+456_519+457dup others(2): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 73877613 | |||||
chr14:73877613
|
G | GTTT | 77 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(74): Show | 90 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.519+455_519+457dup others(3): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 73877613 | |||||
chr14:73877613
|
G | GTTTT | 7 | a0001c0001t0002g0305a0001c0001t0002g0308a0001c0001t0002g0311others(4): Show | 7 | HG00642.hp2 HG02135.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.519+454_519+457dup others(4): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 73877613 | |||||
chr14:73877640
|
TCTTA | T | 3 | a0001c0001t0004g0049a0001c0001t0004g0060a0001c0001t0004g0069 | 3 | HG04115.hp2 HG04199.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.519+475_519+478del others(4): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 73877640 | |||||
chr14:73877912
|
C | A | 2 | a0001c0002t0005g0202a0001c0002t0005g0203 | 2 | HG02165.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.519+744C>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | chr14 | 73877912 | ||||||
chr14:73877971
|
A | G | 60 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(57): Show | 74 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.519+803A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | chr14 | 73877971 | ||||||
chr14:73878019
|
G | A | 1 | a0001c0001t0002g0349 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.519+851G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | chr14 | 73878019 | ||||||
chr14:73878048
|
A | C | 1 | a0001c0002t0001g0281 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.519+880A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | chr14 | 73878048 | ||||||
chr14:73878260
|
C | G | 2 | a0001c0002t0001g0246a0001c0002t0001g0247 | 2 | NA18956.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.520-836C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | chr14 | 73878260 | ||||||
chr14:73878282
|
G | A | 1 | a0001c0001t0002g0332 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.520-814G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | chr14 | 73878282 | ||||||
chr14:73878351
|
T | A | 1 | a0001c0002t0005g0208 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.520-745T>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | chr14 | 73878351 | ||||||
chr14:73878354
|
ATTTAATT others(15): Show |
A | 2 | a0001c0002t0009g0180a0001c0002t0009g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.520-740_520-719del others(22): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 73878354 | |||||
chr14:73878449
|
T | G | 1 | a0001c0001t0004g0039 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.520-647T>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | chr14 | 73878449 | ||||||
chr14:73878718
|
A | T | 3 | a0001c0002t0001g0161a0001c0002t0001g0162a0001c0002t0001g0173 | 3 | HG01081.hp2 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.520-378A>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | chr14 | 73878718 | ||||||
chr14:73879488
|
G | C | 10 | a0001c0002t0001g0013a0001c0002t0001g0153a0001c0002t0001g0154others(7): Show | 11 | HG01070.hp1 HG01192.hp2 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.729+183G>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 6/9 | chr14 | 73879488 | ||||||
chr14:73879591
|
G | A | 2 | a0001c0001t0003g0101a0001c0001t0003g0118 | 2 | HG00642.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.729+286G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 6/9 | chr14 | 73879591 | ||||||
chr14:73879592
|
A | G | 80 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(77): Show | 93 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.729+287A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 6/9 | chr14 | 73879592 | ||||||
chr14:73879645
|
T | TTGCGTAG others(3): Show |
229 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(226): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.729+340_729+341ins others(10): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 6/9 | chr14 | 73879645 | ||||||
chr14:73879678
|
A | G | 1 | a0001c0001t0004g0055 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.729+373A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 6/9 | chr14 | 73879678 | ||||||
chr14:73879726
|
T | C | 1 | a0001c0002t0005g0184 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.730-329T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 6/9 | chr14 | 73879726 | ||||||
chr14:73880294
|
C | T | 2 | a0001c0001t0004g0072a0001c0001t0004g0073 | 2 | HG01891.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.851+118C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 7/9 | chr14 | 73880294 | ||||||
chr14:73880323
|
A | G | 1 | a0001c0002t0001g0373 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.851+147A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 7/9 | chr14 | 73880323 | ||||||
chr14:73880339
|
G | A | 4 | a0001c0001t0003g0096a0001c0001t0003g0112a0001c0001t0003g0116others(1): Show | 4 | HG01358.hp1 HG01952.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.851+163G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 7/9 | chr14 | 73880339 | ||||||
chr14:73880397
|
A | C | 77 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(74): Show | 90 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.851+221A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 7/9 | chr14 | 73880397 | ||||||
chr14:73880418
|
CA | C | 191 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(188): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.851+249delA | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr14 | 73880418 | |||||
chr14:73880587
|
C | CA | 51 | a0001c0001t0002g0327a0001c0001t0004g0027a0001c0001t0004g0028others(48): Show | 51 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.851+424dupA | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr14 | 73880587 | |||||
chr14:73880593
|
A | C | 4 | a0001c0002t0005g0015a0001c0002t0005g0191a0001c0002t0005g0192others(1): Show | 5 | HG02129.hp2 HG02602.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.851+417A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 7/9 | chr14 | 73880593 | ||||||
chr14:73880599
|
A | AC | 56 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(53): Show | 70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.851+423_851+424ins others(1): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 7/9 | chr14 | 73880599 | ||||||
chr14:73880599
|
A | C | 3 | a0001c0001t0011g0134a0001c0001t0012g0369a0001c0001t0013g0370 | 3 | HG01243.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.851+423A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 7/9 | chr14 | 73880599 | ||||||
chr14:73880600
|
A | C | 91 | a0001c0002t0001g0007a0001c0002t0001g0018a0001c0002t0001g0019others(88): Show | 97 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.851+424A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 7/9 | chr14 | 73880600 | ||||||
chr14:73880601
|
C | A | 2 | a0001c0001t0004g0041a0001c0001t0004g0059 | 2 | HG06807.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.851+425C>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 7/9 | chr14 | 73880601 | ||||||
chr14:73880639
|
T | C | 1 | a0001c0001t0008g0085 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.851+463T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 7/9 | chr14 | 73880639 | ||||||
chr14:73880678
|
T | C | 7 | a0001c0002t0001g0005a0001c0002t0001g0158a0001c0002t0001g0159others(4): Show | 9 | HG01081.hp2 HG01884.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.851+502T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 7/9 | chr14 | 73880678 | ||||||
chr14:73880710
|
A | G | 62 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(59): Show | 76 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(73): Show |
intron_variant | MODIFIER | c.852-495A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 7/9 | chr14 | 73880710 | ||||||
chr14:73880736
|
C | T | 117 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(114): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.852-469C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 7/9 | chr14 | 73880736 | ||||||
chr14:73880835
|
C | T | 1 | a0001c0001t0003g0113 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.852-370C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 7/9 | chr14 | 73880835 | ||||||
chr14:73880851
|
A | C | 198 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(195): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.852-354A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 7/9 | chr14 | 73880851 | ||||||
chr14:73880853
|
G | A | 1 | a0001c0001t0003g0106 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.852-352G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 7/9 | chr14 | 73880853 | ||||||
chr14:73881019
|
T | C | 1 | a0001c0001t0003g0118 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.852-186T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 7/9 | chr14 | 73881019 | ||||||
chr14:73881565
|
A | ATTG | 244 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(241): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.939+275_939+276ins others(3): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 73881565 | |||||
chr14:73881728
|
A | C | 1 | a0001c0002t0007g0178 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.939+436A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 8/9 | chr14 | 73881728 | ||||||
chr14:73881772
|
C | CT | 7 | a0001c0002t0001g0141a0001c0002t0001g0143a0001c0002t0001g0144others(4): Show | 7 | HG01106.hp1 HG01123.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.939+509dupT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 73881772 | |||||
chr14:73881772
|
CT | C | 103 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(100): Show | 118 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.939+509delT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 73881772 | |||||
chr14:73881772
|
CTT | C | 168 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0001t0002g0307others(165): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.939+508_939+509del others(2): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 73881772 | |||||
chr14:73881772
|
CTTTTTTT others(3): Show |
C | 36 | a0001c0002t0005g0014a0001c0002t0005g0015a0001c0002t0005g0016others(33): Show | 40 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.939+500_939+509del others(10): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 73881772 | |||||
chr14:73881772
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0002t0005g0187a0001c0002t0005g0188 | 2 | HG01070.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.939+499_939+509del others(11): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 73881772 | |||||
chr14:73881807
|
G | A | 1 | a0001c0002t0001g0151 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.939+515G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 8/9 | chr14 | 73881807 | ||||||
chr14:73881836
|
T | G | 1 | a0001c0001t0004g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.939+544T>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 8/9 | chr14 | 73881836 | ||||||
chr14:73881860
|
T | G | 189 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(186): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.940-539T>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 8/9 | chr14 | 73881860 | ||||||
chr14:73881887
|
A | G | 191 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(188): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.940-512A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 8/9 | chr14 | 73881887 | ||||||
chr14:73881891
|
A | C | 191 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(188): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.940-508A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 8/9 | chr14 | 73881891 | ||||||
chr14:73881949
|
A | T | 1 | a0001c0001t0003g0025 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.940-450A>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 8/9 | chr14 | 73881949 | ||||||
chr14:73882034
|
A | G | 6 | a0001c0001t0002g0307a0001c0001t0002g0323a0001c0001t0002g0337others(3): Show | 6 | NA18944.hp1 NA18947.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.940-365A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 8/9 | chr14 | 73882034 | ||||||
chr14:73882055
|
T | G | 1 | a0001c0002t0005g0192 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.940-344T>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 8/9 | chr14 | 73882055 | ||||||
chr14:73882070
|
GTGCACC | G | 1 | a0001c0002t0001g0005 | 3 | HG02559.hp1 HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.940-326_940-321del others(6): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 73882070 | |||||
chr14:73882105
|
T | G | 1 | a0001c0001t0003g0114 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.940-294T>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 8/9 | chr14 | 73882105 | ||||||
chr14:73882116
|
A | G | 250 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(247): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.940-283A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 8/9 | chr14 | 73882116 | ||||||
chr14:73882241
|
A | G | 1 | a0001c0002t0001g0144 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.940-158A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 8/9 | chr14 | 73882241 | ||||||
chr14:73882390
|
G | T | 2 | a0001c0001t0012g0369a0001c0001t0013g0370 | 2 | HG01243.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.940-9G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 8/9 | chr14 | 73882390 | ||||||
chr14:73882524
|
G | A | 108 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(105): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.979+86G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | chr14 | 73882524 | ||||||
chr14:73882566
|
T | G | 1 | a0001c0002t0001g0281 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.979+128T>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | chr14 | 73882566 | ||||||
chr14:73882610
|
C | T | 191 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(188): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.979+172C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | chr14 | 73882610 | ||||||
chr14:73882636
|
G | T | 7 | a0001c0002t0001g0216a0001c0002t0001g0218a0001c0002t0001g0219others(4): Show | 7 | HG01243.hp1 HG02486.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.979+198G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | chr14 | 73882636 | ||||||
chr14:73882645
|
C | T | 1 | a0001c0001t0002g0336 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.979+207C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | chr14 | 73882645 | ||||||
chr14:73882657
|
C | T | 1 | a0001c0002t0001g0266 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.979+219C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | chr14 | 73882657 | ||||||
chr14:73882668
|
T | G | 1 | a0001c0002t0001g0373 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.979+230T>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | chr14 | 73882668 | ||||||
chr14:73882799
|
CCTTTTTT others(10): Show |
C | 1 | a0001c0001t0011g0134 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.979+362_979+378del others(17): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | chr14 | 73882799 | ||||||
chr14:73882800
|
C | CT | 45 | a0001c0002t0001g0007a0001c0002t0001g0020a0001c0002t0001g0021others(42): Show | 48 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.979+400dupT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | |||||
chr14:73882800
|
C | CTT | 14 | a0001c0002t0001g0216a0001c0002t0001g0218a0001c0002t0001g0231others(11): Show | 14 | HG00280.hp1 HG00735.hp2 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.979+399_979+400dup others(2): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | |||||
chr14:73882800
|
C | CTTT | 12 | a0001c0002t0001g0018a0001c0002t0001g0219a0001c0002t0001g0221others(9): Show | 12 | HG00323.hp2 HG01167.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.979+398_979+400dup others(3): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | |||||
chr14:73882800
|
C | CTTTT | 11 | a0001c0002t0001g0265a0001c0002t0001g0293a0001c0002t0001g0297others(8): Show | 12 | HG00323.hp1 HG02129.hp2 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.979+397_979+400dup others(4): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | |||||
chr14:73882800
|
C | CTTTTT | 7 | a0001c0002t0005g0191a0001c0002t0005g0193a0001c0002t0005g0196others(4): Show | 7 | HG02523.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.979+396_979+400dup others(5): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | |||||
chr14:73882800
|
C | CTTTTTTT others(3): Show |
1 | a0001c0002t0001g0292 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.979+391_979+400dup others(10): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | |||||
chr14:73882800
|
C | CTTTTTTT others(4): Show |
4 | a0001c0002t0005g0184a0001c0002t0005g0186a0001c0002t0005g0187others(1): Show | 4 | HG01070.hp2 HG01257.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.979+390_979+400dup others(11): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | |||||
chr14:73882800
|
C | CTTTTTTT others(5): Show |
5 | a0001c0002t0005g0014a0001c0002t0005g0183a0001c0002t0005g0185others(2): Show | 6 | HG00639.hp2 HG01071.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.979+389_979+400dup others(12): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | |||||
chr14:73882800
|
C | CTTTTTTT others(8): Show |
1 | a0001c0002t0005g0205 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.979+386_979+400dup others(15): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | |||||
chr14:73882800
|
C | CTTTTTTT others(9): Show |
1 | a0001c0002t0005g0016 | 2 | HG01168.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.979+385_979+400dup others(16): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | |||||
chr14:73882800
|
C | CTTTTTTT others(10): Show |
1 | a0001c0002t0005g0206 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.979+384_979+400dup others(17): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | |||||
chr14:73882800
|
C | CTTTTTTT others(11): Show |
1 | a0001c0002t0005g0190 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.979+383_979+400dup others(18): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | |||||
chr14:73882800
|
C | CTTTTTTT others(12): Show |
1 | a0001c0002t0005g0215 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.979+382_979+400dup others(19): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | |||||
chr14:73882800
|
C | CTTTTTTT others(13): Show |
2 | a0001c0002t0005g0017a0001c0002t0005g0197 | 3 | HG01123.hp2 HG01928.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.979+381_979+400dup others(20): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | |||||
chr14:73882800
|
C | CTTTTTTT others(16): Show |
1 | a0001c0002t0005g0207 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.979+378_979+400dup others(23): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | |||||
chr14:73882800
|
CT | C | 12 | a0001c0002t0001g0136a0001c0002t0001g0137a0001c0002t0001g0138others(9): Show | 12 | HG01070.hp1 HG01192.hp2 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.979+400delT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | |||||
chr14:73882800
|
CTT | C | 8 | a0001c0002t0001g0005a0001c0002t0001g0153a0001c0002t0001g0155others(5): Show | 10 | HG01515.hp1 HG02559.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.979+399_979+400del others(2): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | |||||
chr14:73882800
|
CTTT | C | 9 | a0001c0002t0001g0013a0001c0002t0001g0143a0001c0002t0001g0147others(6): Show | 10 | HG01074.hp2 HG01123.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.979+398_979+400del others(3): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | |||||
chr14:73882800
|
CTTTT | C | 10 | a0001c0002t0001g0148a0001c0002t0001g0152a0001c0002t0001g0154others(7): Show | 10 | HG00741.hp1 HG01081.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.979+397_979+400del others(4): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | |||||
chr14:73882800
|
CTTTTTTT others(3): Show |
C | 52 | a0001c0001t0002g0303a0001c0001t0002g0306a0001c0001t0002g0308others(49): Show | 55 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.979+391_979+400del others(10): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | |||||
chr14:73882800
|
CTTTTTTT others(4): Show |
C | 129 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(126): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.979+390_979+400del others(11): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | |||||
chr14:73882800
|
CTTTTTTT others(5): Show |
C | 10 | a0001c0001t0002g0318a0001c0001t0002g0331a0001c0001t0002g0347others(7): Show | 12 | HG01109.hp2 HG01168.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.979+389_979+400del others(12): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | |||||
chr14:73882800
|
CTTTTTTT others(10): Show |
C | 1 | a0001c0002t0001g0229 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.979+384_979+400del others(17): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | |||||
chr14:73882800
|
CTTTTTTT others(15): Show |
C | 1 | a0001c0002t0001g0168 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.979+379_979+400del others(22): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | |||||
chr14:73882844
|
G | A | 2 | a0001c0001t0004g0033a0001c0001t0004g0074 | 2 | HG01074.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.979+406G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | chr14 | 73882844 | ||||||
chr14:73882913
|
C | T | 2 | a0001c0001t0011g0134a0001c0002t0001g0230 | 2 | HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.979+475C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | chr14 | 73882913 | ||||||
chr14:73882965
|
C | T | 1 | a0001c0001t0015g0132 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.979+527C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | chr14 | 73882965 | ||||||
chr14:73883072
|
C | T | 2 | a0001c0001t0014g0133a0001c0001t0015g0132 | 2 | HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.979+634C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | chr14 | 73883072 | ||||||
chr14:73883178
|
C | T | 1 | a0001c0001t0003g0101 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.979+740C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | chr14 | 73883178 | ||||||
chr14:73883180
|
TCACCTC | T | 4 | a0001c0002t0001g0226a0001c0002t0001g0227a0001c0002t0001g0232others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.979+744_979+749del others(6): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883180 | |||||
chr14:73883188
|
C | CTT | 17 | a0001c0001t0004g0028a0001c0002t0001g0020a0001c0002t0001g0179others(14): Show | 18 | HG00621.hp2 HG01256.hp2 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.979+781_979+782dup others(2): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | |||||
chr14:73883188
|
C | CTTT | 32 | a0001c0002t0001g0007a0001c0002t0001g0018a0001c0002t0001g0019others(29): Show | 34 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.979+780_979+782dup others(3): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | |||||
chr14:73883188
|
C | CTTTT | 10 | a0001c0002t0001g0021a0001c0002t0001g0233a0001c0002t0001g0240others(7): Show | 11 | HG00597.hp1 HG01433.hp1 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.979+779_979+782dup others(4): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | |||||
chr14:73883188
|
C | CTTTTT | 12 | a0001c0002t0001g0234a0001c0002t0001g0235a0001c0002t0001g0236others(9): Show | 14 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.979+778_979+782dup others(5): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | |||||
chr14:73883188
|
C | CTTTTTT | 5 | a0001c0001t0002g0008a0001c0001t0002g0320a0001c0001t0002g0329others(2): Show | 7 | HG00438.hp2 HG03486.hp2 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.979+777_979+782dup others(6): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | |||||
chr14:73883188
|
C | CTTTTTTT | 26 | a0001c0001t0002g0001a0001c0001t0002g0303a0001c0001t0002g0304others(23): Show | 34 | HG00438.hp1 HG00544.hp1 HG02523.hp1 others(31): Show |
intron_variant | MODIFIER | c.979+776_979+782dup others(7): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | |||||
chr14:73883188
|
C | CTTTTTTT others(1): Show |
29 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0310others(26): Show | 31 | HG00408.hp1 HG00642.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.979+775_979+782dup others(8): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | |||||
chr14:73883188
|
C | CTTTTTTT others(2): Show |
16 | a0001c0001t0002g0022a0001c0001t0002g0306a0001c0001t0002g0308others(13): Show | 17 | HG00423.hp2 HG00621.hp1 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.979+774_979+782dup others(9): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | |||||
chr14:73883188
|
C | CTTTTTTT others(3): Show |
7 | a0001c0001t0002g0321a0001c0001t0002g0340a0001c0001t0002g0371others(4): Show | 7 | HG02071.hp2 HG02109.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.979+773_979+782dup others(10): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | |||||
chr14:73883188
|
C | CTTTTTTT others(4): Show |
3 | a0001c0001t0004g0035a0001c0001t0004g0047a0001c0001t0004g0070 | 3 | HG02155.hp2 HG02615.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.979+772_979+782dup others(11): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | |||||
chr14:73883188
|
C | CTTTTTTT others(5): Show |
4 | a0001c0001t0002g0313a0001c0001t0004g0050a0001c0001t0004g0051others(1): Show | 4 | HG00408.hp2 HG02602.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.979+771_979+782dup others(12): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | |||||
chr14:73883188
|
C | CTTTTTTT others(6): Show |
4 | a0001c0001t0004g0029a0001c0001t0004g0045a0001c0001t0004g0048others(1): Show | 4 | HG00544.hp2 HG02132.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.979+770_979+782dup others(13): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | |||||
chr14:73883188
|
C | CTTTTTTT others(7): Show |
2 | a0001c0001t0004g0053a0001c0001t0004g0071 | 2 | HG02717.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.979+769_979+782dup others(14): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | |||||
chr14:73883188
|
C | CTTTTTTT others(8): Show |
2 | a0001c0001t0004g0044a0001c0001t0004g0074 | 2 | HG02559.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.979+768_979+782dup others(15): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | |||||
chr14:73883188
|
C | CTTTTTTT others(9): Show |
1 | a0001c0001t0004g0059 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.979+767_979+782dup others(16): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | |||||
chr14:73883188
|
C | CTTTTTTT others(11): Show |
1 | a0001c0001t0004g0036 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.979+765_979+782dup others(18): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | |||||
chr14:73883188
|
C | CTTTTTTT others(12): Show |
4 | a0001c0001t0002g0345a0001c0001t0004g0064a0001c0001t0004g0073others(1): Show | 4 | HG02258.hp2 HG03139.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.979+764_979+782dup others(19): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | |||||
chr14:73883188
|
C | CTTTTTTT others(13): Show |
4 | a0001c0001t0004g0042a0001c0001t0004g0055a0001c0001t0004g0056others(1): Show | 4 | HG00099.hp2 HG00738.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.979+763_979+782dup others(20): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | |||||
chr14:73883188
|
CT | C | 40 | a0001c0001t0004g0031a0001c0001t0004g0032a0001c0001t0004g0061others(37): Show | 43 | HG00280.hp1 HG01074.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.979+782delT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | |||||
chr14:73883188
|
CTT | C | 40 | a0001c0001t0004g0049a0001c0001t0004g0060a0001c0001t0004g0069others(37): Show | 44 | HG00639.hp2 HG00741.hp1 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.979+781_979+782del others(2): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | |||||
chr14:73883188
|
CTTT | C | 9 | a0001c0001t0002g0348a0001c0001t0004g0057a0001c0001t0004g0058others(6): Show | 9 | HG00323.hp1 HG00741.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.979+780_979+782del others(3): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | |||||
chr14:73883188
|
CTTTTTTT others(3): Show |
C | 7 | a0001c0001t0002g0309a0001c0002t0001g0291a0001c0002t0001g0292others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.979+773_979+782del others(10): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | |||||
chr14:73883188
|
CTTTTTTT others(4): Show |
C | 8 | a0001c0002t0001g0216a0001c0002t0001g0218a0001c0002t0001g0219others(5): Show | 8 | HG01243.hp1 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.979+772_979+782del others(11): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | |||||
chr14:73883188
|
CTTTTTTT others(5): Show |
C | 6 | a0001c0001t0003g0004a0001c0001t0003g0081a0001c0001t0004g0037others(3): Show | 8 | HG01109.hp1 HG02451.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.979+771_979+782del others(12): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | |||||
chr14:73883188
|
CTTTTTTT others(6): Show |
C | 55 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0009others(52): Show | 67 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.979+770_979+782del others(13): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | |||||
chr14:73883188
|
CTTTTTTT others(7): Show |
C | 2 | a0001c0001t0003g0099a0001c0001t0003g0107 | 2 | HG01975.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.979+769_979+782del others(14): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | |||||
chr14:73883188
|
CTTTTTTT others(8): Show |
C | 2 | a0001c0001t0011g0134a0001c0002t0001g0238 | 2 | HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.979+768_979+782del others(15): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | |||||
chr14:73883189
|
T | C | 4 | a0001c0002t0001g0226a0001c0002t0001g0227a0001c0002t0001g0232others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.979+751T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | chr14 | 73883189 | ||||||
chr14:73883360
|
CT | C | 190 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(187): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.980-727delT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883360 | |||||
chr14:73883431
|
T | C | 1 | a0001c0001t0014g0133 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.980-670T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | chr14 | 73883431 | ||||||
chr14:73883446
|
A | G | 77 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(74): Show | 90 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.980-655A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | chr14 | 73883446 | ||||||
chr14:73883524
|
C | T | 77 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(74): Show | 90 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.980-577C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | chr14 | 73883524 | ||||||
chr14:73883602
|
T | G | 2 | a0001c0001t0012g0369a0001c0001t0013g0370 | 2 | HG01243.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.980-499T>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | chr14 | 73883602 | ||||||
chr14:73883610
|
C | T | 77 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(74): Show | 90 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.980-491C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | chr14 | 73883610 | ||||||
chr14:73883935
|
G | A | 77 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0022others(74): Show | 90 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.980-166G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | chr14 | 73883935 | ||||||
chr14:73884091
|
CTT | C | 6 | a0001c0002t0007g0006a0001c0002t0007g0174a0001c0002t0007g0175others(3): Show | 8 | HG01109.hp2 HG01496.hp1 HG02145.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.980-6_980-5delTT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73884091 |