geneid | 5737 |
---|---|
ensemblid | ENSG00000122420.10 |
hgncid | 9600 |
symbol | PTGFR |
name | prostaglandin F receptor |
refseq_nuc | NM_000959.4 |
refseq_prot | NP_000950.1 |
ensembl_nuc | ENST00000370757.8 |
ensembl_prot | ENSP00000359793.3 |
mane_status | MANE Select |
chr | chr1 |
start | 78490974 |
end | 78540701 |
strand | + |
ver | v1.2 |
region | chr1:78490974-78540701 |
region5000 | chr1:78485974-78545701 |
regionname0 | PTGFR_chr1_78490974_78540701 |
regionname5000 | PTGFR_chr1_78485974_78545701 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 359 | 375 | 89 | 68 | 161 | 14 | 41 | 122 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0002 | 0/0 | 359 | 6 | 0 | 0 | 6 | 0 | 0 | 6 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0003 | 0/0 | 359 | 4 | 0 | 0 | 1 | 0 | 3 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0004 | 0/0 | 359 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1080 | 351 | 72 | 64 | 161 | 13 | 39 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
c0002 | 0/0 | 1080 | 16 | 16 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
c0003 | 0/0 | 1080 | 8 | 1 | 4 | 0 | 1 | 2 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
c0004 | 0/0 | 1080 | 6 | 0 | 0 | 6 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
c0005 | 0/0 | 1080 | 4 | 0 | 0 | 1 | 0 | 3 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
c0006 | 0/0 | 1080 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 4350 | 272 | 43 | 50 | 131 | 9 | 37 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
t0002 | 0/0 | 4349 | 29 | 17 | 8 | 2 | 1 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
t0003 | 0/0 | 4350 | 26 | 0 | 0 | 26 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
t0004 | 0/0 | 4356 | 12 | 3 | 7 | 0 | 0 | 2 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
t0005 | 0/0 | 4350 | 5 | 2 | 0 | 2 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
t0006 | 0/0 | 4355 | 5 | 0 | 1 | 0 | 2 | 2 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
t0007 | 0/0 | 4356 | 4 | 4 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
t0008 | 0/0 | 4354 | 3 | 2 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
t0009 | 0/0 | 4356 | 3 | 3 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
t0010 | 0/0 | 4350 | 2 | 0 | 0 | 2 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
t0011 | 0/0 | 4351 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
t0012 | 0/0 | 4350 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
t0013 | 0/0 | 4350 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
t0014 | 0/0 | 4350 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
t0015 | 0/0 | 4350 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
t0016 | 0/0 | 4350 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
t0017 | 0/0 | 4350 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
t0018 | 0/0 | 4350 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
t0019 | 0/0 | 4349 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
t0020 | 0/0 | 4350 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
t0021 | 0/0 | 4354 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
t0022 | 0/0 | 4355 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
t0023 | 0/0 | 4355 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
t0024 | 0/0 | 4355 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
t0025 | 0/0 | 4356 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
t0026 | 0/0 | 4355 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
t0027 | 0/0 | 4354 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
t0028 | 0/0 | 4356 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
t0029 | 0/0 | 4356 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
t0030 | 0/0 | 4349 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
t0031 | 0/0 | 4354 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
t0032 | 0/0 | 4355 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
t0033 | 0/0 | 4350 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
t0034 | 0/0 | 4350 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
t0035 | 0/0 | 4350 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0006 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0178 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0244 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1080 | 351 | 72 | 64 | 161 | 13 | 39 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0001c0002 | 0/0 | 1080 | 16 | 16 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0001c0003 | 0/0 | 1080 | 8 | 1 | 4 | 0 | 1 | 2 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0002c0004 | 0/0 | 1080 | 6 | 0 | 0 | 6 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0003c0005 | 0/0 | 1080 | 4 | 0 | 0 | 1 | 0 | 3 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0004c0006 | 0/0 | 1080 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 5429 | 247 | 31 | 48 | 125 | 8 | 33 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0001c0001t0002 | 0/0 | 5428 | 25 | 16 | 6 | 2 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0001c0001t0003 | 0/0 | 5429 | 26 | 0 | 0 | 26 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0001c0001t0004 | 0/0 | 5435 | 12 | 3 | 7 | 0 | 0 | 2 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0001c0001t0005 | 0/0 | 5429 | 5 | 2 | 0 | 2 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0001c0001t0006 | 0/0 | 5434 | 5 | 0 | 1 | 0 | 2 | 2 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0001c0001t0007 | 0/0 | 5435 | 4 | 4 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0001c0001t0008 | 0/0 | 5433 | 3 | 2 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0001c0001t0009 | 0/0 | 5435 | 3 | 3 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0001c0001t0010 | 0/0 | 5429 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0001c0001t0011 | 0/0 | 5430 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0001c0001t0012 | 0/0 | 5429 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0001c0001t0013 | 0/0 | 5429 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0001c0001t0014 | 0/0 | 5429 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0001c0001t0015 | 0/0 | 5429 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0001c0001t0016 | 0/0 | 5429 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0001c0001t0017 | 0/0 | 5429 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0001c0001t0018 | 0/0 | 5429 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0001c0001t0019 | 0/0 | 5428 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0001c0001t0020 | 0/0 | 5429 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0001c0001t0021 | 0/0 | 5433 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0001c0001t0023 | 0/0 | 5434 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0001c0001t0026 | 0/0 | 5434 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0001c0001t0027 | 0/0 | 5433 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0001c0001t0028 | 0/0 | 5435 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0001c0001t0029 | 0/0 | 5435 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0001c0001t0030 | 0/0 | 5428 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0001c0001t0033 | 0/0 | 5429 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0001c0001t0034 | 0/0 | 5429 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0001c0001t0035 | 0/0 | 5429 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0001c0002t0001 | 0/0 | 5429 | 11 | 11 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0001c0002t0002 | 0/0 | 5428 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0001c0002t0022 | 0/0 | 5434 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0001c0002t0024 | 0/0 | 5434 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0001c0002t0025 | 0/0 | 5435 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0001c0002t0031 | 0/0 | 5433 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0001c0003t0001 | 0/0 | 5429 | 6 | 1 | 2 | 0 | 1 | 2 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0001c0003t0002 | 0/0 | 5428 | 2 | 0 | 2 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0002c0004t0001 | 0/0 | 5429 | 6 | 0 | 0 | 6 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0003c0005t0001 | 0/0 | 5429 | 2 | 0 | 0 | 0 | 0 | 2 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0003c0005t0002 | 0/0 | 5428 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0003c0005t0010 | 0/0 | 5429 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
a0004c0006t0032 | 0/0 | 5434 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | copy fasta | chr1 | 78485974 | 78545701 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0178 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0244 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0003g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0004g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0004g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0004g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0004g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0004g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0004g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0004g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0005g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0005g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0005g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0005g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0006g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0006g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0006g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0006g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0007g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0007g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0007g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0007g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0008g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0008g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0008g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0009g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0009g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0009g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0010g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0011g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0012g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0013g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0014g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0015g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0016g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0017g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0018g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0019g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0020g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0021g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0023g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0026g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0027g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0028g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0029g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0030g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0033g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0034g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0001t0035g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0002t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0002t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0002t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0002t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0002t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0002t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0002t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0002t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0002t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0002t0022g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0002t0024g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0002t0025g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0002t0031g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0003t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0003t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0003t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0003t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0003t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0003t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0001c0003t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0002c0004t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0002c0004t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0002c0004t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0002c0004t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0002c0004t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0002c0004t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0003c0005t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0003c0005t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0003c0005t0010g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
a0004c0006t0032g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0006 | EUR | GBR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | GBR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0293 | EUR | GBR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG00140 | hp2 | a0001 | c0001 | t0006 | g0025 | EUR | GBR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0041 | EUR | FIN | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0155 | EUR | FIN | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | CHS | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | CHS | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG00597 | hp1 | a0001 | c0001 | t0018 | g0150 | EAS | CHS | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0255 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG00642 | hp1 | a0001 | c0003 | t0001 | g0246 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG00741 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01069 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01071 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0301 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01168 | hp1 | a0001 | c0001 | t0028 | g0295 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0080 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01175 | hp2 | a0001 | c0001 | t0004 | g0199 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01255 | hp1 | a0001 | c0003 | t0002 | g0006 | AMR | CLM | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | CLM | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | CLM | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | CLM | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01358 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | CLM | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01358 | hp2 | a0001 | c0003 | t0001 | g0269 | AMR | CLM | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01433 | hp1 | a0001 | c0003 | t0002 | g0006 | AMR | CLM | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01496 | hp2 | a0001 | c0001 | t0004 | g0318 | AMR | CLM | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01515 | hp1 | a0001 | c0003 | t0001 | g0283 | EUR | IBS | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0044 | EUR | IBS | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0157 | EUR | IBS | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | IBS | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0300 | AFR | ACB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01891 | hp1 | a0001 | c0001 | t0007 | g0345 | AFR | ACB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0077 | AFR | ACB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01978 | hp2 | a0001 | c0001 | t0004 | g0314 | AMR | PEL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01981 | hp2 | a0001 | c0001 | t0006 | g0025 | AMR | PEL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | KHV | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02055 | hp1 | a0001 | c0002 | t0001 | g0334 | AFR | ACB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0325 | AFR | ACB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0216 | EAS | KHV | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02129 | hp2 | a0003 | c0005 | t0010 | g0288 | EAS | KHV | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CDX | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CDX | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | CDX | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02258 | hp2 | a0001 | c0001 | t0026 | g0261 | AFR | ACB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0317 | AMR | PEL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PEL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0231 | AFR | ACB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | ACB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | KHV | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02602 | hp2 | a0001 | c0001 | t0006 | g0251 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02647 | hp1 | a0001 | c0001 | t0012 | g0114 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02647 | hp2 | a0001 | c0002 | t0002 | g0333 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02683 | hp1 | a0001 | c0001 | t0008 | g0341 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0304 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0296 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02717 | hp1 | a0001 | c0001 | t0008 | g0343 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0321 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0340 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02809 | hp1 | a0001 | c0001 | t0009 | g0088 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02809 | hp2 | a0001 | c0001 | t0023 | g0260 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02818 | hp1 | a0001 | c0002 | t0001 | g0026 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02818 | hp2 | a0001 | c0001 | t0007 | g0287 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02886 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02896 | hp1 | a0001 | c0001 | t0009 | g0089 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | ESN | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02922 | hp2 | a0001 | c0001 | t0013 | g0084 | AFR | ESN | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0338 | AFR | ESN | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02965 | hp2 | a0001 | c0001 | t0021 | g0286 | AFR | ESN | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0079 | AFR | ESN | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0326 | AFR | ESN | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0320 | AFR | ESN | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0254 | AFR | ESN | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03017 | hp2 | a0001 | c0003 | t0001 | g0272 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0289 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | ESN | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03130 | hp2 | a0001 | c0001 | t0005 | g0103 | AFR | ESN | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03139 | hp1 | a0001 | c0002 | t0001 | g0336 | AFR | ESN | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | ESN | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03195 | hp1 | a0001 | c0001 | t0005 | g0346 | AFR | ESN | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | ESN | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03209 | hp1 | a0001 | c0002 | t0025 | g0327 | AFR | MSL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0342 | AFR | MSL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | MSL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03453 | hp2 | a0001 | c0001 | t0011 | g0245 | AFR | MSL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03486 | hp1 | a0001 | c0001 | t0009 | g0092 | AFR | MSL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03486 | hp2 | a0001 | c0002 | t0001 | g0328 | AFR | MSL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03490 | hp2 | a0003 | c0005 | t0002 | g0282 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03491 | hp1 | a0003 | c0005 | t0001 | g0024 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03492 | hp2 | a0003 | c0005 | t0001 | g0024 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03516 | hp2 | a0001 | c0001 | t0029 | g0339 | AFR | ESN | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03540 | hp1 | a0001 | c0001 | t0030 | g0248 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03579 | hp1 | a0001 | c0001 | t0016 | g0247 | AFR | MSL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03579 | hp2 | a0001 | c0002 | t0031 | g0322 | AFR | MSL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03688 | hp1 | a0001 | c0001 | t0004 | g0315 | SAS | STU | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | STU | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | BEB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | BEB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | BEB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | BEB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03927 | hp2 | a0001 | c0001 | t0006 | g0250 | SAS | BEB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0319 | SAS | BEB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03942 | hp2 | a0001 | c0003 | t0001 | g0274 | SAS | BEB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG04115 | hp1 | a0001 | c0001 | t0005 | g0131 | SAS | STU | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG04115 | hp2 | a0001 | c0001 | t0004 | g0313 | SAS | STU | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | STU | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | STU | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | STU | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | STU | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0312 | SAS | STU | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | STU | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18522 | hp1 | a0001 | c0002 | t0001 | g0335 | AFR | YRI | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18522 | hp2 | a0004 | c0006 | t0032 | g0143 | AFR | YRI | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | CHB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18906 | hp1 | a0001 | c0001 | t0014 | g0294 | AFR | YRI | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | YRI | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0226 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18947 | hp1 | a0002 | c0004 | t0001 | g0161 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18956 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18963 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18968 | hp2 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18970 | hp1 | a0001 | c0001 | t0010 | g0239 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18972 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18977 | hp2 | a0002 | c0004 | t0001 | g0075 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18982 | hp1 | a0002 | c0004 | t0001 | g0235 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18983 | hp2 | a0001 | c0001 | t0033 | g0204 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18984 | hp2 | a0001 | c0001 | t0017 | g0164 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18989 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19012 | hp1 | a0002 | c0004 | t0001 | g0203 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19030 | hp1 | a0001 | c0003 | t0001 | g0273 | AFR | LWK | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19030 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | LWK | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | LWK | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19043 | hp2 | a0001 | c0001 | t0007 | g0083 | AFR | LWK | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19059 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19059 | hp2 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19070 | hp2 | a0002 | c0004 | t0001 | g0177 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19075 | hp2 | a0001 | c0001 | t0034 | g0307 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19077 | hp1 | a0001 | c0001 | t0020 | g0039 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19080 | hp2 | a0001 | c0001 | t0005 | g0128 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19085 | hp1 | a0001 | c0001 | t0003 | g0316 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19085 | hp2 | a0001 | c0001 | t0005 | g0130 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19088 | hp2 | a0002 | c0004 | t0001 | g0068 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0262 | AFR | YRI | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0323 | AFR | YRI | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ASW | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0331 | AFR | ASW | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA20752 | hp1 | a0001 | c0001 | t0035 | g0264 | EUR | TSI | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA20752 | hp2 | a0001 | c0001 | t0006 | g0311 | EUR | TSI | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0265 | EUR | TSI | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA20805 | hp2 | a0001 | c0001 | t0019 | g0035 | EUR | TSI | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | GIH | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | GIH | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG01123 | hp2 | a0001 | c0001 | t0015 | g0115 | AMR | CLM | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02109 | hp1 | a0001 | c0002 | t0022 | g0329 | AFR | ACB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | ACB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02486 | hp1 | a0001 | c0001 | t0008 | g0344 | AFR | ACB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02486 | hp2 | a0001 | c0001 | t0027 | g0121 | AFR | ACB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02559 | hp1 | a0001 | c0001 | t0004 | g0337 | AFR | ACB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG02559 | hp2 | a0001 | c0002 | t0001 | g0026 | AFR | ACB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03471 | hp1 | a0001 | c0002 | t0024 | g0330 | AFR | MSL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | MSL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG06807 | hp1 | a0001 | c0001 | t0007 | g0277 | AFR | USA | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
HG06807 | hp2 | a0001 | c0002 | t0001 | g0332 | AFR | USA | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | USA | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | USA | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA21309 | hp1 | a0001 | c0001 | t0004 | g0305 | AFR | LWK | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
NA21309 | hp2 | a0001 | c0001 | t0004 | g0063 | AFR | LWK | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0244 | REF | REF | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0178 | REF | REF | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:78492766
|
A | T | 1 | a0003 | 4 | HG02129.hp2 HG03490.hp2 HG03491.hp1 others(1): Show |
missense_variant | MODERATE | c.23A>T | p.Gln8Leu | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/3 | 358/5429 | 23/1080 | 8/359 | chr1 | 78492766 | ||
chr1:78493396
|
T | C | 1 | a0004 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.653T>C | p.Leu218Ser | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/3 | 988/5429 | 653/1080 | 218/359 | chr1 | 78493396 | ||
chr1:78536545
|
A | G | 1 | a0002 | 6 | NA18947.hp1 NA18977.hp2 NA18982.hp1 others(3): Show |
missense_variant | MODERATE | c.938A>G | p.Lys313Arg | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 1273/5429 | 938/1080 | 313/359 | chr1 | 78536545 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:78492806
|
C | T | 1 | a0001c0003 | 8 | HG00642.hp1 HG01255.hp1 HG01358.hp2 others(5): Show |
synonymous_variant | LOW | c.63C>T | p.Thr21Thr | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/3 | 398/5429 | 63/1080 | 21/359 | chr1 | 78492806 | ||
chr1:78493178
|
G | A | 2 | a0001c0002a0004c0006 | 17 | HG02055.hp1 HG02109.hp1 HG02451.hp2 others(14): Show |
synonymous_variant | LOW | c.435G>A | p.Thr145Thr | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/3 | 770/5429 | 435/1080 | 145/359 | chr1 | 78493178 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:78490975
|
C | G | 1 | a0001c0001t0035 | 1 | NA20752.hp1 | 5_prime_UTR_variant | MODIFIER | c.-334C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/3 | 1769 | chr1 | 78490975 | |||||
chr1:78491096
|
G | T | 1 | a0001c0001t0034 | 1 | NA19075.hp2 | 5_prime_UTR_variant | MODIFIER | c.-213G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/3 | 1648 | chr1 | 78491096 | |||||
chr1:78491117
|
A | G | 1 | a0001c0001t0033 | 1 | NA18983.hp2 | 5_prime_UTR_variant | MODIFIER | c.-192A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/3 | 1627 | chr1 | 78491117 | |||||
chr1:78491125
|
C | T | 3 | a0001c0001t0030a0001c0002t0031a0004c0006t0032 | 3 | HG03540.hp1 HG03579.hp2 NA18522.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-184C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/3 | chr1 | 78491125 | ||||||
chr1:78536859
|
C | T | 16 | a0001c0001t0004a0001c0001t0006a0001c0001t0007others(13): Show | 38 | HG00140.hp2 HG00741.hp2 HG01069.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*172C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 172 | chr1 | 78536859 | |||||
chr1:78536904
|
A | G | 14 | a0001c0001t0004a0001c0001t0006a0001c0001t0007others(11): Show | 34 | HG00140.hp2 HG00741.hp2 HG01069.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*217A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 217 | chr1 | 78536904 | |||||
chr1:78537277
|
C | T | 14 | a0001c0001t0004a0001c0001t0006a0001c0001t0007others(11): Show | 34 | HG00140.hp2 HG00741.hp2 HG01069.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*590C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 590 | chr1 | 78537277 | |||||
chr1:78537346
|
G | A | 4 | a0001c0001t0023a0001c0002t0022a0001c0002t0024others(1): Show | 4 | HG02109.hp1 HG02809.hp2 HG03471.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*659G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 659 | chr1 | 78537346 | |||||
chr1:78537458
|
C | T | 1 | a0001c0001t0020 | 1 | NA19077.hp1 | 3_prime_UTR_variant | MODIFIER | c.*771C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 771 | chr1 | 78537458 | |||||
chr1:78537573
|
A | C | 14 | a0001c0001t0004a0001c0001t0006a0001c0001t0007others(11): Show | 34 | HG00140.hp2 HG00741.hp2 HG01069.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*886A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 886 | chr1 | 78537573 | |||||
chr1:78537603
|
A | C | 1 | a0001c0001t0029 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*916A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 916 | chr1 | 78537603 | |||||
chr1:78537613
|
A | G | 1 | a0001c0001t0019 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*926A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 926 | chr1 | 78537613 | |||||
chr1:78537614
|
A | G | 2 | a0001c0001t0003a0001c0001t0005 | 31 | HG00544.hp1 HG02015.hp1 HG02080.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*927A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 927 | chr1 | 78537614 | |||||
chr1:78537670
|
A | G | 16 | a0001c0001t0004a0001c0001t0006a0001c0001t0007others(13): Show | 38 | HG00140.hp2 HG00741.hp2 HG01069.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*983A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 983 | chr1 | 78537670 | |||||
chr1:78537696
|
T | C | 1 | a0001c0002t0022 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1009T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 1009 | chr1 | 78537696 | |||||
chr1:78537704
|
G | A | 1 | a0001c0001t0019 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1017G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 1017 | chr1 | 78537704 | |||||
chr1:78537838
|
C | G | 3 | a0001c0001t0004a0001c0001t0006a0001c0001t0009 | 20 | HG00140.hp2 HG00741.hp2 HG01069.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1151C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 1151 | chr1 | 78537838 | |||||
chr1:78538168
|
A | G | 1 | a0001c0001t0028 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1481A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 1481 | chr1 | 78538168 | |||||
chr1:78538482
|
C | T | 1 | a0001c0001t0018 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1795C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 1795 | chr1 | 78538482 | |||||
chr1:78538532
|
T | TA | 6 | a0001c0001t0011a0001c0001t0023a0001c0001t0026others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG02809.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1858dupA | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 1859 | INFO_REALIGN_3_PRIME | chr1 | 78538532 | ||||
chr1:78538532
|
T | TAA | 7 | a0001c0001t0004a0001c0001t0006a0001c0001t0007others(4): Show | 27 | HG00140.hp2 HG00741.hp2 HG01069.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1857_*1858dupAA | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 1859 | INFO_REALIGN_3_PRIME | chr1 | 78538532 | ||||
chr1:78538532
|
TA | T | 6 | a0001c0001t0002a0001c0001t0019a0001c0001t0030others(3): Show | 31 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1858delA | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 1858 | INFO_REALIGN_3_PRIME | chr1 | 78538532 | ||||
chr1:78538670
|
T | C | 1 | a0001c0001t0012 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1983T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 1983 | chr1 | 78538670 | |||||
chr1:78538696
|
T | C | 1 | a0001c0001t0013 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2009T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 2009 | chr1 | 78538696 | |||||
chr1:78538725
|
C | T | 1 | a0001c0001t0009 | 3 | HG02809.hp1 HG02896.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2038C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 2038 | chr1 | 78538725 | |||||
chr1:78538789
|
C | T | 14 | a0001c0001t0004a0001c0001t0006a0001c0001t0007others(11): Show | 34 | HG00140.hp2 HG00741.hp2 HG01069.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*2102C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 2102 | chr1 | 78538789 | |||||
chr1:78538827
|
T | G | 14 | a0001c0001t0004a0001c0001t0006a0001c0001t0007others(11): Show | 34 | HG00140.hp2 HG00741.hp2 HG01069.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*2140T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 2140 | chr1 | 78538827 | |||||
chr1:78538833
|
C | G | 1 | a0001c0001t0013 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2146C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 2146 | chr1 | 78538833 | |||||
chr1:78538891
|
A | C | 1 | a0001c0001t0017 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2204A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 2204 | chr1 | 78538891 | |||||
chr1:78539032
|
T | G | 1 | a0001c0001t0014 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2345T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 2345 | chr1 | 78539032 | |||||
chr1:78539063
|
A | AAGAT | 16 | a0001c0001t0004a0001c0001t0006a0001c0001t0007others(13): Show | 38 | HG00140.hp2 HG00741.hp2 HG01069.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2378_*2381dupGATA | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 2382 | INFO_REALIGN_3_PRIME | chr1 | 78539063 | ||||
chr1:78539091
|
G | T | 1 | a0001c0002t0024 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2404G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 2404 | chr1 | 78539091 | |||||
chr1:78539200
|
A | G | 1 | a0001c0001t0016 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2513A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 2513 | chr1 | 78539200 | |||||
chr1:78539235
|
T | C | 14 | a0001c0001t0004a0001c0001t0006a0001c0001t0007others(11): Show | 34 | HG00140.hp2 HG00741.hp2 HG01069.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*2548T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 2548 | chr1 | 78539235 | |||||
chr1:78539618
|
G | A | 1 | a0001c0001t0015 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2931G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 2931 | chr1 | 78539618 | |||||
chr1:78539639
|
G | T | 1 | a0001c0001t0021 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2952G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 2952 | chr1 | 78539639 | |||||
chr1:78539654
|
T | G | 2 | a0001c0001t0008a0001c0001t0021 | 4 | HG02486.hp1 HG02683.hp1 HG02717.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2967T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 2967 | chr1 | 78539654 | |||||
chr1:78539704
|
T | A | 2 | a0001c0001t0010a0003c0005t0010 | 2 | HG02129.hp2 NA18970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3017T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 3017 | chr1 | 78539704 | |||||
chr1:78539796
|
C | T | 2 | a0001c0001t0005a0001c0001t0011 | 6 | HG03130.hp2 HG03195.hp1 HG03453.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3109C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 3109 | chr1 | 78539796 | |||||
chr1:78539799
|
G | A | 10 | a0001c0001t0004a0001c0001t0006a0001c0001t0007others(7): Show | 30 | HG00140.hp2 HG00741.hp2 HG01069.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*3112G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 3112 | chr1 | 78539799 | |||||
chr1:78539863
|
C | T | 2 | a0001c0001t0008a0001c0001t0021 | 4 | HG02486.hp1 HG02683.hp1 HG02717.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3176C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 3176 | chr1 | 78539863 | |||||
chr1:78539866
|
T | C | 10 | a0001c0001t0004a0001c0001t0006a0001c0001t0007others(7): Show | 30 | HG00140.hp2 HG00741.hp2 HG01069.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*3179T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 3179 | chr1 | 78539866 | |||||
chr1:78540023
|
GA | G | 1 | a0001c0001t0006 | 5 | HG00140.hp2 HG01981.hp2 HG02602.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3339delA | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 3339 | INFO_REALIGN_3_PRIME | chr1 | 78540023 | ||||
chr1:78540082
|
T | A | 1 | a0001c0001t0029 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3395T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 3395 | chr1 | 78540082 | |||||
chr1:78540113
|
T | C | 16 | a0001c0001t0004a0001c0001t0006a0001c0001t0007others(13): Show | 38 | HG00140.hp2 HG00741.hp2 HG01069.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*3426T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 3426 | chr1 | 78540113 | |||||
chr1:78540185
|
A | G | 2 | a0001c0001t0007a0001c0001t0027 | 5 | HG01891.hp1 HG02486.hp2 HG02818.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3498A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 3498 | chr1 | 78540185 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:78491506
|
C | G | 1 | a0001c0001t0005g0346 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-73+270C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/2 | chr1 | 78491506 | ||||||
chr1:78491557
|
C | T | 7 | a0001c0001t0001g0010a0001c0001t0001g0340a0001c0001t0001g0342others(4): Show | 9 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-73+321C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/2 | chr1 | 78491557 | ||||||
chr1:78491646
|
T | C | 1 | a0001c0001t0001g0027 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-73+410T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/2 | chr1 | 78491646 | ||||||
chr1:78491670
|
G | T | 1 | a0001c0001t0005g0346 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-73+434G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/2 | chr1 | 78491670 | ||||||
chr1:78491690
|
A | T | 3 | a0001c0001t0001g0338a0001c0001t0004g0337a0001c0001t0029g0339 | 3 | HG02559.hp1 HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-73+454A>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/2 | chr1 | 78491690 | ||||||
chr1:78491713
|
T | G | 1 | a0001c0001t0001g0028 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-73+477T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/2 | chr1 | 78491713 | ||||||
chr1:78491727
|
G | A | 2 | a0001c0001t0001g0340a0001c0001t0008g0341 | 2 | HG02683.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.-73+491G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/2 | chr1 | 78491727 | ||||||
chr1:78491756
|
C | A | 124 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(121): Show | 141 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.-73+520C>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/2 | chr1 | 78491756 | ||||||
chr1:78491784
|
G | A | 3 | a0001c0001t0001g0129a0001c0001t0005g0130a0001c0001t0005g0131 | 3 | HG00621.hp2 HG04115.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-73+548G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/2 | chr1 | 78491784 | ||||||
chr1:78491865
|
G | A | 63 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(60): Show | 65 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.-73+629G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/2 | chr1 | 78491865 | ||||||
chr1:78492055
|
C | G | 12 | a0001c0002t0001g0009a0001c0002t0001g0026a0001c0002t0001g0328others(9): Show | 15 | HG02055.hp1 HG02109.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.-72-617C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/2 | chr1 | 78492055 | ||||||
chr1:78492065
|
A | C | 4 | a0001c0001t0001g0324a0001c0001t0002g0323a0001c0001t0002g0325others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-72-607A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/2 | chr1 | 78492065 | ||||||
chr1:78492174
|
G | T | 45 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(42): Show | 58 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.-72-498G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/2 | chr1 | 78492174 | ||||||
chr1:78492253
|
G | T | 1 | a0001c0002t0031g0322 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-72-419G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/2 | chr1 | 78492253 | ||||||
chr1:78492256
|
C | T | 3 | a0001c0001t0001g0340a0001c0001t0007g0345a0001c0001t0008g0341 | 3 | HG01891.hp1 HG02683.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.-72-416C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/2 | chr1 | 78492256 | ||||||
chr1:78492293
|
G | T | 2 | a0001c0001t0002g0320a0001c0001t0002g0321 | 2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-72-379G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/2 | chr1 | 78492293 | ||||||
chr1:78492402
|
T | C | 1 | a0001c0002t0031g0322 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-72-270T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/2 | chr1 | 78492402 | ||||||
chr1:78492592
|
C | T | 21 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0303others(18): Show | 27 | HG00140.hp2 HG00558.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.-72-80C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/2 | chr1 | 78492592 | ||||||
chr1:78493551
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.798+10T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78493551 | ||||||
chr1:78493598
|
G | C | 1 | a0001c0001t0001g0029 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.798+57G>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78493598 | ||||||
chr1:78493869
|
A | G | 1 | a0001c0001t0001g0302 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.798+328A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78493869 | ||||||
chr1:78493887
|
G | GT | 38 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0292others(35): Show | 44 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.798+347dupT | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78493887 | |||||
chr1:78493928
|
A | T | 3 | a0001c0001t0001g0129a0001c0001t0005g0130a0001c0001t0005g0131 | 3 | HG00621.hp2 HG04115.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.798+387A>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78493928 | ||||||
chr1:78494001
|
A | G | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.798+460A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78494001 | ||||||
chr1:78494029
|
G | A | 5 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(2): Show | 5 | HG02074.hp1 NA18969.hp2 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.798+488G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78494029 | ||||||
chr1:78494249
|
T | C | 5 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(2): Show | 5 | HG01071.hp1 HG01243.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.798+708T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78494249 | ||||||
chr1:78494314
|
T | C | 2 | a0001c0002t0031g0322a0004c0006t0032g0143 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.798+773T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78494314 | ||||||
chr1:78494326
|
G | T | 1 | a0001c0001t0002g0289 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.798+785G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78494326 | ||||||
chr1:78494369
|
CA | C | 7 | a0001c0001t0001g0010a0001c0001t0001g0340a0001c0001t0001g0342others(4): Show | 9 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.798+836delA | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78494369 | |||||
chr1:78494573
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.798+1032G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78494573 | ||||||
chr1:78494591
|
G | T | 2 | a0001c0002t0031g0322a0004c0006t0032g0143 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.798+1050G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78494591 | ||||||
chr1:78494600
|
T | TTTTG | 12 | a0001c0002t0001g0009a0001c0002t0001g0026a0001c0002t0001g0328others(9): Show | 15 | HG02055.hp1 HG02109.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.798+1080_798+1083d others(6): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78494600 | |||||
chr1:78494659
|
A | G | 242 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(239): Show | 273 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.798+1118A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78494659 | ||||||
chr1:78494692
|
G | A | 4 | a0001c0002t0001g0328a0001c0002t0022g0329a0001c0002t0024g0330others(1): Show | 4 | HG02109.hp1 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.798+1151G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78494692 | ||||||
chr1:78494824
|
T | C | 2 | a0001c0002t0031g0322a0004c0006t0032g0143 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.798+1283T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78494824 | ||||||
chr1:78494893
|
C | G | 38 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0292others(35): Show | 44 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.798+1352C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78494893 | ||||||
chr1:78494896
|
G | A | 5 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0240others(2): Show | 5 | HG02040.hp2 NA18952.hp2 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.798+1355G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78494896 | ||||||
chr1:78494900
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.798+1359G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78494900 | ||||||
chr1:78495009
|
C | T | 2 | a0001c0002t0031g0322a0004c0006t0032g0143 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.798+1468C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78495009 | ||||||
chr1:78495057
|
G | A | 52 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0292others(49): Show | 61 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.798+1516G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78495057 | ||||||
chr1:78495079
|
G | C | 2 | a0001c0002t0031g0322a0004c0006t0032g0143 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.798+1538G>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78495079 | ||||||
chr1:78495224
|
G | C | 1 | a0001c0001t0001g0303 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.798+1683G>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78495224 | ||||||
chr1:78495256
|
A | C | 3 | a0001c0002t0001g0328a0001c0002t0022g0329a0001c0002t0024g0330 | 3 | HG02109.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.798+1715A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78495256 | ||||||
chr1:78495511
|
AT | A | 16 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(13): Show | 16 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.798+1971delT | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78495511 | ||||||
chr1:78495635
|
T | G | 1 | a0001c0001t0003g0162 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.798+2094T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78495635 | ||||||
chr1:78495759
|
T | C | 44 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0292others(41): Show | 53 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.798+2218T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78495759 | ||||||
chr1:78495787
|
C | A | 1 | a0001c0001t0001g0304 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.798+2246C>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78495787 | ||||||
chr1:78495900
|
T | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(171): Show | 201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.798+2359T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78495900 | ||||||
chr1:78495966
|
A | T | 44 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0292others(41): Show | 53 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.798+2425A>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78495966 | ||||||
chr1:78496005
|
C | A | 44 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0292others(41): Show | 53 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.798+2464C>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78496005 | ||||||
chr1:78496016
|
A | G | 21 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0303others(18): Show | 27 | HG00140.hp2 HG00558.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.798+2475A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78496016 | ||||||
chr1:78496060
|
G | T | 3 | a0001c0001t0002g0080a0001c0001t0002g0081a0001c0001t0002g0082 | 3 | HG01167.hp2 HG01169.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.798+2519G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78496060 | ||||||
chr1:78496215
|
G | A | 7 | a0001c0001t0001g0010a0001c0001t0001g0340a0001c0001t0001g0342others(4): Show | 9 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.798+2674G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78496215 | ||||||
chr1:78496320
|
A | G | 2 | a0001c0002t0031g0322a0004c0006t0032g0143 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.798+2779A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78496320 | ||||||
chr1:78496372
|
T | G | 1 | a0001c0001t0001g0242 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.798+2831T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78496372 | ||||||
chr1:78496430
|
A | G | 2 | a0001c0002t0031g0322a0004c0006t0032g0143 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.798+2889A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78496430 | ||||||
chr1:78496447
|
A | G | 6 | a0001c0001t0001g0129a0001c0001t0001g0234a0001c0001t0001g0236others(3): Show | 6 | HG00621.hp2 HG04115.hp1 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.798+2906A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78496447 | ||||||
chr1:78496448
|
T | C | 1 | a0001c0001t0001g0029 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.798+2907T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78496448 | ||||||
chr1:78496555
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.798+3014G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78496555 | ||||||
chr1:78496595
|
G | A | 7 | a0001c0001t0001g0010a0001c0001t0001g0340a0001c0001t0001g0342others(4): Show | 9 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.798+3054G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78496595 | ||||||
chr1:78496667
|
T | C | 2 | a0001c0002t0031g0322a0004c0006t0032g0143 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.798+3126T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78496667 | ||||||
chr1:78496724
|
A | G | 1 | a0003c0005t0010g0288 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.798+3183A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78496724 | ||||||
chr1:78496826
|
A | C | 1 | a0001c0001t0001g0299 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.798+3285A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78496826 | ||||||
chr1:78496839
|
T | C | 2 | a0001c0002t0031g0322a0004c0006t0032g0143 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.798+3298T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78496839 | ||||||
chr1:78496936
|
T | TA | 8 | a0001c0002t0001g0009a0001c0002t0001g0026a0001c0002t0001g0331others(5): Show | 11 | HG02055.hp1 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.798+3396dupA | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78496936 | |||||
chr1:78496938
|
T | A | 8 | a0001c0002t0001g0009a0001c0002t0001g0026a0001c0002t0001g0331others(5): Show | 11 | HG02055.hp1 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.798+3397T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78496938 | ||||||
chr1:78496940
|
T | A | 8 | a0001c0002t0001g0009a0001c0002t0001g0026a0001c0002t0001g0331others(5): Show | 11 | HG02055.hp1 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.798+3399T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78496940 | ||||||
chr1:78496949
|
C | T | 1 | a0001c0002t0025g0327 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.798+3408C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78496949 | ||||||
chr1:78496953
|
G | A | 1 | a0001c0001t0001g0003 | 3 | NA18974.hp2 NA19007.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.798+3412G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78496953 | ||||||
chr1:78496989
|
G | T | 4 | a0001c0002t0001g0328a0001c0002t0022g0329a0001c0002t0024g0330others(1): Show | 4 | HG02109.hp1 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.798+3448G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78496989 | ||||||
chr1:78497065
|
A | G | 2 | a0001c0001t0001g0232a0001c0001t0001g0233 | 2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.798+3524A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78497065 | ||||||
chr1:78497170
|
G | A | 3 | a0001c0002t0001g0328a0001c0002t0022g0329a0001c0002t0024g0330 | 3 | HG02109.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.798+3629G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78497170 | ||||||
chr1:78497285
|
C | T | 1 | a0001c0002t0024g0330 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.798+3744C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78497285 | ||||||
chr1:78497318
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.798+3777C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78497318 | ||||||
chr1:78497620
|
A | C | 46 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0292others(43): Show | 55 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.798+4079A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78497620 | ||||||
chr1:78497658
|
T | C | 1 | a0001c0002t0025g0327 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.798+4117T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78497658 | ||||||
chr1:78497752
|
G | A | 52 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0292others(49): Show | 61 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.798+4211G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78497752 | ||||||
chr1:78497798
|
C | T | 1 | a0001c0001t0005g0128 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.798+4257C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78497798 | ||||||
chr1:78497879
|
C | T | 4 | a0001c0002t0001g0328a0001c0002t0022g0329a0001c0002t0024g0330others(1): Show | 4 | HG02109.hp1 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.798+4338C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78497879 | ||||||
chr1:78498027
|
T | A | 7 | a0001c0001t0001g0010a0001c0001t0001g0340a0001c0001t0001g0342others(4): Show | 9 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.798+4486T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78498027 | ||||||
chr1:78498611
|
T | A | 46 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0292others(43): Show | 55 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.798+5070T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78498611 | ||||||
chr1:78498713
|
A | C | 1 | a0001c0001t0009g0092 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.798+5172A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78498713 | ||||||
chr1:78498857
|
T | G | 52 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0292others(49): Show | 61 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.798+5316T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78498857 | ||||||
chr1:78499025
|
C | T | 21 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0303others(18): Show | 27 | HG00140.hp2 HG00558.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.798+5484C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78499025 | ||||||
chr1:78499136
|
A | G | 243 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 273 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.798+5595A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78499136 | ||||||
chr1:78499195
|
G | C | 1 | a0001c0001t0001g0094 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.798+5654G>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78499195 | ||||||
chr1:78499207
|
CTCTT | C | 4 | a0001c0002t0001g0328a0001c0002t0022g0329a0001c0002t0024g0330others(1): Show | 4 | HG02109.hp1 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.798+5671_798+5674d others(6): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78499207 | |||||
chr1:78499337
|
A | G | 1 | a0002c0004t0001g0161 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.798+5796A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78499337 | ||||||
chr1:78499344
|
A | G | 122 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(119): Show | 137 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.798+5803A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78499344 | ||||||
chr1:78499358
|
A | G | 3 | a0001c0001t0002g0077a0001c0001t0002g0078a0001c0001t0002g0079 | 3 | HG01891.hp2 HG02970.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.798+5817A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78499358 | ||||||
chr1:78499390
|
C | T | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.798+5849C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78499390 | ||||||
chr1:78499461
|
T | C | 4 | a0001c0002t0001g0328a0001c0002t0022g0329a0001c0002t0024g0330others(1): Show | 4 | HG02109.hp1 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.798+5920T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78499461 | ||||||
chr1:78499615
|
G | A | 46 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0292others(43): Show | 55 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.798+6074G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78499615 | ||||||
chr1:78499763
|
A | T | 8 | a0001c0002t0001g0009a0001c0002t0001g0026a0001c0002t0001g0331others(5): Show | 11 | HG02055.hp1 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.798+6222A>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78499763 | ||||||
chr1:78499776
|
G | A | 122 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(119): Show | 137 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.798+6235G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78499776 | ||||||
chr1:78500055
|
T | A | 1 | a0001c0001t0001g0129 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.798+6514T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78500055 | ||||||
chr1:78500061
|
A | AT | 48 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0292others(45): Show | 57 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.798+6530dupT | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78500061 | |||||
chr1:78500076
|
T | A | 1 | a0001c0001t0001g0095 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.798+6535T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78500076 | ||||||
chr1:78500093
|
T | A | 56 | a0001c0001t0001g0007a0001c0001t0001g0137a0001c0001t0001g0237others(53): Show | 60 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.798+6552T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78500093 | ||||||
chr1:78500099
|
T | C | 48 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0292others(45): Show | 57 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.798+6558T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78500099 | ||||||
chr1:78500161
|
T | C | 1 | a0001c0001t0004g0305 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.798+6620T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78500161 | ||||||
chr1:78500176
|
G | A | 48 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0292others(45): Show | 57 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.798+6635G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78500176 | ||||||
chr1:78500232
|
C | A | 1 | a0001c0001t0001g0163 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.798+6691C>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78500232 | ||||||
chr1:78500518
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.798+6977C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78500518 | ||||||
chr1:78500650
|
G | A | 8 | a0001c0002t0001g0009a0001c0002t0001g0026a0001c0002t0001g0331others(5): Show | 11 | HG02055.hp1 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.798+7109G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78500650 | ||||||
chr1:78500996
|
A | G | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.798+7455A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78500996 | ||||||
chr1:78501003
|
C | CT | 16 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0296others(13): Show | 16 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.798+7472dupT | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78501003 | |||||
chr1:78501060
|
G | T | 3 | a0001c0001t0009g0088a0001c0001t0009g0089a0001c0001t0009g0092 | 3 | HG02809.hp1 HG02896.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.798+7519G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78501060 | ||||||
chr1:78501117
|
T | G | 2 | a0001c0001t0001g0242a0001c0001t0001g0285 | 2 | HG02630.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.798+7576T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78501117 | ||||||
chr1:78501357
|
A | C | 1 | a0001c0001t0003g0127 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.798+7816A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78501357 | ||||||
chr1:78501467
|
G | C | 1 | a0004c0006t0032g0143 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.798+7926G>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78501467 | ||||||
chr1:78501513
|
T | C | 1 | a0001c0001t0001g0243 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.798+7972T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78501513 | ||||||
chr1:78501520
|
G | A | 2 | a0001c0002t0001g0328a0001c0002t0022g0329 | 2 | HG02109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.798+7979G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78501520 | ||||||
chr1:78501648
|
C | T | 2 | a0001c0002t0031g0322a0004c0006t0032g0143 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.798+8107C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78501648 | ||||||
chr1:78501743
|
C | T | 2 | a0001c0002t0031g0322a0004c0006t0032g0143 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.798+8202C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78501743 | ||||||
chr1:78501783
|
A | G | 4 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(1): Show | 4 | HG02572.hp1 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.798+8242A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78501783 | ||||||
chr1:78501845
|
G | A | 3 | a0001c0002t0001g0328a0001c0002t0022g0329a0001c0002t0024g0330 | 3 | HG02109.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.798+8304G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78501845 | ||||||
chr1:78501963
|
C | A | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | HG03491.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.798+8422C>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78501963 | ||||||
chr1:78501990
|
A | G | 1 | a0001c0001t0003g0126 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.798+8449A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78501990 | ||||||
chr1:78502055
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.798+8514G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78502055 | ||||||
chr1:78502140
|
G | A | 130 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(127): Show | 147 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.798+8599G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78502140 | ||||||
chr1:78502381
|
C | A | 1 | a0001c0001t0001g0165 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.798+8840C>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78502381 | ||||||
chr1:78502637
|
T | A | 21 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0303others(18): Show | 27 | HG00140.hp2 HG00558.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.798+9096T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78502637 | ||||||
chr1:78502656
|
A | G | 36 | a0001c0001t0001g0010a0001c0001t0001g0090a0001c0001t0001g0091others(33): Show | 41 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(38): Show |
intron_variant | MODIFIER | c.798+9115A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78502656 | ||||||
chr1:78502724
|
T | A | 122 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(119): Show | 138 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.798+9183T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78502724 | ||||||
chr1:78502767
|
G | A | 8 | a0001c0002t0001g0009a0001c0002t0001g0026a0001c0002t0001g0331others(5): Show | 11 | HG02055.hp1 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.798+9226G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78502767 | ||||||
chr1:78502824
|
G | A | 1 | a0001c0001t0007g0083 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.798+9283G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78502824 | ||||||
chr1:78502833
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.798+9292C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78502833 | ||||||
chr1:78502846
|
A | C | 1 | a0001c0001t0003g0229 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.798+9305A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78502846 | ||||||
chr1:78502862
|
G | A | 16 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0296others(13): Show | 16 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.798+9321G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78502862 | ||||||
chr1:78502961
|
G | A | 1 | a0001c0001t0001g0244 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.798+9420G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78502961 | ||||||
chr1:78503036
|
C | A | 1 | a0001c0001t0001g0342 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.798+9495C>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78503036 | ||||||
chr1:78503213
|
T | G | 39 | a0001c0001t0001g0010a0001c0001t0001g0090a0001c0001t0001g0091others(36): Show | 44 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(41): Show |
intron_variant | MODIFIER | c.798+9672T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78503213 | ||||||
chr1:78503233
|
T | TAA | 39 | a0001c0001t0001g0010a0001c0001t0001g0090a0001c0001t0001g0091others(36): Show | 44 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(41): Show |
intron_variant | MODIFIER | c.798+9692_798+9693i others(4): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78503233 | ||||||
chr1:78503414
|
A | G | 1 | a0001c0001t0003g0076 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.798+9873A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78503414 | ||||||
chr1:78503609
|
A | G | 16 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0296others(13): Show | 16 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.798+10068A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78503609 | ||||||
chr1:78503712
|
G | A | 2 | a0001c0001t0002g0289a0001c0001t0011g0245 | 2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.798+10171G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78503712 | ||||||
chr1:78503779
|
A | G | 8 | a0001c0002t0001g0009a0001c0002t0001g0026a0001c0002t0001g0331others(5): Show | 11 | HG02055.hp1 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.798+10238A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78503779 | ||||||
chr1:78504078
|
G | A | 22 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0303others(19): Show | 28 | HG00140.hp2 HG00558.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.798+10537G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78504078 | ||||||
chr1:78504082
|
G | C | 1 | a0001c0001t0001g0138 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.798+10541G>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78504082 | ||||||
chr1:78504104
|
C | T | 4 | a0001c0001t0002g0080a0001c0001t0002g0081a0001c0001t0002g0082others(1): Show | 4 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.798+10563C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78504104 | ||||||
chr1:78504189
|
A | G | 1 | a0001c0001t0001g0243 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.798+10648A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78504189 | ||||||
chr1:78504237
|
A | T | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.798+10696A>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78504237 | ||||||
chr1:78504262
|
C | T | 60 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0027others(57): Show | 71 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.798+10721C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78504262 | ||||||
chr1:78504302
|
T | C | 60 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0027others(57): Show | 71 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.798+10761T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78504302 | ||||||
chr1:78504360
|
T | C | 1 | a0001c0001t0005g0346 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.798+10819T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78504360 | ||||||
chr1:78504480
|
T | C | 1 | a0001c0002t0025g0327 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.798+10939T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78504480 | ||||||
chr1:78504677
|
A | G | 1 | a0001c0001t0001g0228 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.798+11136A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78504677 | ||||||
chr1:78504788
|
C | T | 1 | a0001c0002t0001g0336 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.798+11247C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78504788 | ||||||
chr1:78504817
|
C | A | 2 | a0001c0002t0031g0322a0004c0006t0032g0143 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.798+11276C>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78504817 | ||||||
chr1:78504895
|
T | C | 1 | a0001c0003t0001g0246 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.798+11354T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78504895 | ||||||
chr1:78505120
|
C | CT | 138 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(135): Show | 160 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.798+11598dupT | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78505120 | |||||
chr1:78505370
|
A | G | 25 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0296others(22): Show | 28 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.798+11829A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78505370 | ||||||
chr1:78505440
|
A | T | 1 | a0001c0001t0001g0125 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.798+11899A>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78505440 | ||||||
chr1:78505622
|
G | C | 2 | a0001c0002t0031g0322a0004c0006t0032g0143 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.798+12081G>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78505622 | ||||||
chr1:78505742
|
A | G | 17 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(14): Show | 17 | HG00733.hp2 HG01106.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.798+12201A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78505742 | ||||||
chr1:78505772
|
G | A | 6 | a0001c0001t0001g0010a0001c0001t0001g0340a0001c0001t0007g0345others(3): Show | 8 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.798+12231G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78505772 | ||||||
chr1:78505842
|
A | T | 35 | a0001c0001t0001g0010a0001c0001t0001g0090a0001c0001t0001g0091others(32): Show | 40 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.798+12301A>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78505842 | ||||||
chr1:78506004
|
G | T | 1 | a0002c0004t0001g0075 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.798+12463G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78506004 | ||||||
chr1:78506099
|
G | A | 1 | a0001c0001t0019g0035 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.798+12558G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78506099 | ||||||
chr1:78506136
|
T | C | 1 | a0001c0001t0001g0148 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.798+12595T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78506136 | ||||||
chr1:78506158
|
G | A | 1 | a0001c0001t0001g0036 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.798+12617G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78506158 | ||||||
chr1:78506215
|
A | G | 8 | a0001c0002t0001g0009a0001c0002t0001g0026a0001c0002t0001g0331others(5): Show | 11 | HG02055.hp1 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.798+12674A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78506215 | ||||||
chr1:78506242
|
A | C | 57 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0027others(54): Show | 68 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.798+12701A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78506242 | ||||||
chr1:78506434
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.798+12893A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78506434 | ||||||
chr1:78506540
|
AT | A | 4 | a0001c0001t0002g0289a0001c0001t0011g0245a0001c0001t0016g0247others(1): Show | 4 | HG03041.hp1 HG03453.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.798+13006delT | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78506540 | |||||
chr1:78506681
|
A | G | 1 | a0001c0001t0001g0227 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.798+13140A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78506681 | ||||||
chr1:78506833
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.798+13292G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78506833 | ||||||
chr1:78506908
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.798+13367C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78506908 | ||||||
chr1:78506928
|
T | G | 1 | a0001c0002t0025g0327 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.798+13387T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78506928 | ||||||
chr1:78507287
|
G | T | 1 | a0001c0001t0001g0022 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.798+13746G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78507287 | ||||||
chr1:78507343
|
T | C | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.798+13802T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78507343 | ||||||
chr1:78507376
|
C | T | 1 | a0001c0001t0001g0066 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.798+13835C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78507376 | ||||||
chr1:78507390
|
T | C | 122 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(119): Show | 138 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.798+13849T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78507390 | ||||||
chr1:78507391
|
T | G | 21 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0303others(18): Show | 27 | HG00140.hp2 HG00558.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.798+13850T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78507391 | ||||||
chr1:78507712
|
C | T | 2 | a0001c0001t0001g0086a0001c0001t0001g0087 | 2 | HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.798+14171C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78507712 | ||||||
chr1:78508154
|
T | C | 1 | a0001c0001t0001g0022 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.798+14613T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78508154 | ||||||
chr1:78508588
|
C | A | 1 | a0001c0001t0001g0166 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.798+15047C>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78508588 | ||||||
chr1:78508608
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.798+15067A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78508608 | ||||||
chr1:78508805
|
C | T | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.798+15264C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78508805 | ||||||
chr1:78508821
|
G | A | 2 | a0001c0001t0009g0088a0001c0001t0009g0089 | 2 | HG02809.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.798+15280G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78508821 | ||||||
chr1:78508957
|
A | G | 2 | a0001c0001t0003g0225a0001c0001t0003g0226 | 2 | NA18939.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.798+15416A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78508957 | ||||||
chr1:78509050
|
C | G | 8 | a0001c0002t0001g0009a0001c0002t0001g0026a0001c0002t0001g0331others(5): Show | 11 | HG02055.hp1 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.798+15509C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78509050 | ||||||
chr1:78509224
|
G | A | 33 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0292others(30): Show | 36 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.798+15683G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78509224 | ||||||
chr1:78509270
|
G | A | 25 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0296others(22): Show | 28 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.798+15729G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78509270 | ||||||
chr1:78509282
|
C | T | 2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.798+15741C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78509282 | ||||||
chr1:78509347
|
G | A | 1 | a0001c0002t0025g0327 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.798+15806G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78509347 | ||||||
chr1:78509476
|
G | A | 3 | a0001c0001t0001g0338a0001c0001t0004g0337a0001c0001t0029g0339 | 3 | HG02559.hp1 HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.798+15935G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78509476 | ||||||
chr1:78509509
|
T | C | 7 | a0001c0001t0001g0010a0001c0001t0001g0340a0001c0001t0001g0342others(4): Show | 9 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.798+15968T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78509509 | ||||||
chr1:78509539
|
A | T | 3 | a0001c0001t0001g0304a0001c0001t0001g0319a0001c0001t0004g0318 | 3 | HG01496.hp2 HG02683.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.798+15998A>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78509539 | ||||||
chr1:78509593
|
A | G | 1 | a0001c0001t0001g0317 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.798+16052A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78509593 | ||||||
chr1:78509620
|
G | T | 1 | a0001c0001t0001g0222 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.798+16079G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78509620 | ||||||
chr1:78510154
|
C | T | 1 | a0001c0001t0001g0034 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.798+16613C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78510154 | ||||||
chr1:78510170
|
C | A | 2 | a0001c0001t0001g0167a0001c0001t0003g0168 | 2 | NA19058.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.798+16629C>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78510170 | ||||||
chr1:78510177
|
G | A | 1 | a0001c0002t0025g0327 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.798+16636G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78510177 | ||||||
chr1:78510202
|
C | T | 1 | a0001c0001t0001g0221 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.798+16661C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78510202 | ||||||
chr1:78510262
|
G | A | 1 | a0001c0001t0002g0077 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.798+16721G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78510262 | ||||||
chr1:78510322
|
T | A | 1 | a0001c0001t0001g0030 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.798+16781T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78510322 | ||||||
chr1:78510334
|
C | T | 4 | a0001c0001t0001g0242a0001c0001t0001g0285a0001c0001t0007g0287others(1): Show | 4 | HG02630.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.798+16793C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78510334 | ||||||
chr1:78510391
|
G | A | 2 | a0001c0001t0001g0149a0001c0001t0018g0150 | 2 | HG00597.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.798+16850G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78510391 | ||||||
chr1:78510409
|
G | A | 16 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0296others(13): Show | 16 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.798+16868G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78510409 | ||||||
chr1:78510440
|
G | A | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.798+16899G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78510440 | ||||||
chr1:78510525
|
C | G | 9 | a0001c0001t0005g0346a0001c0002t0001g0009a0001c0002t0001g0026others(6): Show | 12 | HG02055.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.798+16984C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78510525 | ||||||
chr1:78510598
|
A | G | 4 | a0001c0001t0001g0242a0001c0001t0001g0285a0001c0001t0007g0287others(1): Show | 4 | HG02630.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.798+17057A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78510598 | ||||||
chr1:78510673
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.798+17132C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78510673 | ||||||
chr1:78510674
|
G | A | 16 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0296others(13): Show | 16 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.798+17133G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78510674 | ||||||
chr1:78510761
|
A | T | 1 | a0001c0001t0001g0030 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.798+17220A>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78510761 | ||||||
chr1:78510885
|
A | G | 245 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(242): Show | 276 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.798+17344A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78510885 | ||||||
chr1:78510929
|
A | G | 2 | a0001c0002t0031g0322a0004c0006t0032g0143 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.798+17388A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78510929 | ||||||
chr1:78511136
|
T | C | 2 | a0001c0001t0002g0320a0001c0001t0002g0321 | 2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.798+17595T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78511136 | ||||||
chr1:78511457
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.798+17916C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78511457 | ||||||
chr1:78511562
|
C | T | 3 | a0001c0002t0001g0026a0001c0002t0001g0334a0001c0002t0001g0335 | 4 | HG02055.hp1 HG02559.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.798+18021C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78511562 | ||||||
chr1:78511581
|
G | A | 1 | a0001c0001t0001g0228 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.798+18040G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78511581 | ||||||
chr1:78511687
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.798+18146T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78511687 | ||||||
chr1:78511702
|
C | T | 16 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0296others(13): Show | 16 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.798+18161C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78511702 | ||||||
chr1:78511789
|
G | T | 25 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0296others(22): Show | 28 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.798+18248G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78511789 | ||||||
chr1:78511833
|
T | C | 1 | a0001c0001t0020g0039 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.798+18292T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78511833 | ||||||
chr1:78511892
|
G | A | 56 | a0001c0001t0001g0007a0001c0001t0001g0137a0001c0001t0001g0237others(53): Show | 60 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.798+18351G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78511892 | ||||||
chr1:78511898
|
T | G | 1 | a0001c0001t0001g0227 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.798+18357T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78511898 | ||||||
chr1:78512030
|
C | T | 51 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0090others(48): Show | 60 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.798+18489C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78512030 | ||||||
chr1:78512100
|
C | T | 4 | a0001c0001t0001g0021a0001c0001t0001g0218a0001c0001t0003g0217others(1): Show | 5 | HG00544.hp1 HG02080.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.798+18559C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78512100 | ||||||
chr1:78512105
|
C | G | 1 | a0004c0006t0032g0143 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.798+18564C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78512105 | ||||||
chr1:78512161
|
T | C | 2 | a0001c0002t0031g0322a0004c0006t0032g0143 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.798+18620T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78512161 | ||||||
chr1:78512213
|
T | C | 2 | a0001c0001t0001g0030a0001c0001t0001g0031 | 2 | NA18983.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.798+18672T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78512213 | ||||||
chr1:78512277
|
G | C | 25 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0296others(22): Show | 28 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.798+18736G>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78512277 | ||||||
chr1:78512335
|
G | A | 29 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0292others(26): Show | 32 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.798+18794G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78512335 | ||||||
chr1:78512625
|
T | G | 4 | a0001c0002t0001g0328a0001c0002t0022g0329a0001c0002t0024g0330others(1): Show | 4 | HG02109.hp1 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.798+19084T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78512625 | ||||||
chr1:78512752
|
G | A | 1 | a0001c0001t0005g0346 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.798+19211G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78512752 | ||||||
chr1:78512828
|
C | T | 54 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0090others(51): Show | 63 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.798+19287C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78512828 | ||||||
chr1:78512841
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.798+19300G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78512841 | ||||||
chr1:78512953
|
C | T | 3 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160 | 3 | HG03654.hp2 HG03834.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.798+19412C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78512953 | ||||||
chr1:78512957
|
T | C | 2 | a0001c0001t0001g0101a0001c0001t0002g0014 | 3 | HG02615.hp2 HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.798+19416T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78512957 | ||||||
chr1:78513020
|
C | A | 1 | a0001c0001t0001g0169 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.798+19479C>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78513020 | ||||||
chr1:78513087
|
G | A | 5 | a0001c0001t0001g0249a0001c0001t0002g0289a0001c0001t0011g0245others(2): Show | 5 | HG01928.hp2 HG03041.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.798+19546G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78513087 | ||||||
chr1:78513186
|
G | A | 1 | a0001c0001t0001g0102 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.798+19645G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78513186 | ||||||
chr1:78513196
|
A | G | 1 | a0001c0002t0025g0327 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.798+19655A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78513196 | ||||||
chr1:78513293
|
G | A | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.798+19752G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78513293 | ||||||
chr1:78513487
|
G | A | 1 | a0001c0001t0001g0290 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.798+19946G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78513487 | ||||||
chr1:78513509
|
A | G | 21 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0303others(18): Show | 27 | HG00140.hp2 HG00558.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.798+19968A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78513509 | ||||||
chr1:78513556
|
T | C | 245 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(242): Show | 277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.798+20015T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78513556 | ||||||
chr1:78513600
|
G | T | 7 | a0001c0001t0001g0010a0001c0001t0001g0340a0001c0001t0001g0342others(4): Show | 9 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.798+20059G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78513600 | ||||||
chr1:78513713
|
C | A | 29 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0292others(26): Show | 32 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.798+20172C>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78513713 | ||||||
chr1:78513764
|
C | G | 1 | a0001c0001t0001g0342 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.798+20223C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78513764 | ||||||
chr1:78513836
|
G | T | 4 | a0001c0002t0001g0328a0001c0002t0022g0329a0001c0002t0024g0330others(1): Show | 4 | HG02109.hp1 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.798+20295G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78513836 | ||||||
chr1:78513930
|
C | G | 3 | a0001c0002t0001g0328a0001c0002t0022g0329a0001c0002t0024g0330 | 3 | HG02109.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.798+20389C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78513930 | ||||||
chr1:78514102
|
C | T | 1 | a0001c0001t0029g0339 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.798+20561C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78514102 | ||||||
chr1:78514119
|
G | A | 2 | a0001c0001t0006g0250a0001c0001t0006g0251 | 2 | HG02602.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.798+20578G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78514119 | ||||||
chr1:78514149
|
G | A | 1 | a0001c0002t0001g0328 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.798+20608G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78514149 | ||||||
chr1:78514240
|
T | C | 7 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0256others(4): Show | 7 | HG00639.hp2 HG02630.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.798+20699T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78514240 | ||||||
chr1:78514253
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.798+20712G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78514253 | ||||||
chr1:78514480
|
C | G | 46 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(43): Show | 60 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.798+20939C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78514480 | ||||||
chr1:78514519
|
A | G | 1 | a0001c0002t0025g0327 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.798+20978A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78514519 | ||||||
chr1:78514530
|
G | A | 3 | a0001c0001t0009g0088a0001c0001t0009g0089a0001c0001t0009g0092 | 3 | HG02809.hp1 HG02896.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.798+20989G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78514530 | ||||||
chr1:78514576
|
C | T | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0002t0002g0333 | 3 | HG00423.hp1 HG02523.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.798+21035C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78514576 | ||||||
chr1:78514639
|
T | A | 1 | a0004c0006t0032g0143 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.798+21098T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78514639 | ||||||
chr1:78514641
|
A | C | 1 | a0001c0001t0001g0304 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.798+21100A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78514641 | ||||||
chr1:78514641
|
A | G | 1 | a0001c0001t0001g0230 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.798+21100A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78514641 | ||||||
chr1:78514731
|
C | G | 54 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0090others(51): Show | 63 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.798+21190C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78514731 | ||||||
chr1:78514791
|
A | G | 2 | a0001c0001t0001g0232a0001c0001t0001g0233 | 2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.798+21250A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78514791 | ||||||
chr1:78514836
|
G | A | 21 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0303others(18): Show | 27 | HG00140.hp2 HG00558.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.798+21295G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78514836 | ||||||
chr1:78514969
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.798+21428C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78514969 | ||||||
chr1:78514970
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.798+21429G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78514970 | ||||||
chr1:78514998
|
G | A | 4 | a0001c0001t0003g0170a0001c0001t0003g0171a0001c0001t0003g0172others(1): Show | 4 | NA18945.hp1 NA18956.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.799-21408G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78514998 | ||||||
chr1:78515046
|
A | AT | 6 | a0001c0001t0001g0242a0001c0001t0001g0285a0001c0001t0005g0131others(3): Show | 6 | HG02630.hp2 HG02818.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.799-21350dupT | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78515046 | |||||
chr1:78515100
|
G | A | 2 | a0001c0001t0023g0260a0001c0001t0026g0261 | 2 | HG02258.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.799-21306G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78515100 | ||||||
chr1:78515125
|
A | G | 2 | a0001c0001t0001g0232a0001c0001t0001g0233 | 2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.799-21281A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78515125 | ||||||
chr1:78515241
|
A | G | 1 | a0001c0002t0025g0327 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.799-21165A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78515241 | ||||||
chr1:78515521
|
C | T | 1 | a0001c0001t0003g0316 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.799-20885C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78515521 | ||||||
chr1:78515594
|
G | A | 54 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0090others(51): Show | 63 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.799-20812G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78515594 | ||||||
chr1:78516235
|
A | G | 1 | a0001c0002t0031g0322 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.799-20171A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78516235 | ||||||
chr1:78516413
|
C | A | 1 | a0001c0001t0001g0151 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.799-19993C>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78516413 | ||||||
chr1:78516618
|
G | C | 2 | a0001c0002t0025g0327a0004c0006t0032g0143 | 2 | HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.799-19788G>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78516618 | ||||||
chr1:78516749
|
T | A | 1 | a0001c0002t0031g0322 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.799-19657T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78516749 | ||||||
chr1:78516999
|
A | T | 3 | a0001c0002t0001g0328a0001c0002t0022g0329a0001c0002t0024g0330 | 3 | HG02109.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.799-19407A>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78516999 | ||||||
chr1:78517114
|
T | A | 4 | a0001c0001t0001g0242a0001c0001t0001g0285a0001c0001t0007g0287others(1): Show | 4 | HG02630.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.799-19292T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78517114 | ||||||
chr1:78517116
|
C | T | 25 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0296others(22): Show | 28 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.799-19290C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78517116 | ||||||
chr1:78517278
|
A | G | 245 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(242): Show | 276 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.799-19128A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78517278 | ||||||
chr1:78517428
|
T | C | 1 | a0004c0006t0032g0143 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.799-18978T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78517428 | ||||||
chr1:78517488
|
A | G | 1 | a0001c0001t0003g0216 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.799-18918A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78517488 | ||||||
chr1:78517535
|
G | A | 3 | a0001c0002t0001g0328a0001c0002t0022g0329a0001c0002t0024g0330 | 3 | HG02109.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.799-18871G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78517535 | ||||||
chr1:78517651
|
G | T | 21 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0303others(18): Show | 27 | HG00140.hp2 HG00558.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.799-18755G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78517651 | ||||||
chr1:78517670
|
T | C | 4 | a0001c0001t0001g0242a0001c0001t0001g0285a0001c0001t0007g0287others(1): Show | 4 | HG02630.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.799-18736T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78517670 | ||||||
chr1:78517762
|
T | C | 2 | a0001c0001t0001g0174a0001c0001t0001g0175 | 2 | HG02273.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.799-18644T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78517762 | ||||||
chr1:78517880
|
C | T | 3 | a0001c0002t0001g0328a0001c0002t0022g0329a0001c0002t0024g0330 | 3 | HG02109.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.799-18526C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78517880 | ||||||
chr1:78517885
|
A | T | 2 | a0001c0002t0025g0327a0004c0006t0032g0143 | 2 | HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.799-18521A>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78517885 | ||||||
chr1:78517888
|
T | G | 1 | a0001c0001t0002g0262 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.799-18518T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78517888 | ||||||
chr1:78517982
|
A | T | 1 | a0001c0001t0004g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.799-18424A>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78517982 | ||||||
chr1:78518078
|
G | T | 1 | a0001c0001t0001g0215 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.799-18328G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78518078 | ||||||
chr1:78518362
|
C | T | 21 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0303others(18): Show | 27 | HG00140.hp2 HG00558.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.799-18044C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78518362 | ||||||
chr1:78518430
|
T | A | 1 | a0001c0001t0002g0014 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.799-17976T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78518430 | ||||||
chr1:78518457
|
A | G | 3 | a0001c0001t0004g0002a0001c0001t0004g0314a0001c0001t0004g0315 | 6 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.799-17949A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78518457 | ||||||
chr1:78518567
|
GAC | G | 18 | a0001c0001t0001g0010a0001c0001t0001g0019a0001c0001t0001g0129others(15): Show | 21 | HG00621.hp2 HG01261.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.799-17787_799-1778 others(6): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78518567 | |||||
chr1:78518567
|
GACAC | G | 42 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0144others(39): Show | 43 | HG00438.hp2 HG00544.hp1 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.799-17789_799-1778 others(8): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78518567 | |||||
chr1:78518567
|
GACACAC | G | 40 | a0001c0001t0001g0022a0001c0001t0001g0138a0001c0001t0001g0140others(37): Show | 41 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.799-17791_799-1778 others(10): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78518567 | |||||
chr1:78518567
|
GACACACA others(1): Show |
G | 58 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0027others(55): Show | 67 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.799-17793_799-1778 others(12): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78518567 | |||||
chr1:78518567
|
GACACACA others(3): Show |
G | 31 | a0001c0001t0001g0156a0001c0001t0001g0165a0001c0001t0001g0212others(28): Show | 34 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.799-17795_799-1778 others(14): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78518567 | |||||
chr1:78518567
|
GACACACA others(5): Show |
G | 17 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0146others(14): Show | 18 | HG00140.hp2 HG00423.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.799-17797_799-1778 others(16): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78518567 | |||||
chr1:78518567
|
GACACACA others(7): Show |
G | 8 | a0001c0001t0001g0007a0001c0001t0001g0243a0001c0001t0001g0279others(5): Show | 10 | HG01069.hp2 HG01192.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.799-17799_799-1778 others(18): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78518567 | |||||
chr1:78518567
|
GACACACA others(9): Show |
G | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0030g0248 | 3 | HG02886.hp1 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.799-17801_799-1778 others(20): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78518567 | |||||
chr1:78518567
|
GACACACA others(11): Show |
G | 3 | a0001c0001t0001g0042a0001c0001t0002g0078a0001c0003t0001g0283 | 3 | HG01515.hp1 HG03471.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.799-17803_799-1778 others(22): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78518567 | |||||
chr1:78518567
|
GACACACA others(13): Show |
G | 73 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(70): Show | 75 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.799-17805_799-1778 others(24): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78518567 | |||||
chr1:78518567
|
GACACACA others(15): Show |
G | 3 | a0001c0001t0001g0095a0001c0002t0025g0327a0004c0006t0032g0143 | 3 | HG02698.hp1 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.799-17807_799-1778 others(26): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78518567 | |||||
chr1:78518567
|
GACACACA others(17): Show |
G | 44 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(41): Show | 57 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.799-17809_799-1778 others(28): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78518567 | |||||
chr1:78518567
|
GACACACA others(19): Show |
G | 1 | a0001c0001t0003g0018 | 2 | NA18972.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.799-17811_799-1778 others(30): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78518567 | |||||
chr1:78518739
|
T | A | 1 | a0001c0001t0001g0043 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.799-17667T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78518739 | ||||||
chr1:78518739
|
T | C | 243 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 274 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.799-17667T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78518739 | ||||||
chr1:78518903
|
C | T | 21 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0303others(18): Show | 27 | HG00140.hp2 HG00558.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.799-17503C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78518903 | ||||||
chr1:78518939
|
C | T | 2 | a0003c0005t0001g0024a0003c0005t0002g0282 | 3 | HG03490.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.799-17467C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78518939 | ||||||
chr1:78518951
|
C | T | 25 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0296others(22): Show | 28 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.799-17455C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78518951 | ||||||
chr1:78519061
|
G | T | 3 | a0001c0002t0001g0328a0001c0002t0022g0329a0001c0002t0024g0330 | 3 | HG02109.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.799-17345G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78519061 | ||||||
chr1:78519087
|
A | C | 8 | a0001c0002t0001g0009a0001c0002t0001g0026a0001c0002t0001g0331others(5): Show | 11 | HG02055.hp1 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.799-17319A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78519087 | ||||||
chr1:78519106
|
T | G | 1 | a0001c0001t0001g0095 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.799-17300T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78519106 | ||||||
chr1:78519164
|
A | G | 1 | a0001c0001t0003g0186 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.799-17242A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78519164 | ||||||
chr1:78519303
|
G | A | 1 | a0001c0001t0007g0083 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.799-17103G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78519303 | ||||||
chr1:78519351
|
T | C | 3 | a0001c0002t0001g0328a0001c0002t0022g0329a0001c0002t0024g0330 | 3 | HG02109.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.799-17055T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78519351 | ||||||
chr1:78519404
|
C | G | 1 | a0001c0001t0021g0286 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.799-17002C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78519404 | ||||||
chr1:78519671
|
C | T | 16 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0296others(13): Show | 16 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.799-16735C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78519671 | ||||||
chr1:78519782
|
C | G | 1 | a0001c0001t0007g0277 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.799-16624C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78519782 | ||||||
chr1:78519964
|
C | T | 1 | a0001c0001t0001g0312 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.799-16442C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78519964 | ||||||
chr1:78520139
|
C | T | 1 | a0001c0001t0027g0121 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.799-16267C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78520139 | ||||||
chr1:78520246
|
G | A | 3 | a0001c0001t0001g0338a0001c0001t0005g0103a0001c0001t0027g0121 | 3 | HG02486.hp2 HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.799-16160G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78520246 | ||||||
chr1:78520375
|
G | A | 2 | a0001c0001t0001g0167a0001c0001t0003g0168 | 2 | NA19058.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.799-16031G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78520375 | ||||||
chr1:78520745
|
T | C | 3 | a0001c0002t0001g0328a0001c0002t0022g0329a0001c0002t0024g0330 | 3 | HG02109.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.799-15661T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78520745 | ||||||
chr1:78520865
|
G | A | 3 | a0001c0002t0001g0328a0001c0002t0022g0329a0001c0002t0024g0330 | 3 | HG02109.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.799-15541G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78520865 | ||||||
chr1:78520935
|
T | C | 2 | a0001c0002t0025g0327a0004c0006t0032g0143 | 2 | HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.799-15471T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78520935 | ||||||
chr1:78520981
|
G | A | 1 | a0001c0001t0035g0264 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.799-15425G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78520981 | ||||||
chr1:78521027
|
T | A | 3 | a0001c0002t0001g0328a0001c0002t0022g0329a0001c0002t0024g0330 | 3 | HG02109.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.799-15379T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78521027 | ||||||
chr1:78521042
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.799-15364C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78521042 | ||||||
chr1:78521052
|
A | G | 2 | a0001c0002t0025g0327a0004c0006t0032g0143 | 2 | HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.799-15354A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78521052 | ||||||
chr1:78521089
|
T | G | 25 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0296others(22): Show | 28 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.799-15317T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78521089 | ||||||
chr1:78521209
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.799-15197C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78521209 | ||||||
chr1:78521211
|
G | A | 1 | a0001c0002t0025g0327 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.799-15195G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78521211 | ||||||
chr1:78521269
|
G | A | 34 | a0001c0001t0001g0010a0001c0001t0001g0090a0001c0001t0001g0091others(31): Show | 39 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.799-15137G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78521269 | ||||||
chr1:78521434
|
T | C | 2 | a0001c0001t0001g0015a0001c0001t0001g0104 | 3 | HG00673.hp1 HG02165.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.799-14972T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78521434 | ||||||
chr1:78521549
|
G | A | 1 | a0001c0001t0001g0310 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.799-14857G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78521549 | ||||||
chr1:78521607
|
T | G | 1 | a0001c0001t0001g0040 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.799-14799T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78521607 | ||||||
chr1:78521617
|
T | C | 60 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0027others(57): Show | 71 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.799-14789T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78521617 | ||||||
chr1:78521658
|
A | G | 18 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(15): Show | 18 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.799-14748A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78521658 | ||||||
chr1:78521703
|
G | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0105 | 2 | NA18612.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.799-14703G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78521703 | ||||||
chr1:78521901
|
G | C | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.799-14505G>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78521901 | ||||||
chr1:78521931
|
G | A | 121 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(118): Show | 137 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.799-14475G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78521931 | ||||||
chr1:78521971
|
TGCA | T | 8 | a0001c0001t0001g0013a0001c0001t0001g0038a0001c0001t0001g0058others(5): Show | 9 | HG00597.hp2 NA18612.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.799-14434_799-1443 others(7): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78521971 | ||||||
chr1:78522042
|
G | GTTAC | 36 | a0001c0001t0001g0010a0001c0001t0001g0090a0001c0001t0001g0091others(33): Show | 41 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(38): Show |
intron_variant | MODIFIER | c.799-14363_799-1436 others(8): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78522042 | |||||
chr1:78522091
|
C | A | 1 | a0001c0001t0003g0126 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.799-14315C>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78522091 | ||||||
chr1:78522137
|
C | T | 1 | a0001c0001t0001g0338 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.799-14269C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78522137 | ||||||
chr1:78522188
|
C | T | 60 | a0001c0001t0001g0007a0001c0001t0001g0137a0001c0001t0001g0237others(57): Show | 64 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.799-14218C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78522188 | ||||||
chr1:78522511
|
T | A | 1 | a0001c0001t0001g0187 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.799-13895T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78522511 | ||||||
chr1:78522655
|
C | T | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.799-13751C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78522655 | ||||||
chr1:78522825
|
T | A | 1 | a0001c0001t0001g0187 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.799-13581T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78522825 | ||||||
chr1:78522860
|
T | G | 27 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0296others(24): Show | 30 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.799-13546T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78522860 | ||||||
chr1:78522946
|
T | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(258): Show | 295 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.799-13460T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78522946 | ||||||
chr1:78522956
|
A | T | 1 | a0001c0001t0001g0187 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.799-13450A>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78522956 | ||||||
chr1:78522957
|
T | A | 1 | a0001c0001t0001g0187 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.799-13449T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78522957 | ||||||
chr1:78523100
|
A | G | 1 | a0001c0002t0001g0331 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.799-13306A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78523100 | ||||||
chr1:78523271
|
T | C | 2 | a0001c0001t0006g0025a0001c0001t0006g0311 | 3 | HG00140.hp2 HG01981.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.799-13135T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78523271 | ||||||
chr1:78523327
|
T | G | 2 | a0001c0001t0008g0343a0001c0001t0008g0344 | 2 | HG02486.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.799-13079T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78523327 | ||||||
chr1:78523382
|
T | C | 1 | a0001c0002t0024g0330 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.799-13024T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78523382 | ||||||
chr1:78523433
|
G | C | 1 | a0001c0001t0001g0102 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.799-12973G>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78523433 | ||||||
chr1:78523462
|
C | T | 1 | a0001c0002t0025g0327 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.799-12944C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78523462 | ||||||
chr1:78523534
|
G | A | 1 | a0003c0005t0010g0288 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.799-12872G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78523534 | ||||||
chr1:78523633
|
T | C | 3 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160 | 3 | HG03654.hp2 HG03834.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.799-12773T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78523633 | ||||||
chr1:78523665
|
A | G | 1 | a0001c0002t0025g0327 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.799-12741A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78523665 | ||||||
chr1:78523778
|
G | T | 1 | a0004c0006t0032g0143 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.799-12628G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78523778 | ||||||
chr1:78523791
|
T | A | 1 | a0001c0002t0031g0322 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.799-12615T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78523791 | ||||||
chr1:78523795
|
T | C | 11 | a0001c0001t0001g0010a0001c0001t0001g0067a0001c0001t0001g0340others(8): Show | 13 | HG01106.hp1 HG01884.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.799-12611T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78523795 | ||||||
chr1:78523816
|
A | G | 1 | a0003c0005t0010g0288 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.799-12590A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78523816 | ||||||
chr1:78523873
|
A | C | 1 | a0001c0002t0025g0327 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.799-12533A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78523873 | ||||||
chr1:78524090
|
G | A | 1 | a0001c0001t0035g0264 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.799-12316G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78524090 | ||||||
chr1:78524153
|
G | A | 4 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0240others(1): Show | 4 | NA18952.hp2 NA18970.hp1 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.799-12253G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78524153 | ||||||
chr1:78524165
|
A | C | 184 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(181): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.799-12241A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78524165 | ||||||
chr1:78524321
|
G | T | 1 | a0001c0001t0001g0096 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.799-12085G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78524321 | ||||||
chr1:78524498
|
C | T | 3 | a0001c0001t0001g0263a0001c0001t0002g0006a0001c0003t0002g0006 | 4 | HG00099.hp1 HG01175.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.799-11908C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78524498 | ||||||
chr1:78524589
|
T | A | 1 | a0001c0001t0018g0150 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.799-11817T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78524589 | ||||||
chr1:78524590
|
C | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(112): Show | 142 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.799-11816C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78524590 | ||||||
chr1:78524655
|
A | G | 7 | a0001c0001t0001g0010a0001c0001t0001g0124a0001c0001t0001g0243others(4): Show | 9 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.799-11751A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78524655 | ||||||
chr1:78524717
|
C | G | 1 | a0001c0001t0001g0042 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.799-11689C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78524717 | ||||||
chr1:78524889
|
CT | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0124a0001c0001t0001g0243 | 5 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.799-11514delT | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78524889 | |||||
chr1:78524906
|
A | AT | 38 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0047others(35): Show | 39 | HG00140.hp1 HG01074.hp2 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.799-11466dupT | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78524906 | |||||
chr1:78524906
|
A | ATT | 16 | a0001c0001t0001g0042a0001c0001t0001g0052a0001c0001t0001g0059others(13): Show | 16 | HG00438.hp2 HG00733.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.799-11467_799-1146 others(6): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78524906 | |||||
chr1:78524906
|
A | ATTT | 11 | a0001c0001t0001g0036a0001c0001t0001g0053a0001c0001t0001g0054others(8): Show | 11 | HG00423.hp1 HG02129.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.799-11468_799-1146 others(7): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78524906 | |||||
chr1:78524906
|
A | ATTTT | 10 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0034others(7): Show | 10 | HG00438.hp1 HG03453.hp2 HG03492.hp1 others(7): Show |
intron_variant | MODIFIER | c.799-11469_799-1146 others(8): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78524906 | |||||
chr1:78524906
|
A | ATTTTT | 10 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0001g0073others(7): Show | 10 | HG00733.hp2 HG02074.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.799-11470_799-1146 others(9): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78524906 | |||||
chr1:78524906
|
AT | A | 58 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0044others(55): Show | 61 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.799-11466delT | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78524906 | |||||
chr1:78524906
|
ATTTTT | A | 9 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0021others(6): Show | 12 | HG01993.hp1 HG02015.hp1 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.799-11470_799-1146 others(9): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78524906 | |||||
chr1:78524906
|
ATTTTTT | A | 29 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0015others(26): Show | 41 | HG00423.hp2 HG00544.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.799-11471_799-1146 others(10): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78524906 | |||||
chr1:78524906
|
ATTTTTTT | A | 6 | a0001c0001t0001g0101a0001c0001t0001g0110a0001c0001t0021g0286others(3): Show | 6 | HG01975.hp1 HG02055.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.799-11472_799-1146 others(11): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78524906 | |||||
chr1:78524906
|
ATTTTTTT others(1): Show |
A | 9 | a0001c0001t0001g0242a0001c0001t0001g0285a0001c0001t0001g0338others(6): Show | 12 | HG02258.hp2 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.799-11473_799-1146 others(12): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78524906 | |||||
chr1:78524906
|
ATTTTTTT others(3): Show |
A | 7 | a0001c0001t0001g0210a0001c0001t0001g0213a0001c0001t0001g0312others(4): Show | 7 | HG00597.hp1 HG02155.hp2 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.799-11475_799-1146 others(14): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78524906 | |||||
chr1:78524906
|
ATTTTTTT others(4): Show |
A | 40 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0023others(37): Show | 46 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.799-11476_799-1146 others(15): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78524906 | |||||
chr1:78524906
|
ATTTTTTT others(5): Show |
A | 25 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0124others(22): Show | 31 | HG00140.hp2 HG00558.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.799-11477_799-1146 others(16): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78524906 | |||||
chr1:78524906
|
ATTTTTTT others(8): Show |
A | 1 | a0001c0002t0001g0331 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.799-11480_799-1146 others(19): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78524906 | |||||
chr1:78524906
|
ATTTTTTT others(11): Show |
A | 10 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0002g0077others(7): Show | 10 | HG01891.hp1 HG01891.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.799-11483_799-1146 others(22): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78524906 | |||||
chr1:78525001
|
C | T | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.799-11405C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78525001 | ||||||
chr1:78525017
|
G | A | 2 | a0001c0001t0002g0014a0001c0001t0002g0118 | 3 | HG02622.hp1 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.799-11389G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78525017 | ||||||
chr1:78525236
|
G | C | 85 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(82): Show | 100 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.799-11170G>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78525236 | ||||||
chr1:78525260
|
C | A | 1 | a0001c0001t0001g0090 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.799-11146C>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78525260 | ||||||
chr1:78525321
|
G | C | 16 | a0001c0001t0001g0101a0001c0001t0001g0242a0001c0001t0001g0285others(13): Show | 19 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.799-11085G>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78525321 | ||||||
chr1:78525378
|
A | G | 143 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(140): Show | 173 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.799-11028A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78525378 | ||||||
chr1:78525454
|
G | T | 1 | a0001c0001t0001g0185 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.799-10952G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78525454 | ||||||
chr1:78525512
|
A | G | 68 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(65): Show | 80 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.799-10894A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78525512 | ||||||
chr1:78525531
|
A | G | 68 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(65): Show | 80 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.799-10875A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78525531 | ||||||
chr1:78525570
|
T | C | 54 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(51): Show | 72 | HG00423.hp2 HG00544.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.799-10836T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78525570 | ||||||
chr1:78525578
|
A | G | 122 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(119): Show | 152 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.799-10828A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78525578 | ||||||
chr1:78525850
|
T | C | 1 | a0001c0001t0001g0050 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.799-10556T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78525850 | ||||||
chr1:78525867
|
A | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(51): Show | 72 | HG00423.hp2 HG00544.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.799-10539A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78525867 | ||||||
chr1:78525919
|
T | C | 1 | a0001c0001t0002g0082 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.799-10487T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78525919 | ||||||
chr1:78525994
|
A | G | 1 | a0001c0001t0002g0300 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.799-10412A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78525994 | ||||||
chr1:78526056
|
C | T | 4 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0011g0245others(1): Show | 4 | HG02280.hp1 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.799-10350C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78526056 | ||||||
chr1:78526058
|
G | T | 4 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0011g0245others(1): Show | 4 | HG02280.hp1 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.799-10348G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78526058 | ||||||
chr1:78526202
|
G | A | 1 | a0001c0001t0001g0293 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.799-10204G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78526202 | ||||||
chr1:78526264
|
G | A | 1 | a0001c0001t0019g0035 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.799-10142G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78526264 | ||||||
chr1:78526376
|
C | G | 68 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(65): Show | 80 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.799-10030C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78526376 | ||||||
chr1:78526436
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.799-9970G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78526436 | ||||||
chr1:78526494
|
A | G | 18 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(15): Show | 18 | HG00733.hp2 HG01106.hp1 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.799-9912A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78526494 | ||||||
chr1:78526517
|
A | G | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(158): Show | 191 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.799-9889A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78526517 | ||||||
chr1:78526714
|
C | G | 2 | a0001c0001t0001g0232a0001c0001t0001g0233 | 2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.799-9692C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78526714 | ||||||
chr1:78526947
|
C | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0122 | 3 | HG00621.hp1 HG02083.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.799-9459C>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78526947 | ||||||
chr1:78527132
|
C | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 169 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.799-9274C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78527132 | ||||||
chr1:78527303
|
A | C | 1 | a0001c0001t0001g0013 | 2 | NA18957.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.799-9103A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78527303 | ||||||
chr1:78527794
|
T | G | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.799-8612T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78527794 | ||||||
chr1:78528041
|
G | A | 17 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0303others(14): Show | 23 | HG00140.hp2 HG00558.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.799-8365G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78528041 | ||||||
chr1:78528135
|
A | C | 1 | a0001c0001t0004g0305 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.799-8271A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78528135 | ||||||
chr1:78528156
|
G | A | 122 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(119): Show | 152 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.799-8250G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78528156 | ||||||
chr1:78528172
|
C | G | 1 | a0001c0002t0025g0327 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.799-8234C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78528172 | ||||||
chr1:78528216
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.799-8190T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78528216 | ||||||
chr1:78528294
|
C | CA | 58 | a0001c0001t0001g0011a0001c0001t0001g0030a0001c0001t0001g0032others(55): Show | 58 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.799-8084dupA | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78528294 | |||||
chr1:78528294
|
CA | C | 33 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0038others(30): Show | 40 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.799-8084delA | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78528294 | |||||
chr1:78528294
|
CAA | C | 49 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(46): Show | 57 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.799-8085_799-8084d others(4): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78528294 | |||||
chr1:78528294
|
CAAA | C | 51 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0015others(48): Show | 67 | HG00423.hp2 HG00544.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.799-8086_799-8084d others(5): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78528294 | |||||
chr1:78528411
|
T | G | 3 | a0001c0001t0009g0088a0001c0001t0009g0089a0001c0001t0009g0092 | 3 | HG02809.hp1 HG02896.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.799-7995T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78528411 | ||||||
chr1:78528428
|
AG | A | 17 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0232others(14): Show | 17 | HG01891.hp1 HG01891.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.799-7975delG | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78528428 | |||||
chr1:78528487
|
T | C | 4 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0011g0245others(1): Show | 4 | HG02280.hp1 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.799-7919T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78528487 | ||||||
chr1:78528572
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.799-7834T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78528572 | ||||||
chr1:78528610
|
T | G | 3 | a0001c0001t0001g0242a0001c0001t0001g0285a0001c0001t0026g0261 | 3 | HG02258.hp2 HG02630.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.799-7796T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78528610 | ||||||
chr1:78528755
|
T | C | 16 | a0001c0001t0001g0101a0001c0001t0001g0242a0001c0001t0001g0285others(13): Show | 19 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.799-7651T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78528755 | ||||||
chr1:78528761
|
C | T | 1 | a0001c0001t0001g0108 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.799-7645C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78528761 | ||||||
chr1:78528908
|
C | T | 1 | a0001c0002t0022g0329 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.799-7498C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78528908 | ||||||
chr1:78528979
|
G | A | 122 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(119): Show | 152 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.799-7427G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78528979 | ||||||
chr1:78529198
|
G | A | 122 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(119): Show | 152 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.799-7208G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78529198 | ||||||
chr1:78529237
|
T | C | 38 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 53 | HG00423.hp2 HG00544.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.799-7169T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78529237 | ||||||
chr1:78529244
|
T | C | 122 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(119): Show | 152 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.799-7162T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78529244 | ||||||
chr1:78529655
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.799-6751G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78529655 | ||||||
chr1:78529754
|
C | T | 1 | a0001c0001t0001g0223 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.799-6652C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78529754 | ||||||
chr1:78529793
|
A | T | 1 | a0001c0002t0001g0332 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.799-6613A>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78529793 | ||||||
chr1:78529803
|
C | T | 15 | a0001c0001t0001g0101a0001c0001t0001g0242a0001c0001t0001g0285others(12): Show | 18 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.799-6603C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78529803 | ||||||
chr1:78529850
|
T | A | 68 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(65): Show | 80 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.799-6556T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78529850 | ||||||
chr1:78529853
|
C | T | 1 | a0001c0001t0006g0251 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.799-6553C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78529853 | ||||||
chr1:78529946
|
A | G | 1 | a0001c0001t0002g0289 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.799-6460A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78529946 | ||||||
chr1:78529949
|
T | C | 3 | a0001c0001t0001g0297a0001c0001t0028g0295a0001c0003t0001g0246 | 3 | HG00642.hp1 HG01168.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.799-6457T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78529949 | ||||||
chr1:78529960
|
A | C | 1 | a0001c0001t0001g0144 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.799-6446A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78529960 | ||||||
chr1:78530095
|
T | C | 3 | a0001c0001t0009g0088a0001c0001t0009g0089a0001c0001t0009g0092 | 3 | HG02809.hp1 HG02896.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.799-6311T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78530095 | ||||||
chr1:78530111
|
TAAG | T | 68 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(65): Show | 80 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.799-6288_799-6286d others(5): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78530111 | |||||
chr1:78530139
|
G | A | 1 | a0001c0001t0001g0193 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.799-6267G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78530139 | ||||||
chr1:78530157
|
T | G | 1 | a0003c0005t0010g0288 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.799-6249T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78530157 | ||||||
chr1:78530253
|
C | A | 17 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0303others(14): Show | 23 | HG00140.hp2 HG00558.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.799-6153C>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78530253 | ||||||
chr1:78530337
|
A | G | 28 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0027others(25): Show | 36 | HG00140.hp2 HG00558.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.799-6069A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78530337 | ||||||
chr1:78530381
|
T | A | 3 | a0001c0001t0001g0297a0001c0001t0028g0295a0001c0003t0001g0246 | 3 | HG00642.hp1 HG01168.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.799-6025T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78530381 | ||||||
chr1:78530757
|
C | A | 1 | a0001c0001t0001g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.799-5649C>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78530757 | ||||||
chr1:78530907
|
C | CT | 27 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0027others(24): Show | 35 | HG00140.hp2 HG00558.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.799-5494dupT | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78530907 | |||||
chr1:78530956
|
G | A | 8 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0045others(5): Show | 9 | HG00639.hp1 HG01069.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.799-5450G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78530956 | ||||||
chr1:78530982
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.799-5424G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78530982 | ||||||
chr1:78531176
|
G | A | 1 | a0001c0001t0004g0313 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.799-5230G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78531176 | ||||||
chr1:78531429
|
T | C | 14 | a0001c0001t0001g0101a0001c0001t0001g0242a0001c0001t0001g0285others(11): Show | 17 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.799-4977T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78531429 | ||||||
chr1:78531469
|
A | T | 4 | a0001c0001t0001g0182a0001c0001t0003g0186a0001c0001t0003g0216others(1): Show | 4 | HG00544.hp1 HG02040.hp1 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.799-4937A>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78531469 | ||||||
chr1:78531776
|
G | C | 85 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 111 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.799-4630G>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78531776 | ||||||
chr1:78531857
|
A | C | 1 | a0001c0001t0003g0018 | 2 | NA18972.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.799-4549A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78531857 | ||||||
chr1:78531875
|
A | G | 1 | a0001c0001t0001g0218 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.799-4531A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78531875 | ||||||
chr1:78531903
|
A | G | 2 | a0002c0004t0001g0068a0002c0004t0001g0075 | 2 | NA18977.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.799-4503A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78531903 | ||||||
chr1:78532020
|
C | T | 1 | a0001c0001t0002g0014 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.799-4386C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532020 | ||||||
chr1:78532228
|
C | T | 11 | a0001c0001t0001g0101a0001c0001t0001g0338a0001c0001t0029g0339others(8): Show | 14 | HG02055.hp1 HG02451.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.799-4178C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532228 | ||||||
chr1:78532313
|
G | A | 2 | a0001c0001t0001g0249a0001c0001t0030g0248 | 2 | HG01928.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.799-4093G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532313 | ||||||
chr1:78532364
|
T | TATA | 5 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0002g0254others(2): Show | 5 | HG01515.hp1 HG02976.hp2 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.799-4042_799-4041i others(5): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532364 | ||||||
chr1:78532364
|
T | TATATATA others(4): Show |
1 | a0001c0001t0003g0127 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.799-4042_799-4041i others(13): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532364 | ||||||
chr1:78532364
|
T | TTA | 85 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(82): Show | 88 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.799-4010_799-4009d others(4): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532364 | |||||
chr1:78532364
|
T | TTATA | 41 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0040others(38): Show | 43 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.799-4012_799-4009d others(6): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532364 | |||||
chr1:78532364
|
T | TTATATA | 13 | a0001c0001t0001g0050a0001c0001t0001g0137a0001c0001t0001g0144others(10): Show | 13 | HG00544.hp1 HG02080.hp1 HG02273.hp2 others(10): Show |
intron_variant | MODIFIER | c.799-4014_799-4009d others(8): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532364 | |||||
chr1:78532364
|
T | TTATATAT others(1): Show |
12 | a0001c0001t0001g0133a0001c0001t0001g0163a0001c0001t0001g0166others(9): Show | 12 | HG02015.hp2 HG02165.hp2 HG03209.hp2 others(9): Show |
intron_variant | MODIFIER | c.799-4016_799-4009d others(10): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532364 | |||||
chr1:78532364
|
T | TTATATAT others(3): Show |
3 | a0001c0001t0003g0076a0001c0001t0003g0201a0001c0001t0003g0211 | 3 | NA18747.hp2 NA18965.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.799-4018_799-4009d others(12): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532364 | |||||
chr1:78532364
|
T | TTATATAT others(5): Show |
5 | a0001c0001t0001g0182a0001c0001t0001g0193a0001c0001t0003g0225others(2): Show | 5 | HG02040.hp1 NA18939.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.799-4020_799-4009d others(14): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532364 | |||||
chr1:78532364
|
T | TTATATAT others(7): Show |
1 | a0001c0001t0003g0018 | 2 | NA18972.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.799-4022_799-4009d others(16): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532364 | |||||
chr1:78532364
|
T | TTATATAT others(9): Show |
2 | a0001c0001t0001g0093a0001c0002t0022g0329 | 2 | HG01109.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.799-4024_799-4009d others(18): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532364 | |||||
chr1:78532364
|
T | TTATATAT others(11): Show |
4 | a0001c0001t0001g0292a0001c0001t0001g0299a0001c0001t0004g0063others(1): Show | 4 | HG02572.hp2 NA18906.hp1 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.799-4026_799-4009d others(20): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532364 | |||||
chr1:78532364
|
T | TTATATAT others(13): Show |
1 | a0001c0002t0024g0330 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.799-4028_799-4009d others(22): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532364 | |||||
chr1:78532364
|
TTA | T | 5 | a0001c0001t0001g0175a0001c0001t0001g0324a0001c0001t0002g0323others(2): Show | 5 | HG02055.hp2 HG03195.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.799-4010_799-4009d others(4): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532364 | |||||
chr1:78532364
|
TTATA | T | 17 | a0001c0001t0001g0010a0001c0001t0001g0030a0001c0001t0001g0031others(14): Show | 19 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.799-4012_799-4009d others(6): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532364 | |||||
chr1:78532364
|
TTATATA | T | 16 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(13): Show | 16 | HG00642.hp1 HG00733.hp2 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.799-4014_799-4009d others(8): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532364 | |||||
chr1:78532382
|
ATATATAT others(93): Show |
A | 6 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0011g0245others(3): Show | 6 | HG02280.hp1 HG02809.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.799-4022_799-3923d others(102): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532382 | |||||
chr1:78532384
|
A | G | 10 | a0001c0001t0001g0101a0001c0001t0001g0338a0001c0002t0001g0009others(7): Show | 13 | HG02055.hp1 HG02451.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.799-4022A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532384 | ||||||
chr1:78532388
|
A | G | 36 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(33): Show | 51 | HG00423.hp2 HG00544.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.799-4018A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532388 | ||||||
chr1:78532390
|
A | ATATATAT others(21): Show |
1 | a0001c0001t0001g0146 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.799-4009_799-4008i others(30): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532390 | |||||
chr1:78532390
|
A | ATATATAT others(19): Show |
3 | a0001c0001t0001g0160a0001c0001t0001g0208a0001c0001t0001g0230 | 3 | HG03831.hp1 HG03834.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.799-4009_799-4008i others(28): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532390 | |||||
chr1:78532390
|
A | ATATATAT others(15): Show |
11 | a0001c0001t0001g0109a0001c0001t0001g0147a0001c0001t0001g0152others(8): Show | 12 | HG01516.hp1 HG02083.hp1 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.799-4009_799-4008i others(24): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532390 | |||||
chr1:78532390
|
A | ATATATAT others(13): Show |
6 | a0001c0001t0001g0153a0001c0001t0001g0207a0001c0001t0001g0209others(3): Show | 6 | HG00597.hp1 HG01192.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.799-4009_799-4008i others(22): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532390 | |||||
chr1:78532390
|
A | ATATATAT others(11): Show |
11 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0038others(8): Show | 14 | HG00408.hp2 HG00597.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.799-4009_799-4008i others(20): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532390 | |||||
chr1:78532390
|
A | ATATATAT others(9): Show |
4 | a0001c0001t0001g0151a0001c0001t0001g0155a0001c0001t0001g0156others(1): Show | 4 | HG00099.hp2 HG00280.hp2 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.799-4009_799-4008i others(18): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532390 | |||||
chr1:78532390
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0159 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.799-4009_799-4008i others(16): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532390 | |||||
chr1:78532390
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0312 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.799-4009_799-4008i others(14): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532390 | |||||
chr1:78532390
|
A | G | 4 | a0001c0001t0001g0100a0001c0001t0001g0113a0001c0001t0001g0306others(1): Show | 4 | HG01496.hp2 HG02523.hp1 NA19076.hp2 others(1): Show |
intron_variant | MODIFIER | c.799-4016A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532390 | ||||||
chr1:78532390
|
ATATATAT others(69): Show |
A | 10 | a0001c0001t0001g0101a0001c0001t0001g0338a0001c0002t0001g0009others(7): Show | 13 | HG02055.hp1 HG02451.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.799-4014_799-3939d others(78): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532390 | |||||
chr1:78532390
|
ATATATAT others(85): Show |
A | 1 | a0001c0001t0007g0277 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.799-4014_799-3923d others(94): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532390 | |||||
chr1:78532394
|
ATATGTAT others(7): Show |
A | 1 | a0001c0001t0003g0194 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.799-4008_799-3995d others(16): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532394 | |||||
chr1:78532394
|
ATATGTAT others(65): Show |
A | 36 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(33): Show | 51 | HG00423.hp2 HG00544.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.799-4010_799-3939d others(74): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532394 | |||||
chr1:78532396
|
ATGTATAT others(63): Show |
A | 4 | a0001c0001t0001g0100a0001c0001t0001g0113a0001c0001t0001g0306others(1): Show | 4 | HG01496.hp2 HG02523.hp1 NA19076.hp2 others(1): Show |
intron_variant | MODIFIER | c.799-4006_799-3937d others(72): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532396 | |||||
chr1:78532396
|
ATGTATAT others(67): Show |
A | 1 | a0001c0001t0002g0262 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.799-3996_799-3923d others(76): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532396 | |||||
chr1:78532398
|
G | A | 19 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0232others(16): Show | 19 | HG01891.hp1 HG01891.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.799-4008G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532398 | ||||||
chr1:78532400
|
ATATATGT others(65): Show |
A | 2 | a0001c0001t0007g0345a0001c0001t0009g0092 | 2 | HG01891.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.799-4000_799-3929d others(74): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532400 | |||||
chr1:78532402
|
ATATGTGT others(39): Show |
A | 2 | a0001c0001t0026g0261a0004c0006t0032g0143 | 2 | HG02258.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.799-4000_799-3955d others(48): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532402 | |||||
chr1:78532402
|
ATATGTGT others(63): Show |
A | 1 | a0001c0001t0009g0089 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.799-4000_799-3931d others(72): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532402 | |||||
chr1:78532404
|
ATGTG | A | 3 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0002g0079 | 3 | HG02572.hp1 HG02615.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.799-4000_799-3997d others(6): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532404 | |||||
chr1:78532404
|
ATGTGTAT others(37): Show |
A | 2 | a0001c0001t0001g0242a0001c0001t0001g0285 | 2 | HG02630.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.799-4000_799-3957d others(46): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532404 | |||||
chr1:78532404
|
ATGTGTAT others(61): Show |
A | 1 | a0001c0001t0005g0346 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.799-4000_799-3933d others(70): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532404 | |||||
chr1:78532404
|
ATGTGTAT others(71): Show |
A | 1 | a0001c0001t0001g0233 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.799-3998_799-3921d others(80): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532404 | |||||
chr1:78532406
|
G | A | 5 | a0001c0001t0001g0232a0001c0001t0002g0077a0001c0001t0002g0078others(2): Show | 5 | HG01891.hp2 HG02809.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.799-4000G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532406 | ||||||
chr1:78532408
|
G | A | 6 | a0001c0001t0001g0232a0001c0001t0002g0077a0001c0001t0002g0078others(3): Show | 6 | HG01891.hp2 HG02809.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.799-3998G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532408 | ||||||
chr1:78532410
|
ATATATAT others(55): Show |
A | 26 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0027others(23): Show | 34 | HG00140.hp2 HG00558.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.799-3914_799-3853d others(64): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532410 | |||||
chr1:78532412
|
ATATATGT others(47): Show |
A | 1 | a0001c0001t0021g0286 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.799-3992_799-3939d others(56): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532412 | |||||
chr1:78532414
|
ATATGTGT others(51): Show |
A | 1 | a0001c0001t0002g0079 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.799-3988_799-3931d others(60): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532414 | |||||
chr1:78532416
|
ATGTGTGT others(25): Show |
A | 1 | a0001c0001t0013g0084 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.799-3988_799-3957d others(34): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532416 | |||||
chr1:78532416
|
ATGTGTGT others(59): Show |
A | 4 | a0001c0001t0001g0232a0001c0001t0002g0077a0001c0001t0002g0078others(1): Show | 4 | HG01891.hp2 HG02809.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.799-3986_799-3921d others(68): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532416 | |||||
chr1:78532418
|
G | A | 3 | a0001c0001t0001g0086a0001c0001t0003g0194a0001c0001t0029g0339 | 3 | HG02615.hp1 HG03516.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.799-3988G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532418 | ||||||
chr1:78532420
|
G | A | 3 | a0001c0001t0001g0086a0001c0001t0003g0194a0001c0001t0029g0339 | 3 | HG02615.hp1 HG03516.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.799-3986G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532420 | ||||||
chr1:78532434
|
ATATATTT others(31): Show |
A | 3 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0029g0339 | 3 | HG02572.hp1 HG02615.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.799-3966_799-3929d others(40): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532434 | |||||
chr1:78532440
|
T | A | 1 | a0001c0001t0003g0194 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.799-3966T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532440 | ||||||
chr1:78532448
|
G | A | 1 | a0001c0001t0003g0194 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.799-3958G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532448 | ||||||
chr1:78532454
|
G | A | 5 | a0001c0001t0001g0242a0001c0001t0001g0285a0001c0001t0013g0084others(2): Show | 5 | HG02258.hp2 HG02630.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.799-3952G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532454 | ||||||
chr1:78532462
|
ATTTG | A | 5 | a0001c0001t0001g0242a0001c0001t0001g0285a0001c0001t0013g0084others(2): Show | 5 | HG02258.hp2 HG02630.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.799-3942_799-3939d others(6): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532462 | |||||
chr1:78532472
|
G | A | 57 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(54): Show | 75 | HG00423.hp2 HG00544.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.799-3934G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532472 | ||||||
chr1:78532472
|
GTATATAT others(7): Show |
G | 1 | a0001c0001t0003g0194 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.799-3928_799-3915d others(16): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532472 | |||||
chr1:78532480
|
G | A | 6 | a0001c0001t0002g0079a0001c0001t0002g0262a0001c0001t0005g0346others(3): Show | 6 | HG01891.hp1 HG02896.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.799-3926G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532480 | ||||||
chr1:78532482
|
G | A | 6 | a0001c0001t0002g0079a0001c0001t0002g0262a0001c0001t0005g0346others(3): Show | 6 | HG01891.hp1 HG02896.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.799-3924G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532482 | ||||||
chr1:78532484
|
GTA | G | 2 | a0001c0001t0001g0023a0001c0001t0001g0038 | 3 | HG00597.hp2 NA18944.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.799-3916_799-3915d others(4): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532484 | |||||
chr1:78532502
|
T | A | 18 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0232others(15): Show | 18 | HG01891.hp1 HG01891.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.799-3904T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532502 | ||||||
chr1:78532510
|
G | A | 18 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0232others(15): Show | 18 | HG01891.hp1 HG01891.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.799-3896G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532510 | ||||||
chr1:78532610
|
G | A | 27 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0027others(24): Show | 35 | HG00140.hp2 HG00558.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.799-3796G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532610 | ||||||
chr1:78532772
|
A | T | 27 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0027others(24): Show | 35 | HG00140.hp2 HG00558.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.799-3634A>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532772 | ||||||
chr1:78532786
|
A | T | 27 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0027others(24): Show | 35 | HG00140.hp2 HG00558.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.799-3620A>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532786 | ||||||
chr1:78532787
|
T | C | 1 | a0001c0001t0023g0260 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.799-3619T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532787 | ||||||
chr1:78532823
|
A | G | 2 | a0001c0001t0023g0260a0001c0002t0031g0322 | 2 | HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.799-3583A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532823 | ||||||
chr1:78532902
|
T | A | 41 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0038others(38): Show | 45 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.799-3504T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532902 | ||||||
chr1:78532929
|
G | C | 1 | a0001c0001t0002g0118 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.799-3477G>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532929 | ||||||
chr1:78532952
|
T | C | 27 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0027others(24): Show | 35 | HG00140.hp2 HG00558.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.799-3454T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532952 | ||||||
chr1:78532953
|
A | G | 3 | a0001c0001t0001g0297a0001c0001t0028g0295a0001c0003t0001g0246 | 3 | HG00642.hp1 HG01168.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.799-3453A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532953 | ||||||
chr1:78532960
|
A | G | 2 | a0001c0001t0003g0076a0001c0001t0003g0194 | 2 | NA18747.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.799-3446A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532960 | ||||||
chr1:78532971
|
G | C | 1 | a0001c0001t0001g0340 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.799-3435G>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532971 | ||||||
chr1:78532996
|
A | G | 1 | a0001c0001t0029g0339 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.799-3410A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532996 | ||||||
chr1:78533074
|
T | C | 27 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0027others(24): Show | 35 | HG00140.hp2 HG00558.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.799-3332T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78533074 | ||||||
chr1:78533189
|
G | A | 4 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0013g0084others(1): Show | 4 | HG02572.hp1 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.799-3217G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78533189 | ||||||
chr1:78533403
|
C | T | 186 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(183): Show | 217 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.799-3003C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78533403 | ||||||
chr1:78533584
|
G | A | 27 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0027others(24): Show | 35 | HG00140.hp2 HG00558.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.799-2822G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78533584 | ||||||
chr1:78533592
|
C | G | 31 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0027others(28): Show | 39 | HG00140.hp2 HG00558.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.799-2814C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78533592 | ||||||
chr1:78533593
|
A | G | 1 | a0001c0002t0031g0322 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.799-2813A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78533593 | ||||||
chr1:78533666
|
A | G | 1 | a0001c0002t0025g0327 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.799-2740A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78533666 | ||||||
chr1:78533682
|
A | G | 168 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(165): Show | 199 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.799-2724A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78533682 | ||||||
chr1:78533880
|
T | G | 1 | a0001c0001t0001g0224 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.799-2526T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78533880 | ||||||
chr1:78534032
|
T | C | 2 | a0001c0001t0001g0149a0001c0001t0018g0150 | 2 | HG00597.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.799-2374T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78534032 | ||||||
chr1:78534111
|
T | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(120): Show | 145 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.799-2295T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78534111 | ||||||
chr1:78534186
|
A | G | 7 | a0001c0001t0002g0077a0001c0001t0002g0078a0001c0001t0002g0079others(4): Show | 7 | HG01891.hp1 HG01891.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.799-2220A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78534186 | ||||||
chr1:78534239
|
C | T | 1 | a0001c0001t0029g0339 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.799-2167C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78534239 | ||||||
chr1:78534249
|
A | C | 1 | a0001c0001t0004g0318 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.799-2157A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78534249 | ||||||
chr1:78534297
|
A | C | 6 | a0001c0001t0001g0029a0001c0001t0001g0052a0001c0001t0001g0072others(3): Show | 6 | HG02738.hp1 HG02738.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.799-2109A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78534297 | ||||||
chr1:78534518
|
T | A | 29 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0067others(26): Show | 35 | HG00140.hp2 HG00558.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.799-1888T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78534518 | ||||||
chr1:78534544
|
A | G | 1 | a0001c0001t0016g0247 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.799-1862A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78534544 | ||||||
chr1:78534616
|
T | C | 1 | a0001c0001t0012g0114 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.799-1790T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78534616 | ||||||
chr1:78534697
|
G | GT | 87 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(84): Show | 99 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.799-1700dupT | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78534697 | |||||
chr1:78534723
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.799-1683C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78534723 | ||||||
chr1:78534888
|
T | C | 21 | a0001c0001t0002g0014a0001c0001t0002g0077a0001c0001t0002g0078others(18): Show | 22 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.799-1518T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78534888 | ||||||
chr1:78534931
|
C | G | 2 | a0001c0001t0001g0085a0001c0001t0001g0278 | 2 | HG02300.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.799-1475C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78534931 | ||||||
chr1:78535272
|
A | G | 1 | a0001c0001t0029g0339 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.799-1134A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78535272 | ||||||
chr1:78535637
|
C | G | 1 | a0001c0001t0029g0339 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.799-769C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78535637 | ||||||
chr1:78535773
|
A | G | 39 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0004g0002others(36): Show | 43 | HG00140.hp2 HG00741.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.799-633A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78535773 | ||||||
chr1:78535913
|
C | G | 27 | a0001c0001t0004g0002a0001c0001t0004g0063a0001c0001t0004g0199others(24): Show | 31 | HG00140.hp2 HG00741.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.799-493C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78535913 | ||||||
chr1:78535950
|
G | A | 27 | a0001c0001t0004g0002a0001c0001t0004g0063a0001c0001t0004g0199others(24): Show | 31 | HG00140.hp2 HG00741.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.799-456G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78535950 | ||||||
chr1:78535952
|
G | C | 1 | a0001c0001t0011g0245 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.799-454G>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78535952 | ||||||
chr1:78536235
|
T | G | 38 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0004g0002others(35): Show | 42 | HG00140.hp2 HG00741.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.799-171T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78536235 | ||||||
chr1:78536282
|
A | AC | 4 | a0001c0001t0004g0002a0001c0001t0004g0199a0001c0001t0004g0314others(1): Show | 7 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.799-124_799-123ins others(1): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78536282 | ||||||
chr1:78536309
|
A | T | 82 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(79): Show | 90 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.799-97A>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78536309 |