geneid | 5738 |
---|---|
ensemblid | ENSG00000134247.10 |
hgncid | 9601 |
symbol | PTGFRN |
name | prostaglandin F2 receptor inhibitor |
refseq_nuc | NM_020440.4 |
refseq_prot | NP_065173.2 |
ensembl_nuc | ENST00000393203.3 |
ensembl_prot | ENSP00000376899.2 |
mane_status | MANE Select |
chr | chr1 |
start | 116909916 |
end | 116990353 |
strand | + |
ver | v1.2 |
region | chr1:116909916-116990353 |
region5000 | chr1:116904916-116995353 |
regionname0 | PTGFRN_chr1_116909916_116990353 |
regionname5000 | PTGFRN_chr1_116904916_116995353 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 879 | 118 | 50 | 22 | 29 | 5 | 12 | 24 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0002 | 0/1 | 879 | 90 | 8 | 26 | 39 | 6 | 10 | 26 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0003 | 0/0 | 879 | 45 | 0 | 3 | 38 | 0 | 4 | 28 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0004 | 1/0 | 879 | 33 | 8 | 3 | 16 | 5 | 0 | 12 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0005 | 0/0 | 879 | 11 | 9 | 0 | 1 | 0 | 1 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0006 | 0/0 | 879 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0007 | 0/0 | 879 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0008 | 0/0 | 879 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0009 | 0/0 | 879 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0010 | 0/0 | 879 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0011 | 0/0 | 879 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0012 | 0/0 | 879 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 2640 | 106 | 40 | 21 | 29 | 5 | 11 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
c0002 | 0/1 | 2640 | 89 | 7 | 26 | 39 | 6 | 10 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
c0003 | 0/0 | 2640 | 45 | 0 | 3 | 38 | 0 | 4 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
c0004 | 1/0 | 2640 | 30 | 8 | 3 | 16 | 2 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
c0005 | 0/0 | 2640 | 11 | 9 | 0 | 1 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
c0006 | 0/0 | 2640 | 4 | 4 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
c0007 | 0/0 | 2640 | 4 | 4 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
c0008 | 0/0 | 2640 | 3 | 2 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
c0009 | 0/0 | 2640 | 3 | 0 | 0 | 0 | 3 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
c0010 | 0/0 | 2640 | 3 | 3 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
c0011 | 0/0 | 2640 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
c0012 | 0/0 | 2640 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
c0013 | 0/0 | 2640 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
c0014 | 0/0 | 2640 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
c0015 | 0/0 | 2640 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
c0016 | 0/0 | 2640 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
c0017 | 0/0 | 2640 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
c0018 | 0/0 | 2640 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
c0019 | 0/0 | 2640 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
c0020 | 0/0 | 2640 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
c0021 | 0/0 | 2640 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
c0022 | 0/0 | 2640 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
c0023 | 0/0 | 2640 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 3675 | 117 | 40 | 19 | 40 | 8 | 9 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
t0002 | 0/0 | 3673 | 46 | 3 | 2 | 39 | 0 | 2 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
t0003 | 0/0 | 3674 | 40 | 1 | 11 | 18 | 3 | 7 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
t0004 | 0/0 | 3673 | 33 | 10 | 7 | 11 | 3 | 2 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
t0005 | 0/0 | 3676 | 9 | 4 | 1 | 3 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
t0006 | 0/0 | 3674 | 6 | 0 | 1 | 5 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
t0007 | 0/0 | 3673 | 5 | 0 | 3 | 0 | 1 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
t0008 | 0/1 | 3673 | 4 | 0 | 2 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
t0009 | 0/0 | 3670 | 3 | 3 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
t0010 | 0/0 | 3674 | 3 | 0 | 1 | 1 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
t0011 | 0/0 | 3674 | 3 | 3 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
t0012 | 0/0 | 3674 | 3 | 3 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
t0013 | 0/0 | 3675 | 3 | 3 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
t0014 | 0/0 | 3673 | 3 | 3 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
t0015 | 0/0 | 3675 | 3 | 0 | 0 | 3 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
t0016 | 0/0 | 3673 | 2 | 0 | 0 | 0 | 0 | 2 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
t0017 | 0/0 | 3674 | 2 | 1 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
t0018 | 0/0 | 3674 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
t0019 | 0/0 | 3675 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
t0020 | 0/0 | 3675 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
t0021 | 0/0 | 3675 | 2 | 1 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
t0022 | 0/0 | 3674 | 2 | 0 | 2 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
t0023 | 0/0 | 3670 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
t0024 | 0/0 | 3673 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
t0025 | 0/0 | 3673 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
t0026 | 0/0 | 3673 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
t0027 | 0/0 | 3673 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
t0028 | 0/0 | 3673 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
t0029 | 0/0 | 3674 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
t0030 | 0/0 | 3674 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
t0031 | 0/0 | 3675 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
t0032 | 0/0 | 3675 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
t0033 | 0/0 | 3675 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
t0034 | 0/0 | 3675 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
t0035 | 0/0 | 3675 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
t0036 | 0/0 | 3676 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
t0037 | 0/0 | 3676 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
t0038 | 0/0 | 3673 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
t0039 | 0/0 | 3674 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
t0040 | 0/0 | 3674 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
t0041 | 0/0 | 3676 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0090 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0174 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2640 | 106 | 40 | 21 | 29 | 5 | 11 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0001c0006 | 0/0 | 2640 | 4 | 4 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0001c0008 | 0/0 | 2640 | 3 | 2 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0001c0011 | 0/0 | 2640 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0001c0017 | 0/0 | 2640 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0001c0018 | 0/0 | 2640 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0001c0020 | 0/0 | 2640 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0002c0002 | 0/1 | 2640 | 89 | 7 | 26 | 39 | 6 | 10 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0002c0019 | 0/0 | 2640 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0003c0003 | 0/0 | 2640 | 45 | 0 | 3 | 38 | 0 | 4 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0004c0004 | 1/0 | 2640 | 30 | 8 | 3 | 16 | 2 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0004c0009 | 0/0 | 2640 | 3 | 0 | 0 | 0 | 3 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0005c0005 | 0/0 | 2640 | 11 | 9 | 0 | 1 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0006c0007 | 0/0 | 2640 | 4 | 4 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0006c0012 | 0/0 | 2640 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0006c0022 | 0/0 | 2640 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0007c0010 | 0/0 | 2640 | 3 | 3 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0007c0013 | 0/0 | 2640 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0008c0014 | 0/0 | 2640 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0009c0015 | 0/0 | 2640 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0010c0016 | 0/0 | 2640 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0011c0023 | 0/0 | 2640 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0012c0021 | 0/0 | 2640 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6314 | 82 | 27 | 16 | 28 | 4 | 7 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0001c0001t0005 | 0/0 | 6315 | 6 | 3 | 1 | 1 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0001c0001t0007 | 0/0 | 6312 | 5 | 0 | 3 | 0 | 1 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0001c0001t0012 | 0/0 | 6313 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0001c0001t0014 | 0/0 | 6312 | 3 | 3 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0001c0001t0016 | 0/0 | 6312 | 2 | 0 | 0 | 0 | 0 | 2 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0001c0001t0018 | 0/0 | 6313 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0001c0001t0019 | 0/0 | 6314 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0001c0001t0020 | 0/0 | 6314 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0001c0001t0037 | 0/0 | 6315 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0001c0001t0038 | 0/0 | 6312 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0001c0006t0009 | 0/0 | 6309 | 3 | 3 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0001c0006t0023 | 0/0 | 6309 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0001c0008t0011 | 0/0 | 6313 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0001c0008t0021 | 0/0 | 6314 | 2 | 1 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0001c0011t0001 | 0/0 | 6314 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0001c0017t0001 | 0/0 | 6314 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0001c0018t0029 | 0/0 | 6313 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0001c0020t0001 | 0/0 | 6314 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0002c0002t0001 | 0/0 | 6314 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0002c0002t0002 | 0/0 | 6312 | 3 | 1 | 0 | 2 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0002c0002t0003 | 0/0 | 6313 | 39 | 1 | 11 | 18 | 3 | 6 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0002c0002t0004 | 0/0 | 6312 | 26 | 3 | 7 | 11 | 3 | 2 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0002c0002t0006 | 0/0 | 6313 | 6 | 0 | 1 | 5 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0002c0002t0008 | 0/1 | 6312 | 4 | 0 | 2 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0002c0002t0015 | 0/0 | 6314 | 2 | 0 | 0 | 2 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0002c0002t0017 | 0/0 | 6313 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0002c0002t0022 | 0/0 | 6313 | 2 | 0 | 2 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0002c0002t0024 | 0/0 | 6312 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0002c0002t0025 | 0/0 | 6312 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0002c0002t0039 | 0/0 | 6313 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0002c0002t0040 | 0/0 | 6313 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0002c0002t0041 | 0/0 | 6315 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0002c0019t0030 | 0/0 | 6313 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0003c0003t0002 | 0/0 | 6312 | 40 | 0 | 2 | 36 | 0 | 2 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0003c0003t0010 | 0/0 | 6313 | 3 | 0 | 1 | 1 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0003c0003t0026 | 0/0 | 6312 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0003c0003t0027 | 0/0 | 6312 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0004c0004t0001 | 1/0 | 6314 | 24 | 6 | 3 | 12 | 2 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0004c0004t0005 | 0/0 | 6315 | 2 | 0 | 0 | 2 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0004c0004t0028 | 0/0 | 6312 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0004c0004t0032 | 0/0 | 6314 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0004c0004t0034 | 0/0 | 6314 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0004c0004t0035 | 0/0 | 6314 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0004c0009t0001 | 0/0 | 6314 | 2 | 0 | 0 | 0 | 2 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0004c0009t0031 | 0/0 | 6314 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0005c0005t0001 | 0/0 | 6314 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0005c0005t0002 | 0/0 | 6312 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0005c0005t0003 | 0/0 | 6313 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0005c0005t0004 | 0/0 | 6312 | 6 | 6 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0005c0005t0015 | 0/0 | 6314 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0006c0007t0001 | 0/0 | 6314 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0006c0007t0005 | 0/0 | 6315 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0006c0007t0012 | 0/0 | 6313 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0006c0012t0011 | 0/0 | 6313 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0006c0012t0018 | 0/0 | 6313 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0006c0022t0011 | 0/0 | 6313 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0007c0010t0013 | 0/0 | 6314 | 3 | 3 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0007c0013t0002 | 0/0 | 6312 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0007c0013t0017 | 0/0 | 6313 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0008c0014t0004 | 0/0 | 6312 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0009c0015t0001 | 0/0 | 6314 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0010c0016t0002 | 0/0 | 6312 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0011c0023t0033 | 0/0 | 6314 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
a0012c0021t0036 | 0/0 | 6315 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | copy fasta | chr1 | 116904916 | 116995353 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0005g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0005g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0005g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0005g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0005g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0007g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0007g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0007g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0007g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0012g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0014g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0014g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0016g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0016g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0018g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0019g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0019g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0020g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0020g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0037g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0001t0038g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0006t0009g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0006t0009g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0006t0009g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0006t0023g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0008t0011g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0008t0021g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0008t0021g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0011t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0017t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0018t0029g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0001c0020t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0003g0001 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0003g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0003g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0003g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0003g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0003g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0003g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0003g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0004g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0004g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0004g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0004g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0004g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0004g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0004g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0004g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0004g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0004g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0004g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0004g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0006g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0006g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0006g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0006g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0006g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0006g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0008g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0008g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0008g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0008g0174 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0015g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0015g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0017g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0022g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0022g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0024g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0025g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0039g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0040g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0002t0041g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0002c0019t0030g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0010g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0010g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0010g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0026g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0003c0003t0027g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0004c0004t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0004c0004t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0004c0004t0001g0090 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0004c0004t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0004c0004t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0004c0004t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0004c0004t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0004c0004t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0004c0004t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0004c0004t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0004c0004t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0004c0004t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0004c0004t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0004c0004t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0004c0004t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0004c0004t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0004c0004t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0004c0004t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0004c0004t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0004c0004t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0004c0004t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0004c0004t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0004c0004t0005g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0004c0004t0005g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0004c0004t0028g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0004c0004t0032g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0004c0004t0034g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0004c0004t0035g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0004c0009t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0004c0009t0031g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0005c0005t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0005c0005t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0005c0005t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0005c0005t0003g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0005c0005t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0005c0005t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0005c0005t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0005c0005t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0005c0005t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0005c0005t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0005c0005t0015g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0006c0007t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0006c0007t0005g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0006c0007t0012g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0006c0012t0011g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0006c0012t0018g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0006c0022t0011g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0007c0010t0013g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0007c0010t0013g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0007c0010t0013g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0007c0013t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0007c0013t0017g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0008c0014t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0009c0015t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0010c0016t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0011c0023t0033g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
a0012c0021t0036g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0003 | g0001 | EUR | GBR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0146 | EUR | GBR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG00280 | hp1 | a0002 | c0002 | t0004 | g0041 | EUR | FIN | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0227 | EUR | FIN | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG00323 | hp1 | a0002 | c0002 | t0003 | g0117 | EUR | FIN | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0093 | EUR | FIN | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG00408 | hp1 | a0002 | c0002 | t0003 | g0001 | EAS | CHS | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG00438 | hp1 | a0003 | c0003 | t0002 | g0124 | EAS | CHS | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG00438 | hp2 | a0004 | c0004 | t0032 | g0255 | EAS | CHS | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG00558 | hp1 | a0002 | c0002 | t0004 | g0068 | EAS | CHS | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG00558 | hp2 | a0003 | c0003 | t0002 | g0098 | EAS | CHS | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG00597 | hp1 | a0002 | c0002 | t0004 | g0103 | EAS | CHS | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG00597 | hp2 | a0003 | c0003 | t0002 | g0045 | EAS | CHS | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG00621 | hp2 | a0002 | c0002 | t0003 | g0133 | EAS | CHS | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG00673 | hp1 | a0003 | c0003 | t0002 | g0078 | EAS | CHS | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG00673 | hp2 | a0003 | c0003 | t0002 | g0069 | EAS | CHS | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG00733 | hp2 | a0002 | c0002 | t0008 | g0109 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG00735 | hp2 | a0002 | c0002 | t0017 | g0179 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG00741 | hp2 | a0001 | c0001 | t0007 | g0012 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01069 | hp1 | a0002 | c0002 | t0003 | g0248 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01071 | hp2 | a0002 | c0002 | t0003 | g0029 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01099 | hp1 | a0002 | c0002 | t0008 | g0110 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01099 | hp2 | a0002 | c0002 | t0041 | g0121 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01106 | hp1 | a0002 | c0002 | t0004 | g0207 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01106 | hp2 | a0002 | c0002 | t0003 | g0017 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01109 | hp1 | a0003 | c0003 | t0010 | g0074 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01109 | hp2 | a0001 | c0001 | t0038 | g0198 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01169 | hp1 | a0004 | c0004 | t0001 | g0063 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01169 | hp2 | a0002 | c0002 | t0003 | g0032 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01192 | hp1 | a0001 | c0001 | t0007 | g0012 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01243 | hp2 | a0002 | c0002 | t0004 | g0062 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01255 | hp1 | a0002 | c0002 | t0003 | g0016 | AMR | CLM | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01255 | hp2 | a0001 | c0001 | t0007 | g0061 | AMR | CLM | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01258 | hp2 | a0002 | c0002 | t0039 | g0022 | AMR | CLM | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01261 | hp1 | a0001 | c0001 | t0005 | g0185 | AMR | CLM | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01261 | hp2 | a0002 | c0002 | t0003 | g0021 | AMR | CLM | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01346 | hp1 | a0002 | c0002 | t0003 | g0039 | AMR | CLM | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01358 | hp2 | a0002 | c0002 | t0003 | g0129 | AMR | CLM | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01433 | hp2 | a0001 | c0008 | t0021 | g0199 | AMR | CLM | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01496 | hp1 | a0002 | c0002 | t0003 | g0018 | AMR | CLM | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01515 | hp1 | a0001 | c0001 | t0007 | g0059 | EUR | IBS | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01515 | hp2 | a0004 | c0009 | t0001 | g0011 | EUR | IBS | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01516 | hp1 | a0004 | c0004 | t0001 | g0250 | EUR | IBS | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01516 | hp2 | a0002 | c0002 | t0004 | g0064 | EUR | IBS | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01517 | hp1 | a0004 | c0004 | t0001 | g0251 | EUR | IBS | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01517 | hp2 | a0004 | c0009 | t0001 | g0011 | EUR | IBS | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01884 | hp1 | a0002 | c0002 | t0004 | g0065 | AFR | ACB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01884 | hp2 | a0001 | c0001 | t0014 | g0014 | AFR | ACB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01891 | hp1 | a0007 | c0013 | t0017 | g0283 | AFR | ACB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01891 | hp2 | a0001 | c0001 | t0005 | g0291 | AFR | ACB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01928 | hp1 | a0003 | c0003 | t0002 | g0171 | AMR | PEL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01928 | hp2 | a0002 | c0002 | t0022 | g0020 | AMR | PEL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01934 | hp1 | a0002 | c0002 | t0004 | g0178 | AMR | PEL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01934 | hp2 | a0002 | c0002 | t0006 | g0139 | AMR | PEL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01943 | hp1 | a0002 | c0002 | t0004 | g0009 | AMR | PEL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01943 | hp2 | a0002 | c0002 | t0003 | g0083 | AMR | PEL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01952 | hp1 | a0002 | c0002 | t0022 | g0019 | AMR | PEL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01952 | hp2 | a0002 | c0002 | t0004 | g0249 | AMR | PEL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01978 | hp1 | a0003 | c0003 | t0002 | g0172 | AMR | PEL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG01978 | hp2 | a0002 | c0002 | t0004 | g0180 | AMR | PEL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02015 | hp1 | a0002 | c0002 | t0015 | g0173 | EAS | KHV | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02015 | hp2 | a0004 | c0004 | t0001 | g0241 | EAS | KHV | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02027 | hp1 | a0003 | c0003 | t0002 | g0206 | EAS | KHV | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02027 | hp2 | a0002 | c0002 | t0003 | g0046 | EAS | KHV | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02055 | hp1 | a0001 | c0001 | t0005 | g0193 | AFR | ACB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02071 | hp1 | a0002 | c0002 | t0002 | g0165 | EAS | KHV | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02071 | hp2 | a0004 | c0004 | t0001 | g0235 | EAS | KHV | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02080 | hp1 | a0002 | c0002 | t0003 | g0001 | EAS | KHV | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02080 | hp2 | a0003 | c0003 | t0002 | g0076 | EAS | KHV | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02083 | hp1 | a0002 | c0002 | t0002 | g0118 | EAS | KHV | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02132 | hp1 | a0004 | c0004 | t0001 | g0256 | EAS | KHV | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02145 | hp1 | a0007 | c0010 | t0013 | g0286 | AFR | ACB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02145 | hp2 | a0004 | c0004 | t0028 | g0112 | AFR | ACB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02155 | hp1 | a0002 | c0002 | t0003 | g0257 | EAS | CDX | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02155 | hp2 | a0003 | c0003 | t0002 | g0080 | EAS | CDX | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02165 | hp1 | a0002 | c0002 | t0003 | g0085 | EAS | CDX | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02165 | hp2 | a0003 | c0003 | t0002 | g0143 | EAS | CDX | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02257 | hp1 | a0011 | c0023 | t0033 | g0281 | AFR | ACB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02273 | hp1 | a0004 | c0004 | t0001 | g0262 | AMR | PEL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02273 | hp2 | a0002 | c0002 | t0004 | g0009 | AMR | PEL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02293 | hp1 | a0004 | c0004 | t0001 | g0261 | AMR | PEL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02293 | hp2 | a0002 | c0002 | t0003 | g0084 | AMR | PEL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02572 | hp1 | a0001 | c0001 | t0012 | g0292 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02615 | hp1 | a0004 | c0004 | t0001 | g0218 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02615 | hp2 | a0001 | c0001 | t0019 | g0196 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02622 | hp1 | a0005 | c0005 | t0004 | g0232 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02622 | hp2 | a0001 | c0008 | t0011 | g0233 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02630 | hp1 | a0007 | c0010 | t0013 | g0284 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02630 | hp2 | a0002 | c0002 | t0001 | g0195 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02698 | hp2 | a0003 | c0003 | t0010 | g0092 | SAS | PJL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02717 | hp1 | a0001 | c0001 | t0014 | g0014 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02717 | hp2 | a0001 | c0008 | t0021 | g0044 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02723 | hp1 | a0001 | c0001 | t0005 | g0038 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02723 | hp2 | a0002 | c0019 | t0030 | g0270 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02735 | hp1 | a0009 | c0015 | t0001 | g0140 | SAS | PJL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02735 | hp2 | a0005 | c0005 | t0003 | g0252 | SAS | PJL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02809 | hp1 | a0008 | c0014 | t0004 | g0114 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02809 | hp2 | a0006 | c0007 | t0001 | g0282 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02818 | hp2 | a0006 | c0012 | t0011 | g0266 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02886 | hp2 | a0005 | c0005 | t0004 | g0210 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02895 | hp2 | a0001 | c0001 | t0020 | g0201 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02896 | hp1 | a0006 | c0007 | t0012 | g0015 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02896 | hp2 | a0004 | c0004 | t0001 | g0219 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02897 | hp1 | a0006 | c0007 | t0012 | g0015 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02922 | hp2 | a0004 | c0004 | t0001 | g0289 | AFR | ESN | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | ESN | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02965 | hp2 | a0001 | c0006 | t0009 | g0212 | AFR | ESN | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02970 | hp1 | a0005 | c0005 | t0004 | g0215 | AFR | ESN | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02976 | hp1 | a0001 | c0001 | t0018 | g0269 | AFR | ESN | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02976 | hp2 | a0004 | c0004 | t0034 | g0223 | AFR | ESN | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG03041 | hp1 | a0001 | c0001 | t0019 | g0148 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG03041 | hp2 | a0001 | c0001 | t0020 | g0200 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG03098 | hp1 | a0001 | c0001 | t0014 | g0279 | AFR | MSL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | MSL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG03139 | hp1 | a0001 | c0006 | t0009 | g0211 | AFR | ESN | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG03139 | hp2 | a0005 | c0005 | t0001 | g0217 | AFR | ESN | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG03195 | hp1 | a0006 | c0012 | t0018 | g0267 | AFR | ESN | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG03195 | hp2 | a0001 | c0011 | t0001 | g0013 | AFR | ESN | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG03209 | hp2 | a0002 | c0002 | t0002 | g0263 | AFR | MSL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG03225 | hp2 | a0001 | c0006 | t0023 | g0214 | AFR | MSL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG03239 | hp2 | a0002 | c0002 | t0003 | g0023 | SAS | PJL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | MSL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG03486 | hp1 | a0005 | c0005 | t0002 | g0272 | AFR | MSL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG03486 | hp2 | a0012 | c0021 | t0036 | g0287 | AFR | MSL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG03516 | hp1 | a0004 | c0004 | t0001 | g0221 | AFR | ESN | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | ESN | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG03540 | hp1 | a0007 | c0013 | t0002 | g0268 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG03540 | hp2 | a0006 | c0022 | t0011 | g0265 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG03579 | hp1 | a0005 | c0005 | t0004 | g0222 | AFR | MSL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG03579 | hp2 | a0002 | c0002 | t0004 | g0253 | AFR | MSL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG03654 | hp2 | a0001 | c0001 | t0016 | g0228 | SAS | PJL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG03669 | hp1 | a0002 | c0002 | t0004 | g0160 | SAS | PJL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG03669 | hp2 | a0001 | c0001 | t0016 | g0229 | SAS | PJL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG03688 | hp1 | a0003 | c0003 | t0026 | g0116 | SAS | STU | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | STU | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG03704 | hp1 | a0002 | c0002 | t0004 | g0115 | SAS | PJL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG03710 | hp1 | a0001 | c0001 | t0007 | g0060 | SAS | PJL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG03710 | hp2 | a0002 | c0002 | t0003 | g0186 | SAS | PJL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG03831 | hp1 | a0001 | c0017 | t0001 | g0048 | SAS | BEB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG03831 | hp2 | a0002 | c0002 | t0003 | g0123 | SAS | BEB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG03942 | hp1 | a0001 | c0001 | t0005 | g0010 | SAS | BEB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG03942 | hp2 | a0002 | c0002 | t0008 | g0108 | SAS | BEB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG04199 | hp1 | a0003 | c0003 | t0002 | g0184 | SAS | STU | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG04199 | hp2 | a0002 | c0002 | t0003 | g0107 | SAS | STU | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG04204 | hp1 | a0003 | c0003 | t0002 | g0089 | SAS | STU | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG04204 | hp2 | a0002 | c0002 | t0003 | g0102 | SAS | STU | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG04228 | hp1 | a0002 | c0002 | t0003 | g0130 | SAS | STU | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | STU | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18612 | hp1 | a0002 | c0002 | t0003 | g0001 | EAS | CHB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18612 | hp2 | a0002 | c0002 | t0004 | g0067 | EAS | CHB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18747 | hp1 | a0003 | c0003 | t0002 | g0087 | EAS | CHB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18906 | hp1 | a0005 | c0005 | t0001 | g0220 | AFR | YRI | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18906 | hp2 | a0006 | c0007 | t0005 | g0280 | AFR | YRI | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18939 | hp1 | a0004 | c0004 | t0001 | g0240 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18939 | hp2 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18944 | hp2 | a0003 | c0003 | t0002 | g0075 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18947 | hp1 | a0002 | c0002 | t0003 | g0030 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18947 | hp2 | a0002 | c0002 | t0004 | g0047 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18950 | hp1 | a0003 | c0003 | t0002 | g0072 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18951 | hp1 | a0003 | c0003 | t0002 | g0055 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18951 | hp2 | a0004 | c0004 | t0001 | g0237 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18956 | hp1 | a0002 | c0002 | t0003 | g0111 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18956 | hp2 | a0003 | c0003 | t0002 | g0007 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18957 | hp1 | a0002 | c0002 | t0004 | g0053 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18957 | hp2 | a0002 | c0002 | t0006 | g0170 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18960 | hp2 | a0003 | c0003 | t0002 | g0086 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18962 | hp2 | a0003 | c0003 | t0002 | g0158 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18963 | hp1 | a0004 | c0004 | t0005 | g0238 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18963 | hp2 | a0003 | c0003 | t0002 | g0007 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18964 | hp1 | a0003 | c0003 | t0027 | g0002 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18968 | hp1 | a0002 | c0002 | t0003 | g0027 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18968 | hp2 | a0002 | c0002 | t0003 | g0008 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18973 | hp1 | a0004 | c0004 | t0001 | g0244 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18973 | hp2 | a0002 | c0002 | t0003 | g0142 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18974 | hp2 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18977 | hp1 | a0002 | c0002 | t0006 | g0104 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18978 | hp2 | a0002 | c0002 | t0006 | g0132 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18982 | hp2 | a0002 | c0002 | t0025 | g0106 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18985 | hp1 | a0004 | c0004 | t0001 | g0264 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18985 | hp2 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18989 | hp1 | a0003 | c0003 | t0002 | g0091 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18990 | hp1 | a0004 | c0004 | t0001 | g0004 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18990 | hp2 | a0003 | c0003 | t0002 | g0088 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18994 | hp1 | a0001 | c0001 | t0005 | g0155 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18994 | hp2 | a0002 | c0002 | t0003 | g0138 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18999 | hp1 | a0003 | c0003 | t0002 | g0051 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA18999 | hp2 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19000 | hp1 | a0003 | c0003 | t0002 | g0054 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19000 | hp2 | a0002 | c0002 | t0004 | g0096 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19001 | hp1 | a0004 | c0004 | t0005 | g0259 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19001 | hp2 | a0003 | c0003 | t0002 | g0079 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19002 | hp1 | a0003 | c0003 | t0002 | g0176 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19004 | hp1 | a0004 | c0004 | t0001 | g0004 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19004 | hp2 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19005 | hp1 | a0003 | c0003 | t0002 | g0177 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19007 | hp1 | a0002 | c0002 | t0003 | g0135 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19009 | hp1 | a0004 | c0004 | t0001 | g0004 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19009 | hp2 | a0003 | c0003 | t0002 | g0099 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19030 | hp1 | a0005 | c0005 | t0004 | g0216 | AFR | LWK | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | LWK | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19043 | hp1 | a0001 | c0001 | t0037 | g0273 | AFR | LWK | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19043 | hp2 | a0004 | c0004 | t0001 | g0224 | AFR | LWK | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19057 | hp2 | a0003 | c0003 | t0002 | g0077 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19058 | hp1 | a0005 | c0005 | t0015 | g0242 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19060 | hp1 | a0004 | c0004 | t0001 | g0239 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19062 | hp1 | a0002 | c0002 | t0003 | g0137 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19062 | hp2 | a0002 | c0002 | t0006 | g0105 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19063 | hp2 | a0003 | c0003 | t0002 | g0050 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19065 | hp1 | a0003 | c0003 | t0002 | g0056 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19065 | hp2 | a0002 | c0002 | t0006 | g0033 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19066 | hp2 | a0003 | c0003 | t0002 | g0128 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19068 | hp1 | a0003 | c0003 | t0002 | g0057 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19074 | hp1 | a0003 | c0003 | t0002 | g0073 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19074 | hp2 | a0002 | c0002 | t0003 | g0169 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19077 | hp1 | a0003 | c0003 | t0002 | g0245 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19077 | hp2 | a0002 | c0002 | t0003 | g0008 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19080 | hp1 | a0002 | c0002 | t0004 | g0095 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19080 | hp2 | a0002 | c0002 | t0015 | g0024 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19081 | hp2 | a0002 | c0002 | t0004 | g0094 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19082 | hp2 | a0003 | c0003 | t0002 | g0071 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19083 | hp1 | a0003 | c0003 | t0010 | g0097 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19083 | hp2 | a0004 | c0004 | t0001 | g0254 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19085 | hp2 | a0010 | c0016 | t0002 | g0049 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19088 | hp2 | a0002 | c0002 | t0003 | g0149 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19091 | hp1 | a0003 | c0003 | t0002 | g0125 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19091 | hp2 | a0004 | c0004 | t0035 | g0247 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19240 | hp1 | a0001 | c0011 | t0001 | g0013 | AFR | YRI | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA19240 | hp2 | a0007 | c0010 | t0013 | g0285 | AFR | YRI | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ASW | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA20129 | hp2 | a0002 | c0002 | t0024 | g0066 | AFR | ASW | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0127 | EUR | TSI | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA20752 | hp2 | a0002 | c0002 | t0004 | g0113 | EUR | TSI | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA20805 | hp1 | a0004 | c0009 | t0031 | g0147 | EUR | TSI | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA20805 | hp2 | a0002 | c0002 | t0003 | g0136 | EUR | TSI | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | GIH | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA20905 | hp2 | a0002 | c0002 | t0040 | g0141 | SAS | GIH | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02109 | hp2 | a0001 | c0006 | t0009 | g0213 | AFR | ACB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | ACB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG03471 | hp1 | a0005 | c0005 | t0004 | g0209 | AFR | MSL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | MSL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | USA | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
HG06807 | hp2 | a0002 | c0002 | t0004 | g0260 | AFR | USA | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA20300 | hp1 | a0004 | c0004 | t0001 | g0271 | AFR | USA | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA20300 | hp2 | a0002 | c0002 | t0003 | g0119 | AFR | USA | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA21309 | hp1 | a0001 | c0018 | t0029 | g0040 | AFR | LWK | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
NA21309 | hp2 | a0001 | c0020 | t0001 | g0187 | AFR | LWK | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0008 | g0174 | REF | REF | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
homoSapiens_grch38 | hp1 | a0004 | c0004 | t0001 | g0090 | REF | REF | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:116910247
|
C | G | 4 | a0006a0007a0011others(1): Show | 14 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(11): Show |
missense_variant | MODERATE | c.44C>G | p.Ser15Trp | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/9 | 332/6314 | 44/2640 | 15/879 | chr1 | 116910247 | ||
chr1:116944717
|
C | A | 1 | a0012 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.457C>A | p.Pro153Thr | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/9 | 745/6314 | 457/2640 | 153/879 | chr1 | 116944717 | ||
chr1:116945089
|
T | A | 8 | a0001a0002a0003others(5): Show | 268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
missense_variant | MODERATE | c.829T>A | p.Ser277Thr | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/9 | 1117/6314 | 829/2640 | 277/879 | chr1 | 116945089 | ||
chr1:116949339
|
G | C | 1 | a0009 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.980G>C | p.Gly327Ala | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/9 | 1268/6314 | 980/2640 | 327/879 | chr1 | 116949339 | ||
chr1:116961318
|
G | A | 2 | a0003a0010 | 46 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(43): Show |
missense_variant | MODERATE | c.1289G>A | p.Arg430Gln | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/9 | 1577/6314 | 1289/2640 | 430/879 | chr1 | 116961318 | ||
chr1:116961399
|
A | G | 1 | a0010 | 1 | NA19085.hp2 | missense_variant | MODERATE | c.1370A>G | p.Asn457Ser | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/9 | 1658/6314 | 1370/2640 | 457/879 | chr1 | 116961399 | ||
chr1:116984919
|
A | G | 1 | a0008 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.2407A>G | p.Thr803Ala | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/9 | 2695/6314 | 2407/2640 | 803/879 | chr1 | 116984919 | ||
chr1:116986836
|
G | A | 6 | a0002a0003a0005others(3): Show | 153 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(150): Show |
missense_variant | MODERATE | c.2509G>A | p.Val837Ile | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 2797/6314 | 2509/2640 | 837/879 | chr1 | 116986836 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:116941959
|
C | T | 1 | a0001c0011 | 2 | HG03195.hp2 NA19240.hp1 |
synonymous_variant | LOW | c.294C>T | p.Ala98Ala | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 2/9 | 582/6314 | 294/2640 | 98/879 | chr1 | 116941959 | ||
chr1:116944722
|
G | A | 3 | a0001c0006a0006c0012a0006c0022 | 7 | HG02109.hp2 HG02818.hp2 HG02965.hp2 others(4): Show |
synonymous_variant | LOW | c.462G>A | p.Pro154Pro | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/9 | 750/6314 | 462/2640 | 154/879 | chr1 | 116944722 | ||
chr1:116944770
|
C | T | 1 | a0004c0009 | 3 | HG01515.hp2 HG01517.hp2 NA20805.hp1 |
synonymous_variant | LOW | c.510C>T | p.Thr170Thr | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/9 | 798/6314 | 510/2640 | 170/879 | chr1 | 116944770 | ||
chr1:116945088
|
A | G | 18 | a0001c0001a0001c0006a0001c0008others(15): Show | 268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
synonymous_variant | LOW | c.828A>G | p.Pro276Pro | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/9 | 1116/6314 | 828/2640 | 276/879 | chr1 | 116945088 | ||
chr1:116949502
|
A | G | 1 | a0007c0010 | 3 | HG02145.hp1 HG02630.hp1 NA19240.hp2 |
synonymous_variant | LOW | c.1143A>G | p.Gly381Gly | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/9 | 1431/6314 | 1143/2640 | 381/879 | chr1 | 116949502 | ||
chr1:116961571
|
C | T | 3 | a0001c0008a0006c0022a0012c0021 | 5 | HG01433.hp2 HG02622.hp2 HG02717.hp2 others(2): Show |
synonymous_variant | LOW | c.1542C>T | p.Tyr514Tyr | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/9 | 1830/6314 | 1542/2640 | 514/879 | chr1 | 116961571 | ||
chr1:116967053
|
C | T | 1 | a0001c0020 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.1782C>T | p.Gly594Gly | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/9 | 2070/6314 | 1782/2640 | 594/879 | chr1 | 116967053 | ||
chr1:116967110
|
G | T | 1 | a0002c0019 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1839G>T | p.Val613Val | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/9 | 2127/6314 | 1839/2640 | 613/879 | chr1 | 116967110 | ||
chr1:116967311
|
G | A | 1 | a0002c0019 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.2040G>A | p.Glu680Glu | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/9 | 2328/6314 | 2040/2640 | 680/879 | chr1 | 116967311 | ||
chr1:116984822
|
C | T | 1 | a0001c0011 | 2 | HG03195.hp2 NA19240.hp1 |
synonymous_variant | LOW | c.2310C>T | p.Arg770Arg | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/9 | 2598/6314 | 2310/2640 | 770/879 | chr1 | 116984822 | ||
chr1:116986829
|
G | T | 1 | a0001c0018 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.2502G>T | p.Leu834Leu | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 2790/6314 | 2502/2640 | 834/879 | chr1 | 116986829 | ||
chr1:116986856
|
C | T | 1 | a0001c0017 | 1 | HG03831.hp1 | synonymous_variant | LOW | c.2529C>T | p.Ile843Ile | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 2817/6314 | 2529/2640 | 843/879 | chr1 | 116986856 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:116910138
|
AGAG | A | 2 | a0001c0006t0009a0001c0006t0023 | 4 | HG02109.hp2 HG02965.hp2 HG03139.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-53_-51delGAG | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/9 | 51 | INFO_REALIGN_3_PRIME | chr1 | 116910138 | ||||
chr1:116987237
|
A | AT | 9 | a0002c0002t0003a0002c0002t0006a0002c0002t0015others(6): Show | 54 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*278dupT | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 279 | INFO_REALIGN_3_PRIME | chr1 | 116987237 | ||||
chr1:116987343
|
A | G | 3 | a0001c0001t0007a0001c0001t0014a0001c0001t0038 | 9 | HG00741.hp2 HG01109.hp2 HG01192.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*376A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 376 | chr1 | 116987343 | |||||
chr1:116987367
|
C | T | 1 | a0001c0006t0023 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*400C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 400 | chr1 | 116987367 | |||||
chr1:116987460
|
C | T | 1 | a0001c0001t0014 | 3 | HG01884.hp2 HG02717.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*493C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 493 | chr1 | 116987460 | |||||
chr1:116987571
|
C | CT | 5 | a0001c0001t0005a0001c0001t0037a0004c0004t0005others(2): Show | 11 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*623dupT | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 624 | INFO_REALIGN_3_PRIME | chr1 | 116987571 | ||||
chr1:116987571
|
CT | C | 14 | a0001c0001t0012a0001c0001t0018a0001c0008t0011others(11): Show | 18 | HG00735.hp2 HG01109.hp1 HG01891.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*623delT | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 623 | INFO_REALIGN_3_PRIME | chr1 | 116987571 | ||||
chr1:116987571
|
CTT | C | 26 | a0001c0001t0007a0001c0001t0014a0001c0001t0016others(23): Show | 153 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(150): Show |
3_prime_UTR_variant | MODIFIER | c.*622_*623delTT | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 622 | INFO_REALIGN_3_PRIME | chr1 | 116987571 | ||||
chr1:116987631
|
T | C | 1 | a0002c0002t0022 | 2 | HG01928.hp2 HG01952.hp1 |
3_prime_UTR_variant | MODIFIER | c.*664T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 664 | chr1 | 116987631 | |||||
chr1:116987651
|
A | G | 49 | a0001c0001t0007a0001c0001t0012a0001c0001t0014others(46): Show | 184 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*684A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 684 | chr1 | 116987651 | |||||
chr1:116987855
|
G | A | 48 | a0001c0001t0007a0001c0001t0012a0001c0001t0014others(45): Show | 183 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*888G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 888 | chr1 | 116987855 | |||||
chr1:116987885
|
C | T | 44 | a0001c0001t0007a0001c0001t0012a0001c0001t0014others(41): Show | 176 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*918C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 918 | chr1 | 116987885 | |||||
chr1:116987889
|
C | T | 48 | a0001c0001t0007a0001c0001t0012a0001c0001t0014others(45): Show | 183 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*922C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 922 | chr1 | 116987889 | |||||
chr1:116987942
|
A | G | 1 | a0002c0019t0030 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*975A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 975 | chr1 | 116987942 | |||||
chr1:116987965
|
T | C | 3 | a0001c0006t0009a0001c0006t0023a0004c0004t0034 | 5 | HG02109.hp2 HG02965.hp2 HG02976.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*998T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 998 | chr1 | 116987965 | |||||
chr1:116987999
|
A | G | 10 | a0002c0002t0003a0002c0002t0006a0002c0002t0015others(7): Show | 55 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*1032A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 1032 | chr1 | 116987999 | |||||
chr1:116988040
|
C | A | 1 | a0004c0009t0031 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1073C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 1073 | chr1 | 116988040 | |||||
chr1:116988081
|
G | A | 1 | a0004c0004t0032 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1114G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 1114 | chr1 | 116988081 | |||||
chr1:116988105
|
T | C | 1 | a0002c0002t0024 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1138T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 1138 | chr1 | 116988105 | |||||
chr1:116988179
|
A | G | 2 | a0001c0001t0020a0011c0023t0033 | 3 | HG02257.hp1 HG02895.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1212A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 1212 | chr1 | 116988179 | |||||
chr1:116988418
|
C | T | 1 | a0001c0001t0038 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1451C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 1451 | chr1 | 116988418 | |||||
chr1:116988500
|
A | G | 4 | a0001c0001t0007a0001c0001t0014a0001c0001t0016others(1): Show | 11 | HG00741.hp2 HG01109.hp2 HG01192.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1533A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 1533 | chr1 | 116988500 | |||||
chr1:116988705
|
C | T | 1 | a0001c0001t0019 | 2 | HG02615.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1738C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 1738 | chr1 | 116988705 | |||||
chr1:116988811
|
C | G | 1 | a0002c0019t0030 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1844C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 1844 | chr1 | 116988811 | |||||
chr1:116988813
|
C | T | 1 | a0001c0001t0016 | 2 | HG03654.hp2 HG03669.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1846C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 1846 | chr1 | 116988813 | |||||
chr1:116988998
|
G | A | 31 | a0001c0001t0016a0001c0006t0009a0001c0006t0023others(28): Show | 155 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*2031G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 2031 | chr1 | 116988998 | |||||
chr1:116988999
|
A | G | 9 | a0002c0002t0002a0003c0003t0002a0003c0003t0010others(6): Show | 52 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*2032A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 2032 | chr1 | 116988999 | |||||
chr1:116989005
|
A | G | 4 | a0001c0001t0007a0001c0001t0014a0001c0001t0016others(1): Show | 11 | HG00741.hp2 HG01109.hp2 HG01192.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2038A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 2038 | chr1 | 116989005 | |||||
chr1:116989191
|
T | C | 49 | a0001c0001t0007a0001c0001t0012a0001c0001t0014others(46): Show | 184 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*2224T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 2224 | chr1 | 116989191 | |||||
chr1:116989289
|
A | G | 32 | a0001c0001t0007a0001c0001t0014a0001c0001t0020others(29): Show | 161 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*2322A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 2322 | chr1 | 116989289 | |||||
chr1:116989409
|
T | C | 1 | a0012c0021t0036 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2442T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 2442 | chr1 | 116989409 | |||||
chr1:116989533
|
C | T | 1 | a0007c0010t0013 | 3 | HG02145.hp1 HG02630.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2566C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 2566 | chr1 | 116989533 | |||||
chr1:116989534
|
G | A | 1 | a0002c0002t0039 | 1 | HG01258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2567G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 2567 | chr1 | 116989534 | |||||
chr1:116989669
|
A | G | 19 | a0001c0001t0012a0001c0001t0016a0001c0001t0018others(16): Show | 68 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*2702A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 2702 | chr1 | 116989669 | |||||
chr1:116989690
|
T | G | 1 | a0002c0002t0025 | 1 | NA18982.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2723T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 2723 | chr1 | 116989690 | |||||
chr1:116989750
|
G | T | 27 | a0001c0001t0007a0001c0001t0014a0001c0001t0018others(24): Show | 112 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*2783G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 2783 | chr1 | 116989750 | |||||
chr1:116989755
|
A | T | 1 | a0002c0002t0006 | 6 | HG01934.hp2 NA18957.hp2 NA18977.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2788A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 2788 | chr1 | 116989755 | |||||
chr1:116989887
|
C | A | 3 | a0001c0001t0007a0001c0001t0014a0001c0001t0038 | 9 | HG00741.hp2 HG01109.hp2 HG01192.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2920C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 2920 | chr1 | 116989887 | |||||
chr1:116989897
|
C | G | 1 | a0002c0002t0008 | 4 | HG00733.hp2 HG01099.hp1 HG03942.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2930C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 2930 | chr1 | 116989897 | |||||
chr1:116989912
|
C | T | 1 | a0004c0004t0028 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2945C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 2945 | chr1 | 116989912 | |||||
chr1:116989927
|
C | T | 1 | a0002c0002t0040 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2960C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 2960 | chr1 | 116989927 | |||||
chr1:116990168
|
C | T | 32 | a0001c0001t0012a0001c0001t0016a0001c0001t0018others(29): Show | 114 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*3201C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 3201 | chr1 | 116990168 | |||||
chr1:116990176
|
C | G | 15 | a0001c0001t0012a0001c0001t0016a0001c0001t0018others(12): Show | 63 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*3209C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 3209 | chr1 | 116990176 | |||||
chr1:116990193
|
A | G | 1 | a0003c0003t0027 | 1 | NA18964.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3226A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 3226 | chr1 | 116990193 | |||||
chr1:116990207
|
A | G | 1 | a0003c0003t0026 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3240A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 3240 | chr1 | 116990207 | |||||
chr1:116990269
|
T | C | 11 | a0001c0001t0007a0001c0001t0014a0001c0001t0020others(8): Show | 23 | HG00741.hp2 HG01109.hp2 HG01192.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3302T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 3302 | chr1 | 116990269 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:116910638
|
G | C | 7 | a0002c0002t0003g0016a0002c0002t0003g0017a0002c0002t0003g0018others(4): Show | 7 | HG01106.hp2 HG01255.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.49+386G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116910638 | ||||||
chr1:116910668
|
C | T | 5 | a0001c0001t0001g0290a0001c0001t0001g0293a0001c0001t0005g0291others(2): Show | 5 | HG01891.hp2 HG02486.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+416C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116910668 | ||||||
chr1:116910720
|
G | T | 1 | a0001c0001t0001g0288 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.49+468G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116910720 | ||||||
chr1:116910911
|
A | G | 71 | a0001c0001t0001g0005a0001c0001t0001g0227a0001c0001t0001g0230others(68): Show | 78 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(75): Show |
intron_variant | MODIFIER | c.49+659A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116910911 | ||||||
chr1:116911063
|
C | T | 1 | a0001c0001t0001g0226 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.49+811C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116911063 | ||||||
chr1:116911080
|
A | G | 9 | a0006c0007t0001g0282a0006c0007t0005g0280a0006c0007t0012g0015others(6): Show | 10 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.49+828A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116911080 | ||||||
chr1:116911133
|
G | A | 39 | a0001c0001t0001g0227a0001c0001t0001g0230a0001c0001t0001g0231others(36): Show | 41 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.49+881G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116911133 | ||||||
chr1:116911165
|
C | G | 58 | a0001c0001t0001g0005a0001c0001t0001g0227a0001c0001t0001g0230others(55): Show | 64 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(61): Show |
intron_variant | MODIFIER | c.49+913C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116911165 | ||||||
chr1:116911173
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.49+921C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116911173 | ||||||
chr1:116911321
|
C | T | 16 | a0001c0006t0009g0211a0001c0006t0009g0212a0001c0006t0009g0213others(13): Show | 16 | HG02109.hp2 HG02615.hp1 HG02886.hp2 others(13): Show |
intron_variant | MODIFIER | c.49+1069C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116911321 | ||||||
chr1:116911402
|
A | G | 13 | a0006c0007t0001g0282a0006c0007t0005g0280a0006c0007t0012g0015others(10): Show | 14 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.49+1150A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116911402 | ||||||
chr1:116911403
|
T | C | 71 | a0001c0001t0001g0005a0001c0001t0001g0227a0001c0001t0001g0230others(68): Show | 78 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(75): Show |
intron_variant | MODIFIER | c.49+1151T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116911403 | ||||||
chr1:116911407
|
T | C | 58 | a0001c0001t0001g0005a0001c0001t0001g0227a0001c0001t0001g0230others(55): Show | 64 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(61): Show |
intron_variant | MODIFIER | c.49+1155T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116911407 | ||||||
chr1:116911478
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.49+1226C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116911478 | ||||||
chr1:116911502
|
C | T | 1 | a0004c0004t0001g0264 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.49+1250C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116911502 | ||||||
chr1:116911508
|
C | T | 1 | a0002c0002t0002g0263 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.49+1256C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116911508 | ||||||
chr1:116911590
|
T | G | 1 | a0002c0002t0003g0023 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.49+1338T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116911590 | ||||||
chr1:116911686
|
A | G | 13 | a0006c0007t0001g0282a0006c0007t0005g0280a0006c0007t0012g0015others(10): Show | 14 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.49+1434A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116911686 | ||||||
chr1:116911717
|
A | C | 9 | a0006c0007t0001g0282a0006c0007t0005g0280a0006c0007t0012g0015others(6): Show | 10 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.49+1465A>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116911717 | ||||||
chr1:116911803
|
C | T | 3 | a0001c0001t0001g0278a0001c0001t0014g0014a0001c0001t0014g0279 | 4 | HG01884.hp2 HG02055.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+1551C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116911803 | ||||||
chr1:116911866
|
C | T | 58 | a0001c0001t0001g0005a0001c0001t0001g0227a0001c0001t0001g0230others(55): Show | 64 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(61): Show |
intron_variant | MODIFIER | c.49+1614C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116911866 | ||||||
chr1:116911948
|
G | T | 58 | a0001c0001t0001g0005a0001c0001t0001g0227a0001c0001t0001g0230others(55): Show | 64 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(61): Show |
intron_variant | MODIFIER | c.49+1696G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116911948 | ||||||
chr1:116912190
|
C | T | 1 | a0002c0002t0004g0207 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.49+1938C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116912190 | ||||||
chr1:116912296
|
A | G | 1 | a0003c0003t0002g0206 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.49+2044A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116912296 | ||||||
chr1:116912367
|
G | A | 1 | a0002c0002t0015g0024 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.49+2115G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116912367 | ||||||
chr1:116912431
|
A | G | 9 | a0006c0007t0001g0282a0006c0007t0005g0280a0006c0007t0012g0015others(6): Show | 10 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.49+2179A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116912431 | ||||||
chr1:116912472
|
C | T | 1 | a0004c0004t0001g0224 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.49+2220C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116912472 | ||||||
chr1:116912499
|
C | T | 4 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0204others(1): Show | 4 | HG01192.hp2 HG01358.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+2247C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116912499 | ||||||
chr1:116912820
|
C | T | 3 | a0001c0001t0020g0200a0001c0001t0020g0201a0001c0008t0021g0199 | 3 | HG01433.hp2 HG02895.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.49+2568C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116912820 | ||||||
chr1:116912866
|
G | C | 1 | a0001c0001t0001g0025 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.49+2614G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116912866 | ||||||
chr1:116912927
|
C | T | 13 | a0001c0001t0001g0005a0001c0001t0001g0274a0001c0001t0001g0275others(10): Show | 17 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.49+2675C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116912927 | ||||||
chr1:116912931
|
C | T | 44 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0234others(41): Show | 46 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.49+2679C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116912931 | ||||||
chr1:116913214
|
A | C | 1 | a0001c0001t0038g0198 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.49+2962A>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116913214 | ||||||
chr1:116913379
|
C | T | 1 | a0001c0001t0007g0012 | 2 | HG00741.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.49+3127C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116913379 | ||||||
chr1:116913413
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.49+3161G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116913413 | ||||||
chr1:116913588
|
A | G | 1 | a0004c0004t0034g0223 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.49+3336A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116913588 | ||||||
chr1:116913778
|
A | G | 3 | a0001c0001t0020g0200a0001c0001t0020g0201a0001c0008t0021g0199 | 3 | HG01433.hp2 HG02895.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.49+3526A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116913778 | ||||||
chr1:116913805
|
A | G | 16 | a0001c0006t0009g0211a0001c0006t0009g0212a0001c0006t0009g0213others(13): Show | 16 | HG02109.hp2 HG02615.hp1 HG02886.hp2 others(13): Show |
intron_variant | MODIFIER | c.49+3553A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116913805 | ||||||
chr1:116913822
|
G | C | 15 | a0001c0006t0009g0211a0001c0006t0009g0212a0001c0006t0009g0213others(12): Show | 15 | HG02109.hp2 HG02615.hp1 HG02886.hp2 others(12): Show |
intron_variant | MODIFIER | c.49+3570G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116913822 | ||||||
chr1:116913884
|
G | A | 6 | a0001c0001t0001g0028a0001c0001t0001g0031a0002c0002t0003g0027others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+3632G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116913884 | ||||||
chr1:116914003
|
T | G | 4 | a0001c0001t0001g0005a0001c0001t0037g0273a0004c0004t0001g0271others(1): Show | 6 | HG02109.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+3751T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116914003 | ||||||
chr1:116914217
|
C | T | 5 | a0001c0001t0001g0194a0001c0001t0001g0197a0001c0001t0005g0193others(2): Show | 5 | HG02055.hp1 HG02559.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+3965C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116914217 | ||||||
chr1:116914309
|
G | A | 1 | a0002c0002t0006g0033 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.49+4057G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116914309 | ||||||
chr1:116914314
|
A | G | 19 | a0001c0001t0001g0005a0001c0001t0037g0273a0001c0006t0009g0211others(16): Show | 21 | HG02109.hp1 HG02109.hp2 HG02615.hp1 others(18): Show |
intron_variant | MODIFIER | c.49+4062A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116914314 | ||||||
chr1:116914331
|
C | A | 6 | a0001c0001t0001g0006a0001c0001t0001g0034a0001c0001t0001g0035others(3): Show | 7 | HG02257.hp2 HG02572.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+4079C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116914331 | ||||||
chr1:116914393
|
G | C | 3 | a0006c0012t0011g0266a0006c0012t0018g0267a0006c0022t0011g0265 | 3 | HG02818.hp2 HG03195.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.49+4141G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116914393 | ||||||
chr1:116914505
|
C | G | 2 | a0004c0004t0001g0261a0004c0004t0001g0262 | 2 | HG02273.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.49+4253C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116914505 | ||||||
chr1:116914800
|
A | G | 1 | a0002c0002t0004g0260 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.49+4548A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116914800 | ||||||
chr1:116914822
|
T | A | 1 | a0005c0005t0004g0209 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.49+4570T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116914822 | ||||||
chr1:116914856
|
TC | T | 25 | a0001c0001t0001g0026a0001c0001t0001g0175a0001c0001t0001g0181others(22): Show | 26 | HG00621.hp1 HG00733.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.49+4606delC | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116914856 | |||||
chr1:116915029
|
T | G | 1 | a0002c0002t0004g0207 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.49+4777T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116915029 | ||||||
chr1:116915164
|
T | G | 2 | a0001c0001t0016g0228a0001c0001t0016g0229 | 2 | HG03654.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.49+4912T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116915164 | ||||||
chr1:116915242
|
G | A | 86 | a0001c0001t0001g0005a0001c0001t0001g0230a0001c0001t0001g0231others(83): Show | 93 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(90): Show |
intron_variant | MODIFIER | c.49+4990G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116915242 | ||||||
chr1:116915477
|
T | A | 1 | a0004c0004t0034g0223 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.49+5225T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116915477 | ||||||
chr1:116915670
|
C | G | 3 | a0001c0001t0020g0200a0001c0001t0020g0201a0001c0008t0021g0199 | 3 | HG01433.hp2 HG02895.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.49+5418C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116915670 | ||||||
chr1:116915753
|
G | A | 89 | a0001c0001t0001g0005a0001c0001t0001g0230a0001c0001t0001g0231others(86): Show | 96 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(93): Show |
intron_variant | MODIFIER | c.49+5501G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116915753 | ||||||
chr1:116915862
|
T | A | 5 | a0001c0001t0001g0290a0001c0001t0001g0293a0001c0001t0005g0291others(2): Show | 5 | HG01891.hp2 HG02486.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+5610T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116915862 | ||||||
chr1:116915937
|
G | T | 2 | a0004c0004t0001g0261a0004c0004t0001g0262 | 2 | HG02273.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.49+5685G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116915937 | ||||||
chr1:116915975
|
C | T | 1 | a0002c0002t0008g0174 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.49+5723C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116915975 | ||||||
chr1:116916077
|
C | T | 1 | a0002c0002t0015g0173 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.49+5825C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116916077 | ||||||
chr1:116916108
|
T | C | 25 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0276others(22): Show | 27 | HG01891.hp1 HG01891.hp2 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.49+5856T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116916108 | ||||||
chr1:116916184
|
A | G | 6 | a0001c0001t0001g0290a0001c0001t0001g0293a0001c0001t0005g0291others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+5932A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116916184 | ||||||
chr1:116916553
|
G | T | 2 | a0003c0003t0002g0171a0003c0003t0002g0172 | 2 | HG01928.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.49+6301G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116916553 | ||||||
chr1:116916610
|
G | A | 2 | a0001c0001t0001g0175a0001c0008t0021g0199 | 2 | HG01258.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.49+6358G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116916610 | ||||||
chr1:116916664
|
G | A | 1 | a0002c0002t0003g0023 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.49+6412G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116916664 | ||||||
chr1:116916766
|
G | T | 1 | a0002c0002t0002g0263 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.49+6514G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116916766 | ||||||
chr1:116916769
|
A | C | 1 | a0001c0001t0018g0269 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.49+6517A>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116916769 | ||||||
chr1:116916977
|
G | A | 1 | a0002c0019t0030g0270 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.49+6725G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116916977 | ||||||
chr1:116917154
|
A | G | 1 | a0002c0002t0006g0170 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.49+6902A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116917154 | ||||||
chr1:116917213
|
T | C | 61 | a0001c0001t0001g0005a0001c0001t0001g0230a0001c0001t0001g0231others(58): Show | 66 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(63): Show |
intron_variant | MODIFIER | c.49+6961T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116917213 | ||||||
chr1:116917289
|
G | A | 1 | a0002c0002t0003g0039 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.49+7037G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116917289 | ||||||
chr1:116917309
|
AAC | A | 61 | a0001c0001t0001g0005a0001c0001t0001g0230a0001c0001t0001g0231others(58): Show | 66 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(63): Show |
intron_variant | MODIFIER | c.49+7059_49+7060del others(2): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116917309 | |||||
chr1:116917662
|
C | G | 82 | a0001c0001t0001g0010a0001c0001t0001g0025a0001c0001t0001g0028others(79): Show | 87 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.49+7410C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116917662 | ||||||
chr1:116917794
|
T | C | 1 | a0001c0018t0029g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.49+7542T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116917794 | ||||||
chr1:116917832
|
G | A | 7 | a0001c0001t0001g0005a0001c0001t0001g0230a0001c0001t0001g0231others(4): Show | 9 | HG02109.hp1 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.49+7580G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116917832 | ||||||
chr1:116917902
|
C | T | 12 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0276others(9): Show | 13 | HG01891.hp2 HG02486.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.49+7650C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116917902 | ||||||
chr1:116917961
|
C | T | 1 | a0002c0002t0002g0263 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.49+7709C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116917961 | ||||||
chr1:116918121
|
A | G | 11 | a0004c0004t0001g0218a0004c0004t0001g0219a0004c0004t0001g0221others(8): Show | 11 | HG02615.hp1 HG02809.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.49+7869A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116918121 | ||||||
chr1:116918165
|
G | C | 1 | a0002c0002t0004g0041 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.49+7913G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116918165 | ||||||
chr1:116918278
|
T | C | 4 | a0001c0001t0001g0278a0001c0001t0014g0014a0001c0001t0014g0279others(1): Show | 5 | HG01884.hp2 HG02055.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+8026T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116918278 | ||||||
chr1:116918312
|
T | C | 40 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0194others(37): Show | 43 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.49+8060T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116918312 | ||||||
chr1:116918476
|
A | G | 4 | a0001c0006t0023g0214a0006c0012t0011g0266a0006c0012t0018g0267others(1): Show | 4 | HG02818.hp2 HG03195.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+8224A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116918476 | ||||||
chr1:116918483
|
G | A | 3 | a0001c0001t0001g0290a0001c0001t0005g0291a0004c0004t0001g0289 | 3 | HG01891.hp2 HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.49+8231G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116918483 | ||||||
chr1:116918568
|
A | G | 6 | a0001c0001t0001g0290a0001c0001t0001g0293a0001c0001t0005g0291others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+8316A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116918568 | ||||||
chr1:116918653
|
G | A | 6 | a0001c0001t0001g0230a0001c0001t0001g0274a0001c0001t0001g0275others(3): Show | 7 | HG02280.hp2 HG02965.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.49+8401G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116918653 | ||||||
chr1:116918720
|
A | C | 1 | a0002c0002t0004g0113 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.49+8468A>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116918720 | ||||||
chr1:116918978
|
T | C | 12 | a0004c0004t0001g0218a0004c0004t0001g0219a0004c0004t0001g0221others(9): Show | 12 | HG02615.hp1 HG02809.hp1 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.49+8726T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116918978 | ||||||
chr1:116919291
|
G | A | 15 | a0001c0001t0001g0230a0001c0001t0001g0274a0001c0001t0001g0275others(12): Show | 16 | HG01433.hp2 HG01891.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.49+9039G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116919291 | ||||||
chr1:116919313
|
A | G | 2 | a0001c0001t0020g0200a0001c0001t0020g0201 | 2 | HG02895.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.49+9061A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116919313 | ||||||
chr1:116919392
|
G | A | 1 | a0002c0002t0004g0115 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.49+9140G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116919392 | ||||||
chr1:116919417
|
A | T | 3 | a0001c0001t0037g0273a0004c0004t0001g0271a0005c0005t0002g0272 | 3 | HG03486.hp1 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.49+9165A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116919417 | ||||||
chr1:116919428
|
G | T | 74 | a0001c0001t0001g0005a0001c0001t0001g0227a0001c0001t0001g0231others(71): Show | 79 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(76): Show |
intron_variant | MODIFIER | c.49+9176G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116919428 | ||||||
chr1:116919460
|
C | T | 4 | a0001c0001t0020g0200a0001c0001t0020g0201a0001c0008t0021g0044others(1): Show | 4 | HG01433.hp2 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+9208C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116919460 | ||||||
chr1:116919484
|
A | G | 2 | a0004c0004t0001g0004a0004c0004t0005g0259 | 4 | NA18990.hp1 NA19001.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+9232A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116919484 | ||||||
chr1:116919491
|
T | A | 74 | a0001c0001t0001g0005a0001c0001t0001g0227a0001c0001t0001g0231others(71): Show | 79 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(76): Show |
intron_variant | MODIFIER | c.49+9239T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116919491 | ||||||
chr1:116919496
|
G | C | 74 | a0001c0001t0001g0005a0001c0001t0001g0227a0001c0001t0001g0231others(71): Show | 79 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(76): Show |
intron_variant | MODIFIER | c.49+9244G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116919496 | ||||||
chr1:116919530
|
C | T | 74 | a0001c0001t0001g0005a0001c0001t0001g0227a0001c0001t0001g0231others(71): Show | 79 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(76): Show |
intron_variant | MODIFIER | c.49+9278C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116919530 | ||||||
chr1:116919856
|
T | G | 4 | a0001c0001t0001g0278a0001c0001t0014g0014a0001c0001t0014g0279others(1): Show | 5 | HG01884.hp2 HG02055.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+9604T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116919856 | ||||||
chr1:116919920
|
C | T | 4 | a0001c0001t0020g0200a0001c0001t0020g0201a0001c0008t0021g0044others(1): Show | 4 | HG01433.hp2 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+9668C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116919920 | ||||||
chr1:116920026
|
C | G | 15 | a0001c0001t0001g0230a0001c0001t0001g0274a0001c0001t0001g0275others(12): Show | 16 | HG01433.hp2 HG01891.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.49+9774C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116920026 | ||||||
chr1:116920069
|
C | T | 74 | a0001c0001t0001g0005a0001c0001t0001g0227a0001c0001t0001g0231others(71): Show | 79 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(76): Show |
intron_variant | MODIFIER | c.49+9817C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116920069 | ||||||
chr1:116920178
|
C | T | 74 | a0001c0001t0001g0005a0001c0001t0001g0227a0001c0001t0001g0231others(71): Show | 79 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(76): Show |
intron_variant | MODIFIER | c.49+9926C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116920178 | ||||||
chr1:116920319
|
T | C | 74 | a0001c0001t0001g0005a0001c0001t0001g0227a0001c0001t0001g0231others(71): Show | 79 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(76): Show |
intron_variant | MODIFIER | c.49+10067T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116920319 | ||||||
chr1:116920518
|
C | T | 67 | a0001c0001t0001g0005a0001c0001t0001g0227a0001c0001t0001g0231others(64): Show | 72 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(69): Show |
intron_variant | MODIFIER | c.49+10266C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116920518 | ||||||
chr1:116920532
|
C | A | 74 | a0001c0001t0001g0005a0001c0001t0001g0227a0001c0001t0001g0231others(71): Show | 79 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(76): Show |
intron_variant | MODIFIER | c.49+10280C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116920532 | ||||||
chr1:116920596
|
A | G | 74 | a0001c0001t0001g0005a0001c0001t0001g0227a0001c0001t0001g0231others(71): Show | 79 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(76): Show |
intron_variant | MODIFIER | c.49+10344A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116920596 | ||||||
chr1:116920706
|
C | T | 2 | a0001c0001t0016g0228a0001c0001t0016g0229 | 2 | HG03654.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.49+10454C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116920706 | ||||||
chr1:116920731
|
C | A | 74 | a0001c0001t0001g0005a0001c0001t0001g0227a0001c0001t0001g0231others(71): Show | 79 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(76): Show |
intron_variant | MODIFIER | c.49+10479C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116920731 | ||||||
chr1:116920894
|
G | A | 54 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0031others(51): Show | 59 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.49+10642G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116920894 | ||||||
chr1:116920915
|
T | C | 156 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0025others(153): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.49+10663T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116920915 | ||||||
chr1:116921093
|
T | C | 93 | a0001c0001t0001g0005a0001c0001t0001g0227a0001c0001t0001g0230others(90): Show | 100 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(97): Show |
intron_variant | MODIFIER | c.49+10841T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116921093 | ||||||
chr1:116921228
|
G | A | 1 | a0001c0018t0029g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.49+10976G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116921228 | ||||||
chr1:116921260
|
G | A | 1 | a0007c0013t0002g0268 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.49+11008G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116921260 | ||||||
chr1:116921273
|
A | G | 74 | a0001c0001t0001g0005a0001c0001t0001g0227a0001c0001t0001g0231others(71): Show | 79 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(76): Show |
intron_variant | MODIFIER | c.49+11021A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116921273 | ||||||
chr1:116921275
|
C | T | 7 | a0001c0001t0001g0290a0001c0001t0001g0293a0001c0001t0005g0291others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+11023C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116921275 | ||||||
chr1:116921550
|
A | C | 1 | a0012c0021t0036g0287 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.49+11298A>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116921550 | ||||||
chr1:116921630
|
C | CTT | 6 | a0001c0001t0001g0230a0001c0001t0001g0274a0001c0001t0001g0275others(3): Show | 7 | HG02280.hp2 HG02965.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.49+11390_49+11391d others(4): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116921630 | |||||
chr1:116921676
|
C | A | 1 | a0004c0004t0028g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.49+11424C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116921676 | ||||||
chr1:116921797
|
G | A | 5 | a0001c0001t0001g0290a0001c0001t0001g0293a0001c0001t0005g0291others(2): Show | 5 | HG01891.hp2 HG02486.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+11545G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116921797 | ||||||
chr1:116921840
|
A | G | 4 | a0001c0001t0001g0278a0001c0001t0014g0014a0001c0001t0014g0279others(1): Show | 5 | HG01884.hp2 HG02055.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+11588A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116921840 | ||||||
chr1:116921915
|
C | T | 1 | a0001c0001t0001g0192 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.49+11663C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116921915 | ||||||
chr1:116922106
|
A | G | 7 | a0001c0006t0009g0211a0001c0006t0009g0212a0001c0006t0009g0213others(4): Show | 7 | HG02109.hp2 HG02818.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.49+11854A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116922106 | ||||||
chr1:116922125
|
C | T | 1 | a0002c0019t0030g0270 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.49+11873C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116922125 | ||||||
chr1:116922147
|
C | T | 1 | a0001c0001t0001g0005 | 3 | HG02109.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.49+11895C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116922147 | ||||||
chr1:116922291
|
A | G | 1 | a0004c0004t0001g0224 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.49+12039A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116922291 | ||||||
chr1:116922578
|
G | A | 4 | a0001c0001t0001g0278a0001c0001t0014g0014a0001c0001t0014g0279others(1): Show | 5 | HG01884.hp2 HG02055.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+12326G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116922578 | ||||||
chr1:116922630
|
T | C | 15 | a0001c0001t0001g0230a0001c0001t0001g0274a0001c0001t0001g0275others(12): Show | 16 | HG01433.hp2 HG01891.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.49+12378T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116922630 | ||||||
chr1:116922709
|
G | A | 1 | a0002c0002t0004g0113 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.49+12457G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116922709 | ||||||
chr1:116922921
|
T | C | 1 | a0007c0013t0017g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.49+12669T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116922921 | ||||||
chr1:116922926
|
T | G | 1 | a0002c0002t0004g0047 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.49+12674T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116922926 | ||||||
chr1:116923094
|
T | C | 1 | a0003c0003t0026g0116 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.49+12842T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116923094 | ||||||
chr1:116923097
|
G | C | 1 | a0001c0017t0001g0048 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.49+12845G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116923097 | ||||||
chr1:116923143
|
A | G | 73 | a0001c0001t0001g0005a0001c0001t0001g0231a0001c0001t0001g0234others(70): Show | 78 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(75): Show |
intron_variant | MODIFIER | c.49+12891A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116923143 | ||||||
chr1:116923200
|
T | C | 1 | a0010c0016t0002g0049 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.49+12948T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116923200 | ||||||
chr1:116923211
|
A | G | 1 | a0003c0003t0002g0172 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.49+12959A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116923211 | ||||||
chr1:116923240
|
G | A | 73 | a0001c0001t0001g0005a0001c0001t0001g0231a0001c0001t0001g0234others(70): Show | 78 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(75): Show |
intron_variant | MODIFIER | c.49+12988G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116923240 | ||||||
chr1:116923263
|
G | A | 4 | a0001c0001t0020g0200a0001c0001t0020g0201a0001c0008t0021g0044others(1): Show | 4 | HG01433.hp2 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+13011G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116923263 | ||||||
chr1:116923281
|
C | T | 6 | a0001c0001t0001g0230a0001c0001t0001g0274a0001c0001t0001g0275others(3): Show | 7 | HG02280.hp2 HG02965.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.49+13029C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116923281 | ||||||
chr1:116923282
|
A | G | 92 | a0001c0001t0001g0005a0001c0001t0001g0230a0001c0001t0001g0231others(89): Show | 99 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(96): Show |
intron_variant | MODIFIER | c.49+13030A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116923282 | ||||||
chr1:116923315
|
A | G | 1 | a0002c0002t0003g0111 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.49+13063A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116923315 | ||||||
chr1:116923390
|
T | A | 4 | a0003c0003t0002g0002a0003c0003t0002g0050a0003c0003t0002g0051others(1): Show | 5 | NA18939.hp2 NA18964.hp1 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+13138T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116923390 | ||||||
chr1:116923428
|
T | A | 73 | a0001c0001t0001g0005a0001c0001t0001g0231a0001c0001t0001g0234others(70): Show | 78 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(75): Show |
intron_variant | MODIFIER | c.49+13176T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116923428 | ||||||
chr1:116923484
|
T | C | 2 | a0001c0001t0001g0052a0001c0001t0001g0208 | 2 | HG01243.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.49+13232T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116923484 | ||||||
chr1:116923531
|
T | C | 4 | a0001c0001t0001g0278a0001c0001t0014g0014a0001c0001t0014g0279others(1): Show | 5 | HG01884.hp2 HG02055.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+13279T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116923531 | ||||||
chr1:116923580
|
G | A | 6 | a0001c0001t0001g0230a0001c0001t0001g0274a0001c0001t0001g0275others(3): Show | 7 | HG02280.hp2 HG02965.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.49+13328G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116923580 | ||||||
chr1:116923621
|
G | A | 73 | a0001c0001t0001g0005a0001c0001t0001g0231a0001c0001t0001g0234others(70): Show | 78 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(75): Show |
intron_variant | MODIFIER | c.49+13369G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116923621 | ||||||
chr1:116923718
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.49+13466G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116923718 | ||||||
chr1:116923930
|
A | G | 1 | a0002c0002t0002g0263 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.49+13678A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116923930 | ||||||
chr1:116924054
|
T | C | 1 | a0001c0001t0001g0144 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.49+13802T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116924054 | ||||||
chr1:116924143
|
A | AT | 8 | a0001c0001t0001g0168a0001c0001t0001g0190a0001c0001t0001g0191others(5): Show | 8 | HG00741.hp1 HG02965.hp1 HG04228.hp2 others(5): Show |
intron_variant | MODIFIER | c.49+13913dupT | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116924143 | |||||
chr1:116924143
|
A | ATT | 9 | a0001c0001t0001g0230a0001c0001t0001g0275a0001c0001t0001g0276others(6): Show | 11 | HG01884.hp2 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.49+13912_49+13913d others(4): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116924143 | |||||
chr1:116924143
|
AT | A | 15 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0226others(12): Show | 15 | HG00099.hp2 HG00323.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.49+13913delT | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116924143 | |||||
chr1:116924143
|
ATT | A | 30 | a0001c0001t0001g0231a0001c0001t0001g0234a0001c0001t0018g0269others(27): Show | 30 | HG00438.hp2 HG02109.hp2 HG02273.hp1 others(27): Show |
intron_variant | MODIFIER | c.49+13912_49+13913d others(4): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116924143 | |||||
chr1:116924143
|
ATTT | A | 34 | a0001c0001t0001g0005a0001c0001t0001g0236a0001c0001t0001g0243others(31): Show | 39 | HG01069.hp1 HG01516.hp1 HG01517.hp1 others(36): Show |
intron_variant | MODIFIER | c.49+13911_49+13913d others(5): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116924143 | |||||
chr1:116924184
|
T | G | 73 | a0001c0001t0001g0005a0001c0001t0001g0231a0001c0001t0001g0234others(70): Show | 78 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(75): Show |
intron_variant | MODIFIER | c.49+13932T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116924184 | ||||||
chr1:116924233
|
C | T | 1 | a0004c0004t0001g0224 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.49+13981C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116924233 | ||||||
chr1:116924303
|
CACCCG | C | 73 | a0001c0001t0001g0005a0001c0001t0001g0231a0001c0001t0001g0234others(70): Show | 78 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(75): Show |
intron_variant | MODIFIER | c.49+14052_49+14056d others(7): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116924303 | ||||||
chr1:116924387
|
T | TA | 5 | a0007c0010t0013g0284a0007c0010t0013g0285a0007c0010t0013g0286others(2): Show | 5 | HG01891.hp1 HG02145.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+14136dupA | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116924387 | |||||
chr1:116924551
|
G | A | 92 | a0001c0001t0001g0005a0001c0001t0001g0230a0001c0001t0001g0231others(89): Show | 99 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(96): Show |
intron_variant | MODIFIER | c.49+14299G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116924551 | ||||||
chr1:116924624
|
T | C | 2 | a0003c0003t0002g0054a0003c0003t0002g0055 | 2 | NA18951.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.49+14372T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116924624 | ||||||
chr1:116924636
|
C | T | 5 | a0002c0002t0003g0107a0002c0002t0008g0108a0002c0002t0008g0109others(2): Show | 5 | HG00733.hp2 HG01099.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+14384C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116924636 | ||||||
chr1:116924704
|
T | G | 1 | a0002c0019t0030g0270 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.49+14452T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116924704 | ||||||
chr1:116925068
|
G | C | 73 | a0001c0001t0001g0005a0001c0001t0001g0231a0001c0001t0001g0234others(70): Show | 78 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(75): Show |
intron_variant | MODIFIER | c.49+14816G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116925068 | ||||||
chr1:116925069
|
A | T | 1 | a0004c0004t0001g0254 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.49+14817A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116925069 | ||||||
chr1:116925156
|
AG | A | 4 | a0001c0001t0001g0231a0001c0001t0001g0234a0001c0008t0011g0233others(1): Show | 4 | HG02486.hp2 HG02622.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+14905delG | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116925156 | ||||||
chr1:116925212
|
G | T | 73 | a0001c0001t0001g0005a0001c0001t0001g0231a0001c0001t0001g0234others(70): Show | 78 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(75): Show |
intron_variant | MODIFIER | c.49+14960G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116925212 | ||||||
chr1:116925435
|
G | GA | 72 | a0001c0001t0001g0005a0001c0001t0001g0231a0001c0001t0001g0234others(69): Show | 77 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(74): Show |
intron_variant | MODIFIER | c.49+15193dupA | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116925435 | |||||
chr1:116925759
|
A | C | 1 | a0009c0015t0001g0140 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.49+15507A>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116925759 | ||||||
chr1:116925954
|
G | A | 6 | a0001c0001t0001g0230a0001c0001t0001g0274a0001c0001t0001g0275others(3): Show | 7 | HG02280.hp2 HG02965.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.49+15702G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116925954 | ||||||
chr1:116925995
|
T | A | 1 | a0002c0019t0030g0270 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.50-15720T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116925995 | ||||||
chr1:116926063
|
C | T | 1 | a0012c0021t0036g0287 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.50-15652C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116926063 | ||||||
chr1:116926064
|
AG | A | 73 | a0001c0001t0001g0005a0001c0001t0001g0231a0001c0001t0001g0234others(70): Show | 78 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(75): Show |
intron_variant | MODIFIER | c.50-15649delG | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116926064 | |||||
chr1:116926073
|
GTGT | G | 73 | a0001c0001t0001g0005a0001c0001t0001g0231a0001c0001t0001g0234others(70): Show | 78 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(75): Show |
intron_variant | MODIFIER | c.50-15636_50-15634d others(5): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116926073 | |||||
chr1:116926130
|
G | T | 38 | a0001c0001t0001g0005a0001c0001t0001g0236a0001c0001t0001g0243others(35): Show | 43 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.50-15585G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116926130 | ||||||
chr1:116926145
|
G | A | 1 | a0001c0018t0029g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.50-15570G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116926145 | ||||||
chr1:116926202
|
A | G | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG03239.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.50-15513A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116926202 | ||||||
chr1:116926284
|
G | C | 6 | a0001c0001t0001g0230a0001c0001t0001g0274a0001c0001t0001g0275others(3): Show | 7 | HG02280.hp2 HG02965.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.50-15431G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116926284 | ||||||
chr1:116926286
|
G | C | 7 | a0001c0001t0001g0290a0001c0001t0001g0293a0001c0001t0005g0291others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.50-15429G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116926286 | ||||||
chr1:116926361
|
C | T | 73 | a0001c0001t0001g0005a0001c0001t0001g0231a0001c0001t0001g0234others(70): Show | 78 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(75): Show |
intron_variant | MODIFIER | c.50-15354C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116926361 | ||||||
chr1:116926418
|
C | A | 1 | a0004c0004t0001g0235 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.50-15297C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116926418 | ||||||
chr1:116926686
|
G | A | 6 | a0001c0001t0001g0058a0002c0002t0003g0169a0003c0003t0002g0054others(3): Show | 6 | NA18951.hp1 NA18964.hp2 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-15029G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116926686 | ||||||
chr1:116926700
|
T | A | 73 | a0001c0001t0001g0005a0001c0001t0001g0231a0001c0001t0001g0234others(70): Show | 78 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(75): Show |
intron_variant | MODIFIER | c.50-15015T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116926700 | ||||||
chr1:116926740
|
C | G | 2 | a0001c0001t0001g0194a0002c0002t0001g0195 | 2 | HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.50-14975C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116926740 | ||||||
chr1:116926779
|
C | G | 27 | a0001c0001t0001g0231a0001c0001t0001g0234a0001c0001t0037g0273others(24): Show | 27 | HG02109.hp2 HG02145.hp2 HG02486.hp2 others(24): Show |
intron_variant | MODIFIER | c.50-14936C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116926779 | ||||||
chr1:116926891
|
A | G | 73 | a0001c0001t0001g0005a0001c0001t0001g0231a0001c0001t0001g0234others(70): Show | 78 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(75): Show |
intron_variant | MODIFIER | c.50-14824A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116926891 | ||||||
chr1:116927015
|
C | T | 92 | a0001c0001t0001g0005a0001c0001t0001g0230a0001c0001t0001g0231others(89): Show | 99 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(96): Show |
intron_variant | MODIFIER | c.50-14700C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116927015 | ||||||
chr1:116927113
|
C | T | 1 | a0005c0005t0004g0209 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.50-14602C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116927113 | ||||||
chr1:116927159
|
C | G | 77 | a0001c0001t0001g0005a0001c0001t0001g0231a0001c0001t0001g0234others(74): Show | 82 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(79): Show |
intron_variant | MODIFIER | c.50-14556C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116927159 | ||||||
chr1:116927167
|
A | G | 1 | a0002c0002t0025g0106 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.50-14548A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116927167 | ||||||
chr1:116927254
|
A | G | 1 | a0001c0006t0023g0214 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.50-14461A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116927254 | ||||||
chr1:116927401
|
A | G | 7 | a0001c0001t0001g0290a0001c0001t0001g0293a0001c0001t0005g0291others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.50-14314A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116927401 | ||||||
chr1:116927469
|
G | A | 1 | a0002c0002t0003g0111 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.50-14246G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116927469 | ||||||
chr1:116927525
|
C | CTTTTTTT others(2): Show |
12 | a0001c0001t0001g0230a0001c0001t0001g0274a0001c0001t0001g0275others(9): Show | 14 | HG01884.hp2 HG02145.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.50-14179_50-14171d others(11): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116927525 | |||||
chr1:116927525
|
C | CTTTTTTT others(3): Show |
32 | a0001c0001t0001g0231a0001c0001t0001g0277a0001c0001t0001g0278others(29): Show | 32 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(29): Show |
intron_variant | MODIFIER | c.50-14180_50-14171d others(12): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116927525 | |||||
chr1:116927525
|
C | CTTTTTTT others(4): Show |
5 | a0001c0001t0001g0234a0001c0001t0037g0273a0004c0004t0001g0221others(2): Show | 5 | HG02486.hp2 HG03486.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.50-14181_50-14171d others(13): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116927525 | |||||
chr1:116927525
|
CT | C | 6 | a0001c0001t0020g0200a0001c0001t0020g0201a0001c0008t0021g0044others(3): Show | 6 | HG01433.hp2 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-14171delT | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116927525 | |||||
chr1:116927525
|
CTT | C | 37 | a0001c0001t0001g0005a0001c0001t0001g0236a0001c0001t0001g0243others(34): Show | 42 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.50-14172_50-14171d others(4): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116927525 | |||||
chr1:116927543
|
T | C | 37 | a0001c0001t0001g0005a0001c0001t0001g0236a0001c0001t0001g0243others(34): Show | 42 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.50-14172T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116927543 | ||||||
chr1:116927598
|
A | G | 3 | a0001c0001t0037g0273a0004c0004t0001g0271a0005c0005t0002g0272 | 3 | HG03486.hp1 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.50-14117A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116927598 | ||||||
chr1:116927690
|
T | C | 75 | a0001c0001t0001g0005a0001c0001t0001g0231a0001c0001t0001g0234others(72): Show | 80 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(77): Show |
intron_variant | MODIFIER | c.50-14025T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116927690 | ||||||
chr1:116927872
|
T | G | 37 | a0001c0001t0001g0005a0001c0001t0001g0236a0001c0001t0001g0243others(34): Show | 42 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.50-13843T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116927872 | ||||||
chr1:116927988
|
G | A | 1 | a0002c0002t0002g0263 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.50-13727G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116927988 | ||||||
chr1:116927990
|
A | T | 13 | a0004c0004t0001g0218a0004c0004t0001g0219a0004c0004t0001g0221others(10): Show | 13 | HG02145.hp2 HG02615.hp1 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.50-13725A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116927990 | ||||||
chr1:116928207
|
G | A | 1 | a0005c0005t0004g0209 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.50-13508G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116928207 | ||||||
chr1:116928223
|
G | C | 1 | a0004c0009t0031g0147 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.50-13492G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116928223 | ||||||
chr1:116928228
|
C | A | 10 | a0001c0001t0037g0273a0001c0006t0009g0211a0001c0006t0009g0212others(7): Show | 10 | HG02109.hp2 HG02818.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.50-13487C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116928228 | ||||||
chr1:116928266
|
A | G | 4 | a0007c0010t0013g0284a0007c0010t0013g0285a0007c0010t0013g0286others(1): Show | 4 | HG02145.hp1 HG02630.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-13449A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116928266 | ||||||
chr1:116928285
|
C | T | 4 | a0001c0001t0001g0278a0001c0001t0014g0014a0001c0001t0014g0279others(1): Show | 5 | HG01884.hp2 HG02055.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.50-13430C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116928285 | ||||||
chr1:116928332
|
C | G | 49 | a0001c0001t0001g0005a0001c0001t0001g0230a0001c0001t0001g0236others(46): Show | 55 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-13383C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116928332 | ||||||
chr1:116928336
|
T | C | 1 | a0001c0001t0001g0192 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.50-13379T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116928336 | ||||||
chr1:116928472
|
T | C | 39 | a0001c0001t0001g0231a0001c0001t0001g0234a0001c0001t0001g0290others(36): Show | 39 | HG01433.hp2 HG01891.hp2 HG02109.hp2 others(36): Show |
intron_variant | MODIFIER | c.50-13243T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116928472 | ||||||
chr1:116928631
|
G | A | 7 | a0001c0006t0009g0211a0001c0006t0009g0212a0001c0006t0009g0213others(4): Show | 7 | HG02109.hp2 HG02818.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.50-13084G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116928631 | ||||||
chr1:116928642
|
C | CA | 6 | a0001c0001t0001g0227a0001c0001t0007g0012a0001c0001t0007g0059others(3): Show | 7 | HG00280.hp2 HG00741.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.50-13073_50-13072i others(3): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116928642 | ||||||
chr1:116928805
|
T | G | 1 | a0001c0011t0001g0013 | 2 | HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.50-12910T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116928805 | ||||||
chr1:116928887
|
C | T | 38 | a0001c0001t0001g0231a0001c0001t0001g0234a0001c0001t0001g0290others(35): Show | 38 | HG01433.hp2 HG01891.hp2 HG02109.hp2 others(35): Show |
intron_variant | MODIFIER | c.50-12828C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116928887 | ||||||
chr1:116929292
|
C | T | 4 | a0001c0001t0001g0231a0001c0001t0001g0234a0001c0008t0011g0233others(1): Show | 4 | HG02486.hp2 HG02622.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-12423C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116929292 | ||||||
chr1:116929334
|
A | G | 1 | a0001c0001t0001g0293 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.50-12381A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116929334 | ||||||
chr1:116929353
|
C | T | 1 | a0004c0004t0001g0224 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.50-12362C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116929353 | ||||||
chr1:116929404
|
C | G | 1 | a0001c0001t0001g0167 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.50-12311C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116929404 | ||||||
chr1:116929427
|
G | A | 54 | a0001c0001t0001g0005a0001c0001t0001g0230a0001c0001t0001g0236others(51): Show | 61 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(58): Show |
intron_variant | MODIFIER | c.50-12288G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116929427 | ||||||
chr1:116929503
|
G | A | 1 | a0002c0002t0002g0118 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.50-12212G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116929503 | ||||||
chr1:116929532
|
C | T | 2 | a0001c0001t0016g0228a0001c0001t0016g0229 | 2 | HG03654.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.50-12183C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116929532 | ||||||
chr1:116929641
|
A | G | 1 | a0002c0019t0030g0270 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.50-12074A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116929641 | ||||||
chr1:116929796
|
G | C | 1 | a0001c0001t0038g0198 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.50-11919G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116929796 | ||||||
chr1:116929906
|
C | G | 6 | a0001c0001t0001g0230a0001c0001t0001g0274a0001c0001t0001g0275others(3): Show | 7 | HG02280.hp2 HG02965.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.50-11809C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116929906 | ||||||
chr1:116929939
|
C | T | 1 | a0007c0013t0002g0268 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.50-11776C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116929939 | ||||||
chr1:116930080
|
T | G | 1 | a0002c0002t0025g0106 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.50-11635T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116930080 | ||||||
chr1:116930081
|
A | G | 41 | a0001c0001t0001g0231a0001c0001t0001g0234a0001c0001t0001g0290others(38): Show | 41 | HG01433.hp2 HG01891.hp2 HG02109.hp2 others(38): Show |
intron_variant | MODIFIER | c.50-11634A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116930081 | ||||||
chr1:116930193
|
A | G | 54 | a0001c0001t0001g0005a0001c0001t0001g0230a0001c0001t0001g0243others(51): Show | 58 | HG00438.hp2 HG00597.hp1 HG01069.hp1 others(55): Show |
intron_variant | MODIFIER | c.50-11522A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116930193 | ||||||
chr1:116930284
|
T | C | 32 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0231others(29): Show | 32 | HG01433.hp2 HG01891.hp1 HG02145.hp2 others(29): Show |
intron_variant | MODIFIER | c.50-11431T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116930284 | ||||||
chr1:116930342
|
A | G | 2 | a0001c0001t0001g0146a0002c0002t0003g0039 | 2 | HG00099.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.50-11373A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116930342 | ||||||
chr1:116930377
|
A | G | 128 | a0001c0001t0001g0010a0001c0001t0001g0025a0001c0001t0001g0028others(125): Show | 137 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.50-11338A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116930377 | ||||||
chr1:116930457
|
C | T | 1 | a0002c0002t0006g0139 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.50-11258C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116930457 | ||||||
chr1:116930663
|
C | T | 2 | a0001c0001t0037g0273a0007c0010t0013g0284 | 2 | HG02630.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.50-11052C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116930663 | ||||||
chr1:116930714
|
C | G | 1 | a0002c0002t0015g0024 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.50-11001C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116930714 | ||||||
chr1:116930719
|
A | G | 11 | a0001c0001t0001g0035a0001c0001t0001g0293a0001c0008t0011g0233others(8): Show | 12 | HG01891.hp1 HG02145.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.50-10996A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116930719 | ||||||
chr1:116930797
|
G | A | 64 | a0001c0001t0001g0006a0001c0001t0001g0025a0001c0001t0001g0028others(61): Show | 68 | HG00735.hp1 HG00741.hp2 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.50-10918G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116930797 | ||||||
chr1:116930813
|
GC | G | 3 | a0006c0012t0011g0266a0006c0012t0018g0267a0006c0022t0011g0265 | 3 | HG02818.hp2 HG03195.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.50-10900delC | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116930813 | |||||
chr1:116930826
|
G | A | 2 | a0001c0001t0001g0028a0002c0002t0003g0029 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.50-10889G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116930826 | ||||||
chr1:116930841
|
C | G | 2 | a0003c0003t0002g0054a0003c0003t0002g0055 | 2 | NA18951.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.50-10874C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116930841 | ||||||
chr1:116930966
|
A | G | 43 | a0001c0001t0001g0146a0001c0001t0001g0150a0001c0001t0001g0156others(40): Show | 46 | HG00099.hp2 HG00735.hp1 HG01433.hp2 others(43): Show |
intron_variant | MODIFIER | c.50-10749A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116930966 | ||||||
chr1:116931130
|
A | G | 1 | a0003c0003t0010g0092 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.50-10585A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116931130 | ||||||
chr1:116931133
|
C | T | 1 | a0003c0003t0002g0091 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.50-10582C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116931133 | ||||||
chr1:116931218
|
G | A | 293 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(290): Show | 312 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.50-10497G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116931218 | ||||||
chr1:116931403
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.50-10312C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116931403 | ||||||
chr1:116931496
|
C | CT | 8 | a0001c0001t0001g0293a0001c0001t0012g0292a0001c0001t0016g0228others(5): Show | 8 | HG02145.hp1 HG02572.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.50-10204dupT | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116931496 | |||||
chr1:116931496
|
CTTT | C | 55 | a0001c0001t0001g0231a0001c0001t0001g0234a0001c0001t0001g0243others(52): Show | 57 | HG00438.hp2 HG01071.hp1 HG01169.hp1 others(54): Show |
intron_variant | MODIFIER | c.50-10206_50-10204d others(5): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116931496 | |||||
chr1:116931524
|
C | T | 57 | a0001c0001t0001g0231a0001c0001t0001g0234a0001c0001t0001g0243others(54): Show | 59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-10191C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116931524 | ||||||
chr1:116931541
|
C | T | 57 | a0001c0001t0001g0231a0001c0001t0001g0234a0001c0001t0001g0243others(54): Show | 59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-10174C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116931541 | ||||||
chr1:116931588
|
C | T | 57 | a0001c0001t0001g0231a0001c0001t0001g0234a0001c0001t0001g0243others(54): Show | 59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-10127C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116931588 | ||||||
chr1:116931607
|
T | G | 57 | a0001c0001t0001g0231a0001c0001t0001g0234a0001c0001t0001g0243others(54): Show | 59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-10108T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116931607 | ||||||
chr1:116931775
|
A | G | 199 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0025others(196): Show | 209 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.50-9940A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116931775 | ||||||
chr1:116931849
|
G | A | 7 | a0001c0006t0009g0211a0001c0006t0009g0212a0001c0006t0009g0213others(4): Show | 7 | HG02109.hp2 HG02818.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.50-9866G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116931849 | ||||||
chr1:116931986
|
C | A | 8 | a0001c0001t0001g0005a0001c0001t0001g0278a0001c0001t0014g0014others(5): Show | 12 | HG01515.hp2 HG01517.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.50-9729C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116931986 | ||||||
chr1:116932185
|
G | C | 1 | a0011c0023t0033g0281 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.50-9530G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116932185 | ||||||
chr1:116932254
|
G | A | 57 | a0001c0001t0001g0231a0001c0001t0001g0234a0001c0001t0001g0243others(54): Show | 59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-9461G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116932254 | ||||||
chr1:116932321
|
A | G | 1 | a0001c0001t0018g0269 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.50-9394A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116932321 | ||||||
chr1:116932334
|
G | A | 57 | a0001c0001t0001g0231a0001c0001t0001g0234a0001c0001t0001g0243others(54): Show | 59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-9381G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116932334 | ||||||
chr1:116932344
|
G | A | 1 | a0004c0004t0001g0224 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.50-9371G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116932344 | ||||||
chr1:116932358
|
G | A | 57 | a0001c0001t0001g0231a0001c0001t0001g0234a0001c0001t0001g0243others(54): Show | 59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-9357G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116932358 | ||||||
chr1:116932392
|
G | A | 1 | a0007c0013t0017g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.50-9323G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116932392 | ||||||
chr1:116932535
|
C | T | 57 | a0001c0001t0001g0231a0001c0001t0001g0234a0001c0001t0001g0243others(54): Show | 59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-9180C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116932535 | ||||||
chr1:116932553
|
A | G | 190 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0025others(187): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.50-9162A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116932553 | ||||||
chr1:116932619
|
C | A | 1 | a0003c0003t0002g0069 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.50-9096C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116932619 | ||||||
chr1:116932624
|
A | AT | 57 | a0001c0001t0001g0231a0001c0001t0001g0234a0001c0001t0001g0243others(54): Show | 59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-9089dupT | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116932624 | |||||
chr1:116932636
|
G | A | 57 | a0001c0001t0001g0231a0001c0001t0001g0234a0001c0001t0001g0243others(54): Show | 59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-9079G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116932636 | ||||||
chr1:116932839
|
G | A | 57 | a0001c0001t0001g0231a0001c0001t0001g0234a0001c0001t0001g0243others(54): Show | 59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-8876G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116932839 | ||||||
chr1:116932943
|
T | A | 1 | a0012c0021t0036g0287 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.50-8772T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116932943 | ||||||
chr1:116933093
|
A | G | 190 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0025others(187): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.50-8622A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116933093 | ||||||
chr1:116933170
|
A | G | 237 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(234): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.50-8545A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116933170 | ||||||
chr1:116933360
|
G | T | 237 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(234): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.50-8355G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116933360 | ||||||
chr1:116933371
|
C | A | 1 | a0001c0001t0001g0025 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.50-8344C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116933371 | ||||||
chr1:116933619
|
G | T | 1 | a0004c0004t0001g0224 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.50-8096G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116933619 | ||||||
chr1:116933822
|
T | G | 57 | a0001c0001t0001g0231a0001c0001t0001g0234a0001c0001t0001g0243others(54): Show | 59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-7893T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116933822 | ||||||
chr1:116933844
|
A | G | 184 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0025others(181): Show | 193 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.50-7871A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116933844 | ||||||
chr1:116934200
|
C | G | 57 | a0001c0001t0001g0231a0001c0001t0001g0234a0001c0001t0001g0243others(54): Show | 59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-7515C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116934200 | ||||||
chr1:116934224
|
C | T | 7 | a0001c0001t0016g0228a0001c0001t0016g0229a0001c0001t0018g0269others(4): Show | 7 | HG02145.hp1 HG02630.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.50-7491C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116934224 | ||||||
chr1:116934486
|
C | G | 45 | a0001c0001t0001g0243a0001c0001t0001g0258a0001c0006t0009g0211others(42): Show | 47 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.50-7229C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116934486 | ||||||
chr1:116934619
|
G | A | 57 | a0001c0001t0001g0231a0001c0001t0001g0234a0001c0001t0001g0243others(54): Show | 59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-7096G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116934619 | ||||||
chr1:116934630
|
G | A | 57 | a0001c0001t0001g0231a0001c0001t0001g0234a0001c0001t0001g0243others(54): Show | 59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-7085G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116934630 | ||||||
chr1:116934674
|
A | G | 1 | a0002c0002t0003g0142 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.50-7041A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116934674 | ||||||
chr1:116934675
|
T | C | 1 | a0003c0003t0002g0158 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.50-7040T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116934675 | ||||||
chr1:116934679
|
CT | C | 57 | a0001c0001t0001g0231a0001c0001t0001g0234a0001c0001t0001g0243others(54): Show | 59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-7034delT | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116934679 | |||||
chr1:116934764
|
G | T | 184 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0025others(181): Show | 193 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.50-6951G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116934764 | ||||||
chr1:116934852
|
A | G | 57 | a0001c0001t0001g0231a0001c0001t0001g0234a0001c0001t0001g0243others(54): Show | 59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-6863A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116934852 | ||||||
chr1:116934950
|
A | G | 251 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0025others(248): Show | 262 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.50-6765A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116934950 | ||||||
chr1:116935198
|
G | C | 251 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0025others(248): Show | 262 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.50-6517G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116935198 | ||||||
chr1:116935248
|
G | A | 10 | a0001c0001t0001g0293a0001c0001t0012g0292a0001c0001t0016g0228others(7): Show | 10 | HG02145.hp1 HG02572.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.50-6467G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116935248 | ||||||
chr1:116935423
|
T | G | 1 | a0001c0001t0001g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.50-6292T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116935423 | ||||||
chr1:116935484
|
G | A | 57 | a0001c0001t0001g0231a0001c0001t0001g0234a0001c0001t0001g0243others(54): Show | 59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-6231G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116935484 | ||||||
chr1:116935662
|
T | C | 57 | a0001c0001t0001g0231a0001c0001t0001g0234a0001c0001t0001g0243others(54): Show | 59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-6053T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116935662 | ||||||
chr1:116935735
|
G | A | 2 | a0004c0004t0001g0224a0011c0023t0033g0281 | 2 | HG02257.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.50-5980G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116935735 | ||||||
chr1:116935860
|
T | C | 1 | a0002c0002t0004g0249 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.50-5855T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116935860 | ||||||
chr1:116935954
|
G | A | 1 | a0001c0001t0018g0269 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.50-5761G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116935954 | ||||||
chr1:116935961
|
T | A | 1 | a0005c0005t0004g0210 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.50-5754T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116935961 | ||||||
chr1:116936242
|
TAAC | T | 183 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0025others(180): Show | 192 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.50-5470_50-5468del others(3): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116936242 | |||||
chr1:116936359
|
T | C | 11 | a0001c0001t0001g0035a0001c0001t0001g0042a0001c0001t0001g0230others(8): Show | 12 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.50-5356T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116936359 | ||||||
chr1:116936571
|
T | C | 57 | a0001c0001t0001g0231a0001c0001t0001g0234a0001c0001t0001g0243others(54): Show | 59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-5144T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116936571 | ||||||
chr1:116936623
|
C | T | 45 | a0001c0001t0001g0243a0001c0001t0001g0258a0001c0006t0009g0211others(42): Show | 47 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.50-5092C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116936623 | ||||||
chr1:116936669
|
A | G | 1 | a0004c0004t0001g0244 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.50-5046A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116936669 | ||||||
chr1:116936749
|
C | T | 57 | a0001c0001t0001g0231a0001c0001t0001g0234a0001c0001t0001g0243others(54): Show | 59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-4966C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116936749 | ||||||
chr1:116936871
|
G | A | 1 | a0002c0002t0004g0249 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.50-4844G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116936871 | ||||||
chr1:116936953
|
T | C | 45 | a0001c0001t0001g0243a0001c0001t0001g0258a0001c0006t0009g0211others(42): Show | 47 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.50-4762T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116936953 | ||||||
chr1:116936958
|
G | A | 1 | a0002c0019t0030g0270 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.50-4757G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116936958 | ||||||
chr1:116937072
|
A | C | 1 | a0001c0001t0018g0269 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.50-4643A>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116937072 | ||||||
chr1:116937130
|
T | C | 264 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(261): Show | 280 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(277): Show |
intron_variant | MODIFIER | c.50-4585T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116937130 | ||||||
chr1:116937541
|
G | T | 45 | a0001c0001t0001g0243a0001c0001t0001g0258a0001c0006t0009g0211others(42): Show | 47 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.50-4174G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116937541 | ||||||
chr1:116937658
|
G | T | 1 | a0002c0002t0006g0105 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.50-4057G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116937658 | ||||||
chr1:116937694
|
G | A | 24 | a0001c0001t0001g0005a0001c0001t0001g0227a0001c0001t0001g0278others(21): Show | 29 | HG00280.hp2 HG00741.hp2 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.50-4021G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116937694 | ||||||
chr1:116937703
|
C | G | 1 | a0003c0003t0002g0089 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.50-4012C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116937703 | ||||||
chr1:116938079
|
A | G | 1 | a0003c0003t0002g0089 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.50-3636A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116938079 | ||||||
chr1:116938268
|
A | G | 250 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(247): Show | 267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.50-3447A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116938268 | ||||||
chr1:116938371
|
A | T | 9 | a0002c0002t0004g0003a0002c0002t0004g0009a0002c0002t0004g0047others(6): Show | 12 | HG00558.hp1 HG00597.hp1 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.50-3344A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116938371 | ||||||
chr1:116938673
|
C | T | 1 | a0001c0001t0016g0229 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.50-3042C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116938673 | ||||||
chr1:116938700
|
A | G | 1 | a0001c0006t0009g0213 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.50-3015A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116938700 | ||||||
chr1:116938743
|
G | C | 4 | a0001c0008t0021g0044a0001c0008t0021g0199a0004c0004t0001g0224others(1): Show | 4 | HG01433.hp2 HG02257.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-2972G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116938743 | ||||||
chr1:116938763
|
T | G | 1 | a0001c0001t0001g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.50-2952T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116938763 | ||||||
chr1:116938833
|
A | G | 7 | a0001c0006t0009g0211a0001c0006t0009g0212a0001c0006t0009g0213others(4): Show | 7 | HG02109.hp2 HG02818.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.50-2882A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116938833 | ||||||
chr1:116939040
|
G | A | 1 | a0005c0005t0004g0209 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.50-2675G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116939040 | ||||||
chr1:116939124
|
C | T | 1 | a0002c0002t0003g0102 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.50-2591C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116939124 | ||||||
chr1:116939185
|
C | T | 2 | a0003c0003t0002g0088a0003c0003t0002g0177 | 2 | NA18990.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.50-2530C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116939185 | ||||||
chr1:116939200
|
A | G | 1 | a0007c0010t0013g0284 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.50-2515A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116939200 | ||||||
chr1:116939204
|
C | T | 1 | a0012c0021t0036g0287 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.50-2511C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116939204 | ||||||
chr1:116939462
|
T | C | 249 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(246): Show | 266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.50-2253T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116939462 | ||||||
chr1:116939973
|
A | G | 2 | a0003c0003t0002g0086a0003c0003t0002g0087 | 2 | NA18747.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.50-1742A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116939973 | ||||||
chr1:116939974
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.50-1741A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116939974 | ||||||
chr1:116940001
|
T | C | 1 | a0001c0001t0001g0231 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.50-1714T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116940001 | ||||||
chr1:116940143
|
C | T | 183 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0025others(180): Show | 192 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.50-1572C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116940143 | ||||||
chr1:116940181
|
A | C | 3 | a0001c0001t0001g0293a0001c0001t0012g0292a0001c0001t0037g0273 | 3 | HG02572.hp1 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.50-1534A>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116940181 | ||||||
chr1:116940192
|
C | T | 1 | a0007c0013t0017g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.50-1523C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116940192 | ||||||
chr1:116940196
|
A | G | 30 | a0001c0001t0001g0005a0001c0001t0001g0227a0001c0001t0001g0231others(27): Show | 35 | HG00280.hp2 HG00741.hp2 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.50-1519A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116940196 | ||||||
chr1:116940279
|
C | T | 1 | a0011c0023t0033g0281 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.50-1436C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116940279 | ||||||
chr1:116940447
|
T | C | 2 | a0002c0019t0030g0270a0012c0021t0036g0287 | 2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.50-1268T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116940447 | ||||||
chr1:116940491
|
C | G | 8 | a0001c0008t0021g0044a0001c0008t0021g0199a0004c0004t0001g0224others(5): Show | 8 | HG01433.hp2 HG02145.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.50-1224C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116940491 | ||||||
chr1:116940651
|
C | T | 7 | a0001c0001t0001g0005a0001c0001t0001g0278a0001c0001t0014g0014others(4): Show | 11 | HG01515.hp2 HG01517.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.50-1064C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116940651 | ||||||
chr1:116940739
|
G | A | 183 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0025others(180): Show | 192 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.50-976G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116940739 | ||||||
chr1:116941583
|
A | T | 1 | a0001c0001t0001g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.50-132A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116941583 | ||||||
chr1:116942215
|
T | G | 1 | a0007c0013t0002g0268 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.418+132T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 2/8 | chr1 | 116942215 | ||||||
chr1:116942364
|
G | C | 1 | a0011c0023t0033g0281 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.418+281G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 2/8 | chr1 | 116942364 | ||||||
chr1:116943096
|
A | G | 2 | a0004c0004t0001g0004a0004c0004t0005g0259 | 4 | NA18990.hp1 NA19001.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.418+1013A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 2/8 | chr1 | 116943096 | ||||||
chr1:116943203
|
A | G | 1 | a0002c0002t0004g0068 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.418+1120A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 2/8 | chr1 | 116943203 | ||||||
chr1:116943276
|
A | G | 1 | a0004c0004t0001g0224 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.418+1193A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 2/8 | chr1 | 116943276 | ||||||
chr1:116943298
|
A | T | 2 | a0002c0019t0030g0270a0012c0021t0036g0287 | 2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.418+1215A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 2/8 | chr1 | 116943298 | ||||||
chr1:116943347
|
G | A | 49 | a0001c0001t0001g0005a0001c0001t0001g0093a0001c0001t0001g0157others(46): Show | 57 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.418+1264G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 2/8 | chr1 | 116943347 | ||||||
chr1:116943563
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0278a0001c0001t0014g0014others(1): Show | 7 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.419-1116G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 2/8 | chr1 | 116943563 | ||||||
chr1:116943732
|
G | A | 6 | a0001c0001t0001g0227a0001c0001t0007g0012a0001c0001t0007g0059others(3): Show | 7 | HG00280.hp2 HG00741.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.419-947G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 2/8 | chr1 | 116943732 | ||||||
chr1:116943828
|
G | A | 190 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0025others(187): Show | 200 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.419-851G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 2/8 | chr1 | 116943828 | ||||||
chr1:116943840
|
A | T | 1 | a0012c0021t0036g0287 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.419-839A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 2/8 | chr1 | 116943840 | ||||||
chr1:116943934
|
C | T | 1 | a0002c0002t0024g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.419-745C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 2/8 | chr1 | 116943934 | ||||||
chr1:116944197
|
C | T | 1 | a0003c0003t0002g0206 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.419-482C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 2/8 | chr1 | 116944197 | ||||||
chr1:116944477
|
G | T | 28 | a0001c0001t0001g0093a0001c0001t0001g0157a0001c0018t0029g0040others(25): Show | 31 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.419-202G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 2/8 | chr1 | 116944477 | ||||||
chr1:116944521
|
A | G | 4 | a0001c0001t0012g0292a0001c0001t0018g0269a0001c0001t0037g0273others(1): Show | 4 | HG02572.hp1 HG02976.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.419-158A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 2/8 | chr1 | 116944521 | ||||||
chr1:116944543
|
G | A | 42 | a0001c0001t0001g0093a0001c0001t0001g0157a0001c0001t0001g0234others(39): Show | 45 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.419-136G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 2/8 | chr1 | 116944543 | ||||||
chr1:116944648
|
G | A | 94 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0036others(91): Show | 98 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.419-31G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 2/8 | chr1 | 116944648 | ||||||
chr1:116945262
|
G | A | 190 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(187): Show | 202 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.832+170G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116945262 | ||||||
chr1:116945484
|
C | T | 2 | a0002c0002t0008g0109a0002c0002t0008g0110 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.832+392C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116945484 | ||||||
chr1:116945569
|
C | T | 1 | a0002c0002t0022g0019 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.832+477C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116945569 | ||||||
chr1:116945744
|
C | CT | 10 | a0001c0001t0001g0208a0001c0001t0001g0234a0001c0008t0011g0233others(7): Show | 10 | HG01243.hp1 HG01433.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.832+669dupT | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 116945744 | |||||
chr1:116945744
|
CT | C | 46 | a0001c0001t0001g0006a0001c0001t0001g0034a0001c0001t0001g0043others(43): Show | 50 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.832+669delT | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 116945744 | |||||
chr1:116945778
|
A | G | 1 | a0003c0003t0002g0089 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.832+686A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116945778 | ||||||
chr1:116945861
|
T | G | 7 | a0001c0006t0009g0211a0001c0006t0009g0212a0001c0006t0009g0213others(4): Show | 7 | HG02109.hp2 HG02818.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.832+769T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116945861 | ||||||
chr1:116945877
|
A | G | 9 | a0001c0001t0001g0276a0001c0001t0012g0292a0001c0001t0016g0228others(6): Show | 9 | HG01891.hp1 HG02572.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.832+785A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116945877 | ||||||
chr1:116946133
|
C | T | 1 | a0007c0010t0013g0284 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.832+1041C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116946133 | ||||||
chr1:116946142
|
A | T | 1 | a0002c0002t0008g0108 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.832+1050A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116946142 | ||||||
chr1:116946442
|
G | A | 1 | a0001c0001t0001g0151 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.832+1350G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116946442 | ||||||
chr1:116946794
|
G | A | 1 | a0003c0003t0002g0045 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.832+1702G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116946794 | ||||||
chr1:116947275
|
C | T | 1 | a0012c0021t0036g0287 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.833-1917C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116947275 | ||||||
chr1:116947577
|
T | G | 3 | a0001c0001t0001g0052a0001c0001t0001g0208a0001c0001t0001g0293 | 3 | HG01243.hp1 HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.833-1615T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116947577 | ||||||
chr1:116947638
|
C | T | 4 | a0005c0005t0004g0210a0005c0005t0004g0215a0005c0005t0004g0216others(1): Show | 4 | HG02886.hp2 HG02970.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.833-1554C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116947638 | ||||||
chr1:116947639
|
G | T | 244 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(241): Show | 259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.833-1553G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116947639 | ||||||
chr1:116948009
|
C | T | 3 | a0007c0010t0013g0284a0007c0010t0013g0285a0007c0010t0013g0286 | 3 | HG02145.hp1 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.833-1183C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116948009 | ||||||
chr1:116948038
|
C | T | 53 | a0001c0001t0001g0093a0001c0001t0001g0157a0001c0001t0001g0234others(50): Show | 56 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.833-1154C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116948038 | ||||||
chr1:116948071
|
C | G | 1 | a0002c0002t0002g0263 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.833-1121C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116948071 | ||||||
chr1:116948195
|
G | A | 6 | a0001c0001t0001g0234a0001c0008t0011g0233a0001c0008t0021g0044others(3): Show | 6 | HG01433.hp2 HG02486.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.833-997G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116948195 | ||||||
chr1:116948366
|
C | G | 2 | a0004c0004t0001g0224a0011c0023t0033g0281 | 2 | HG02257.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.833-826C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116948366 | ||||||
chr1:116948501
|
A | G | 93 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0028others(90): Show | 99 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.833-691A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116948501 | ||||||
chr1:116948520
|
A | G | 1 | a0004c0009t0001g0011 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.833-672A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116948520 | ||||||
chr1:116948628
|
C | T | 3 | a0007c0010t0013g0284a0007c0010t0013g0285a0007c0010t0013g0286 | 3 | HG02145.hp1 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.833-564C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116948628 | ||||||
chr1:116948746
|
T | G | 3 | a0007c0010t0013g0284a0007c0010t0013g0285a0007c0010t0013g0286 | 3 | HG02145.hp1 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.833-446T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116948746 | ||||||
chr1:116948842
|
T | C | 3 | a0001c0001t0012g0292a0001c0001t0037g0273a0006c0007t0012g0015 | 4 | HG02572.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.833-350T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116948842 | ||||||
chr1:116948967
|
T | C | 192 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(189): Show | 203 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.833-225T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116948967 | ||||||
chr1:116949015
|
G | A | 1 | a0006c0007t0001g0282 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.833-177G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116949015 | ||||||
chr1:116949807
|
A | G | 6 | a0001c0001t0001g0234a0001c0008t0011g0233a0001c0008t0021g0044others(3): Show | 6 | HG01433.hp2 HG02486.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1213+235A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116949807 | ||||||
chr1:116949942
|
G | A | 4 | a0004c0004t0001g0004a0004c0004t0001g0254a0004c0004t0001g0264others(1): Show | 6 | NA18985.hp1 NA18990.hp1 NA19001.hp1 others(3): Show |
intron_variant | MODIFIER | c.1213+370G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116949942 | ||||||
chr1:116950002
|
A | AT | 7 | a0001c0006t0009g0211a0001c0006t0009g0212a0001c0006t0009g0213others(4): Show | 7 | HG02109.hp2 HG02818.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1213+440dupT | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 116950002 | |||||
chr1:116950130
|
T | C | 2 | a0001c0001t0016g0228a0001c0001t0016g0229 | 2 | HG03654.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1213+558T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116950130 | ||||||
chr1:116950217
|
C | A | 2 | a0001c0001t0001g0031a0002c0002t0003g0030 | 2 | NA18947.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1213+645C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116950217 | ||||||
chr1:116950390
|
T | C | 31 | a0001c0001t0001g0070a0001c0001t0001g0093a0001c0001t0001g0157others(28): Show | 34 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1213+818T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116950390 | ||||||
chr1:116950430
|
CT | C | 51 | a0001c0001t0001g0070a0001c0001t0001g0093a0001c0001t0001g0157others(48): Show | 56 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.1213+859delT | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116950430 | ||||||
chr1:116950453
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1213+881G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116950453 | ||||||
chr1:116950547
|
T | C | 2 | a0001c0001t0016g0228a0001c0001t0016g0229 | 2 | HG03654.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1213+975T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116950547 | ||||||
chr1:116950585
|
T | C | 8 | a0001c0001t0001g0006a0001c0001t0001g0034a0001c0006t0009g0211others(5): Show | 9 | HG02109.hp2 HG02257.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1213+1013T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116950585 | ||||||
chr1:116950630
|
A | G | 5 | a0003c0003t0002g0080a0003c0003t0002g0088a0003c0003t0002g0143others(2): Show | 5 | HG02155.hp2 HG02165.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.1213+1058A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116950630 | ||||||
chr1:116950741
|
C | T | 1 | a0002c0002t0006g0033 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1213+1169C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116950741 | ||||||
chr1:116950787
|
C | A | 2 | a0001c0001t0016g0228a0001c0001t0016g0229 | 2 | HG03654.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1213+1215C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116950787 | ||||||
chr1:116950809
|
C | T | 18 | a0002c0002t0001g0195a0003c0003t0002g0076a0003c0003t0002g0077others(15): Show | 18 | HG00558.hp2 HG00673.hp1 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.1213+1237C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116950809 | ||||||
chr1:116951109
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1213+1537G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116951109 | ||||||
chr1:116951120
|
T | G | 4 | a0001c0008t0011g0233a0006c0022t0011g0265a0007c0013t0002g0268others(1): Show | 4 | HG02622.hp2 HG03486.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1213+1548T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116951120 | ||||||
chr1:116951189
|
G | A | 31 | a0001c0001t0001g0070a0001c0001t0001g0093a0001c0001t0001g0157others(28): Show | 34 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1213+1617G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116951189 | ||||||
chr1:116951266
|
A | G | 7 | a0002c0002t0003g0016a0002c0002t0003g0017a0002c0002t0003g0018others(4): Show | 7 | HG01106.hp2 HG01255.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1213+1694A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116951266 | ||||||
chr1:116951524
|
T | A | 2 | a0001c0001t0016g0228a0001c0001t0016g0229 | 2 | HG03654.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1213+1952T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116951524 | ||||||
chr1:116951627
|
A | T | 3 | a0007c0010t0013g0284a0007c0010t0013g0285a0007c0010t0013g0286 | 3 | HG02145.hp1 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1213+2055A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116951627 | ||||||
chr1:116951657
|
G | A | 30 | a0001c0001t0001g0070a0001c0001t0001g0093a0001c0001t0001g0157others(27): Show | 33 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.1213+2085G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116951657 | ||||||
chr1:116951677
|
CT | C | 5 | a0001c0001t0001g0276a0004c0009t0001g0011a0004c0009t0031g0147others(2): Show | 6 | HG01515.hp2 HG01517.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1213+2106delT | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116951677 | ||||||
chr1:116951699
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1213+2127C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116951699 | ||||||
chr1:116951725
|
A | G | 1 | a0003c0003t0002g0099 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1213+2153A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116951725 | ||||||
chr1:116951901
|
T | C | 1 | a0004c0004t0032g0255 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1213+2329T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116951901 | ||||||
chr1:116951953
|
C | T | 2 | a0001c0001t0016g0228a0001c0001t0016g0229 | 2 | HG03654.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1213+2381C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116951953 | ||||||
chr1:116952049
|
G | A | 1 | a0007c0013t0017g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1213+2477G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116952049 | ||||||
chr1:116952198
|
T | C | 148 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(145): Show | 157 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.1213+2626T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116952198 | ||||||
chr1:116952282
|
T | C | 1 | a0001c0006t0009g0213 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1213+2710T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116952282 | ||||||
chr1:116952474
|
A | G | 1 | a0004c0004t0001g0224 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1213+2902A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116952474 | ||||||
chr1:116952479
|
T | C | 1 | a0003c0003t0002g0184 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1213+2907T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116952479 | ||||||
chr1:116952588
|
ATTATAT | A | 103 | a0001c0001t0001g0070a0001c0001t0001g0093a0001c0001t0001g0157others(100): Show | 110 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.1213+3019_1213+302 others(10): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 116952588 | |||||
chr1:116952710
|
C | T | 2 | a0001c0001t0016g0228a0001c0001t0016g0229 | 2 | HG03654.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1213+3138C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116952710 | ||||||
chr1:116952762
|
A | G | 2 | a0001c0001t0001g0166a0002c0002t0002g0165 | 2 | HG02071.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.1213+3190A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116952762 | ||||||
chr1:116952802
|
C | G | 1 | a0002c0002t0003g0117 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1213+3230C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116952802 | ||||||
chr1:116953081
|
A | T | 2 | a0001c0001t0012g0292a0006c0007t0012g0015 | 3 | HG02572.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1213+3509A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116953081 | ||||||
chr1:116953399
|
G | A | 149 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(146): Show | 158 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.1213+3827G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116953399 | ||||||
chr1:116953550
|
C | G | 30 | a0001c0001t0001g0093a0001c0001t0001g0157a0001c0001t0018g0269others(27): Show | 33 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.1213+3978C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116953550 | ||||||
chr1:116953775
|
T | C | 293 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(290): Show | 312 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.1213+4203T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116953775 | ||||||
chr1:116953847
|
A | G | 252 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(249): Show | 268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.1213+4275A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116953847 | ||||||
chr1:116953853
|
C | CT | 48 | a0002c0002t0003g0018a0002c0002t0008g0108a0003c0003t0002g0002others(45): Show | 51 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.1213+4298dupT | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 116953853 | |||||
chr1:116953883
|
C | T | 7 | a0002c0002t0003g0016a0002c0002t0003g0017a0002c0002t0003g0018others(4): Show | 7 | HG01106.hp2 HG01255.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1213+4311C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116953883 | ||||||
chr1:116953892
|
G | A | 1 | a0001c0001t0001g0153 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1213+4320G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116953892 | ||||||
chr1:116953955
|
C | A | 2 | a0001c0001t0016g0228a0001c0001t0016g0229 | 2 | HG03654.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1213+4383C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116953955 | ||||||
chr1:116954119
|
A | G | 5 | a0001c0001t0012g0292a0001c0001t0016g0228a0001c0001t0016g0229others(2): Show | 6 | HG02572.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1213+4547A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116954119 | ||||||
chr1:116954123
|
G | C | 1 | a0004c0004t0028g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1213+4551G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116954123 | ||||||
chr1:116954298
|
C | G | 1 | a0004c0004t0028g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1213+4726C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116954298 | ||||||
chr1:116954557
|
G | A | 1 | a0002c0002t0003g0142 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1213+4985G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116954557 | ||||||
chr1:116954721
|
A | G | 2 | a0001c0008t0021g0044a0001c0008t0021g0199 | 2 | HG01433.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1213+5149A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116954721 | ||||||
chr1:116954767
|
C | CT | 150 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(147): Show | 159 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1213+5197dupT | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 116954767 | |||||
chr1:116954857
|
T | C | 7 | a0001c0006t0009g0211a0001c0006t0009g0212a0001c0006t0009g0213others(4): Show | 7 | HG02109.hp2 HG02818.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1213+5285T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116954857 | ||||||
chr1:116954881
|
A | G | 1 | a0003c0003t0002g0079 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1213+5309A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116954881 | ||||||
chr1:116955788
|
C | T | 149 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(146): Show | 158 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.1214-5455C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116955788 | ||||||
chr1:116955800
|
C | A | 1 | a0004c0004t0028g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1214-5443C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116955800 | ||||||
chr1:116955880
|
A | G | 11 | a0002c0002t0001g0195a0004c0004t0001g0271a0004c0004t0001g0289others(8): Show | 11 | HG02622.hp1 HG02630.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.1214-5363A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116955880 | ||||||
chr1:116955964
|
G | A | 149 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(146): Show | 158 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.1214-5279G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116955964 | ||||||
chr1:116956158
|
G | A | 1 | a0004c0004t0028g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1214-5085G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116956158 | ||||||
chr1:116956167
|
G | A | 2 | a0001c0001t0001g0258a0002c0002t0003g0248 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1214-5076G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116956167 | ||||||
chr1:116956333
|
G | T | 3 | a0007c0010t0013g0284a0007c0010t0013g0285a0007c0010t0013g0286 | 3 | HG02145.hp1 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1214-4910G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116956333 | ||||||
chr1:116956421
|
C | T | 2 | a0003c0003t0002g0171a0003c0003t0002g0172 | 2 | HG01928.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1214-4822C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116956421 | ||||||
chr1:116956532
|
C | T | 1 | a0002c0002t0003g0017 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1214-4711C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116956532 | ||||||
chr1:116956544
|
G | A | 1 | a0003c0003t0002g0124 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1214-4699G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116956544 | ||||||
chr1:116956570
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1214-4673G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116956570 | ||||||
chr1:116956575
|
A | G | 8 | a0001c0001t0001g0058a0001c0001t0001g0144a0001c0001t0001g0152others(5): Show | 8 | NA18944.hp1 NA18950.hp2 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.1214-4668A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116956575 | ||||||
chr1:116956615
|
G | T | 6 | a0001c0001t0016g0228a0001c0001t0016g0229a0001c0008t0011g0233others(3): Show | 6 | HG02622.hp2 HG03486.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.1214-4628G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116956615 | ||||||
chr1:116956616
|
G | T | 6 | a0001c0001t0016g0228a0001c0001t0016g0229a0001c0008t0011g0233others(3): Show | 6 | HG02622.hp2 HG03486.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.1214-4627G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116956616 | ||||||
chr1:116956637
|
C | T | 7 | a0001c0006t0009g0211a0001c0006t0009g0212a0001c0006t0009g0213others(4): Show | 7 | HG02109.hp2 HG02818.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1214-4606C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116956637 | ||||||
chr1:116956681
|
G | T | 3 | a0007c0010t0013g0284a0007c0010t0013g0285a0007c0010t0013g0286 | 3 | HG02145.hp1 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1214-4562G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116956681 | ||||||
chr1:116956926
|
A | T | 46 | a0001c0001t0001g0276a0003c0003t0002g0002a0003c0003t0002g0007others(43): Show | 48 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.1214-4317A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116956926 | ||||||
chr1:116956955
|
C | CA | 4 | a0001c0008t0011g0233a0006c0022t0011g0265a0007c0013t0002g0268others(1): Show | 4 | HG02622.hp2 HG03486.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1214-4287dupA | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 116956955 | |||||
chr1:116957026
|
A | G | 33 | a0001c0001t0001g0070a0001c0001t0001g0093a0001c0001t0001g0157others(30): Show | 36 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.1214-4217A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116957026 | ||||||
chr1:116957104
|
ACT | A | 248 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(245): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.1214-4118_1214-411 others(6): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 116957104 | |||||
chr1:116957104
|
ACTCTCT | A | 3 | a0001c0001t0020g0200a0001c0001t0020g0201a0004c0004t0001g0241 | 3 | HG02015.hp2 HG02895.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1214-4122_1214-411 others(10): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 116957104 | |||||
chr1:116957106
|
T | A | 5 | a0001c0008t0021g0044a0001c0008t0021g0199a0007c0010t0013g0284others(2): Show | 5 | HG01433.hp2 HG02145.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1214-4137T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116957106 | ||||||
chr1:116957151
|
C | CTG | 57 | a0001c0001t0001g0227a0001c0001t0007g0012a0001c0001t0007g0059others(54): Show | 61 | HG00280.hp2 HG00558.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.1214-4068_1214-406 others(6): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 116957151 | |||||
chr1:116957151
|
CTG | C | 6 | a0001c0001t0005g0038a0001c0001t0014g0014a0001c0001t0014g0279others(3): Show | 7 | HG01884.hp2 HG02145.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1214-4068_1214-406 others(6): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 116957151 | |||||
chr1:116957151
|
CTGTGTG | C | 6 | a0001c0001t0001g0127a0001c0001t0001g0163a0001c0008t0011g0233others(3): Show | 6 | HG00639.hp1 HG02622.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1214-4072_1214-406 others(10): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 116957151 | |||||
chr1:116957222
|
C | T | 1 | a0003c0003t0026g0116 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1214-4021C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116957222 | ||||||
chr1:116957248
|
C | T | 3 | a0007c0010t0013g0284a0007c0010t0013g0285a0007c0010t0013g0286 | 3 | HG02145.hp1 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1214-3995C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116957248 | ||||||
chr1:116957249
|
G | A | 1 | a0001c0006t0009g0211 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1214-3994G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116957249 | ||||||
chr1:116957355
|
G | A | 2 | a0003c0003t0002g0088a0003c0003t0002g0177 | 2 | NA18990.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1214-3888G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116957355 | ||||||
chr1:116957492
|
T | A | 2 | a0001c0008t0021g0044a0001c0008t0021g0199 | 2 | HG01433.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1214-3751T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116957492 | ||||||
chr1:116957494
|
A | G | 11 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0042others(8): Show | 12 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1214-3749A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116957494 | ||||||
chr1:116957613
|
A | G | 53 | a0001c0001t0001g0276a0001c0001t0012g0292a0001c0001t0037g0273others(50): Show | 56 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.1214-3630A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116957613 | ||||||
chr1:116957715
|
G | A | 1 | a0003c0003t0026g0116 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1214-3528G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116957715 | ||||||
chr1:116957808
|
T | C | 1 | a0002c0002t0006g0033 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1214-3435T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116957808 | ||||||
chr1:116957864
|
G | A | 45 | a0003c0003t0002g0002a0003c0003t0002g0007a0003c0003t0002g0045others(42): Show | 47 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.1214-3379G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116957864 | ||||||
chr1:116957921
|
G | T | 2 | a0001c0008t0021g0044a0001c0008t0021g0199 | 2 | HG01433.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1214-3322G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116957921 | ||||||
chr1:116957929
|
G | A | 1 | a0001c0001t0001g0159 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1214-3314G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116957929 | ||||||
chr1:116958142
|
G | A | 32 | a0001c0001t0001g0093a0001c0001t0001g0157a0001c0018t0029g0040others(29): Show | 35 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.1214-3101G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116958142 | ||||||
chr1:116958693
|
T | G | 12 | a0002c0002t0001g0195a0002c0002t0002g0263a0004c0004t0001g0271others(9): Show | 12 | HG02622.hp1 HG02630.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.1214-2550T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116958693 | ||||||
chr1:116958788
|
C | A | 79 | a0001c0001t0001g0093a0001c0001t0001g0157a0001c0018t0029g0040others(76): Show | 84 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.1214-2455C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116958788 | ||||||
chr1:116959046
|
C | G | 2 | a0001c0001t0018g0269a0004c0004t0028g0112 | 2 | HG02145.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1214-2197C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116959046 | ||||||
chr1:116959228
|
C | A | 1 | a0011c0023t0033g0281 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1214-2015C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116959228 | ||||||
chr1:116959266
|
G | A | 1 | a0002c0002t0003g0130 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1214-1977G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116959266 | ||||||
chr1:116959330
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1214-1913A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116959330 | ||||||
chr1:116959521
|
C | T | 1 | a0001c0001t0016g0228 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1214-1722C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116959521 | ||||||
chr1:116959561
|
T | C | 1 | a0003c0003t0002g0054 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1214-1682T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116959561 | ||||||
chr1:116959732
|
G | A | 1 | a0002c0002t0004g0041 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1214-1511G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116959732 | ||||||
chr1:116959745
|
G | T | 1 | a0001c0001t0001g0166 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1214-1498G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116959745 | ||||||
chr1:116959938
|
A | C | 1 | a0001c0001t0001g0150 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1214-1305A>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116959938 | ||||||
chr1:116959999
|
T | C | 6 | a0001c0001t0001g0101a0001c0001t0001g0131a0001c0001t0001g0183others(3): Show | 6 | HG00621.hp1 NA18747.hp2 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.1214-1244T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116959999 | ||||||
chr1:116960001
|
T | A | 1 | a0012c0021t0036g0287 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1214-1242T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116960001 | ||||||
chr1:116960137
|
A | G | 3 | a0001c0008t0011g0233a0006c0022t0011g0265a0012c0021t0036g0287 | 3 | HG02622.hp2 HG03486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1214-1106A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116960137 | ||||||
chr1:116960144
|
A | G | 3 | a0001c0008t0021g0044a0001c0008t0021g0199a0007c0013t0017g0283 | 3 | HG01433.hp2 HG01891.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1214-1099A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116960144 | ||||||
chr1:116960223
|
T | C | 1 | a0008c0014t0004g0114 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1214-1020T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116960223 | ||||||
chr1:116960393
|
A | G | 2 | a0001c0008t0021g0044a0001c0008t0021g0199 | 2 | HG01433.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1214-850A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116960393 | ||||||
chr1:116960473
|
G | A | 2 | a0001c0001t0014g0014a0001c0001t0014g0279 | 3 | HG01884.hp2 HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1214-770G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116960473 | ||||||
chr1:116960553
|
G | A | 1 | a0001c0001t0020g0200 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1214-690G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116960553 | ||||||
chr1:116960569
|
C | G | 7 | a0001c0001t0018g0269a0001c0008t0011g0233a0001c0008t0021g0044others(4): Show | 7 | HG01433.hp2 HG02257.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1214-674C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116960569 | ||||||
chr1:116960676
|
C | T | 3 | a0007c0010t0013g0284a0007c0010t0013g0285a0007c0010t0013g0286 | 3 | HG02145.hp1 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1214-567C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116960676 | ||||||
chr1:116960692
|
T | G | 294 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(291): Show | 313 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.1214-551T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116960692 | ||||||
chr1:116960814
|
G | T | 1 | a0001c0001t0001g0225 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1214-429G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116960814 | ||||||
chr1:116960825
|
C | G | 1 | a0002c0019t0030g0270 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1214-418C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116960825 | ||||||
chr1:116960900
|
G | C | 5 | a0001c0008t0011g0233a0001c0008t0021g0044a0001c0008t0021g0199others(2): Show | 5 | HG01433.hp2 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1214-343G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116960900 | ||||||
chr1:116961048
|
C | T | 1 | a0011c0023t0033g0281 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1214-195C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116961048 | ||||||
chr1:116961096
|
T | C | 1 | a0011c0023t0033g0281 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1214-147T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116961096 | ||||||
chr1:116961808
|
C | T | 1 | a0003c0003t0002g0073 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1639+140C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116961808 | ||||||
chr1:116961982
|
C | T | 1 | a0002c0002t0015g0173 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1639+314C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116961982 | ||||||
chr1:116962250
|
G | A | 3 | a0007c0010t0013g0284a0007c0010t0013g0285a0007c0010t0013g0286 | 3 | HG02145.hp1 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1639+582G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116962250 | ||||||
chr1:116962272
|
C | G | 3 | a0007c0010t0013g0284a0007c0010t0013g0285a0007c0010t0013g0286 | 3 | HG02145.hp1 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1639+604C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116962272 | ||||||
chr1:116962466
|
A | G | 1 | a0001c0001t0001g0276 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1639+798A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116962466 | ||||||
chr1:116962641
|
T | A | 1 | a0003c0003t0002g0051 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1639+973T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116962641 | ||||||
chr1:116962690
|
C | T | 88 | a0001c0001t0001g0093a0001c0001t0001g0157a0001c0001t0001g0276others(85): Show | 93 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.1639+1022C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116962690 | ||||||
chr1:116962691
|
C | T | 1 | a0003c0003t0002g0099 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1639+1023C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116962691 | ||||||
chr1:116962695
|
C | G | 1 | a0002c0002t0002g0263 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1639+1027C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116962695 | ||||||
chr1:116962826
|
T | C | 2 | a0001c0001t0001g0146a0001c0001t0001g0150 | 2 | HG00099.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1639+1158T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116962826 | ||||||
chr1:116962888
|
C | T | 1 | a0003c0003t0002g0124 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1639+1220C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116962888 | ||||||
chr1:116962889
|
G | A | 1 | a0002c0019t0030g0270 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1639+1221G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116962889 | ||||||
chr1:116962933
|
C | G | 1 | a0003c0003t0002g0124 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1639+1265C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116962933 | ||||||
chr1:116963036
|
G | GCTTC | 3 | a0002c0002t0003g0137a0002c0002t0003g0169a0002c0002t0006g0105 | 3 | NA19062.hp1 NA19062.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1639+1374_1639+137 others(8): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 116963036 | |||||
chr1:116963049
|
C | T | 4 | a0001c0008t0011g0233a0001c0008t0021g0044a0001c0008t0021g0199others(1): Show | 4 | HG01433.hp2 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1639+1381C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116963049 | ||||||
chr1:116963116
|
C | T | 5 | a0001c0008t0011g0233a0001c0008t0021g0044a0001c0008t0021g0199others(2): Show | 5 | HG01433.hp2 HG02257.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1639+1448C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116963116 | ||||||
chr1:116963210
|
C | T | 5 | a0001c0001t0012g0292a0001c0001t0018g0269a0001c0001t0037g0273others(2): Show | 6 | HG02572.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1639+1542C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116963210 | ||||||
chr1:116963290
|
C | T | 6 | a0001c0001t0001g0037a0001c0001t0001g0052a0001c0001t0001g0208others(3): Show | 6 | HG01243.hp1 HG02922.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1639+1622C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116963290 | ||||||
chr1:116963564
|
A | T | 47 | a0001c0001t0001g0093a0001c0001t0001g0157a0001c0001t0001g0276others(44): Show | 51 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.1639+1896A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116963564 | ||||||
chr1:116963579
|
G | A | 1 | a0011c0023t0033g0281 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1639+1911G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116963579 | ||||||
chr1:116963619
|
G | A | 1 | a0002c0002t0006g0132 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1639+1951G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116963619 | ||||||
chr1:116963689
|
C | G | 1 | a0004c0004t0028g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1639+2021C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116963689 | ||||||
chr1:116963732
|
C | T | 4 | a0001c0008t0011g0233a0001c0008t0021g0044a0001c0008t0021g0199others(1): Show | 4 | HG01433.hp2 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1639+2064C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116963732 | ||||||
chr1:116963774
|
A | AT | 41 | a0001c0001t0001g0093a0001c0001t0001g0157a0001c0001t0001g0276others(38): Show | 45 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.1639+2121dupT | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 116963774 | |||||
chr1:116963924
|
A | G | 1 | a0002c0002t0004g0094 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1639+2256A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116963924 | ||||||
chr1:116964000
|
G | T | 30 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0058others(27): Show | 32 | HG00099.hp2 HG00408.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1639+2332G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116964000 | ||||||
chr1:116964018
|
G | A | 1 | a0004c0004t0028g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1639+2350G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116964018 | ||||||
chr1:116964076
|
G | GAC | 2 | a0001c0001t0012g0292a0006c0007t0012g0015 | 3 | HG02572.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1639+2408_1639+240 others(6): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116964076 | ||||||
chr1:116964079
|
G | C | 2 | a0001c0001t0012g0292a0006c0007t0012g0015 | 3 | HG02572.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1639+2411G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116964079 | ||||||
chr1:116964079
|
G | GC | 80 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0204others(77): Show | 83 | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.1639+2418dupC | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 116964079 | |||||
chr1:116964079
|
G | GCC | 41 | a0001c0001t0001g0093a0001c0001t0001g0276a0001c0001t0018g0269others(38): Show | 44 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.1639+2417_1639+241 others(6): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 116964079 | |||||
chr1:116964084
|
C | CG | 3 | a0007c0010t0013g0284a0007c0010t0013g0285a0007c0010t0013g0286 | 3 | HG02145.hp1 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1639+2416_1639+241 others(5): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116964084 | ||||||
chr1:116964110
|
C | G | 47 | a0001c0001t0001g0093a0001c0001t0001g0157a0001c0001t0001g0276others(44): Show | 51 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.1639+2442C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116964110 | ||||||
chr1:116964188
|
C | T | 1 | a0004c0004t0001g0219 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1639+2520C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116964188 | ||||||
chr1:116964230
|
C | T | 7 | a0001c0006t0009g0211a0001c0006t0009g0212a0001c0006t0009g0213others(4): Show | 7 | HG02109.hp2 HG02818.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1639+2562C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116964230 | ||||||
chr1:116964231
|
T | G | 7 | a0001c0006t0009g0211a0001c0006t0009g0212a0001c0006t0009g0213others(4): Show | 7 | HG02109.hp2 HG02818.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1639+2563T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116964231 | ||||||
chr1:116964270
|
T | A | 27 | a0001c0001t0001g0025a0001c0001t0001g0058a0001c0001t0001g0081others(24): Show | 27 | HG00099.hp2 HG00408.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.1639+2602T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116964270 | ||||||
chr1:116964395
|
G | A | 3 | a0007c0010t0013g0284a0007c0010t0013g0285a0007c0010t0013g0286 | 3 | HG02145.hp1 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1640-2516G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116964395 | ||||||
chr1:116964542
|
T | A | 12 | a0002c0002t0001g0195a0004c0004t0001g0271a0005c0005t0001g0217others(9): Show | 12 | HG01891.hp1 HG02622.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1640-2369T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116964542 | ||||||
chr1:116964548
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1640-2363A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116964548 | ||||||
chr1:116964582
|
T | C | 1 | a0004c0004t0001g0256 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1640-2329T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116964582 | ||||||
chr1:116964599
|
A | G | 46 | a0001c0001t0001g0093a0001c0001t0001g0157a0001c0001t0001g0276others(43): Show | 50 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.1640-2312A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116964599 | ||||||
chr1:116964780
|
T | C | 55 | a0001c0001t0001g0093a0001c0001t0001g0157a0001c0001t0001g0227others(52): Show | 60 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.1640-2131T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116964780 | ||||||
chr1:116964893
|
T | C | 7 | a0001c0006t0009g0211a0001c0006t0009g0212a0001c0006t0009g0213others(4): Show | 7 | HG02109.hp2 HG02818.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1640-2018T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116964893 | ||||||
chr1:116965013
|
C | T | 1 | a0002c0002t0003g0142 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1640-1898C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116965013 | ||||||
chr1:116965043
|
C | G | 38 | a0001c0001t0001g0093a0001c0001t0001g0157a0001c0001t0001g0276others(35): Show | 41 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1640-1868C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116965043 | ||||||
chr1:116965171
|
C | T | 13 | a0002c0002t0001g0195a0004c0004t0001g0271a0004c0004t0028g0112others(10): Show | 13 | HG01891.hp1 HG02145.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1640-1740C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116965171 | ||||||
chr1:116965226
|
A | G | 7 | a0001c0001t0001g0227a0001c0001t0007g0012a0001c0001t0007g0059others(4): Show | 8 | HG00280.hp2 HG00741.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.1640-1685A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116965226 | ||||||
chr1:116965258
|
G | A | 7 | a0001c0001t0001g0227a0001c0001t0007g0012a0001c0001t0007g0059others(4): Show | 8 | HG00280.hp2 HG00741.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.1640-1653G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116965258 | ||||||
chr1:116965379
|
G | A | 1 | a0011c0023t0033g0281 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1640-1532G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116965379 | ||||||
chr1:116965524
|
A | G | 2 | a0001c0001t0016g0228a0001c0001t0016g0229 | 2 | HG03654.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1640-1387A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116965524 | ||||||
chr1:116965548
|
T | C | 2 | a0001c0001t0016g0228a0001c0001t0016g0229 | 2 | HG03654.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1640-1363T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116965548 | ||||||
chr1:116965564
|
A | C | 47 | a0001c0001t0001g0093a0001c0001t0001g0157a0001c0001t0001g0276others(44): Show | 51 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.1640-1347A>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116965564 | ||||||
chr1:116965623
|
TC | T | 50 | a0001c0001t0001g0031a0001c0001t0001g0134a0001c0001t0001g0166others(47): Show | 54 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1640-1285delC | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 116965623 | |||||
chr1:116965682
|
C | T | 53 | a0001c0001t0001g0227a0001c0001t0007g0012a0001c0001t0007g0059others(50): Show | 56 | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.1640-1229C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116965682 | ||||||
chr1:116965852
|
G | C | 5 | a0001c0001t0001g0070a0001c0001t0001g0202a0001c0001t0001g0203others(2): Show | 5 | HG01192.hp2 HG01346.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.1640-1059G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116965852 | ||||||
chr1:116966499
|
A | G | 33 | a0001c0001t0001g0093a0001c0001t0001g0157a0001c0018t0029g0040others(30): Show | 36 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.1640-412A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116966499 | ||||||
chr1:116966548
|
C | T | 7 | a0001c0006t0009g0211a0001c0006t0009g0212a0001c0006t0009g0213others(4): Show | 7 | HG02109.hp2 HG02818.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1640-363C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116966548 | ||||||
chr1:116966760
|
T | G | 1 | a0001c0001t0001g0154 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1640-151T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116966760 | ||||||
chr1:116966789
|
G | A | 2 | a0003c0003t0002g0057a0007c0013t0017g0283 | 2 | HG01891.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1640-122G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116966789 | ||||||
chr1:116967359
|
G | A | 42 | a0001c0001t0001g0093a0001c0001t0001g0157a0001c0001t0018g0269others(39): Show | 45 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.2059+29G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116967359 | ||||||
chr1:116967365
|
C | T | 42 | a0001c0001t0001g0093a0001c0001t0001g0157a0001c0001t0018g0269others(39): Show | 45 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.2059+35C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116967365 | ||||||
chr1:116967439
|
C | T | 42 | a0001c0001t0001g0093a0001c0001t0001g0157a0001c0001t0018g0269others(39): Show | 45 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.2059+109C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116967439 | ||||||
chr1:116967714
|
GC | G | 3 | a0001c0001t0001g0081a0001c0001t0001g0100a0001c0001t0001g0236 | 3 | HG00408.hp2 HG02083.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.2059+385delC | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116967714 | ||||||
chr1:116967895
|
G | A | 64 | a0001c0001t0001g0227a0001c0001t0007g0012a0001c0001t0007g0059others(61): Show | 68 | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.2059+565G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116967895 | ||||||
chr1:116968182
|
G | A | 123 | a0001c0001t0001g0093a0001c0001t0001g0157a0001c0001t0001g0227others(120): Show | 130 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.2059+852G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116968182 | ||||||
chr1:116968283
|
A | AG | 42 | a0001c0001t0001g0093a0001c0001t0001g0157a0001c0001t0018g0269others(39): Show | 45 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.2059+953_2059+954i others(3): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116968283 | ||||||
chr1:116968355
|
A | C | 5 | a0001c0001t0001g0227a0001c0001t0007g0012a0001c0001t0007g0059others(2): Show | 6 | HG00280.hp2 HG00741.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.2059+1025A>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116968355 | ||||||
chr1:116968387
|
A | G | 1 | a0003c0003t0002g0099 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2059+1057A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116968387 | ||||||
chr1:116968573
|
T | G | 1 | a0005c0005t0002g0272 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2059+1243T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116968573 | ||||||
chr1:116968639
|
A | G | 1 | a0004c0004t0001g0240 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2059+1309A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116968639 | ||||||
chr1:116968819
|
C | G | 2 | a0001c0001t0001g0234a0001c0001t0005g0193 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2059+1489C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116968819 | ||||||
chr1:116968861
|
A | C | 41 | a0001c0001t0001g0093a0001c0001t0001g0157a0001c0001t0018g0269others(38): Show | 44 | HG00323.hp2 HG00558.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.2059+1531A>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116968861 | ||||||
chr1:116968992
|
T | C | 1 | a0004c0004t0001g0261 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2059+1662T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116968992 | ||||||
chr1:116969036
|
G | C | 124 | a0001c0001t0001g0093a0001c0001t0001g0157a0001c0001t0001g0227others(121): Show | 131 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.2059+1706G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116969036 | ||||||
chr1:116969120
|
GTT | G | 38 | a0001c0001t0001g0093a0001c0001t0001g0157a0001c0001t0020g0200others(35): Show | 41 | HG00323.hp2 HG00558.hp1 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.2059+1803_2059+180 others(6): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr1 | 116969120 | |||||
chr1:116969159
|
A | G | 109 | a0001c0001t0001g0093a0001c0001t0001g0157a0001c0001t0001g0227others(106): Show | 116 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.2059+1829A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116969159 | ||||||
chr1:116969182
|
T | C | 67 | a0001c0001t0001g0227a0001c0001t0001g0276a0001c0001t0007g0012others(64): Show | 71 | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.2059+1852T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116969182 | ||||||
chr1:116969218
|
T | C | 42 | a0001c0001t0001g0093a0001c0001t0001g0157a0001c0001t0018g0269others(39): Show | 45 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.2059+1888T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116969218 | ||||||
chr1:116969274
|
G | A | 5 | a0001c0001t0001g0227a0001c0001t0007g0012a0001c0001t0007g0059others(2): Show | 6 | HG00280.hp2 HG00741.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.2059+1944G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116969274 | ||||||
chr1:116969322
|
T | C | 1 | a0011c0023t0033g0281 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2059+1992T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116969322 | ||||||
chr1:116969508
|
A | G | 3 | a0001c0001t0001g0036a0001c0001t0001g0230a0001c0001t0001g0277 | 3 | HG02280.hp2 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2059+2178A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116969508 | ||||||
chr1:116969570
|
A | G | 42 | a0001c0001t0001g0093a0001c0001t0001g0157a0001c0001t0018g0269others(39): Show | 45 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.2059+2240A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116969570 | ||||||
chr1:116969612
|
C | T | 9 | a0002c0002t0004g0003a0002c0002t0004g0009a0002c0002t0004g0047others(6): Show | 12 | HG00558.hp1 HG00597.hp1 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.2059+2282C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116969612 | ||||||
chr1:116969679
|
A | G | 2 | a0001c0008t0011g0233a0006c0022t0011g0265 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2059+2349A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116969679 | ||||||
chr1:116969752
|
G | A | 1 | a0001c0001t0001g0276 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2059+2422G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116969752 | ||||||
chr1:116969860
|
A | T | 2 | a0003c0003t0002g0071a0003c0003t0002g0072 | 2 | NA18950.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.2059+2530A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116969860 | ||||||
chr1:116969883
|
T | C | 46 | a0001c0001t0001g0093a0001c0001t0001g0157a0001c0001t0012g0292others(43): Show | 50 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.2059+2553T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116969883 | ||||||
chr1:116969924
|
G | C | 41 | a0001c0001t0001g0093a0001c0001t0001g0157a0001c0001t0018g0269others(38): Show | 44 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.2059+2594G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116969924 | ||||||
chr1:116970165
|
CT | C | 3 | a0001c0001t0001g0031a0001c0001t0005g0185a0002c0002t0003g0123 | 3 | HG01261.hp1 HG03831.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.2059+2837delT | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr1 | 116970165 | |||||
chr1:116970165
|
CTT | C | 48 | a0001c0001t0001g0028a0001c0001t0001g0134a0001c0001t0001g0166others(45): Show | 52 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.2059+2836_2059+283 others(6): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116970165 | ||||||
chr1:116970179
|
T | C | 3 | a0001c0001t0005g0038a0001c0001t0019g0148a0001c0001t0019g0196 | 3 | HG02615.hp2 HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2059+2849T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116970179 | ||||||
chr1:116970304
|
T | A | 1 | a0003c0003t0002g0089 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2059+2974T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116970304 | ||||||
chr1:116970364
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2059+3034A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116970364 | ||||||
chr1:116970379
|
G | T | 1 | a0001c0001t0001g0276 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2059+3049G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116970379 | ||||||
chr1:116970537
|
T | A | 1 | a0001c0001t0001g0276 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2059+3207T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116970537 | ||||||
chr1:116970639
|
G | T | 2 | a0001c0001t0016g0228a0001c0001t0016g0229 | 2 | HG03654.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.2059+3309G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116970639 | ||||||
chr1:116970816
|
G | A | 11 | a0002c0002t0001g0195a0004c0004t0001g0271a0005c0005t0001g0217others(8): Show | 11 | HG02622.hp1 HG02630.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.2060-3400G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116970816 | ||||||
chr1:116970830
|
C | G | 79 | a0001c0001t0001g0227a0001c0001t0001g0276a0001c0001t0007g0012others(76): Show | 83 | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.2060-3386C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116970830 | ||||||
chr1:116970998
|
A | T | 2 | a0002c0002t0003g0039a0002c0002t0003g0136 | 2 | HG01346.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2060-3218A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116970998 | ||||||
chr1:116971198
|
T | TA | 3 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0205 | 3 | HG01358.hp1 HG01433.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.2060-3017dupA | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr1 | 116971198 | |||||
chr1:116971281
|
C | T | 4 | a0002c0002t0004g0003a0002c0002t0004g0094a0002c0002t0004g0095others(1): Show | 6 | NA18974.hp2 NA18985.hp2 NA18999.hp2 others(3): Show |
intron_variant | MODIFIER | c.2060-2935C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116971281 | ||||||
chr1:116971282
|
T | TTAGCCAT others(17): Show |
1 | a0001c0001t0018g0269 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2060-2913_2060-291 others(28): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr1 | 116971282 | |||||
chr1:116971363
|
T | G | 32 | a0001c0001t0001g0093a0001c0001t0001g0157a0001c0018t0029g0040others(29): Show | 35 | HG00323.hp2 HG00558.hp1 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.2060-2853T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116971363 | ||||||
chr1:116971426
|
A | G | 47 | a0003c0003t0002g0002a0003c0003t0002g0007a0003c0003t0002g0045others(44): Show | 49 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.2060-2790A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116971426 | ||||||
chr1:116971500
|
C | G | 2 | a0001c0001t0001g0234a0001c0001t0005g0193 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2060-2716C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116971500 | ||||||
chr1:116971712
|
A | G | 85 | a0001c0001t0001g0025a0001c0001t0001g0081a0001c0001t0001g0100others(82): Show | 89 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.2060-2504A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116971712 | ||||||
chr1:116971936
|
G | A | 1 | a0004c0009t0001g0011 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2060-2280G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116971936 | ||||||
chr1:116971998
|
C | T | 2 | a0001c0008t0021g0044a0001c0008t0021g0199 | 2 | HG01433.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2060-2218C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116971998 | ||||||
chr1:116972053
|
G | A | 24 | a0001c0001t0001g0157a0001c0001t0012g0292a0001c0001t0016g0228others(21): Show | 25 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.2060-2163G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116972053 | ||||||
chr1:116972058
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.2060-2158C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116972058 | ||||||
chr1:116972102
|
C | T | 1 | a0002c0002t0006g0132 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2060-2114C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116972102 | ||||||
chr1:116972161
|
A | G | 4 | a0002c0019t0030g0270a0007c0010t0013g0284a0007c0010t0013g0285others(1): Show | 4 | HG02145.hp1 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2060-2055A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116972161 | ||||||
chr1:116972310
|
G | A | 2 | a0001c0001t0037g0273a0012c0021t0036g0287 | 2 | HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2060-1906G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116972310 | ||||||
chr1:116972493
|
A | G | 123 | a0001c0001t0001g0227a0001c0001t0007g0012a0001c0001t0007g0059others(120): Show | 131 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.2060-1723A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116972493 | ||||||
chr1:116972662
|
C | A | 45 | a0002c0002t0002g0118a0003c0003t0002g0002a0003c0003t0002g0007others(42): Show | 47 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.2060-1554C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116972662 | ||||||
chr1:116972678
|
C | T | 1 | a0001c0001t0001g0293 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2060-1538C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116972678 | ||||||
chr1:116972694
|
G | A | 2 | a0001c0001t0012g0292a0006c0007t0012g0015 | 3 | HG02572.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2060-1522G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116972694 | ||||||
chr1:116972902
|
G | T | 5 | a0001c0006t0009g0211a0001c0006t0009g0212a0001c0006t0009g0213others(2): Show | 5 | HG02109.hp2 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2060-1314G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116972902 | ||||||
chr1:116972986
|
C | T | 2 | a0001c0008t0021g0044a0001c0008t0021g0199 | 2 | HG01433.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2060-1230C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116972986 | ||||||
chr1:116973026
|
C | A | 5 | a0001c0006t0009g0211a0001c0006t0009g0212a0001c0006t0009g0213others(2): Show | 5 | HG02109.hp2 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2060-1190C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116973026 | ||||||
chr1:116973044
|
A | G | 1 | a0001c0018t0029g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2060-1172A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116973044 | ||||||
chr1:116973052
|
G | C | 1 | a0006c0012t0018g0267 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2060-1164G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116973052 | ||||||
chr1:116973104
|
G | T | 2 | a0001c0001t0001g0234a0001c0001t0005g0193 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2060-1112G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116973104 | ||||||
chr1:116973135
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2060-1081C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116973135 | ||||||
chr1:116973309
|
A | T | 1 | a0002c0002t0002g0118 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2060-907A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116973309 | ||||||
chr1:116973488
|
C | T | 1 | a0001c0018t0029g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2060-728C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116973488 | ||||||
chr1:116973535
|
G | T | 1 | a0001c0001t0001g0182 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2060-681G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116973535 | ||||||
chr1:116973581
|
C | G | 26 | a0001c0001t0007g0012a0001c0001t0007g0059a0001c0001t0007g0060others(23): Show | 29 | HG00741.hp2 HG01109.hp2 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.2060-635C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116973581 | ||||||
chr1:116973581
|
C | T | 1 | a0002c0002t0008g0108 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2060-635C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116973581 | ||||||
chr1:116973604
|
CA | C | 71 | a0001c0001t0001g0152a0001c0001t0005g0038a0001c0001t0007g0012others(68): Show | 75 | HG00438.hp1 HG00597.hp2 HG00741.hp2 others(72): Show |
intron_variant | MODIFIER | c.2060-593delA | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr1 | 116973604 | |||||
chr1:116973604
|
CAA | C | 45 | a0001c0001t0012g0292a0001c0018t0029g0040a0002c0002t0001g0195others(42): Show | 49 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.2060-594_2060-593d others(4): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr1 | 116973604 | |||||
chr1:116973719
|
A | G | 33 | a0001c0001t0007g0012a0001c0001t0007g0059a0001c0001t0007g0060others(30): Show | 36 | HG00741.hp2 HG01109.hp2 HG01192.hp1 others(33): Show |
intron_variant | MODIFIER | c.2060-497A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116973719 | ||||||
chr1:116973882
|
C | G | 2 | a0001c0001t0012g0292a0006c0007t0012g0015 | 3 | HG02572.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2060-334C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116973882 | ||||||
chr1:116974386
|
C | T | 1 | a0002c0002t0003g0130 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2167+63C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116974386 | ||||||
chr1:116974387
|
G | A | 1 | a0007c0013t0002g0268 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2167+64G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116974387 | ||||||
chr1:116974387
|
G | T | 1 | a0001c0001t0001g0005 | 3 | HG02109.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2167+64G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116974387 | ||||||
chr1:116974479
|
T | G | 1 | a0002c0019t0030g0270 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2167+156T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116974479 | ||||||
chr1:116974491
|
G | A | 2 | a0001c0008t0021g0044a0001c0008t0021g0199 | 2 | HG01433.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2167+168G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116974491 | ||||||
chr1:116974510
|
C | T | 2 | a0001c0001t0037g0273a0012c0021t0036g0287 | 2 | HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2167+187C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116974510 | ||||||
chr1:116974657
|
C | T | 1 | a0011c0023t0033g0281 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2167+334C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116974657 | ||||||
chr1:116974740
|
G | A | 1 | a0002c0002t0003g0083 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2167+417G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116974740 | ||||||
chr1:116974798
|
C | T | 1 | a0002c0002t0003g0027 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2167+475C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116974798 | ||||||
chr1:116974901
|
G | A | 2 | a0001c0001t0001g0127a0001c0001t0001g0163 | 2 | HG00639.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2167+578G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116974901 | ||||||
chr1:116974904
|
C | T | 3 | a0001c0008t0011g0233a0006c0012t0011g0266a0006c0022t0011g0265 | 3 | HG02622.hp2 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2167+581C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116974904 | ||||||
chr1:116974916
|
C | T | 1 | a0002c0002t0004g0095 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2167+593C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116974916 | ||||||
chr1:116974938
|
C | T | 1 | a0006c0012t0018g0267 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2167+615C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116974938 | ||||||
chr1:116974945
|
C | T | 5 | a0001c0006t0009g0211a0001c0006t0009g0212a0001c0006t0009g0213others(2): Show | 5 | HG02109.hp2 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2167+622C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116974945 | ||||||
chr1:116975013
|
G | A | 1 | a0001c0018t0029g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2167+690G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116975013 | ||||||
chr1:116975047
|
G | T | 1 | a0001c0001t0001g0122 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2167+724G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116975047 | ||||||
chr1:116975076
|
T | C | 1 | a0001c0001t0001g0131 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2167+753T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116975076 | ||||||
chr1:116975087
|
T | C | 5 | a0001c0006t0009g0211a0001c0006t0009g0212a0001c0006t0009g0213others(2): Show | 5 | HG02109.hp2 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2167+764T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116975087 | ||||||
chr1:116975118
|
C | T | 2 | a0001c0008t0021g0044a0001c0008t0021g0199 | 2 | HG01433.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2167+795C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116975118 | ||||||
chr1:116975186
|
C | T | 1 | a0001c0018t0029g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2167+863C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116975186 | ||||||
chr1:116975211
|
A | G | 1 | a0002c0019t0030g0270 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2167+888A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116975211 | ||||||
chr1:116975296
|
G | A | 2 | a0004c0004t0001g0237a0004c0004t0001g0244 | 2 | NA18951.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.2167+973G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116975296 | ||||||
chr1:116975411
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2167+1088C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116975411 | ||||||
chr1:116975553
|
T | A | 1 | a0004c0004t0001g0271 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2167+1230T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116975553 | ||||||
chr1:116975636
|
A | G | 2 | a0001c0001t0012g0292a0006c0007t0012g0015 | 3 | HG02572.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2167+1313A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116975636 | ||||||
chr1:116975755
|
C | T | 1 | a0002c0002t0001g0195 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2167+1432C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116975755 | ||||||
chr1:116975777
|
A | G | 4 | a0001c0001t0020g0200a0001c0001t0020g0201a0001c0018t0029g0040others(1): Show | 4 | HG02257.hp1 HG02895.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2167+1454A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116975777 | ||||||
chr1:116976027
|
A | G | 1 | a0003c0003t0002g0206 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2167+1704A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116976027 | ||||||
chr1:116976057
|
T | C | 4 | a0002c0019t0030g0270a0007c0010t0013g0284a0007c0010t0013g0285others(1): Show | 4 | HG02145.hp1 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2167+1734T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116976057 | ||||||
chr1:116976139
|
C | T | 20 | a0001c0001t0007g0012a0001c0001t0007g0059a0001c0001t0007g0060others(17): Show | 22 | HG00741.hp2 HG01109.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.2167+1816C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116976139 | ||||||
chr1:116976154
|
G | A | 3 | a0001c0001t0020g0200a0001c0001t0020g0201a0011c0023t0033g0281 | 3 | HG02257.hp1 HG02895.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2167+1831G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116976154 | ||||||
chr1:116976187
|
G | T | 1 | a0004c0004t0028g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2167+1864G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116976187 | ||||||
chr1:116976374
|
G | A | 8 | a0002c0002t0001g0195a0005c0005t0001g0217a0005c0005t0001g0220others(5): Show | 8 | HG02622.hp1 HG02630.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.2167+2051G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116976374 | ||||||
chr1:116976491
|
C | G | 1 | a0003c0003t0002g0245 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2167+2168C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116976491 | ||||||
chr1:116976544
|
C | A | 5 | a0001c0001t0007g0012a0001c0001t0007g0059a0001c0001t0007g0060others(2): Show | 6 | HG00741.hp2 HG01109.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.2167+2221C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116976544 | ||||||
chr1:116976608
|
A | G | 1 | a0001c0001t0037g0273 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2167+2285A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116976608 | ||||||
chr1:116976769
|
A | G | 1 | a0004c0004t0028g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2167+2446A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116976769 | ||||||
chr1:116977120
|
CAAAG | C | 48 | a0002c0002t0002g0118a0002c0002t0002g0263a0003c0003t0002g0002others(45): Show | 50 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2167+2800_2167+280 others(8): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 116977120 | |||||
chr1:116977125
|
A | G | 3 | a0007c0010t0013g0284a0007c0010t0013g0285a0007c0010t0013g0286 | 3 | HG02145.hp1 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2167+2802A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116977125 | ||||||
chr1:116977186
|
A | G | 1 | a0002c0002t0003g0169 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2167+2863A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116977186 | ||||||
chr1:116977195
|
C | T | 1 | a0001c0008t0011g0233 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2167+2872C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116977195 | ||||||
chr1:116977197
|
A | G | 1 | a0001c0001t0005g0155 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2167+2874A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116977197 | ||||||
chr1:116977252
|
A | G | 1 | a0001c0018t0029g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2167+2929A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116977252 | ||||||
chr1:116977432
|
A | C | 124 | a0001c0001t0001g0227a0001c0001t0007g0012a0001c0001t0007g0059others(121): Show | 132 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.2167+3109A>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116977432 | ||||||
chr1:116977596
|
C | A | 24 | a0001c0001t0007g0012a0001c0001t0007g0059a0001c0001t0007g0060others(21): Show | 26 | HG00741.hp2 HG01109.hp2 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.2167+3273C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116977596 | ||||||
chr1:116977610
|
C | T | 5 | a0001c0006t0009g0211a0001c0006t0009g0212a0001c0006t0009g0213others(2): Show | 5 | HG02109.hp2 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2167+3287C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116977610 | ||||||
chr1:116977626
|
G | A | 3 | a0001c0001t0020g0200a0001c0001t0020g0201a0011c0023t0033g0281 | 3 | HG02257.hp1 HG02895.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2167+3303G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116977626 | ||||||
chr1:116977794
|
A | T | 1 | a0002c0002t0041g0121 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2167+3471A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116977794 | ||||||
chr1:116978019
|
A | G | 2 | a0004c0004t0001g0250a0004c0004t0001g0251 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2167+3696A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116978019 | ||||||
chr1:116978043
|
C | T | 31 | a0002c0002t0004g0003a0002c0002t0004g0009a0002c0002t0004g0041others(28): Show | 34 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.2167+3720C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116978043 | ||||||
chr1:116978064
|
A | G | 1 | a0003c0003t0002g0245 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2167+3741A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116978064 | ||||||
chr1:116978325
|
G | C | 96 | a0001c0001t0018g0269a0001c0001t0020g0200a0001c0001t0020g0201others(93): Show | 101 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.2167+4002G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116978325 | ||||||
chr1:116978494
|
TCCAGCAG others(21): Show |
T | 2 | a0001c0008t0021g0044a0001c0008t0021g0199 | 2 | HG01433.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2167+4173_2167+420 others(32): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 116978494 | |||||
chr1:116978514
|
C | G | 27 | a0001c0001t0001g0227a0001c0001t0007g0012a0001c0001t0007g0059others(24): Show | 30 | HG00280.hp2 HG00741.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.2167+4191C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116978514 | ||||||
chr1:116978535
|
G | A | 25 | a0001c0001t0001g0227a0001c0001t0007g0012a0001c0001t0007g0059others(22): Show | 28 | HG00280.hp2 HG00741.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.2167+4212G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116978535 | ||||||
chr1:116978577
|
T | C | 1 | a0004c0004t0034g0223 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2167+4254T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116978577 | ||||||
chr1:116978641
|
A | G | 2 | a0001c0008t0021g0044a0001c0008t0021g0199 | 2 | HG01433.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2167+4318A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116978641 | ||||||
chr1:116978772
|
A | G | 1 | a0011c0023t0033g0281 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2167+4449A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116978772 | ||||||
chr1:116978815
|
G | A | 4 | a0001c0001t0020g0200a0001c0001t0020g0201a0001c0018t0029g0040others(1): Show | 4 | HG02257.hp1 HG02895.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2167+4492G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116978815 | ||||||
chr1:116978853
|
T | G | 125 | a0001c0001t0001g0227a0001c0001t0007g0012a0001c0001t0007g0059others(122): Show | 133 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.2167+4530T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116978853 | ||||||
chr1:116978909
|
A | G | 120 | a0001c0001t0001g0227a0001c0001t0007g0012a0001c0001t0007g0059others(117): Show | 128 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.2167+4586A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116978909 | ||||||
chr1:116979079
|
GACAA | G | 3 | a0003c0003t0002g0075a0003c0003t0002g0080a0003c0003t0002g0143 | 3 | HG02155.hp2 HG02165.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.2167+4760_2167+476 others(8): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 116979079 | |||||
chr1:116979102
|
A | G | 1 | a0001c0001t0001g0167 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2167+4779A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116979102 | ||||||
chr1:116979120
|
G | A | 119 | a0001c0001t0001g0227a0001c0001t0007g0012a0001c0001t0007g0059others(116): Show | 127 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.2167+4797G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116979120 | ||||||
chr1:116979124
|
C | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0100 | 2 | HG00408.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.2167+4801C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116979124 | ||||||
chr1:116979175
|
A | T | 1 | a0001c0020t0001g0187 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2167+4852A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116979175 | ||||||
chr1:116979260
|
A | G | 8 | a0001c0001t0001g0227a0001c0001t0007g0012a0001c0001t0007g0059others(5): Show | 10 | HG00280.hp2 HG00741.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2167+4937A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116979260 | ||||||
chr1:116979275
|
C | T | 3 | a0002c0002t0004g0178a0002c0002t0004g0180a0002c0002t0017g0179 | 3 | HG00735.hp2 HG01934.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.2167+4952C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116979275 | ||||||
chr1:116979276
|
A | G | 3 | a0002c0002t0004g0178a0002c0002t0004g0180a0002c0002t0017g0179 | 3 | HG00735.hp2 HG01934.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.2167+4953A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116979276 | ||||||
chr1:116979307
|
A | G | 1 | a0004c0004t0001g0271 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2167+4984A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116979307 | ||||||
chr1:116979316
|
A | G | 125 | a0001c0001t0001g0227a0001c0001t0007g0012a0001c0001t0007g0059others(122): Show | 133 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.2167+4993A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116979316 | ||||||
chr1:116979690
|
C | T | 117 | a0001c0001t0001g0227a0001c0001t0007g0012a0001c0001t0007g0059others(114): Show | 124 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.2168-4990C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116979690 | ||||||
chr1:116979743
|
T | C | 1 | a0001c0001t0020g0201 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2168-4937T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116979743 | ||||||
chr1:116979787
|
G | A | 125 | a0001c0001t0001g0227a0001c0001t0007g0012a0001c0001t0007g0059others(122): Show | 133 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.2168-4893G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116979787 | ||||||
chr1:116979846
|
G | T | 1 | a0001c0018t0029g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2168-4834G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116979846 | ||||||
chr1:116979880
|
TTAAAC | T | 4 | a0001c0001t0016g0228a0001c0001t0016g0229a0003c0003t0002g0171others(1): Show | 4 | HG01928.hp1 HG01978.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.2168-4795_2168-479 others(9): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 116979880 | |||||
chr1:116980021
|
G | GAAGA | 5 | a0001c0006t0009g0211a0001c0006t0009g0212a0001c0006t0009g0213others(2): Show | 5 | HG02109.hp2 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2168-4657_2168-465 others(8): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 116980021 | |||||
chr1:116980025
|
A | AAAAC | 114 | a0001c0001t0001g0227a0001c0001t0007g0012a0001c0001t0007g0059others(111): Show | 122 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.2168-4652_2168-464 others(8): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 116980025 | |||||
chr1:116980025
|
A | C | 5 | a0001c0006t0009g0211a0001c0006t0009g0212a0001c0006t0009g0213others(2): Show | 5 | HG02109.hp2 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2168-4655A>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116980025 | ||||||
chr1:116980114
|
C | T | 48 | a0002c0002t0002g0118a0002c0002t0002g0263a0003c0003t0002g0002others(45): Show | 50 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2168-4566C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116980114 | ||||||
chr1:116980120
|
T | C | 10 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0230others(7): Show | 11 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2168-4560T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116980120 | ||||||
chr1:116980155
|
C | T | 10 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0230others(7): Show | 11 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2168-4525C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116980155 | ||||||
chr1:116980159
|
A | G | 5 | a0001c0006t0009g0211a0001c0006t0009g0212a0001c0006t0009g0213others(2): Show | 5 | HG02109.hp2 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2168-4521A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116980159 | ||||||
chr1:116980162
|
C | A | 10 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0230others(7): Show | 11 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2168-4518C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116980162 | ||||||
chr1:116980163
|
A | G | 10 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0230others(7): Show | 11 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2168-4517A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116980163 | ||||||
chr1:116980165
|
C | T | 10 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0230others(7): Show | 11 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2168-4515C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116980165 | ||||||
chr1:116980171
|
C | T | 10 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0230others(7): Show | 11 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2168-4509C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116980171 | ||||||
chr1:116980243
|
G | A | 2 | a0003c0003t0002g0007a0003c0003t0002g0073 | 3 | NA18956.hp2 NA18963.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.2168-4437G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116980243 | ||||||
chr1:116980379
|
A | G | 115 | a0001c0001t0001g0227a0001c0001t0007g0012a0001c0001t0007g0059others(112): Show | 123 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.2168-4301A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116980379 | ||||||
chr1:116980537
|
G | A | 2 | a0003c0003t0002g0054a0003c0003t0002g0055 | 2 | NA18951.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.2168-4143G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116980537 | ||||||
chr1:116980573
|
G | C | 2 | a0001c0001t0037g0273a0012c0021t0036g0287 | 2 | HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2168-4107G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116980573 | ||||||
chr1:116980711
|
C | T | 49 | a0002c0002t0002g0118a0002c0002t0002g0263a0003c0003t0002g0002others(46): Show | 51 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.2168-3969C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116980711 | ||||||
chr1:116980736
|
A | C | 1 | a0007c0013t0002g0268 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2168-3944A>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116980736 | ||||||
chr1:116980850
|
A | G | 5 | a0002c0019t0030g0270a0004c0004t0028g0112a0007c0010t0013g0284others(2): Show | 5 | HG02145.hp1 HG02145.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2168-3830A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116980850 | ||||||
chr1:116980876
|
G | A | 114 | a0001c0001t0007g0012a0001c0001t0007g0059a0001c0001t0007g0060others(111): Show | 122 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.2168-3804G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116980876 | ||||||
chr1:116981107
|
T | C | 4 | a0001c0001t0018g0269a0001c0008t0021g0044a0001c0008t0021g0199others(1): Show | 4 | HG01433.hp2 HG02717.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2168-3573T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116981107 | ||||||
chr1:116981186
|
C | CATT | 6 | a0001c0001t0001g0162a0001c0001t0001g0288a0004c0004t0001g0237others(3): Show | 6 | HG02015.hp2 NA18939.hp1 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.2168-3492_2168-349 others(7): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 116981186 | |||||
chr1:116981270
|
A | G | 2 | a0001c0001t0020g0200a0001c0001t0020g0201 | 2 | HG02895.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2168-3410A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116981270 | ||||||
chr1:116981400
|
T | G | 117 | a0001c0001t0001g0227a0001c0001t0007g0012a0001c0001t0007g0059others(114): Show | 125 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.2168-3280T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116981400 | ||||||
chr1:116981560
|
G | C | 6 | a0001c0001t0001g0036a0001c0001t0001g0230a0001c0001t0001g0274others(3): Show | 7 | HG02280.hp2 HG02922.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.2168-3120G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116981560 | ||||||
chr1:116981601
|
C | A | 4 | a0001c0001t0020g0200a0001c0001t0020g0201a0001c0018t0029g0040others(1): Show | 4 | HG02257.hp1 HG02895.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2168-3079C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116981601 | ||||||
chr1:116981623
|
T | G | 1 | a0002c0019t0030g0270 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2168-3057T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116981623 | ||||||
chr1:116981641
|
A | T | 1 | a0003c0003t0002g0087 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2168-3039A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116981641 | ||||||
chr1:116981775
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2168-2905C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116981775 | ||||||
chr1:116981850
|
C | A | 1 | a0005c0005t0002g0272 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2168-2830C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116981850 | ||||||
chr1:116981975
|
C | T | 41 | a0002c0002t0001g0195a0002c0002t0004g0003a0002c0002t0004g0009others(38): Show | 44 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.2168-2705C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116981975 | ||||||
chr1:116982005
|
A | C | 1 | a0001c0001t0007g0061 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2168-2675A>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116982005 | ||||||
chr1:116982011
|
G | C | 1 | a0002c0002t0006g0033 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2168-2669G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116982011 | ||||||
chr1:116982033
|
C | T | 1 | a0004c0009t0001g0011 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2168-2647C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116982033 | ||||||
chr1:116982045
|
T | C | 3 | a0001c0008t0011g0233a0006c0012t0011g0266a0006c0022t0011g0265 | 3 | HG02622.hp2 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2168-2635T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116982045 | ||||||
chr1:116982112
|
C | T | 4 | a0001c0001t0020g0200a0001c0001t0020g0201a0001c0018t0029g0040others(1): Show | 4 | HG02257.hp1 HG02895.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2168-2568C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116982112 | ||||||
chr1:116982113
|
G | A | 4 | a0001c0001t0012g0292a0001c0001t0016g0228a0001c0001t0016g0229others(1): Show | 5 | HG02572.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.2168-2567G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116982113 | ||||||
chr1:116982451
|
A | G | 4 | a0003c0003t0002g0002a0003c0003t0002g0050a0003c0003t0002g0051others(1): Show | 5 | NA18939.hp2 NA18964.hp1 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.2168-2229A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116982451 | ||||||
chr1:116982577
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0122a0001c0001t0005g0010 | 3 | HG02698.hp1 HG03688.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.2168-2103G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116982577 | ||||||
chr1:116982614
|
C | A | 1 | a0004c0009t0001g0011 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2168-2066C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116982614 | ||||||
chr1:116982670
|
A | T | 4 | a0002c0019t0030g0270a0007c0010t0013g0284a0007c0010t0013g0285others(1): Show | 4 | HG02145.hp1 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2168-2010A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116982670 | ||||||
chr1:116982694
|
C | T | 3 | a0002c0002t0003g0023a0002c0002t0003g0119a0005c0005t0003g0252 | 3 | HG02735.hp2 HG03239.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2168-1986C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116982694 | ||||||
chr1:116982703
|
C | G | 1 | a0003c0003t0002g0078 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2168-1977C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116982703 | ||||||
chr1:116982784
|
G | T | 2 | a0001c0001t0018g0269a0006c0012t0018g0267 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2168-1896G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116982784 | ||||||
chr1:116982796
|
A | G | 1 | a0003c0003t0002g0054 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2168-1884A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116982796 | ||||||
chr1:116982836
|
C | A | 114 | a0001c0001t0007g0012a0001c0001t0007g0059a0001c0001t0007g0060others(111): Show | 122 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.2168-1844C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116982836 | ||||||
chr1:116982887
|
G | A | 4 | a0002c0019t0030g0270a0007c0010t0013g0284a0007c0010t0013g0285others(1): Show | 4 | HG02145.hp1 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2168-1793G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116982887 | ||||||
chr1:116982906
|
A | G | 2 | a0001c0001t0018g0269a0006c0012t0018g0267 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2168-1774A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116982906 | ||||||
chr1:116982935
|
A | C | 4 | a0002c0019t0030g0270a0007c0010t0013g0284a0007c0010t0013g0285others(1): Show | 4 | HG02145.hp1 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2168-1745A>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116982935 | ||||||
chr1:116983158
|
G | T | 1 | a0004c0004t0028g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2168-1522G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983158 | ||||||
chr1:116983188
|
C | T | 38 | a0002c0002t0003g0001a0002c0002t0003g0016a0002c0002t0003g0017others(35): Show | 41 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(38): Show |
intron_variant | MODIFIER | c.2168-1492C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983188 | ||||||
chr1:116983189
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2168-1491G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983189 | ||||||
chr1:116983240
|
G | T | 2 | a0001c0001t0037g0273a0012c0021t0036g0287 | 2 | HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2168-1440G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983240 | ||||||
chr1:116983433
|
A | G | 38 | a0002c0002t0003g0001a0002c0002t0003g0016a0002c0002t0003g0017others(35): Show | 41 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(38): Show |
intron_variant | MODIFIER | c.2168-1247A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983433 | ||||||
chr1:116983498
|
C | CA | 8 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0197others(5): Show | 8 | HG01433.hp1 HG02559.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.2168-1158dupA | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 116983498 | |||||
chr1:116983498
|
CA | C | 17 | a0001c0001t0001g0144a0001c0001t0037g0273a0001c0006t0009g0211others(14): Show | 17 | HG01069.hp1 HG01433.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.2168-1158delA | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 116983498 | |||||
chr1:116983498
|
CAA | C | 57 | a0001c0001t0007g0012a0001c0001t0007g0059a0001c0001t0007g0060others(54): Show | 63 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.2168-1159_2168-115 others(6): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 116983498 | |||||
chr1:116983498
|
CAAA | C | 85 | a0002c0002t0001g0195a0002c0002t0002g0118a0002c0002t0002g0165others(82): Show | 90 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.2168-1160_2168-115 others(7): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 116983498 | |||||
chr1:116983498
|
CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0001g0146a0001c0001t0001g0150 | 2 | HG00099.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2168-1170_2168-115 others(17): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 116983498 | |||||
chr1:116983585
|
G | C | 49 | a0002c0002t0002g0118a0002c0002t0002g0165a0002c0002t0002g0263others(46): Show | 51 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.2168-1095G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983585 | ||||||
chr1:116983638
|
T | A | 11 | a0001c0001t0007g0012a0001c0001t0007g0059a0001c0001t0007g0060others(8): Show | 14 | HG00741.hp2 HG01109.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.2168-1042T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983638 | ||||||
chr1:116983789
|
T | C | 1 | a0003c0003t0002g0076 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2168-891T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983789 | ||||||
chr1:116983790
|
C | T | 1 | a0003c0003t0002g0076 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2168-890C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983790 | ||||||
chr1:116983795
|
G | C | 1 | a0003c0003t0002g0076 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2168-885G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983795 | ||||||
chr1:116983797
|
G | T | 1 | a0003c0003t0002g0076 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2168-883G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983797 | ||||||
chr1:116983798
|
G | C | 1 | a0003c0003t0002g0076 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2168-882G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983798 | ||||||
chr1:116983802
|
T | G | 1 | a0003c0003t0002g0076 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2168-878T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983802 | ||||||
chr1:116983803
|
A | T | 1 | a0003c0003t0002g0076 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2168-877A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983803 | ||||||
chr1:116983808
|
A | C | 1 | a0003c0003t0002g0076 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2168-872A>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983808 | ||||||
chr1:116983809
|
A | T | 1 | a0003c0003t0002g0076 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2168-871A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983809 | ||||||
chr1:116983828
|
C | A | 1 | a0003c0003t0002g0076 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2168-852C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983828 | ||||||
chr1:116983829
|
T | C | 1 | a0003c0003t0002g0076 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2168-851T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983829 | ||||||
chr1:116983855
|
C | T | 1 | a0003c0003t0010g0074 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2168-825C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983855 | ||||||
chr1:116983868
|
A | C | 1 | a0003c0003t0002g0076 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2168-812A>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983868 | ||||||
chr1:116983898
|
A | C | 1 | a0003c0003t0002g0076 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2168-782A>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983898 | ||||||
chr1:116984135
|
C | A | 1 | a0001c0001t0001g0005 | 3 | HG02109.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2168-545C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116984135 | ||||||
chr1:116984145
|
A | G | 1 | a0001c0018t0029g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2168-535A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116984145 | ||||||
chr1:116984179
|
G | A | 1 | a0011c0023t0033g0281 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2168-501G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116984179 | ||||||
chr1:116984283
|
G | C | 168 | a0001c0001t0001g0227a0001c0001t0007g0012a0001c0001t0007g0059others(165): Show | 180 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.2168-397G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116984283 | ||||||
chr1:116984477
|
A | T | 38 | a0002c0002t0003g0001a0002c0002t0003g0016a0002c0002t0003g0017others(35): Show | 41 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(38): Show |
intron_variant | MODIFIER | c.2168-203A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116984477 | ||||||
chr1:116984508
|
A | G | 2 | a0001c0001t0016g0228a0001c0001t0016g0229 | 2 | HG03654.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.2168-172A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116984508 | ||||||
chr1:116984530
|
A | T | 44 | a0001c0001t0001g0010a0001c0001t0001g0026a0001c0001t0001g0028others(41): Show | 46 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.2168-150A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116984530 | ||||||
chr1:116984574
|
G | A | 11 | a0001c0001t0007g0012a0001c0001t0007g0059a0001c0001t0007g0060others(8): Show | 14 | HG00741.hp2 HG01109.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.2168-106G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116984574 | ||||||
chr1:116984605
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2168-75C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116984605 | ||||||
chr1:116984626
|
A | G | 1 | a0002c0002t0003g0135 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2168-54A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116984626 | ||||||
chr1:116985023
|
GTCT | G | 116 | a0001c0001t0007g0012a0001c0001t0007g0059a0001c0001t0007g0060others(113): Show | 124 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.2473+46_2473+48del others(3): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 116985023 | |||||
chr1:116985079
|
A | G | 1 | a0002c0002t0004g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2473+94A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116985079 | ||||||
chr1:116985094
|
G | A | 1 | a0001c0001t0001g0278 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2473+109G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116985094 | ||||||
chr1:116985117
|
G | T | 1 | a0004c0004t0028g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2473+132G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116985117 | ||||||
chr1:116985470
|
G | A | 2 | a0001c0001t0037g0273a0012c0021t0036g0287 | 2 | HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2473+485G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116985470 | ||||||
chr1:116985473
|
C | T | 2 | a0001c0001t0012g0292a0006c0007t0012g0015 | 3 | HG02572.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2473+488C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116985473 | ||||||
chr1:116985555
|
C | A | 153 | a0001c0001t0007g0012a0001c0001t0007g0059a0001c0001t0007g0060others(150): Show | 163 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.2473+570C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116985555 | ||||||
chr1:116985617
|
A | G | 41 | a0002c0002t0001g0195a0002c0002t0004g0003a0002c0002t0004g0009others(38): Show | 44 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.2473+632A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116985617 | ||||||
chr1:116985657
|
G | A | 90 | a0002c0002t0001g0195a0002c0002t0002g0118a0002c0002t0002g0165others(87): Show | 95 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.2473+672G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116985657 | ||||||
chr1:116985703
|
A | G | 2 | a0001c0001t0018g0269a0006c0012t0018g0267 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2473+718A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116985703 | ||||||
chr1:116985707
|
C | CA | 26 | a0001c0001t0007g0012a0001c0001t0007g0059a0001c0001t0007g0060others(23): Show | 29 | HG00741.hp2 HG01069.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.2473+736dupA | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 116985707 | |||||
chr1:116985707
|
C | CAA | 50 | a0002c0002t0003g0001a0002c0002t0003g0008a0002c0002t0003g0016others(47): Show | 54 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.2473+735_2473+736d others(4): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 116985707 | |||||
chr1:116985722
|
G | A | 90 | a0002c0002t0001g0195a0002c0002t0002g0118a0002c0002t0002g0165others(87): Show | 95 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.2473+737G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116985722 | ||||||
chr1:116985744
|
G | A | 50 | a0002c0002t0003g0001a0002c0002t0003g0008a0002c0002t0003g0016others(47): Show | 54 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.2473+759G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116985744 | ||||||
chr1:116985818
|
C | G | 3 | a0001c0008t0011g0233a0006c0012t0011g0266a0006c0022t0011g0265 | 3 | HG02622.hp2 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2473+833C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116985818 | ||||||
chr1:116985885
|
CT | C | 4 | a0001c0001t0012g0292a0001c0001t0016g0228a0001c0001t0016g0229others(1): Show | 5 | HG02572.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.2473+902delT | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 116985885 | |||||
chr1:116985888
|
G | C | 1 | a0011c0023t0033g0281 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2473+903G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116985888 | ||||||
chr1:116985889
|
G | A | 3 | a0001c0008t0011g0233a0006c0012t0011g0266a0006c0022t0011g0265 | 3 | HG02622.hp2 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2473+904G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116985889 | ||||||
chr1:116985909
|
C | A | 1 | a0003c0003t0002g0057 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2474-892C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116985909 | ||||||
chr1:116985994
|
A | G | 166 | a0001c0001t0007g0012a0001c0001t0007g0059a0001c0001t0007g0060others(163): Show | 178 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.2474-807A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116985994 | ||||||
chr1:116986024
|
G | C | 4 | a0001c0001t0020g0200a0001c0001t0020g0201a0001c0018t0029g0040others(1): Show | 4 | HG02257.hp1 HG02895.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2474-777G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116986024 | ||||||
chr1:116986071
|
T | C | 2 | a0001c0001t0018g0269a0006c0012t0018g0267 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2474-730T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116986071 | ||||||
chr1:116986188
|
T | TG | 166 | a0001c0001t0007g0012a0001c0001t0007g0059a0001c0001t0007g0060others(163): Show | 178 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.2474-610dupG | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 116986188 | |||||
chr1:116986554
|
C | T | 3 | a0007c0010t0013g0284a0007c0010t0013g0285a0007c0010t0013g0286 | 3 | HG02145.hp1 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2474-247C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116986554 | ||||||
chr1:116986589
|
G | A | 1 | a0001c0001t0001g0226 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2474-212G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116986589 | ||||||
chr1:116986600
|
T | A | 2 | a0002c0002t0003g0102a0002c0002t0003g0186 | 2 | HG03710.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.2474-201T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116986600 | ||||||
chr1:116986757
|
C | T | 1 | a0006c0007t0012g0015 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2474-44C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116986757 |