geneid | 134359 |
---|---|
ensemblid | ENSG00000152359.15 |
hgncid | 26658 |
symbol | POC5 |
name | POC5 centriolar protein |
refseq_nuc | NM_001099271.2 |
refseq_prot | NP_001092741.1 |
ensembl_nuc | ENST00000428202.7 |
ensembl_prot | ENSP00000410216.2 |
mane_status | MANE Select |
chr | chr5 |
start | 75674124 |
end | 75717437 |
strand | - |
ver | v1.2 |
region | chr5:75674124-75717437 |
region5000 | chr5:75669124-75722437 |
regionname0 | POC5_chr5_75674124_75717437 |
regionname5000 | POC5_chr5_75669124_75722437 |
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 | 575 | 137 | 45 | 28 | 46 | 5 | 13 | 34 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
a0002 | 1/1 | 575 | 111 | 5 | 21 | 65 | 6 | 12 | 52 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
a0003 | 0/0 | 575 | 96 | 15 | 11 | 59 | 1 | 10 | 48 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
a0004 | 0/0 | 575 | 22 | 17 | 5 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
a0005 | 0/0 | 575 | 5 | 0 | 0 | 4 | 0 | 1 | 3 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
a0006 | 0/0 | 575 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
a0007 | 0/0 | 575 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
a0008 | 0/0 | 575 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
a0009 | 0/0 | 575 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
a0010 | 0/0 | 575 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
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 | 1728 | 113 | 36 | 24 | 40 | 4 | 9 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
c0002 | 1/1 | 1728 | 110 | 5 | 21 | 64 | 6 | 12 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
c0003 | 0/0 | 1728 | 96 | 15 | 11 | 59 | 1 | 10 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
c0004 | 0/0 | 1728 | 23 | 8 | 4 | 6 | 1 | 4 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
c0005 | 0/0 | 1728 | 21 | 16 | 5 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
c0006 | 0/0 | 1728 | 5 | 0 | 0 | 4 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
c0007 | 0/0 | 1728 | 4 | 0 | 0 | 4 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
c0008 | 0/0 | 1728 | 2 | 0 | 1 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
c0009 | 0/0 | 1728 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
c0010 | 0/0 | 1728 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
c0011 | 0/0 | 1728 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
c0012 | 0/0 | 1728 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
c0013 | 0/0 | 1728 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
c0014 | 0/0 | 1728 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
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 | 1/1 | 458 | 218 | 39 | 46 | 96 | 10 | 25 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
t0002 | 0/0 | 458 | 113 | 26 | 15 | 59 | 2 | 11 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
t0003 | 0/0 | 458 | 22 | 17 | 5 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
t0004 | 0/0 | 458 | 20 | 0 | 0 | 18 | 0 | 2 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
t0005 | 0/0 | 461 | 7 | 0 | 0 | 7 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
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 | 18 | 0 | 4 | 13 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0002 | 0/0 | 11 | 0 | 2 | 7 | 0 | 2 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0003 | 0/0 | 8 | 1 | 2 | 5 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0005 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0006 | 0/0 | 4 | 2 | 1 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0009 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0012 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0018 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0021 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0032 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0146 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0148 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
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 | 1728 | 113 | 36 | 24 | 40 | 4 | 9 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
a0001c0004 | 0/0 | 1728 | 23 | 8 | 4 | 6 | 1 | 4 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
a0001c0011 | 0/0 | 1728 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
a0002c0002 | 1/1 | 1728 | 110 | 5 | 21 | 64 | 6 | 12 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
a0002c0009 | 0/0 | 1728 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
a0003c0003 | 0/0 | 1728 | 96 | 15 | 11 | 59 | 1 | 10 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
a0004c0005 | 0/0 | 1728 | 21 | 16 | 5 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
a0004c0014 | 0/0 | 1728 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
a0005c0006 | 0/0 | 1728 | 5 | 0 | 0 | 4 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
a0006c0007 | 0/0 | 1728 | 4 | 0 | 0 | 4 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
a0007c0008 | 0/0 | 1728 | 2 | 0 | 1 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
a0008c0012 | 0/0 | 1728 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
a0009c0013 | 0/0 | 1728 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
a0010c0010 | 0/0 | 1728 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2185 | 101 | 31 | 23 | 34 | 4 | 9 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
a0001c0001t0002 | 0/0 | 2185 | 12 | 5 | 1 | 6 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
a0001c0004t0001 | 0/0 | 2185 | 5 | 2 | 0 | 0 | 0 | 3 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
a0001c0004t0002 | 0/0 | 2185 | 18 | 6 | 4 | 6 | 1 | 1 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
a0001c0011t0001 | 0/0 | 2185 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
a0002c0002t0001 | 1/1 | 2185 | 103 | 5 | 21 | 57 | 6 | 12 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
a0002c0002t0005 | 0/0 | 2188 | 7 | 0 | 0 | 7 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
a0002c0009t0001 | 0/0 | 2185 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
a0003c0003t0001 | 0/0 | 2185 | 4 | 0 | 1 | 3 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
a0003c0003t0002 | 0/0 | 2185 | 77 | 15 | 10 | 43 | 1 | 8 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
a0003c0003t0004 | 0/0 | 2185 | 15 | 0 | 0 | 13 | 0 | 2 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
a0004c0005t0003 | 0/0 | 2185 | 21 | 16 | 5 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
a0004c0014t0003 | 0/0 | 2185 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
a0005c0006t0002 | 0/0 | 2185 | 5 | 0 | 0 | 4 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
a0006c0007t0004 | 0/0 | 2185 | 4 | 0 | 0 | 4 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
a0007c0008t0001 | 0/0 | 2185 | 2 | 0 | 1 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
a0008c0012t0001 | 0/0 | 2185 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
a0009c0013t0002 | 0/0 | 2185 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
a0010c0010t0004 | 0/0 | 2185 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | copy fasta | chr5 | 75669124 | 75722437 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 11 | 0 | 2 | 7 | 0 | 2 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0005 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0004t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0004t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0004t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0004t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0004t0002g0003 | 0/0 | 8 | 1 | 2 | 5 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0004t0002g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0004t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0004t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0004t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0004t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0004t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0004t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0004t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0004t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0001c0011t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0006 | 0/0 | 4 | 2 | 1 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0012 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0146 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0148 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0005g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0005g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0005g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0002t0005g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0002c0009t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0001 | 0/0 | 18 | 0 | 4 | 13 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0018 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0032 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0004g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0004g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0004g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0003c0003t0004g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0004c0005t0003g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0004c0005t0003g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0004c0005t0003g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0004c0005t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0004c0005t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0004c0005t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0004c0005t0003g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0004c0005t0003g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0004c0005t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0004c0005t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0004c0005t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0004c0005t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0004c0005t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0004c0005t0003g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0004c0005t0003g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0004c0005t0003g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0004c0014t0003g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0005c0006t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0005c0006t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0005c0006t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0005c0006t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0005c0006t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0006c0007t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0006c0007t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0006c0007t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0006c0007t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0007c0008t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0007c0008t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0008c0012t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0009c0013t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
a0010c0010t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0220 | EUR | GBR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0102 | EUR | GBR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG00140 | hp1 | a0002 | c0002 | t0001 | g0024 | EUR | GBR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0092 | EUR | GBR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG00280 | hp1 | a0001 | c0004 | t0002 | g0019 | EUR | FIN | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0021 | EUR | FIN | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG00323 | hp1 | a0002 | c0002 | t0001 | g0201 | EUR | FIN | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0174 | EUR | FIN | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG00408 | hp1 | a0002 | c0002 | t0001 | g0126 | EAS | CHS | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG00408 | hp2 | a0001 | c0004 | t0002 | g0003 | EAS | CHS | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG00423 | hp1 | a0003 | c0003 | t0002 | g0268 | EAS | CHS | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | CHS | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0207 | EAS | CHS | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG00544 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | CHS | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG00558 | hp1 | a0003 | c0003 | t0002 | g0256 | EAS | CHS | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | CHS | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG00609 | hp1 | a0002 | c0002 | t0001 | g0157 | EAS | CHS | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG00609 | hp2 | a0003 | c0003 | t0002 | g0014 | EAS | CHS | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG00621 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | CHS | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG00621 | hp2 | a0003 | c0003 | t0002 | g0033 | EAS | CHS | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG00639 | hp2 | a0002 | c0002 | t0001 | g0231 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG00642 | hp2 | a0002 | c0002 | t0001 | g0074 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG00733 | hp1 | a0002 | c0002 | t0001 | g0225 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG00733 | hp2 | a0003 | c0003 | t0001 | g0066 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG00735 | hp1 | a0004 | c0005 | t0003 | g0285 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG00735 | hp2 | a0002 | c0002 | t0001 | g0155 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01069 | hp1 | a0003 | c0003 | t0002 | g0031 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0175 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01071 | hp1 | a0007 | c0008 | t0001 | g0143 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01071 | hp2 | a0003 | c0003 | t0002 | g0031 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01099 | hp1 | a0001 | c0004 | t0002 | g0110 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01099 | hp2 | a0002 | c0002 | t0001 | g0224 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01106 | hp2 | a0002 | c0002 | t0001 | g0237 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01109 | hp1 | a0004 | c0005 | t0003 | g0293 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01167 | hp2 | a0004 | c0005 | t0003 | g0294 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0191 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01169 | hp1 | a0002 | c0002 | t0001 | g0190 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01169 | hp2 | a0004 | c0005 | t0003 | g0292 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0202 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01243 | hp1 | a0004 | c0005 | t0003 | g0035 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01255 | hp1 | a0001 | c0004 | t0002 | g0019 | AMR | CLM | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01256 | hp1 | a0002 | c0002 | t0001 | g0235 | AMR | CLM | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0025 | AMR | CLM | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0156 | AMR | CLM | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01358 | hp2 | a0003 | c0003 | t0002 | g0067 | AMR | CLM | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0024 | AMR | CLM | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01361 | hp2 | a0001 | c0004 | t0002 | g0003 | AMR | CLM | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0025 | AMR | CLM | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01496 | hp1 | a0003 | c0003 | t0002 | g0258 | AMR | CLM | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01516 | hp1 | a0002 | c0002 | t0001 | g0192 | EUR | IBS | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01516 | hp2 | a0003 | c0003 | t0002 | g0018 | EUR | IBS | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0210 | AFR | ACB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01884 | hp2 | a0004 | c0005 | t0003 | g0290 | AFR | ACB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01891 | hp2 | a0004 | c0005 | t0003 | g0007 | AFR | ACB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01934 | hp2 | a0003 | c0003 | t0002 | g0254 | AMR | PEL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01943 | hp1 | a0003 | c0003 | t0002 | g0001 | AMR | PEL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01952 | hp1 | a0001 | c0004 | t0002 | g0003 | AMR | PEL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01952 | hp2 | a0002 | c0002 | t0001 | g0196 | AMR | PEL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01975 | hp1 | a0003 | c0003 | t0002 | g0001 | AMR | PEL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01975 | hp2 | a0002 | c0002 | t0001 | g0151 | AMR | PEL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01981 | hp1 | a0003 | c0003 | t0002 | g0001 | AMR | PEL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01981 | hp2 | a0002 | c0002 | t0001 | g0029 | AMR | PEL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02015 | hp1 | a0008 | c0012 | t0001 | g0119 | EAS | KHV | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02015 | hp2 | a0002 | c0002 | t0001 | g0185 | EAS | KHV | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | KHV | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02027 | hp2 | a0003 | c0003 | t0002 | g0257 | EAS | KHV | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | KHV | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02040 | hp2 | a0005 | c0006 | t0002 | g0039 | EAS | KHV | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02056 | hp1 | a0003 | c0003 | t0002 | g0013 | EAS | KHV | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | KHV | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02071 | hp2 | a0002 | c0002 | t0001 | g0144 | EAS | KHV | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02080 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | KHV | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02080 | hp2 | a0002 | c0002 | t0001 | g0236 | EAS | KHV | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | KHV | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | KHV | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02145 | hp1 | a0004 | c0014 | t0003 | g0291 | AFR | ACB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02145 | hp2 | a0001 | c0004 | t0002 | g0085 | AFR | ACB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02148 | hp1 | a0002 | c0002 | t0001 | g0199 | AMR | PEL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CDX | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | CDX | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02257 | hp1 | a0002 | c0002 | t0001 | g0238 | AFR | ACB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02257 | hp2 | a0004 | c0005 | t0003 | g0036 | AFR | ACB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02258 | hp1 | a0004 | c0005 | t0003 | g0036 | AFR | ACB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02293 | hp1 | a0003 | c0003 | t0002 | g0001 | AMR | PEL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02451 | hp1 | a0001 | c0004 | t0002 | g0003 | AFR | ACB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02451 | hp2 | a0003 | c0003 | t0002 | g0261 | AFR | ACB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02523 | hp1 | a0002 | c0002 | t0001 | g0195 | EAS | KHV | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02523 | hp2 | a0003 | c0003 | t0002 | g0265 | EAS | KHV | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02572 | hp1 | a0004 | c0005 | t0003 | g0284 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02572 | hp2 | a0001 | c0004 | t0002 | g0084 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02602 | hp1 | a0003 | c0003 | t0002 | g0058 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0183 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02647 | hp1 | a0004 | c0005 | t0003 | g0007 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02683 | hp2 | a0002 | c0002 | t0001 | g0233 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02698 | hp1 | a0003 | c0003 | t0002 | g0055 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02698 | hp2 | a0007 | c0008 | t0001 | g0073 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02723 | hp2 | a0004 | c0005 | t0003 | g0007 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02735 | hp2 | a0003 | c0003 | t0002 | g0065 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02809 | hp2 | a0001 | c0011 | t0001 | g0095 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02818 | hp1 | a0003 | c0003 | t0002 | g0056 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02886 | hp1 | a0003 | c0003 | t0002 | g0260 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02895 | hp1 | a0001 | c0004 | t0001 | g0078 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02896 | hp2 | a0004 | c0005 | t0003 | g0286 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ESN | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02922 | hp2 | a0003 | c0003 | t0002 | g0051 | AFR | ESN | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ESN | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02970 | hp2 | a0004 | c0005 | t0003 | g0007 | AFR | ESN | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03041 | hp2 | a0004 | c0005 | t0003 | g0283 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | MSL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03098 | hp2 | a0003 | c0003 | t0002 | g0273 | AFR | MSL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03130 | hp1 | a0004 | c0005 | t0003 | g0035 | AFR | ESN | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03130 | hp2 | a0004 | c0005 | t0003 | g0288 | AFR | ESN | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | ESN | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03139 | hp2 | a0003 | c0003 | t0002 | g0052 | AFR | ESN | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03195 | hp2 | a0001 | c0004 | t0002 | g0080 | AFR | ESN | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0249 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03453 | hp1 | a0004 | c0005 | t0003 | g0289 | AFR | MSL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03453 | hp2 | a0003 | c0003 | t0002 | g0269 | AFR | MSL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03486 | hp1 | a0001 | c0004 | t0001 | g0075 | AFR | MSL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | MSL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03490 | hp2 | a0001 | c0004 | t0001 | g0167 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03491 | hp1 | a0003 | c0003 | t0002 | g0064 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03492 | hp1 | a0001 | c0004 | t0001 | g0028 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03516 | hp1 | a0003 | c0003 | t0002 | g0050 | AFR | ESN | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03516 | hp2 | a0003 | c0003 | t0002 | g0054 | AFR | ESN | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03540 | hp2 | a0003 | c0003 | t0002 | g0057 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0248 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03688 | hp1 | a0009 | c0013 | t0002 | g0086 | SAS | STU | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03688 | hp2 | a0003 | c0003 | t0002 | g0079 | SAS | STU | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03704 | hp2 | a0003 | c0003 | t0004 | g0069 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0152 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0029 | SAS | BEB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03834 | hp2 | a0002 | c0002 | t0001 | g0182 | SAS | BEB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03927 | hp1 | a0002 | c0002 | t0001 | g0012 | SAS | BEB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03927 | hp2 | a0003 | c0003 | t0004 | g0048 | SAS | BEB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0193 | SAS | STU | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0203 | SAS | STU | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG04199 | hp1 | a0003 | c0003 | t0002 | g0018 | SAS | STU | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG04199 | hp2 | a0002 | c0002 | t0001 | g0223 | SAS | STU | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG04204 | hp1 | a0001 | c0004 | t0002 | g0082 | SAS | STU | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG04204 | hp2 | a0003 | c0003 | t0002 | g0001 | SAS | STU | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG04228 | hp1 | a0003 | c0003 | t0002 | g0032 | SAS | STU | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG04228 | hp2 | a0001 | c0004 | t0001 | g0028 | SAS | STU | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18522 | hp1 | a0003 | c0003 | t0002 | g0047 | AFR | YRI | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | YRI | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18612 | hp2 | a0003 | c0003 | t0002 | g0253 | EAS | CHB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18747 | hp1 | a0003 | c0003 | t0004 | g0004 | EAS | CHB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18747 | hp2 | a0003 | c0003 | t0002 | g0255 | EAS | CHB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18906 | hp1 | a0003 | c0003 | t0002 | g0266 | AFR | YRI | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18906 | hp2 | a0004 | c0005 | t0003 | g0287 | AFR | YRI | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18940 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18940 | hp2 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18941 | hp2 | a0002 | c0002 | t0001 | g0153 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18942 | hp1 | a0003 | c0003 | t0004 | g0059 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18942 | hp2 | a0002 | c0002 | t0005 | g0280 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18943 | hp2 | a0003 | c0003 | t0002 | g0267 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18944 | hp1 | a0002 | c0002 | t0005 | g0017 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18944 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18947 | hp1 | a0002 | c0002 | t0001 | g0278 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18948 | hp1 | a0006 | c0007 | t0004 | g0071 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18948 | hp2 | a0003 | c0003 | t0002 | g0252 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18950 | hp1 | a0003 | c0003 | t0002 | g0014 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18950 | hp2 | a0002 | c0009 | t0001 | g0229 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18951 | hp2 | a0003 | c0003 | t0001 | g0272 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0186 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18953 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18953 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18954 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18956 | hp1 | a0002 | c0002 | t0001 | g0197 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18956 | hp2 | a0003 | c0003 | t0002 | g0262 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18959 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18959 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18960 | hp2 | a0002 | c0002 | t0005 | g0017 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18962 | hp1 | a0003 | c0003 | t0004 | g0004 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18963 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18965 | hp1 | a0003 | c0003 | t0002 | g0015 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18965 | hp2 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18966 | hp1 | a0003 | c0003 | t0002 | g0277 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18966 | hp2 | a0001 | c0004 | t0002 | g0003 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18967 | hp1 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18967 | hp2 | a0003 | c0003 | t0004 | g0063 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18968 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18968 | hp2 | a0003 | c0003 | t0004 | g0053 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18970 | hp1 | a0003 | c0003 | t0002 | g0016 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0184 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18971 | hp1 | a0010 | c0010 | t0004 | g0070 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18971 | hp2 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18972 | hp1 | a0001 | c0004 | t0002 | g0003 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18972 | hp2 | a0003 | c0003 | t0002 | g0015 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18973 | hp1 | a0003 | c0003 | t0002 | g0014 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18974 | hp1 | a0005 | c0006 | t0002 | g0038 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18974 | hp2 | a0003 | c0003 | t0004 | g0008 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18975 | hp1 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18975 | hp2 | a0003 | c0003 | t0004 | g0004 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18977 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18978 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18978 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18979 | hp1 | a0003 | c0003 | t0002 | g0016 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18983 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0189 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18985 | hp1 | a0003 | c0003 | t0002 | g0271 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18985 | hp2 | a0003 | c0003 | t0004 | g0060 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18986 | hp1 | a0002 | c0002 | t0001 | g0154 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18986 | hp2 | a0003 | c0003 | t0002 | g0016 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18989 | hp2 | a0002 | c0002 | t0001 | g0165 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18991 | hp1 | a0006 | c0007 | t0004 | g0061 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18991 | hp2 | a0002 | c0002 | t0005 | g0279 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18992 | hp1 | a0003 | c0003 | t0002 | g0264 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18992 | hp2 | a0002 | c0002 | t0005 | g0017 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18993 | hp1 | a0003 | c0003 | t0002 | g0033 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18993 | hp2 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18998 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18998 | hp2 | a0003 | c0003 | t0004 | g0008 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA18999 | hp2 | a0002 | c0002 | t0001 | g0226 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19000 | hp1 | a0002 | c0002 | t0001 | g0206 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19000 | hp2 | a0003 | c0003 | t0002 | g0270 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19001 | hp1 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19001 | hp2 | a0003 | c0003 | t0002 | g0274 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19002 | hp1 | a0003 | c0003 | t0004 | g0004 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19004 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19005 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19005 | hp2 | a0005 | c0006 | t0002 | g0040 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19006 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19006 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19007 | hp1 | a0001 | c0004 | t0002 | g0003 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19009 | hp1 | a0006 | c0007 | t0004 | g0049 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19009 | hp2 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19011 | hp1 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19011 | hp2 | a0001 | c0004 | t0002 | g0003 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19030 | hp1 | a0002 | c0002 | t0001 | g0171 | AFR | LWK | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19030 | hp2 | a0004 | c0005 | t0003 | g0282 | AFR | LWK | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19043 | hp1 | a0001 | c0004 | t0002 | g0081 | AFR | LWK | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | LWK | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19054 | hp1 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19056 | hp2 | a0003 | c0003 | t0002 | g0263 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19058 | hp1 | a0002 | c0002 | t0005 | g0034 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19058 | hp2 | a0003 | c0003 | t0004 | g0046 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19059 | hp1 | a0002 | c0002 | t0001 | g0205 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19060 | hp1 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19060 | hp2 | a0006 | c0007 | t0004 | g0062 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19063 | hp1 | a0003 | c0003 | t0004 | g0008 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19064 | hp1 | a0002 | c0002 | t0005 | g0034 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19064 | hp2 | a0003 | c0003 | t0002 | g0015 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19066 | hp1 | a0003 | c0003 | t0002 | g0013 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19066 | hp2 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19067 | hp1 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19067 | hp2 | a0005 | c0006 | t0002 | g0041 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0234 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19070 | hp1 | a0003 | c0003 | t0004 | g0004 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19075 | hp1 | a0003 | c0003 | t0002 | g0259 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19077 | hp1 | a0001 | c0004 | t0002 | g0076 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19077 | hp2 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19079 | hp1 | a0002 | c0002 | t0001 | g0232 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19079 | hp2 | a0003 | c0003 | t0002 | g0013 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19081 | hp2 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19082 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19083 | hp1 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19083 | hp2 | a0003 | c0003 | t0001 | g0275 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19086 | hp1 | a0002 | c0002 | t0001 | g0221 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19088 | hp1 | a0003 | c0003 | t0001 | g0276 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19088 | hp2 | a0002 | c0002 | t0001 | g0228 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19089 | hp1 | a0002 | c0002 | t0001 | g0204 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0222 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19240 | hp1 | a0001 | c0004 | t0002 | g0083 | AFR | YRI | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | YRI | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0158 | EUR | TSI | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | TSI | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA20905 | hp1 | a0005 | c0006 | t0002 | g0044 | SAS | GIH | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0219 | SAS | GIH | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0128 | AMR | CLM | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG01123 | hp2 | a0003 | c0003 | t0002 | g0068 | AMR | CLM | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02109 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | ACB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | ACB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG02559 | hp2 | a0003 | c0003 | t0002 | g0072 | AFR | ACB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | MSL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG03471 | hp2 | a0003 | c0003 | t0002 | g0045 | AFR | MSL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0198 | AFR | USA | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
HG06807 | hp2 | a0003 | c0003 | t0002 | g0032 | AFR | USA | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | USA | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
NA20300 | hp2 | a0004 | c0005 | t0003 | g0281 | AFR | USA | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0146 | REF | REF | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0148 | REF | REF | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:75685263
|
C | T | 1 | a0009 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.1351G>A | p.Val451Ile | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/12 | 1497/2185 | 1351/1728 | 451/575 | chr5 | 75685263 | ||
chr5:75685328
|
G | A | 1 | a0007 | 2 | HG01071.hp1 HG02698.hp2 |
missense_variant | MODERATE | c.1286C>T | p.Ala429Val | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/12 | 1432/2185 | 1286/1728 | 429/575 | chr5 | 75685328 | ||
chr5:75690483
|
A | G | 1 | a0010 | 1 | NA18971.hp1 | missense_variant | MODERATE | c.875T>C | p.Val292Ala | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 8/12 | 1021/2185 | 875/1728 | 292/575 | chr5 | 75690483 | ||
chr5:75690501
|
T | C | 1 | a0009 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.857A>G | p.Lys286Arg | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 8/12 | 1003/2185 | 857/1728 | 286/575 | chr5 | 75690501 | ||
chr5:75690523
|
T | C | 1 | a0008 | 1 | HG02015.hp1 | missense_variant | MODERATE | c.835A>G | p.Thr279Ala | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 8/12 | 981/2185 | 835/1728 | 279/575 | chr5 | 75690523 | ||
chr5:75692424
|
C | T | 1 | a0006 | 4 | NA18948.hp1 NA18991.hp1 NA19009.hp1 others(1): Show |
missense_variant | MODERATE | c.767G>A | p.Arg256Gln | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 7/12 | 913/2185 | 767/1728 | 256/575 | chr5 | 75692424 | ||
chr5:75702781
|
G | A | 1 | a0005 | 5 | HG02040.hp2 NA18974.hp1 NA19005.hp2 others(2): Show |
missense_variant | MODERATE | c.337C>T | p.Pro113Ser | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/12 | 483/2185 | 337/1728 | 113/575 | chr5 | 75702781 | ||
chr5:75705757
|
A | G | 3 | a0003a0006a0010 | 101 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(98): Show |
missense_variant | MODERATE | c.254T>C | p.Ile85Thr | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/12 | 400/2185 | 254/1728 | 85/575 | chr5 | 75705757 | ||
chr5:75705765
|
T | A | 1 | a0004 | 22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
missense_variant | MODERATE | c.246A>T | p.Glu82Asp | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/12 | 392/2185 | 246/1728 | 82/575 | chr5 | 75705765 | ||
chr5:75707853
|
T | C | 8 | a0001a0003a0004others(5): Show | 267 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(264): Show |
missense_variant | MODERATE | c.107A>G | p.His36Arg | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/12 | 253/2185 | 107/1728 | 36/575 | chr5 | 75707853 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:75685219
|
T | G | 1 | a0002c0009 | 1 | NA18950.hp2 | synonymous_variant | LOW | c.1395A>C | p.Ala465Ala | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/12 | 1541/2185 | 1395/1728 | 465/575 | chr5 | 75685219 | ||
chr5:75685435
|
T | C | 1 | a0001c0011 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.1179A>G | p.Gln393Gln | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/12 | 1325/2185 | 1179/1728 | 393/575 | chr5 | 75685435 | ||
chr5:75702650
|
A | G | 1 | a0004c0014 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.468T>C | p.Leu156Leu | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/12 | 614/2185 | 468/1728 | 156/575 | chr5 | 75702650 | ||
chr5:75702773
|
G | A | 2 | a0001c0004a0009c0013 | 24 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(21): Show |
synonymous_variant | LOW | c.345C>T | p.His115His | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/12 | 491/2185 | 345/1728 | 115/575 | chr5 | 75702773 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:75674199
|
T | C | 10 | a0001c0001t0002a0001c0004t0002a0003c0003t0002others(7): Show | 155 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*236A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 12/12 | 236 | chr5 | 75674199 | |||||
chr5:75674411
|
G | A | 3 | a0003c0003t0004a0006c0007t0004a0010c0010t0004 | 20 | HG03704.hp2 HG03927.hp2 NA18747.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*24C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 12/12 | 24 | chr5 | 75674411 | |||||
chr5:75717388
|
T | TCAG | 1 | a0002c0002t0005 | 7 | NA18942.hp2 NA18944.hp1 NA18960.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-100_-98dupCTG | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/12 | 4452 | chr5 | 75717388 | |||||
chr5:75717414
|
G | A | 2 | a0004c0005t0003a0004c0014t0003 | 22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-123C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/12 | chr5 | 75717414 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:75674731
|
T | G | 11 | a0001c0004t0002g0003a0001c0004t0002g0019a0001c0004t0002g0076others(8): Show | 19 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.1585-153A>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75674731 | ||||||
chr5:75674747
|
A | T | 14 | a0003c0003t0004g0004a0003c0003t0004g0008a0003c0003t0004g0046others(11): Show | 20 | HG03704.hp2 HG03927.hp2 NA18747.hp1 others(17): Show |
intron_variant | MODIFIER | c.1585-169T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75674747 | ||||||
chr5:75674834
|
C | T | 1 | a0003c0003t0002g0072 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1585-256G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75674834 | ||||||
chr5:75675025
|
G | A | 106 | a0001c0001t0002g0037a0001c0001t0002g0042a0001c0001t0002g0043others(103): Show | 154 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.1585-447C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75675025 | ||||||
chr5:75675150
|
C | G | 107 | a0001c0001t0002g0037a0001c0001t0002g0042a0001c0001t0002g0043others(104): Show | 155 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.1585-572G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75675150 | ||||||
chr5:75675190
|
A | T | 1 | a0001c0001t0001g0132 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1585-612T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75675190 | ||||||
chr5:75675193
|
T | C | 120 | a0001c0001t0001g0113a0001c0001t0001g0163a0001c0001t0001g0168others(117): Show | 168 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.1585-615A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75675193 | ||||||
chr5:75675200
|
C | T | 106 | a0001c0001t0002g0037a0001c0001t0002g0042a0001c0001t0002g0043others(103): Show | 154 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.1585-622G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75675200 | ||||||
chr5:75675203
|
A | T | 1 | a0003c0003t0002g0051 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1585-625T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75675203 | ||||||
chr5:75675263
|
C | CAT | 107 | a0001c0001t0002g0037a0001c0001t0002g0042a0001c0001t0002g0043others(104): Show | 155 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.1585-687_1585-686d others(4): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75675263 | ||||||
chr5:75675342
|
T | C | 11 | a0001c0004t0002g0003a0001c0004t0002g0019a0001c0004t0002g0076others(8): Show | 19 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.1585-764A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75675342 | ||||||
chr5:75675443
|
T | G | 1 | a0004c0005t0003g0281 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1585-865A>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75675443 | ||||||
chr5:75675549
|
A | G | 107 | a0001c0001t0002g0037a0001c0001t0002g0042a0001c0001t0002g0043others(104): Show | 155 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.1585-971T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75675549 | ||||||
chr5:75675694
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1585-1116G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75675694 | ||||||
chr5:75675884
|
G | A | 1 | a0001c0001t0002g0037 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1585-1306C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75675884 | ||||||
chr5:75676021
|
A | G | 115 | a0001c0001t0001g0005a0001c0001t0001g0077a0001c0001t0001g0124others(112): Show | 135 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.1585-1443T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676021 | ||||||
chr5:75676165
|
C | G | 117 | a0001c0001t0001g0163a0001c0001t0001g0173a0001c0001t0001g0178others(114): Show | 165 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.1585-1587G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676165 | ||||||
chr5:75676469
|
AGGTCCCA others(6): Show |
A | 1 | a0001c0001t0001g0077 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1584+1292_1584+130 others(17): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676469 | ||||||
chr5:75676503
|
A | G | 1 | a0001c0001t0001g0214 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1584+1271T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676503 | ||||||
chr5:75676547
|
C | CG | 111 | a0001c0001t0001g0005a0001c0001t0001g0077a0001c0001t0001g0124others(108): Show | 130 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.1584+1226dupC | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676547 | ||||||
chr5:75676548
|
G | A | 11 | a0001c0004t0002g0003a0001c0004t0002g0019a0001c0004t0002g0076others(8): Show | 19 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.1584+1226C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676548 | ||||||
chr5:75676548
|
G | C | 104 | a0001c0001t0001g0163a0001c0001t0001g0173a0001c0001t0001g0178others(101): Show | 144 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(141): Show |
intron_variant | MODIFIER | c.1584+1226C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676548 | ||||||
chr5:75676682
|
G | T | 117 | a0001c0001t0001g0163a0001c0001t0001g0173a0001c0001t0001g0178others(114): Show | 165 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.1584+1092C>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676682 | ||||||
chr5:75676748
|
G | A | 15 | a0003c0003t0002g0058a0003c0003t0004g0004a0003c0003t0004g0008others(12): Show | 21 | HG02602.hp1 HG03704.hp2 HG03927.hp2 others(18): Show |
intron_variant | MODIFIER | c.1584+1026C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676748 | ||||||
chr5:75676759
|
T | C | 8 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0134others(5): Show | 8 | HG01243.hp2 HG02040.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1584+1015A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676759 | ||||||
chr5:75676767
|
C | T | 51 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0133others(48): Show | 79 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.1584+1007G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676767 | ||||||
chr5:75676821
|
T | C | 118 | a0001c0001t0001g0163a0001c0001t0001g0173a0001c0001t0001g0178others(115): Show | 166 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.1584+953A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676821 | ||||||
chr5:75676826
|
CA | C | 6 | a0001c0004t0002g0083a0001c0004t0002g0084a0002c0002t0005g0017others(3): Show | 9 | HG02572.hp2 NA18942.hp2 NA18944.hp1 others(6): Show |
intron_variant | MODIFIER | c.1584+947delT | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676826 | ||||||
chr5:75676831
|
A | G | 104 | a0001c0001t0001g0163a0001c0001t0001g0173a0001c0001t0001g0178others(101): Show | 144 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(141): Show |
intron_variant | MODIFIER | c.1584+943T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676831 | ||||||
chr5:75676836
|
AAT | A | 104 | a0001c0001t0001g0163a0001c0001t0001g0173a0001c0001t0001g0178others(101): Show | 144 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(141): Show |
intron_variant | MODIFIER | c.1584+936_1584+937d others(4): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676836 | ||||||
chr5:75676845
|
AAAAT | A | 14 | a0001c0001t0001g0020a0001c0004t0001g0075a0001c0004t0001g0078others(11): Show | 23 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.1584+925_1584+928d others(6): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676845 | ||||||
chr5:75676846
|
A | T | 104 | a0001c0001t0001g0163a0001c0001t0001g0173a0001c0001t0001g0178others(101): Show | 144 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(141): Show |
intron_variant | MODIFIER | c.1584+928T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676846 | ||||||
chr5:75676849
|
T | A | 104 | a0001c0001t0001g0163a0001c0001t0001g0173a0001c0001t0001g0178others(101): Show | 144 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(141): Show |
intron_variant | MODIFIER | c.1584+925A>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676849 | ||||||
chr5:75676874
|
C | A | 1 | a0003c0003t0001g0066 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1584+900G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676874 | ||||||
chr5:75676924
|
A | G | 104 | a0001c0001t0001g0163a0001c0001t0001g0173a0001c0001t0001g0178others(101): Show | 144 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(141): Show |
intron_variant | MODIFIER | c.1584+850T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676924 | ||||||
chr5:75676941
|
C | A | 11 | a0001c0004t0002g0003a0001c0004t0002g0019a0001c0004t0002g0076others(8): Show | 19 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.1584+833G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676941 | ||||||
chr5:75677052
|
G | A | 104 | a0001c0001t0001g0163a0001c0001t0001g0173a0001c0001t0001g0178others(101): Show | 144 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(141): Show |
intron_variant | MODIFIER | c.1584+722C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75677052 | ||||||
chr5:75677217
|
T | G | 104 | a0001c0001t0001g0163a0001c0001t0001g0173a0001c0001t0001g0178others(101): Show | 144 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(141): Show |
intron_variant | MODIFIER | c.1584+557A>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75677217 | ||||||
chr5:75677482
|
C | T | 1 | a0004c0005t0003g0281 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1584+292G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75677482 | ||||||
chr5:75677574
|
C | T | 1 | a0003c0003t0002g0264 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1584+200G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75677574 | ||||||
chr5:75677580
|
C | A | 104 | a0001c0001t0001g0163a0001c0001t0001g0173a0001c0001t0001g0178others(101): Show | 144 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(141): Show |
intron_variant | MODIFIER | c.1584+194G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75677580 | ||||||
chr5:75677621
|
T | TA | 15 | a0001c0001t0001g0130a0001c0001t0001g0176a0001c0001t0001g0181others(12): Show | 23 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.1584+152dupT | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75677621 | ||||||
chr5:75677621
|
TA | T | 161 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(158): Show | 218 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.1584+152delT | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75677621 | ||||||
chr5:75677623
|
A | T | 26 | a0001c0001t0001g0163a0001c0001t0001g0173a0001c0001t0001g0178others(23): Show | 31 | HG00735.hp1 HG01109.hp1 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.1584+151T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75677623 | ||||||
chr5:75678054
|
C | T | 104 | a0001c0001t0001g0163a0001c0001t0001g0173a0001c0001t0001g0178others(101): Show | 144 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(141): Show |
intron_variant | MODIFIER | c.1408-104G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75678054 | ||||||
chr5:75678056
|
G | T | 6 | a0001c0001t0002g0133a0001c0001t0002g0166a0001c0001t0002g0215others(3): Show | 6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1408-106C>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75678056 | ||||||
chr5:75678124
|
C | T | 78 | a0001c0001t0002g0037a0001c0001t0002g0042a0001c0001t0002g0043others(75): Show | 113 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.1408-174G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75678124 | ||||||
chr5:75678157
|
C | T | 1 | a0002c0002t0001g0144 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1408-207G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75678157 | ||||||
chr5:75678265
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1408-315G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75678265 | ||||||
chr5:75678318
|
C | T | 4 | a0002c0002t0001g0029a0002c0002t0001g0151a0002c0002t0001g0196others(1): Show | 5 | HG01952.hp2 HG01975.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.1408-368G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75678318 | ||||||
chr5:75678328
|
C | T | 4 | a0004c0005t0003g0035a0004c0005t0003g0281a0004c0005t0003g0282others(1): Show | 5 | HG01243.hp1 HG03130.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1408-378G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75678328 | ||||||
chr5:75678506
|
T | C | 105 | a0001c0001t0001g0163a0001c0001t0001g0173a0001c0001t0001g0178others(102): Show | 145 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(142): Show |
intron_variant | MODIFIER | c.1408-556A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75678506 | ||||||
chr5:75678609
|
C | CT | 110 | a0001c0001t0001g0005a0001c0001t0001g0077a0001c0001t0001g0124others(107): Show | 129 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.1408-660dupA | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75678609 | ||||||
chr5:75678612
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1408-662A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75678612 | ||||||
chr5:75678629
|
C | G | 1 | a0003c0003t0002g0277 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1408-679G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75678629 | ||||||
chr5:75678683
|
G | A | 105 | a0001c0001t0001g0163a0001c0001t0001g0173a0001c0001t0001g0178others(102): Show | 145 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(142): Show |
intron_variant | MODIFIER | c.1408-733C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75678683 | ||||||
chr5:75678715
|
T | C | 105 | a0001c0001t0001g0163a0001c0001t0001g0173a0001c0001t0001g0178others(102): Show | 145 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(142): Show |
intron_variant | MODIFIER | c.1408-765A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75678715 | ||||||
chr5:75678812
|
T | C | 5 | a0004c0005t0003g0290a0004c0005t0003g0292a0004c0005t0003g0293others(2): Show | 5 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.1408-862A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75678812 | ||||||
chr5:75678822
|
T | G | 1 | a0001c0001t0001g0116 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1408-872A>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75678822 | ||||||
chr5:75678829
|
C | T | 2 | a0003c0003t0002g0269a0003c0003t0002g0273 | 2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1408-879G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75678829 | ||||||
chr5:75678853
|
A | G | 6 | a0001c0001t0002g0133a0001c0001t0002g0166a0001c0001t0002g0215others(3): Show | 6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1408-903T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75678853 | ||||||
chr5:75678913
|
C | T | 1 | a0003c0003t0002g0079 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1408-963G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75678913 | ||||||
chr5:75679057
|
C | T | 2 | a0001c0001t0001g0093a0002c0002t0001g0203 | 2 | HG04115.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1408-1107G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75679057 | ||||||
chr5:75679205
|
T | C | 13 | a0001c0004t0001g0075a0001c0004t0001g0078a0001c0004t0002g0003others(10): Show | 21 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.1408-1255A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75679205 | ||||||
chr5:75679443
|
C | T | 228 | a0001c0001t0001g0005a0001c0001t0001g0077a0001c0001t0001g0124others(225): Show | 295 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.1408-1493G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75679443 | ||||||
chr5:75679519
|
A | T | 104 | a0001c0001t0001g0163a0001c0001t0001g0173a0001c0001t0001g0178others(101): Show | 144 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(141): Show |
intron_variant | MODIFIER | c.1408-1569T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75679519 | ||||||
chr5:75679604
|
G | A | 77 | a0001c0001t0002g0037a0001c0001t0002g0042a0001c0001t0002g0043others(74): Show | 112 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.1408-1654C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75679604 | ||||||
chr5:75679662
|
T | C | 1 | a0004c0005t0003g0281 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1408-1712A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75679662 | ||||||
chr5:75679837
|
G | C | 4 | a0002c0002t0001g0029a0002c0002t0001g0151a0002c0002t0001g0196others(1): Show | 5 | HG01952.hp2 HG01975.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.1408-1887C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75679837 | ||||||
chr5:75680087
|
A | G | 216 | a0001c0001t0001g0005a0001c0001t0001g0077a0001c0001t0001g0124others(213): Show | 276 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.1408-2137T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75680087 | ||||||
chr5:75680186
|
G | T | 2 | a0001c0004t0001g0075a0001c0004t0001g0078 | 2 | HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1408-2236C>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75680186 | ||||||
chr5:75680252
|
A | G | 1 | a0001c0001t0002g0043 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1408-2302T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75680252 | ||||||
chr5:75680280
|
G | A | 25 | a0001c0001t0001g0094a0001c0001t0001g0117a0001c0001t0002g0037others(22): Show | 30 | HG00733.hp2 HG01516.hp2 HG02559.hp2 others(27): Show |
intron_variant | MODIFIER | c.1408-2330C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75680280 | ||||||
chr5:75680404
|
G | A | 31 | a0003c0003t0002g0001a0003c0003t0002g0013a0003c0003t0002g0014others(28): Show | 59 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.1408-2454C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75680404 | ||||||
chr5:75680468
|
C | G | 1 | a0004c0005t0003g0286 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1408-2518G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75680468 | ||||||
chr5:75680782
|
T | C | 1 | a0002c0002t0001g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1408-2832A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75680782 | ||||||
chr5:75680989
|
A | G | 2 | a0001c0004t0001g0075a0001c0004t0001g0078 | 2 | HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1408-3039T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75680989 | ||||||
chr5:75681060
|
C | A | 1 | a0001c0001t0001g0162 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1408-3110G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75681060 | ||||||
chr5:75681080
|
GGAGT | G | 6 | a0001c0001t0002g0133a0001c0001t0002g0166a0001c0001t0002g0215others(3): Show | 6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1408-3134_1408-313 others(8): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75681080 | ||||||
chr5:75681236
|
T | G | 14 | a0001c0004t0001g0075a0001c0004t0001g0078a0001c0004t0002g0003others(11): Show | 22 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.1408-3286A>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75681236 | ||||||
chr5:75681282
|
C | T | 1 | a0003c0003t0002g0057 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1408-3332G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75681282 | ||||||
chr5:75681292
|
A | G | 9 | a0001c0001t0002g0037a0001c0001t0002g0042a0001c0001t0002g0043others(6): Show | 9 | HG01243.hp2 HG02040.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1408-3342T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75681292 | ||||||
chr5:75681324
|
A | G | 229 | a0001c0001t0001g0005a0001c0001t0001g0077a0001c0001t0001g0124others(226): Show | 291 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.1408-3374T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75681324 | ||||||
chr5:75681358
|
A | G | 1 | a0003c0003t0002g0260 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1408-3408T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75681358 | ||||||
chr5:75681374
|
T | C | 1 | a0001c0004t0002g0019 | 2 | HG00280.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1408-3424A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75681374 | ||||||
chr5:75681625
|
A | AT | 12 | a0004c0005t0003g0007a0004c0005t0003g0035a0004c0005t0003g0036others(9): Show | 17 | HG00735.hp1 HG01243.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.1407+3581dupA | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75681625 | ||||||
chr5:75681632
|
A | T | 229 | a0001c0001t0001g0005a0001c0001t0001g0077a0001c0001t0001g0124others(226): Show | 291 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.1407+3575T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75681632 | ||||||
chr5:75681633
|
A | T | 229 | a0001c0001t0001g0005a0001c0001t0001g0077a0001c0001t0001g0124others(226): Show | 291 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.1407+3574T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75681633 | ||||||
chr5:75681774
|
T | A | 6 | a0001c0001t0002g0133a0001c0001t0002g0166a0001c0001t0002g0215others(3): Show | 6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1407+3433A>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75681774 | ||||||
chr5:75681836
|
T | C | 212 | a0001c0001t0001g0005a0001c0001t0001g0077a0001c0001t0001g0124others(209): Show | 269 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.1407+3371A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75681836 | ||||||
chr5:75681842
|
ATC | A | 8 | a0003c0003t0002g0013a0003c0003t0002g0016a0003c0003t0002g0255others(5): Show | 12 | HG02027.hp2 HG02056.hp1 NA18747.hp2 others(9): Show |
intron_variant | MODIFIER | c.1407+3363_1407+336 others(6): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75681842 | ||||||
chr5:75682020
|
T | C | 229 | a0001c0001t0001g0005a0001c0001t0001g0077a0001c0001t0001g0124others(226): Show | 291 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.1407+3187A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75682020 | ||||||
chr5:75682029
|
T | C | 212 | a0001c0001t0001g0005a0001c0001t0001g0077a0001c0001t0001g0124others(209): Show | 269 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.1407+3178A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75682029 | ||||||
chr5:75682084
|
G | T | 1 | a0001c0001t0001g0244 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1407+3123C>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75682084 | ||||||
chr5:75682125
|
A | G | 242 | a0001c0001t0001g0005a0001c0001t0001g0077a0001c0001t0001g0124others(239): Show | 312 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.1407+3082T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75682125 | ||||||
chr5:75682210
|
TCAAAA | T | 229 | a0001c0001t0001g0005a0001c0001t0001g0077a0001c0001t0001g0124others(226): Show | 291 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.1407+2992_1407+299 others(9): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75682210 | ||||||
chr5:75682509
|
A | C | 9 | a0001c0001t0002g0037a0001c0001t0002g0042a0001c0001t0002g0043others(6): Show | 9 | HG01243.hp2 HG02040.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1407+2698T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75682509 | ||||||
chr5:75682513
|
C | A | 3 | a0002c0002t0001g0172a0002c0002t0001g0207a0003c0003t0002g0252 | 3 | HG00438.hp1 NA18940.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.1407+2694G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75682513 | ||||||
chr5:75682517
|
C | CTT | 199 | a0001c0001t0001g0005a0001c0001t0001g0124a0001c0001t0001g0129others(196): Show | 257 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.1407+2688_1407+268 others(6): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75682517 | ||||||
chr5:75682517
|
C | CTTT | 23 | a0001c0001t0001g0077a0001c0001t0002g0037a0001c0001t0002g0042others(20): Show | 27 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.1407+2687_1407+268 others(7): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75682517 | ||||||
chr5:75682688
|
T | C | 3 | a0002c0002t0001g0192a0002c0002t0001g0231a0002c0002t0001g0237 | 3 | HG00639.hp2 HG01106.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1407+2519A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75682688 | ||||||
chr5:75682724
|
C | G | 3 | a0001c0001t0001g0162a0001c0001t0001g0208a0001c0001t0001g0244 | 3 | HG02615.hp2 HG02818.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1407+2483G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75682724 | ||||||
chr5:75682759
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1407+2448G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75682759 | ||||||
chr5:75682790
|
C | T | 2 | a0001c0001t0001g0208a0001c0001t0001g0244 | 2 | HG02615.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1407+2417G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75682790 | ||||||
chr5:75682897
|
A | G | 3 | a0003c0003t0002g0260a0003c0003t0002g0261a0003c0003t0002g0266 | 3 | HG02451.hp2 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1407+2310T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75682897 | ||||||
chr5:75683032
|
G | A | 229 | a0001c0001t0001g0005a0001c0001t0001g0077a0001c0001t0001g0124others(226): Show | 291 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.1407+2175C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75683032 | ||||||
chr5:75683054
|
G | C | 1 | a0009c0013t0002g0086 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1407+2153C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75683054 | ||||||
chr5:75683137
|
A | G | 2 | a0001c0004t0001g0075a0001c0004t0001g0078 | 2 | HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1407+2070T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75683137 | ||||||
chr5:75683239
|
GT | G | 13 | a0001c0004t0001g0075a0001c0004t0001g0078a0001c0004t0002g0003others(10): Show | 21 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.1407+1967delA | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75683239 | ||||||
chr5:75683239
|
GTT | G | 15 | a0003c0003t0002g0270a0004c0005t0003g0007a0004c0005t0003g0036others(12): Show | 19 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.1407+1966_1407+196 others(6): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75683239 | ||||||
chr5:75683239
|
GTTT | G | 214 | a0001c0001t0001g0005a0001c0001t0001g0077a0001c0001t0001g0124others(211): Show | 272 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.1407+1965_1407+196 others(7): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75683239 | ||||||
chr5:75683335
|
A | G | 9 | a0004c0005t0003g0007a0004c0005t0003g0036a0004c0005t0003g0283others(6): Show | 13 | HG00735.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1407+1872T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75683335 | ||||||
chr5:75683394
|
C | T | 6 | a0001c0001t0002g0133a0001c0001t0002g0166a0001c0001t0002g0215others(3): Show | 6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1407+1813G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75683394 | ||||||
chr5:75683445
|
G | A | 13 | a0001c0004t0001g0075a0001c0004t0001g0078a0001c0004t0002g0003others(10): Show | 21 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.1407+1762C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75683445 | ||||||
chr5:75683527
|
A | C | 13 | a0001c0004t0001g0075a0001c0004t0001g0078a0001c0004t0002g0003others(10): Show | 21 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.1407+1680T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75683527 | ||||||
chr5:75683678
|
G | A | 2 | a0002c0002t0001g0174a0002c0002t0001g0175 | 2 | HG00323.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.1407+1529C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75683678 | ||||||
chr5:75683703
|
T | TA | 10 | a0002c0002t0001g0172a0004c0005t0003g0007a0004c0005t0003g0036others(7): Show | 14 | HG00735.hp1 HG01891.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1407+1503dupT | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75683703 | ||||||
chr5:75683703
|
TA | T | 18 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0115others(15): Show | 26 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(23): Show |
intron_variant | MODIFIER | c.1407+1503delT | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75683703 | ||||||
chr5:75683727
|
C | T | 1 | a0001c0004t0002g0082 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1407+1480G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75683727 | ||||||
chr5:75683806
|
C | T | 65 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(62): Show | 89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.1407+1401G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75683806 | ||||||
chr5:75683823
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1407+1384G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75683823 | ||||||
chr5:75683867
|
C | A | 1 | a0003c0003t0002g0257 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1407+1340G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75683867 | ||||||
chr5:75683912
|
C | T | 1 | a0001c0001t0002g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1407+1295G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75683912 | ||||||
chr5:75684041
|
G | C | 51 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(48): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.1407+1166C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684041 | ||||||
chr5:75684097
|
C | G | 5 | a0004c0005t0003g0290a0004c0005t0003g0292a0004c0005t0003g0293others(2): Show | 5 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.1407+1110G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684097 | ||||||
chr5:75684194
|
A | G | 51 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(48): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.1407+1013T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684194 | ||||||
chr5:75684299
|
T | C | 1 | a0004c0005t0003g0281 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1407+908A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684299 | ||||||
chr5:75684313
|
C | T | 1 | a0003c0003t0002g0274 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1407+894G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684313 | ||||||
chr5:75684315
|
T | TAA | 87 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(84): Show | 116 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.1407+891_1407+892i others(4): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684315 | ||||||
chr5:75684363
|
A | AT | 17 | a0001c0001t0002g0166a0001c0001t0002g0215a0001c0001t0002g0216others(14): Show | 17 | HG00438.hp1 HG02027.hp1 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.1407+843dupA | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684363 | ||||||
chr5:75684363
|
A | ATTTTTTT others(12): Show |
2 | a0001c0004t0001g0075a0001c0004t0001g0078 | 2 | HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1407+825_1407+843d others(21): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684363 | ||||||
chr5:75684363
|
AT | A | 50 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(47): Show | 66 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.1407+843delA | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684363 | ||||||
chr5:75684363
|
ATT | A | 11 | a0001c0004t0002g0003a0001c0004t0002g0019a0001c0004t0002g0076others(8): Show | 19 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.1407+842_1407+843d others(4): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684363 | ||||||
chr5:75684385
|
G | A | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.1407+822C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684385 | ||||||
chr5:75684427
|
A | G | 13 | a0001c0004t0001g0075a0001c0004t0001g0078a0001c0004t0002g0003others(10): Show | 21 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.1407+780T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684427 | ||||||
chr5:75684449
|
T | TC | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.1407+757dupG | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684449 | ||||||
chr5:75684489
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1407+718G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684489 | ||||||
chr5:75684497
|
T | C | 1 | a0002c0002t0001g0193 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1407+710A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684497 | ||||||
chr5:75684521
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1407+686G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684521 | ||||||
chr5:75684614
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1407+593G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684614 | ||||||
chr5:75684615
|
G | A | 34 | a0003c0003t0001g0272a0003c0003t0001g0275a0003c0003t0001g0276others(31): Show | 62 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1407+592C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684615 | ||||||
chr5:75684651
|
C | A | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.1407+556G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684651 | ||||||
chr5:75684665
|
T | C | 2 | a0002c0002t0001g0179a0002c0002t0001g0228 | 2 | NA19067.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1407+542A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684665 | ||||||
chr5:75684747
|
A | G | 51 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(48): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.1407+460T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684747 | ||||||
chr5:75684809
|
AT | A | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.1407+397delA | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684809 | ||||||
chr5:75684870
|
CT | C | 13 | a0001c0004t0001g0075a0001c0004t0001g0078a0001c0004t0002g0003others(10): Show | 21 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.1407+336delA | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684870 | ||||||
chr5:75684870
|
CTT | C | 50 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(47): Show | 66 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.1407+335_1407+336d others(4): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684870 | ||||||
chr5:75684899
|
G | A | 51 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(48): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.1407+308C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684899 | ||||||
chr5:75685005
|
C | T | 51 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(48): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.1407+202G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75685005 | ||||||
chr5:75685050
|
G | A | 1 | a0003c0003t0002g0058 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1407+157C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75685050 | ||||||
chr5:75685067
|
C | T | 34 | a0003c0003t0001g0272a0003c0003t0001g0275a0003c0003t0001g0276others(31): Show | 62 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1407+140G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75685067 | ||||||
chr5:75685118
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1407+89G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75685118 | ||||||
chr5:75685497
|
A | T | 51 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(48): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.1130-13T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75685497 | ||||||
chr5:75685519
|
C | T | 3 | a0004c0005t0003g0035a0004c0005t0003g0281a0004c0005t0003g0282 | 4 | HG01243.hp1 HG03130.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1130-35G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75685519 | ||||||
chr5:75685720
|
T | C | 1 | a0004c0005t0003g0281 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1130-236A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75685720 | ||||||
chr5:75685978
|
C | T | 6 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0213others(3): Show | 6 | HG02055.hp1 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1130-494G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75685978 | ||||||
chr5:75686176
|
G | A | 1 | a0001c0004t0002g0084 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1130-692C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75686176 | ||||||
chr5:75686382
|
T | C | 162 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(159): Show | 226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1130-898A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75686382 | ||||||
chr5:75686657
|
T | C | 9 | a0002c0002t0001g0011a0002c0002t0001g0125a0002c0002t0001g0155others(6): Show | 11 | HG00558.hp2 HG00609.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.1130-1173A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75686657 | ||||||
chr5:75686842
|
G | A | 4 | a0002c0002t0001g0146a0002c0002t0001g0156a0002c0002t0001g0201others(1): Show | 4 | HG00323.hp1 HG01192.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.1130-1358C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75686842 | ||||||
chr5:75686865
|
C | A | 5 | a0005c0006t0002g0038a0005c0006t0002g0039a0005c0006t0002g0040others(2): Show | 5 | HG02040.hp2 NA18974.hp1 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.1130-1381G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75686865 | ||||||
chr5:75686961
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1130-1477G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75686961 | ||||||
chr5:75687033
|
AAC | A | 17 | a0004c0005t0003g0007a0004c0005t0003g0035a0004c0005t0003g0036others(14): Show | 22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.1130-1551_1130-155 others(6): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75687033 | ||||||
chr5:75687037
|
A | AT | 14 | a0001c0001t0001g0112a0001c0004t0001g0075a0001c0004t0001g0078others(11): Show | 22 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.1130-1554dupA | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75687037 | ||||||
chr5:75687037
|
A | T | 17 | a0004c0005t0003g0007a0004c0005t0003g0035a0004c0005t0003g0036others(14): Show | 22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.1130-1553T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75687037 | ||||||
chr5:75687055
|
T | TAG | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.1130-1573_1130-157 others(6): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75687055 | ||||||
chr5:75687112
|
C | T | 17 | a0004c0005t0003g0007a0004c0005t0003g0035a0004c0005t0003g0036others(14): Show | 22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.1130-1628G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75687112 | ||||||
chr5:75687155
|
T | C | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.1130-1671A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75687155 | ||||||
chr5:75687192
|
G | A | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.1130-1708C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75687192 | ||||||
chr5:75687241
|
A | G | 51 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(48): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.1130-1757T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75687241 | ||||||
chr5:75687256
|
T | G | 35 | a0003c0003t0001g0272a0003c0003t0001g0275a0003c0003t0001g0276others(32): Show | 63 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1129+1756A>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75687256 | ||||||
chr5:75687303
|
T | C | 1 | a0002c0002t0001g0249 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1129+1709A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75687303 | ||||||
chr5:75687321
|
C | T | 3 | a0002c0002t0001g0170a0002c0002t0001g0185a0002c0002t0001g0227 | 3 | HG02015.hp2 NA18964.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1129+1691G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75687321 | ||||||
chr5:75687391
|
T | TA | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.1129+1620dupT | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75687391 | ||||||
chr5:75687736
|
G | A | 2 | a0002c0002t0001g0199a0002c0002t0001g0235 | 2 | HG01256.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.1129+1276C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75687736 | ||||||
chr5:75687737
|
G | A | 1 | a0003c0003t0002g0265 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1129+1275C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75687737 | ||||||
chr5:75687927
|
A | G | 1 | a0002c0002t0001g0203 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1129+1085T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75687927 | ||||||
chr5:75688204
|
T | C | 11 | a0001c0004t0002g0003a0001c0004t0002g0019a0001c0004t0002g0076others(8): Show | 19 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.1129+808A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75688204 | ||||||
chr5:75688255
|
G | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0118 | 2 | NA18964.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1129+757C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75688255 | ||||||
chr5:75688263
|
G | A | 17 | a0004c0005t0003g0007a0004c0005t0003g0035a0004c0005t0003g0036others(14): Show | 22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.1129+749C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75688263 | ||||||
chr5:75688444
|
C | T | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.1129+568G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75688444 | ||||||
chr5:75688503
|
T | A | 1 | a0003c0003t0002g0047 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1129+509A>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75688503 | ||||||
chr5:75688583
|
A | T | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.1129+429T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75688583 | ||||||
chr5:75688737
|
A | G | 5 | a0004c0005t0003g0290a0004c0005t0003g0292a0004c0005t0003g0293others(2): Show | 5 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.1129+275T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75688737 | ||||||
chr5:75688794
|
G | A | 13 | a0001c0004t0001g0075a0001c0004t0001g0078a0001c0004t0002g0003others(10): Show | 21 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.1129+218C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75688794 | ||||||
chr5:75688878
|
T | C | 1 | a0002c0002t0001g0200 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1129+134A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75688878 | ||||||
chr5:75688993
|
A | T | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.1129+19T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75688993 | ||||||
chr5:75689390
|
G | C | 1 | a0001c0001t0002g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.976-225C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 8/11 | chr5 | 75689390 | ||||||
chr5:75689479
|
G | A | 1 | a0002c0002t0001g0170 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.976-314C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 8/11 | chr5 | 75689479 | ||||||
chr5:75689526
|
A | AAAAAT | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.976-366_976-362dup others(5): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 8/11 | chr5 | 75689526 | ||||||
chr5:75689537
|
A | G | 1 | a0002c0002t0001g0194 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.976-372T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 8/11 | chr5 | 75689537 | ||||||
chr5:75689591
|
G | A | 8 | a0001c0001t0002g0037a0001c0001t0002g0042a0001c0001t0002g0043others(5): Show | 8 | HG01243.hp2 HG02040.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.976-426C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 8/11 | chr5 | 75689591 | ||||||
chr5:75689635
|
T | C | 6 | a0001c0001t0002g0133a0001c0001t0002g0166a0001c0001t0002g0215others(3): Show | 6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.976-470A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 8/11 | chr5 | 75689635 | ||||||
chr5:75689689
|
A | G | 3 | a0004c0005t0003g0035a0004c0005t0003g0281a0004c0005t0003g0282 | 4 | HG01243.hp1 HG03130.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.976-524T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 8/11 | chr5 | 75689689 | ||||||
chr5:75689918
|
C | T | 9 | a0004c0005t0003g0007a0004c0005t0003g0036a0004c0005t0003g0283others(6): Show | 13 | HG00735.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.975+465G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 8/11 | chr5 | 75689918 | ||||||
chr5:75689959
|
C | T | 11 | a0001c0004t0002g0003a0001c0004t0002g0019a0001c0004t0002g0076others(8): Show | 19 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.975+424G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 8/11 | chr5 | 75689959 | ||||||
chr5:75690042
|
T | C | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.975+341A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 8/11 | chr5 | 75690042 | ||||||
chr5:75690169
|
G | A | 1 | a0003c0003t0002g0266 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.975+214C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 8/11 | chr5 | 75690169 | ||||||
chr5:75690220
|
A | G | 51 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(48): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.975+163T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 8/11 | chr5 | 75690220 | ||||||
chr5:75690656
|
T | C | 153 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(150): Show | 217 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.796-94A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 7/11 | chr5 | 75690656 | ||||||
chr5:75690751
|
G | A | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.796-189C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 7/11 | chr5 | 75690751 | ||||||
chr5:75690877
|
A | G | 11 | a0001c0004t0002g0003a0001c0004t0002g0019a0001c0004t0002g0076others(8): Show | 19 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.796-315T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 7/11 | chr5 | 75690877 | ||||||
chr5:75691152
|
G | A | 17 | a0004c0005t0003g0007a0004c0005t0003g0035a0004c0005t0003g0036others(14): Show | 22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.796-590C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 7/11 | chr5 | 75691152 | ||||||
chr5:75691176
|
G | A | 1 | a0001c0001t0002g0216 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.796-614C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 7/11 | chr5 | 75691176 | ||||||
chr5:75691198
|
G | A | 1 | a0003c0003t0001g0066 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.796-636C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 7/11 | chr5 | 75691198 | ||||||
chr5:75691283
|
C | T | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.796-721G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 7/11 | chr5 | 75691283 | ||||||
chr5:75691624
|
A | T | 1 | a0001c0001t0001g0115 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.795+772T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 7/11 | chr5 | 75691624 | ||||||
chr5:75691708
|
C | CAT | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.795+686_795+687dup others(2): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 7/11 | chr5 | 75691708 | ||||||
chr5:75691955
|
C | G | 1 | a0001c0001t0001g0161 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.795+441G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 7/11 | chr5 | 75691955 | ||||||
chr5:75692151
|
T | A | 17 | a0004c0005t0003g0007a0004c0005t0003g0035a0004c0005t0003g0036others(14): Show | 22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.795+245A>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 7/11 | chr5 | 75692151 | ||||||
chr5:75692166
|
T | A | 13 | a0001c0004t0001g0075a0001c0004t0001g0078a0001c0004t0002g0003others(10): Show | 21 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.795+230A>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 7/11 | chr5 | 75692166 | ||||||
chr5:75692205
|
T | C | 1 | a0002c0002t0001g0125 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.795+191A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 7/11 | chr5 | 75692205 | ||||||
chr5:75692241
|
C | A | 1 | a0005c0006t0002g0041 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.795+155G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 7/11 | chr5 | 75692241 | ||||||
chr5:75692325
|
A | G | 1 | a0002c0002t0001g0201 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.795+71T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 7/11 | chr5 | 75692325 | ||||||
chr5:75692365
|
T | C | 1 | a0002c0002t0001g0157 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.795+31A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 7/11 | chr5 | 75692365 | ||||||
chr5:75692373
|
C | A | 1 | a0001c0001t0001g0213 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.795+23G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 7/11 | chr5 | 75692373 | ||||||
chr5:75692511
|
C | T | 51 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(48): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.691-11G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75692511 | ||||||
chr5:75692544
|
A | G | 162 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(159): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.691-44T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75692544 | ||||||
chr5:75692570
|
A | C | 17 | a0004c0005t0003g0007a0004c0005t0003g0035a0004c0005t0003g0036others(14): Show | 22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.691-70T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75692570 | ||||||
chr5:75692753
|
G | T | 1 | a0005c0006t0002g0041 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.691-253C>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75692753 | ||||||
chr5:75692933
|
C | T | 2 | a0001c0001t0001g0099a0001c0001t0001g0112 | 2 | HG03654.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.691-433G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75692933 | ||||||
chr5:75693014
|
TTATATA | T | 17 | a0004c0005t0003g0007a0004c0005t0003g0035a0004c0005t0003g0036others(14): Show | 22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.691-520_691-515del others(6): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75693014 | ||||||
chr5:75693026
|
CTATATAT | C | 6 | a0001c0001t0002g0133a0001c0001t0002g0166a0001c0001t0002g0215others(3): Show | 6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.691-533_691-527del others(7): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75693026 | ||||||
chr5:75693081
|
TTAA | T | 6 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0213others(3): Show | 6 | HG02055.hp1 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.691-584_691-582del others(3): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75693081 | ||||||
chr5:75693097
|
C | CATGTT | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.691-598_691-597ins others(5): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75693097 | ||||||
chr5:75693103
|
T | C | 1 | a0002c0002t0001g0226 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.691-603A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75693103 | ||||||
chr5:75693161
|
CAT | C | 13 | a0001c0004t0001g0075a0001c0004t0001g0078a0001c0004t0002g0003others(10): Show | 21 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.691-663_691-662del others(2): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75693161 | ||||||
chr5:75693184
|
CTAA | C | 51 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(48): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.691-687_691-685del others(3): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75693184 | ||||||
chr5:75693212
|
T | C | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.691-712A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75693212 | ||||||
chr5:75693320
|
T | G | 2 | a0002c0002t0001g0201a0002c0002t0001g0202 | 2 | HG00323.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.691-820A>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75693320 | ||||||
chr5:75693532
|
T | C | 8 | a0001c0001t0002g0037a0001c0001t0002g0042a0001c0001t0002g0043others(5): Show | 8 | HG01243.hp2 HG02040.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.691-1032A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75693532 | ||||||
chr5:75693584
|
A | C | 1 | a0003c0003t0002g0067 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.690+1071T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75693584 | ||||||
chr5:75693625
|
C | CA | 65 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(62): Show | 89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.690+1029dupT | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75693625 | ||||||
chr5:75693658
|
C | T | 1 | a0004c0005t0003g0283 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.690+997G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75693658 | ||||||
chr5:75693659
|
G | A | 8 | a0001c0001t0001g0212a0001c0001t0002g0133a0001c0001t0002g0166others(5): Show | 8 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.690+996C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75693659 | ||||||
chr5:75693806
|
G | A | 4 | a0001c0001t0002g0133a0001c0001t0002g0166a0001c0001t0002g0217others(1): Show | 4 | HG02132.hp1 HG02135.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.690+849C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75693806 | ||||||
chr5:75693823
|
C | T | 1 | a0003c0003t0002g0258 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.690+832G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75693823 | ||||||
chr5:75693904
|
C | A | 2 | a0003c0003t0002g0067a0003c0003t0002g0068 | 2 | HG01123.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.690+751G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75693904 | ||||||
chr5:75693905
|
C | A | 7 | a0001c0001t0002g0133a0001c0001t0002g0166a0001c0001t0002g0215others(4): Show | 7 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.690+750G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75693905 | ||||||
chr5:75694071
|
G | C | 1 | a0002c0002t0001g0144 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.690+584C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75694071 | ||||||
chr5:75694072
|
A | C | 1 | a0002c0002t0001g0144 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.690+583T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75694072 | ||||||
chr5:75694073
|
G | T | 1 | a0002c0002t0001g0144 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.690+582C>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75694073 | ||||||
chr5:75694126
|
T | C | 17 | a0004c0005t0003g0007a0004c0005t0003g0035a0004c0005t0003g0036others(14): Show | 22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.690+529A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75694126 | ||||||
chr5:75694300
|
G | C | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.690+355C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75694300 | ||||||
chr5:75694313
|
T | C | 1 | a0002c0002t0001g0237 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.690+342A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75694313 | ||||||
chr5:75694352
|
A | T | 11 | a0001c0004t0002g0003a0001c0004t0002g0019a0001c0004t0002g0076others(8): Show | 19 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.690+303T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75694352 | ||||||
chr5:75694353
|
A | T | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.690+302T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75694353 | ||||||
chr5:75694389
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.690+266G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75694389 | ||||||
chr5:75694523
|
T | C | 51 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(48): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.690+132A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75694523 | ||||||
chr5:75694910
|
A | G | 1 | a0001c0001t0001g0103 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.514-79T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75694910 | ||||||
chr5:75694954
|
A | C | 35 | a0003c0003t0001g0272a0003c0003t0001g0275a0003c0003t0001g0276others(32): Show | 63 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.514-123T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75694954 | ||||||
chr5:75694989
|
C | A | 1 | a0005c0006t0002g0041 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.514-158G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75694989 | ||||||
chr5:75694996
|
C | A | 1 | a0002c0002t0001g0223 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.514-165G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75694996 | ||||||
chr5:75695067
|
G | A | 1 | a0002c0002t0001g0128 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.514-236C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75695067 | ||||||
chr5:75695221
|
G | A | 1 | a0002c0002t0001g0236 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.514-390C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75695221 | ||||||
chr5:75695297
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.514-466C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75695297 | ||||||
chr5:75695341
|
A | C | 3 | a0001c0001t0001g0109a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | HG00639.hp1 HG01109.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.514-510T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75695341 | ||||||
chr5:75695556
|
C | T | 1 | a0003c0003t0002g0047 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.514-725G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75695556 | ||||||
chr5:75695618
|
G | A | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.514-787C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75695618 | ||||||
chr5:75695676
|
C | A | 1 | a0005c0006t0002g0041 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.514-845G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75695676 | ||||||
chr5:75695719
|
C | T | 1 | a0003c0003t0002g0014 | 3 | HG00609.hp2 NA18950.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.514-888G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75695719 | ||||||
chr5:75695720
|
G | A | 9 | a0004c0005t0003g0007a0004c0005t0003g0036a0004c0005t0003g0283others(6): Show | 13 | HG00735.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.514-889C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75695720 | ||||||
chr5:75695761
|
T | C | 30 | a0001c0004t0001g0075a0001c0004t0001g0078a0001c0004t0002g0003others(27): Show | 43 | HG00280.hp1 HG00408.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.514-930A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75695761 | ||||||
chr5:75695770
|
C | T | 17 | a0004c0005t0003g0007a0004c0005t0003g0035a0004c0005t0003g0036others(14): Show | 22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.514-939G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75695770 | ||||||
chr5:75695853
|
A | G | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.514-1022T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75695853 | ||||||
chr5:75695854
|
T | C | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.514-1023A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75695854 | ||||||
chr5:75695859
|
C | T | 1 | a0005c0006t0002g0039 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.514-1028G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75695859 | ||||||
chr5:75695893
|
T | C | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.514-1062A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75695893 | ||||||
chr5:75695904
|
T | C | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.514-1073A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75695904 | ||||||
chr5:75695923
|
C | A | 1 | a0004c0005t0003g0285 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.514-1092G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75695923 | ||||||
chr5:75695969
|
C | T | 1 | a0003c0003t0004g0059 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.514-1138G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75695969 | ||||||
chr5:75695985
|
G | A | 1 | a0002c0002t0001g0203 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.514-1154C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75695985 | ||||||
chr5:75695993
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.514-1162G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75695993 | ||||||
chr5:75696021
|
G | A | 1 | a0003c0003t0002g0267 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.514-1190C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696021 | ||||||
chr5:75696024
|
A | C | 162 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(159): Show | 226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.514-1193T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696024 | ||||||
chr5:75696039
|
C | A | 5 | a0004c0005t0003g0290a0004c0005t0003g0292a0004c0005t0003g0293others(2): Show | 5 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.514-1208G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696039 | ||||||
chr5:75696078
|
A | G | 81 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(78): Show | 110 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.514-1247T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696078 | ||||||
chr5:75696118
|
C | T | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.514-1287G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696118 | ||||||
chr5:75696142
|
A | G | 2 | a0003c0003t0002g0269a0003c0003t0002g0273 | 2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.514-1311T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696142 | ||||||
chr5:75696183
|
C | A | 6 | a0001c0001t0002g0133a0001c0001t0002g0166a0001c0001t0002g0215others(3): Show | 6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.514-1352G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696183 | ||||||
chr5:75696183
|
C | T | 51 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(48): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.514-1352G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696183 | ||||||
chr5:75696191
|
C | G | 1 | a0003c0003t0002g0257 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.514-1360G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696191 | ||||||
chr5:75696225
|
C | T | 2 | a0001c0004t0002g0080a0001c0004t0002g0081 | 2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.514-1394G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696225 | ||||||
chr5:75696238
|
G | A | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.514-1407C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696238 | ||||||
chr5:75696265
|
C | A | 11 | a0001c0004t0002g0003a0001c0004t0002g0019a0001c0004t0002g0076others(8): Show | 19 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.514-1434G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696265 | ||||||
chr5:75696328
|
A | G | 17 | a0004c0005t0003g0007a0004c0005t0003g0035a0004c0005t0003g0036others(14): Show | 22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.514-1497T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696328 | ||||||
chr5:75696331
|
G | C | 1 | a0001c0001t0001g0077 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.514-1500C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696331 | ||||||
chr5:75696337
|
T | C | 11 | a0001c0004t0002g0003a0001c0004t0002g0019a0001c0004t0002g0076others(8): Show | 19 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.514-1506A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696337 | ||||||
chr5:75696371
|
C | T | 6 | a0001c0001t0002g0133a0001c0001t0002g0166a0001c0001t0002g0215others(3): Show | 6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.514-1540G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696371 | ||||||
chr5:75696378
|
C | A | 3 | a0002c0002t0001g0189a0002c0002t0001g0230a0002c0009t0001g0229 | 3 | NA18950.hp2 NA18984.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.514-1547G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696378 | ||||||
chr5:75696418
|
C | T | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.514-1587G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696418 | ||||||
chr5:75696420
|
T | A | 51 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(48): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.514-1589A>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696420 | ||||||
chr5:75696449
|
G | C | 2 | a0003c0003t0002g0056a0003c0003t0002g0057 | 2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.514-1618C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696449 | ||||||
chr5:75696452
|
T | G | 1 | a0001c0004t0002g0019 | 2 | HG00280.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.514-1621A>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696452 | ||||||
chr5:75696454
|
A | G | 1 | a0003c0003t0002g0256 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.514-1623T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696454 | ||||||
chr5:75696468
|
C | A | 53 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(50): Show | 69 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.514-1637G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696468 | ||||||
chr5:75696474
|
C | T | 51 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(48): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.514-1643G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696474 | ||||||
chr5:75696582
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.514-1751T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696582 | ||||||
chr5:75696591
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.514-1760T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696591 | ||||||
chr5:75696653
|
C | T | 2 | a0002c0002t0001g0125a0002c0002t0001g0226 | 2 | NA18999.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.514-1822G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696653 | ||||||
chr5:75696671
|
T | A | 2 | a0002c0002t0001g0204a0002c0002t0001g0205 | 2 | NA19059.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.514-1840A>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696671 | ||||||
chr5:75696673
|
G | A | 8 | a0001c0001t0002g0133a0001c0001t0002g0166a0001c0001t0002g0215others(5): Show | 8 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.514-1842C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696673 | ||||||
chr5:75696701
|
C | A | 5 | a0004c0005t0003g0290a0004c0005t0003g0292a0004c0005t0003g0293others(2): Show | 5 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.514-1870G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696701 | ||||||
chr5:75696743
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.514-1912C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696743 | ||||||
chr5:75696756
|
C | T | 5 | a0004c0005t0003g0290a0004c0005t0003g0292a0004c0005t0003g0293others(2): Show | 5 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.514-1925G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696756 | ||||||
chr5:75696802
|
T | C | 1 | a0002c0002t0001g0128 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.514-1971A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696802 | ||||||
chr5:75696863
|
A | G | 1 | a0001c0001t0001g0089 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.514-2032T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696863 | ||||||
chr5:75696957
|
A | C | 1 | a0002c0002t0001g0185 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.514-2126T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696957 | ||||||
chr5:75696957
|
A | G | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.514-2126T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696957 | ||||||
chr5:75697053
|
C | T | 6 | a0001c0001t0002g0133a0001c0001t0002g0166a0001c0001t0002g0215others(3): Show | 6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.514-2222G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697053 | ||||||
chr5:75697054
|
G | A | 1 | a0002c0002t0001g0230 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.514-2223C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697054 | ||||||
chr5:75697078
|
A | G | 1 | a0002c0002t0001g0029 | 2 | HG01981.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.514-2247T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697078 | ||||||
chr5:75697079
|
T | C | 1 | a0002c0002t0001g0237 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.514-2248A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697079 | ||||||
chr5:75697126
|
A | C | 1 | a0003c0003t0002g0255 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.514-2295T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697126 | ||||||
chr5:75697159
|
T | C | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.514-2328A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697159 | ||||||
chr5:75697261
|
C | T | 15 | a0001c0001t0002g0134a0002c0002t0001g0006a0002c0002t0001g0012others(12): Show | 21 | HG00423.hp2 HG01257.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.514-2430G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697261 | ||||||
chr5:75697262
|
G | A | 1 | a0004c0005t0003g0281 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.514-2431C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697262 | ||||||
chr5:75697291
|
A | G | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.514-2460T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697291 | ||||||
chr5:75697313
|
C | T | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.514-2482G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697313 | ||||||
chr5:75697334
|
C | A | 1 | a0002c0002t0001g0179 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.514-2503G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697334 | ||||||
chr5:75697359
|
C | T | 2 | a0002c0002t0001g0125a0002c0002t0001g0226 | 2 | NA18999.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.514-2528G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697359 | ||||||
chr5:75697360
|
A | C | 9 | a0004c0005t0003g0007a0004c0005t0003g0036a0004c0005t0003g0283others(6): Show | 13 | HG00735.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.514-2529T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697360 | ||||||
chr5:75697360
|
A | G | 2 | a0002c0002t0001g0125a0002c0002t0001g0226 | 2 | NA18999.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.514-2529T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697360 | ||||||
chr5:75697387
|
GT | G | 51 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(48): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.514-2557delA | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697387 | ||||||
chr5:75697454
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.514-2623G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697454 | ||||||
chr5:75697521
|
C | T | 2 | a0003c0003t0002g0056a0003c0003t0002g0057 | 2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.514-2690G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697521 | ||||||
chr5:75697563
|
C | T | 1 | a0001c0001t0002g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.514-2732G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697563 | ||||||
chr5:75697580
|
G | A | 2 | a0003c0003t0002g0031a0003c0003t0002g0032 | 4 | HG01069.hp1 HG01071.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.514-2749C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697580 | ||||||
chr5:75697661
|
A | C | 51 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(48): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.514-2830T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697661 | ||||||
chr5:75697663
|
T | C | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.514-2832A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697663 | ||||||
chr5:75697740
|
G | A | 3 | a0004c0005t0003g0035a0004c0005t0003g0281a0004c0005t0003g0282 | 4 | HG01243.hp1 HG03130.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.514-2909C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697740 | ||||||
chr5:75697787
|
G | C | 5 | a0004c0005t0003g0290a0004c0005t0003g0292a0004c0005t0003g0293others(2): Show | 5 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.514-2956C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697787 | ||||||
chr5:75697794
|
T | C | 65 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(62): Show | 89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.514-2963A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697794 | ||||||
chr5:75697884
|
C | A | 87 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(84): Show | 116 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.514-3053G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697884 | ||||||
chr5:75697903
|
G | A | 1 | a0003c0003t0004g0069 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.514-3072C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697903 | ||||||
chr5:75697910
|
T | C | 2 | a0004c0005t0003g0286a0004c0005t0003g0287 | 2 | HG02896.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.514-3079A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697910 | ||||||
chr5:75697975
|
C | A | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.514-3144G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697975 | ||||||
chr5:75697983
|
A | C | 87 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(84): Show | 116 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.514-3152T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697983 | ||||||
chr5:75698032
|
T | C | 13 | a0001c0004t0001g0075a0001c0004t0001g0078a0001c0004t0002g0003others(10): Show | 21 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.514-3201A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698032 | ||||||
chr5:75698108
|
T | C | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.514-3277A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698108 | ||||||
chr5:75698214
|
A | G | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.514-3383T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698214 | ||||||
chr5:75698226
|
T | C | 81 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(78): Show | 110 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.514-3395A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698226 | ||||||
chr5:75698270
|
T | C | 11 | a0001c0004t0002g0003a0001c0004t0002g0019a0001c0004t0002g0076others(8): Show | 19 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.514-3439A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698270 | ||||||
chr5:75698301
|
T | A | 2 | a0004c0005t0003g0292a0004c0005t0003g0294 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.514-3470A>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698301 | ||||||
chr5:75698429
|
A | C | 13 | a0001c0004t0001g0075a0001c0004t0001g0078a0001c0004t0002g0003others(10): Show | 21 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.514-3598T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698429 | ||||||
chr5:75698453
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.514-3622C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698453 | ||||||
chr5:75698468
|
C | T | 1 | a0002c0002t0001g0146 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.514-3637G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698468 | ||||||
chr5:75698498
|
A | G | 2 | a0001c0001t0001g0113a0001c0001t0001g0168 | 2 | HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.514-3667T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698498 | ||||||
chr5:75698518
|
C | A | 3 | a0001c0001t0001g0022a0001c0001t0001g0097a0001c0001t0001g0098 | 4 | NA18960.hp1 NA18984.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.514-3687G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698518 | ||||||
chr5:75698530
|
A | T | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.514-3699T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698530 | ||||||
chr5:75698536
|
C | T | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.514-3705G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698536 | ||||||
chr5:75698642
|
T | A | 1 | a0002c0002t0001g0206 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.514-3811A>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698642 | ||||||
chr5:75698653
|
A | T | 1 | a0002c0002t0001g0145 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.514-3822T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698653 | ||||||
chr5:75698745
|
C | T | 8 | a0001c0001t0002g0037a0001c0001t0002g0042a0001c0001t0002g0043others(5): Show | 8 | HG01243.hp2 HG02040.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.513+3860G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698745 | ||||||
chr5:75698746
|
A | T | 8 | a0001c0001t0002g0037a0001c0001t0002g0042a0001c0001t0002g0043others(5): Show | 8 | HG01243.hp2 HG02040.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.513+3859T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698746 | ||||||
chr5:75698793
|
A | G | 1 | a0002c0002t0001g0179 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.513+3812T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698793 | ||||||
chr5:75698798
|
G | C | 81 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(78): Show | 110 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.513+3807C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698798 | ||||||
chr5:75698843
|
C | T | 1 | a0003c0003t0004g0059 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.513+3762G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698843 | ||||||
chr5:75698845
|
A | G | 1 | a0002c0002t0001g0225 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.513+3760T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698845 | ||||||
chr5:75698914
|
G | C | 1 | a0001c0001t0001g0020 | 2 | HG01255.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.513+3691C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698914 | ||||||
chr5:75698926
|
A | G | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.513+3679T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698926 | ||||||
chr5:75698988
|
G | A | 51 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(48): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.513+3617C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698988 | ||||||
chr5:75699038
|
T | TAGACCAA others(13): Show |
1 | a0005c0006t0002g0041 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.513+3547_513+3566d others(22): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699038 | ||||||
chr5:75699063
|
G | A | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.513+3542C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699063 | ||||||
chr5:75699088
|
T | C | 122 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(119): Show | 179 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.513+3517A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699088 | ||||||
chr5:75699099
|
C | T | 5 | a0004c0005t0003g0290a0004c0005t0003g0292a0004c0005t0003g0293others(2): Show | 5 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.513+3506G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699099 | ||||||
chr5:75699122
|
T | C | 6 | a0001c0001t0002g0133a0001c0001t0002g0166a0001c0001t0002g0215others(3): Show | 6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.513+3483A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699122 | ||||||
chr5:75699184
|
T | C | 1 | a0002c0002t0001g0128 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.513+3421A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699184 | ||||||
chr5:75699236
|
G | A | 1 | a0001c0001t0002g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.513+3369C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699236 | ||||||
chr5:75699247
|
C | T | 17 | a0004c0005t0003g0007a0004c0005t0003g0035a0004c0005t0003g0036others(14): Show | 22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.513+3358G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699247 | ||||||
chr5:75699365
|
C | G | 1 | a0001c0001t0001g0138 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.513+3240G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699365 | ||||||
chr5:75699366
|
C | G | 1 | a0001c0004t0002g0080 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.513+3239G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699366 | ||||||
chr5:75699367
|
A | G | 13 | a0001c0004t0001g0075a0001c0004t0001g0078a0001c0004t0002g0003others(10): Show | 21 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.513+3238T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699367 | ||||||
chr5:75699368
|
C | A | 1 | a0001c0001t0001g0138 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.513+3237G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699368 | ||||||
chr5:75699418
|
A | G | 1 | a0002c0002t0001g0144 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.513+3187T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699418 | ||||||
chr5:75699443
|
A | G | 3 | a0002c0002t0001g0183a0002c0002t0001g0219a0002c0002t0001g0248 | 3 | HG02602.hp2 HG03654.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.513+3162T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699443 | ||||||
chr5:75699452
|
A | G | 1 | a0002c0002t0001g0144 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.513+3153T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699452 | ||||||
chr5:75699533
|
T | A | 162 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(159): Show | 226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.513+3072A>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699533 | ||||||
chr5:75699561
|
T | C | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.513+3044A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699561 | ||||||
chr5:75699584
|
A | G | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.513+3021T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699584 | ||||||
chr5:75699655
|
T | C | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.513+2950A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699655 | ||||||
chr5:75699680
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.513+2925G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699680 | ||||||
chr5:75699682
|
A | G | 1 | a0003c0003t0002g0047 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.513+2923T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699682 | ||||||
chr5:75699712
|
G | A | 51 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(48): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.513+2893C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699712 | ||||||
chr5:75699722
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.513+2883T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699722 | ||||||
chr5:75699778
|
C | G | 32 | a0001c0001t0002g0134a0003c0003t0001g0066a0003c0003t0002g0018others(29): Show | 39 | HG00733.hp2 HG01123.hp2 HG01358.hp2 others(36): Show |
intron_variant | MODIFIER | c.513+2827G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699778 | ||||||
chr5:75699793
|
C | G | 1 | a0003c0003t0002g0079 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.513+2812G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699793 | ||||||
chr5:75699793
|
C | T | 65 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(62): Show | 89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.513+2812G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699793 | ||||||
chr5:75699794
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.513+2811C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699794 | ||||||
chr5:75699803
|
G | A | 1 | a0003c0003t0002g0047 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.513+2802C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699803 | ||||||
chr5:75699809
|
C | T | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.513+2796G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699809 | ||||||
chr5:75699816
|
AC | A | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.513+2788delG | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699816 | ||||||
chr5:75699823
|
T | C | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.513+2782A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699823 | ||||||
chr5:75699918
|
T | C | 1 | a0002c0002t0001g0238 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.513+2687A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699918 | ||||||
chr5:75700044
|
G | A | 80 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(77): Show | 109 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.513+2561C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700044 | ||||||
chr5:75700046
|
C | A | 1 | a0001c0001t0001g0088 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.513+2559G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700046 | ||||||
chr5:75700184
|
C | T | 34 | a0003c0003t0001g0272a0003c0003t0001g0275a0003c0003t0001g0276others(31): Show | 62 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.513+2421G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700184 | ||||||
chr5:75700185
|
C | G | 1 | a0001c0001t0001g0250 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.513+2420G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700185 | ||||||
chr5:75700221
|
T | G | 53 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(50): Show | 69 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.513+2384A>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700221 | ||||||
chr5:75700250
|
C | T | 18 | a0003c0003t0002g0254a0004c0005t0003g0007a0004c0005t0003g0035others(15): Show | 23 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.513+2355G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700250 | ||||||
chr5:75700256
|
A | G | 1 | a0003c0003t0002g0013 | 3 | HG02056.hp1 NA19066.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.513+2349T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700256 | ||||||
chr5:75700344
|
C | G | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.513+2261G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700344 | ||||||
chr5:75700372
|
T | C | 1 | a0001c0001t0001g0130 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.513+2233A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700372 | ||||||
chr5:75700374
|
T | C | 1 | a0002c0002t0001g0074 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.513+2231A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700374 | ||||||
chr5:75700413
|
C | T | 81 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(78): Show | 110 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.513+2192G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700413 | ||||||
chr5:75700470
|
A | C | 3 | a0004c0005t0003g0035a0004c0005t0003g0281a0004c0005t0003g0282 | 4 | HG01243.hp1 HG03130.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.513+2135T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700470 | ||||||
chr5:75700573
|
A | G | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.513+2032T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700573 | ||||||
chr5:75700589
|
A | C | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.513+2016T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700589 | ||||||
chr5:75700626
|
A | C | 1 | a0001c0001t0001g0088 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.513+1979T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700626 | ||||||
chr5:75700650
|
C | T | 8 | a0001c0001t0002g0037a0001c0001t0002g0042a0001c0001t0002g0043others(5): Show | 8 | HG01243.hp2 HG02040.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.513+1955G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700650 | ||||||
chr5:75700655
|
A | C | 1 | a0001c0001t0001g0101 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.513+1950T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700655 | ||||||
chr5:75700704
|
C | A | 6 | a0001c0001t0002g0133a0001c0001t0002g0166a0001c0001t0002g0215others(3): Show | 6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.513+1901G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700704 | ||||||
chr5:75700726
|
A | C | 17 | a0004c0005t0003g0007a0004c0005t0003g0035a0004c0005t0003g0036others(14): Show | 22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.513+1879T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700726 | ||||||
chr5:75700757
|
C | G | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.513+1848G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700757 | ||||||
chr5:75700793
|
C | T | 65 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(62): Show | 89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.513+1812G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700793 | ||||||
chr5:75700801
|
A | C | 51 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(48): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.513+1804T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700801 | ||||||
chr5:75700856
|
C | T | 1 | a0004c0005t0003g0281 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.513+1749G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700856 | ||||||
chr5:75700880
|
G | A | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.513+1725C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700880 | ||||||
chr5:75700900
|
G | C | 8 | a0001c0001t0002g0037a0001c0001t0002g0042a0001c0001t0002g0043others(5): Show | 8 | HG01243.hp2 HG02040.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.513+1705C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700900 | ||||||
chr5:75700908
|
A | T | 8 | a0001c0001t0002g0037a0001c0001t0002g0042a0001c0001t0002g0043others(5): Show | 8 | HG01243.hp2 HG02040.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.513+1697T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700908 | ||||||
chr5:75700914
|
T | C | 17 | a0004c0005t0003g0007a0004c0005t0003g0035a0004c0005t0003g0036others(14): Show | 22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.513+1691A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700914 | ||||||
chr5:75700965
|
A | G | 2 | a0001c0004t0001g0075a0001c0004t0001g0078 | 2 | HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.513+1640T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700965 | ||||||
chr5:75701016
|
T | C | 31 | a0003c0003t0001g0066a0003c0003t0002g0018a0003c0003t0002g0045others(28): Show | 38 | HG00733.hp2 HG01123.hp2 HG01358.hp2 others(35): Show |
intron_variant | MODIFIER | c.513+1589A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701016 | ||||||
chr5:75701103
|
C | G | 2 | a0004c0005t0003g0036a0004c0005t0003g0283 | 3 | HG02257.hp2 HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.513+1502G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701103 | ||||||
chr5:75701152
|
G | T | 1 | a0003c0003t0002g0058 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.513+1453C>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701152 | ||||||
chr5:75701163
|
G | A | 1 | a0003c0003t0002g0047 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.513+1442C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701163 | ||||||
chr5:75701186
|
C | G | 51 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(48): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.513+1419G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701186 | ||||||
chr5:75701216
|
C | T | 3 | a0004c0005t0003g0035a0004c0005t0003g0281a0004c0005t0003g0282 | 4 | HG01243.hp1 HG03130.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.513+1389G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701216 | ||||||
chr5:75701264
|
T | C | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.513+1341A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701264 | ||||||
chr5:75701270
|
C | G | 2 | a0001c0004t0001g0075a0001c0004t0001g0078 | 2 | HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.513+1335G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701270 | ||||||
chr5:75701283
|
C | T | 63 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(60): Show | 87 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.513+1322G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701283 | ||||||
chr5:75701284
|
G | T | 1 | a0001c0001t0001g0101 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.513+1321C>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701284 | ||||||
chr5:75701365
|
A | G | 11 | a0001c0004t0002g0003a0001c0004t0002g0019a0001c0004t0002g0076others(8): Show | 19 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.513+1240T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701365 | ||||||
chr5:75701435
|
C | T | 51 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(48): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.513+1170G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701435 | ||||||
chr5:75701464
|
G | T | 1 | a0001c0001t0002g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.513+1141C>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701464 | ||||||
chr5:75701475
|
A | G | 5 | a0004c0005t0003g0290a0004c0005t0003g0292a0004c0005t0003g0293others(2): Show | 5 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.513+1130T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701475 | ||||||
chr5:75701480
|
C | A | 65 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(62): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.513+1125G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701480 | ||||||
chr5:75701486
|
C | T | 1 | a0003c0003t0002g0253 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.513+1119G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701486 | ||||||
chr5:75701500
|
G | C | 64 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(61): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.513+1105C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701500 | ||||||
chr5:75701507
|
G | T | 1 | a0001c0001t0001g0101 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.513+1098C>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701507 | ||||||
chr5:75701599
|
T | C | 66 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(63): Show | 91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.513+1006A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701599 | ||||||
chr5:75701701
|
C | T | 9 | a0004c0005t0003g0007a0004c0005t0003g0036a0004c0005t0003g0283others(6): Show | 13 | HG00735.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.513+904G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701701 | ||||||
chr5:75701708
|
C | G | 2 | a0003c0003t0002g0056a0003c0003t0002g0057 | 2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.513+897G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701708 | ||||||
chr5:75701728
|
A | AAAAT | 3 | a0002c0002t0001g0187a0007c0008t0001g0073a0007c0008t0001g0143 | 3 | HG01071.hp1 HG02698.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.513+873_513+876dup others(4): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701728 | ||||||
chr5:75701728
|
AAAAT | A | 155 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(152): Show | 220 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.513+873_513+876del others(4): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701728 | ||||||
chr5:75701839
|
C | G | 1 | a0001c0001t0001g0124 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.513+766G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701839 | ||||||
chr5:75701911
|
T | C | 66 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(63): Show | 91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.513+694A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701911 | ||||||
chr5:75701931
|
T | C | 155 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(152): Show | 220 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.513+674A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701931 | ||||||
chr5:75702007
|
T | C | 66 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(63): Show | 91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.513+598A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75702007 | ||||||
chr5:75702016
|
A | G | 9 | a0004c0005t0003g0007a0004c0005t0003g0036a0004c0005t0003g0283others(6): Show | 13 | HG00735.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.513+589T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75702016 | ||||||
chr5:75702170
|
A | G | 66 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(63): Show | 91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.513+435T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75702170 | ||||||
chr5:75702172
|
G | A | 1 | a0003c0003t0002g0072 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.513+433C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75702172 | ||||||
chr5:75702358
|
A | G | 1 | a0001c0001t0001g0088 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.513+247T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75702358 | ||||||
chr5:75702438
|
C | T | 1 | a0002c0002t0001g0186 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.513+167G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75702438 | ||||||
chr5:75702439
|
G | A | 66 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(63): Show | 91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.513+166C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75702439 | ||||||
chr5:75702444
|
T | G | 3 | a0004c0005t0003g0035a0004c0005t0003g0281a0004c0005t0003g0282 | 4 | HG01243.hp1 HG03130.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.513+161A>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75702444 | ||||||
chr5:75702509
|
G | A | 66 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(63): Show | 91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.513+96C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75702509 | ||||||
chr5:75702560
|
C | T | 6 | a0001c0001t0002g0133a0001c0001t0002g0166a0001c0001t0002g0215others(3): Show | 6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.513+45G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75702560 | ||||||
chr5:75702601
|
G | A | 51 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(48): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
splice_region_variant&intron_variant | LOW | c.513+4C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75702601 | ||||||
chr5:75703067
|
C | T | 51 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(48): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.308-257G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75703067 | ||||||
chr5:75703285
|
T | C | 17 | a0004c0005t0003g0007a0004c0005t0003g0035a0004c0005t0003g0036others(14): Show | 22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.308-475A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75703285 | ||||||
chr5:75703350
|
G | A | 4 | a0001c0001t0001g0087a0001c0001t0001g0099a0001c0001t0001g0122others(1): Show | 4 | HG01943.hp2 HG02148.hp2 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.308-540C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75703350 | ||||||
chr5:75703464
|
A | G | 1 | a0001c0001t0001g0111 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.308-654T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75703464 | ||||||
chr5:75703573
|
C | G | 9 | a0004c0005t0003g0007a0004c0005t0003g0036a0004c0005t0003g0283others(6): Show | 13 | HG00735.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.308-763G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75703573 | ||||||
chr5:75703580
|
C | A | 6 | a0001c0001t0002g0133a0001c0001t0002g0166a0001c0001t0002g0215others(3): Show | 6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.308-770G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75703580 | ||||||
chr5:75703739
|
G | T | 57 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(54): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.308-929C>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75703739 | ||||||
chr5:75703751
|
G | A | 165 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(162): Show | 230 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.308-941C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75703751 | ||||||
chr5:75703875
|
G | A | 1 | a0001c0004t0002g0085 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.308-1065C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75703875 | ||||||
chr5:75703889
|
C | G | 1 | a0001c0001t0001g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.308-1079G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75703889 | ||||||
chr5:75703930
|
C | T | 7 | a0001c0001t0002g0133a0001c0001t0002g0160a0001c0001t0002g0166others(4): Show | 7 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.308-1120G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75703930 | ||||||
chr5:75703972
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.308-1162C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75703972 | ||||||
chr5:75704026
|
G | A | 1 | a0010c0010t0004g0070 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.308-1216C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75704026 | ||||||
chr5:75704110
|
G | A | 13 | a0001c0004t0001g0028a0001c0004t0001g0167a0001c0004t0002g0003others(10): Show | 22 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.308-1300C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75704110 | ||||||
chr5:75704140
|
C | T | 1 | a0002c0002t0001g0185 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.308-1330G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75704140 | ||||||
chr5:75704153
|
C | CA | 8 | a0001c0001t0001g0164a0002c0002t0001g0159a0002c0002t0001g0172others(5): Show | 8 | HG00423.hp1 HG02896.hp1 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.308-1344dupT | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75704153 | ||||||
chr5:75704153
|
CA | C | 23 | a0001c0001t0001g0101a0001c0001t0001g0120a0001c0001t0002g0133others(20): Show | 27 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.308-1344delT | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75704153 | ||||||
chr5:75704153
|
CAA | C | 48 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(45): Show | 64 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.308-1345_308-1344d others(4): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75704153 | ||||||
chr5:75704925
|
C | G | 1 | a0002c0002t0001g0142 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.307+779G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75704925 | ||||||
chr5:75704931
|
G | A | 6 | a0001c0001t0002g0133a0001c0001t0002g0166a0001c0001t0002g0215others(3): Show | 6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.307+773C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75704931 | ||||||
chr5:75704967
|
G | A | 57 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(54): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.307+737C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75704967 | ||||||
chr5:75704981
|
C | T | 17 | a0004c0005t0003g0007a0004c0005t0003g0035a0004c0005t0003g0036others(14): Show | 22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.307+723G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75704981 | ||||||
chr5:75705094
|
G | T | 1 | a0002c0002t0001g0184 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.307+610C>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75705094 | ||||||
chr5:75705103
|
C | T | 6 | a0001c0001t0001g0124a0001c0001t0001g0141a0001c0001t0001g0176others(3): Show | 6 | HG01192.hp2 HG01261.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.307+601G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75705103 | ||||||
chr5:75705173
|
G | A | 6 | a0001c0001t0002g0133a0001c0001t0002g0166a0001c0001t0002g0215others(3): Show | 6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.307+531C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75705173 | ||||||
chr5:75705200
|
C | A | 74 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(71): Show | 95 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.307+504G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75705200 | ||||||
chr5:75705209
|
T | TA | 23 | a0001c0001t0002g0133a0001c0001t0002g0166a0001c0001t0002g0215others(20): Show | 28 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.307+494_307+495ins others(1): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75705209 | ||||||
chr5:75705209
|
T | TAA | 48 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(45): Show | 64 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.307+494_307+495ins others(2): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75705209 | ||||||
chr5:75705210
|
T | A | 74 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(71): Show | 95 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.307+494A>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75705210 | ||||||
chr5:75705211
|
A | T | 13 | a0001c0004t0001g0028a0001c0004t0001g0167a0001c0004t0002g0003others(10): Show | 22 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.307+493T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75705211 | ||||||
chr5:75705218
|
T | A | 74 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(71): Show | 95 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.307+486A>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75705218 | ||||||
chr5:75705236
|
C | A | 1 | a0003c0003t0002g0274 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.307+468G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75705236 | ||||||
chr5:75705427
|
T | C | 51 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(48): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.307+277A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75705427 | ||||||
chr5:75705496
|
C | T | 51 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(48): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.307+208G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75705496 | ||||||
chr5:75705569
|
A | G | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | NA18954.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.307+135T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75705569 | ||||||
chr5:75705607
|
A | G | 89 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(86): Show | 119 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.307+97T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75705607 | ||||||
chr5:75705852
|
A | G | 1 | a0003c0003t0004g0048 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.224-65T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75705852 | ||||||
chr5:75705891
|
A | G | 5 | a0004c0005t0003g0290a0004c0005t0003g0292a0004c0005t0003g0293others(2): Show | 5 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.224-104T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75705891 | ||||||
chr5:75705934
|
G | A | 1 | a0002c0002t0001g0224 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.224-147C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75705934 | ||||||
chr5:75705969
|
GACTT | G | 6 | a0001c0001t0002g0133a0001c0001t0002g0166a0001c0001t0002g0215others(3): Show | 6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.224-186_224-183del others(4): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75705969 | ||||||
chr5:75706562
|
GTTTT | G | 49 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(46): Show | 65 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.224-779_224-776del others(4): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75706562 | ||||||
chr5:75706565
|
T | C | 1 | a0001c0001t0001g0088 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.224-778A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75706565 | ||||||
chr5:75706570
|
T | C | 1 | a0001c0001t0001g0101 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.224-783A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75706570 | ||||||
chr5:75706638
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.224-851T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75706638 | ||||||
chr5:75706736
|
A | C | 1 | a0002c0002t0001g0224 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.224-949T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75706736 | ||||||
chr5:75706807
|
T | C | 1 | a0003c0003t0002g0047 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.223+930A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75706807 | ||||||
chr5:75706810
|
G | C | 74 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(71): Show | 95 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.223+927C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75706810 | ||||||
chr5:75706867
|
T | C | 1 | a0003c0003t0002g0054 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.223+870A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75706867 | ||||||
chr5:75707018
|
T | C | 2 | a0002c0002t0001g0172a0002c0002t0001g0207 | 2 | HG00438.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.223+719A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75707018 | ||||||
chr5:75707020
|
C | T | 57 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(54): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.223+717G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75707020 | ||||||
chr5:75707023
|
C | T | 6 | a0001c0001t0002g0133a0001c0001t0002g0166a0001c0001t0002g0215others(3): Show | 6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.223+714G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75707023 | ||||||
chr5:75707070
|
G | T | 74 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(71): Show | 95 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.223+667C>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75707070 | ||||||
chr5:75707111
|
T | C | 1 | a0003c0003t0002g0047 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.223+626A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75707111 | ||||||
chr5:75707134
|
T | C | 2 | a0003c0003t0002g0031a0003c0003t0002g0032 | 4 | HG01069.hp1 HG01071.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.223+603A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75707134 | ||||||
chr5:75707141
|
T | C | 6 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0213others(3): Show | 6 | HG02055.hp1 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.223+596A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75707141 | ||||||
chr5:75707185
|
C | T | 6 | a0001c0001t0002g0133a0001c0001t0002g0166a0001c0001t0002g0215others(3): Show | 6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.223+552G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75707185 | ||||||
chr5:75707231
|
A | G | 155 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(152): Show | 220 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.223+506T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75707231 | ||||||
chr5:75707384
|
C | CT | 3 | a0002c0002t0001g0183a0002c0002t0001g0219a0002c0002t0001g0248 | 3 | HG02602.hp2 HG03654.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.223+352dupA | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75707384 | ||||||
chr5:75707588
|
A | C | 57 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(54): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.223+149T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75707588 | ||||||
chr5:75707624
|
A | T | 13 | a0001c0004t0001g0028a0001c0004t0001g0167a0001c0004t0002g0003others(10): Show | 22 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.223+113T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75707624 | ||||||
chr5:75707626
|
A | T | 13 | a0001c0004t0001g0028a0001c0004t0001g0167a0001c0004t0002g0003others(10): Show | 22 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.223+111T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75707626 | ||||||
chr5:75707627
|
T | TC | 13 | a0001c0004t0001g0028a0001c0004t0001g0167a0001c0004t0002g0003others(10): Show | 22 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.223+109_223+110ins others(1): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75707627 | ||||||
chr5:75707644
|
T | C | 13 | a0001c0004t0001g0028a0001c0004t0001g0167a0001c0004t0002g0003others(10): Show | 22 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.223+93A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75707644 | ||||||
chr5:75707906
|
G | A | 4 | a0001c0001t0001g0088a0001c0001t0001g0100a0001c0001t0001g0101others(1): Show | 4 | NA18999.hp1 NA19059.hp2 NA19075.hp2 others(1): Show |
intron_variant | MODIFIER | c.85-31C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75707906 | ||||||
chr5:75707964
|
CCA | C | 6 | a0001c0001t0002g0133a0001c0001t0002g0166a0001c0001t0002g0215others(3): Show | 6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.85-91_85-90delTG | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75707964 | ||||||
chr5:75708053
|
T | C | 57 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(54): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.85-178A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75708053 | ||||||
chr5:75708282
|
A | G | 57 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(54): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.85-407T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75708282 | ||||||
chr5:75708350
|
G | A | 51 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(48): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.85-475C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75708350 | ||||||
chr5:75709154
|
C | G | 1 | a0004c0005t0003g0290 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.85-1279G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75709154 | ||||||
chr5:75709270
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.85-1395C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75709270 | ||||||
chr5:75709492
|
T | TA | 66 | a0003c0003t0001g0066a0003c0003t0001g0272a0003c0003t0001g0275others(63): Show | 101 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.85-1618dupT | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75709492 | ||||||
chr5:75709515
|
A | G | 6 | a0001c0001t0002g0133a0001c0001t0002g0166a0001c0001t0002g0215others(3): Show | 6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.85-1640T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75709515 | ||||||
chr5:75709781
|
G | T | 2 | a0001c0004t0001g0075a0001c0004t0001g0078 | 2 | HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.85-1906C>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75709781 | ||||||
chr5:75709790
|
T | C | 5 | a0004c0005t0003g0290a0004c0005t0003g0292a0004c0005t0003g0293others(2): Show | 5 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.85-1915A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75709790 | ||||||
chr5:75709969
|
T | C | 2 | a0001c0004t0001g0075a0001c0004t0001g0078 | 2 | HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.85-2094A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75709969 | ||||||
chr5:75710074
|
A | G | 57 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(54): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.85-2199T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75710074 | ||||||
chr5:75710288
|
T | A | 87 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(84): Show | 116 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.85-2413A>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75710288 | ||||||
chr5:75710331
|
T | C | 51 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(48): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.85-2456A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75710331 | ||||||
chr5:75710448
|
G | A | 8 | a0001c0001t0002g0037a0001c0001t0002g0042a0001c0001t0002g0043others(5): Show | 8 | HG01243.hp2 HG02040.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.84+2406C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75710448 | ||||||
chr5:75710451
|
C | A | 2 | a0003c0003t0002g0269a0003c0003t0002g0273 | 2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.84+2403G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75710451 | ||||||
chr5:75710558
|
C | T | 6 | a0001c0001t0002g0133a0001c0001t0002g0166a0001c0001t0002g0215others(3): Show | 6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.84+2296G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75710558 | ||||||
chr5:75710559
|
A | G | 57 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(54): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.84+2295T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75710559 | ||||||
chr5:75710624
|
T | A | 57 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(54): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.84+2230A>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75710624 | ||||||
chr5:75710824
|
T | C | 1 | a0003c0003t0002g0055 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.84+2030A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75710824 | ||||||
chr5:75710828
|
C | T | 5 | a0004c0005t0003g0290a0004c0005t0003g0292a0004c0005t0003g0293others(2): Show | 5 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.84+2026G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75710828 | ||||||
chr5:75710858
|
T | C | 2 | a0001c0004t0001g0075a0001c0004t0001g0078 | 2 | HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.84+1996A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75710858 | ||||||
chr5:75710986
|
T | C | 2 | a0001c0004t0001g0075a0001c0004t0001g0078 | 2 | HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.84+1868A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75710986 | ||||||
chr5:75710996
|
T | A | 6 | a0001c0001t0002g0133a0001c0001t0002g0166a0001c0001t0002g0215others(3): Show | 6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.84+1858A>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75710996 | ||||||
chr5:75711033
|
G | A | 3 | a0004c0005t0003g0035a0004c0005t0003g0281a0004c0005t0003g0282 | 4 | HG01243.hp1 HG03130.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.84+1821C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75711033 | ||||||
chr5:75711119
|
T | A | 1 | a0001c0001t0002g0037 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.84+1735A>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75711119 | ||||||
chr5:75711581
|
T | A | 33 | a0003c0003t0001g0272a0003c0003t0001g0275a0003c0003t0001g0276others(30): Show | 60 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.84+1273A>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75711581 | ||||||
chr5:75711632
|
A | C | 34 | a0003c0003t0001g0272a0003c0003t0001g0275a0003c0003t0001g0276others(31): Show | 62 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.84+1222T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75711632 | ||||||
chr5:75711731
|
A | G | 57 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(54): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.84+1123T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75711731 | ||||||
chr5:75711753
|
A | C | 57 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(54): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.84+1101T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75711753 | ||||||
chr5:75711768
|
A | G | 1 | a0003c0003t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.84+1086T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75711768 | ||||||
chr5:75711776
|
G | A | 51 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(48): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.84+1078C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75711776 | ||||||
chr5:75711833
|
A | G | 6 | a0001c0001t0002g0133a0001c0001t0002g0166a0001c0001t0002g0215others(3): Show | 6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.84+1021T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75711833 | ||||||
chr5:75711896
|
A | G | 1 | a0003c0003t0002g0079 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.84+958T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75711896 | ||||||
chr5:75711943
|
G | A | 6 | a0001c0001t0002g0133a0001c0001t0002g0166a0001c0001t0002g0215others(3): Show | 6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.84+911C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75711943 | ||||||
chr5:75712033
|
C | T | 2 | a0002c0002t0001g0182a0002c0002t0001g0223 | 2 | HG03834.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.84+821G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75712033 | ||||||
chr5:75712107
|
G | A | 17 | a0004c0005t0003g0007a0004c0005t0003g0035a0004c0005t0003g0036others(14): Show | 22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.84+747C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75712107 | ||||||
chr5:75712323
|
A | G | 6 | a0001c0001t0001g0124a0001c0001t0001g0141a0001c0001t0001g0176others(3): Show | 6 | HG01192.hp2 HG01261.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.84+531T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75712323 | ||||||
chr5:75712368
|
T | C | 92 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(89): Show | 121 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.84+486A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75712368 | ||||||
chr5:75712461
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.84+393A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75712461 | ||||||
chr5:75712490
|
A | G | 6 | a0001c0001t0002g0133a0001c0001t0002g0166a0001c0001t0002g0215others(3): Show | 6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.84+364T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75712490 | ||||||
chr5:75712556
|
T | A | 2 | a0001c0004t0001g0075a0001c0004t0001g0078 | 2 | HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.84+298A>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75712556 | ||||||
chr5:75712683
|
T | C | 1 | a0001c0001t0001g0214 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.84+171A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75712683 | ||||||
chr5:75712684
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.84+170C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75712684 | ||||||
chr5:75712694
|
T | G | 1 | a0001c0001t0001g0088 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.84+160A>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75712694 | ||||||
chr5:75712703
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.84+151C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75712703 | ||||||
chr5:75712789
|
TTTTCCCT others(8): Show |
T | 1 | a0001c0001t0001g0108 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.84+50_84+64delTGAA others(11): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75712789 | ||||||
chr5:75712851
|
T | G | 1 | a0004c0005t0003g0289 | 1 | HG03453.hp1 | splice_region_variant&intron_variant | LOW | c.84+3A>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75712851 | ||||||
chr5:75713133
|
C | T | 51 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(48): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.-14-182G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75713133 | ||||||
chr5:75713242
|
C | A | 1 | a0009c0013t0002g0086 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-14-291G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75713242 | ||||||
chr5:75713255
|
G | C | 1 | a0002c0002t0001g0220 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-14-304C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75713255 | ||||||
chr5:75713259
|
A | ACTTT | 11 | a0001c0004t0002g0003a0001c0004t0002g0019a0001c0004t0002g0076others(8): Show | 19 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.-14-312_-14-309dup others(4): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75713259 | ||||||
chr5:75713288
|
G | C | 6 | a0001c0001t0002g0133a0001c0001t0002g0166a0001c0001t0002g0215others(3): Show | 6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14-337C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75713288 | ||||||
chr5:75713473
|
T | C | 66 | a0003c0003t0001g0066a0003c0003t0001g0272a0003c0003t0001g0275others(63): Show | 101 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.-14-522A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75713473 | ||||||
chr5:75713486
|
A | T | 11 | a0001c0004t0002g0003a0001c0004t0002g0019a0001c0004t0002g0076others(8): Show | 19 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.-14-535T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75713486 | ||||||
chr5:75713636
|
A | T | 3 | a0002c0002t0001g0140a0002c0002t0001g0165a0002c0002t0001g0222 | 3 | NA18971.hp2 NA18989.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-14-685T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75713636 | ||||||
chr5:75713698
|
G | A | 1 | a0003c0003t0002g0047 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-14-747C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75713698 | ||||||
chr5:75713814
|
G | A | 9 | a0004c0005t0003g0007a0004c0005t0003g0036a0004c0005t0003g0283others(6): Show | 13 | HG00735.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-14-863C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75713814 | ||||||
chr5:75713864
|
A | G | 1 | a0001c0001t0001g0089 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-14-913T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75713864 | ||||||
chr5:75713866
|
G | A | 6 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(3): Show | 6 | HG00741.hp1 HG02004.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-915C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75713866 | ||||||
chr5:75714009
|
C | G | 6 | a0001c0001t0002g0133a0001c0001t0002g0166a0001c0001t0002g0215others(3): Show | 6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14-1058G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75714009 | ||||||
chr5:75714087
|
A | G | 1 | a0001c0001t0001g0108 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-14-1136T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75714087 | ||||||
chr5:75714089
|
G | C | 1 | a0002c0002t0001g0165 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-14-1138C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75714089 | ||||||
chr5:75714177
|
T | C | 163 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(160): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.-14-1226A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75714177 | ||||||
chr5:75714242
|
C | G | 1 | a0002c0002t0001g0179 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-14-1291G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75714242 | ||||||
chr5:75714255
|
G | T | 34 | a0003c0003t0001g0272a0003c0003t0001g0275a0003c0003t0001g0276others(31): Show | 62 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-14-1304C>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75714255 | ||||||
chr5:75714284
|
A | G | 1 | a0001c0001t0001g0108 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-14-1333T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75714284 | ||||||
chr5:75714285
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-14-1334C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75714285 | ||||||
chr5:75714392
|
G | A | 1 | a0006c0007t0004g0071 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-14-1441C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75714392 | ||||||
chr5:75714694
|
C | T | 31 | a0003c0003t0001g0066a0003c0003t0002g0018a0003c0003t0002g0045others(28): Show | 38 | HG00733.hp2 HG01123.hp2 HG01358.hp2 others(35): Show |
intron_variant | MODIFIER | c.-14-1743G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75714694 | ||||||
chr5:75714708
|
C | T | 17 | a0004c0005t0003g0007a0004c0005t0003g0035a0004c0005t0003g0036others(14): Show | 22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.-14-1757G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75714708 | ||||||
chr5:75714727
|
T | G | 1 | a0003c0003t0002g0047 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-14-1776A>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75714727 | ||||||
chr5:75714859
|
G | C | 17 | a0004c0005t0003g0007a0004c0005t0003g0035a0004c0005t0003g0036others(14): Show | 22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.-14-1908C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75714859 | ||||||
chr5:75714936
|
G | A | 2 | a0001c0004t0001g0028a0001c0004t0001g0167 | 3 | HG03490.hp2 HG03492.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-14-1985C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75714936 | ||||||
chr5:75714988
|
CCTGTATT others(28): Show |
C | 2 | a0001c0004t0001g0075a0001c0004t0001g0078 | 2 | HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-14-2072_-14-2038d others(37): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75714988 | ||||||
chr5:75715028
|
C | T | 3 | a0004c0005t0003g0035a0004c0005t0003g0281a0004c0005t0003g0282 | 4 | HG01243.hp1 HG03130.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-2077G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75715028 | ||||||
chr5:75715067
|
CT | C | 3 | a0004c0005t0003g0035a0004c0005t0003g0281a0004c0005t0003g0282 | 4 | HG01243.hp1 HG03130.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-2117delA | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75715067 | ||||||
chr5:75715087
|
A | C | 17 | a0004c0005t0003g0007a0004c0005t0003g0035a0004c0005t0003g0036others(14): Show | 22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.-14-2136T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75715087 | ||||||
chr5:75715234
|
C | T | 51 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(48): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.-15+2072G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75715234 | ||||||
chr5:75715264
|
C | T | 1 | a0002c0002t0001g0025 | 2 | HG01257.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.-15+2042G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75715264 | ||||||
chr5:75715301
|
C | T | 73 | a0001c0001t0002g0037a0001c0001t0002g0042a0001c0001t0002g0043others(70): Show | 108 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.-15+2005G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75715301 | ||||||
chr5:75715309
|
C | CA | 13 | a0001c0001t0001g0077a0001c0001t0001g0168a0001c0001t0001g0169others(10): Show | 13 | HG00099.hp1 HG02055.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-15+1996dupT | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75715309 | ||||||
chr5:75715309
|
C | CAA | 14 | a0001c0004t0001g0078a0001c0004t0002g0003a0001c0004t0002g0019others(11): Show | 23 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.-15+1995_-15+1996d others(4): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75715309 | ||||||
chr5:75715309
|
C | CAAAAAA | 4 | a0004c0005t0003g0007a0004c0005t0003g0036a0004c0005t0003g0288others(1): Show | 8 | HG01891.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-15+1991_-15+1996d others(8): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75715309 | ||||||
chr5:75715309
|
CA | C | 8 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0109others(5): Show | 8 | HG01256.hp2 HG01943.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15+1996delT | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75715309 | ||||||
chr5:75715476
|
TGA | T | 15 | a0001c0001t0001g0077a0001c0004t0001g0075a0001c0004t0001g0078others(12): Show | 23 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.-15+1828_-15+1829d others(4): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75715476 | ||||||
chr5:75715724
|
C | A | 3 | a0001c0001t0001g0109a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | HG00639.hp1 HG01109.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.-15+1582G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75715724 | ||||||
chr5:75715738
|
A | T | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-15+1568T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75715738 | ||||||
chr5:75715948
|
G | A | 9 | a0004c0005t0003g0007a0004c0005t0003g0036a0004c0005t0003g0283others(6): Show | 13 | HG00735.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-15+1358C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75715948 | ||||||
chr5:75715989
|
G | A | 8 | a0004c0005t0003g0035a0004c0005t0003g0281a0004c0005t0003g0282others(5): Show | 9 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.-15+1317C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75715989 | ||||||
chr5:75716003
|
T | C | 2 | a0002c0002t0001g0174a0002c0002t0001g0175 | 2 | HG00323.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.-15+1303A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75716003 | ||||||
chr5:75716383
|
T | TG | 56 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(53): Show | 67 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.-15+922dupC | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75716383 | ||||||
chr5:75716383
|
T | TGG | 34 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(31): Show | 39 | HG00544.hp1 HG00639.hp2 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.-15+921_-15+922dup others(2): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75716383 | ||||||
chr5:75716383
|
TG | T | 53 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(50): Show | 63 | HG00280.hp2 HG00408.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.-15+922delC | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75716383 | ||||||
chr5:75716383
|
TGG | T | 35 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0087others(32): Show | 47 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.-15+921_-15+922del others(2): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75716383 | ||||||
chr5:75716383
|
TGGG | T | 44 | a0001c0001t0001g0077a0001c0001t0002g0037a0001c0004t0001g0075others(41): Show | 79 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.-15+920_-15+922del others(3): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75716383 | ||||||
chr5:75716384
|
G | C | 9 | a0003c0003t0002g0018a0003c0003t0002g0050a0003c0003t0002g0051others(6): Show | 10 | HG01516.hp2 HG02698.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.-15+922C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75716384 | ||||||
chr5:75716385
|
G | C | 19 | a0003c0003t0001g0066a0003c0003t0002g0056a0003c0003t0002g0057others(16): Show | 25 | HG00733.hp2 HG01123.hp2 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.-15+921C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75716385 | ||||||
chr5:75716388
|
G | C | 1 | a0001c0001t0001g0250 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-15+918C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75716388 | ||||||
chr5:75716392
|
G | C | 1 | a0003c0003t0002g0072 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-15+914C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75716392 | ||||||
chr5:75716396
|
G | T | 2 | a0002c0002t0001g0074a0007c0008t0001g0073 | 2 | HG00642.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.-15+910C>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75716396 | ||||||
chr5:75716492
|
C | T | 73 | a0001c0001t0002g0037a0001c0001t0002g0042a0001c0001t0002g0043others(70): Show | 108 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.-15+814G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75716492 | ||||||
chr5:75716999
|
C | A | 17 | a0004c0005t0003g0007a0004c0005t0003g0035a0004c0005t0003g0036others(14): Show | 22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.-15+307G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75716999 | ||||||
chr5:75717008
|
A | G | 1 | a0001c0001t0001g0251 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-15+298T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75717008 | ||||||
chr5:75717009
|
G | A | 1 | a0001c0001t0001g0251 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-15+297C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75717009 | ||||||
chr5:75717211
|
G | A | 34 | a0003c0003t0001g0272a0003c0003t0001g0275a0003c0003t0001g0276others(31): Show | 62 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-15+95C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75717211 | ||||||
chr5:75717253
|
A | G | 3 | a0004c0005t0003g0035a0004c0005t0003g0281a0004c0005t0003g0282 | 4 | HG01243.hp1 HG03130.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+53T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75717253 | ||||||
chr5:75717290
|
G | A | 1 | a0002c0002t0001g0278 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-15+16C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75717290 |