geneid | 79810 |
---|---|
ensemblid | ENSG00000049883.15 |
hgncid | 25734 |
symbol | PTCD2 |
name | pentatricopeptide repeat domain 2 |
refseq_nuc | NM_024754.5 |
refseq_prot | NP_079030.3 |
ensembl_nuc | ENST00000380639.10 |
ensembl_prot | ENSP00000370013.4 |
mane_status | MANE Select |
chr | chr5 |
start | 72320373 |
end | 72368395 |
strand | + |
ver | v1.2 |
region | chr5:72320373-72368395 |
region5000 | chr5:72315373-72373395 |
regionname0 | PTCD2_chr5_72320373_72368395 |
regionname5000 | PTCD2_chr5_72315373_72373395 |
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 | 1/1 | 388 | 327 | 82 | 60 | 131 | 14 | 38 | 101 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0002 | 0/0 | 388 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
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 | 1/1 | 1167 | 326 | 82 | 60 | 130 | 14 | 38 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
c0002 | 0/0 | 1167 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
c0003 | 0/0 | 1167 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 9979 | 90 | 3 | 20 | 53 | 3 | 10 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0002 | 0/0 | 9979 | 51 | 0 | 6 | 41 | 0 | 4 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0003 | 0/0 | 9979 | 20 | 2 | 2 | 12 | 0 | 4 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0004 | 0/0 | 9979 | 16 | 2 | 5 | 4 | 2 | 3 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0005 | 0/0 | 9979 | 12 | 7 | 1 | 1 | 2 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0006 | 0/0 | 9979 | 10 | 0 | 5 | 0 | 2 | 3 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0007 | 0/0 | 9971 | 8 | 8 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0008 | 0/0 | 9979 | 8 | 1 | 3 | 0 | 1 | 3 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0009 | 0/0 | 9979 | 8 | 7 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0010 | 0/0 | 9979 | 6 | 6 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0011 | 0/0 | 9979 | 6 | 5 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0012 | 0/0 | 9979 | 5 | 0 | 0 | 5 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0013 | 0/0 | 9979 | 4 | 2 | 2 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0014 | 0/0 | 9979 | 4 | 1 | 2 | 0 | 1 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0015 | 0/0 | 9979 | 4 | 4 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0016 | 0/0 | 9979 | 3 | 0 | 2 | 0 | 1 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0017 | 0/0 | 9979 | 3 | 2 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0018 | 0/0 | 9979 | 3 | 3 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0019 | 0/0 | 9979 | 3 | 3 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0020 | 0/0 | 9979 | 3 | 2 | 0 | 0 | 1 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0021 | 0/0 | 9978 | 3 | 3 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0022 | 0/0 | 9979 | 2 | 0 | 0 | 0 | 0 | 2 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0023 | 0/0 | 9979 | 2 | 2 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0024 | 0/0 | 9979 | 2 | 2 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0025 | 0/0 | 9979 | 2 | 2 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0026 | 0/0 | 9979 | 2 | 0 | 2 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0027 | 0/1 | 9979 | 2 | 0 | 0 | 0 | 1 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0028 | 0/0 | 9979 | 2 | 0 | 0 | 0 | 0 | 2 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0029 | 0/0 | 9979 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0030 | 0/0 | 9979 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0031 | 0/0 | 9979 | 2 | 0 | 0 | 1 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0032 | 0/0 | 9978 | 2 | 2 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0033 | 0/0 | 9979 | 2 | 0 | 2 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0034 | 0/0 | 9979 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0035 | 0/0 | 9970 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0036 | 0/0 | 9971 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0037 | 0/0 | 9970 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0038 | 0/0 | 9979 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0039 | 0/0 | 9979 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0040 | 0/0 | 9979 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0041 | 0/0 | 9979 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0042 | 0/0 | 9979 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0043 | 0/0 | 9979 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0044 | 0/0 | 9979 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0045 | 0/0 | 9979 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0046 | 0/0 | 9979 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0047 | 0/0 | 9979 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0048 | 0/0 | 9979 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0049 | 0/0 | 9979 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0050 | 0/0 | 9979 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0051 | 0/0 | 9979 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0052 | 0/0 | 9979 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0053 | 0/0 | 9979 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0054 | 0/0 | 9979 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0055 | 0/0 | 9979 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0056 | 0/0 | 9979 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0057 | 0/0 | 9979 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0058 | 0/0 | 9979 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0059 | 0/0 | 9979 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0060 | 0/0 | 9979 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0061 | 0/0 | 9978 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0062 | 0/0 | 9979 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0063 | 0/0 | 9979 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0064 | 0/0 | 9979 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0065 | 0/0 | 9979 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0066 | 0/0 | 9979 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
t0067 | 0/0 | 9979 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
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 | 27 | 0 | 2 | 22 | 0 | 3 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0002 | 0/0 | 18 | 1 | 6 | 8 | 1 | 2 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0003 | 0/0 | 16 | 0 | 4 | 9 | 2 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0004 | 0/0 | 11 | 1 | 2 | 3 | 2 | 3 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0005 | 0/0 | 10 | 2 | 3 | 0 | 2 | 3 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0006 | 0/0 | 7 | 0 | 1 | 5 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0007 | 0/0 | 6 | 2 | 1 | 1 | 1 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0008 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0011 | 0/0 | 3 | 2 | 0 | 0 | 1 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0013 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0015 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0021 | 0/1 | 3 | 0 | 2 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0136 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
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 | 1/1 | 1167 | 326 | 82 | 60 | 130 | 14 | 38 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0003 | 0/0 | 1167 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0002c0002 | 0/0 | 1167 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 11145 | 90 | 3 | 20 | 53 | 3 | 10 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0002 | 0/0 | 11145 | 49 | 0 | 6 | 39 | 0 | 4 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0003 | 0/0 | 11145 | 20 | 2 | 2 | 12 | 0 | 4 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0004 | 0/0 | 11145 | 16 | 2 | 5 | 4 | 2 | 3 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0005 | 0/0 | 11145 | 12 | 7 | 1 | 1 | 2 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0006 | 0/0 | 11145 | 10 | 0 | 5 | 0 | 2 | 3 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0007 | 0/0 | 11137 | 8 | 8 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0008 | 0/0 | 11145 | 8 | 1 | 3 | 0 | 1 | 3 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0009 | 0/0 | 11145 | 8 | 7 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0010 | 0/0 | 11145 | 6 | 6 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0011 | 0/0 | 11145 | 6 | 5 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0012 | 0/0 | 11145 | 5 | 0 | 0 | 5 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0013 | 0/0 | 11145 | 4 | 2 | 2 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0014 | 0/0 | 11145 | 4 | 1 | 2 | 0 | 1 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0015 | 0/0 | 11145 | 4 | 4 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0016 | 0/0 | 11145 | 3 | 0 | 2 | 0 | 1 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0017 | 0/0 | 11145 | 3 | 2 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0018 | 0/0 | 11145 | 3 | 3 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0019 | 0/0 | 11145 | 3 | 3 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0020 | 0/0 | 11145 | 3 | 2 | 0 | 0 | 1 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0021 | 0/0 | 11144 | 3 | 3 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0022 | 0/0 | 11145 | 2 | 0 | 0 | 0 | 0 | 2 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0023 | 0/0 | 11145 | 2 | 2 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0024 | 0/0 | 11145 | 2 | 2 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0025 | 0/0 | 11145 | 2 | 2 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0026 | 0/0 | 11145 | 2 | 0 | 2 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0027 | 0/1 | 11145 | 2 | 0 | 0 | 0 | 1 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0028 | 0/0 | 11145 | 2 | 0 | 0 | 0 | 0 | 2 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0029 | 0/0 | 11145 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0030 | 0/0 | 11145 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0031 | 0/0 | 11145 | 2 | 0 | 0 | 1 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0032 | 0/0 | 11144 | 2 | 2 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0033 | 0/0 | 11145 | 2 | 0 | 2 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0034 | 0/0 | 11145 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0035 | 0/0 | 11136 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0036 | 0/0 | 11137 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0037 | 0/0 | 11136 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0038 | 0/0 | 11145 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0039 | 0/0 | 11145 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0040 | 0/0 | 11145 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0041 | 0/0 | 11145 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0042 | 0/0 | 11145 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0043 | 0/0 | 11145 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0044 | 0/0 | 11145 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0045 | 0/0 | 11145 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0046 | 0/0 | 11145 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0047 | 0/0 | 11145 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0048 | 0/0 | 11145 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0049 | 0/0 | 11145 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0050 | 0/0 | 11145 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0051 | 0/0 | 11145 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0052 | 0/0 | 11145 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0053 | 0/0 | 11145 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0054 | 0/0 | 11145 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0055 | 0/0 | 11145 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0056 | 0/0 | 11145 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0057 | 0/0 | 11145 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0058 | 0/0 | 11145 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0059 | 0/0 | 11145 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0060 | 0/0 | 11145 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0061 | 0/0 | 11144 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0062 | 0/0 | 11145 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0063 | 0/0 | 11145 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0064 | 0/0 | 11145 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0065 | 0/0 | 11145 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0066 | 0/0 | 11145 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0001t0067 | 0/0 | 11145 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0001c0003t0002 | 0/0 | 11145 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
a0002c0002t0002 | 0/0 | 11145 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | copy fasta | chr5 | 72315373 | 72373395 |
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 | 15 | 1 | 6 | 7 | 1 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0003 | 0/0 | 14 | 0 | 3 | 9 | 1 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0136 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0002g0001 | 0/0 | 23 | 0 | 2 | 19 | 0 | 2 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0002g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0002g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0002g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0003g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0003g0004 | 0/0 | 6 | 1 | 1 | 3 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0003g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0004g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0004g0007 | 0/0 | 4 | 0 | 1 | 1 | 1 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0004g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0004g0013 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0004g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0004g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0005g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0005g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0005g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0005g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0005g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0005g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0006g0005 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0006g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0006g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0006g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0006g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0006g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0007g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0007g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0007g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0007g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0007g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0008g0005 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0008g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0008g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0008g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0008g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0008g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0009g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0009g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0009g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0009g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0009g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0009g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0010g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0010g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0010g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0010g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0010g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0010g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0011g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0011g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0011g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0011g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0011g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0011g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0012g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0012g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0012g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0012g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0013g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0013g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0013g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0013g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0014g0005 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0014g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0014g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0015g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0015g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0015g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0015g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0016g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0016g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0017g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0017g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0018g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0019g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0019g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0019g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0020g0011 | 0/0 | 3 | 2 | 0 | 0 | 1 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0021g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0022g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0023g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0023g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0024g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0024g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0025g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0026g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0026g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0027g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0027g0021 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0028g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0028g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0029g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0029g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0030g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0030g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0031g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0031g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0032g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0032g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0033g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0033g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0034g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0035g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0036g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0037g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0038g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0039g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0040g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0041g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0042g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0043g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0044g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0045g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0046g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0047g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0048g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0049g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0050g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0051g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0052g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0053g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0054g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0055g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0056g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0057g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0058g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0059g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0060g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0061g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0062g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0063g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0064g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0065g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0066g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0001t0067g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0001c0003t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0006 | g0125 | EUR | GBR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG00140 | hp1 | a0001 | c0001 | t0016 | g0004 | EUR | GBR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0137 | EUR | FIN | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG00280 | hp2 | a0001 | c0001 | t0004 | g0007 | EUR | FIN | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | CHS | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG00438 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | CHS | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0112 | EAS | CHS | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG00558 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | CHS | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG00621 | hp1 | a0001 | c0001 | t0012 | g0152 | EAS | CHS | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG00642 | hp1 | a0001 | c0001 | t0005 | g0077 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG00642 | hp2 | a0001 | c0001 | t0008 | g0192 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG00673 | hp1 | a0001 | c0001 | t0004 | g0091 | EAS | CHS | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG00673 | hp2 | a0001 | c0001 | t0052 | g0172 | EAS | CHS | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG00735 | hp2 | a0001 | c0001 | t0006 | g0016 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG00738 | hp2 | a0001 | c0001 | t0004 | g0007 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG00741 | hp1 | a0001 | c0001 | t0009 | g0050 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG00741 | hp2 | a0001 | c0001 | t0004 | g0013 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01069 | hp2 | a0001 | c0001 | t0026 | g0121 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01071 | hp1 | a0001 | c0001 | t0026 | g0005 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01074 | hp2 | a0001 | c0001 | t0017 | g0039 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01081 | hp2 | a0001 | c0001 | t0006 | g0016 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01099 | hp1 | a0001 | c0001 | t0055 | g0003 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0090 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01109 | hp1 | a0001 | c0001 | t0008 | g0030 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01167 | hp1 | a0001 | c0001 | t0013 | g0094 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01168 | hp1 | a0001 | c0001 | t0016 | g0109 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01168 | hp2 | a0001 | c0001 | t0004 | g0079 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01169 | hp1 | a0001 | c0001 | t0016 | g0004 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01175 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01192 | hp1 | a0001 | c0001 | t0065 | g0113 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01192 | hp2 | a0001 | c0001 | t0008 | g0005 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01243 | hp1 | a0001 | c0001 | t0011 | g0066 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01243 | hp2 | a0001 | c0001 | t0013 | g0092 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01255 | hp1 | a0001 | c0001 | t0006 | g0005 | AMR | CLM | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01261 | hp1 | a0001 | c0001 | t0033 | g0111 | AMR | CLM | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01346 | hp1 | a0001 | c0001 | t0014 | g0030 | AMR | CLM | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01358 | hp2 | a0001 | c0001 | t0043 | g0118 | AMR | CLM | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01361 | hp1 | a0001 | c0001 | t0014 | g0015 | AMR | CLM | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01433 | hp2 | a0001 | c0001 | t0063 | g0064 | AMR | CLM | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01515 | hp1 | a0001 | c0001 | t0004 | g0100 | EUR | IBS | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01515 | hp2 | a0001 | c0001 | t0005 | g0004 | EUR | IBS | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01517 | hp1 | a0001 | c0001 | t0008 | g0122 | EUR | IBS | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01517 | hp2 | a0001 | c0001 | t0005 | g0027 | EUR | IBS | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01884 | hp1 | a0001 | c0001 | t0011 | g0061 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01884 | hp2 | a0001 | c0001 | t0018 | g0020 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01891 | hp1 | a0001 | c0001 | t0066 | g0067 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01891 | hp2 | a0001 | c0001 | t0019 | g0151 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0119 | AMR | PEL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01934 | hp2 | a0001 | c0001 | t0006 | g0016 | AMR | PEL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01978 | hp1 | a0001 | c0001 | t0053 | g0179 | AMR | PEL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01978 | hp2 | a0001 | c0001 | t0033 | g0029 | AMR | PEL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02055 | hp1 | a0001 | c0001 | t0010 | g0057 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02055 | hp2 | a0001 | c0001 | t0005 | g0008 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | KHV | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | KHV | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02074 | hp2 | a0001 | c0001 | t0031 | g0148 | EAS | KHV | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | KHV | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02080 | hp2 | a0001 | c0001 | t0039 | g0080 | EAS | KHV | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | KHV | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02145 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02145 | hp2 | a0001 | c0001 | t0011 | g0063 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02148 | hp1 | a0001 | c0001 | t0004 | g0082 | AMR | PEL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | CDX | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CDX | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02257 | hp1 | a0001 | c0001 | t0023 | g0054 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02257 | hp2 | a0001 | c0001 | t0020 | g0011 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02258 | hp1 | a0001 | c0001 | t0011 | g0062 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02258 | hp2 | a0001 | c0001 | t0010 | g0055 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02280 | hp1 | a0001 | c0001 | t0032 | g0117 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02280 | hp2 | a0001 | c0001 | t0045 | g0007 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02451 | hp1 | a0001 | c0001 | t0023 | g0042 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02451 | hp2 | a0001 | c0001 | t0007 | g0031 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02615 | hp1 | a0001 | c0001 | t0011 | g0068 | AFR | GWD | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02615 | hp2 | a0001 | c0001 | t0036 | g0120 | AFR | GWD | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02622 | hp1 | a0001 | c0001 | t0015 | g0046 | AFR | GWD | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02630 | hp1 | a0001 | c0001 | t0010 | g0022 | AFR | GWD | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02630 | hp2 | a0001 | c0001 | t0005 | g0104 | AFR | GWD | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02647 | hp1 | a0001 | c0001 | t0009 | g0010 | AFR | GWD | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02647 | hp2 | a0001 | c0001 | t0021 | g0014 | AFR | GWD | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02683 | hp1 | a0001 | c0001 | t0008 | g0124 | SAS | PJL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02698 | hp2 | a0001 | c0001 | t0058 | g0135 | SAS | PJL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02717 | hp1 | a0001 | c0001 | t0024 | g0130 | AFR | GWD | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02717 | hp2 | a0001 | c0001 | t0007 | g0127 | AFR | GWD | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02723 | hp1 | a0001 | c0001 | t0035 | g0126 | AFR | GWD | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0107 | SAS | PJL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02735 | hp2 | a0001 | c0001 | t0054 | g0002 | SAS | PJL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0108 | SAS | PJL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02738 | hp2 | a0001 | c0001 | t0028 | g0164 | SAS | PJL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02818 | hp1 | a0001 | c0001 | t0009 | g0048 | AFR | GWD | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02818 | hp2 | a0001 | c0001 | t0047 | g0022 | AFR | GWD | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02886 | hp1 | a0001 | c0001 | t0009 | g0044 | AFR | GWD | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02886 | hp2 | a0001 | c0001 | t0020 | g0011 | AFR | GWD | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02922 | hp1 | a0001 | c0001 | t0018 | g0020 | AFR | ESN | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02922 | hp2 | a0001 | c0001 | t0021 | g0014 | AFR | ESN | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02965 | hp1 | a0001 | c0001 | t0017 | g0190 | AFR | ESN | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02965 | hp2 | a0001 | c0001 | t0011 | g0059 | AFR | ESN | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03041 | hp1 | a0001 | c0001 | t0015 | g0045 | AFR | GWD | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03041 | hp2 | a0001 | c0001 | t0024 | g0131 | AFR | GWD | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03098 | hp1 | a0001 | c0001 | t0007 | g0133 | AFR | MSL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03098 | hp2 | a0001 | c0001 | t0009 | g0010 | AFR | MSL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03130 | hp1 | a0001 | c0001 | t0015 | g0053 | AFR | ESN | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03130 | hp2 | a0001 | c0001 | t0007 | g0017 | AFR | ESN | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03139 | hp1 | a0001 | c0001 | t0009 | g0010 | AFR | ESN | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03139 | hp2 | a0001 | c0001 | t0025 | g0032 | AFR | ESN | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03195 | hp1 | a0001 | c0001 | t0025 | g0032 | AFR | ESN | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03195 | hp2 | a0001 | c0001 | t0010 | g0056 | AFR | ESN | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03209 | hp1 | a0001 | c0001 | t0038 | g0114 | AFR | MSL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03209 | hp2 | a0001 | c0001 | t0009 | g0049 | AFR | MSL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03225 | hp1 | a0001 | c0001 | t0005 | g0008 | AFR | MSL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03225 | hp2 | a0001 | c0001 | t0048 | g0129 | AFR | MSL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03239 | hp1 | a0001 | c0001 | t0005 | g0029 | SAS | PJL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | MSL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03453 | hp2 | a0001 | c0001 | t0019 | g0146 | AFR | MSL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03490 | hp2 | a0001 | c0001 | t0006 | g0123 | SAS | PJL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0189 | SAS | PJL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03516 | hp1 | a0001 | c0001 | t0015 | g0047 | AFR | ESN | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03516 | hp2 | a0001 | c0001 | t0013 | g0095 | AFR | ESN | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03540 | hp1 | a0001 | c0001 | t0037 | g0052 | AFR | GWD | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03540 | hp2 | a0001 | c0001 | t0051 | g0018 | AFR | GWD | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03579 | hp1 | a0001 | c0001 | t0009 | g0051 | AFR | MSL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03579 | hp2 | a0001 | c0001 | t0014 | g0005 | AFR | MSL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03654 | hp1 | a0001 | c0001 | t0050 | g0005 | SAS | PJL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0083 | SAS | PJL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03669 | hp2 | a0001 | c0001 | t0006 | g0005 | SAS | PJL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03688 | hp1 | a0001 | c0001 | t0004 | g0087 | SAS | STU | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | STU | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03710 | hp1 | a0001 | c0001 | t0008 | g0015 | SAS | PJL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03710 | hp2 | a0001 | c0001 | t0022 | g0004 | SAS | PJL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03831 | hp1 | a0001 | c0001 | t0042 | g0084 | SAS | BEB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | BEB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03834 | hp1 | a0001 | c0001 | t0006 | g0128 | SAS | BEB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03927 | hp1 | a0001 | c0001 | t0044 | g0001 | SAS | BEB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03927 | hp2 | a0001 | c0001 | t0031 | g0006 | SAS | BEB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0086 | SAS | BEB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG03942 | hp2 | a0001 | c0001 | t0022 | g0004 | SAS | BEB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG04199 | hp1 | a0001 | c0001 | t0008 | g0005 | SAS | STU | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | STU | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG04204 | hp1 | a0001 | c0001 | t0004 | g0013 | SAS | STU | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | STU | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG04228 | hp1 | a0001 | c0001 | t0028 | g0002 | SAS | STU | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG04228 | hp2 | a0001 | c0001 | t0004 | g0007 | SAS | STU | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18522 | hp1 | a0001 | c0001 | t0010 | g0041 | AFR | YRI | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18522 | hp2 | a0001 | c0001 | t0019 | g0018 | AFR | YRI | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18906 | hp1 | a0001 | c0001 | t0017 | g0039 | AFR | YRI | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18906 | hp2 | a0001 | c0001 | t0018 | g0020 | AFR | YRI | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18943 | hp1 | a0001 | c0001 | t0041 | g0001 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18946 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18952 | hp2 | a0001 | c0001 | t0030 | g0154 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18954 | hp2 | a0001 | c0001 | t0005 | g0102 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18957 | hp1 | a0001 | c0001 | t0059 | g0165 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18967 | hp2 | a0001 | c0001 | t0046 | g0009 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18968 | hp1 | a0001 | c0001 | t0060 | g0037 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18982 | hp2 | a0001 | c0001 | t0040 | g0081 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18983 | hp1 | a0001 | c0001 | t0012 | g0006 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18986 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18989 | hp1 | a0001 | c0001 | t0029 | g0141 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18990 | hp1 | a0001 | c0001 | t0056 | g0037 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18991 | hp1 | a0001 | c0001 | t0034 | g0098 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18992 | hp2 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19000 | hp2 | a0001 | c0001 | t0067 | g0138 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19006 | hp1 | a0001 | c0001 | t0057 | g0144 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19006 | hp2 | a0001 | c0001 | t0004 | g0078 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19011 | hp1 | a0001 | c0001 | t0030 | g0178 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19011 | hp2 | a0001 | c0001 | t0012 | g0002 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | LWK | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19030 | hp2 | a0001 | c0001 | t0007 | g0017 | AFR | LWK | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19043 | hp1 | a0001 | c0001 | t0064 | g0115 | AFR | LWK | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19043 | hp2 | a0001 | c0001 | t0049 | g0069 | AFR | LWK | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19054 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19055 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19068 | hp1 | a0001 | c0001 | t0012 | g0006 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19068 | hp2 | a0002 | c0002 | t0002 | g0073 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19080 | hp1 | a0001 | c0001 | t0012 | g0072 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19083 | hp2 | a0001 | c0001 | t0029 | g0181 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19091 | hp1 | a0001 | c0003 | t0002 | g0085 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19240 | hp1 | a0001 | c0001 | t0021 | g0014 | AFR | YRI | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA19240 | hp2 | a0001 | c0001 | t0007 | g0017 | AFR | YRI | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA20129 | hp1 | a0001 | c0001 | t0061 | g0182 | AFR | ASW | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA20129 | hp2 | a0001 | c0001 | t0007 | g0031 | AFR | ASW | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA20752 | hp1 | a0001 | c0001 | t0027 | g0003 | EUR | TSI | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA20752 | hp2 | a0001 | c0001 | t0014 | g0005 | EUR | TSI | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA20805 | hp1 | a0001 | c0001 | t0020 | g0011 | EUR | TSI | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA20805 | hp2 | a0001 | c0001 | t0006 | g0005 | EUR | TSI | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | GIH | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | GIH | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0027 | AMR | CLM | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG01123 | hp2 | a0001 | c0001 | t0006 | g0015 | AMR | CLM | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02109 | hp1 | a0001 | c0001 | t0005 | g0105 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02109 | hp2 | a0001 | c0001 | t0010 | g0043 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02486 | hp1 | a0001 | c0001 | t0005 | g0099 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02486 | hp2 | a0001 | c0001 | t0007 | g0132 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02559 | hp1 | a0001 | c0001 | t0032 | g0116 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG02559 | hp2 | a0001 | c0001 | t0062 | g0065 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG06807 | hp1 | a0001 | c0001 | t0008 | g0005 | AFR | USA | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | USA | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA20300 | hp1 | a0001 | c0001 | t0005 | g0007 | AFR | USA | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | USA | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA21309 | hp1 | a0001 | c0001 | t0005 | g0060 | AFR | LWK | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
NA21309 | hp2 | a0001 | c0001 | t0013 | g0093 | AFR | LWK | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0027 | g0021 | REF | REF | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0136 | REF | REF | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:72331317
|
T | C | 1 | a0002 | 1 | NA19068.hp2 | missense_variant | MODERATE | c.410T>C | p.Val137Ala | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/10 | 420/11145 | 410/1167 | 137/388 | chr5 | 72331317 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:72358361
|
A | G | 1 | a0001c0003 | 1 | NA19091.hp1 | synonymous_variant | LOW | c.1101A>G | p.Leu367Leu | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 1111/11145 | 1101/1167 | 367/388 | chr5 | 72358361 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:72358590
|
G | T | 1 | a0001c0001t0067 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*163G>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 163 | chr5 | 72358590 | |||||
chr5:72358592
|
T | C | 1 | a0001c0001t0034 | 1 | NA18991.hp1 | 3_prime_UTR_variant | MODIFIER | c.*165T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 165 | chr5 | 72358592 | |||||
chr5:72358602
|
C | A | 1 | a0001c0001t0035 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*175C>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 175 | chr5 | 72358602 | |||||
chr5:72358670
|
C | T | 1 | a0001c0001t0033 | 2 | HG01261.hp1 HG01978.hp2 |
3_prime_UTR_variant | MODIFIER | c.*243C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 243 | chr5 | 72358670 | |||||
chr5:72358695
|
G | T | 1 | a0001c0001t0066 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*268G>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 268 | chr5 | 72358695 | |||||
chr5:72358755
|
C | T | 1 | a0001c0001t0065 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*328C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 328 | chr5 | 72358755 | |||||
chr5:72358899
|
A | C | 3 | a0001c0001t0021a0001c0001t0032a0001c0001t0064 | 6 | HG02280.hp1 HG02559.hp1 HG02647.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*472A>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 472 | chr5 | 72358899 | |||||
chr5:72358931
|
A | G | 5 | a0001c0001t0011a0001c0001t0020a0001c0001t0062others(2): Show | 12 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*504A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 504 | chr5 | 72358931 | |||||
chr5:72359028
|
G | C | 48 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(45): Show | 205 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*601G>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 601 | chr5 | 72359028 | |||||
chr5:72359110
|
G | A | 5 | a0001c0001t0011a0001c0001t0020a0001c0001t0062others(2): Show | 12 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*683G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 683 | chr5 | 72359110 | |||||
chr5:72359200
|
C | G | 1 | a0001c0001t0035 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*773C>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 773 | chr5 | 72359200 | |||||
chr5:72359203
|
T | C | 3 | a0001c0001t0007a0001c0001t0036a0001c0001t0037 | 10 | HG02451.hp2 HG02486.hp2 HG02615.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*776T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 776 | chr5 | 72359203 | |||||
chr5:72359356
|
G | A | 21 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(18): Show | 121 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*929G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 929 | chr5 | 72359356 | |||||
chr5:72359423
|
A | C | 3 | a0001c0001t0021a0001c0001t0032a0001c0001t0064 | 6 | HG02280.hp1 HG02559.hp1 HG02647.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*996A>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 996 | chr5 | 72359423 | |||||
chr5:72359473
|
G | T | 1 | a0001c0001t0022 | 2 | HG03710.hp2 HG03942.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1046G>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 1046 | chr5 | 72359473 | |||||
chr5:72359529
|
C | G | 1 | a0001c0001t0050 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1102C>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 1102 | chr5 | 72359529 | |||||
chr5:72360005
|
T | C | 1 | a0001c0001t0022 | 2 | HG03710.hp2 HG03942.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1578T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 1578 | chr5 | 72360005 | |||||
chr5:72360016
|
A | G | 3 | a0001c0001t0021a0001c0001t0032a0001c0001t0064 | 6 | HG02280.hp1 HG02559.hp1 HG02647.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1589A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 1589 | chr5 | 72360016 | |||||
chr5:72360209
|
CA | C | 5 | a0001c0001t0021a0001c0001t0032a0001c0001t0035others(2): Show | 8 | HG02280.hp1 HG02559.hp1 HG02647.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1798delA | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 1798 | INFO_REALIGN_3_PRIME | chr5 | 72360209 | ||||
chr5:72360346
|
T | C | 1 | a0001c0001t0051 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1919T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 1919 | chr5 | 72360346 | |||||
chr5:72360381
|
G | A | 1 | a0001c0001t0062 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1954G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 1954 | chr5 | 72360381 | |||||
chr5:72360531
|
G | A | 1 | a0001c0001t0017 | 3 | HG01074.hp2 HG02965.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2104G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 2104 | chr5 | 72360531 | |||||
chr5:72360735
|
AGTGCAGT others(1): Show |
A | 4 | a0001c0001t0007a0001c0001t0035a0001c0001t0036others(1): Show | 11 | HG02451.hp2 HG02486.hp2 HG02615.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2312_*2319delCAGT others(4): Show |
PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 2312 | INFO_REALIGN_3_PRIME | chr5 | 72360735 | ||||
chr5:72360780
|
G | A | 1 | a0001c0001t0012 | 5 | HG00621.hp1 NA18983.hp1 NA19011.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2353G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 2353 | chr5 | 72360780 | |||||
chr5:72360795
|
A | G | 1 | a0001c0001t0026 | 2 | HG01069.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2368A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 2368 | chr5 | 72360795 | |||||
chr5:72360822
|
A | G | 1 | a0001c0001t0050 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2395A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 2395 | chr5 | 72360822 | |||||
chr5:72361065
|
T | C | 1 | a0001c0001t0038 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2638T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 2638 | chr5 | 72361065 | |||||
chr5:72361194
|
T | G | 3 | a0001c0001t0007a0001c0001t0036a0001c0001t0037 | 10 | HG02451.hp2 HG02486.hp2 HG02615.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2767T>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 2767 | chr5 | 72361194 | |||||
chr5:72361367
|
G | A | 1 | a0001c0001t0039 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2940G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 2940 | chr5 | 72361367 | |||||
chr5:72361488
|
G | A | 3 | a0001c0001t0016a0001c0001t0022a0001c0001t0065 | 6 | HG00140.hp1 HG01168.hp1 HG01169.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3061G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 3061 | chr5 | 72361488 | |||||
chr5:72361552
|
A | G | 1 | a0001c0001t0060 | 1 | NA18968.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3125A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 3125 | chr5 | 72361552 | |||||
chr5:72361587
|
G | A | 5 | a0001c0001t0006a0001c0001t0008a0001c0001t0014others(2): Show | 25 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*3160G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 3160 | chr5 | 72361587 | |||||
chr5:72361609
|
A | G | 1 | a0001c0001t0059 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3182A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 3182 | chr5 | 72361609 | |||||
chr5:72361725
|
G | A | 5 | a0001c0001t0009a0001c0001t0010a0001c0001t0015others(2): Show | 21 | HG00741.hp1 HG02055.hp1 HG02109.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*3298G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 3298 | chr5 | 72361725 | |||||
chr5:72361833
|
T | G | 1 | a0001c0001t0040 | 1 | NA18982.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3406T>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 3406 | chr5 | 72361833 | |||||
chr5:72362137
|
T | C | 1 | a0001c0001t0048 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3710T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 3710 | chr5 | 72362137 | |||||
chr5:72362278
|
G | C | 5 | a0001c0001t0011a0001c0001t0020a0001c0001t0062others(2): Show | 12 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3851G>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 3851 | chr5 | 72362278 | |||||
chr5:72362653
|
A | G | 1 | a0001c0001t0058 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4226A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 4226 | chr5 | 72362653 | |||||
chr5:72362674
|
T | C | 1 | a0001c0001t0015 | 4 | HG02622.hp1 HG03041.hp1 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4247T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 4247 | chr5 | 72362674 | |||||
chr5:72362705
|
A | G | 1 | a0001c0001t0057 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4278A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 4278 | chr5 | 72362705 | |||||
chr5:72362760
|
A | G | 1 | a0001c0001t0035 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4333A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 4333 | chr5 | 72362760 | |||||
chr5:72362823
|
C | G | 2 | a0001c0001t0016a0001c0001t0065 | 4 | HG00140.hp1 HG01168.hp1 HG01169.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4396C>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 4396 | chr5 | 72362823 | |||||
chr5:72363007
|
T | C | 5 | a0001c0001t0009a0001c0001t0010a0001c0001t0015others(2): Show | 21 | HG00741.hp1 HG02055.hp1 HG02109.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*4580T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 4580 | chr5 | 72363007 | |||||
chr5:72363103
|
T | C | 3 | a0001c0001t0021a0001c0001t0032a0001c0001t0064 | 6 | HG02280.hp1 HG02559.hp1 HG02647.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4676T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 4676 | chr5 | 72363103 | |||||
chr5:72363629
|
C | T | 5 | a0001c0001t0011a0001c0001t0020a0001c0001t0062others(2): Show | 12 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*5202C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 5202 | chr5 | 72363629 | |||||
chr5:72364262
|
C | T | 1 | a0001c0001t0046 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5835C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 5835 | chr5 | 72364262 | |||||
chr5:72364279
|
G | A | 5 | a0001c0001t0009a0001c0001t0010a0001c0001t0015others(2): Show | 21 | HG00741.hp1 HG02055.hp1 HG02109.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*5852G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 5852 | chr5 | 72364279 | |||||
chr5:72364404
|
G | C | 2 | a0001c0001t0024a0001c0001t0025 | 4 | HG02717.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5977G>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 5977 | chr5 | 72364404 | |||||
chr5:72364538
|
C | A | 1 | a0001c0001t0052 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6111C>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 6111 | chr5 | 72364538 | |||||
chr5:72364582
|
T | A | 1 | a0001c0001t0041 | 1 | NA18943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6155T>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 6155 | chr5 | 72364582 | |||||
chr5:72364619
|
C | T | 1 | a0001c0001t0017 | 3 | HG01074.hp2 HG02965.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6192C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 6192 | chr5 | 72364619 | |||||
chr5:72364685
|
A | T | 2 | a0001c0001t0024a0001c0001t0025 | 4 | HG02717.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6258A>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 6258 | chr5 | 72364685 | |||||
chr5:72364923
|
C | A | 1 | a0001c0001t0017 | 3 | HG01074.hp2 HG02965.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6496C>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 6496 | chr5 | 72364923 | |||||
chr5:72364924
|
G | T | 1 | a0001c0001t0017 | 3 | HG01074.hp2 HG02965.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6497G>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 6497 | chr5 | 72364924 | |||||
chr5:72365012
|
T | A | 15 | a0001c0001t0002a0001c0001t0004a0001c0001t0013others(12): Show | 82 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*6585T>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 6585 | chr5 | 72365012 | |||||
chr5:72365080
|
G | T | 1 | a0001c0001t0066 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6653G>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 6653 | chr5 | 72365080 | |||||
chr5:72365304
|
T | C | 1 | a0001c0001t0027 | 2 | NA20752.hp1 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6877T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 6877 | chr5 | 72365304 | |||||
chr5:72365568
|
A | G | 1 | a0001c0001t0056 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7141A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 7141 | chr5 | 72365568 | |||||
chr5:72365584
|
G | A | 1 | a0001c0001t0042 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7157G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 7157 | chr5 | 72365584 | |||||
chr5:72365688
|
G | A | 1 | a0001c0001t0053 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7261G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 7261 | chr5 | 72365688 | |||||
chr5:72365761
|
A | G | 22 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(19): Show | 123 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*7334A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 7334 | chr5 | 72365761 | |||||
chr5:72365771
|
A | G | 6 | a0001c0001t0011a0001c0001t0020a0001c0001t0048others(3): Show | 13 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*7344A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 7344 | chr5 | 72365771 | |||||
chr5:72366000
|
G | C | 6 | a0001c0001t0011a0001c0001t0020a0001c0001t0048others(3): Show | 13 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*7573G>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 7573 | chr5 | 72366000 | |||||
chr5:72366007
|
G | A | 6 | a0001c0001t0011a0001c0001t0020a0001c0001t0048others(3): Show | 13 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*7580G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 7580 | chr5 | 72366007 | |||||
chr5:72366066
|
A | T | 2 | a0001c0001t0008a0001c0001t0026 | 10 | HG00642.hp2 HG01069.hp2 HG01071.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*7639A>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 7639 | chr5 | 72366066 | |||||
chr5:72366108
|
C | T | 1 | a0001c0001t0023 | 2 | HG02257.hp1 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7681C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 7681 | chr5 | 72366108 | |||||
chr5:72366483
|
A | G | 1 | a0001c0001t0036 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8056A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 8056 | chr5 | 72366483 | |||||
chr5:72366590
|
G | A | 1 | a0001c0001t0043 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8163G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 8163 | chr5 | 72366590 | |||||
chr5:72366641
|
T | A | 1 | a0001c0001t0028 | 2 | HG02738.hp2 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8214T>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 8214 | chr5 | 72366641 | |||||
chr5:72366687
|
A | G | 2 | a0001c0001t0036a0001c0001t0048 | 2 | HG02615.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8260A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 8260 | chr5 | 72366687 | |||||
chr5:72367125
|
C | A | 3 | a0001c0001t0007a0001c0001t0013a0001c0001t0049 | 13 | HG01167.hp1 HG01243.hp2 HG02451.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*8698C>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 8698 | chr5 | 72367125 | |||||
chr5:72367172
|
T | C | 1 | a0001c0001t0029 | 2 | NA18989.hp1 NA19083.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8745T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 8745 | chr5 | 72367172 | |||||
chr5:72367355
|
A | G | 1 | a0001c0001t0055 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8928A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 8928 | chr5 | 72367355 | |||||
chr5:72367522
|
A | G | 1 | a0001c0001t0054 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9095A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 9095 | chr5 | 72367522 | |||||
chr5:72367569
|
C | T | 2 | a0001c0001t0019a0001c0001t0051 | 4 | HG01891.hp2 HG03453.hp2 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*9142C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 9142 | chr5 | 72367569 | |||||
chr5:72367643
|
T | G | 4 | a0001c0001t0007a0001c0001t0013a0001c0001t0035others(1): Show | 14 | HG01167.hp1 HG01243.hp2 HG02451.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*9216T>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 9216 | chr5 | 72367643 | |||||
chr5:72367759
|
G | A | 1 | a0001c0001t0044 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9332G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 9332 | chr5 | 72367759 | |||||
chr5:72367771
|
G | A | 19 | a0001c0001t0002a0001c0001t0003a0001c0001t0011others(16): Show | 98 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*9344G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 9344 | chr5 | 72367771 | |||||
chr5:72368204
|
G | A | 7 | a0001c0001t0006a0001c0001t0008a0001c0001t0026others(4): Show | 24 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*9777G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 9777 | chr5 | 72368204 | |||||
chr5:72368358
|
C | T | 6 | a0001c0001t0009a0001c0001t0018a0001c0001t0025others(3): Show | 16 | HG00741.hp1 HG01884.hp2 HG02615.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*9931C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 9931 | chr5 | 72368358 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:72320651
|
G | A | 1 | a0001c0001t0003g0040 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.127+142G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 1/9 | chr5 | 72320651 | ||||||
chr5:72320690
|
C | T | 1 | a0001c0001t0008g0192 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.127+181C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 1/9 | chr5 | 72320690 | ||||||
chr5:72320743
|
T | C | 20 | a0001c0001t0009g0010a0001c0001t0009g0044a0001c0001t0009g0048others(17): Show | 22 | HG00741.hp1 HG02055.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.127+234T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 1/9 | chr5 | 72320743 | ||||||
chr5:72320787
|
C | T | 1 | a0001c0001t0001g0191 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.127+278C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 1/9 | chr5 | 72320787 | ||||||
chr5:72320907
|
G | A | 1 | a0001c0001t0001g0058 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.127+398G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 1/9 | chr5 | 72320907 | ||||||
chr5:72320993
|
G | A | 11 | a0001c0001t0005g0060a0001c0001t0011g0059a0001c0001t0011g0061others(8): Show | 13 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.127+484G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 1/9 | chr5 | 72320993 | ||||||
chr5:72321428
|
C | T | 2 | a0001c0001t0017g0039a0001c0001t0017g0190 | 3 | HG01074.hp2 HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.128-744C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 1/9 | chr5 | 72321428 | ||||||
chr5:72321472
|
G | T | 1 | a0001c0001t0003g0189 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.128-700G>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 1/9 | chr5 | 72321472 | ||||||
chr5:72321735
|
T | C | 144 | a0001c0001t0001g0110a0001c0001t0002g0001a0001c0001t0002g0009others(141): Show | 206 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.128-437T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 1/9 | chr5 | 72321735 | ||||||
chr5:72321833
|
G | A | 1 | a0001c0001t0049g0069 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.128-339G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 1/9 | chr5 | 72321833 | ||||||
chr5:72321862
|
G | A | 1 | a0001c0001t0010g0041 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.128-310G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 1/9 | chr5 | 72321862 | ||||||
chr5:72322009
|
T | G | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.128-163T>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 1/9 | chr5 | 72322009 | ||||||
chr5:72322082
|
A | G | 4 | a0001c0001t0010g0041a0001c0001t0010g0055a0001c0001t0010g0056others(1): Show | 4 | HG02055.hp1 HG02258.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-90A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 1/9 | chr5 | 72322082 | ||||||
chr5:72322449
|
C | A | 75 | a0001c0001t0001g0110a0001c0001t0002g0001a0001c0001t0002g0009others(72): Show | 119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.220+185C>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | chr5 | 72322449 | ||||||
chr5:72322640
|
A | G | 2 | a0001c0001t0017g0039a0001c0001t0017g0190 | 3 | HG01074.hp2 HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.220+376A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | chr5 | 72322640 | ||||||
chr5:72322728
|
T | C | 1 | a0001c0001t0003g0070 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.220+464T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | chr5 | 72322728 | ||||||
chr5:72322857
|
C | G | 1 | a0001c0001t0038g0114 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.220+593C>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | chr5 | 72322857 | ||||||
chr5:72322946
|
G | C | 4 | a0001c0001t0021g0014a0001c0001t0032g0116a0001c0001t0032g0117others(1): Show | 6 | HG02280.hp1 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.220+682G>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | chr5 | 72322946 | ||||||
chr5:72323148
|
T | C | 1 | a0001c0001t0058g0135 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.220+884T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | chr5 | 72323148 | ||||||
chr5:72323849
|
G | C | 2 | a0001c0001t0017g0039a0001c0001t0017g0190 | 3 | HG01074.hp2 HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.220+1585G>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | chr5 | 72323849 | ||||||
chr5:72323892
|
C | T | 1 | a0001c0001t0001g0188 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.220+1628C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | chr5 | 72323892 | ||||||
chr5:72323893
|
G | A | 3 | a0001c0001t0002g0023a0001c0001t0002g0071a0001c0001t0012g0072 | 4 | NA18968.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+1629G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | chr5 | 72323893 | ||||||
chr5:72324170
|
A | G | 1 | a0001c0001t0023g0054 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.220+1906A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | chr5 | 72324170 | ||||||
chr5:72324418
|
A | G | 223 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(220): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.220+2154A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | chr5 | 72324418 | ||||||
chr5:72324695
|
T | C | 1 | a0002c0002t0002g0073 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.221-1917T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | chr5 | 72324695 | ||||||
chr5:72324926
|
G | GT | 5 | a0001c0001t0007g0017a0001c0001t0007g0132a0001c0001t0007g0133others(2): Show | 7 | HG02055.hp1 HG02486.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.221-1674dupT | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 72324926 | |||||
chr5:72325067
|
C | T | 3 | a0001c0001t0024g0130a0001c0001t0024g0131a0001c0001t0025g0032 | 4 | HG02717.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-1545C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | chr5 | 72325067 | ||||||
chr5:72325549
|
C | T | 1 | a0001c0001t0001g0187 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.221-1063C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | chr5 | 72325549 | ||||||
chr5:72325601
|
G | A | 52 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0012others(49): Show | 88 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.221-1011G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | chr5 | 72325601 | ||||||
chr5:72325838
|
C | G | 3 | a0001c0001t0024g0130a0001c0001t0024g0131a0001c0001t0025g0032 | 4 | HG02717.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-774C>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | chr5 | 72325838 | ||||||
chr5:72325862
|
C | G | 3 | a0001c0001t0024g0130a0001c0001t0024g0131a0001c0001t0025g0032 | 4 | HG02717.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-750C>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | chr5 | 72325862 | ||||||
chr5:72325916
|
G | A | 2 | a0001c0001t0023g0042a0001c0001t0023g0054 | 2 | HG02257.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.221-696G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | chr5 | 72325916 | ||||||
chr5:72326067
|
G | C | 3 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0067g0138 | 3 | NA18948.hp2 NA19000.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.221-545G>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | chr5 | 72326067 | ||||||
chr5:72326111
|
A | G | 2 | a0001c0001t0001g0185a0001c0001t0001g0186 | 2 | HG02698.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.221-501A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | chr5 | 72326111 | ||||||
chr5:72326817
|
T | G | 1 | a0001c0001t0010g0043 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.350+76T>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72326817 | ||||||
chr5:72326949
|
TA | T | 4 | a0001c0001t0021g0014a0001c0001t0032g0116a0001c0001t0032g0117others(1): Show | 6 | HG02280.hp1 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.350+210delA | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 72326949 | |||||
chr5:72327210
|
C | T | 1 | a0001c0001t0049g0069 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.350+469C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72327210 | ||||||
chr5:72327313
|
A | G | 1 | a0001c0001t0004g0100 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.350+572A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72327313 | ||||||
chr5:72327353
|
T | A | 3 | a0001c0001t0005g0060a0001c0001t0011g0059a0001c0001t0011g0061 | 3 | HG01884.hp1 HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.350+612T>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72327353 | ||||||
chr5:72327472
|
A | AT | 115 | a0001c0001t0001g0110a0001c0001t0001g0134a0001c0001t0001g0183others(112): Show | 167 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.350+748dupT | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 72327472 | |||||
chr5:72327472
|
A | ATT | 4 | a0001c0001t0004g0013a0001c0001t0032g0116a0001c0001t0032g0117others(1): Show | 6 | HG00741.hp2 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.350+747_350+748dup others(2): Show |
PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 72327472 | |||||
chr5:72327679
|
G | T | 22 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0038others(19): Show | 37 | HG00140.hp2 HG00621.hp2 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.350+938G>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72327679 | ||||||
chr5:72328386
|
A | C | 1 | a0001c0001t0001g0166 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.350+1645A>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72328386 | ||||||
chr5:72328542
|
A | G | 1 | a0001c0001t0005g0099 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.350+1801A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72328542 | ||||||
chr5:72328847
|
T | A | 1 | a0001c0001t0035g0126 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.350+2106T>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72328847 | ||||||
chr5:72328869
|
C | T | 2 | a0001c0001t0017g0039a0001c0001t0017g0190 | 3 | HG01074.hp2 HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.350+2128C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72328869 | ||||||
chr5:72328871
|
C | T | 1 | a0001c0001t0059g0165 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.350+2130C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72328871 | ||||||
chr5:72328872
|
G | A | 1 | a0001c0001t0009g0044 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.350+2131G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72328872 | ||||||
chr5:72329013
|
C | T | 223 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(220): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.351-2245C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72329013 | ||||||
chr5:72329085
|
T | C | 1 | a0001c0001t0002g0076 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.351-2173T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72329085 | ||||||
chr5:72329168
|
A | C | 20 | a0001c0001t0009g0010a0001c0001t0009g0044a0001c0001t0009g0048others(17): Show | 22 | HG00741.hp1 HG02055.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.351-2090A>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72329168 | ||||||
chr5:72329179
|
C | A | 4 | a0001c0001t0021g0014a0001c0001t0032g0116a0001c0001t0032g0117others(1): Show | 6 | HG02280.hp1 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.351-2079C>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72329179 | ||||||
chr5:72329314
|
C | T | 1 | a0001c0001t0025g0032 | 2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.351-1944C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72329314 | ||||||
chr5:72329438
|
C | G | 4 | a0001c0001t0021g0014a0001c0001t0032g0116a0001c0001t0032g0117others(1): Show | 6 | HG02280.hp1 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.351-1820C>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72329438 | ||||||
chr5:72329681
|
GC | G | 73 | a0001c0001t0001g0110a0001c0001t0002g0001a0001c0001t0002g0009others(70): Show | 117 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.351-1575delC | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 72329681 | |||||
chr5:72329712
|
A | G | 1 | a0001c0001t0049g0069 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.351-1546A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72329712 | ||||||
chr5:72329734
|
T | C | 11 | a0001c0001t0005g0060a0001c0001t0011g0059a0001c0001t0011g0061others(8): Show | 13 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.351-1524T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72329734 | ||||||
chr5:72329936
|
C | CT | 80 | a0001c0001t0001g0110a0001c0001t0001g0162a0001c0001t0001g0163others(77): Show | 124 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.351-1308dupT | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 72329936 | |||||
chr5:72330038
|
T | C | 2 | a0001c0001t0017g0039a0001c0001t0017g0190 | 3 | HG01074.hp2 HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.351-1220T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72330038 | ||||||
chr5:72330081
|
C | T | 11 | a0001c0001t0005g0060a0001c0001t0011g0059a0001c0001t0011g0061others(8): Show | 13 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.351-1177C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72330081 | ||||||
chr5:72330162
|
G | A | 2 | a0001c0001t0001g0033a0001c0001t0029g0141 | 3 | NA18942.hp1 NA18989.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.351-1096G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72330162 | ||||||
chr5:72330191
|
C | T | 1 | a0001c0001t0002g0096 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.351-1067C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72330191 | ||||||
chr5:72330235
|
C | T | 1 | a0001c0001t0053g0179 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.351-1023C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72330235 | ||||||
chr5:72330782
|
G | C | 11 | a0001c0001t0005g0060a0001c0001t0011g0059a0001c0001t0011g0061others(8): Show | 13 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.351-476G>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72330782 | ||||||
chr5:72330969
|
C | T | 1 | a0001c0001t0030g0178 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.351-289C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72330969 | ||||||
chr5:72330975
|
G | T | 1 | a0001c0001t0003g0112 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.351-283G>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72330975 | ||||||
chr5:72331098
|
A | G | 1 | a0001c0001t0015g0053 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.351-160A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72331098 | ||||||
chr5:72331427
|
T | C | 1 | a0001c0001t0001g0142 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.468+52T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72331427 | ||||||
chr5:72331486
|
G | T | 1 | a0001c0001t0001g0140 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.468+111G>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72331486 | ||||||
chr5:72331776
|
C | T | 4 | a0001c0001t0013g0092a0001c0001t0013g0093a0001c0001t0013g0094others(1): Show | 4 | HG01167.hp1 HG01243.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.468+401C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72331776 | ||||||
chr5:72331921
|
T | C | 1 | a0001c0001t0005g0077 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.468+546T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72331921 | ||||||
chr5:72332025
|
AC | A | 1 | a0001c0001t0002g0012 | 3 | HG00408.hp1 HG02074.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.468+651delC | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72332025 | ||||||
chr5:72332361
|
T | A | 1 | a0001c0001t0001g0143 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.468+986T>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72332361 | ||||||
chr5:72332449
|
C | A | 1 | a0001c0001t0001g0143 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.468+1074C>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72332449 | ||||||
chr5:72332473
|
G | A | 2 | a0001c0001t0032g0116a0001c0001t0032g0117 | 2 | HG02280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.468+1098G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72332473 | ||||||
chr5:72332528
|
CTA | C | 15 | a0001c0001t0001g0161a0001c0001t0006g0005a0001c0001t0006g0016others(12): Show | 22 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.468+1155_468+1156d others(4): Show |
PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 72332528 | |||||
chr5:72332614
|
AT | A | 3 | a0001c0001t0024g0130a0001c0001t0024g0131a0001c0001t0025g0032 | 4 | HG02717.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.468+1240delT | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72332614 | ||||||
chr5:72332757
|
G | A | 11 | a0001c0001t0005g0060a0001c0001t0011g0059a0001c0001t0011g0061others(8): Show | 13 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.468+1382G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72332757 | ||||||
chr5:72332931
|
A | G | 7 | a0001c0001t0009g0010a0001c0001t0009g0044a0001c0001t0009g0048others(4): Show | 9 | HG00741.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.468+1556A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72332931 | ||||||
chr5:72332944
|
A | G | 2 | a0001c0001t0017g0039a0001c0001t0017g0190 | 3 | HG01074.hp2 HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.468+1569A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72332944 | ||||||
chr5:72333128
|
C | T | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | NA18983.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.468+1753C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72333128 | ||||||
chr5:72333198
|
G | A | 1 | a0001c0001t0013g0092 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.469-1820G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72333198 | ||||||
chr5:72333329
|
A | G | 1 | a0001c0001t0033g0111 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.469-1689A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72333329 | ||||||
chr5:72333348
|
C | T | 1 | a0001c0001t0004g0091 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.469-1670C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72333348 | ||||||
chr5:72333529
|
C | G | 2 | a0001c0001t0032g0116a0001c0001t0032g0117 | 2 | HG02280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.469-1489C>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72333529 | ||||||
chr5:72333529
|
C | T | 1 | a0001c0001t0049g0069 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.469-1489C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72333529 | ||||||
chr5:72333542
|
A | G | 1 | a0001c0001t0011g0061 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.469-1476A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72333542 | ||||||
chr5:72334042
|
A | AT | 4 | a0001c0001t0021g0014a0001c0001t0032g0116a0001c0001t0032g0117others(1): Show | 6 | HG02280.hp1 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.469-968dupT | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 72334042 | |||||
chr5:72334167
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.469-851A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72334167 | ||||||
chr5:72334176
|
A | G | 1 | a0001c0001t0001g0058 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.469-842A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72334176 | ||||||
chr5:72334550
|
CT | C | 144 | a0001c0001t0001g0033a0001c0001t0001g0110a0001c0001t0001g0161others(141): Show | 205 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.469-455delT | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 72334550 | |||||
chr5:72334621
|
G | A | 2 | a0001c0001t0017g0039a0001c0001t0017g0190 | 3 | HG01074.hp2 HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.469-397G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72334621 | ||||||
chr5:72334755
|
T | C | 1 | a0001c0001t0009g0048 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.469-263T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72334755 | ||||||
chr5:72334941
|
A | G | 1 | a0001c0001t0037g0052 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.469-77A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72334941 | ||||||
chr5:72334966
|
C | T | 1 | a0001c0001t0001g0160 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.469-52C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72334966 | ||||||
chr5:72335455
|
C | CA | 108 | a0001c0001t0001g0110a0001c0001t0001g0147a0001c0001t0001g0149others(105): Show | 138 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.548-320dupA | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 72335455 | |||||
chr5:72336710
|
CA | C | 35 | a0001c0001t0001g0175a0001c0001t0002g0026a0001c0001t0002g0083others(32): Show | 46 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.639+845delA | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 72336710 | |||||
chr5:72337758
|
A | G | 1 | a0001c0001t0004g0082 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.640-864A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 6/9 | chr5 | 72337758 | ||||||
chr5:72338014
|
A | G | 1 | a0001c0001t0035g0126 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.640-608A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 6/9 | chr5 | 72338014 | ||||||
chr5:72338095
|
G | T | 22 | a0001c0001t0001g0110a0001c0001t0003g0004a0001c0001t0003g0027others(19): Show | 30 | HG00140.hp1 HG00558.hp1 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.640-527G>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 6/9 | chr5 | 72338095 | ||||||
chr5:72338304
|
C | T | 1 | a0001c0001t0036g0120 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.640-318C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 6/9 | chr5 | 72338304 | ||||||
chr5:72338354
|
C | G | 47 | a0001c0001t0005g0060a0001c0001t0007g0017a0001c0001t0007g0031others(44): Show | 58 | HG00741.hp1 HG01074.hp2 HG01243.hp1 others(55): Show |
intron_variant | MODIFIER | c.640-268C>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 6/9 | chr5 | 72338354 | ||||||
chr5:72338373
|
T | G | 1 | a0001c0001t0010g0055 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.640-249T>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 6/9 | chr5 | 72338373 | ||||||
chr5:72338786
|
T | C | 3 | a0001c0001t0024g0130a0001c0001t0024g0131a0001c0001t0025g0032 | 4 | HG02717.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.753+51T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72338786 | ||||||
chr5:72338797
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.753+62G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72338797 | ||||||
chr5:72338880
|
A | G | 1 | a0001c0001t0001g0142 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.753+145A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72338880 | ||||||
chr5:72338885
|
A | G | 22 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0038others(19): Show | 37 | HG00140.hp2 HG00621.hp2 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.753+150A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72338885 | ||||||
chr5:72339320
|
G | C | 20 | a0001c0001t0009g0010a0001c0001t0009g0044a0001c0001t0009g0048others(17): Show | 22 | HG00741.hp1 HG02055.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.753+585G>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72339320 | ||||||
chr5:72339350
|
A | T | 4 | a0001c0001t0001g0168a0001c0001t0001g0174a0001c0001t0001g0176others(1): Show | 4 | NA18983.hp2 NA19003.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.753+615A>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72339350 | ||||||
chr5:72339419
|
T | A | 6 | a0001c0001t0007g0017a0001c0001t0007g0031a0001c0001t0007g0127others(3): Show | 9 | HG02451.hp2 HG02486.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.753+684T>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72339419 | ||||||
chr5:72339479
|
G | A | 2 | a0001c0001t0023g0042a0001c0001t0023g0054 | 2 | HG02257.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.753+744G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72339479 | ||||||
chr5:72339706
|
T | TAGTTTTT others(304): Show |
9 | a0001c0001t0005g0060a0001c0001t0011g0059a0001c0001t0011g0062others(6): Show | 11 | HG01433.hp2 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.753+982_753+983ins others(311): Show |
PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 72339706 | |||||
chr5:72339706
|
T | TAGTTTTT others(305): Show |
2 | a0001c0001t0011g0061a0001c0001t0011g0066 | 2 | HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.753+982_753+983ins others(312): Show |
PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 72339706 | |||||
chr5:72339771
|
C | T | 2 | a0001c0001t0032g0116a0001c0001t0032g0117 | 2 | HG02280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.753+1036C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72339771 | ||||||
chr5:72339986
|
G | A | 143 | a0001c0001t0001g0110a0001c0001t0002g0001a0001c0001t0002g0009others(140): Show | 205 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.753+1251G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72339986 | ||||||
chr5:72340422
|
G | C | 1 | a0001c0001t0001g0142 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.753+1687G>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72340422 | ||||||
chr5:72340492
|
T | C | 1 | a0001c0001t0004g0078 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.753+1757T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72340492 | ||||||
chr5:72340685
|
T | G | 1 | a0001c0001t0004g0079 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.753+1950T>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72340685 | ||||||
chr5:72340751
|
T | G | 48 | a0001c0001t0005g0060a0001c0001t0007g0017a0001c0001t0007g0031others(45): Show | 59 | HG00741.hp1 HG01074.hp2 HG01243.hp1 others(56): Show |
intron_variant | MODIFIER | c.753+2016T>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72340751 | ||||||
chr5:72340841
|
G | A | 18 | a0001c0001t0006g0005a0001c0001t0006g0015a0001c0001t0006g0016others(15): Show | 25 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.753+2106G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72340841 | ||||||
chr5:72340870
|
C | T | 1 | a0001c0001t0018g0020 | 3 | HG01884.hp2 HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.754-2092C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72340870 | ||||||
chr5:72340969
|
GT | G | 145 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0002g0001others(142): Show | 207 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.754-1980delT | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 72340969 | |||||
chr5:72341028
|
G | A | 11 | a0001c0001t0005g0060a0001c0001t0011g0059a0001c0001t0011g0061others(8): Show | 13 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.754-1934G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72341028 | ||||||
chr5:72341033
|
C | T | 1 | a0001c0001t0001g0188 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.754-1929C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72341033 | ||||||
chr5:72341143
|
C | T | 1 | a0001c0001t0001g0159 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.754-1819C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72341143 | ||||||
chr5:72341161
|
T | C | 11 | a0001c0001t0005g0060a0001c0001t0011g0059a0001c0001t0011g0061others(8): Show | 13 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.754-1801T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72341161 | ||||||
chr5:72341180
|
A | G | 3 | a0001c0001t0024g0130a0001c0001t0024g0131a0001c0001t0025g0032 | 4 | HG02717.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.754-1782A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72341180 | ||||||
chr5:72341324
|
G | A | 4 | a0001c0001t0021g0014a0001c0001t0032g0116a0001c0001t0032g0117others(1): Show | 6 | HG02280.hp1 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.754-1638G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72341324 | ||||||
chr5:72341516
|
T | C | 1 | a0001c0001t0001g0176 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.754-1446T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72341516 | ||||||
chr5:72341812
|
G | A | 3 | a0001c0001t0002g0097a0001c0001t0039g0080a0001c0001t0040g0081 | 3 | HG02080.hp2 NA18982.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.754-1150G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72341812 | ||||||
chr5:72342016
|
G | A | 1 | a0001c0001t0004g0079 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.754-946G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72342016 | ||||||
chr5:72342030
|
G | A | 2 | a0001c0001t0011g0062a0001c0001t0011g0063 | 2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.754-932G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72342030 | ||||||
chr5:72342063
|
TAAA | T | 6 | a0001c0001t0007g0017a0001c0001t0007g0031a0001c0001t0007g0127others(3): Show | 9 | HG02451.hp2 HG02486.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.754-897_754-895del others(3): Show |
PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 72342063 | |||||
chr5:72342227
|
G | A | 1 | a0001c0001t0035g0126 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.754-735G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72342227 | ||||||
chr5:72342399
|
A | T | 3 | a0001c0001t0024g0130a0001c0001t0024g0131a0001c0001t0025g0032 | 4 | HG02717.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.754-563A>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72342399 | ||||||
chr5:72342463
|
T | A | 1 | a0001c0001t0001g0150 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.754-499T>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72342463 | ||||||
chr5:72342620
|
G | A | 3 | a0001c0001t0024g0130a0001c0001t0024g0131a0001c0001t0025g0032 | 4 | HG02717.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.754-342G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72342620 | ||||||
chr5:72342629
|
A | C | 6 | a0001c0001t0007g0017a0001c0001t0007g0031a0001c0001t0007g0127others(3): Show | 9 | HG02451.hp2 HG02486.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.754-333A>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72342629 | ||||||
chr5:72342629
|
A | G | 1 | a0001c0001t0048g0129 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.754-333A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72342629 | ||||||
chr5:72342798
|
G | T | 1 | a0001c0001t0001g0161 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.754-164G>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72342798 | ||||||
chr5:72342843
|
T | C | 5 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0142others(2): Show | 7 | HG00408.hp2 HG00597.hp1 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.754-119T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72342843 | ||||||
chr5:72343228
|
C | G | 1 | a0001c0001t0036g0120 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.828+192C>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72343228 | ||||||
chr5:72343288
|
AG | A | 2 | a0001c0001t0017g0039a0001c0001t0017g0190 | 3 | HG01074.hp2 HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.828+253delG | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72343288 | ||||||
chr5:72343350
|
G | C | 18 | a0001c0001t0006g0005a0001c0001t0006g0015a0001c0001t0006g0016others(15): Show | 25 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.828+314G>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72343350 | ||||||
chr5:72343416
|
G | A | 1 | a0001c0001t0003g0040 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.828+380G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72343416 | ||||||
chr5:72343428
|
G | A | 2 | a0001c0001t0017g0039a0001c0001t0017g0190 | 3 | HG01074.hp2 HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.828+392G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72343428 | ||||||
chr5:72343550
|
G | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0169 | 3 | NA18964.hp1 NA19000.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.828+514G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72343550 | ||||||
chr5:72343724
|
C | T | 18 | a0001c0001t0006g0005a0001c0001t0006g0015a0001c0001t0006g0016others(15): Show | 25 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.828+688C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72343724 | ||||||
chr5:72343768
|
A | G | 1 | a0001c0001t0035g0126 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.828+732A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72343768 | ||||||
chr5:72343817
|
TTA | T | 11 | a0001c0001t0005g0060a0001c0001t0011g0059a0001c0001t0011g0061others(8): Show | 13 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.828+783_828+784del others(2): Show |
PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr5 | 72343817 | |||||
chr5:72343874
|
T | C | 1 | a0001c0001t0048g0129 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.828+838T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72343874 | ||||||
chr5:72343950
|
G | A | 18 | a0001c0001t0006g0005a0001c0001t0006g0015a0001c0001t0006g0016others(15): Show | 25 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.828+914G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72343950 | ||||||
chr5:72344005
|
C | T | 1 | a0001c0001t0025g0032 | 2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.828+969C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72344005 | ||||||
chr5:72344106
|
C | T | 1 | a0001c0001t0005g0105 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.828+1070C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72344106 | ||||||
chr5:72344112
|
C | T | 3 | a0001c0001t0005g0029a0001c0001t0033g0029a0001c0001t0033g0111 | 3 | HG01261.hp1 HG01978.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.828+1076C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72344112 | ||||||
chr5:72344242
|
G | A | 1 | a0001c0001t0058g0135 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.828+1206G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72344242 | ||||||
chr5:72344654
|
G | A | 36 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0012others(33): Show | 65 | HG00408.hp1 HG00438.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.828+1618G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72344654 | ||||||
chr5:72344730
|
T | A | 1 | a0001c0001t0049g0069 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.828+1694T>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72344730 | ||||||
chr5:72344744
|
C | T | 6 | a0001c0001t0007g0017a0001c0001t0007g0031a0001c0001t0007g0127others(3): Show | 9 | HG02451.hp2 HG02486.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.828+1708C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72344744 | ||||||
chr5:72344749
|
G | T | 3 | a0001c0001t0005g0029a0001c0001t0033g0029a0001c0001t0033g0111 | 3 | HG01261.hp1 HG01978.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.828+1713G>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72344749 | ||||||
chr5:72344790
|
C | G | 6 | a0001c0001t0007g0017a0001c0001t0007g0031a0001c0001t0007g0127others(3): Show | 9 | HG02451.hp2 HG02486.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.828+1754C>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72344790 | ||||||
chr5:72344830
|
A | G | 1 | a0001c0001t0048g0129 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.828+1794A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72344830 | ||||||
chr5:72344877
|
A | G | 15 | a0001c0001t0005g0060a0001c0001t0011g0059a0001c0001t0011g0061others(12): Show | 18 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.828+1841A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72344877 | ||||||
chr5:72344968
|
G | A | 1 | a0001c0001t0002g0088 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.828+1932G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72344968 | ||||||
chr5:72345015
|
G | A | 1 | a0001c0001t0009g0049 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.828+1979G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72345015 | ||||||
chr5:72345024
|
A | G | 1 | a0001c0001t0036g0120 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.828+1988A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72345024 | ||||||
chr5:72345293
|
A | C | 48 | a0001c0001t0005g0060a0001c0001t0007g0017a0001c0001t0007g0031others(45): Show | 59 | HG00741.hp1 HG01074.hp2 HG01243.hp1 others(56): Show |
intron_variant | MODIFIER | c.828+2257A>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72345293 | ||||||
chr5:72345469
|
C | T | 12 | a0001c0001t0005g0060a0001c0001t0011g0059a0001c0001t0011g0061others(9): Show | 14 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.828+2433C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72345469 | ||||||
chr5:72345493
|
C | T | 3 | a0001c0001t0001g0158a0001c0001t0056g0037a0001c0001t0060g0037 | 3 | NA18968.hp1 NA18990.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.828+2457C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72345493 | ||||||
chr5:72345664
|
G | A | 7 | a0001c0001t0001g0018a0001c0001t0001g0162a0001c0001t0001g0187others(4): Show | 7 | HG01891.hp2 HG02622.hp2 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.828+2628G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72345664 | ||||||
chr5:72345714
|
G | T | 1 | a0001c0001t0049g0069 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.828+2678G>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72345714 | ||||||
chr5:72346216
|
A | C | 1 | a0001c0001t0001g0157 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.828+3180A>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72346216 | ||||||
chr5:72346462
|
C | T | 1 | a0001c0001t0015g0053 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.828+3426C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72346462 | ||||||
chr5:72346550
|
C | T | 6 | a0001c0001t0007g0017a0001c0001t0007g0031a0001c0001t0007g0127others(3): Show | 9 | HG02451.hp2 HG02486.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.828+3514C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72346550 | ||||||
chr5:72347043
|
A | G | 1 | a0001c0001t0038g0114 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.828+4007A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72347043 | ||||||
chr5:72347135
|
A | G | 1 | a0001c0001t0002g0090 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.828+4099A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72347135 | ||||||
chr5:72347191
|
G | A | 1 | a0001c0001t0048g0129 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.828+4155G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72347191 | ||||||
chr5:72347198
|
C | T | 11 | a0001c0001t0005g0060a0001c0001t0011g0059a0001c0001t0011g0061others(8): Show | 13 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.828+4162C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72347198 | ||||||
chr5:72347267
|
C | T | 1 | a0001c0001t0064g0115 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.828+4231C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72347267 | ||||||
chr5:72347359
|
C | T | 1 | a0001c0001t0025g0032 | 2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.828+4323C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72347359 | ||||||
chr5:72347374
|
A | G | 1 | a0001c0001t0005g0104 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.828+4338A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72347374 | ||||||
chr5:72347386
|
T | C | 1 | a0001c0001t0011g0068 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.828+4350T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72347386 | ||||||
chr5:72347388
|
C | T | 25 | a0001c0001t0005g0060a0001c0001t0007g0017a0001c0001t0007g0031others(22): Show | 32 | HG01074.hp2 HG01243.hp1 HG01433.hp2 others(29): Show |
intron_variant | MODIFIER | c.828+4352C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72347388 | ||||||
chr5:72347413
|
C | T | 1 | a0001c0001t0002g0086 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.828+4377C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72347413 | ||||||
chr5:72347866
|
G | T | 1 | a0001c0001t0001g0156 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.829-4775G>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72347866 | ||||||
chr5:72348534
|
A | G | 2 | a0001c0001t0017g0039a0001c0001t0017g0190 | 3 | HG01074.hp2 HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.829-4107A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72348534 | ||||||
chr5:72348924
|
G | A | 1 | a0001c0001t0015g0045 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.829-3717G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72348924 | ||||||
chr5:72348974
|
G | A | 21 | a0001c0001t0003g0004a0001c0001t0003g0027a0001c0001t0003g0028others(18): Show | 29 | HG00140.hp1 HG00558.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.829-3667G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72348974 | ||||||
chr5:72349384
|
G | A | 3 | a0001c0001t0024g0130a0001c0001t0024g0131a0001c0001t0025g0032 | 4 | HG02717.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.829-3257G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72349384 | ||||||
chr5:72349600
|
G | T | 6 | a0001c0001t0007g0017a0001c0001t0007g0031a0001c0001t0007g0127others(3): Show | 9 | HG02451.hp2 HG02486.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.829-3041G>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72349600 | ||||||
chr5:72349747
|
C | T | 5 | a0001c0001t0007g0017a0001c0001t0007g0031a0001c0001t0007g0127others(2): Show | 8 | HG02451.hp2 HG02486.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.829-2894C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72349747 | ||||||
chr5:72349826
|
T | C | 6 | a0001c0001t0007g0017a0001c0001t0007g0031a0001c0001t0007g0127others(3): Show | 9 | HG02451.hp2 HG02486.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.829-2815T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72349826 | ||||||
chr5:72350253
|
C | T | 1 | a0001c0001t0007g0031 | 2 | HG02451.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.829-2388C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72350253 | ||||||
chr5:72350295
|
AATTT | A | 18 | a0001c0001t0001g0147a0001c0001t0006g0005a0001c0001t0006g0015others(15): Show | 25 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.829-2342_829-2339d others(6): Show |
PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr5 | 72350295 | |||||
chr5:72350403
|
G | C | 3 | a0001c0001t0005g0104a0001c0001t0005g0105a0001c0001t0038g0114 | 3 | HG02109.hp1 HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.829-2238G>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72350403 | ||||||
chr5:72350516
|
A | G | 4 | a0001c0001t0021g0014a0001c0001t0032g0116a0001c0001t0032g0117others(1): Show | 6 | HG02280.hp1 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.829-2125A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72350516 | ||||||
chr5:72350604
|
G | T | 1 | a0001c0001t0005g0105 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.829-2037G>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72350604 | ||||||
chr5:72350662
|
T | C | 3 | a0001c0001t0020g0011a0001c0001t0063g0064a0001c0001t0066g0067 | 5 | HG01433.hp2 HG01891.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.829-1979T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72350662 | ||||||
chr5:72350717
|
A | G | 2 | a0001c0001t0021g0014a0001c0001t0064g0115 | 4 | HG02647.hp2 HG02922.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.829-1924A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72350717 | ||||||
chr5:72350770
|
G | T | 3 | a0001c0001t0024g0130a0001c0001t0024g0131a0001c0001t0025g0032 | 4 | HG02717.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.829-1871G>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72350770 | ||||||
chr5:72350937
|
A | G | 3 | a0001c0001t0024g0130a0001c0001t0024g0131a0001c0001t0025g0032 | 4 | HG02717.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.829-1704A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72350937 | ||||||
chr5:72350988
|
G | A | 1 | a0001c0001t0008g0122 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.829-1653G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72350988 | ||||||
chr5:72351274
|
T | G | 6 | a0001c0001t0009g0010a0001c0001t0009g0044a0001c0001t0009g0048others(3): Show | 8 | HG00741.hp1 HG02647.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.829-1367T>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72351274 | ||||||
chr5:72351296
|
G | A | 1 | a0001c0001t0007g0132 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.829-1345G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72351296 | ||||||
chr5:72351331
|
C | T | 3 | a0001c0001t0001g0036a0001c0001t0001g0157a0001c0001t0058g0135 | 4 | HG01070.hp1 HG02698.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.829-1310C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72351331 | ||||||
chr5:72351473
|
G | A | 1 | a0001c0001t0038g0114 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.829-1168G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72351473 | ||||||
chr5:72351589
|
A | G | 1 | a0001c0001t0008g0124 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.829-1052A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72351589 | ||||||
chr5:72351793
|
T | A | 3 | a0001c0001t0024g0130a0001c0001t0024g0131a0001c0001t0025g0032 | 4 | HG02717.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.829-848T>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72351793 | ||||||
chr5:72351798
|
C | G | 1 | a0001c0001t0013g0095 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.829-843C>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72351798 | ||||||
chr5:72351920
|
G | A | 4 | a0001c0001t0021g0014a0001c0001t0032g0116a0001c0001t0032g0117others(1): Show | 6 | HG02280.hp1 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.829-721G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72351920 | ||||||
chr5:72351988
|
T | C | 1 | a0001c0001t0006g0123 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.829-653T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72351988 | ||||||
chr5:72352208
|
C | T | 2 | a0001c0001t0001g0185a0001c0001t0001g0186 | 2 | HG02698.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.829-433C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72352208 | ||||||
chr5:72352229
|
C | A | 1 | a0001c0001t0010g0043 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.829-412C>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72352229 | ||||||
chr5:72352308
|
C | T | 1 | a0001c0001t0028g0164 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.829-333C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72352308 | ||||||
chr5:72352394
|
C | A | 2 | a0001c0001t0003g0101a0001c0001t0003g0106 | 2 | NA19054.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.829-247C>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72352394 | ||||||
chr5:72352405
|
C | T | 2 | a0001c0001t0017g0039a0001c0001t0017g0190 | 3 | HG01074.hp2 HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.829-236C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72352405 | ||||||
chr5:72352471
|
G | A | 2 | a0001c0001t0003g0107a0001c0001t0003g0108 | 2 | HG02735.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.829-170G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72352471 | ||||||
chr5:72352482
|
T | C | 1 | a0001c0001t0012g0152 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.829-159T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72352482 | ||||||
chr5:72352763
|
G | A | 11 | a0001c0001t0005g0060a0001c0001t0011g0059a0001c0001t0011g0061others(8): Show | 13 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.942+9G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72352763 | ||||||
chr5:72353018
|
T | C | 1 | a0001c0001t0003g0107 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.942+264T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72353018 | ||||||
chr5:72353019
|
T | C | 1 | a0001c0001t0052g0172 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.942+265T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72353019 | ||||||
chr5:72353080
|
C | T | 1 | a0001c0001t0004g0091 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.942+326C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72353080 | ||||||
chr5:72353127
|
A | G | 7 | a0001c0001t0007g0017a0001c0001t0007g0031a0001c0001t0007g0127others(4): Show | 10 | HG02451.hp2 HG02486.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.942+373A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72353127 | ||||||
chr5:72353157
|
A | G | 7 | a0001c0001t0007g0017a0001c0001t0007g0031a0001c0001t0007g0127others(4): Show | 10 | HG02451.hp2 HG02486.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.942+403A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72353157 | ||||||
chr5:72353504
|
CTT | C | 1 | a0001c0001t0018g0020 | 3 | HG01884.hp2 HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.942+752_942+753del others(2): Show |
PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 72353504 | |||||
chr5:72354133
|
C | T | 1 | a0001c0001t0011g0068 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.942+1379C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72354133 | ||||||
chr5:72354175
|
G | A | 3 | a0001c0001t0024g0130a0001c0001t0024g0131a0001c0001t0025g0032 | 4 | HG02717.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.942+1421G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72354175 | ||||||
chr5:72354382
|
G | GA | 110 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0034others(107): Show | 176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.942+1654dupA | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 72354382 | |||||
chr5:72354382
|
G | GAA | 48 | a0001c0001t0001g0021a0001c0001t0001g0169a0001c0001t0001g0188others(45): Show | 59 | HG00642.hp2 HG00673.hp2 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.942+1653_942+1654d others(4): Show |
PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 72354382 | |||||
chr5:72354382
|
G | GAAA | 11 | a0001c0001t0005g0099a0001c0001t0009g0048a0001c0001t0009g0050others(8): Show | 13 | HG00741.hp1 HG01243.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.942+1652_942+1654d others(5): Show |
PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 72354382 | |||||
chr5:72354428
|
A | T | 4 | a0001c0001t0021g0014a0001c0001t0032g0116a0001c0001t0032g0117others(1): Show | 6 | HG02280.hp1 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.942+1674A>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72354428 | ||||||
chr5:72354443
|
A | G | 1 | a0001c0001t0001g0155 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.942+1689A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72354443 | ||||||
chr5:72354668
|
G | A | 1 | a0001c0001t0004g0078 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.942+1914G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72354668 | ||||||
chr5:72354901
|
G | T | 1 | a0001c0001t0001g0019 | 3 | HG01167.hp2 HG01169.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.942+2147G>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72354901 | ||||||
chr5:72354974
|
A | T | 3 | a0001c0001t0024g0130a0001c0001t0024g0131a0001c0001t0025g0032 | 4 | HG02717.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.942+2220A>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72354974 | ||||||
chr5:72355234
|
C | T | 1 | a0001c0001t0006g0123 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.942+2480C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72355234 | ||||||
chr5:72355475
|
C | T | 5 | a0001c0001t0001g0018a0001c0001t0019g0018a0001c0001t0019g0146others(2): Show | 5 | HG01891.hp2 HG02622.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.942+2721C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72355475 | ||||||
chr5:72355731
|
G | A | 1 | a0001c0001t0001g0188 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.943-2472G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72355731 | ||||||
chr5:72355793
|
G | A | 1 | a0001c0001t0042g0084 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.943-2410G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72355793 | ||||||
chr5:72355934
|
T | C | 2 | a0001c0001t0001g0153a0001c0001t0001g0160 | 2 | NA18939.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.943-2269T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72355934 | ||||||
chr5:72356171
|
G | A | 5 | a0001c0001t0001g0018a0001c0001t0019g0018a0001c0001t0019g0146others(2): Show | 5 | HG01891.hp2 HG02622.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.943-2032G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72356171 | ||||||
chr5:72356280
|
T | C | 2 | a0001c0001t0017g0039a0001c0001t0017g0190 | 3 | HG01074.hp2 HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.943-1923T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72356280 | ||||||
chr5:72356418
|
A | T | 8 | a0001c0001t0007g0017a0001c0001t0007g0031a0001c0001t0007g0127others(5): Show | 11 | HG02451.hp2 HG02486.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.943-1785A>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72356418 | ||||||
chr5:72356513
|
A | ATG | 224 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(221): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.943-1690_943-1689i others(4): Show |
PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72356513 | ||||||
chr5:72356626
|
T | A | 1 | a0001c0001t0005g0102 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.943-1577T>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72356626 | ||||||
chr5:72356835
|
A | G | 1 | a0001c0001t0030g0154 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.943-1368A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72356835 | ||||||
chr5:72356927
|
C | T | 1 | a0001c0001t0001g0019 | 3 | HG01167.hp2 HG01169.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.943-1276C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72356927 | ||||||
chr5:72357077
|
C | G | 1 | a0001c0001t0004g0082 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.943-1126C>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72357077 | ||||||
chr5:72357363
|
C | T | 3 | a0001c0001t0005g0029a0001c0001t0033g0029a0001c0001t0033g0111 | 3 | HG01261.hp1 HG01978.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.943-840C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72357363 | ||||||
chr5:72357657
|
A | T | 4 | a0001c0001t0021g0014a0001c0001t0032g0116a0001c0001t0032g0117others(1): Show | 6 | HG02280.hp1 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.943-546A>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72357657 | ||||||
chr5:72357847
|
CT | C | 10 | a0001c0001t0011g0059a0001c0001t0011g0061a0001c0001t0011g0062others(7): Show | 12 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.943-342delT | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 72357847 | |||||
chr5:72357860
|
T | G | 10 | a0001c0001t0011g0059a0001c0001t0011g0061a0001c0001t0011g0062others(7): Show | 12 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.943-343T>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72357860 | ||||||
chr5:72358054
|
C | T | 6 | a0001c0001t0009g0010a0001c0001t0009g0044a0001c0001t0009g0048others(3): Show | 8 | HG00741.hp1 HG02647.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.943-149C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72358054 |