geneid | 63929 |
---|---|
ensemblid | ENSG00000196236.13 |
hgncid | 28052 |
symbol | XPNPEP3 |
name | X-prolyl aminopeptidase 3 |
refseq_nuc | NM_022098.4 |
refseq_prot | NP_071381.1 |
ensembl_nuc | ENST00000357137.9 |
ensembl_prot | ENSP00000349658.4 |
mane_status | MANE Select |
chr | chr22 |
start | 40857148 |
end | 40932815 |
strand | + |
ver | v1.2 |
region | chr22:40857148-40932815 |
region5000 | chr22:40852148-40937815 |
regionname0 | XPNPEP3_chr22_40857148_40932815 |
regionname5000 | XPNPEP3_chr22_40852148_40937815 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 507 | 246 | 82 | 40 | 84 | 10 | 28 | 61 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0002 | 0/0 | 507 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0003 | 0/0 | 507 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1524 | 241 | 77 | 40 | 84 | 10 | 28 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
c0002 | 0/0 | 1524 | 4 | 4 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
c0003 | 0/0 | 1524 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
c0004 | 0/0 | 1524 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
c0005 | 0/0 | 1524 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 6416 | 60 | 5 | 10 | 31 | 4 | 10 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0002 | 1/0 | 6415 | 55 | 12 | 16 | 12 | 4 | 10 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0003 | 0/0 | 6415 | 22 | 17 | 2 | 3 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0004 | 0/0 | 6414 | 17 | 0 | 0 | 17 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0005 | 0/0 | 6414 | 10 | 10 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0006 | 0/0 | 6417 | 7 | 1 | 2 | 3 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0007 | 0/0 | 6416 | 6 | 1 | 2 | 3 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0008 | 0/0 | 6413 | 6 | 4 | 2 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0009 | 0/0 | 6416 | 4 | 3 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0010 | 0/0 | 6415 | 4 | 0 | 0 | 4 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0011 | 0/0 | 6401 | 4 | 3 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0012 | 0/0 | 6415 | 3 | 1 | 1 | 0 | 1 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0013 | 0/0 | 6415 | 3 | 3 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0014 | 0/0 | 6416 | 3 | 1 | 0 | 0 | 0 | 2 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0015 | 0/0 | 6415 | 2 | 0 | 0 | 2 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0016 | 0/0 | 6415 | 2 | 0 | 0 | 2 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0017 | 0/0 | 6414 | 2 | 2 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0018 | 0/1 | 6415 | 2 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0019 | 0/0 | 6415 | 2 | 2 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0020 | 0/0 | 6415 | 2 | 0 | 0 | 0 | 0 | 2 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0021 | 0/0 | 6414 | 2 | 2 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0022 | 0/0 | 6415 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0023 | 0/0 | 6415 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0024 | 0/0 | 6416 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0025 | 0/0 | 6415 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0026 | 0/0 | 6418 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0027 | 0/0 | 6416 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0028 | 0/0 | 6415 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0029 | 0/0 | 6415 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0030 | 0/0 | 6415 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0031 | 0/0 | 6414 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0032 | 0/0 | 6415 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0033 | 0/0 | 6415 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0034 | 0/0 | 6416 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0035 | 0/0 | 6415 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0036 | 0/0 | 6417 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0037 | 0/0 | 6416 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0038 | 0/0 | 6416 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0039 | 0/0 | 6417 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0040 | 0/0 | 6417 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0041 | 0/0 | 6413 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0042 | 0/0 | 6414 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0043 | 0/0 | 6414 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0044 | 0/0 | 6414 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0045 | 0/0 | 6416 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0046 | 0/0 | 6414 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0047 | 0/0 | 6414 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0048 | 0/0 | 6414 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0049 | 0/0 | 6414 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0050 | 0/0 | 6415 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
t0051 | 0/0 | 6416 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0101 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0137 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1524 | 241 | 77 | 40 | 84 | 10 | 28 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0002 | 0/0 | 1524 | 4 | 4 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0005 | 0/0 | 1524 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0002c0003 | 0/0 | 1524 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0003c0004 | 0/0 | 1524 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 7939 | 60 | 5 | 10 | 31 | 4 | 10 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0002 | 1/0 | 7938 | 55 | 12 | 16 | 12 | 4 | 10 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0003 | 0/0 | 7938 | 21 | 16 | 2 | 3 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0004 | 0/0 | 7937 | 15 | 0 | 0 | 15 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0005 | 0/0 | 7937 | 9 | 9 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0006 | 0/0 | 7940 | 7 | 1 | 2 | 3 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0007 | 0/0 | 7939 | 6 | 1 | 2 | 3 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0008 | 0/0 | 7936 | 6 | 4 | 2 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0009 | 0/0 | 7939 | 4 | 3 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0010 | 0/0 | 7938 | 4 | 0 | 0 | 4 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0011 | 0/0 | 7924 | 4 | 3 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0012 | 0/0 | 7938 | 3 | 1 | 1 | 0 | 1 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0013 | 0/0 | 7938 | 3 | 3 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0014 | 0/0 | 7939 | 3 | 1 | 0 | 0 | 0 | 2 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0015 | 0/0 | 7938 | 2 | 0 | 0 | 2 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0016 | 0/0 | 7938 | 2 | 0 | 0 | 2 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0017 | 0/0 | 7937 | 2 | 2 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0018 | 0/1 | 7938 | 2 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0019 | 0/0 | 7938 | 2 | 2 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0020 | 0/0 | 7938 | 2 | 0 | 0 | 0 | 0 | 2 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0021 | 0/0 | 7937 | 2 | 2 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0022 | 0/0 | 7938 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0023 | 0/0 | 7938 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0024 | 0/0 | 7939 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0025 | 0/0 | 7938 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0026 | 0/0 | 7941 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0027 | 0/0 | 7939 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0028 | 0/0 | 7938 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0029 | 0/0 | 7938 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0030 | 0/0 | 7938 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0031 | 0/0 | 7937 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0032 | 0/0 | 7938 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0033 | 0/0 | 7938 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0034 | 0/0 | 7939 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0035 | 0/0 | 7938 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0036 | 0/0 | 7940 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0037 | 0/0 | 7939 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0038 | 0/0 | 7939 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0039 | 0/0 | 7940 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0040 | 0/0 | 7940 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0041 | 0/0 | 7936 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0042 | 0/0 | 7937 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0043 | 0/0 | 7937 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0044 | 0/0 | 7937 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0045 | 0/0 | 7939 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0047 | 0/0 | 7937 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0049 | 0/0 | 7937 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0001t0051 | 0/0 | 7939 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0002t0005 | 0/0 | 7937 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0002t0046 | 0/0 | 7937 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0002t0048 | 0/0 | 7937 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0002t0050 | 0/0 | 7938 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0001c0005t0003 | 0/0 | 7938 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0002c0003t0004 | 0/0 | 7937 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
a0003c0004t0004 | 0/0 | 7937 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | copy fasta | chr22 | 40852148 | 40937815 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0101 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0004g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0004g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0004g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0005g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0005g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0006g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0006g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0006g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0006g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0006g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0006g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0006g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0007g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0007g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0007g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0007g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0007g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0007g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0008g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0008g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0008g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0008g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0008g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0008g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0009g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0009g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0009g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0009g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0010g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0010g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0010g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0010g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0011g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0011g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0011g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0011g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0012g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0012g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0012g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0013g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0013g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0013g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0014g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0014g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0014g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0015g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0015g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0016g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0016g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0017g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0017g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0018g0137 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0018g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0019g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0019g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0020g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0020g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0021g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0021g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0022g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0023g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0024g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0025g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0026g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0027g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0028g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0029g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0030g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0031g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0032g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0033g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0034g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0035g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0036g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0037g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0038g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0039g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0040g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0041g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0042g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0043g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0044g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0045g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0047g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0049g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0001t0051g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0002t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0002t0046g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0002t0048g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0002t0050g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0001c0005t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0002c0003t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
a0003c0004t0004g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0012 | g0038 | EUR | GBR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0144 | EUR | GBR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0152 | EUR | GBR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0093 | EUR | GBR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | CHS | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG00544 | hp1 | a0001 | c0001 | t0004 | g0053 | EAS | CHS | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG00597 | hp1 | a0001 | c0001 | t0016 | g0046 | EAS | CHS | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG00597 | hp2 | a0001 | c0001 | t0006 | g0178 | EAS | CHS | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG00609 | hp1 | a0001 | c0001 | t0010 | g0051 | EAS | CHS | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG00639 | hp2 | a0001 | c0001 | t0011 | g0225 | AMR | PUR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | PUR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0147 | AMR | PUR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0181 | AMR | PUR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG01106 | hp1 | a0001 | c0001 | t0006 | g0017 | AMR | PUR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0182 | AMR | PUR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG01109 | hp2 | a0001 | c0001 | t0025 | g0173 | AMR | PUR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG01192 | hp1 | a0001 | c0001 | t0007 | g0188 | AMR | PUR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG01192 | hp2 | a0001 | c0001 | t0007 | g0187 | AMR | PUR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG01243 | hp2 | a0001 | c0001 | t0008 | g0170 | AMR | PUR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0156 | AMR | CLM | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | CLM | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0191 | AMR | CLM | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0125 | AMR | CLM | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG01346 | hp2 | a0001 | c0001 | t0037 | g0032 | AMR | CLM | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0158 | AMR | CLM | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0124 | AMR | CLM | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG01433 | hp1 | a0001 | c0001 | t0012 | g0035 | AMR | CLM | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0153 | AMR | CLM | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG01496 | hp2 | a0001 | c0001 | t0008 | g0069 | AMR | CLM | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0071 | EUR | IBS | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0159 | EUR | IBS | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG01884 | hp1 | a0001 | c0001 | t0035 | g0033 | AFR | ACB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG01884 | hp2 | a0001 | c0002 | t0046 | g0217 | AFR | ACB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0120 | AMR | PEL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG01934 | hp2 | a0001 | c0001 | t0009 | g0218 | AMR | PEL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | PEL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0117 | AMR | PEL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0029 | AMR | PEL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02015 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | KHV | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | KHV | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02027 | hp2 | a0001 | c0001 | t0004 | g0054 | EAS | KHV | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02040 | hp2 | a0001 | c0001 | t0004 | g0043 | EAS | KHV | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0063 | AFR | ACB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02055 | hp2 | a0001 | c0001 | t0008 | g0165 | AFR | ACB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02056 | hp2 | a0001 | c0001 | t0004 | g0169 | EAS | KHV | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02080 | hp1 | a0001 | c0001 | t0004 | g0049 | EAS | KHV | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02132 | hp1 | a0002 | c0003 | t0004 | g0045 | EAS | KHV | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02257 | hp1 | a0001 | c0001 | t0006 | g0083 | AFR | ACB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02257 | hp2 | a0001 | c0001 | t0024 | g0145 | AFR | ACB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0056 | AFR | ACB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0155 | AFR | ACB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0194 | AFR | ACB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02293 | hp1 | a0001 | c0001 | t0006 | g0074 | AMR | PEL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02293 | hp2 | a0001 | c0001 | t0030 | g0119 | AMR | PEL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0095 | AFR | ACB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02451 | hp2 | a0001 | c0005 | t0003 | g0196 | AFR | ACB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0201 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02572 | hp2 | a0001 | c0001 | t0008 | g0066 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02602 | hp2 | a0001 | c0001 | t0020 | g0143 | SAS | PJL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0059 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02615 | hp2 | a0001 | c0001 | t0005 | g0207 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02622 | hp1 | a0001 | c0001 | t0008 | g0067 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02622 | hp2 | a0001 | c0001 | t0005 | g0205 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02630 | hp1 | a0001 | c0002 | t0048 | g0214 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0202 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0162 | SAS | PJL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02683 | hp2 | a0001 | c0001 | t0014 | g0027 | SAS | PJL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0061 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0062 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02738 | hp1 | a0001 | c0001 | t0014 | g0189 | SAS | PJL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02738 | hp2 | a0001 | c0001 | t0006 | g0086 | SAS | PJL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02809 | hp1 | a0001 | c0001 | t0049 | g0209 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02809 | hp2 | a0001 | c0001 | t0009 | g0220 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02886 | hp1 | a0001 | c0001 | t0022 | g0009 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02886 | hp2 | a0001 | c0001 | t0005 | g0203 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0127 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02895 | hp2 | a0001 | c0001 | t0019 | g0010 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02897 | hp1 | a0001 | c0001 | t0019 | g0011 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02897 | hp2 | a0001 | c0001 | t0014 | g0012 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0195 | AFR | ESN | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02965 | hp2 | a0001 | c0001 | t0013 | g0129 | AFR | ESN | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02976 | hp1 | a0001 | c0001 | t0013 | g0130 | AFR | ESN | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02976 | hp2 | a0001 | c0001 | t0033 | g0057 | AFR | ESN | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG03041 | hp2 | a0001 | c0001 | t0011 | g0226 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG03098 | hp1 | a0001 | c0001 | t0009 | g0223 | AFR | MSL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG03098 | hp2 | a0001 | c0001 | t0047 | g0008 | AFR | MSL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0193 | AFR | ESN | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG03195 | hp1 | a0001 | c0001 | t0008 | g0068 | AFR | ESN | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG03195 | hp2 | a0001 | c0001 | t0007 | g0149 | AFR | ESN | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG03209 | hp1 | a0001 | c0002 | t0005 | g0215 | AFR | MSL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG03209 | hp2 | a0001 | c0001 | t0029 | g0222 | AFR | MSL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG03225 | hp1 | a0001 | c0001 | t0005 | g0212 | AFR | MSL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG03225 | hp2 | a0001 | c0001 | t0005 | g0204 | AFR | MSL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0160 | SAS | PJL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG03453 | hp1 | a0001 | c0001 | t0021 | g0211 | AFR | MSL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG03453 | hp2 | a0001 | c0001 | t0031 | g0174 | AFR | MSL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG03486 | hp1 | a0001 | c0001 | t0021 | g0210 | AFR | MSL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0199 | AFR | MSL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0131 | SAS | PJL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0171 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG03579 | hp1 | a0001 | c0001 | t0027 | g0228 | AFR | MSL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG03579 | hp2 | a0001 | c0001 | t0017 | g0221 | AFR | MSL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG03654 | hp2 | a0001 | c0001 | t0020 | g0186 | SAS | PJL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0151 | SAS | PJL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG03669 | hp2 | a0001 | c0001 | t0034 | g0091 | SAS | PJL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG03704 | hp2 | a0001 | c0001 | t0028 | g0142 | SAS | PJL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0150 | SAS | BEB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG03831 | hp2 | a0001 | c0001 | t0026 | g0028 | SAS | BEB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | BEB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0190 | SAS | BEB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | STU | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0141 | SAS | STU | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0139 | SAS | BEB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0116 | SAS | STU | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | STU | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18522 | hp1 | a0001 | c0001 | t0011 | g0224 | AFR | YRI | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0058 | AFR | YRI | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | CHB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18906 | hp1 | a0001 | c0001 | t0045 | g0034 | AFR | YRI | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0060 | AFR | YRI | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18942 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18942 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18944 | hp1 | a0001 | c0001 | t0023 | g0089 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18949 | hp2 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18960 | hp1 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18961 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18964 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18968 | hp2 | a0001 | c0001 | t0004 | g0047 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18970 | hp1 | a0001 | c0001 | t0004 | g0048 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18975 | hp1 | a0001 | c0001 | t0036 | g0179 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18975 | hp2 | a0001 | c0001 | t0007 | g0229 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18980 | hp1 | a0001 | c0001 | t0015 | g0122 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18994 | hp1 | a0003 | c0004 | t0004 | g0002 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18995 | hp1 | a0001 | c0001 | t0010 | g0166 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18995 | hp2 | a0001 | c0001 | t0038 | g0097 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA18997 | hp2 | a0001 | c0001 | t0010 | g0042 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA19000 | hp2 | a0001 | c0001 | t0007 | g0237 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA19009 | hp2 | a0001 | c0001 | t0044 | g0050 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA19010 | hp1 | a0001 | c0001 | t0010 | g0192 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA19030 | hp1 | a0001 | c0001 | t0005 | g0216 | AFR | LWK | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA19030 | hp2 | a0001 | c0001 | t0040 | g0100 | AFR | LWK | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA19043 | hp1 | a0001 | c0002 | t0050 | g0213 | AFR | LWK | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | LWK | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA19054 | hp1 | a0001 | c0001 | t0042 | g0167 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA19057 | hp1 | a0001 | c0001 | t0004 | g0052 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA19060 | hp1 | a0001 | c0001 | t0043 | g0001 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA19060 | hp2 | a0001 | c0001 | t0051 | g0024 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA19063 | hp2 | a0001 | c0001 | t0039 | g0168 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA19065 | hp2 | a0001 | c0001 | t0015 | g0123 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA19077 | hp1 | a0001 | c0001 | t0004 | g0055 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA19083 | hp1 | a0001 | c0001 | t0006 | g0197 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA19087 | hp1 | a0001 | c0001 | t0007 | g0236 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA19087 | hp2 | a0001 | c0001 | t0041 | g0039 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA19090 | hp1 | a0001 | c0001 | t0006 | g0005 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA19090 | hp2 | a0001 | c0001 | t0016 | g0044 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | YRI | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA19240 | hp2 | a0001 | c0001 | t0013 | g0185 | AFR | YRI | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0240 | AFR | ASW | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA20129 | hp2 | a0001 | c0001 | t0005 | g0206 | AFR | ASW | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0113 | EUR | TSI | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA20752 | hp2 | a0001 | c0001 | t0032 | g0037 | EUR | TSI | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | TSI | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0140 | EUR | TSI | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | GIH | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0115 | SAS | GIH | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02109 | hp1 | a0001 | c0001 | t0005 | g0208 | AFR | ACB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG02559 | hp2 | a0001 | c0001 | t0012 | g0036 | AFR | ACB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0200 | AFR | MSL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG03471 | hp2 | a0001 | c0001 | t0011 | g0227 | AFR | MSL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0239 | AFR | USA | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0134 | AFR | USA | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA20300 | hp1 | a0001 | c0001 | t0018 | g0138 | AFR | USA | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA20300 | hp2 | a0001 | c0001 | t0009 | g0219 | AFR | USA | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA21309 | hp1 | a0001 | c0001 | t0017 | g0136 | AFR | LWK | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
NA21309 | hp2 | a0001 | c0001 | t0005 | g0241 | AFR | LWK | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0018 | g0137 | REF | REF | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0101 | REF | REF | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:40881790
|
T | C | 1 | a0002 | 1 | HG02132.hp1 | missense_variant | MODERATE | c.202T>C | p.Ser68Pro | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/10 | 236/7938 | 202/1524 | 68/507 | chr22 | 40881790 | ||
chr22:40886424
|
G | A | 1 | a0003 | 1 | NA18994.hp1 | missense_variant | MODERATE | c.701G>A | p.Arg234Gln | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/10 | 735/7938 | 701/1524 | 234/507 | chr22 | 40886424 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:40857244
|
A | G | 1 | a0001c0005 | 1 | HG02451.hp2 | splice_region_variant&synonymous_variant | LOW | c.63A>G | p.Ser21Ser | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/10 | 97/7938 | 63/1524 | 21/507 | chr22 | 40857244 | ||
chr22:40869045
|
A | G | 1 | a0001c0002 | 4 | HG01884.hp2 HG02630.hp1 HG03209.hp1 others(1): Show |
synonymous_variant | LOW | c.111A>G | p.Pro37Pro | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/10 | 145/7938 | 111/1524 | 37/507 | chr22 | 40869045 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:40857159
|
C | T | 1 | a0001c0001t0051 | 1 | NA19060.hp2 | 5_prime_UTR_variant | MODIFIER | c.-23C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/10 | 23 | chr22 | 40857159 | |||||
chr22:40926825
|
A | G | 1 | a0001c0002t0050 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*390A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 390 | chr22 | 40926825 | |||||
chr22:40926902
|
C | T | 8 | a0001c0001t0005a0001c0001t0021a0001c0001t0047others(5): Show | 17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*467C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 467 | chr22 | 40926902 | |||||
chr22:40926966
|
T | G | 1 | a0001c0001t0022 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*531T>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 531 | chr22 | 40926966 | |||||
chr22:40927312
|
A | G | 2 | a0001c0001t0011a0001c0001t0045 | 5 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*877A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 877 | chr22 | 40927312 | |||||
chr22:40927331
|
G | C | 1 | a0001c0001t0023 | 1 | NA18944.hp1 | 3_prime_UTR_variant | MODIFIER | c.*896G>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 896 | chr22 | 40927331 | |||||
chr22:40927485
|
T | C | 1 | a0001c0002t0046 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1050T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 1050 | chr22 | 40927485 | |||||
chr22:40927638
|
G | A | 2 | a0001c0001t0021a0001c0001t0047 | 3 | HG03098.hp2 HG03453.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1203G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 1203 | chr22 | 40927638 | |||||
chr22:40927650
|
G | A | 1 | a0001c0001t0047 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1215G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 1215 | chr22 | 40927650 | |||||
chr22:40927651
|
G | A | 1 | a0001c0001t0015 | 2 | NA18980.hp1 NA19065.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1216G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 1216 | chr22 | 40927651 | |||||
chr22:40927670
|
T | C | 1 | a0001c0001t0015 | 2 | NA18980.hp1 NA19065.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1235T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 1235 | chr22 | 40927670 | |||||
chr22:40927671
|
G | A | 1 | a0001c0001t0015 | 2 | NA18980.hp1 NA19065.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1236G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 1236 | chr22 | 40927671 | |||||
chr22:40927874
|
C | CA | 7 | a0001c0001t0006a0001c0001t0007a0001c0001t0016others(4): Show | 19 | HG00597.hp1 HG00597.hp2 HG01106.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1457dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 1458 | INFO_REALIGN_3_PRIME | chr22 | 40927874 | ||||
chr22:40927874
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0011 | 4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1445_*1457delAAAA others(9): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 1445 | INFO_REALIGN_3_PRIME | chr22 | 40927874 | ||||
chr22:40927887
|
A | G | 1 | a0001c0001t0020 | 2 | HG02602.hp2 HG03654.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1452A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 1452 | chr22 | 40927887 | |||||
chr22:40927966
|
A | G | 1 | a0001c0001t0027 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1531A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 1531 | chr22 | 40927966 | |||||
chr22:40928041
|
GC | G | 10 | a0001c0001t0004a0001c0001t0008a0001c0001t0010others(7): Show | 33 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1607delC | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 1607 | chr22 | 40928041 | |||||
chr22:40928201
|
C | CT | 13 | a0001c0001t0001a0001c0001t0006a0001c0001t0010others(10): Show | 83 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*1784dupT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 1785 | INFO_REALIGN_3_PRIME | chr22 | 40928201 | ||||
chr22:40928201
|
CT | C | 11 | a0001c0001t0005a0001c0001t0011a0001c0001t0021others(8): Show | 23 | HG00639.hp2 HG01884.hp2 HG02109.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1784delT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 1784 | INFO_REALIGN_3_PRIME | chr22 | 40928201 | ||||
chr22:40928683
|
A | G | 1 | a0001c0001t0033 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2248A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 2248 | chr22 | 40928683 | |||||
chr22:40929046
|
G | T | 2 | a0001c0001t0019a0001c0001t0022 | 3 | HG02886.hp1 HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2611G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 2611 | chr22 | 40929046 | |||||
chr22:40929064
|
G | A | 43 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(40): Show | 170 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*2629G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 2629 | chr22 | 40929064 | |||||
chr22:40929192
|
C | CT | 4 | a0001c0001t0019a0001c0001t0022a0001c0001t0040others(1): Show | 5 | HG02886.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2774dupT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 2775 | INFO_REALIGN_3_PRIME | chr22 | 40929192 | ||||
chr22:40929197
|
T | C | 1 | a0001c0001t0013 | 3 | HG02965.hp2 HG02976.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2762T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 2762 | chr22 | 40929197 | |||||
chr22:40929316
|
C | G | 8 | a0001c0001t0005a0001c0001t0021a0001c0001t0047others(5): Show | 17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2881C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 2881 | chr22 | 40929316 | |||||
chr22:40929393
|
G | A | 10 | a0001c0001t0005a0001c0001t0011a0001c0001t0021others(7): Show | 22 | HG00639.hp2 HG01884.hp2 HG02109.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2958G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 2958 | chr22 | 40929393 | |||||
chr22:40929413
|
G | A | 8 | a0001c0001t0005a0001c0001t0021a0001c0001t0047others(5): Show | 17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2978G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 2978 | chr22 | 40929413 | |||||
chr22:40929438
|
G | A | 1 | a0001c0001t0008 | 6 | HG01243.hp2 HG01496.hp2 HG02055.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3003G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 3003 | chr22 | 40929438 | |||||
chr22:40929562
|
A | G | 1 | a0001c0002t0046 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3127A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 3127 | chr22 | 40929562 | |||||
chr22:40929572
|
C | G | 10 | a0001c0001t0005a0001c0001t0011a0001c0001t0021others(7): Show | 22 | HG00639.hp2 HG01884.hp2 HG02109.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*3137C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 3137 | chr22 | 40929572 | |||||
chr22:40929611
|
T | C | 1 | a0001c0001t0042 | 1 | NA19054.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3176T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 3176 | chr22 | 40929611 | |||||
chr22:40929755
|
T | G | 1 | a0001c0001t0043 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3320T>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 3320 | chr22 | 40929755 | |||||
chr22:40929767
|
G | A | 1 | a0001c0001t0034 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3332G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 3332 | chr22 | 40929767 | |||||
chr22:40929786
|
C | T | 2 | a0001c0001t0012a0001c0001t0032 | 4 | HG00099.hp1 HG01433.hp1 HG02559.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3351C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 3351 | chr22 | 40929786 | |||||
chr22:40929801
|
C | T | 10 | a0001c0001t0005a0001c0001t0011a0001c0001t0021others(7): Show | 22 | HG00639.hp2 HG01884.hp2 HG02109.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*3366C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 3366 | chr22 | 40929801 | |||||
chr22:40929846
|
T | C | 4 | a0001c0001t0009a0001c0001t0019a0001c0001t0022others(1): Show | 8 | HG01934.hp2 HG02809.hp2 HG02886.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3411T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 3411 | chr22 | 40929846 | |||||
chr22:40930125
|
G | T | 9 | a0001c0001t0005a0001c0001t0011a0001c0001t0021others(6): Show | 21 | HG00639.hp2 HG01884.hp2 HG02109.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*3690G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 3690 | chr22 | 40930125 | |||||
chr22:40930133
|
G | GT | 4 | a0001c0001t0011a0001c0001t0026a0001c0001t0028others(1): Show | 7 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3712dupT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 3713 | INFO_REALIGN_3_PRIME | chr22 | 40930133 | ||||
chr22:40930240
|
C | T | 1 | a0001c0001t0038 | 1 | NA18995.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3805C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 3805 | chr22 | 40930240 | |||||
chr22:40930390
|
A | G | 2 | a0001c0001t0019a0001c0001t0022 | 3 | HG02886.hp1 HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3955A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 3955 | chr22 | 40930390 | |||||
chr22:40930797
|
C | G | 9 | a0001c0001t0005a0001c0001t0011a0001c0001t0021others(6): Show | 21 | HG00639.hp2 HG01884.hp2 HG02109.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*4362C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 4362 | chr22 | 40930797 | |||||
chr22:40930965
|
C | T | 2 | a0001c0001t0025a0001c0001t0031 | 2 | HG01109.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4530C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 4530 | chr22 | 40930965 | |||||
chr22:40930996
|
G | A | 2 | a0001c0001t0012a0001c0001t0032 | 4 | HG00099.hp1 HG01433.hp1 HG02559.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4561G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 4561 | chr22 | 40930996 | |||||
chr22:40931021
|
G | A | 8 | a0001c0001t0005a0001c0001t0021a0001c0001t0047others(5): Show | 17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*4586G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 4586 | chr22 | 40931021 | |||||
chr22:40931137
|
G | A | 11 | a0001c0001t0004a0001c0001t0008a0001c0001t0010others(8): Show | 34 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*4702G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 4702 | chr22 | 40931137 | |||||
chr22:40931806
|
T | C | 1 | a0001c0001t0044 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5371T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 5371 | chr22 | 40931806 | |||||
chr22:40931880
|
G | A | 1 | a0001c0001t0027 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5445G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 5445 | chr22 | 40931880 | |||||
chr22:40931962
|
A | G | 1 | a0001c0001t0037 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5527A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 5527 | chr22 | 40931962 | |||||
chr22:40931982
|
C | G | 1 | a0001c0001t0018 | 2 | NA20300.hp1 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5547C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 5547 | chr22 | 40931982 | |||||
chr22:40932049
|
C | A | 1 | a0001c0002t0048 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5614C>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 5614 | chr22 | 40932049 | |||||
chr22:40932078
|
C | G | 1 | a0001c0001t0011 | 4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5643C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 5643 | chr22 | 40932078 | |||||
chr22:40932204
|
T | A | 1 | a0001c0001t0049 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5769T>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 5769 | chr22 | 40932204 | |||||
chr22:40932206
|
C | A | 1 | a0001c0001t0049 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5771C>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 5771 | chr22 | 40932206 | |||||
chr22:40932337
|
G | GT | 3 | a0001c0001t0009a0001c0001t0036a0001c0001t0045 | 6 | HG01934.hp2 HG02809.hp2 HG03098.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5915dupT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 5916 | INFO_REALIGN_3_PRIME | chr22 | 40932337 | ||||
chr22:40932337
|
GT | G | 8 | a0001c0001t0008a0001c0001t0011a0001c0001t0017others(5): Show | 18 | HG00639.hp2 HG01109.hp2 HG01243.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*5915delT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 5915 | INFO_REALIGN_3_PRIME | chr22 | 40932337 | ||||
chr22:40932350
|
T | A | 1 | a0001c0001t0030 | 1 | HG02293.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5915T>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 5915 | chr22 | 40932350 | |||||
chr22:40932490
|
A | C | 1 | a0001c0001t0013 | 3 | HG02965.hp2 HG02976.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6055A>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 6055 | chr22 | 40932490 | |||||
chr22:40932614
|
G | A | 2 | a0001c0001t0025a0001c0001t0031 | 2 | HG01109.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6179G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 6179 | chr22 | 40932614 | |||||
chr22:40932636
|
A | T | 8 | a0001c0001t0005a0001c0001t0021a0001c0001t0047others(5): Show | 17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*6201A>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 6201 | chr22 | 40932636 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:40857280
|
G | T | 1 | a0001c0001t0005g0241 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.64+35G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40857280 | ||||||
chr22:40857362
|
C | T | 3 | a0001c0001t0002g0007a0001c0001t0002g0239a0001c0001t0002g0240 | 4 | HG03130.hp1 HG03139.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+117C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40857362 | ||||||
chr22:40857708
|
C | G | 1 | a0001c0001t0002g0238 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.64+463C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40857708 | ||||||
chr22:40857811
|
A | C | 9 | a0001c0001t0002g0230a0001c0001t0002g0231a0001c0001t0002g0232others(6): Show | 9 | NA18949.hp1 NA18969.hp2 NA18975.hp2 others(6): Show |
intron_variant | MODIFIER | c.64+566A>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40857811 | ||||||
chr22:40857818
|
C | A | 1 | a0001c0001t0047g0008 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.64+573C>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40857818 | ||||||
chr22:40858242
|
G | C | 3 | a0001c0001t0019g0010a0001c0001t0019g0011a0001c0001t0022g0009 | 3 | HG02886.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.64+997G>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40858242 | ||||||
chr22:40858293
|
A | G | 31 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(28): Show | 31 | HG00639.hp2 HG01884.hp2 HG01934.hp2 others(28): Show |
intron_variant | MODIFIER | c.64+1048A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40858293 | ||||||
chr22:40858303
|
TGCCACGT others(2): Show |
T | 17 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(14): Show | 17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.64+1063_64+1071del others(9): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 40858303 | |||||
chr22:40858373
|
C | G | 1 | a0001c0001t0027g0228 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.64+1128C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40858373 | ||||||
chr22:40858522
|
C | CT | 23 | a0001c0001t0001g0180a0001c0001t0002g0181a0001c0001t0002g0182others(20): Show | 23 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.64+1301dupT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 40858522 | |||||
chr22:40858522
|
C | CTT | 5 | a0001c0001t0002g0198a0001c0001t0003g0199a0001c0001t0003g0200others(2): Show | 5 | HG02572.hp1 HG02630.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+1300_64+1301dup others(2): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 40858522 | |||||
chr22:40858522
|
CT | C | 69 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(66): Show | 70 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.64+1301delT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 40858522 | |||||
chr22:40858522
|
CTT | C | 13 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(10): Show | 13 | HG02109.hp1 HG02615.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.64+1300_64+1301del others(2): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 40858522 | |||||
chr22:40858546
|
T | G | 6 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0008g0066others(3): Show | 6 | HG00733.hp1 HG01496.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.64+1301T>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40858546 | ||||||
chr22:40858646
|
C | T | 1 | a0001c0001t0047g0008 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.64+1401C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40858646 | ||||||
chr22:40858980
|
G | T | 4 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177others(1): Show | 4 | NA18967.hp1 NA18968.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+1735G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40858980 | ||||||
chr22:40859030
|
A | G | 4 | a0001c0001t0011g0224a0001c0001t0011g0225a0001c0001t0011g0226others(1): Show | 4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+1785A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40859030 | ||||||
chr22:40859159
|
G | A | 17 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(14): Show | 17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.64+1914G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40859159 | ||||||
chr22:40859233
|
G | A | 1 | a0001c0001t0027g0228 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.64+1988G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40859233 | ||||||
chr22:40859386
|
A | T | 2 | a0001c0001t0025g0173a0001c0001t0031g0174 | 2 | HG01109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.64+2141A>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40859386 | ||||||
chr22:40859557
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.64+2312A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40859557 | ||||||
chr22:40859667
|
A | G | 17 | a0001c0001t0003g0056a0001c0001t0003g0058a0001c0001t0003g0059others(14): Show | 17 | HG02055.hp1 HG02258.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.64+2422A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40859667 | ||||||
chr22:40859741
|
C | T | 1 | a0001c0001t0005g0216 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.64+2496C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40859741 | ||||||
chr22:40859815
|
G | C | 17 | a0001c0001t0003g0056a0001c0001t0003g0058a0001c0001t0003g0059others(14): Show | 17 | HG02055.hp1 HG02258.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.64+2570G>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40859815 | ||||||
chr22:40859957
|
G | A | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG01515.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.64+2712G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40859957 | ||||||
chr22:40860157
|
A | C | 2 | a0001c0001t0025g0173a0001c0001t0031g0174 | 2 | HG01109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.64+2912A>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40860157 | ||||||
chr22:40860181
|
A | G | 1 | a0001c0001t0008g0170 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.64+2936A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40860181 | ||||||
chr22:40860363
|
C | T | 33 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(30): Show | 34 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.64+3118C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40860363 | ||||||
chr22:40860656
|
CT | C | 8 | a0001c0001t0001g0004a0001c0001t0001g0072a0001c0001t0005g0212others(5): Show | 9 | HG00639.hp2 HG03041.hp2 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.64+3425delT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 40860656 | |||||
chr22:40860676
|
A | G | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG02015.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.64+3431A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40860676 | ||||||
chr22:40860708
|
A | G | 4 | a0001c0001t0011g0224a0001c0001t0011g0225a0001c0001t0011g0226others(1): Show | 4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+3463A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40860708 | ||||||
chr22:40860798
|
A | G | 164 | a0001c0001t0001g0146a0001c0001t0002g0006a0001c0001t0002g0007others(161): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.64+3553A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40860798 | ||||||
chr22:40860879
|
C | G | 1 | a0001c0001t0005g0212 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.64+3634C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40860879 | ||||||
chr22:40861047
|
T | C | 17 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(14): Show | 17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.64+3802T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40861047 | ||||||
chr22:40861209
|
G | A | 5 | a0001c0001t0002g0115a0001c0001t0009g0218a0001c0001t0009g0219others(2): Show | 5 | HG01934.hp2 HG02809.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+3964G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40861209 | ||||||
chr22:40861389
|
C | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0064a0001c0001t0001g0065 | 3 | HG00733.hp1 HG01109.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.64+4144C>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40861389 | ||||||
chr22:40861616
|
A | C | 4 | a0001c0001t0005g0212a0001c0001t0021g0210a0001c0001t0021g0211others(1): Show | 4 | HG03098.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+4371A>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40861616 | ||||||
chr22:40861655
|
C | A | 1 | a0001c0001t0002g0116 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.64+4410C>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40861655 | ||||||
chr22:40861735
|
C | G | 1 | a0001c0001t0001g0031 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.64+4490C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40861735 | ||||||
chr22:40861830
|
T | TA | 7 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0002g0120others(4): Show | 7 | HG00423.hp1 HG00735.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.64+4586dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 40861830 | |||||
chr22:40861873
|
T | G | 15 | a0001c0001t0002g0116a0001c0001t0002g0121a0001c0001t0002g0184others(12): Show | 15 | HG01167.hp1 HG04228.hp1 NA18949.hp1 others(12): Show |
intron_variant | MODIFIER | c.64+4628T>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40861873 | ||||||
chr22:40862140
|
A | G | 69 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(66): Show | 70 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.64+4895A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40862140 | ||||||
chr22:40862404
|
G | A | 6 | a0001c0001t0008g0066a0001c0001t0008g0067a0001c0001t0008g0068others(3): Show | 6 | HG01243.hp2 HG01496.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.64+5159G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40862404 | ||||||
chr22:40862427
|
C | G | 2 | a0001c0001t0015g0122a0001c0001t0015g0123 | 2 | NA18980.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.64+5182C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40862427 | ||||||
chr22:40862657
|
T | C | 8 | a0001c0001t0004g0001a0001c0001t0004g0040a0001c0001t0004g0041others(5): Show | 8 | NA18949.hp2 NA18960.hp1 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.64+5412T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40862657 | ||||||
chr22:40862673
|
GC | G | 4 | a0001c0001t0011g0224a0001c0001t0011g0225a0001c0001t0011g0226others(1): Show | 4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+5430delC | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 40862673 | |||||
chr22:40863619
|
A | G | 4 | a0001c0001t0011g0224a0001c0001t0011g0225a0001c0001t0011g0226others(1): Show | 4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-5380A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40863619 | ||||||
chr22:40864133
|
G | C | 4 | a0001c0001t0009g0218a0001c0001t0009g0219a0001c0001t0009g0220others(1): Show | 4 | HG01934.hp2 HG02809.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-4866G>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40864133 | ||||||
chr22:40864420
|
A | G | 2 | a0001c0001t0025g0173a0001c0001t0031g0174 | 2 | HG01109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.65-4579A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40864420 | ||||||
chr22:40864701
|
T | C | 1 | a0001c0001t0037g0032 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.65-4298T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40864701 | ||||||
chr22:40864708
|
G | A | 4 | a0001c0001t0011g0224a0001c0001t0011g0225a0001c0001t0011g0226others(1): Show | 4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-4291G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40864708 | ||||||
chr22:40864822
|
T | A | 1 | a0001c0001t0002g0124 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.65-4177T>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40864822 | ||||||
chr22:40864842
|
C | G | 5 | a0001c0001t0012g0035a0001c0001t0012g0036a0001c0001t0012g0038others(2): Show | 5 | HG00099.hp1 HG01433.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-4157C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40864842 | ||||||
chr22:40864927
|
C | T | 1 | a0001c0001t0002g0162 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.65-4072C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40864927 | ||||||
chr22:40864989
|
C | A | 1 | a0001c0001t0002g0125 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.65-4010C>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40864989 | ||||||
chr22:40865005
|
A | C | 1 | a0001c0001t0001g0114 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.65-3994A>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40865005 | ||||||
chr22:40865311
|
G | A | 1 | a0001c0001t0045g0034 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.65-3688G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40865311 | ||||||
chr22:40865325
|
CT | C | 140 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(137): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.65-3654delT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 40865325 | |||||
chr22:40865325
|
CTT | C | 33 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(30): Show | 33 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.65-3655_65-3654del others(2): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 40865325 | |||||
chr22:40865555
|
C | T | 1 | a0001c0001t0002g0161 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.65-3444C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40865555 | ||||||
chr22:40865699
|
G | T | 2 | a0001c0001t0002g0159a0001c0001t0002g0160 | 2 | HG01515.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.65-3300G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40865699 | ||||||
chr22:40865742
|
G | T | 1 | a0001c0001t0002g0158 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.65-3257G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40865742 | ||||||
chr22:40865743
|
C | T | 1 | a0001c0001t0002g0158 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.65-3256C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40865743 | ||||||
chr22:40865815
|
A | G | 22 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(19): Show | 22 | HG00639.hp2 HG01884.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.65-3184A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40865815 | ||||||
chr22:40866099
|
A | G | 4 | a0001c0001t0012g0035a0001c0001t0012g0036a0001c0001t0012g0038others(1): Show | 4 | HG00099.hp1 HG01433.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-2900A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40866099 | ||||||
chr22:40866123
|
A | T | 6 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0110others(3): Show | 6 | HG00639.hp1 HG01515.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-2876A>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40866123 | ||||||
chr22:40866149
|
T | C | 17 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(14): Show | 17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.65-2850T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40866149 | ||||||
chr22:40866353
|
G | A | 6 | a0001c0001t0009g0218a0001c0001t0009g0219a0001c0001t0009g0220others(3): Show | 6 | HG01934.hp2 HG02809.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-2646G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40866353 | ||||||
chr22:40866460
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.65-2539C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40866460 | ||||||
chr22:40866575
|
A | G | 1 | a0001c0001t0001g0030 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.65-2424A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40866575 | ||||||
chr22:40866644
|
A | G | 1 | a0001c0001t0002g0157 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.65-2355A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40866644 | ||||||
chr22:40866847
|
G | A | 1 | a0001c0001t0010g0166 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.65-2152G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40866847 | ||||||
chr22:40866848
|
C | T | 22 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0126others(19): Show | 24 | HG00140.hp1 HG00733.hp2 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.65-2151C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40866848 | ||||||
chr22:40866947
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.65-2052C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40866947 | ||||||
chr22:40866994
|
G | A | 4 | a0001c0001t0009g0218a0001c0001t0009g0219a0001c0001t0009g0220others(1): Show | 4 | HG01934.hp2 HG02809.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-2005G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40866994 | ||||||
chr22:40867363
|
A | G | 2 | a0001c0001t0025g0173a0001c0001t0031g0174 | 2 | HG01109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.65-1636A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40867363 | ||||||
chr22:40867368
|
C | T | 17 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(14): Show | 17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.65-1631C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40867368 | ||||||
chr22:40867419
|
A | G | 1 | a0001c0001t0001g0031 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.65-1580A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40867419 | ||||||
chr22:40867769
|
T | C | 3 | a0001c0001t0001g0004a0001c0001t0001g0072a0001c0001t0001g0079 | 4 | HG00544.hp2 NA18964.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-1230T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40867769 | ||||||
chr22:40867936
|
C | CA | 17 | a0001c0001t0001g0016a0001c0001t0001g0109a0001c0001t0001g0114others(14): Show | 17 | HG00438.hp2 HG00639.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.65-1045dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 40867936 | |||||
chr22:40867936
|
CA | C | 15 | a0001c0001t0002g0128a0001c0001t0005g0203a0001c0001t0005g0204others(12): Show | 15 | HG01167.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.65-1045delA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 40867936 | |||||
chr22:40868139
|
T | G | 3 | a0001c0001t0013g0129a0001c0001t0013g0130a0001c0001t0013g0185 | 3 | HG02965.hp2 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.65-860T>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40868139 | ||||||
chr22:40868428
|
C | CGT | 53 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0003g0202others(50): Show | 54 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.65-546_65-545dupGT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 40868428 | |||||
chr22:40868428
|
C | CGTGT | 3 | a0001c0001t0003g0029a0001c0001t0011g0226a0001c0001t0011g0227 | 3 | HG01981.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-548_65-545dupGT others(2): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 40868428 | |||||
chr22:40868428
|
CGT | C | 14 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(11): Show | 14 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.65-546_65-545delGT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 40868428 | |||||
chr22:40868446
|
T | TGA | 9 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(6): Show | 9 | HG02109.hp1 HG02615.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.65-552_65-551insAG | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 40868446 | |||||
chr22:40868537
|
T | G | 2 | a0001c0001t0001g0110a0001c0001t0001g0111 | 2 | HG03492.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.65-462T>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40868537 | ||||||
chr22:40868658
|
C | G | 4 | a0001c0001t0001g0005a0001c0001t0001g0105a0001c0001t0001g0106others(1): Show | 4 | NA18961.hp1 NA19054.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-341C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40868658 | ||||||
chr22:40868705
|
A | G | 22 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(19): Show | 22 | HG00639.hp2 HG01884.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.65-294A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40868705 | ||||||
chr22:40869139
|
C | T | 17 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(14): Show | 17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.181+24C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40869139 | ||||||
chr22:40869331
|
T | C | 1 | a0001c0001t0001g0022 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.181+216T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40869331 | ||||||
chr22:40869770
|
T | C | 1 | a0001c0001t0002g0118 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.181+655T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40869770 | ||||||
chr22:40869816
|
G | A | 22 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(19): Show | 22 | HG00639.hp2 HG01884.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.181+701G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40869816 | ||||||
chr22:40869896
|
A | G | 1 | a0001c0001t0027g0228 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.181+781A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40869896 | ||||||
chr22:40869999
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.181+884T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40869999 | ||||||
chr22:40870406
|
A | G | 1 | a0001c0001t0045g0034 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.181+1291A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40870406 | ||||||
chr22:40870526
|
A | G | 2 | a0001c0001t0002g0148a0001c0001t0007g0188 | 2 | HG01192.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.181+1411A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40870526 | ||||||
chr22:40870968
|
G | C | 5 | a0001c0001t0003g0193a0001c0001t0003g0194a0001c0001t0003g0195others(2): Show | 5 | HG02280.hp2 HG02965.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.181+1853G>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40870968 | ||||||
chr22:40871034
|
A | G | 1 | a0001c0001t0027g0228 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.181+1919A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40871034 | ||||||
chr22:40871058
|
T | C | 1 | a0001c0001t0003g0029 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.181+1943T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40871058 | ||||||
chr22:40871360
|
C | A | 22 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(19): Show | 22 | HG00639.hp2 HG01884.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.181+2245C>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40871360 | ||||||
chr22:40871665
|
G | C | 2 | a0001c0001t0003g0062a0001c0001t0003g0063 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.181+2550G>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40871665 | ||||||
chr22:40872215
|
G | T | 2 | a0001c0002t0005g0215a0001c0002t0048g0214 | 2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.181+3100G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40872215 | ||||||
chr22:40872489
|
C | T | 18 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(15): Show | 18 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.181+3374C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40872489 | ||||||
chr22:40872611
|
C | T | 2 | a0001c0001t0002g0118a0001c0001t0002g0120 | 2 | HG01934.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.181+3496C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40872611 | ||||||
chr22:40872921
|
T | G | 189 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(186): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.181+3806T>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40872921 | ||||||
chr22:40872980
|
G | A | 1 | a0001c0001t0045g0034 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.181+3865G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40872980 | ||||||
chr22:40873098
|
C | CT | 13 | a0001c0001t0001g0030a0001c0001t0001g0104a0001c0001t0001g0180others(10): Show | 13 | HG00423.hp2 HG01192.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.181+4008dupT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr22 | 40873098 | |||||
chr22:40873098
|
CT | C | 43 | a0001c0001t0001g0013a0001c0001t0001g0064a0001c0001t0001g0073others(40): Show | 44 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.181+4008delT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr22 | 40873098 | |||||
chr22:40873098
|
CTT | C | 22 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(19): Show | 22 | HG01884.hp2 HG01934.hp2 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.181+4007_181+4008d others(4): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr22 | 40873098 | |||||
chr22:40873103
|
T | C | 3 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0049g0209 | 3 | HG02109.hp1 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.181+3988T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40873103 | ||||||
chr22:40873104
|
T | C | 14 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(11): Show | 14 | HG01884.hp2 HG02622.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.181+3989T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40873104 | ||||||
chr22:40873208
|
A | G | 22 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(19): Show | 22 | HG00639.hp2 HG01884.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.181+4093A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40873208 | ||||||
chr22:40873877
|
A | G | 17 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(14): Show | 17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.181+4762A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40873877 | ||||||
chr22:40873924
|
A | G | 1 | a0001c0001t0001g0103 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.181+4809A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40873924 | ||||||
chr22:40874164
|
A | G | 1 | a0001c0001t0003g0085 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.181+5049A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40874164 | ||||||
chr22:40874421
|
G | GTGTTTT | 29 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(26): Show | 29 | HG00639.hp2 HG01884.hp2 HG01934.hp2 others(26): Show |
intron_variant | MODIFIER | c.181+5320_181+5325d others(8): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr22 | 40874421 | |||||
chr22:40874435
|
G | GT | 33 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(30): Show | 34 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.181+5328dupT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr22 | 40874435 | |||||
chr22:40874518
|
G | T | 29 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(26): Show | 29 | HG00639.hp2 HG01884.hp2 HG01934.hp2 others(26): Show |
intron_variant | MODIFIER | c.181+5403G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40874518 | ||||||
chr22:40874632
|
C | T | 4 | a0001c0001t0011g0224a0001c0001t0011g0225a0001c0001t0011g0226others(1): Show | 4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.181+5517C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40874632 | ||||||
chr22:40874713
|
A | G | 1 | a0001c0001t0005g0206 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.181+5598A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40874713 | ||||||
chr22:40874726
|
G | A | 4 | a0001c0001t0012g0035a0001c0001t0012g0036a0001c0001t0012g0038others(1): Show | 4 | HG00099.hp1 HG01433.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.181+5611G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40874726 | ||||||
chr22:40874960
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.181+5845A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40874960 | ||||||
chr22:40875144
|
C | A | 1 | a0001c0001t0002g0198 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.181+6029C>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40875144 | ||||||
chr22:40875229
|
G | T | 1 | a0001c0001t0022g0009 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.181+6114G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40875229 | ||||||
chr22:40875273
|
G | A | 1 | a0001c0001t0002g0157 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.181+6158G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40875273 | ||||||
chr22:40875663
|
T | C | 1 | a0001c0001t0001g0087 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.182-6107T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40875663 | ||||||
chr22:40875850
|
T | TA | 6 | a0001c0001t0001g0104a0001c0001t0001g0176a0001c0001t0002g0132others(3): Show | 6 | HG02027.hp1 HG03654.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.182-5900dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr22 | 40875850 | |||||
chr22:40875850
|
TA | T | 30 | a0001c0001t0004g0052a0001c0001t0005g0203a0001c0001t0005g0204others(27): Show | 30 | HG00639.hp2 HG01884.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.182-5900delA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr22 | 40875850 | |||||
chr22:40875931
|
A | G | 5 | a0001c0001t0002g0156a0001c0001t0002g0159a0001c0001t0002g0160others(2): Show | 5 | HG01256.hp2 HG01258.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.182-5839A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40875931 | ||||||
chr22:40876072
|
T | G | 1 | a0001c0001t0002g0121 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.182-5698T>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40876072 | ||||||
chr22:40876139
|
T | C | 160 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0115others(157): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.182-5631T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40876139 | ||||||
chr22:40876260
|
T | G | 1 | a0001c0001t0004g0043 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.182-5510T>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40876260 | ||||||
chr22:40876411
|
C | T | 22 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(19): Show | 22 | HG00639.hp2 HG01884.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.182-5359C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40876411 | ||||||
chr22:40876556
|
TAGTGAAT others(104): Show |
T | 1 | a0001c0001t0001g0073 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.182-5139_182-5029d others(2): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr22 | 40876556 | |||||
chr22:40876585
|
C | T | 1 | a0001c0001t0014g0189 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.182-5185C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40876585 | ||||||
chr22:40876879
|
T | A | 2 | a0001c0001t0003g0088a0001c0001t0023g0089 | 2 | NA18942.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.182-4891T>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40876879 | ||||||
chr22:40877194
|
C | G | 4 | a0001c0001t0001g0005a0001c0001t0001g0105a0001c0001t0001g0106others(1): Show | 4 | NA18961.hp1 NA19054.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.182-4576C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40877194 | ||||||
chr22:40877219
|
C | G | 4 | a0001c0001t0011g0224a0001c0001t0011g0225a0001c0001t0011g0226others(1): Show | 4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.182-4551C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40877219 | ||||||
chr22:40877350
|
A | G | 1 | a0001c0001t0002g0155 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.182-4420A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40877350 | ||||||
chr22:40877356
|
C | T | 3 | a0001c0001t0010g0166a0001c0001t0010g0192a0001c0001t0042g0167 | 3 | NA18995.hp1 NA19010.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.182-4414C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40877356 | ||||||
chr22:40877717
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.182-4053T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40877717 | ||||||
chr22:40877762
|
A | G | 17 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(14): Show | 17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.182-4008A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40877762 | ||||||
chr22:40877926
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.182-3844T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40877926 | ||||||
chr22:40877979
|
G | A | 1 | a0001c0001t0006g0083 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.182-3791G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40877979 | ||||||
chr22:40878137
|
C | T | 1 | a0001c0001t0006g0086 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.182-3633C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40878137 | ||||||
chr22:40878206
|
C | CA | 20 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(17): Show | 20 | HG00639.hp2 HG01884.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.182-3547dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr22 | 40878206 | |||||
chr22:40878388
|
CAT | C | 4 | a0001c0001t0011g0224a0001c0001t0011g0225a0001c0001t0011g0226others(1): Show | 4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.182-3380_182-3379d others(4): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr22 | 40878388 | |||||
chr22:40878523
|
CAT | C | 4 | a0001c0001t0011g0224a0001c0001t0011g0225a0001c0001t0011g0226others(1): Show | 4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.182-3245_182-3244d others(4): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr22 | 40878523 | |||||
chr22:40878840
|
G | A | 1 | a0001c0001t0017g0221 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.182-2930G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40878840 | ||||||
chr22:40879120
|
A | C | 4 | a0001c0001t0012g0035a0001c0001t0012g0036a0001c0001t0012g0038others(1): Show | 4 | HG00099.hp1 HG01433.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.182-2650A>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40879120 | ||||||
chr22:40879241
|
T | C | 4 | a0001c0001t0011g0224a0001c0001t0011g0225a0001c0001t0011g0226others(1): Show | 4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.182-2529T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40879241 | ||||||
chr22:40879255
|
C | G | 3 | a0001c0001t0013g0129a0001c0001t0013g0130a0001c0001t0013g0185 | 3 | HG02965.hp2 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.182-2515C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40879255 | ||||||
chr22:40880028
|
C | CA | 22 | a0001c0001t0001g0018a0001c0001t0001g0090a0001c0001t0001g0176others(19): Show | 22 | HG00639.hp2 HG01192.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.182-1720dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr22 | 40880028 | |||||
chr22:40880117
|
G | A | 1 | a0001c0001t0045g0034 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.182-1653G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40880117 | ||||||
chr22:40880264
|
AG | A | 4 | a0001c0001t0011g0224a0001c0001t0011g0225a0001c0001t0011g0226others(1): Show | 4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.182-1505delG | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40880264 | ||||||
chr22:40880267
|
T | G | 4 | a0001c0001t0011g0224a0001c0001t0011g0225a0001c0001t0011g0226others(1): Show | 4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.182-1503T>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40880267 | ||||||
chr22:40880268
|
A | G | 4 | a0001c0001t0011g0224a0001c0001t0011g0225a0001c0001t0011g0226others(1): Show | 4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.182-1502A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40880268 | ||||||
chr22:40880271
|
G | A | 4 | a0001c0001t0011g0224a0001c0001t0011g0225a0001c0001t0011g0226others(1): Show | 4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.182-1499G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40880271 | ||||||
chr22:40880273
|
C | T | 4 | a0001c0001t0011g0224a0001c0001t0011g0225a0001c0001t0011g0226others(1): Show | 4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.182-1497C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40880273 | ||||||
chr22:40880657
|
G | A | 4 | a0001c0001t0011g0224a0001c0001t0011g0225a0001c0001t0011g0226others(1): Show | 4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.182-1113G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40880657 | ||||||
chr22:40880712
|
C | T | 4 | a0001c0001t0005g0212a0001c0001t0021g0210a0001c0001t0021g0211others(1): Show | 4 | HG03098.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.182-1058C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40880712 | ||||||
chr22:40880772
|
A | T | 33 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(30): Show | 34 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.182-998A>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40880772 | ||||||
chr22:40880784
|
T | A | 1 | a0001c0001t0002g0133 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.182-986T>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40880784 | ||||||
chr22:40880787
|
C | CA | 25 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0090others(22): Show | 26 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.182-966dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr22 | 40880787 | |||||
chr22:40880787
|
CA | C | 12 | a0001c0001t0002g0127a0001c0001t0009g0220a0001c0001t0011g0224others(9): Show | 12 | HG00639.hp2 HG02809.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.182-966delA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr22 | 40880787 | |||||
chr22:40880956
|
G | A | 4 | a0001c0001t0011g0224a0001c0001t0011g0225a0001c0001t0011g0226others(1): Show | 4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.182-814G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40880956 | ||||||
chr22:40881162
|
C | T | 1 | a0001c0001t0027g0228 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.182-608C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40881162 | ||||||
chr22:40881170
|
C | G | 1 | a0001c0001t0004g0041 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.182-600C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40881170 | ||||||
chr22:40881456
|
C | CA | 15 | a0001c0001t0001g0023a0001c0001t0002g0126a0001c0001t0002g0128others(12): Show | 15 | HG00140.hp1 HG00733.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.182-298dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr22 | 40881456 | |||||
chr22:40881456
|
CA | C | 37 | a0001c0001t0001g0005a0001c0001t0001g0114a0001c0001t0002g0127others(34): Show | 37 | HG00639.hp2 HG01884.hp2 HG01934.hp2 others(34): Show |
intron_variant | MODIFIER | c.182-298delA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr22 | 40881456 | |||||
chr22:40882243
|
A | C | 9 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(6): Show | 9 | HG02109.hp1 HG02615.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.589+66A>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40882243 | ||||||
chr22:40882322
|
C | T | 17 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(14): Show | 17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.589+145C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40882322 | ||||||
chr22:40882491
|
G | T | 1 | a0001c0001t0001g0087 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.589+314G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40882491 | ||||||
chr22:40882503
|
C | A | 4 | a0001c0001t0002g0132a0001c0001t0002g0135a0001c0001t0002g0158others(1): Show | 4 | HG01361.hp1 HG02027.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.589+326C>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40882503 | ||||||
chr22:40882527
|
C | T | 4 | a0001c0001t0011g0224a0001c0001t0011g0225a0001c0001t0011g0226others(1): Show | 4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.589+350C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40882527 | ||||||
chr22:40882634
|
T | TA | 33 | a0001c0001t0003g0056a0001c0001t0003g0058a0001c0001t0003g0059others(30): Show | 33 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.589+470dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr22 | 40882634 | |||||
chr22:40882752
|
T | A | 9 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(6): Show | 9 | HG02109.hp1 HG02615.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.589+575T>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40882752 | ||||||
chr22:40882971
|
C | A | 1 | a0001c0001t0013g0129 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.589+794C>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40882971 | ||||||
chr22:40883598
|
G | A | 3 | a0001c0001t0019g0010a0001c0001t0019g0011a0001c0001t0022g0009 | 3 | HG02886.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.589+1421G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40883598 | ||||||
chr22:40883665
|
G | C | 1 | a0001c0001t0001g0090 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.589+1488G>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40883665 | ||||||
chr22:40883904
|
G | T | 9 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(6): Show | 9 | HG02109.hp1 HG02615.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.589+1727G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40883904 | ||||||
chr22:40884494
|
G | A | 1 | a0001c0001t0022g0009 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.590-1819G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40884494 | ||||||
chr22:40884722
|
C | G | 1 | a0001c0001t0012g0036 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.590-1591C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40884722 | ||||||
chr22:40884855
|
G | A | 4 | a0001c0002t0005g0215a0001c0002t0046g0217a0001c0002t0048g0214others(1): Show | 4 | HG01884.hp2 HG02630.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.590-1458G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40884855 | ||||||
chr22:40884889
|
G | A | 3 | a0001c0001t0002g0007a0001c0001t0002g0239a0001c0001t0002g0240 | 4 | HG03130.hp1 HG03139.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.590-1424G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40884889 | ||||||
chr22:40884963
|
G | A | 6 | a0001c0001t0008g0066a0001c0001t0008g0067a0001c0001t0008g0068others(3): Show | 6 | HG01243.hp2 HG01496.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.590-1350G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40884963 | ||||||
chr22:40885091
|
A | G | 1 | a0001c0001t0027g0228 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.590-1222A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40885091 | ||||||
chr22:40885418
|
A | G | 4 | a0001c0001t0011g0224a0001c0001t0011g0225a0001c0001t0011g0226others(1): Show | 4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.590-895A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40885418 | ||||||
chr22:40885588
|
A | T | 1 | a0001c0001t0006g0017 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.590-725A>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40885588 | ||||||
chr22:40885647
|
C | T | 6 | a0001c0001t0009g0218a0001c0001t0009g0219a0001c0001t0009g0220others(3): Show | 6 | HG01934.hp2 HG02809.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.590-666C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40885647 | ||||||
chr22:40885760
|
G | A | 2 | a0001c0001t0017g0136a0001c0001t0024g0145 | 2 | HG02257.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.590-553G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40885760 | ||||||
chr22:40885880
|
G | T | 9 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(6): Show | 9 | HG02109.hp1 HG02615.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.590-433G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40885880 | ||||||
chr22:40885977
|
A | G | 4 | a0001c0001t0011g0224a0001c0001t0011g0225a0001c0001t0011g0226others(1): Show | 4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.590-336A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40885977 | ||||||
chr22:40885987
|
TAAAG | T | 4 | a0001c0001t0001g0073a0001c0001t0001g0078a0001c0001t0001g0163others(1): Show | 4 | HG02015.hp2 NA18747.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.590-324_590-321del others(4): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr22 | 40885987 | |||||
chr22:40886043
|
C | A | 5 | a0001c0001t0002g0117a0001c0001t0002g0181a0001c0001t0002g0182others(2): Show | 5 | HG00423.hp1 HG00735.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.590-270C>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40886043 | ||||||
chr22:40886061
|
C | G | 1 | a0001c0001t0001g0102 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.590-252C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40886061 | ||||||
chr22:40886246
|
T | C | 1 | a0001c0001t0003g0092 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.590-67T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40886246 | ||||||
chr22:40886304
|
C | T | 4 | a0001c0001t0011g0224a0001c0001t0011g0225a0001c0001t0011g0226others(1): Show | 4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.590-9C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40886304 | ||||||
chr22:40886305
|
A | G | 1 | a0001c0001t0001g0113 | 1 | NA20752.hp1 | splice_region_variant&intron_variant | LOW | c.590-8A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40886305 | ||||||
chr22:40886588
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.792+73G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40886588 | ||||||
chr22:40886783
|
G | T | 33 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(30): Show | 34 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.792+268G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40886783 | ||||||
chr22:40886826
|
C | CA | 17 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(14): Show | 17 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.792+328dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40886826 | |||||
chr22:40886826
|
CA | C | 29 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(26): Show | 29 | HG00639.hp2 HG01884.hp2 HG01934.hp2 others(26): Show |
intron_variant | MODIFIER | c.792+328delA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40886826 | |||||
chr22:40886902
|
A | G | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG00733.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.792+387A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40886902 | ||||||
chr22:40886974
|
A | G | 9 | a0001c0001t0009g0218a0001c0001t0009g0219a0001c0001t0009g0220others(6): Show | 9 | HG01934.hp2 HG02809.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.792+459A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40886974 | ||||||
chr22:40887197
|
G | C | 6 | a0001c0001t0009g0218a0001c0001t0009g0219a0001c0001t0009g0220others(3): Show | 6 | HG01934.hp2 HG02809.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.792+682G>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40887197 | ||||||
chr22:40887480
|
C | T | 2 | a0001c0001t0001g0030a0001c0001t0014g0012 | 2 | HG02559.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.792+965C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40887480 | ||||||
chr22:40887705
|
C | A | 31 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(28): Show | 31 | HG00639.hp2 HG01884.hp2 HG01934.hp2 others(28): Show |
intron_variant | MODIFIER | c.792+1190C>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40887705 | ||||||
chr22:40887747
|
G | C | 2 | a0001c0001t0018g0137a0001c0001t0018g0138 | 2 | NA20300.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.792+1232G>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40887747 | ||||||
chr22:40887845
|
CT | C | 9 | a0001c0001t0009g0218a0001c0001t0009g0219a0001c0001t0009g0220others(6): Show | 9 | HG01934.hp2 HG02809.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.792+1331delT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40887845 | ||||||
chr22:40887980
|
G | A | 170 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(167): Show | 172 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.792+1465G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40887980 | ||||||
chr22:40888000
|
A | G | 1 | a0001c0001t0001g0078 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.792+1485A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40888000 | ||||||
chr22:40888005
|
A | G | 1 | a0001c0001t0005g0212 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.792+1490A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40888005 | ||||||
chr22:40888042
|
G | A | 4 | a0001c0001t0011g0224a0001c0001t0011g0225a0001c0001t0011g0226others(1): Show | 4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.792+1527G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40888042 | ||||||
chr22:40888531
|
G | T | 1 | a0001c0001t0001g0018 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.792+2016G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40888531 | ||||||
chr22:40888636
|
CT | C | 13 | a0001c0001t0005g0212a0001c0001t0009g0218a0001c0001t0009g0219others(10): Show | 13 | HG01934.hp2 HG02809.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.792+2135delT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40888636 | |||||
chr22:40888832
|
C | A | 5 | a0001c0001t0002g0006a0001c0001t0002g0127a0001c0001t0002g0153others(2): Show | 6 | HG01433.hp2 HG02280.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.792+2317C>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40888832 | ||||||
chr22:40888864
|
C | G | 3 | a0001c0001t0011g0225a0001c0001t0011g0226a0001c0001t0011g0227 | 3 | HG00639.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.792+2349C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40888864 | ||||||
chr22:40889014
|
T | G | 33 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(30): Show | 34 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.792+2499T>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40889014 | ||||||
chr22:40889192
|
G | GGCTCAT | 31 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(28): Show | 31 | HG00639.hp2 HG01884.hp2 HG01934.hp2 others(28): Show |
intron_variant | MODIFIER | c.792+2677_792+2678i others(8): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40889192 | ||||||
chr22:40889555
|
T | C | 1 | a0001c0001t0014g0027 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.792+3040T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40889555 | ||||||
chr22:40889938
|
G | A | 1 | a0001c0001t0002g0182 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.792+3423G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40889938 | ||||||
chr22:40890163
|
T | C | 17 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(14): Show | 17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.792+3648T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40890163 | ||||||
chr22:40890187
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.792+3672A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40890187 | ||||||
chr22:40890392
|
A | T | 1 | a0001c0001t0024g0145 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.792+3877A>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40890392 | ||||||
chr22:40890413
|
G | GTGGT | 5 | a0001c0001t0001g0030a0001c0001t0001g0099a0001c0001t0014g0012others(2): Show | 5 | HG01884.hp1 HG02109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.792+3899_792+3902d others(6): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40890413 | |||||
chr22:40890740
|
ACCTGTAG others(486): Show |
A | 1 | a0001c0001t0006g0197 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.792+4244_792+4736d others(2): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40890740 | |||||
chr22:40890972
|
G | A | 6 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(3): Show | 6 | HG02622.hp2 HG02886.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.792+4457G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40890972 | ||||||
chr22:40891179
|
C | CA | 15 | a0001c0001t0001g0079a0001c0001t0001g0104a0001c0001t0001g0180others(12): Show | 15 | HG00423.hp2 HG00544.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.792+4687dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40891179 | |||||
chr22:40891179
|
CA | C | 14 | a0001c0001t0001g0070a0001c0001t0001g0114a0001c0001t0002g0117others(11): Show | 14 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(11): Show |
intron_variant | MODIFIER | c.792+4687delA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40891179 | |||||
chr22:40891264
|
A | T | 1 | a0001c0001t0002g0124 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.792+4749A>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40891264 | ||||||
chr22:40891514
|
G | A | 1 | a0001c0001t0010g0042 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.792+4999G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40891514 | ||||||
chr22:40891532
|
A | G | 2 | a0001c0001t0005g0216a0001c0001t0005g0241 | 2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.792+5017A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40891532 | ||||||
chr22:40892006
|
C | T | 1 | a0001c0001t0027g0228 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.792+5491C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40892006 | ||||||
chr22:40892023
|
T | G | 243 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(240): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.792+5508T>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40892023 | ||||||
chr22:40892274
|
T | C | 1 | a0001c0001t0007g0187 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.792+5759T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40892274 | ||||||
chr22:40892375
|
C | T | 2 | a0001c0001t0003g0088a0001c0001t0023g0089 | 2 | NA18942.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.792+5860C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40892375 | ||||||
chr22:40892477
|
G | A | 17 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(14): Show | 17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.792+5962G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40892477 | ||||||
chr22:40892882
|
T | G | 33 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(30): Show | 34 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.792+6367T>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40892882 | ||||||
chr22:40892931
|
CATATT | C | 17 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(14): Show | 17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.792+6420_792+6424d others(7): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40892931 | |||||
chr22:40892950
|
C | T | 2 | a0001c0001t0001g0112a0001c0001t0001g0113 | 2 | HG00639.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.792+6435C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40892950 | ||||||
chr22:40893039
|
T | C | 17 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(14): Show | 17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.792+6524T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40893039 | ||||||
chr22:40893064
|
A | G | 2 | a0001c0001t0001g0112a0001c0001t0001g0113 | 2 | HG00639.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.792+6549A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40893064 | ||||||
chr22:40893096
|
TTATATAT others(3): Show |
T | 29 | a0001c0001t0001g0087a0001c0001t0004g0001a0001c0001t0004g0002others(26): Show | 30 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.792+6599_792+6608d others(12): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40893096 | |||||
chr22:40893105
|
AAT | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0072 | 3 | NA18964.hp1 NA18970.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.792+6598_792+6599d others(4): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40893105 | |||||
chr22:40893505
|
C | CA | 27 | a0001c0001t0001g0094a0001c0001t0001g0176a0001c0001t0002g0139others(24): Show | 27 | HG00733.hp2 HG00735.hp2 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.792+7013dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40893505 | |||||
chr22:40893505
|
CA | C | 6 | a0001c0001t0001g0077a0001c0001t0001g0164a0001c0001t0002g0148others(3): Show | 6 | HG01257.hp2 HG02015.hp2 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.792+7013delA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40893505 | |||||
chr22:40893822
|
G | A | 4 | a0001c0002t0005g0215a0001c0002t0046g0217a0001c0002t0048g0214others(1): Show | 4 | HG01884.hp2 HG02630.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.792+7307G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40893822 | ||||||
chr22:40894466
|
C | G | 4 | a0001c0001t0011g0224a0001c0001t0011g0225a0001c0001t0011g0226others(1): Show | 4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.792+7951C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40894466 | ||||||
chr22:40894624
|
A | G | 6 | a0001c0001t0009g0218a0001c0001t0009g0219a0001c0001t0009g0220others(3): Show | 6 | HG01934.hp2 HG02809.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.792+8109A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40894624 | ||||||
chr22:40894909
|
C | T | 6 | a0001c0001t0009g0218a0001c0001t0009g0219a0001c0001t0009g0220others(3): Show | 6 | HG01934.hp2 HG02809.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.792+8394C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40894909 | ||||||
chr22:40895100
|
T | G | 1 | a0001c0001t0002g0198 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.792+8585T>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40895100 | ||||||
chr22:40895104
|
A | T | 1 | a0001c0001t0017g0221 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.792+8589A>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40895104 | ||||||
chr22:40895126
|
AATTGCCT others(342): Show |
A | 2 | a0001c0001t0002g0184a0001c0001t0002g0198 | 2 | NA18967.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.792+8613_792+8961d others(2): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40895126 | |||||
chr22:40895288
|
T | A | 1 | a0001c0001t0002g0140 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.792+8773T>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40895288 | ||||||
chr22:40895342
|
C | CT | 6 | a0001c0001t0012g0035a0001c0001t0012g0036a0001c0001t0012g0038others(3): Show | 6 | HG00099.hp1 HG01433.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.792+8838dupT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40895342 | |||||
chr22:40895392
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.792+8877A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40895392 | ||||||
chr22:40895726
|
T | C | 170 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(167): Show | 172 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.792+9211T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40895726 | ||||||
chr22:40895985
|
G | A | 1 | a0001c0001t0021g0211 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.792+9470G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40895985 | ||||||
chr22:40895998
|
T | C | 1 | a0001c0001t0007g0229 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.792+9483T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40895998 | ||||||
chr22:40896205
|
A | C | 1 | a0001c0001t0002g0159 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.792+9690A>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40896205 | ||||||
chr22:40896244
|
C | A | 16 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(13): Show | 16 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.792+9729C>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40896244 | ||||||
chr22:40896351
|
G | A | 10 | a0001c0001t0009g0218a0001c0001t0009g0219a0001c0001t0009g0220others(7): Show | 10 | HG01934.hp2 HG02630.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.792+9836G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40896351 | ||||||
chr22:40896399
|
C | T | 1 | a0001c0001t0045g0034 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.792+9884C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40896399 | ||||||
chr22:40896440
|
C | T | 5 | a0001c0001t0004g0001a0001c0001t0004g0040a0001c0001t0004g0041others(2): Show | 5 | NA18949.hp2 NA18960.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.792+9925C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40896440 | ||||||
chr22:40896524
|
G | C | 2 | a0001c0001t0002g0121a0001c0001t0002g0126 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.792+10009G>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40896524 | ||||||
chr22:40896659
|
A | G | 7 | a0001c0001t0009g0218a0001c0001t0009g0219a0001c0001t0009g0220others(4): Show | 7 | HG01934.hp2 HG02630.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.792+10144A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40896659 | ||||||
chr22:40896702
|
A | G | 16 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(13): Show | 16 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.792+10187A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40896702 | ||||||
chr22:40896817
|
C | T | 2 | a0001c0001t0012g0035a0001c0001t0012g0038 | 2 | HG00099.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.792+10302C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40896817 | ||||||
chr22:40896834
|
A | G | 4 | a0001c0001t0011g0224a0001c0001t0011g0225a0001c0001t0011g0226others(1): Show | 4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.792+10319A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40896834 | ||||||
chr22:40896918
|
TACTTC | T | 3 | a0001c0001t0013g0129a0001c0001t0013g0130a0001c0001t0013g0185 | 3 | HG02965.hp2 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.792+10408_792+1041 others(9): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40896918 | |||||
chr22:40897029
|
C | CT | 82 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(79): Show | 83 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.792+10536dupT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40897029 | |||||
chr22:40897029
|
C | CTT | 7 | a0001c0001t0001g0104a0001c0001t0001g0108a0001c0001t0002g0184others(4): Show | 7 | HG01884.hp1 HG02602.hp2 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.792+10535_792+1053 others(6): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40897029 | |||||
chr22:40897071
|
G | T | 1 | a0001c0001t0035g0033 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.793-10516G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40897071 | ||||||
chr22:40897113
|
G | C | 4 | a0001c0001t0012g0035a0001c0001t0012g0036a0001c0001t0012g0038others(1): Show | 4 | HG00099.hp1 HG01433.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.793-10474G>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40897113 | ||||||
chr22:40897401
|
A | G | 1 | a0001c0001t0001g0078 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.793-10186A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40897401 | ||||||
chr22:40898095
|
G | GTTT | 5 | a0001c0001t0011g0224a0001c0001t0011g0225a0001c0001t0011g0226others(2): Show | 5 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.793-9487_793-9485d others(5): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898095 | |||||
chr22:40898100
|
T | TTTG | 17 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(14): Show | 17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.793-9478_793-9476d others(5): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898100 | |||||
chr22:40898167
|
G | A | 3 | a0001c0001t0021g0210a0001c0001t0021g0211a0001c0001t0047g0008 | 3 | HG03098.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.793-9420G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40898167 | ||||||
chr22:40898219
|
TGACCCAT others(326): Show |
T | 32 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(29): Show | 32 | HG00639.hp2 HG01884.hp2 HG01934.hp2 others(29): Show |
intron_variant | MODIFIER | c.793-9357_793-9025d others(2): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898219 | |||||
chr22:40898225
|
A | AT | 18 | a0001c0001t0002g0006a0001c0001t0002g0133a0001c0001t0002g0150others(15): Show | 19 | HG00140.hp1 HG00733.hp2 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.793-9323dupT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | |||||
chr22:40898225
|
A | ATT | 9 | a0001c0001t0002g0007a0001c0001t0002g0127a0001c0001t0002g0131others(6): Show | 10 | HG02280.hp2 HG02451.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.793-9324_793-9323d others(4): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | |||||
chr22:40898225
|
A | ATTT | 10 | a0001c0001t0001g0105a0001c0001t0003g0059a0001c0001t0003g0061others(7): Show | 10 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.793-9325_793-9323d others(5): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | |||||
chr22:40898225
|
A | ATTTTT | 6 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0004g0053others(3): Show | 6 | HG00544.hp1 HG00609.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.793-9327_793-9323d others(7): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | |||||
chr22:40898225
|
A | ATTTTTT | 9 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0080others(6): Show | 9 | HG01257.hp1 HG01257.hp2 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.793-9328_793-9323d others(8): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | |||||
chr22:40898225
|
A | ATTTTTTT | 18 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0022others(15): Show | 18 | HG00438.hp1 HG00438.hp2 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.793-9329_793-9323d others(9): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | |||||
chr22:40898225
|
A | ATTTTTTT others(1): Show |
8 | a0001c0001t0001g0020a0001c0001t0001g0030a0001c0001t0001g0081others(5): Show | 8 | HG02257.hp1 HG02559.hp1 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.793-9330_793-9323d others(10): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | |||||
chr22:40898225
|
A | ATTTTTTT others(3): Show |
3 | a0001c0001t0001g0090a0001c0001t0002g0156a0001c0001t0003g0063 | 3 | HG01256.hp2 HG02055.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.793-9332_793-9323d others(12): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | |||||
chr22:40898225
|
A | ATTTTTTT others(4): Show |
2 | a0001c0001t0001g0065a0001c0001t0001g0103 | 2 | HG03654.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.793-9333_793-9323d others(13): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | |||||
chr22:40898225
|
A | ATTTTTTT others(5): Show |
5 | a0001c0001t0001g0013a0001c0001t0001g0025a0001c0001t0001g0098others(2): Show | 5 | HG01109.hp1 HG01258.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.793-9334_793-9323d others(14): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | |||||
chr22:40898225
|
A | ATTTTTTT others(6): Show |
2 | a0001c0001t0001g0078a0001c0001t0001g0108 | 2 | HG03704.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.793-9335_793-9323d others(15): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | |||||
chr22:40898225
|
A | ATTTTTTT others(7): Show |
7 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0070others(4): Show | 7 | HG00544.hp2 HG01943.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.793-9336_793-9323d others(16): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | |||||
chr22:40898225
|
A | ATTTTTTT others(8): Show |
5 | a0001c0001t0001g0021a0001c0001t0001g0076a0001c0001t0001g0084others(2): Show | 5 | HG01169.hp1 NA18944.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.793-9337_793-9323d others(17): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | |||||
chr22:40898225
|
A | ATTTTTTT others(9): Show |
2 | a0001c0001t0001g0111a0001c0001t0003g0092 | 2 | HG03492.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.793-9338_793-9323d others(18): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | |||||
chr22:40898225
|
A | ATTTTTTT others(10): Show |
1 | a0001c0001t0001g0093 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.793-9339_793-9323d others(19): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | |||||
chr22:40898225
|
A | ATTTTTTT others(13): Show |
2 | a0001c0001t0001g0018a0001c0001t0001g0109 | 2 | HG01243.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.793-9342_793-9323d others(22): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | |||||
chr22:40898225
|
A | ATTTTTTT others(14): Show |
1 | a0001c0001t0036g0179 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.793-9343_793-9323d others(23): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | |||||
chr22:40898225
|
A | ATTTTTTT others(16): Show |
1 | a0001c0001t0003g0029 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.793-9345_793-9323d others(25): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | |||||
chr22:40898225
|
A | ATTTTTTT others(18): Show |
1 | a0001c0001t0001g0071 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.793-9347_793-9323d others(27): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | |||||
chr22:40898225
|
AT | A | 17 | a0001c0001t0001g0019a0001c0001t0002g0115a0001c0001t0002g0117others(14): Show | 17 | HG01943.hp2 HG01981.hp1 HG02293.hp1 others(14): Show |
intron_variant | MODIFIER | c.793-9323delT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | |||||
chr22:40898225
|
ATT | A | 23 | a0001c0001t0002g0124a0001c0001t0002g0128a0001c0001t0002g0132others(20): Show | 23 | HG00099.hp2 HG00423.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.793-9324_793-9323d others(4): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | |||||
chr22:40898225
|
ATTT | A | 12 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0135others(9): Show | 12 | HG00099.hp1 HG01934.hp1 HG03654.hp2 others(9): Show |
intron_variant | MODIFIER | c.793-9325_793-9323d others(5): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | |||||
chr22:40898225
|
ATTTTTTT others(3): Show |
A | 2 | a0001c0001t0006g0178a0001c0001t0035g0033 | 2 | HG00597.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.793-9332_793-9323d others(12): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | |||||
chr22:40898225
|
ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0001g0104 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.793-9334_793-9323d others(14): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | |||||
chr22:40898225
|
ATTTTTTT others(6): Show |
A | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG02015.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.793-9335_793-9323d others(15): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | |||||
chr22:40898225
|
ATTTTTTT others(8): Show |
A | 2 | a0001c0001t0001g0102a0001c0001t0003g0056 | 2 | HG02258.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.793-9337_793-9323d others(17): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | |||||
chr22:40898225
|
ATTTTTTT others(9): Show |
A | 2 | a0001c0001t0001g0004a0001c0001t0001g0072 | 3 | NA18964.hp1 NA18970.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.793-9338_793-9323d others(18): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | |||||
chr22:40898225
|
ATTTTTTT others(10): Show |
A | 1 | a0001c0001t0001g0180 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.793-9339_793-9323d others(19): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | |||||
chr22:40898225
|
ATTTTTTT others(11): Show |
A | 3 | a0001c0001t0001g0146a0001c0001t0003g0147a0001c0001t0051g0024 | 3 | HG00735.hp1 HG01256.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.793-9340_793-9323d others(20): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | |||||
chr22:40898225
|
ATTTTTTT others(12): Show |
A | 2 | a0001c0001t0001g0175a0001c0001t0006g0197 | 2 | NA18989.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.793-9341_793-9323d others(21): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | |||||
chr22:40898225
|
ATTTTTTT others(13): Show |
A | 1 | a0001c0001t0033g0057 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.793-9342_793-9323d others(22): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | |||||
chr22:40898277
|
C | T | 1 | a0001c0001t0001g0104 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.793-9310C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40898277 | ||||||
chr22:40898285
|
C | T | 4 | a0001c0001t0001g0090a0001c0001t0001g0096a0001c0001t0001g0146others(1): Show | 4 | HG00735.hp1 HG01256.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.793-9302C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40898285 | ||||||
chr22:40898474
|
T | C | 198 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(195): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.793-9113T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40898474 | ||||||
chr22:40898994
|
C | T | 4 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(1): Show | 4 | HG01243.hp1 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.793-8593C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40898994 | ||||||
chr22:40899085
|
G | T | 5 | a0001c0001t0011g0224a0001c0001t0011g0225a0001c0001t0011g0226others(2): Show | 5 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.793-8502G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40899085 | ||||||
chr22:40899145
|
T | C | 1 | a0001c0001t0001g0075 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.793-8442T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40899145 | ||||||
chr22:40899208
|
C | T | 1 | a0001c0001t0045g0034 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.793-8379C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40899208 | ||||||
chr22:40899220
|
C | CA | 5 | a0001c0001t0010g0166a0001c0001t0011g0224a0001c0001t0011g0225others(2): Show | 5 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.793-8360dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40899220 | |||||
chr22:40899380
|
C | G | 1 | a0001c0001t0027g0228 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.793-8207C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40899380 | ||||||
chr22:40899430
|
A | G | 1 | a0001c0001t0002g0198 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.793-8157A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40899430 | ||||||
chr22:40899616
|
T | C | 1 | a0001c0001t0027g0228 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.793-7971T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40899616 | ||||||
chr22:40899623
|
A | G | 1 | a0001c0001t0003g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.793-7964A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40899623 | ||||||
chr22:40899680
|
G | A | 3 | a0001c0001t0013g0129a0001c0001t0013g0130a0001c0001t0013g0185 | 3 | HG02965.hp2 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.793-7907G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40899680 | ||||||
chr22:40899767
|
G | A | 1 | a0001c0001t0021g0211 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.793-7820G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40899767 | ||||||
chr22:40899812
|
T | C | 1 | a0001c0001t0002g0159 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.793-7775T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40899812 | ||||||
chr22:40899817
|
C | CA | 13 | a0001c0001t0002g0150a0001c0001t0009g0223a0001c0001t0010g0166others(10): Show | 13 | HG00639.hp2 HG01884.hp2 HG03041.hp2 others(10): Show |
intron_variant | MODIFIER | c.793-7750dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40899817 | |||||
chr22:40899817
|
CA | C | 22 | a0001c0001t0003g0056a0001c0001t0003g0058a0001c0001t0003g0059others(19): Show | 22 | HG01496.hp2 HG02055.hp1 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.793-7750delA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40899817 | |||||
chr22:40899837
|
AG | A | 77 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(74): Show | 78 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.793-7748delG | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40899837 | |||||
chr22:40899838
|
G | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0087a0001c0001t0001g0094others(1): Show | 4 | HG01109.hp1 HG02056.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.793-7749G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40899838 | ||||||
chr22:40900307
|
G | GA | 10 | a0001c0001t0002g0150a0001c0001t0007g0188a0001c0001t0007g0237others(7): Show | 10 | HG00639.hp2 HG01109.hp2 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.793-7265dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40900307 | |||||
chr22:40900308
|
A | G | 2 | a0001c0001t0003g0062a0001c0001t0003g0063 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.793-7279A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40900308 | ||||||
chr22:40900330
|
T | C | 17 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(14): Show | 17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.793-7257T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40900330 | ||||||
chr22:40900407
|
C | A | 3 | a0001c0001t0012g0035a0001c0001t0012g0038a0001c0001t0032g0037 | 3 | HG00099.hp1 HG01433.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.793-7180C>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40900407 | ||||||
chr22:40900474
|
C | T | 1 | a0001c0001t0002g0117 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.793-7113C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40900474 | ||||||
chr22:40900555
|
G | A | 22 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(19): Show | 22 | HG00639.hp2 HG01884.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.793-7032G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40900555 | ||||||
chr22:40900757
|
C | T | 1 | a0001c0001t0003g0201 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.793-6830C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40900757 | ||||||
chr22:40901097
|
A | T | 85 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(82): Show | 86 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.793-6490A>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40901097 | ||||||
chr22:40901233
|
G | T | 1 | a0001c0001t0003g0202 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.793-6354G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40901233 | ||||||
chr22:40901236
|
C | CTTTTTT | 218 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(215): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.793-6343_793-6338d others(8): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40901236 | |||||
chr22:40901236
|
C | CTTTTTTT | 22 | a0001c0001t0001g0023a0001c0001t0002g0152a0001c0001t0002g0230others(19): Show | 22 | HG00140.hp1 HG02257.hp2 HG02738.hp2 others(19): Show |
intron_variant | MODIFIER | c.793-6344_793-6338d others(9): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40901236 | |||||
chr22:40901299
|
A | G | 1 | a0001c0001t0033g0057 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.793-6288A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40901299 | ||||||
chr22:40901301
|
C | G | 85 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(82): Show | 86 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.793-6286C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40901301 | ||||||
chr22:40901493
|
C | G | 1 | a0001c0001t0027g0228 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.793-6094C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40901493 | ||||||
chr22:40901501
|
C | G | 1 | a0001c0001t0045g0034 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.793-6086C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40901501 | ||||||
chr22:40901915
|
G | T | 5 | a0001c0001t0011g0224a0001c0001t0011g0225a0001c0001t0011g0226others(2): Show | 5 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.793-5672G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40901915 | ||||||
chr22:40901916
|
G | A | 17 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(14): Show | 17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.793-5671G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40901916 | ||||||
chr22:40901920
|
C | G | 1 | a0001c0001t0045g0034 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.793-5667C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40901920 | ||||||
chr22:40901931
|
TG | T | 4 | a0001c0001t0002g0007a0001c0001t0002g0134a0001c0001t0002g0239others(1): Show | 5 | HG03130.hp1 HG03139.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.793-5654delG | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40901931 | |||||
chr22:40902071
|
C | CTTT | 17 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(14): Show | 17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.793-5499_793-5497d others(5): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40902071 | |||||
chr22:40902071
|
C | CTTTTT | 12 | a0001c0001t0009g0218a0001c0001t0009g0219a0001c0001t0009g0220others(9): Show | 12 | HG00639.hp2 HG01934.hp2 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.793-5501_793-5497d others(7): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40902071 | |||||
chr22:40902111
|
C | T | 1 | a0001c0001t0027g0228 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.793-5476C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40902111 | ||||||
chr22:40902134
|
G | A | 69 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(66): Show | 70 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.793-5453G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40902134 | ||||||
chr22:40902246
|
A | AT | 24 | a0001c0001t0002g0121a0001c0001t0002g0126a0001c0001t0002g0181others(21): Show | 24 | HG00735.hp2 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.793-5319dupT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40902246 | |||||
chr22:40902246
|
A | ATT | 6 | a0001c0001t0005g0205a0001c0001t0011g0224a0001c0001t0011g0225others(3): Show | 6 | HG00639.hp2 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.793-5320_793-5319d others(4): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40902246 | |||||
chr22:40902246
|
AT | A | 80 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(77): Show | 81 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.793-5319delT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40902246 | |||||
chr22:40902485
|
C | T | 3 | a0001c0001t0001g0102a0001c0001t0001g0172a0001c0001t0038g0097 | 3 | HG02080.hp2 NA18995.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.793-5102C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40902485 | ||||||
chr22:40902649
|
T | C | 1 | a0001c0001t0012g0036 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.793-4938T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40902649 | ||||||
chr22:40902651
|
G | A | 1 | a0001c0001t0045g0034 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.793-4936G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40902651 | ||||||
chr22:40902733
|
G | A | 6 | a0001c0001t0004g0003a0001c0001t0004g0054a0001c0001t0010g0042others(3): Show | 7 | HG02015.hp1 HG02027.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.793-4854G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40902733 | ||||||
chr22:40902847
|
G | A | 5 | a0001c0001t0011g0224a0001c0001t0011g0225a0001c0001t0011g0226others(2): Show | 5 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.793-4740G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40902847 | ||||||
chr22:40902871
|
CCT | C | 168 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(165): Show | 170 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.793-4713_793-4712d others(4): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40902871 | |||||
chr22:40902969
|
T | C | 1 | a0002c0003t0004g0045 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.793-4618T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40902969 | ||||||
chr22:40902973
|
A | G | 4 | a0001c0001t0012g0035a0001c0001t0012g0036a0001c0001t0012g0038others(1): Show | 4 | HG00099.hp1 HG01433.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.793-4614A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40902973 | ||||||
chr22:40903042
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.793-4545C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40903042 | ||||||
chr22:40903062
|
A | G | 1 | a0001c0001t0001g0084 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.793-4525A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40903062 | ||||||
chr22:40903483
|
C | G | 5 | a0001c0001t0009g0218a0001c0001t0009g0219a0001c0001t0009g0220others(2): Show | 5 | HG01934.hp2 HG02809.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.793-4104C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40903483 | ||||||
chr22:40903530
|
G | A | 1 | a0001c0001t0003g0171 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.793-4057G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40903530 | ||||||
chr22:40903688
|
C | T | 1 | a0001c0001t0011g0226 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.793-3899C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40903688 | ||||||
chr22:40903874
|
T | TCA | 4 | a0001c0001t0003g0060a0001c0001t0004g0047a0001c0001t0014g0189others(1): Show | 4 | HG02738.hp1 HG03579.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.793-3676_793-3675d others(4): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40903874 | |||||
chr22:40903874
|
T | TCACA | 6 | a0001c0001t0003g0058a0001c0001t0003g0059a0001c0001t0003g0063others(3): Show | 6 | HG02055.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.793-3678_793-3675d others(6): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40903874 | |||||
chr22:40903874
|
T | TCACACA | 11 | a0001c0001t0003g0056a0001c0001t0003g0062a0001c0001t0003g0193others(8): Show | 11 | HG02258.hp1 HG02280.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.793-3680_793-3675d others(8): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40903874 | |||||
chr22:40903874
|
T | TCACACAC others(3): Show |
3 | a0001c0001t0011g0224a0001c0001t0011g0227a0001c0005t0003g0196 | 3 | HG02451.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.793-3684_793-3675d others(12): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40903874 | |||||
chr22:40903874
|
TCA | T | 81 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0020others(78): Show | 82 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.793-3676_793-3675d others(4): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40903874 | |||||
chr22:40903874
|
TCACA | T | 75 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(72): Show | 76 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.793-3678_793-3675d others(6): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40903874 | |||||
chr22:40903874
|
TCACACA | T | 5 | a0001c0001t0009g0218a0001c0001t0009g0219a0001c0001t0009g0220others(2): Show | 5 | HG01934.hp2 HG02809.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.793-3680_793-3675d others(8): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40903874 | |||||
chr22:40903989
|
A | C | 3 | a0001c0001t0001g0102a0001c0001t0001g0172a0001c0001t0038g0097 | 3 | HG02080.hp2 NA18995.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.793-3598A>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40903989 | ||||||
chr22:40904181
|
A | T | 1 | a0001c0001t0001g0022 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.793-3406A>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40904181 | ||||||
chr22:40904232
|
A | G | 3 | a0001c0001t0002g0159a0001c0001t0002g0160a0001c0001t0014g0189 | 3 | HG01515.hp2 HG02738.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.793-3355A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40904232 | ||||||
chr22:40904308
|
G | A | 1 | a0001c0001t0002g0240 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.793-3279G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40904308 | ||||||
chr22:40904366
|
A | G | 2 | a0001c0001t0012g0035a0001c0001t0012g0038 | 2 | HG00099.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.793-3221A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40904366 | ||||||
chr22:40904423
|
A | G | 1 | a0001c0001t0036g0179 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.793-3164A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40904423 | ||||||
chr22:40905084
|
T | A | 1 | a0001c0001t0001g0018 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.793-2503T>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40905084 | ||||||
chr22:40905237
|
G | A | 1 | a0001c0001t0005g0212 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.793-2350G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40905237 | ||||||
chr22:40905501
|
C | T | 5 | a0001c0001t0011g0224a0001c0001t0011g0225a0001c0001t0011g0226others(2): Show | 5 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.793-2086C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40905501 | ||||||
chr22:40905728
|
C | G | 2 | a0001c0001t0018g0137a0001c0001t0018g0138 | 2 | NA20300.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.793-1859C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40905728 | ||||||
chr22:40905765
|
C | T | 1 | a0001c0001t0030g0119 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.793-1822C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40905765 | ||||||
chr22:40905926
|
G | A | 1 | a0001c0001t0002g0125 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.793-1661G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40905926 | ||||||
chr22:40905940
|
C | T | 1 | a0001c0001t0003g0202 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.793-1647C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40905940 | ||||||
chr22:40905983
|
G | T | 3 | a0001c0001t0019g0010a0001c0001t0019g0011a0001c0001t0022g0009 | 3 | HG02886.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.793-1604G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40905983 | ||||||
chr22:40906067
|
A | G | 7 | a0001c0001t0001g0005a0001c0001t0001g0105a0001c0001t0001g0106others(4): Show | 7 | HG02132.hp2 NA18942.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.793-1520A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40906067 | ||||||
chr22:40906090
|
C | CTGTT | 18 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(15): Show | 18 | HG01934.hp2 HG02109.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.793-1471_793-1468d others(6): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40906090 | |||||
chr22:40906215
|
C | T | 1 | a0001c0001t0034g0091 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.793-1372C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40906215 | ||||||
chr22:40906420
|
C | CA | 10 | a0001c0001t0001g0026a0001c0001t0002g0131a0001c0001t0002g0139others(7): Show | 10 | HG01106.hp1 HG01884.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.793-1151dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40906420 | |||||
chr22:40906420
|
C | CAA | 13 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(10): Show | 13 | HG02109.hp1 HG02615.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.793-1152_793-1151d others(4): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40906420 | |||||
chr22:40906588
|
A | G | 1 | a0001c0001t0002g0128 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.793-999A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40906588 | ||||||
chr22:40906628
|
C | T | 1 | a0001c0001t0027g0228 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.793-959C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40906628 | ||||||
chr22:40906784
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.793-803A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40906784 | ||||||
chr22:40906907
|
T | A | 1 | a0001c0001t0045g0034 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.793-680T>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40906907 | ||||||
chr22:40906969
|
A | T | 171 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(168): Show | 173 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.793-618A>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40906969 | ||||||
chr22:40907159
|
C | T | 2 | a0001c0001t0002g0121a0001c0001t0002g0126 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.793-428C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40907159 | ||||||
chr22:40907217
|
C | G | 1 | a0001c0001t0027g0228 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.793-370C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40907217 | ||||||
chr22:40907256
|
C | T | 1 | a0001c0001t0002g0158 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.793-331C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40907256 | ||||||
chr22:40907290
|
G | A | 3 | a0001c0001t0019g0010a0001c0001t0019g0011a0001c0001t0022g0009 | 3 | HG02886.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.793-297G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40907290 | ||||||
chr22:40907382
|
C | T | 17 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(14): Show | 17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.793-205C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40907382 | ||||||
chr22:40907420
|
C | CA | 7 | a0001c0001t0001g0025a0001c0001t0002g0139a0001c0001t0002g0150others(4): Show | 7 | HG01496.hp1 HG02615.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.793-157dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40907420 | |||||
chr22:40907918
|
G | A | 32 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(29): Show | 32 | HG00639.hp2 HG01884.hp2 HG01934.hp2 others(29): Show |
intron_variant | MODIFIER | c.855+269G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 5/9 | chr22 | 40907918 | ||||||
chr22:40908121
|
C | T | 1 | a0001c0001t0027g0228 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.855+472C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 5/9 | chr22 | 40908121 | ||||||
chr22:40908301
|
C | G | 2 | a0001c0001t0017g0136a0001c0001t0024g0145 | 2 | HG02257.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.855+652C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 5/9 | chr22 | 40908301 | ||||||
chr22:40908459
|
A | G | 4 | a0001c0001t0009g0218a0001c0001t0009g0219a0001c0001t0009g0220others(1): Show | 4 | HG01934.hp2 HG02809.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.856-663A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 5/9 | chr22 | 40908459 | ||||||
chr22:40909625
|
C | T | 1 | a0001c0001t0045g0034 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.969+390C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40909625 | ||||||
chr22:40909631
|
G | A | 2 | a0001c0001t0001g0105a0001c0001t0001g0106 | 2 | NA18961.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.969+396G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40909631 | ||||||
chr22:40909691
|
G | A | 5 | a0001c0001t0009g0218a0001c0001t0009g0219a0001c0001t0009g0220others(2): Show | 5 | HG01934.hp2 HG02809.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.969+456G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40909691 | ||||||
chr22:40909772
|
CTAAA | C | 4 | a0001c0001t0002g0007a0001c0001t0002g0155a0001c0001t0002g0239others(1): Show | 5 | HG02258.hp2 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.969+560_969+563del others(4): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr22 | 40909772 | |||||
chr22:40909791
|
A | T | 4 | a0001c0001t0001g0090a0001c0001t0001g0096a0001c0001t0001g0146others(1): Show | 4 | HG00735.hp1 HG01256.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.969+556A>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40909791 | ||||||
chr22:40909792
|
A | T | 4 | a0001c0001t0001g0090a0001c0001t0001g0096a0001c0001t0001g0146others(1): Show | 4 | HG00735.hp1 HG01256.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.969+557A>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40909792 | ||||||
chr22:40909899
|
C | T | 1 | a0001c0001t0027g0228 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.969+664C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40909899 | ||||||
chr22:40910175
|
G | A | 5 | a0001c0001t0004g0002a0001c0001t0004g0047a0001c0001t0004g0052others(2): Show | 5 | NA18961.hp2 NA18968.hp2 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.969+940G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40910175 | ||||||
chr22:40910541
|
C | CA | 7 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0002g0120others(4): Show | 7 | HG00423.hp1 HG00735.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.969+1313dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr22 | 40910541 | |||||
chr22:40910583
|
C | G | 1 | a0001c0001t0029g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.969+1348C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40910583 | ||||||
chr22:40910724
|
G | A | 5 | a0001c0001t0011g0224a0001c0001t0011g0225a0001c0001t0011g0226others(2): Show | 5 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.969+1489G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40910724 | ||||||
chr22:40910956
|
C | T | 37 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(34): Show | 38 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.969+1721C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40910956 | ||||||
chr22:40911481
|
G | A | 1 | a0001c0001t0034g0091 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.969+2246G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40911481 | ||||||
chr22:40911789
|
C | G | 1 | a0001c0001t0002g0139 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.970-2450C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40911789 | ||||||
chr22:40911803
|
G | A | 2 | a0001c0001t0001g0112a0001c0001t0001g0113 | 2 | HG00639.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.970-2436G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40911803 | ||||||
chr22:40912000
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.970-2239C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40912000 | ||||||
chr22:40912585
|
G | A | 3 | a0001c0001t0019g0010a0001c0001t0019g0011a0001c0001t0022g0009 | 3 | HG02886.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.970-1654G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40912585 | ||||||
chr22:40912699
|
A | G | 33 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(30): Show | 34 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.970-1540A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40912699 | ||||||
chr22:40912731
|
G | T | 4 | a0001c0002t0005g0215a0001c0002t0046g0217a0001c0002t0048g0214others(1): Show | 4 | HG01884.hp2 HG02630.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.970-1508G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40912731 | ||||||
chr22:40912794
|
CAGGAGGC others(13): Show |
C | 1 | a0001c0001t0002g0158 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.970-1442_970-1423d others(22): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr22 | 40912794 | |||||
chr22:40912936
|
T | G | 1 | a0001c0001t0003g0088 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.970-1303T>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40912936 | ||||||
chr22:40913131
|
A | G | 1 | a0001c0001t0003g0095 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.970-1108A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40913131 | ||||||
chr22:40913348
|
G | C | 1 | a0002c0003t0004g0045 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.970-891G>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40913348 | ||||||
chr22:40913426
|
A | C | 2 | a0001c0001t0012g0035a0001c0001t0012g0038 | 2 | HG00099.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.970-813A>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40913426 | ||||||
chr22:40913437
|
C | CA | 7 | a0001c0001t0001g0104a0001c0001t0009g0218a0001c0001t0009g0219others(4): Show | 7 | HG01934.hp2 HG02809.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.970-785dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr22 | 40913437 | |||||
chr22:40913456
|
A | C | 1 | a0001c0002t0048g0214 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.970-783A>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40913456 | ||||||
chr22:40913693
|
C | G | 1 | a0001c0001t0005g0203 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.970-546C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40913693 | ||||||
chr22:40913698
|
C | T | 13 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(10): Show | 13 | HG02109.hp1 HG02615.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.970-541C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40913698 | ||||||
chr22:40913882
|
C | T | 1 | a0001c0001t0002g0151 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.970-357C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40913882 | ||||||
chr22:40913896
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.970-343G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40913896 | ||||||
chr22:40914003
|
TGTG | T | 22 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(19): Show | 22 | HG00639.hp2 HG01884.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.970-231_970-229del others(3): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr22 | 40914003 | |||||
chr22:40914056
|
C | T | 2 | a0001c0001t0009g0220a0001c0001t0009g0223 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.970-183C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40914056 | ||||||
chr22:40914059
|
T | C | 4 | a0001c0001t0012g0035a0001c0001t0012g0036a0001c0001t0012g0038others(1): Show | 4 | HG00099.hp1 HG01433.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.970-180T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40914059 | ||||||
chr22:40914064
|
C | T | 1 | a0001c0001t0014g0012 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.970-175C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40914064 | ||||||
chr22:40914144
|
G | GA | 7 | a0001c0001t0001g0023a0001c0001t0001g0110a0001c0001t0001g0111others(4): Show | 7 | HG00099.hp1 HG01433.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.970-79dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr22 | 40914144 | |||||
chr22:40914180
|
AC | A | 4 | a0001c0001t0002g0007a0001c0001t0002g0155a0001c0001t0002g0239others(1): Show | 5 | HG02258.hp2 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.970-58delC | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40914180 | ||||||
chr22:40914199
|
C | G | 17 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(14): Show | 17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.970-40C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40914199 | ||||||
chr22:40914218
|
A | T | 2 | a0001c0001t0020g0143a0001c0001t0020g0186 | 2 | HG02602.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.970-21A>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40914218 | ||||||
chr22:40914339
|
G | A | 5 | a0001c0001t0011g0224a0001c0001t0011g0225a0001c0001t0011g0226others(2): Show | 5 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1055+15G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40914339 | ||||||
chr22:40914404
|
C | A | 1 | a0001c0001t0007g0188 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1055+80C>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40914404 | ||||||
chr22:40914528
|
A | G | 1 | a0001c0001t0027g0228 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1055+204A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40914528 | ||||||
chr22:40914531
|
A | AT | 46 | a0001c0001t0001g0099a0001c0001t0001g0104a0001c0001t0001g0106others(43): Show | 46 | HG00140.hp1 HG00544.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.1055+238dupT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr22 | 40914531 | |||||
chr22:40914531
|
A | ATT | 5 | a0001c0001t0004g0049a0001c0001t0015g0123a0001c0001t0019g0011others(2): Show | 5 | HG02080.hp1 HG02897.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1055+237_1055+238d others(4): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr22 | 40914531 | |||||
chr22:40914531
|
AT | A | 53 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(50): Show | 54 | HG00140.hp2 HG00544.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.1055+238delT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr22 | 40914531 | |||||
chr22:40914531
|
ATT | A | 14 | a0001c0001t0001g0031a0001c0001t0001g0071a0001c0001t0001g0081others(11): Show | 14 | HG00609.hp2 HG01515.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1055+237_1055+238d others(4): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr22 | 40914531 | |||||
chr22:40914531
|
ATTT | A | 5 | a0001c0001t0011g0224a0001c0001t0011g0225a0001c0001t0011g0226others(2): Show | 5 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1055+236_1055+238d others(5): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr22 | 40914531 | |||||
chr22:40914572
|
C | T | 17 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(14): Show | 17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.1055+248C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40914572 | ||||||
chr22:40914890
|
G | T | 3 | a0001c0001t0019g0010a0001c0001t0019g0011a0001c0001t0022g0009 | 3 | HG02886.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1055+566G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40914890 | ||||||
chr22:40915050
|
C | CT | 207 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(204): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.1055+745dupT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr22 | 40915050 | |||||
chr22:40915050
|
C | CTT | 12 | a0001c0001t0003g0171a0001c0001t0005g0204a0001c0001t0005g0212others(9): Show | 12 | HG00639.hp2 HG03041.hp2 HG03098.hp2 others(9): Show |
intron_variant | MODIFIER | c.1055+744_1055+745d others(4): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr22 | 40915050 | |||||
chr22:40915116
|
A | T | 7 | a0001c0001t0004g0002a0001c0001t0004g0047a0001c0001t0004g0048others(4): Show | 7 | HG00597.hp1 NA18961.hp2 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.1055+792A>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40915116 | ||||||
chr22:40915233
|
G | A | 2 | a0001c0001t0006g0017a0001c0001t0006g0083 | 2 | HG01106.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1055+909G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40915233 | ||||||
chr22:40915512
|
T | C | 1 | a0001c0001t0027g0228 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1055+1188T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40915512 | ||||||
chr22:40915732
|
C | T | 1 | a0001c0001t0002g0157 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1055+1408C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40915732 | ||||||
chr22:40915869
|
A | T | 5 | a0001c0001t0011g0224a0001c0001t0011g0225a0001c0001t0011g0226others(2): Show | 5 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1055+1545A>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40915869 | ||||||
chr22:40916058
|
C | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0072a0001c0001t0001g0079 | 4 | HG00544.hp2 NA18964.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1055+1734C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40916058 | ||||||
chr22:40916308
|
A | G | 1 | a0001c0002t0050g0213 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1055+1984A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40916308 | ||||||
chr22:40916313
|
A | G | 3 | a0001c0001t0006g0086a0001c0001t0026g0028a0001c0001t0037g0032 | 3 | HG01346.hp2 HG02738.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1055+1989A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40916313 | ||||||
chr22:40916346
|
A | G | 69 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(66): Show | 70 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.1055+2022A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40916346 | ||||||
chr22:40916578
|
T | C | 5 | a0001c0001t0008g0066a0001c0001t0008g0067a0001c0001t0008g0068others(2): Show | 5 | HG01243.hp2 HG01496.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1055+2254T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40916578 | ||||||
chr22:40916764
|
G | A | 3 | a0001c0001t0013g0129a0001c0001t0013g0130a0001c0001t0013g0185 | 3 | HG02965.hp2 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1055+2440G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40916764 | ||||||
chr22:40917088
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1055+2764A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40917088 | ||||||
chr22:40917201
|
C | T | 1 | a0001c0001t0028g0142 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1055+2877C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40917201 | ||||||
chr22:40917570
|
TATG | T | 5 | a0001c0001t0003g0193a0001c0001t0003g0194a0001c0001t0003g0195others(2): Show | 5 | HG02280.hp2 HG02965.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1055+3249_1055+325 others(7): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr22 | 40917570 | |||||
chr22:40917610
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1055+3286G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40917610 | ||||||
chr22:40917698
|
C | T | 3 | a0001c0001t0017g0136a0001c0001t0017g0221a0001c0001t0024g0145 | 3 | HG02257.hp2 HG03579.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1055+3374C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40917698 | ||||||
chr22:40917720
|
A | G | 1 | a0001c0001t0017g0221 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1055+3396A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40917720 | ||||||
chr22:40917776
|
G | A | 3 | a0001c0001t0002g0134a0001c0001t0002g0140a0001c0001t0007g0187 | 3 | HG01192.hp2 HG06807.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1055+3452G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40917776 | ||||||
chr22:40917839
|
A | T | 4 | a0001c0001t0012g0035a0001c0001t0012g0036a0001c0001t0012g0038others(1): Show | 4 | HG00099.hp1 HG01433.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1055+3515A>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40917839 | ||||||
chr22:40917998
|
G | T | 4 | a0001c0001t0012g0035a0001c0001t0012g0036a0001c0001t0012g0038others(1): Show | 4 | HG00099.hp1 HG01433.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1055+3674G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40917998 | ||||||
chr22:40918006
|
G | GT | 5 | a0001c0001t0001g0013a0001c0001t0001g0103a0001c0001t0001g0177others(2): Show | 5 | HG01109.hp1 HG01981.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.1055+3683dupT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr22 | 40918006 | |||||
chr22:40918007
|
TC | T | 4 | a0001c0001t0001g0026a0001c0001t0001g0172a0001c0001t0038g0097others(1): Show | 4 | HG02080.hp2 NA18984.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.1055+3684delC | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40918007 | ||||||
chr22:40918008
|
C | A | 5 | a0001c0001t0001g0013a0001c0001t0001g0103a0001c0001t0001g0177others(2): Show | 5 | HG01109.hp1 HG01981.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.1055+3684C>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40918008 | ||||||
chr22:40918008
|
C | T | 73 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(70): Show | 74 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1055+3684C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40918008 | ||||||
chr22:40918009
|
T | A | 78 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(75): Show | 79 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.1055+3685T>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40918009 | ||||||
chr22:40918009
|
T | TA | 7 | a0001c0001t0002g0120a0001c0001t0002g0141a0001c0001t0002g0162others(4): Show | 7 | HG01934.hp1 HG02683.hp1 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.1055+3705dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr22 | 40918009 | |||||
chr22:40918009
|
TA | T | 86 | a0001c0001t0002g0006a0001c0001t0002g0127a0001c0001t0002g0153others(83): Show | 88 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.1055+3705delA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr22 | 40918009 | |||||
chr22:40918029
|
A | G | 1 | a0001c0001t0012g0036 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1055+3705A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40918029 | ||||||
chr22:40918242
|
C | T | 4 | a0001c0001t0012g0035a0001c0001t0012g0036a0001c0001t0012g0038others(1): Show | 4 | HG00099.hp1 HG01433.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1055+3918C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40918242 | ||||||
chr22:40918633
|
G | A | 2 | a0001c0001t0002g0153a0001c0001t0002g0154 | 2 | HG01433.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1056-3700G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40918633 | ||||||
chr22:40918764
|
G | A | 5 | a0001c0001t0011g0224a0001c0001t0011g0225a0001c0001t0011g0226others(2): Show | 5 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1056-3569G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40918764 | ||||||
chr22:40918783
|
G | GT | 90 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(87): Show | 91 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.1056-3540dupT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr22 | 40918783 | |||||
chr22:40918783
|
G | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1056-3550G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40918783 | ||||||
chr22:40918875
|
C | T | 5 | a0001c0001t0011g0224a0001c0001t0011g0225a0001c0001t0011g0226others(2): Show | 5 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1056-3458C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40918875 | ||||||
chr22:40919079
|
T | C | 175 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(172): Show | 177 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.1056-3254T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40919079 | ||||||
chr22:40919081
|
A | G | 1 | a0001c0001t0027g0228 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1056-3252A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40919081 | ||||||
chr22:40919151
|
C | T | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | NA18967.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.1056-3182C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40919151 | ||||||
chr22:40919326
|
G | A | 1 | a0001c0001t0004g0049 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1056-3007G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40919326 | ||||||
chr22:40919373
|
G | T | 1 | a0001c0001t0004g0049 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1056-2960G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40919373 | ||||||
chr22:40919526
|
G | A | 17 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(14): Show | 17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.1056-2807G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40919526 | ||||||
chr22:40919534
|
T | C | 5 | a0001c0001t0004g0001a0001c0001t0004g0040a0001c0001t0004g0041others(2): Show | 5 | NA18949.hp2 NA18960.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.1056-2799T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40919534 | ||||||
chr22:40919590
|
C | T | 85 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(82): Show | 86 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1056-2743C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40919590 | ||||||
chr22:40919856
|
G | A | 3 | a0001c0001t0013g0129a0001c0001t0013g0130a0001c0001t0013g0185 | 3 | HG02965.hp2 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1056-2477G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40919856 | ||||||
chr22:40920241
|
G | A | 1 | a0001c0001t0027g0228 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1056-2092G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40920241 | ||||||
chr22:40920534
|
GT | G | 3 | a0001c0001t0013g0129a0001c0001t0013g0130a0001c0001t0013g0185 | 3 | HG02965.hp2 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1056-1797delT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr22 | 40920534 | |||||
chr22:40920904
|
T | A | 17 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(14): Show | 17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.1056-1429T>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40920904 | ||||||
chr22:40921012
|
G | A | 17 | a0001c0001t0003g0056a0001c0001t0003g0058a0001c0001t0003g0059others(14): Show | 17 | HG02055.hp1 HG02258.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.1056-1321G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40921012 | ||||||
chr22:40921079
|
A | C | 83 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(80): Show | 84 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.1056-1254A>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40921079 | ||||||
chr22:40921221
|
T | C | 9 | a0001c0001t0009g0218a0001c0001t0009g0219a0001c0001t0009g0220others(6): Show | 9 | HG01934.hp2 HG02809.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1056-1112T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40921221 | ||||||
chr22:40921393
|
G | A | 1 | a0001c0001t0003g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1056-940G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40921393 | ||||||
chr22:40921440
|
T | C | 32 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(29): Show | 32 | HG00639.hp2 HG01884.hp2 HG01934.hp2 others(29): Show |
intron_variant | MODIFIER | c.1056-893T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40921440 | ||||||
chr22:40921486
|
T | TA | 34 | a0001c0001t0001g0094a0001c0001t0001g0104a0001c0001t0001g0176others(31): Show | 34 | HG00639.hp2 HG01106.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.1056-827dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr22 | 40921486 | |||||
chr22:40921507
|
C | A | 1 | a0001c0001t0027g0228 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1056-826C>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40921507 | ||||||
chr22:40921536
|
T | TGTG | 5 | a0001c0001t0011g0224a0001c0001t0011g0225a0001c0001t0011g0226others(2): Show | 5 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1056-792_1056-790d others(5): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr22 | 40921536 | |||||
chr22:40921812
|
A | G | 1 | a0001c0001t0001g0031 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1056-521A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40921812 | ||||||
chr22:40922150
|
C | T | 4 | a0001c0002t0005g0215a0001c0002t0046g0217a0001c0002t0048g0214others(1): Show | 4 | HG01884.hp2 HG02630.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1056-183C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40922150 | ||||||
chr22:40922273
|
G | A | 5 | a0001c0001t0011g0224a0001c0001t0011g0225a0001c0001t0011g0226others(2): Show | 5 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1056-60G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40922273 | ||||||
chr22:40922669
|
T | C | 3 | a0001c0001t0017g0136a0001c0001t0017g0221a0001c0001t0024g0145 | 3 | HG02257.hp2 HG03579.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1236+156T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 8/9 | chr22 | 40922669 | ||||||
chr22:40922715
|
GAT | G | 9 | a0001c0001t0003g0056a0001c0001t0003g0058a0001c0001t0003g0059others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1236+208_1236+209d others(4): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr22 | 40922715 | |||||
chr22:40922719
|
TATAC | T | 8 | a0001c0001t0003g0193a0001c0001t0003g0194a0001c0001t0003g0195others(5): Show | 8 | HG02280.hp2 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1236+208_1236+211d others(6): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr22 | 40922719 | |||||
chr22:40922721
|
T | C | 5 | a0001c0001t0002g0116a0001c0001t0002g0124a0001c0001t0002g0128others(2): Show | 5 | HG01167.hp2 HG01361.hp2 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.1236+208T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 8/9 | chr22 | 40922721 | ||||||
chr22:40922721
|
T | TAC | 6 | a0001c0001t0001g0102a0001c0001t0002g0133a0001c0001t0002g0240others(3): Show | 6 | HG02723.hp1 HG02886.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1236+232_1236+233d others(4): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr22 | 40922721 | |||||
chr22:40922721
|
T | TACAC | 3 | a0001c0001t0006g0086a0001c0001t0026g0028a0001c0001t0037g0032 | 3 | HG01346.hp2 HG02738.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1236+230_1236+233d others(6): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr22 | 40922721 | |||||
chr22:40922721
|
TAC | T | 18 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(15): Show | 18 | HG01934.hp2 HG02109.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.1236+232_1236+233d others(4): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr22 | 40922721 | |||||
chr22:40922747
|
T | C | 17 | a0001c0001t0003g0056a0001c0001t0003g0058a0001c0001t0003g0059others(14): Show | 17 | HG02055.hp1 HG02258.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.1236+234T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 8/9 | chr22 | 40922747 | ||||||
chr22:40922767
|
C | T | 1 | a0001c0001t0027g0228 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1236+254C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 8/9 | chr22 | 40922767 | ||||||
chr22:40922795
|
G | GT | 4 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(1): Show | 4 | HG01243.hp1 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1236+288dupT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr22 | 40922795 | |||||
chr22:40922893
|
T | C | 2 | a0001c0001t0001g0082a0001c0001t0006g0178 | 2 | HG00597.hp2 HG00609.hp2 |
intron_variant | MODIFIER | c.1236+380T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 8/9 | chr22 | 40922893 | ||||||
chr22:40922955
|
C | T | 1 | a0001c0001t0003g0171 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1236+442C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 8/9 | chr22 | 40922955 | ||||||
chr22:40923313
|
C | G | 23 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(20): Show | 23 | HG00639.hp2 HG01884.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.1236+800C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 8/9 | chr22 | 40923313 | ||||||
chr22:40923649
|
C | T | 8 | a0001c0001t0009g0218a0001c0001t0009g0219a0001c0001t0009g0220others(5): Show | 8 | HG01934.hp2 HG02809.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1237-713C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 8/9 | chr22 | 40923649 | ||||||
chr22:40924116
|
T | A | 23 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(20): Show | 23 | HG00639.hp2 HG01884.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.1237-246T>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 8/9 | chr22 | 40924116 | ||||||
chr22:40924142
|
G | A | 4 | a0001c0002t0005g0215a0001c0002t0046g0217a0001c0002t0048g0214others(1): Show | 4 | HG01884.hp2 HG02630.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1237-220G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 8/9 | chr22 | 40924142 | ||||||
chr22:40924670
|
C | T | 9 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0205others(6): Show | 9 | HG02109.hp1 HG02615.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1357+188C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 9/9 | chr22 | 40924670 | ||||||
chr22:40924790
|
T | G | 1 | a0001c0001t0003g0092 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1357+308T>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 9/9 | chr22 | 40924790 | ||||||
chr22:40924895
|
A | G | 4 | a0001c0001t0002g0115a0001c0001t0002g0139a0001c0001t0020g0143others(1): Show | 4 | HG02602.hp2 HG03654.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1357+413A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 9/9 | chr22 | 40924895 | ||||||
chr22:40925377
|
G | A | 1 | a0001c0001t0002g0124 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1358-892G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 9/9 | chr22 | 40925377 | ||||||
chr22:40925674
|
G | C | 1 | a0001c0001t0014g0027 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1358-595G>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 9/9 | chr22 | 40925674 | ||||||
chr22:40925690
|
C | T | 7 | a0001c0001t0003g0056a0001c0001t0003g0058a0001c0001t0003g0059others(4): Show | 7 | HG02258.hp1 HG02615.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1358-579C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 9/9 | chr22 | 40925690 | ||||||
chr22:40925756
|
T | C | 1 | a0001c0001t0002g0162 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1358-513T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 9/9 | chr22 | 40925756 | ||||||
chr22:40925890
|
G | A | 4 | a0001c0001t0012g0035a0001c0001t0012g0036a0001c0001t0012g0038others(1): Show | 4 | HG00099.hp1 HG01433.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1358-379G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 9/9 | chr22 | 40925890 | ||||||
chr22:40925892
|
A | G | 4 | a0001c0001t0012g0035a0001c0001t0012g0036a0001c0001t0012g0038others(1): Show | 4 | HG00099.hp1 HG01433.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1358-377A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 9/9 | chr22 | 40925892 | ||||||
chr22:40925944
|
A | C | 3 | a0001c0001t0002g0007a0001c0001t0002g0239a0001c0001t0002g0240 | 4 | HG03130.hp1 HG03139.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1358-325A>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 9/9 | chr22 | 40925944 |