geneid | 5817 |
---|---|
ensemblid | ENSG00000073008.16 |
hgncid | 9705 |
symbol | PVR |
name | PVR cell adhesion molecule |
refseq_nuc | NM_006505.5 |
refseq_prot | NP_006496.4 |
ensembl_nuc | ENST00000425690.8 |
ensembl_prot | ENSP00000402060.2 |
mane_status | MANE Select |
chr | chr19 |
start | 44643910 |
end | 44666162 |
strand | + |
ver | v1.2 |
region | chr19:44643910-44666162 |
region5000 | chr19:44638910-44671162 |
regionname0 | PVR_chr19_44643910_44666162 |
regionname5000 | PVR_chr19_44638910_44671162 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 417 | 313 | 61 | 61 | 139 | 13 | 37 | 103 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0002 | 0/0 | 417 | 63 | 4 | 12 | 39 | 1 | 7 | 35 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0003 | 0/0 | 417 | 23 | 22 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0004 | 0/0 | 417 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0005 | 0/0 | 417 | 3 | 0 | 1 | 0 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0006 | 0/0 | 417 | 3 | 0 | 0 | 3 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0007 | 0/0 | 417 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0008 | 0/0 | 416 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0009 | 0/0 | 417 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0010 | 0/0 | 417 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1254 | 303 | 51 | 61 | 139 | 13 | 37 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
c0002 | 0/0 | 1254 | 63 | 4 | 12 | 39 | 1 | 7 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
c0003 | 0/0 | 1254 | 23 | 22 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
c0004 | 0/0 | 1254 | 10 | 10 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
c0005 | 0/0 | 1254 | 3 | 0 | 0 | 3 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
c0006 | 0/0 | 1254 | 3 | 0 | 1 | 0 | 2 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
c0007 | 0/0 | 1254 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
c0008 | 0/0 | 1254 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
c0009 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
c0010 | 0/0 | 1254 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
c0011 | 0/0 | 1254 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
c0012 | 0/0 | 1254 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 4538 | 49 | 2 | 3 | 37 | 2 | 5 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0002 | 0/0 | 4539 | 48 | 1 | 10 | 29 | 1 | 7 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0003 | 0/0 | 4539 | 28 | 0 | 6 | 17 | 2 | 3 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0004 | 0/0 | 4537 | 27 | 0 | 10 | 15 | 0 | 2 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0005 | 0/0 | 4540 | 19 | 2 | 6 | 8 | 0 | 3 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0006 | 0/0 | 4538 | 15 | 0 | 3 | 11 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0007 | 0/0 | 4539 | 14 | 9 | 1 | 4 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0008 | 0/0 | 4539 | 13 | 3 | 0 | 7 | 1 | 2 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0009 | 0/0 | 4540 | 10 | 0 | 1 | 4 | 3 | 2 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0010 | 0/0 | 4539 | 10 | 0 | 1 | 4 | 0 | 5 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0011 | 0/0 | 4539 | 7 | 0 | 0 | 7 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0012 | 1/0 | 4539 | 5 | 1 | 2 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0013 | 0/0 | 4539 | 5 | 1 | 3 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0014 | 0/0 | 4539 | 5 | 0 | 0 | 4 | 1 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0015 | 0/0 | 4539 | 5 | 0 | 4 | 0 | 1 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0016 | 0/0 | 4539 | 5 | 1 | 0 | 2 | 0 | 2 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0017 | 0/0 | 4538 | 4 | 0 | 0 | 4 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0018 | 0/0 | 4540 | 4 | 0 | 3 | 0 | 1 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0019 | 0/0 | 4540 | 4 | 1 | 0 | 2 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0020 | 0/0 | 4541 | 3 | 0 | 3 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0021 | 0/0 | 4538 | 3 | 0 | 0 | 3 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0022 | 0/0 | 4538 | 3 | 0 | 2 | 0 | 1 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0023 | 0/1 | 4541 | 3 | 0 | 2 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0024 | 0/0 | 4540 | 3 | 0 | 1 | 0 | 2 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0025 | 0/0 | 4537 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0026 | 0/0 | 4539 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0027 | 0/0 | 4538 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0028 | 0/0 | 4538 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0029 | 0/0 | 4538 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0030 | 0/0 | 4538 | 2 | 0 | 1 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0031 | 0/0 | 4540 | 2 | 0 | 1 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0032 | 0/0 | 4529 | 2 | 0 | 0 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0033 | 0/0 | 4540 | 2 | 0 | 1 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0034 | 0/0 | 4541 | 2 | 0 | 1 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0035 | 0/0 | 4538 | 2 | 0 | 2 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0036 | 0/0 | 4541 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0037 | 0/0 | 4540 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0038 | 0/0 | 4539 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0039 | 0/0 | 4534 | 2 | 1 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0040 | 0/0 | 4538 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0041 | 0/0 | 4528 | 2 | 0 | 0 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0042 | 0/0 | 4527 | 2 | 0 | 0 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0043 | 0/0 | 4540 | 2 | 1 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0044 | 0/0 | 4541 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0045 | 0/0 | 4540 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0046 | 0/0 | 4535 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0047 | 0/0 | 4540 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0048 | 0/0 | 4539 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0049 | 0/0 | 4539 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0050 | 0/0 | 4540 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0051 | 0/0 | 4537 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0052 | 0/0 | 4539 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0053 | 0/0 | 4538 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0054 | 0/0 | 4539 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0055 | 0/0 | 4540 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0056 | 0/0 | 4538 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0057 | 0/0 | 4541 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0058 | 0/0 | 4540 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0059 | 0/0 | 4541 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0060 | 0/0 | 4538 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0061 | 0/0 | 4527 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0062 | 0/0 | 4540 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0063 | 0/0 | 4539 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0064 | 0/0 | 4540 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0065 | 0/0 | 4539 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0066 | 0/0 | 4539 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0067 | 0/0 | 4539 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0068 | 0/0 | 4537 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0069 | 0/0 | 4538 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0070 | 0/0 | 4539 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0071 | 0/0 | 4541 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0072 | 0/0 | 4539 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0073 | 0/0 | 4541 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0074 | 0/0 | 4541 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0075 | 0/0 | 4540 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0076 | 0/0 | 4539 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0077 | 0/0 | 4540 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0078 | 0/0 | 4537 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0079 | 0/0 | 4509 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0080 | 0/0 | 4538 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0081 | 0/0 | 4540 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0082 | 0/0 | 4540 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0083 | 0/0 | 4538 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0084 | 0/0 | 4539 | 1 | 0 | 0 | 0 | 1 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0085 | 0/0 | 4534 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0086 | 0/0 | 4539 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0087 | 0/0 | 4539 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0088 | 0/0 | 4539 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0089 | 0/0 | 4539 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0090 | 0/0 | 4538 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0091 | 0/0 | 4535 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0092 | 0/0 | 4538 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0093 | 0/0 | 4539 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0094 | 0/0 | 4538 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0095 | 0/0 | 4536 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0096 | 0/0 | 4538 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0097 | 0/0 | 4540 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0098 | 0/0 | 4538 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0099 | 0/0 | 4584 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0100 | 0/0 | 4538 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0101 | 0/0 | 4538 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0102 | 0/0 | 4538 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0103 | 0/0 | 4539 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0104 | 0/0 | 4541 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0105 | 0/0 | 4539 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0106 | 0/0 | 4538 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0107 | 0/0 | 4539 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0108 | 0/0 | 4539 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0109 | 0/0 | 4539 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0110 | 0/0 | 4538 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0111 | 0/0 | 4539 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0112 | 0/0 | 4541 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0113 | 0/0 | 4539 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0114 | 0/0 | 4538 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0115 | 0/0 | 4538 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0116 | 0/0 | 4540 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0117 | 0/0 | 4537 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0118 | 0/0 | 4538 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0119 | 0/0 | 4538 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0120 | 0/0 | 4525 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
t0121 | 0/0 | 4538 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 27 | 2 | 6 | 15 | 1 | 3 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0002 | 0/0 | 19 | 0 | 9 | 9 | 1 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0003 | 0/0 | 15 | 0 | 2 | 12 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0004 | 0/0 | 13 | 0 | 4 | 8 | 1 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0005 | 0/0 | 11 | 0 | 2 | 7 | 1 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0006 | 0/0 | 9 | 0 | 2 | 4 | 0 | 3 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0007 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0008 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0009 | 0/0 | 5 | 0 | 1 | 1 | 0 | 3 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0010 | 0/0 | 5 | 1 | 0 | 1 | 0 | 3 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0011 | 0/0 | 5 | 1 | 2 | 0 | 1 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0012 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0014 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0015 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0017 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0019 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0021 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0024 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0027 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0028 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0038 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0044 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0045 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0046 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0047 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0048 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0052 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0053 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0089 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0198 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1254 | 303 | 51 | 61 | 139 | 13 | 37 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0004 | 0/0 | 1254 | 10 | 10 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0002c0002 | 0/0 | 1254 | 63 | 4 | 12 | 39 | 1 | 7 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0003c0003 | 0/0 | 1254 | 23 | 22 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0004c0007 | 0/0 | 1254 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0004c0012 | 0/0 | 1254 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0005c0006 | 0/0 | 1254 | 3 | 0 | 1 | 0 | 2 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0006c0005 | 0/0 | 1254 | 3 | 0 | 0 | 3 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0007c0010 | 0/0 | 1254 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0008c0009 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0009c0011 | 0/0 | 1254 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0010c0008 | 0/0 | 1254 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5791 | 49 | 2 | 3 | 37 | 2 | 5 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0002 | 0/0 | 5792 | 45 | 1 | 10 | 26 | 1 | 7 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0003 | 0/0 | 5792 | 27 | 0 | 6 | 16 | 2 | 3 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0004 | 0/0 | 5790 | 2 | 0 | 2 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0005 | 0/0 | 5793 | 18 | 2 | 6 | 7 | 0 | 3 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0006 | 0/0 | 5791 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0007 | 0/0 | 5792 | 10 | 6 | 0 | 4 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0008 | 0/0 | 5792 | 8 | 3 | 0 | 3 | 1 | 1 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0009 | 0/0 | 5793 | 8 | 0 | 1 | 4 | 1 | 2 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0010 | 0/0 | 5792 | 10 | 0 | 1 | 4 | 0 | 5 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0011 | 0/0 | 5792 | 7 | 0 | 0 | 7 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0012 | 1/0 | 5792 | 5 | 1 | 2 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0013 | 0/0 | 5792 | 5 | 1 | 3 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0014 | 0/0 | 5792 | 5 | 0 | 0 | 4 | 1 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0015 | 0/0 | 5792 | 5 | 0 | 4 | 0 | 1 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0017 | 0/0 | 5791 | 4 | 0 | 0 | 4 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0018 | 0/0 | 5793 | 4 | 0 | 3 | 0 | 1 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0019 | 0/0 | 5793 | 2 | 1 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0020 | 0/0 | 5794 | 3 | 0 | 3 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0021 | 0/0 | 5791 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0022 | 0/0 | 5791 | 2 | 0 | 2 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0023 | 0/1 | 5794 | 3 | 0 | 2 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0024 | 0/0 | 5793 | 3 | 0 | 1 | 0 | 2 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0028 | 0/0 | 5791 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0030 | 0/0 | 5791 | 2 | 0 | 1 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0031 | 0/0 | 5793 | 2 | 0 | 1 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0032 | 0/0 | 5782 | 2 | 0 | 0 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0033 | 0/0 | 5793 | 2 | 0 | 1 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0034 | 0/0 | 5794 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0036 | 0/0 | 5794 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0037 | 0/0 | 5793 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0038 | 0/0 | 5792 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0039 | 0/0 | 5787 | 2 | 1 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0040 | 0/0 | 5791 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0041 | 0/0 | 5781 | 2 | 0 | 0 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0042 | 0/0 | 5780 | 2 | 0 | 0 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0043 | 0/0 | 5793 | 2 | 1 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0046 | 0/0 | 5788 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0048 | 0/0 | 5792 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0049 | 0/0 | 5792 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0054 | 0/0 | 5792 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0055 | 0/0 | 5793 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0057 | 0/0 | 5794 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0058 | 0/0 | 5793 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0059 | 0/0 | 5794 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0060 | 0/0 | 5791 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0063 | 0/0 | 5792 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0064 | 0/0 | 5793 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0065 | 0/0 | 5792 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0066 | 0/0 | 5792 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0067 | 0/0 | 5792 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0068 | 0/0 | 5790 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0069 | 0/0 | 5791 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0070 | 0/0 | 5792 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0072 | 0/0 | 5792 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0073 | 0/0 | 5794 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0074 | 0/0 | 5794 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0075 | 0/0 | 5793 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0076 | 0/0 | 5792 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0077 | 0/0 | 5793 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0080 | 0/0 | 5791 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0081 | 0/0 | 5793 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0082 | 0/0 | 5793 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0084 | 0/0 | 5792 | 1 | 0 | 0 | 0 | 1 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0086 | 0/0 | 5792 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0087 | 0/0 | 5792 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0088 | 0/0 | 5792 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0089 | 0/0 | 5792 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0090 | 0/0 | 5791 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0091 | 0/0 | 5788 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0092 | 0/0 | 5791 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0093 | 0/0 | 5792 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0094 | 0/0 | 5791 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0095 | 0/0 | 5789 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0096 | 0/0 | 5791 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0097 | 0/0 | 5793 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0098 | 0/0 | 5791 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0100 | 0/0 | 5791 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0101 | 0/0 | 5791 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0102 | 0/0 | 5791 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0103 | 0/0 | 5792 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0105 | 0/0 | 5792 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0106 | 0/0 | 5791 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0114 | 0/0 | 5791 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0116 | 0/0 | 5793 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0120 | 0/0 | 5778 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0001t0121 | 0/0 | 5791 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0004t0025 | 0/0 | 5790 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0004t0026 | 0/0 | 5792 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0004t0027 | 0/0 | 5791 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0004t0050 | 0/0 | 5793 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0004t0051 | 0/0 | 5790 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0004t0052 | 0/0 | 5792 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0001c0004t0053 | 0/0 | 5791 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0002c0002t0003 | 0/0 | 5792 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0002c0002t0004 | 0/0 | 5790 | 24 | 0 | 8 | 14 | 0 | 2 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0002c0002t0006 | 0/0 | 5791 | 14 | 0 | 2 | 11 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0002c0002t0008 | 0/0 | 5792 | 5 | 0 | 0 | 4 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0002c0002t0016 | 0/0 | 5792 | 5 | 1 | 0 | 2 | 0 | 2 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0002c0002t0019 | 0/0 | 5793 | 2 | 0 | 0 | 1 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0002c0002t0021 | 0/0 | 5791 | 2 | 0 | 0 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0002c0002t0022 | 0/0 | 5791 | 1 | 0 | 0 | 0 | 1 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0002c0002t0035 | 0/0 | 5791 | 2 | 0 | 2 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0002c0002t0036 | 0/0 | 5794 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0002c0002t0061 | 0/0 | 5780 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0002c0002t0062 | 0/0 | 5793 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0002c0002t0078 | 0/0 | 5790 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0002c0002t0079 | 0/0 | 5762 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0002c0002t0083 | 0/0 | 5791 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0002c0002t0085 | 0/0 | 5787 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0003c0003t0007 | 0/0 | 5792 | 4 | 3 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0003c0003t0044 | 0/0 | 5794 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0003c0003t0045 | 0/0 | 5793 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0003c0003t0046 | 0/0 | 5788 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0003c0003t0047 | 0/0 | 5793 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0003c0003t0104 | 0/0 | 5794 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0003c0003t0107 | 0/0 | 5792 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0003c0003t0108 | 0/0 | 5792 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0003c0003t0109 | 0/0 | 5792 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0003c0003t0110 | 0/0 | 5791 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0003c0003t0111 | 0/0 | 5792 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0003c0003t0112 | 0/0 | 5794 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0003c0003t0113 | 0/0 | 5792 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0003c0003t0115 | 0/0 | 5791 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0003c0003t0117 | 0/0 | 5790 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0003c0003t0118 | 0/0 | 5791 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0003c0003t0119 | 0/0 | 5791 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0004c0007t0029 | 0/0 | 5791 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0004c0007t0056 | 0/0 | 5791 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0004c0012t0029 | 0/0 | 5791 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0005c0006t0009 | 0/0 | 5793 | 2 | 0 | 0 | 0 | 2 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0005c0006t0034 | 0/0 | 5794 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0006c0005t0002 | 0/0 | 5792 | 2 | 0 | 0 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0006c0005t0005 | 0/0 | 5793 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0007c0010t0071 | 0/0 | 5794 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0008c0009t0099 | 0/0 | 5834 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0009c0011t0002 | 0/0 | 5792 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
a0010c0008t0004 | 0/0 | 5790 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | copy fasta | chr19 | 44638910 | 44671162 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0010 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0002g0001 | 0/0 | 7 | 0 | 3 | 4 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0002g0003 | 0/0 | 9 | 0 | 2 | 7 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0002g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0002g0021 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0002g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0003g0001 | 0/0 | 12 | 0 | 2 | 7 | 1 | 2 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0003g0005 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0004g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0005g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0005g0004 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0005g0006 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0005g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0005g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0005g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0005g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0005g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0005g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0005g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0005g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0005g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0005g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0005g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0006g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0007g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0007g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0007g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0007g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0007g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0007g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0007g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0007g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0008g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0008g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0008g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0008g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0008g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0008g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0008g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0009g0001 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0009g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0009g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0009g0053 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0009g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0010g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0010g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0010g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0010g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0010g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0010g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0010g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0010g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0010g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0011g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0011g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0011g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0011g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0012g0011 | 0/0 | 4 | 1 | 2 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0012g0198 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0013g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0013g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0013g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0013g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0014g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0014g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0014g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0014g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0015g0012 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0015g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0015g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0017g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0017g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0017g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0017g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0018g0004 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0018g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0019g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0019g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0020g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0020g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0021g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0022g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0022g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0023g0089 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0023g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0023g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0024g0038 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0024g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0028g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0028g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0030g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0030g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0031g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0031g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0032g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0032g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0033g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0033g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0034g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0036g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0037g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0037g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0038g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0039g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0039g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0040g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0040g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0041g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0041g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0042g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0042g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0043g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0043g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0046g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0048g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0049g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0054g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0055g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0057g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0058g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0059g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0060g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0063g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0064g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0065g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0066g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0067g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0068g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0069g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0070g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0072g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0073g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0074g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0075g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0076g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0077g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0080g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0081g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0082g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0084g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0086g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0087g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0088g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0089g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0090g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0091g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0092g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0093g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0094g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0095g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0096g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0097g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0098g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0100g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0101g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0102g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0103g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0105g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0106g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0114g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0116g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0120g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0121g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0004t0025g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0004t0025g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0004t0026g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0004t0026g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0004t0027g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0004t0027g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0004t0050g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0004t0051g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0004t0052g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0004t0053g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0004g0002 | 0/0 | 10 | 0 | 6 | 4 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0004g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0004g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0004g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0004g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0004g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0006g0002 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0006g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0006g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0006g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0006g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0006g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0006g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0006g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0006g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0008g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0008g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0008g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0008g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0008g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0016g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0016g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0016g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0016g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0016g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0019g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0019g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0021g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0022g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0035g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0036g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0061g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0062g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0078g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0079g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0083g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0085g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0007g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0007g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0007g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0007g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0044g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0045g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0045g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0046g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0047g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0047g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0104g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0107g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0108g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0109g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0110g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0111g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0112g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0113g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0115g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0117g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0118g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0119g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0004c0007t0029g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0004c0007t0056g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0004c0012t0029g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0005c0006t0009g0052 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0005c0006t0034g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0006c0005t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0006c0005t0005g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0007c0010t0071g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0008c0009t0099g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0009c0011t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0010c0008t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0218 | EUR | GBR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00099 | hp2 | a0005 | c0006 | t0009 | g0052 | EUR | GBR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00140 | hp1 | a0002 | c0002 | t0022 | g0002 | EUR | GBR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0076 | EUR | GBR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00280 | hp1 | a0001 | c0001 | t0015 | g0012 | EUR | FIN | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | FIN | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00323 | hp1 | a0001 | c0001 | t0008 | g0209 | EUR | FIN | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00323 | hp2 | a0001 | c0001 | t0018 | g0004 | EUR | FIN | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00423 | hp1 | a0001 | c0001 | t0041 | g0072 | EAS | CHS | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00423 | hp2 | a0001 | c0001 | t0017 | g0205 | EAS | CHS | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00438 | hp1 | a0001 | c0001 | t0007 | g0073 | EAS | CHS | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00438 | hp2 | a0001 | c0001 | t0011 | g0187 | EAS | CHS | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00558 | hp1 | a0001 | c0001 | t0007 | g0058 | EAS | CHS | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | CHS | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00609 | hp1 | a0001 | c0001 | t0008 | g0020 | EAS | CHS | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00621 | hp1 | a0001 | c0001 | t0010 | g0091 | EAS | CHS | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00621 | hp2 | a0001 | c0001 | t0005 | g0051 | EAS | CHS | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00642 | hp1 | a0002 | c0002 | t0004 | g0002 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00642 | hp2 | a0001 | c0001 | t0063 | g0176 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00673 | hp1 | a0001 | c0001 | t0005 | g0004 | EAS | CHS | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00733 | hp2 | a0001 | c0001 | t0070 | g0006 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00735 | hp1 | a0001 | c0001 | t0073 | g0188 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00735 | hp2 | a0005 | c0006 | t0034 | g0215 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00738 | hp1 | a0001 | c0001 | t0039 | g0150 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00738 | hp2 | a0001 | c0001 | t0009 | g0053 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00741 | hp1 | a0001 | c0001 | t0023 | g0115 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0217 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01069 | hp2 | a0001 | c0001 | t0022 | g0212 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01070 | hp1 | a0001 | c0001 | t0015 | g0195 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01070 | hp2 | a0001 | c0001 | t0013 | g0179 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01071 | hp1 | a0001 | c0001 | t0022 | g0005 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01071 | hp2 | a0001 | c0001 | t0013 | g0027 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01074 | hp2 | a0001 | c0001 | t0033 | g0028 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01081 | hp1 | a0001 | c0001 | t0004 | g0049 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01099 | hp1 | a0001 | c0001 | t0090 | g0103 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01106 | hp1 | a0001 | c0001 | t0005 | g0044 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0200 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01109 | hp1 | a0001 | c0001 | t0088 | g0004 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01109 | hp2 | a0003 | c0003 | t0007 | g0014 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01167 | hp2 | a0001 | c0001 | t0018 | g0004 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01168 | hp1 | a0001 | c0001 | t0015 | g0196 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01168 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01169 | hp1 | a0001 | c0001 | t0015 | g0012 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01169 | hp2 | a0001 | c0001 | t0005 | g0185 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01175 | hp1 | a0001 | c0001 | t0013 | g0183 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01175 | hp2 | a0001 | c0001 | t0010 | g0085 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01192 | hp1 | a0001 | c0001 | t0005 | g0004 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01192 | hp2 | a0001 | c0001 | t0024 | g0114 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01243 | hp1 | a0001 | c0001 | t0020 | g0028 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01243 | hp2 | a0001 | c0001 | t0005 | g0017 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0201 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0204 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01256 | hp2 | a0001 | c0001 | t0018 | g0046 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01257 | hp1 | a0001 | c0001 | t0015 | g0012 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01257 | hp2 | a0002 | c0002 | t0006 | g0136 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01258 | hp1 | a0001 | c0001 | t0075 | g0012 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01258 | hp2 | a0001 | c0001 | t0018 | g0004 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01261 | hp1 | a0001 | c0001 | t0020 | g0012 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01261 | hp2 | a0001 | c0001 | t0020 | g0028 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01346 | hp2 | a0001 | c0001 | t0004 | g0049 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01358 | hp1 | a0001 | c0001 | t0012 | g0011 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01358 | hp2 | a0002 | c0002 | t0035 | g0002 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0024 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01361 | hp2 | a0002 | c0002 | t0035 | g0002 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01433 | hp1 | a0001 | c0001 | t0006 | g0208 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01433 | hp2 | a0001 | c0001 | t0012 | g0011 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01496 | hp1 | a0001 | c0001 | t0023 | g0116 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0021 | EUR | IBS | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01516 | hp2 | a0001 | c0001 | t0024 | g0038 | EUR | IBS | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01517 | hp1 | a0001 | c0001 | t0024 | g0038 | EUR | IBS | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01517 | hp2 | a0005 | c0006 | t0009 | g0052 | EUR | IBS | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01884 | hp1 | a0001 | c0001 | t0120 | g0149 | AFR | ACB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01884 | hp2 | a0001 | c0001 | t0028 | g0126 | AFR | ACB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01891 | hp1 | a0001 | c0001 | t0038 | g0035 | AFR | ACB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01891 | hp2 | a0003 | c0003 | t0118 | g0069 | AFR | ACB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01928 | hp1 | a0002 | c0002 | t0006 | g0002 | AMR | PEL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01928 | hp2 | a0007 | c0010 | t0071 | g0024 | AMR | PEL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PEL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01943 | hp1 | a0001 | c0001 | t0031 | g0001 | AMR | PEL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01943 | hp2 | a0002 | c0002 | t0004 | g0002 | AMR | PEL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01952 | hp2 | a0002 | c0002 | t0004 | g0019 | AMR | PEL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01993 | hp1 | a0002 | c0002 | t0004 | g0002 | AMR | PEL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01993 | hp2 | a0001 | c0001 | t0030 | g0045 | AMR | PEL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02004 | hp1 | a0001 | c0001 | t0005 | g0214 | AMR | PEL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02004 | hp2 | a0002 | c0002 | t0004 | g0002 | AMR | PEL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02015 | hp1 | a0006 | c0005 | t0002 | g0003 | EAS | KHV | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02055 | hp1 | a0001 | c0001 | t0077 | g0168 | AFR | ACB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02055 | hp2 | a0002 | c0002 | t0036 | g0139 | AFR | ACB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02056 | hp1 | a0002 | c0002 | t0006 | g0002 | EAS | KHV | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02056 | hp2 | a0001 | c0001 | t0008 | g0005 | EAS | KHV | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02071 | hp1 | a0006 | c0005 | t0005 | g0003 | EAS | KHV | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02074 | hp1 | a0001 | c0001 | t0100 | g0106 | EAS | KHV | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | KHV | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02080 | hp2 | a0001 | c0001 | t0009 | g0203 | EAS | KHV | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02129 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | KHV | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | KHV | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02132 | hp2 | a0001 | c0001 | t0014 | g0222 | EAS | KHV | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02135 | hp1 | a0001 | c0001 | t0010 | g0083 | EAS | KHV | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02135 | hp2 | a0001 | c0001 | t0009 | g0005 | EAS | KHV | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02145 | hp1 | a0003 | c0003 | t0112 | g0034 | AFR | ACB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02145 | hp2 | a0001 | c0001 | t0005 | g0171 | AFR | ACB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02155 | hp1 | a0002 | c0002 | t0004 | g0007 | EAS | CDX | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02155 | hp2 | a0001 | c0001 | t0066 | g0005 | EAS | CDX | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02165 | hp1 | a0001 | c0001 | t0096 | g0090 | EAS | CDX | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02165 | hp2 | a0001 | c0001 | t0065 | g0219 | EAS | CDX | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02257 | hp1 | a0003 | c0003 | t0047 | g0068 | AFR | ACB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02257 | hp2 | a0001 | c0001 | t0036 | g0043 | AFR | ACB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02258 | hp1 | a0003 | c0003 | t0115 | g0033 | AFR | ACB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02258 | hp2 | a0001 | c0001 | t0114 | g0111 | AFR | ACB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02273 | hp2 | a0002 | c0002 | t0004 | g0135 | AMR | PEL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02280 | hp2 | a0001 | c0001 | t0028 | g0057 | AFR | ACB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02293 | hp2 | a0002 | c0002 | t0004 | g0002 | AMR | PEL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02451 | hp1 | a0002 | c0002 | t0085 | g0064 | AFR | ACB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02451 | hp2 | a0001 | c0004 | t0027 | g0022 | AFR | ACB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02572 | hp1 | a0003 | c0003 | t0045 | g0034 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02572 | hp2 | a0001 | c0004 | t0026 | g0023 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0044 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02615 | hp1 | a0003 | c0003 | t0111 | g0032 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02615 | hp2 | a0001 | c0001 | t0007 | g0013 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02622 | hp1 | a0001 | c0001 | t0007 | g0063 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02622 | hp2 | a0001 | c0001 | t0106 | g0098 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02630 | hp1 | a0001 | c0001 | t0105 | g0099 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02630 | hp2 | a0001 | c0004 | t0052 | g0023 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02647 | hp1 | a0001 | c0004 | t0027 | g0173 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02647 | hp2 | a0001 | c0001 | t0043 | g0013 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02698 | hp1 | a0001 | c0001 | t0005 | g0006 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02717 | hp1 | a0001 | c0001 | t0101 | g0030 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02717 | hp2 | a0001 | c0001 | t0094 | g0154 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02723 | hp1 | a0001 | c0004 | t0053 | g0022 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02723 | hp2 | a0001 | c0001 | t0082 | g0001 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02738 | hp1 | a0001 | c0001 | t0009 | g0001 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02738 | hp2 | a0001 | c0001 | t0005 | g0191 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02809 | hp1 | a0003 | c0003 | t0044 | g0014 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02809 | hp2 | a0002 | c0002 | t0083 | g0131 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02818 | hp1 | a0001 | c0001 | t0091 | g0151 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02818 | hp2 | a0003 | c0003 | t0007 | g0033 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02895 | hp1 | a0003 | c0003 | t0007 | g0065 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02895 | hp2 | a0001 | c0001 | t0007 | g0013 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02896 | hp1 | a0001 | c0004 | t0025 | g0023 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02896 | hp2 | a0004 | c0007 | t0029 | g0163 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02897 | hp1 | a0001 | c0004 | t0025 | g0175 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02897 | hp2 | a0003 | c0003 | t0007 | g0066 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02922 | hp1 | a0003 | c0003 | t0117 | g0071 | AFR | ESN | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02922 | hp2 | a0001 | c0001 | t0037 | g0161 | AFR | ESN | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02965 | hp1 | a0001 | c0001 | t0007 | g0013 | AFR | ESN | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02965 | hp2 | a0004 | c0012 | t0029 | g0162 | AFR | ESN | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02970 | hp1 | a0001 | c0004 | t0051 | g0174 | AFR | ESN | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02970 | hp2 | a0003 | c0003 | t0119 | g0070 | AFR | ESN | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03017 | hp1 | a0001 | c0001 | t0008 | g0006 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03041 | hp1 | a0004 | c0007 | t0056 | g0164 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03041 | hp2 | a0001 | c0001 | t0072 | g0166 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03098 | hp1 | a0001 | c0004 | t0026 | g0172 | AFR | MSL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03098 | hp2 | a0003 | c0003 | t0108 | g0113 | AFR | MSL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03130 | hp1 | a0001 | c0001 | t0008 | g0227 | AFR | ESN | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03130 | hp2 | a0001 | c0001 | t0048 | g0165 | AFR | ESN | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03139 | hp1 | a0003 | c0003 | t0107 | g0032 | AFR | ESN | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03139 | hp2 | a0001 | c0001 | t0040 | g0152 | AFR | ESN | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03195 | hp1 | a0001 | c0001 | t0058 | g0233 | AFR | ESN | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03195 | hp2 | a0001 | c0001 | t0102 | g0030 | AFR | ESN | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03209 | hp1 | a0003 | c0003 | t0045 | g0096 | AFR | MSL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03209 | hp2 | a0001 | c0001 | t0092 | g0155 | AFR | MSL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03225 | hp1 | a0001 | c0001 | t0069 | g0230 | AFR | MSL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03225 | hp2 | a0003 | c0003 | t0110 | g0128 | AFR | MSL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0021 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03453 | hp1 | a0001 | c0001 | t0040 | g0153 | AFR | MSL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03453 | hp2 | a0003 | c0003 | t0047 | g0067 | AFR | MSL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03486 | hp1 | a0001 | c0001 | t0008 | g0225 | AFR | MSL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03486 | hp2 | a0003 | c0003 | t0044 | g0014 | AFR | MSL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03490 | hp1 | a0001 | c0001 | t0054 | g0220 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03490 | hp2 | a0001 | c0001 | t0009 | g0053 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03491 | hp1 | a0001 | c0001 | t0013 | g0159 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03491 | hp2 | a0001 | c0001 | t0086 | g0048 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03516 | hp1 | a0001 | c0001 | t0057 | g0228 | AFR | ESN | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03516 | hp2 | a0001 | c0001 | t0074 | g0167 | AFR | ESN | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03540 | hp2 | a0001 | c0001 | t0039 | g0148 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03654 | hp1 | a0002 | c0002 | t0016 | g0008 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03654 | hp2 | a0001 | c0001 | t0010 | g0009 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03669 | hp1 | a0002 | c0002 | t0004 | g0147 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0182 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | STU | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03688 | hp2 | a0001 | c0001 | t0055 | g0027 | SAS | STU | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03704 | hp2 | a0002 | c0002 | t0004 | g0138 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03710 | hp1 | a0001 | c0001 | t0010 | g0092 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03710 | hp2 | a0001 | c0001 | t0097 | g0010 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03831 | hp1 | a0002 | c0002 | t0016 | g0041 | SAS | BEB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03831 | hp2 | a0001 | c0001 | t0005 | g0006 | SAS | BEB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03834 | hp1 | a0001 | c0001 | t0067 | g0003 | SAS | BEB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03834 | hp2 | a0001 | c0001 | t0030 | g0047 | SAS | BEB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0180 | SAS | BEB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03927 | hp2 | a0001 | c0001 | t0012 | g0011 | SAS | BEB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03942 | hp1 | a0001 | c0001 | t0034 | g0216 | SAS | BEB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03942 | hp2 | a0001 | c0001 | t0010 | g0009 | SAS | BEB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG04115 | hp1 | a0001 | c0001 | t0010 | g0094 | SAS | STU | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG04115 | hp2 | a0001 | c0001 | t0095 | g0010 | SAS | STU | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG04184 | hp1 | a0001 | c0001 | t0010 | g0080 | SAS | BEB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0199 | SAS | BEB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | STU | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG04199 | hp2 | a0002 | c0002 | t0019 | g0133 | SAS | STU | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG04228 | hp1 | a0002 | c0002 | t0008 | g0146 | SAS | STU | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG04228 | hp2 | a0001 | c0001 | t0033 | g0197 | SAS | STU | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18522 | hp1 | a0001 | c0001 | t0076 | g0232 | AFR | YRI | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18522 | hp2 | a0003 | c0003 | t0109 | g0100 | AFR | YRI | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18612 | hp1 | a0002 | c0002 | t0004 | g0145 | EAS | CHB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | CHB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18747 | hp2 | a0002 | c0002 | t0004 | g0007 | EAS | CHB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18906 | hp1 | a0001 | c0004 | t0050 | g0022 | AFR | YRI | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18906 | hp2 | a0001 | c0001 | t0059 | g0229 | AFR | YRI | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18939 | hp1 | a0001 | c0001 | t0041 | g0075 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18939 | hp2 | a0001 | c0001 | t0032 | g0006 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18941 | hp1 | a0002 | c0002 | t0004 | g0002 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18942 | hp2 | a0001 | c0001 | t0021 | g0001 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18945 | hp1 | a0001 | c0001 | t0116 | g0015 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18945 | hp2 | a0002 | c0002 | t0016 | g0002 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18946 | hp2 | a0002 | c0002 | t0021 | g0008 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18947 | hp2 | a0002 | c0002 | t0006 | g0002 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18949 | hp1 | a0002 | c0002 | t0016 | g0130 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18949 | hp2 | a0001 | c0001 | t0064 | g0025 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18950 | hp1 | a0002 | c0002 | t0003 | g0042 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18950 | hp2 | a0001 | c0001 | t0011 | g0025 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18951 | hp2 | a0002 | c0002 | t0006 | g0129 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18953 | hp1 | a0001 | c0001 | t0011 | g0025 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18954 | hp1 | a0006 | c0005 | t0002 | g0003 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18956 | hp1 | a0001 | c0001 | t0049 | g0189 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18956 | hp2 | a0002 | c0002 | t0004 | g0002 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18957 | hp1 | a0002 | c0002 | t0004 | g0007 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18959 | hp1 | a0002 | c0002 | t0008 | g0134 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18959 | hp2 | a0001 | c0001 | t0011 | g0178 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18965 | hp1 | a0002 | c0002 | t0004 | g0142 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18966 | hp2 | a0001 | c0001 | t0007 | g0117 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18968 | hp1 | a0002 | c0002 | t0004 | g0019 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18969 | hp1 | a0001 | c0001 | t0014 | g0221 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18969 | hp2 | a0002 | c0002 | t0004 | g0140 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18970 | hp2 | a0002 | c0002 | t0008 | g0143 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18972 | hp1 | a0001 | c0001 | t0043 | g0015 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18972 | hp2 | a0001 | c0001 | t0005 | g0045 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18973 | hp2 | a0002 | c0002 | t0006 | g0008 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18975 | hp1 | a0002 | c0002 | t0078 | g0002 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18975 | hp2 | a0002 | c0002 | t0006 | g0007 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18977 | hp2 | a0002 | c0002 | t0004 | g0007 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18979 | hp1 | a0001 | c0001 | t0017 | g0003 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18979 | hp2 | a0002 | c0002 | t0004 | g0002 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18980 | hp1 | a0002 | c0002 | t0006 | g0008 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18980 | hp2 | a0001 | c0001 | t0087 | g0003 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18982 | hp1 | a0002 | c0002 | t0019 | g0137 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18983 | hp1 | a0001 | c0001 | t0042 | g0009 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18989 | hp2 | a0002 | c0002 | t0079 | g0040 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18990 | hp2 | a0001 | c0001 | t0007 | g0118 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18991 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18993 | hp1 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18993 | hp2 | a0010 | c0008 | t0004 | g0042 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18994 | hp1 | a0001 | c0001 | t0010 | g0055 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18995 | hp1 | a0001 | c0001 | t0008 | g0020 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18999 | hp1 | a0001 | c0001 | t0017 | g0006 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18999 | hp2 | a0001 | c0001 | t0017 | g0001 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19000 | hp1 | a0001 | c0001 | t0011 | g0026 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19000 | hp2 | a0001 | c0001 | t0081 | g0050 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19001 | hp1 | a0002 | c0002 | t0006 | g0141 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19002 | hp1 | a0002 | c0002 | t0062 | g0007 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19002 | hp2 | a0001 | c0001 | t0005 | g0177 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19003 | hp2 | a0001 | c0001 | t0098 | g0101 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19005 | hp2 | a0001 | c0001 | t0011 | g0026 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19006 | hp2 | a0001 | c0001 | t0060 | g0004 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19010 | hp2 | a0002 | c0002 | t0021 | g0008 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19030 | hp1 | a0003 | c0003 | t0104 | g0014 | AFR | LWK | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19030 | hp2 | a0001 | c0001 | t0068 | g0231 | AFR | LWK | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19043 | hp1 | a0001 | c0001 | t0007 | g0062 | AFR | LWK | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19043 | hp2 | a0001 | c0001 | t0089 | g0001 | AFR | LWK | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19054 | hp1 | a0002 | c0002 | t0006 | g0008 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19054 | hp2 | a0008 | c0009 | t0099 | g0087 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19058 | hp1 | a0001 | c0001 | t0042 | g0078 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19058 | hp2 | a0001 | c0001 | t0121 | g0193 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19060 | hp1 | a0001 | c0001 | t0032 | g0048 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19064 | hp1 | a0002 | c0002 | t0004 | g0040 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19064 | hp2 | a0001 | c0001 | t0009 | g0001 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19065 | hp2 | a0002 | c0002 | t0004 | g0007 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19066 | hp1 | a0002 | c0002 | t0008 | g0156 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19067 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19067 | hp2 | a0001 | c0001 | t0011 | g0026 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19068 | hp1 | a0001 | c0001 | t0009 | g0005 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19068 | hp2 | a0001 | c0001 | t0014 | g0029 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19072 | hp1 | a0001 | c0001 | t0010 | g0015 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19072 | hp2 | a0001 | c0001 | t0080 | g0206 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19077 | hp1 | a0001 | c0001 | t0019 | g0020 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19077 | hp2 | a0001 | c0001 | t0014 | g0029 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19078 | hp1 | a0002 | c0002 | t0006 | g0019 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19078 | hp2 | a0009 | c0011 | t0002 | g0234 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19079 | hp1 | a0002 | c0002 | t0006 | g0132 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19082 | hp2 | a0001 | c0001 | t0005 | g0194 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19083 | hp2 | a0002 | c0002 | t0004 | g0002 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19084 | hp1 | a0002 | c0002 | t0061 | g0157 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19084 | hp2 | a0002 | c0002 | t0006 | g0002 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19086 | hp1 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19086 | hp2 | a0001 | c0001 | t0031 | g0029 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19087 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19088 | hp2 | a0002 | c0002 | t0008 | g0054 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19240 | hp1 | a0001 | c0001 | t0038 | g0035 | AFR | YRI | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0170 | AFR | YRI | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA20129 | hp1 | a0001 | c0001 | t0008 | g0169 | AFR | ASW | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ASW | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0001 | EUR | TSI | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA20752 | hp2 | a0001 | c0001 | t0014 | g0017 | EUR | TSI | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA20805 | hp1 | a0001 | c0001 | t0009 | g0011 | EUR | TSI | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA20805 | hp2 | a0001 | c0001 | t0084 | g0005 | EUR | TSI | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA20905 | hp1 | a0002 | c0002 | t0006 | g0041 | SAS | GIH | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0186 | SAS | GIH | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01123 | hp1 | a0001 | c0001 | t0103 | g0223 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01123 | hp2 | a0002 | c0002 | t0004 | g0002 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02109 | hp1 | a0001 | c0001 | t0019 | g0226 | AFR | ACB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02109 | hp2 | a0001 | c0001 | t0093 | g0224 | AFR | ACB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02559 | hp1 | a0003 | c0003 | t0113 | g0112 | AFR | ACB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02559 | hp2 | a0001 | c0001 | t0012 | g0011 | AFR | ACB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03471 | hp1 | a0002 | c0002 | t0016 | g0144 | AFR | MSL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03471 | hp2 | a0001 | c0001 | t0037 | g0043 | AFR | MSL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG06807 | hp1 | a0001 | c0001 | t0007 | g0061 | AFR | USA | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG06807 | hp2 | a0001 | c0001 | t0013 | g0027 | AFR | USA | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA20300 | hp1 | a0001 | c0001 | t0046 | g0095 | AFR | USA | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA20300 | hp2 | a0003 | c0003 | t0046 | g0097 | AFR | USA | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0023 | g0089 | REF | REF | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0012 | g0198 | REF | REF | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:44647342
|
G | A | 2 | a0002a0010 | 64 | HG00140.hp1 HG00642.hp1 HG01123.hp2 others(61): Show |
missense_variant | MODERATE | c.199G>A | p.Ala67Thr | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/8 | 386/5792 | 199/1254 | 67/417 | chr19 | 44647342 | ||
chr19:44649958
|
C | G | 1 | a0004 | 3 | HG02896.hp2 HG02965.hp2 HG03041.hp1 |
missense_variant | MODERATE | c.577C>G | p.Pro193Ala | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/8 | 764/5792 | 577/1254 | 193/417 | chr19 | 44649958 | ||
chr19:44650057
|
G | A | 1 | a0006 | 3 | HG02015.hp1 HG02071.hp1 NA18954.hp1 |
missense_variant | MODERATE | c.676G>A | p.Glu226Lys | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/8 | 863/5792 | 676/1254 | 226/417 | chr19 | 44650057 | ||
chr19:44653980
|
C | G | 1 | a0010 | 1 | NA18993.hp2 | missense_variant | MODERATE | c.805C>G | p.Arg269Gly | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/8 | 992/5792 | 805/1254 | 269/417 | chr19 | 44653980 | ||
chr19:44657802
|
G | A | 1 | a0003 | 23 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(20): Show |
missense_variant | MODERATE | c.883G>A | p.Ala295Thr | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 5/8 | 1070/5792 | 883/1254 | 295/417 | chr19 | 44657802 | ||
chr19:44657831
|
A | C | 1 | a0009 | 1 | NA19078.hp2 | missense_variant | MODERATE | c.912A>C | p.Lys304Asn | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 5/8 | 1099/5792 | 912/1254 | 304/417 | chr19 | 44657831 | ||
chr19:44657841
|
A | G | 1 | a0007 | 1 | HG01928.hp2 | missense_variant | MODERATE | c.922A>G | p.Thr308Ala | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 5/8 | 1109/5792 | 922/1254 | 308/417 | chr19 | 44657841 | ||
chr19:44658770
|
G | A | 1 | a0005 | 3 | HG00099.hp2 HG00735.hp2 HG01517.hp2 |
missense_variant | MODERATE | c.1020G>A | p.Met340Ile | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/8 | 1207/5792 | 1020/1254 | 340/417 | chr19 | 44658770 | ||
chr19:44661248
|
CCAGCATT others(39): Show |
C | 1 | a0008 | 1 | NA19054.hp2 | splice_acceptor_variant&disruptive_inframe_deletion&splice_region_variant&intron_variant | HIGH | c.1151-40_1156delCAT others(43): Show |
p.Ser384_Glu386delin others(4): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 7/8 | 1151/1254 | 384/417 | INFO_REALIGN_3_PRIME | chr19 | 44661248 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:44647491
|
G | A | 1 | a0003c0003 | 23 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(20): Show |
synonymous_variant | LOW | c.348G>A | p.Glu116Glu | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/8 | 535/5792 | 348/1254 | 116/417 | chr19 | 44647491 | ||
chr19:44653979
|
T | A | 1 | a0004c0007 | 2 | HG02896.hp2 HG03041.hp1 |
synonymous_variant | LOW | c.804T>A | p.Ala268Ala | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/8 | 991/5792 | 804/1254 | 268/417 | chr19 | 44653979 | ||
chr19:44657871
|
C | T | 1 | a0001c0004 | 10 | HG02451.hp2 HG02572.hp2 HG02630.hp2 others(7): Show |
synonymous_variant | LOW | c.952C>T | p.Leu318Leu | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 5/8 | 1139/5792 | 952/1254 | 318/417 | chr19 | 44657871 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:44643944
|
C | T | 1 | a0001c0001t0121 | 1 | NA19058.hp2 | 5_prime_UTR_variant | MODIFIER | c.-153C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/8 | 153 | chr19 | 44643944 | |||||
chr19:44643990
|
AGGACCTG others(7): Show |
A | 1 | a0001c0001t0120 | 1 | HG01884.hp1 | 5_prime_UTR_variant | MODIFIER | c.-103_-90delCCTGAGC others(7): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/8 | 90 | INFO_REALIGN_3_PRIME | chr19 | 44643990 | ||||
chr19:44644040
|
G | T | 48 | a0001c0001t0001a0001c0001t0007a0001c0001t0010others(45): Show | 130 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(127): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-57G>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/8 | chr19 | 44644040 | ||||||
chr19:44661968
|
G | C | 1 | a0001c0001t0048 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*157G>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 157 | chr19 | 44661968 | |||||
chr19:44662053
|
C | T | 1 | a0001c0001t0089 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*242C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 242 | chr19 | 44662053 | |||||
chr19:44662231
|
C | A | 1 | a0001c0001t0049 | 1 | NA18956.hp1 | 3_prime_UTR_variant | MODIFIER | c.*420C>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 420 | chr19 | 44662231 | |||||
chr19:44662246
|
C | T | 1 | a0001c0001t0048 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*435C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 435 | chr19 | 44662246 | |||||
chr19:44662259
|
GT | G | 9 | a0001c0001t0038a0001c0001t0090a0001c0004t0025others(6): Show | 13 | HG01099.hp1 HG01891.hp1 HG02451.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*454delT | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 454 | INFO_REALIGN_3_PRIME | chr19 | 44662259 | ||||
chr19:44662261
|
T | G | 9 | a0001c0001t0038a0001c0001t0090a0001c0004t0025others(6): Show | 13 | HG01099.hp1 HG01891.hp1 HG02451.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*450T>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 450 | chr19 | 44662261 | |||||
chr19:44662346
|
C | G | 4 | a0003c0003t0047a0003c0003t0117a0003c0003t0118others(1): Show | 5 | HG01891.hp2 HG02257.hp1 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*535C>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 535 | chr19 | 44662346 | |||||
chr19:44662645
|
A | C | 137 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(134): Show | 407 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(404): Show |
3_prime_UTR_variant | MODIFIER | c.*834A>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 834 | chr19 | 44662645 | |||||
chr19:44662655
|
A | G | 1 | a0001c0001t0088 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*844A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 844 | chr19 | 44662655 | |||||
chr19:44662751
|
T | C | 1 | a0001c0001t0054 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*940T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 940 | chr19 | 44662751 | |||||
chr19:44662921
|
G | A | 1 | a0001c0001t0028 | 2 | HG01884.hp2 HG02280.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1110G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 1110 | chr19 | 44662921 | |||||
chr19:44663108
|
G | C | 3 | a0001c0001t0039a0001c0001t0091a0001c0001t0120 | 4 | HG00738.hp1 HG01884.hp1 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1297G>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 1297 | chr19 | 44663108 | |||||
chr19:44663135
|
C | T | 1 | a0001c0004t0053 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1324C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 1324 | chr19 | 44663135 | |||||
chr19:44663180
|
C | G | 1 | a0001c0001t0116 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1369C>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 1369 | chr19 | 44663180 | |||||
chr19:44663185
|
T | G | 2 | a0001c0001t0023a0001c0001t0024 | 6 | HG00741.hp1 HG01192.hp2 HG01496.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1374T>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 1374 | chr19 | 44663185 | |||||
chr19:44663199
|
G | A | 2 | a0001c0001t0013a0001c0001t0055 | 6 | HG01070.hp2 HG01071.hp2 HG01175.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1388G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 1388 | chr19 | 44663199 | |||||
chr19:44663400
|
A | G | 1 | a0003c0003t0115 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1589A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 1589 | chr19 | 44663400 | |||||
chr19:44663481
|
G | A | 4 | a0001c0001t0048a0004c0007t0029a0004c0007t0056others(1): Show | 4 | HG02896.hp2 HG02965.hp2 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1670G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 1670 | chr19 | 44663481 | |||||
chr19:44663491
|
G | A | 1 | a0001c0001t0089 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1680G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 1680 | chr19 | 44663491 | |||||
chr19:44663522
|
G | A | 7 | a0001c0001t0040a0001c0001t0057a0001c0001t0058others(4): Show | 8 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1711G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 1711 | chr19 | 44663522 | |||||
chr19:44663585
|
C | T | 1 | a0001c0001t0087 | 1 | NA18980.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1774C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 1774 | chr19 | 44663585 | |||||
chr19:44663684
|
C | T | 1 | a0001c0001t0086 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1873C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 1873 | chr19 | 44663684 | |||||
chr19:44663742
|
CT | C | 15 | a0001c0001t0001a0001c0001t0010a0001c0001t0041others(12): Show | 74 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*1942delT | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 1942 | INFO_REALIGN_3_PRIME | chr19 | 44663742 | ||||
chr19:44663791
|
G | A | 1 | a0002c0002t0062 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1980G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 1980 | chr19 | 44663791 | |||||
chr19:44663847
|
G | C | 1 | a0001c0001t0063 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2036G>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 2036 | chr19 | 44663847 | |||||
chr19:44663948
|
G | A | 3 | a0001c0001t0011a0001c0001t0064a0001c0001t0065 | 9 | HG00438.hp2 HG02165.hp2 NA18949.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2137G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 2137 | chr19 | 44663948 | |||||
chr19:44663975
|
T | C | 1 | a0001c0001t0066 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2164T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 2164 | chr19 | 44663975 | |||||
chr19:44664149
|
AAATT | A | 5 | a0001c0001t0039a0001c0001t0046a0001c0001t0091others(2): Show | 6 | HG00738.hp1 HG02451.hp1 HG02818.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2344_*2347delATTA | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 2344 | INFO_REALIGN_3_PRIME | chr19 | 44664149 | ||||
chr19:44664264
|
A | G | 50 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(47): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*2453A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 2453 | chr19 | 44664264 | |||||
chr19:44664357
|
C | T | 1 | a0001c0001t0084 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2546C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 2546 | chr19 | 44664357 | |||||
chr19:44664435
|
A | G | 1 | a0001c0001t0114 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2624A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 2624 | chr19 | 44664435 | |||||
chr19:44664491
|
A | C | 23 | a0001c0001t0046a0001c0001t0048a0001c0001t0076others(20): Show | 23 | HG01884.hp1 HG02055.hp1 HG02145.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2680A>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 2680 | chr19 | 44664491 | |||||
chr19:44664502
|
C | G | 4 | a0001c0001t0015a0001c0001t0020a0001c0001t0033others(1): Show | 11 | HG00280.hp1 HG01070.hp1 HG01074.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2691C>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 2691 | chr19 | 44664502 | |||||
chr19:44664711
|
C | CT | 11 | a0001c0001t0036a0001c0001t0037a0001c0001t0074others(8): Show | 14 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2914dupT | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 2915 | INFO_REALIGN_3_PRIME | chr19 | 44664711 | ||||
chr19:44664711
|
CT | C | 20 | a0001c0001t0004a0001c0001t0006a0001c0001t0015others(17): Show | 68 | HG00280.hp1 HG00642.hp1 HG01070.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*2914delT | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 2914 | INFO_REALIGN_3_PRIME | chr19 | 44664711 | ||||
chr19:44664826
|
A | T | 3 | a0001c0001t0046a0002c0002t0085a0003c0003t0046 | 3 | HG02451.hp1 NA20300.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3015A>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3015 | chr19 | 44664826 | |||||
chr19:44664895
|
A | G | 1 | a0001c0001t0059 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3084A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3084 | chr19 | 44664895 | |||||
chr19:44664963
|
T | C | 4 | a0001c0001t0068a0001c0001t0069a0001c0001t0076others(1): Show | 4 | HG01123.hp1 HG03225.hp1 NA18522.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3152T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3152 | chr19 | 44664963 | |||||
chr19:44665105
|
A | G | 1 | a0001c0001t0081 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3294A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3294 | chr19 | 44665105 | |||||
chr19:44665131
|
G | A | 4 | a0001c0001t0015a0001c0001t0020a0001c0001t0033others(1): Show | 11 | HG00280.hp1 HG01070.hp1 HG01074.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3320G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3320 | chr19 | 44665131 | |||||
chr19:44665156
|
C | CG | 5 | a0001c0001t0018a0001c0001t0023a0001c0001t0024others(2): Show | 12 | HG00323.hp2 HG00735.hp1 HG00741.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3351dupG | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3352 | INFO_REALIGN_3_PRIME | chr19 | 44665156 | ||||
chr19:44665156
|
C | T | 3 | a0003c0003t0045a0003c0003t0108a0003c0003t0113 | 4 | HG02559.hp1 HG02572.hp1 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3345C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3345 | chr19 | 44665156 | |||||
chr19:44665157
|
G | A | 1 | a0001c0001t0070 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3346G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3346 | chr19 | 44665157 | |||||
chr19:44665196
|
C | T | 1 | a0001c0001t0072 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3385C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3385 | chr19 | 44665196 | |||||
chr19:44665230
|
G | A | 16 | a0001c0001t0003a0001c0001t0009a0001c0001t0014others(13): Show | 56 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*3419G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3419 | chr19 | 44665230 | |||||
chr19:44665466
|
C | G | 4 | a0001c0001t0105a0001c0001t0106a0003c0003t0112others(1): Show | 4 | HG02145.hp1 HG02258.hp1 HG02622.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3655C>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3655 | chr19 | 44665466 | |||||
chr19:44665467
|
G | A | 1 | a0002c0002t0078 | 1 | NA18975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3656G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3656 | chr19 | 44665467 | |||||
chr19:44665574
|
G | C | 14 | a0001c0001t0028a0001c0001t0046a0001c0004t0025others(11): Show | 18 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3763G>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3763 | chr19 | 44665574 | |||||
chr19:44665619
|
AGT | A | 3 | a0001c0001t0068a0001c0001t0076a0001c0001t0103 | 3 | HG01123.hp1 NA18522.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3810_*3811delTG | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3810 | INFO_REALIGN_3_PRIME | chr19 | 44665619 | ||||
chr19:44665635
|
C | CA | 30 | a0001c0001t0005a0001c0001t0009a0001c0001t0010others(27): Show | 83 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*3849dupA | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3850 | INFO_REALIGN_3_PRIME | chr19 | 44665635 | ||||
chr19:44665635
|
C | CAA | 13 | a0001c0001t0020a0001c0001t0034a0001c0001t0057others(10): Show | 15 | HG00735.hp2 HG01123.hp1 HG01243.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3848_*3849dupAA | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3850 | INFO_REALIGN_3_PRIME | chr19 | 44665635 | ||||
chr19:44665635
|
CA | C | 31 | a0001c0001t0004a0001c0001t0017a0001c0001t0022others(28): Show | 63 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*3849delA | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3849 | INFO_REALIGN_3_PRIME | chr19 | 44665635 | ||||
chr19:44665635
|
CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0032a0001c0001t0041 | 4 | HG00423.hp1 NA18939.hp1 NA18939.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3840_*3849delAAAA others(6): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3840 | INFO_REALIGN_3_PRIME | chr19 | 44665635 | ||||
chr19:44665635
|
CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0042a0002c0002t0061 | 3 | NA18983.hp1 NA19058.hp1 NA19084.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3839_*3849delAAAA others(7): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3839 | INFO_REALIGN_3_PRIME | chr19 | 44665635 | ||||
chr19:44665670
|
C | T | 1 | a0001c0001t0100 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3859C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3859 | chr19 | 44665670 | |||||
chr19:44665681
|
C | CTTTTTTA others(39): Show |
1 | a0008c0009t0099 | 1 | NA19054.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3870_*3871insTTTT others(42): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3871 | chr19 | 44665681 | |||||
chr19:44665683
|
G | T | 1 | a0008c0009t0099 | 1 | NA19054.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3872G>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3872 | chr19 | 44665683 | |||||
chr19:44665686
|
C | T | 1 | a0008c0009t0099 | 1 | NA19054.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3875C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3875 | chr19 | 44665686 | |||||
chr19:44665687
|
A | T | 1 | a0008c0009t0099 | 1 | NA19054.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3876A>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3876 | chr19 | 44665687 | |||||
chr19:44665688
|
C | G | 1 | a0008c0009t0099 | 1 | NA19054.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3877C>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3877 | chr19 | 44665688 | |||||
chr19:44665694
|
G | T | 1 | a0008c0009t0099 | 1 | NA19054.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3883G>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3883 | chr19 | 44665694 | |||||
chr19:44665701
|
C | T | 1 | a0001c0001t0092 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3890C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3890 | chr19 | 44665701 | |||||
chr19:44665757
|
TGGTGCCA others(22): Show |
T | 1 | a0002c0002t0079 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3947_*3975delGGTG others(25): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3947 | chr19 | 44665757 | |||||
chr19:44665943
|
C | A | 1 | a0001c0001t0098 | 1 | NA19003.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4132C>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 4132 | chr19 | 44665943 | |||||
chr19:44665957
|
C | T | 2 | a0003c0003t0107a0003c0003t0111 | 2 | HG02615.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4146C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 4146 | chr19 | 44665957 | |||||
chr19:44665974
|
C | A | 1 | a0003c0003t0113 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4163C>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 4163 | chr19 | 44665974 | |||||
chr19:44666140
|
A | T | 1 | a0002c0002t0035 | 2 | HG01358.hp2 HG01361.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4329A>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 4329 | chr19 | 44666140 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:44644235
|
C | G | 1 | a0009c0011t0002g0234 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.79+60C>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44644235 | ||||||
chr19:44644272
|
C | T | 7 | a0001c0001t0008g0227a0001c0001t0057g0228a0001c0001t0058g0233others(4): Show | 7 | HG03130.hp1 HG03195.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.79+97C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44644272 | ||||||
chr19:44644307
|
G | T | 2 | a0001c0001t0008g0225a0001c0001t0019g0226 | 2 | HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.79+132G>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44644307 | ||||||
chr19:44644386
|
A | T | 2 | a0001c0001t0093g0224a0001c0001t0103g0223 | 2 | HG01123.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.79+211A>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44644386 | ||||||
chr19:44644419
|
T | G | 157 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(154): Show | 196 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.79+244T>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44644419 | ||||||
chr19:44644420
|
C | G | 2 | a0002c0002t0008g0156a0002c0002t0061g0157 | 2 | NA19066.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.79+245C>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44644420 | ||||||
chr19:44644468
|
G | A | 3 | a0002c0002t0008g0054a0002c0002t0008g0156a0002c0002t0061g0157 | 3 | NA19066.hp1 NA19084.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.79+293G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44644468 | ||||||
chr19:44644612
|
G | T | 6 | a0001c0001t0040g0152a0001c0001t0040g0153a0001c0001t0092g0155others(3): Show | 6 | HG01123.hp1 HG02109.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+437G>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44644612 | ||||||
chr19:44644676
|
A | G | 6 | a0001c0001t0014g0221a0001c0001t0014g0222a0001c0001t0039g0148others(3): Show | 6 | HG00738.hp1 HG01884.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+501A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44644676 | ||||||
chr19:44644692
|
G | T | 1 | a0001c0001t0054g0220 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.79+517G>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44644692 | ||||||
chr19:44644719
|
CT | C | 6 | a0001c0001t0001g0056a0001c0001t0002g0158a0001c0001t0003g0160others(3): Show | 6 | HG01074.hp1 HG02280.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+560delT | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44644719 | |||||
chr19:44644818
|
C | A | 1 | a0001c0001t0007g0058 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.79+643C>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44644818 | ||||||
chr19:44644819
|
G | A | 2 | a0001c0001t0008g0020a0001c0001t0019g0020 | 3 | HG00609.hp1 NA18995.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.79+644G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44644819 | ||||||
chr19:44644850
|
G | A | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG02074.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.79+675G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44644850 | ||||||
chr19:44644925
|
C | A | 3 | a0001c0001t0036g0043a0001c0001t0037g0043a0001c0001t0037g0161 | 3 | HG02257.hp2 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.79+750C>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44644925 | ||||||
chr19:44645003
|
TA | T | 42 | a0002c0002t0003g0042a0002c0002t0004g0002a0002c0002t0004g0007others(39): Show | 63 | HG00140.hp1 HG00642.hp1 HG01123.hp2 others(60): Show |
intron_variant | MODIFIER | c.79+833delA | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645003 | |||||
chr19:44645004
|
AAAAATAT others(34): Show |
A | 1 | a0001c0001t0065g0219 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.79+909_79+949delAA others(39): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645004 | |||||
chr19:44645057
|
T | C | 5 | a0001c0001t0007g0013a0001c0001t0007g0061a0001c0001t0007g0062others(2): Show | 7 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+882T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645057 | ||||||
chr19:44645068
|
GTAATATA | G | 43 | a0002c0002t0003g0042a0002c0002t0004g0002a0002c0002t0004g0007others(40): Show | 64 | HG00140.hp1 HG00642.hp1 HG01123.hp2 others(61): Show |
intron_variant | MODIFIER | c.79+906_79+912delTA others(5): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645068 | |||||
chr19:44645080
|
A | G | 1 | a0003c0003t0110g0128 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.79+905A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645080 | ||||||
chr19:44645083
|
TAA | T | 5 | a0001c0001t0040g0152a0001c0001t0040g0153a0001c0001t0092g0155others(2): Show | 5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+909_79+910delAA | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645083 | ||||||
chr19:44645088
|
A | T | 5 | a0001c0001t0040g0152a0001c0001t0040g0153a0001c0001t0092g0155others(2): Show | 5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+913A>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645088 | ||||||
chr19:44645098
|
T | C | 5 | a0001c0001t0007g0013a0001c0001t0007g0061a0001c0001t0007g0062others(2): Show | 7 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+923T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645098 | ||||||
chr19:44645100
|
T | TATTATAA others(6): Show |
1 | a0001c0001t0001g0127 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.79+927_79+928insTA others(11): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645100 | |||||
chr19:44645106
|
ATAG | A | 5 | a0001c0001t0040g0152a0001c0001t0040g0153a0001c0001t0092g0155others(2): Show | 5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+934_79+936delGT others(1): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645106 | |||||
chr19:44645107
|
TA | T | 43 | a0002c0002t0003g0042a0002c0002t0004g0002a0002c0002t0004g0007others(40): Show | 64 | HG00140.hp1 HG00642.hp1 HG01123.hp2 others(61): Show |
intron_variant | MODIFIER | c.79+933delA | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645107 | ||||||
chr19:44645108
|
A | T | 1 | a0001c0001t0001g0127 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.79+933A>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645108 | ||||||
chr19:44645109
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.79+934G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645109 | ||||||
chr19:44645119
|
A | T | 2 | a0001c0001t0028g0057a0001c0001t0028g0126 | 2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.79+944A>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645119 | ||||||
chr19:44645121
|
ATATTATA others(55): Show |
A | 2 | a0002c0002t0003g0042a0010c0008t0004g0042 | 2 | NA18950.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.79+960_79+1021delT others(61): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645121 | |||||
chr19:44645122
|
TA | T | 5 | a0001c0001t0040g0152a0001c0001t0040g0153a0001c0001t0092g0155others(2): Show | 5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+948delA | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645122 | ||||||
chr19:44645123
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.79+948A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645123 | ||||||
chr19:44645124
|
T | G | 5 | a0001c0001t0040g0152a0001c0001t0040g0153a0001c0001t0092g0155others(2): Show | 5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+949T>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645124 | ||||||
chr19:44645124
|
T | TAATAAAA others(71): Show |
5 | a0001c0001t0007g0013a0001c0001t0007g0061a0001c0001t0007g0062others(2): Show | 7 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+949_79+950insAA others(76): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645124 | ||||||
chr19:44645128
|
A | AATATATA others(33): Show |
8 | a0001c0001t0008g0227a0001c0001t0057g0228a0001c0001t0058g0233others(5): Show | 8 | HG01123.hp1 HG03130.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.79+959_79+960insAA others(38): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645128 | |||||
chr19:44645128
|
A | AATATATA others(30): Show |
54 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(51): Show | 59 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.79+959_79+960insAA others(35): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645128 | |||||
chr19:44645128
|
A | AATATATA others(70): Show |
20 | a0001c0001t0001g0016a0001c0001t0001g0036a0001c0001t0001g0037others(17): Show | 24 | HG00423.hp1 HG00609.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.79+959_79+960insAA others(75): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645128 | |||||
chr19:44645128
|
A | AATATATA others(68): Show |
4 | a0001c0001t0039g0148a0001c0001t0039g0150a0001c0001t0091g0151others(1): Show | 4 | HG00738.hp1 HG01884.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+959_79+960insAA others(73): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645128 | |||||
chr19:44645128
|
A | AATATATT others(30): Show |
11 | a0001c0001t0001g0018a0001c0001t0001g0039a0001c0001t0001g0119others(8): Show | 14 | HG00597.hp2 HG00673.hp2 NA18944.hp1 others(11): Show |
intron_variant | MODIFIER | c.79+971_79+972insAA others(35): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645128 | |||||
chr19:44645128
|
A | AATATATT others(33): Show |
2 | a0001c0004t0026g0172a0001c0004t0027g0173 | 2 | HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.79+1031_79+1070dup others(40): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645128 | |||||
chr19:44645128
|
A | T | 6 | a0001c0001t0001g0127a0001c0001t0007g0013a0001c0001t0007g0061others(3): Show | 8 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.79+953A>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645128 | ||||||
chr19:44645128
|
AATATATT others(33): Show |
A | 51 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0047others(48): Show | 77 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.79+1031_79+1070del others(40): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645128 | |||||
chr19:44645129
|
A | T | 5 | a0001c0001t0040g0152a0001c0001t0040g0153a0001c0001t0092g0155others(2): Show | 5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+954A>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645129 | ||||||
chr19:44645135
|
T | A | 77 | a0001c0001t0002g0021a0001c0001t0002g0044a0001c0001t0002g0158others(74): Show | 102 | HG00140.hp1 HG00642.hp1 HG00741.hp1 others(99): Show |
intron_variant | MODIFIER | c.79+960T>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645135 | ||||||
chr19:44645136
|
A | ATATATAT others(28): Show |
4 | a0001c0001t0023g0115a0001c0001t0023g0116a0001c0001t0024g0038others(1): Show | 5 | HG00741.hp1 HG01192.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+971_79+972insAA others(33): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645136 | |||||
chr19:44645136
|
A | T | 5 | a0001c0001t0040g0152a0001c0001t0040g0153a0001c0001t0092g0155others(2): Show | 5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+961A>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645136 | ||||||
chr19:44645137
|
T | TA | 57 | a0001c0001t0002g0021a0001c0001t0002g0044a0001c0001t0002g0158others(54): Show | 80 | HG00140.hp1 HG00642.hp1 HG01081.hp2 others(77): Show |
intron_variant | MODIFIER | c.79+963dupA | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645137 | |||||
chr19:44645140
|
ATAT | A | 11 | a0003c0003t0007g0014a0003c0003t0007g0065a0003c0003t0007g0066others(8): Show | 12 | HG01109.hp2 HG01891.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.79+972_79+974delTA others(1): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645140 | |||||
chr19:44645142
|
AT | A | 57 | a0001c0001t0002g0021a0001c0001t0002g0044a0001c0001t0002g0158others(54): Show | 80 | HG00140.hp1 HG00642.hp1 HG01081.hp2 others(77): Show |
intron_variant | MODIFIER | c.79+969delT | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645142 | |||||
chr19:44645162
|
G | A | 4 | a0001c0001t0048g0165a0004c0007t0029g0163a0004c0007t0056g0164others(1): Show | 4 | HG02896.hp2 HG02965.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+987G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645162 | ||||||
chr19:44645163
|
T | C | 4 | a0001c0001t0048g0165a0004c0007t0029g0163a0004c0007t0056g0164others(1): Show | 4 | HG02896.hp2 HG02965.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+988T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645163 | ||||||
chr19:44645178
|
AT | A | 4 | a0001c0001t0048g0165a0004c0007t0029g0163a0004c0007t0056g0164others(1): Show | 4 | HG02896.hp2 HG02965.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+1004delT | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645178 | ||||||
chr19:44645183
|
T | A | 4 | a0001c0001t0048g0165a0004c0007t0029g0163a0004c0007t0056g0164others(1): Show | 4 | HG02896.hp2 HG02965.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+1008T>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645183 | ||||||
chr19:44645183
|
T | TTATTATT others(30): Show |
38 | a0002c0002t0004g0002a0002c0002t0004g0007a0002c0002t0004g0019others(35): Show | 59 | HG00140.hp1 HG00642.hp1 HG01123.hp2 others(56): Show |
intron_variant | MODIFIER | c.79+1014_79+1015ins others(37): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645183 | |||||
chr19:44645183
|
T | TTATTATT others(67): Show |
1 | a0002c0002t0004g0147 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.79+1014_79+1015ins others(74): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645183 | |||||
chr19:44645186
|
T | TA | 4 | a0001c0001t0048g0165a0004c0007t0029g0163a0004c0007t0056g0164others(1): Show | 4 | HG02896.hp2 HG02965.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+1011_79+1012ins others(1): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645186 | ||||||
chr19:44645187
|
T | A | 1 | a0001c0001t0041g0072 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.79+1012T>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645187 | ||||||
chr19:44645192
|
T | A | 1 | a0001c0001t0041g0072 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.79+1017T>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645192 | ||||||
chr19:44645202
|
G | A | 4 | a0001c0001t0048g0165a0004c0007t0029g0163a0004c0007t0056g0164others(1): Show | 4 | HG02896.hp2 HG02965.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+1027G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645202 | ||||||
chr19:44645203
|
T | C | 4 | a0001c0001t0048g0165a0004c0007t0029g0163a0004c0007t0056g0164others(1): Show | 4 | HG02896.hp2 HG02965.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+1028T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645203 | ||||||
chr19:44645227
|
T | A | 151 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(148): Show | 188 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.79+1052T>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645227 | ||||||
chr19:44645227
|
T | TATAATAT others(33): Show |
5 | a0001c0001t0040g0152a0001c0001t0040g0153a0001c0001t0092g0155others(2): Show | 5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+1070_79+1071ins others(40): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645227 | |||||
chr19:44645232
|
T | A | 67 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(64): Show | 79 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.79+1057T>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645232 | ||||||
chr19:44645232
|
T | TATATAAT others(33): Show |
2 | a0001c0001t0001g0016a0001c0001t0001g0036 | 2 | NA18965.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.79+1070_79+1071ins others(40): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645232 | |||||
chr19:44645276
|
ATAT | A | 5 | a0001c0001t0040g0152a0001c0001t0040g0153a0001c0001t0092g0155others(2): Show | 5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+1102_79+1104del others(3): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645276 | ||||||
chr19:44645285
|
TTAA | T | 9 | a0001c0001t0039g0148a0001c0001t0039g0150a0001c0001t0040g0152others(6): Show | 9 | HG00738.hp1 HG01884.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.79+1114_79+1116del others(3): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645285 | |||||
chr19:44645303
|
ATATAT | A | 6 | a0001c0001t0040g0152a0001c0001t0040g0153a0001c0001t0092g0155others(3): Show | 6 | HG02109.hp2 HG02451.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+1134_79+1138del others(5): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645303 | |||||
chr19:44645404
|
A | G | 1 | a0001c0001t0002g0199 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.79+1229A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645404 | ||||||
chr19:44645408
|
G | A | 312 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(309): Show | 411 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(408): Show |
intron_variant | MODIFIER | c.79+1233G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645408 | ||||||
chr19:44645413
|
G | GTATATAT others(5): Show |
1 | a0001c0001t0046g0095 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.79+1239_79+1240ins others(12): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645413 | |||||
chr19:44645413
|
G | GTATATAT others(7): Show |
4 | a0001c0004t0027g0022a0001c0004t0050g0022a0001c0004t0051g0174others(1): Show | 4 | HG02451.hp2 HG02723.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+1239_79+1240ins others(14): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645413 | |||||
chr19:44645413
|
G | GTATATAT others(9): Show |
5 | a0001c0004t0025g0023a0001c0004t0025g0175a0001c0004t0026g0023others(2): Show | 5 | HG02572.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+1239_79+1240ins others(16): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645413 | |||||
chr19:44645413
|
GTGTATAT others(1): Show |
G | 3 | a0002c0002t0006g0008a0002c0002t0016g0008a0002c0002t0021g0008 | 6 | HG03654.hp1 NA18946.hp2 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+1240_79+1247del others(8): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645413 | |||||
chr19:44645413
|
GTGTATAT others(3): Show |
G | 39 | a0002c0002t0003g0042a0002c0002t0004g0002a0002c0002t0004g0007others(36): Show | 57 | HG00140.hp1 HG00642.hp1 HG01123.hp2 others(54): Show |
intron_variant | MODIFIER | c.79+1240_79+1249del others(10): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645413 | |||||
chr19:44645415
|
G | A | 12 | a0001c0001t0046g0095a0001c0001t0114g0111a0001c0004t0025g0023others(9): Show | 12 | HG02258.hp2 HG02451.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.79+1240G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645415 | ||||||
chr19:44645415
|
G | GTA | 11 | a0001c0001t0002g0190a0001c0001t0002g0192a0001c0001t0005g0191others(8): Show | 12 | HG00099.hp2 HG00558.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.79+1269_79+1270dup others(2): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645415 | |||||
chr19:44645415
|
G | GTATA | 8 | a0001c0001t0005g0194a0001c0001t0007g0013a0001c0001t0007g0061others(5): Show | 10 | HG02615.hp2 HG02647.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.79+1267_79+1270dup others(4): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645415 | |||||
chr19:44645415
|
G | GTATACAT others(5): Show |
2 | a0001c0001t0007g0073a0001c0001t0041g0072 | 2 | HG00423.hp1 HG00438.hp1 |
intron_variant | MODIFIER | c.79+1244_79+1245ins others(12): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645415 | |||||
chr19:44645415
|
G | GTATATA | 8 | a0001c0001t0015g0012a0001c0001t0015g0195a0001c0001t0015g0196others(5): Show | 11 | HG00280.hp1 HG01070.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.79+1265_79+1270dup others(6): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645415 | |||||
chr19:44645415
|
G | GTATATAT others(1): Show |
11 | a0001c0001t0001g0074a0001c0001t0001g0102a0001c0001t0002g0021others(8): Show | 13 | HG01081.hp2 HG01346.hp1 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.79+1263_79+1270dup others(8): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645415 | |||||
chr19:44645415
|
G | GTATATAT others(3): Show |
16 | a0001c0001t0001g0009a0001c0001t0001g0076a0001c0001t0001g0077others(13): Show | 20 | HG00140.hp2 HG00738.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.79+1261_79+1270dup others(10): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645415 | |||||
chr19:44645415
|
G | GTATATAT others(5): Show |
31 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0036others(28): Show | 37 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.79+1259_79+1270dup others(12): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645415 | |||||
chr19:44645415
|
G | GTATATAT others(7): Show |
20 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0031others(17): Show | 25 | HG00280.hp2 HG00544.hp1 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.79+1257_79+1270dup others(14): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645415 | |||||
chr19:44645415
|
G | GTATATAT others(9): Show |
8 | a0001c0001t0001g0037a0001c0001t0001g0107a0001c0001t0001g0108others(5): Show | 9 | HG00609.hp2 HG02145.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.79+1255_79+1270dup others(16): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645415 | |||||
chr19:44645415
|
G | GTATATAT others(11): Show |
3 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0124 | 3 | NA18942.hp1 NA18952.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.79+1253_79+1270dup others(18): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645415 | |||||
chr19:44645415
|
G | GTATATAT others(13): Show |
1 | a0001c0001t0010g0091 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.79+1251_79+1270dup others(20): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645415 | |||||
chr19:44645415
|
G | GTATATAT others(17): Show |
1 | a0001c0001t0001g0125 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.79+1247_79+1270dup others(24): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645415 | |||||
chr19:44645415
|
G | GTGTATA | 4 | a0001c0001t0057g0228a0001c0001t0059g0229a0001c0001t0068g0231others(1): Show | 4 | HG03225.hp1 HG03516.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+1241_79+1242ins others(6): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645415 | |||||
chr19:44645415
|
G | GTGTATAT others(1): Show |
3 | a0001c0001t0048g0165a0001c0001t0076g0232a0001c0001t0103g0223 | 3 | HG01123.hp1 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.79+1241_79+1242ins others(8): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645415 | |||||
chr19:44645415
|
G | GTGTATAT others(3): Show |
3 | a0001c0001t0001g0093a0001c0001t0010g0092a0001c0001t0058g0233 | 3 | HG03195.hp1 HG03688.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.79+1241_79+1242ins others(10): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645415 | |||||
chr19:44645415
|
G | GTGTATAT others(5): Show |
1 | a0001c0001t0010g0094 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.79+1241_79+1242ins others(12): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645415 | |||||
chr19:44645415
|
GTA | G | 77 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0006others(74): Show | 118 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.79+1269_79+1270del others(2): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645415 | |||||
chr19:44645415
|
GTATA | G | 7 | a0001c0001t0005g0177a0001c0001t0063g0176a0003c0003t0007g0033others(4): Show | 7 | HG00642.hp2 HG02258.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.79+1267_79+1270del others(4): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645415 | |||||
chr19:44645417
|
A | G | 2 | a0001c0001t0008g0225a0001c0001t0019g0226 | 2 | HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.79+1242A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645417 | ||||||
chr19:44645419
|
A | G | 2 | a0001c0001t0003g0217a0001c0001t0003g0218 | 2 | HG00099.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.79+1244A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645419 | ||||||
chr19:44645421
|
A | G | 1 | a0001c0001t0003g0218 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.79+1246A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645421 | ||||||
chr19:44645443
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0024g0038 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.79+1270_79+1271ins others(13): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645443 | |||||
chr19:44645443
|
A | ATATATAT others(8): Show |
3 | a0001c0001t0023g0115a0001c0001t0023g0116a0001c0001t0024g0114 | 3 | HG00741.hp1 HG01192.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.79+1270_79+1271ins others(15): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645443 | |||||
chr19:44645456
|
G | T | 4 | a0001c0001t0023g0115a0001c0001t0023g0116a0001c0001t0024g0038others(1): Show | 5 | HG00741.hp1 HG01192.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+1281G>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645456 | ||||||
chr19:44645458
|
G | A | 1 | a0001c0001t0003g0200 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.79+1283G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645458 | ||||||
chr19:44645477
|
T | TGAGA | 156 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(153): Show | 195 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.79+1307_79+1310dup others(4): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645477 | |||||
chr19:44645671
|
C | T | 89 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(86): Show | 104 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.79+1496C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645671 | ||||||
chr19:44645742
|
C | T | 1 | a0003c0003t0109g0100 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.80-1481C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645742 | ||||||
chr19:44645842
|
A | G | 43 | a0002c0002t0003g0042a0002c0002t0004g0002a0002c0002t0004g0007others(40): Show | 64 | HG00140.hp1 HG00642.hp1 HG01123.hp2 others(61): Show |
intron_variant | MODIFIER | c.80-1381A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645842 | ||||||
chr19:44645964
|
G | A | 156 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(153): Show | 195 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.80-1259G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645964 | ||||||
chr19:44646144
|
C | A | 1 | a0002c0002t0083g0131 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.80-1079C>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44646144 | ||||||
chr19:44646217
|
AC | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0044a0001c0001t0005g0044 | 5 | HG01081.hp2 HG01106.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-1004delC | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44646217 | |||||
chr19:44646220
|
G | A | 1 | a0001c0001t0008g0225 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.80-1003G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44646220 | ||||||
chr19:44646342
|
T | C | 310 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(307): Show | 406 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(403): Show |
intron_variant | MODIFIER | c.80-881T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44646342 | ||||||
chr19:44646377
|
G | A | 3 | a0004c0007t0029g0163a0004c0007t0056g0164a0004c0012t0029g0162 | 3 | HG02896.hp2 HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.80-846G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44646377 | ||||||
chr19:44646456
|
C | T | 1 | a0003c0003t0118g0069 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.80-767C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44646456 | ||||||
chr19:44646467
|
C | A | 2 | a0001c0001t0008g0225a0001c0001t0019g0226 | 2 | HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.80-756C>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44646467 | ||||||
chr19:44646497
|
G | T | 2 | a0001c0001t0028g0057a0001c0001t0028g0126 | 2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.80-726G>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44646497 | ||||||
chr19:44646569
|
A | C | 5 | a0001c0001t0040g0152a0001c0001t0040g0153a0001c0001t0092g0155others(2): Show | 5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.80-654A>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44646569 | ||||||
chr19:44646633
|
G | A | 3 | a0004c0007t0029g0163a0004c0007t0056g0164a0004c0012t0029g0162 | 3 | HG02896.hp2 HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.80-590G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44646633 | ||||||
chr19:44646664
|
C | T | 1 | a0001c0001t0008g0209 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.80-559C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44646664 | ||||||
chr19:44646686
|
C | G | 2 | a0001c0001t0028g0057a0001c0001t0028g0126 | 2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.80-537C>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44646686 | ||||||
chr19:44646698
|
A | G | 8 | a0001c0001t0008g0227a0001c0001t0057g0228a0001c0001t0058g0233others(5): Show | 8 | HG01123.hp1 HG03130.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.80-525A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44646698 | ||||||
chr19:44646730
|
C | G | 10 | a0001c0001t0008g0225a0001c0001t0008g0227a0001c0001t0019g0226others(7): Show | 10 | HG01123.hp1 HG02109.hp1 HG03130.hp1 others(7): Show |
intron_variant | MODIFIER | c.80-493C>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44646730 | ||||||
chr19:44646935
|
G | A | 1 | a0001c0001t0003g0201 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.80-288G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44646935 | ||||||
chr19:44647083
|
T | C | 1 | a0009c0011t0002g0234 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.80-140T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44647083 | ||||||
chr19:44647161
|
G | A | 43 | a0002c0002t0003g0042a0002c0002t0004g0002a0002c0002t0004g0007others(40): Show | 64 | HG00140.hp1 HG00642.hp1 HG01123.hp2 others(61): Show |
intron_variant | MODIFIER | c.80-62G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44647161 | ||||||
chr19:44647186
|
GC | G | 8 | a0001c0001t0008g0227a0001c0001t0057g0228a0001c0001t0058g0233others(5): Show | 8 | HG01123.hp1 HG03130.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.80-33delC | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44647186 | |||||
chr19:44647709
|
G | A | 8 | a0001c0001t0008g0227a0001c0001t0057g0228a0001c0001t0058g0233others(5): Show | 8 | HG01123.hp1 HG03130.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.427+139G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44647709 | ||||||
chr19:44647895
|
G | T | 1 | a0009c0011t0002g0234 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.427+325G>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44647895 | ||||||
chr19:44648008
|
C | A | 43 | a0002c0002t0003g0042a0002c0002t0004g0002a0002c0002t0004g0007others(40): Show | 64 | HG00140.hp1 HG00642.hp1 HG01123.hp2 others(61): Show |
intron_variant | MODIFIER | c.427+438C>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44648008 | ||||||
chr19:44648013
|
T | G | 8 | a0001c0001t0002g0024a0001c0001t0002g0184a0001c0001t0002g0190others(5): Show | 9 | HG00642.hp2 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.427+443T>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44648013 | ||||||
chr19:44648040
|
C | T | 2 | a0001c0001t0046g0095a0001c0001t0114g0111 | 2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.427+470C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44648040 | ||||||
chr19:44648041
|
G | A | 1 | a0002c0002t0006g0132 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.427+471G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44648041 | ||||||
chr19:44648225
|
T | C | 4 | a0001c0001t0001g0076a0001c0001t0001g0127a0001c0001t0010g0085others(1): Show | 4 | HG00140.hp2 HG01175.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.427+655T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44648225 | ||||||
chr19:44648244
|
C | T | 2 | a0001c0001t0046g0095a0001c0001t0114g0111 | 2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.427+674C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44648244 | ||||||
chr19:44648304
|
G | C | 1 | a0001c0001t0007g0061 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.427+734G>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44648304 | ||||||
chr19:44648484
|
A | C | 3 | a0001c0001t0068g0231a0001c0001t0069g0230a0001c0001t0076g0232 | 3 | HG03225.hp1 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.427+914A>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44648484 | ||||||
chr19:44648488
|
T | C | 1 | a0001c0001t0114g0111 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.427+918T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44648488 | ||||||
chr19:44648567
|
G | C | 1 | a0002c0002t0019g0133 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.427+997G>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44648567 | ||||||
chr19:44648593
|
G | A | 2 | a0001c0001t0001g0077a0001c0001t0001g0081 | 2 | NA18953.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.427+1023G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44648593 | ||||||
chr19:44648652
|
C | CTGTTT | 56 | a0001c0001t0007g0013a0001c0001t0007g0061a0001c0001t0007g0062others(53): Show | 80 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(77): Show |
intron_variant | MODIFIER | c.427+1104_427+1108d others(7): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 44648652 | |||||
chr19:44648652
|
C | CTGTTTTG others(3): Show |
10 | a0001c0001t0028g0057a0001c0001t0028g0126a0001c0001t0040g0152others(7): Show | 10 | HG01884.hp2 HG02109.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.427+1099_427+1108d others(12): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 44648652 | |||||
chr19:44648652
|
C | CTGTTTTG others(8): Show |
1 | a0002c0002t0085g0064 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.427+1094_427+1108d others(17): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 44648652 | |||||
chr19:44648652
|
CTGTTT | C | 8 | a0001c0001t0015g0012a0001c0001t0015g0195a0001c0001t0015g0196others(5): Show | 11 | HG00280.hp1 HG01070.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.427+1104_427+1108d others(7): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 44648652 | |||||
chr19:44648674
|
G | C | 10 | a0001c0001t0003g0202a0001c0001t0015g0012a0001c0001t0015g0195others(7): Show | 13 | HG00280.hp1 HG01070.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.427+1104G>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44648674 | ||||||
chr19:44648679
|
C | G | 160 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(157): Show | 198 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.427+1109C>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44648679 | ||||||
chr19:44648684
|
C | G | 152 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(149): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.427+1114C>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44648684 | ||||||
chr19:44648990
|
T | C | 10 | a0001c0001t0002g0021a0001c0001t0002g0044a0001c0001t0002g0158others(7): Show | 12 | HG01081.hp2 HG01106.hp1 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.428-819T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44648990 | ||||||
chr19:44649122
|
T | C | 177 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(174): Show | 218 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.428-687T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44649122 | ||||||
chr19:44649140
|
G | A | 2 | a0001c0001t0028g0057a0001c0001t0028g0126 | 2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.428-669G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44649140 | ||||||
chr19:44649247
|
A | G | 5 | a0001c0001t0040g0152a0001c0001t0040g0153a0001c0001t0092g0155others(2): Show | 5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.428-562A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44649247 | ||||||
chr19:44649316
|
G | T | 11 | a0003c0003t0007g0014a0003c0003t0007g0065a0003c0003t0007g0066others(8): Show | 12 | HG01109.hp2 HG01891.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.428-493G>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44649316 | ||||||
chr19:44649418
|
A | G | 9 | a0002c0002t0004g0007a0002c0002t0004g0040a0002c0002t0004g0140others(6): Show | 13 | HG02155.hp1 NA18612.hp1 NA18747.hp2 others(10): Show |
intron_variant | MODIFIER | c.428-391A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44649418 | ||||||
chr19:44649427
|
C | CT | 148 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(145): Show | 186 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.428-362dupT | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 44649427 | |||||
chr19:44649427
|
C | CTT | 6 | a0001c0001t0001g0031a0001c0001t0010g0085a0001c0001t0041g0075others(3): Show | 7 | HG01175.hp2 HG02055.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.428-363_428-362dup others(2): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 44649427 | |||||
chr19:44649451
|
A | G | 50 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0047others(47): Show | 76 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.428-358A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44649451 | ||||||
chr19:44649468
|
C | T | 2 | a0001c0001t0046g0095a0001c0001t0114g0111 | 2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.428-341C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44649468 | ||||||
chr19:44649486
|
G | A | 2 | a0001c0001t0014g0029a0001c0001t0031g0029 | 3 | NA19068.hp2 NA19077.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.428-323G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44649486 | ||||||
chr19:44649651
|
C | G | 10 | a0001c0001t0002g0021a0001c0001t0002g0044a0001c0001t0002g0158others(7): Show | 12 | HG01081.hp2 HG01106.hp1 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.428-158C>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44649651 | ||||||
chr19:44649701
|
G | A | 1 | a0001c0001t0009g0203 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.428-108G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44649701 | ||||||
chr19:44649712
|
C | T | 2 | a0001c0004t0026g0172a0001c0004t0027g0173 | 2 | HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.428-97C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44649712 | ||||||
chr19:44650157
|
C | T | 2 | a0001c0001t0105g0099a0001c0001t0106g0098 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.724+52C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44650157 | ||||||
chr19:44650190
|
G | A | 1 | a0001c0001t0002g0186 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.724+85G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44650190 | ||||||
chr19:44650274
|
C | T | 2 | a0001c0001t0028g0057a0001c0001t0028g0126 | 2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.724+169C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44650274 | ||||||
chr19:44650283
|
C | A | 1 | a0002c0002t0016g0130 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.724+178C>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44650283 | ||||||
chr19:44650353
|
G | C | 2 | a0001c0001t0024g0038a0001c0001t0024g0114 | 3 | HG01192.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.724+248G>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44650353 | ||||||
chr19:44650530
|
A | T | 9 | a0001c0001t0039g0148a0001c0001t0039g0150a0001c0001t0040g0152others(6): Show | 9 | HG00738.hp1 HG01884.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.724+425A>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44650530 | ||||||
chr19:44650561
|
C | CT | 22 | a0001c0001t0008g0169a0001c0001t0039g0150a0001c0001t0040g0152others(19): Show | 22 | HG00735.hp1 HG00738.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.724+475dupT | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr19 | 44650561 | |||||
chr19:44650561
|
CT | C | 21 | a0001c0001t0001g0086a0001c0001t0002g0184a0001c0001t0002g0211others(18): Show | 23 | HG01069.hp2 HG01070.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.724+475delT | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr19 | 44650561 | |||||
chr19:44650632
|
G | A | 12 | a0001c0001t0002g0017a0001c0001t0005g0017a0001c0001t0005g0191others(9): Show | 17 | HG00438.hp2 HG00609.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.724+527G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44650632 | ||||||
chr19:44650860
|
C | T | 2 | a0001c0001t0028g0057a0001c0001t0028g0126 | 2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.724+755C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44650860 | ||||||
chr19:44650894
|
A | G | 1 | a0001c0001t0001g0088 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.724+789A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44650894 | ||||||
chr19:44651013
|
G | T | 2 | a0001c0001t0028g0057a0001c0001t0028g0126 | 2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.724+908G>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44651013 | ||||||
chr19:44651068
|
G | A | 152 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(149): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.724+963G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44651068 | ||||||
chr19:44651276
|
G | A | 1 | a0001c0001t0005g0177 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.724+1171G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44651276 | ||||||
chr19:44651342
|
A | G | 4 | a0001c0001t0023g0115a0001c0001t0023g0116a0001c0001t0024g0038others(1): Show | 5 | HG00741.hp1 HG01192.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.724+1237A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44651342 | ||||||
chr19:44651466
|
G | A | 2 | a0001c0001t0008g0225a0001c0001t0019g0226 | 2 | HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.724+1361G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44651466 | ||||||
chr19:44651843
|
C | T | 11 | a0003c0003t0007g0014a0003c0003t0007g0065a0003c0003t0007g0066others(8): Show | 12 | HG01109.hp2 HG01891.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.724+1738C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44651843 | ||||||
chr19:44651853
|
A | T | 43 | a0002c0002t0003g0042a0002c0002t0004g0002a0002c0002t0004g0007others(40): Show | 64 | HG00140.hp1 HG00642.hp1 HG01123.hp2 others(61): Show |
intron_variant | MODIFIER | c.724+1748A>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44651853 | ||||||
chr19:44652119
|
G | T | 3 | a0001c0001t0002g0021a0001c0001t0002g0044a0001c0001t0005g0044 | 5 | HG01081.hp2 HG01106.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.725-1781G>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44652119 | ||||||
chr19:44652365
|
A | ATTTTTG | 10 | a0001c0004t0025g0023a0001c0004t0025g0175a0001c0004t0026g0023others(7): Show | 10 | HG02451.hp2 HG02572.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.725-1511_725-1506d others(8): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr19 | 44652365 | |||||
chr19:44652443
|
G | T | 10 | a0001c0004t0025g0023a0001c0004t0025g0175a0001c0004t0026g0023others(7): Show | 10 | HG02451.hp2 HG02572.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.725-1457G>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44652443 | ||||||
chr19:44652506
|
C | T | 3 | a0004c0007t0029g0163a0004c0007t0056g0164a0004c0012t0029g0162 | 3 | HG02896.hp2 HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.725-1394C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44652506 | ||||||
chr19:44652765
|
T | C | 1 | a0009c0011t0002g0234 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.725-1135T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44652765 | ||||||
chr19:44652771
|
T | C | 1 | a0009c0011t0002g0234 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.725-1129T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44652771 | ||||||
chr19:44652889
|
T | C | 1 | a0001c0001t0040g0153 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.725-1011T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44652889 | ||||||
chr19:44652891
|
A | T | 2 | a0002c0002t0006g0041a0002c0002t0016g0041 | 2 | HG03831.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.725-1009A>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44652891 | ||||||
chr19:44653041
|
C | T | 1 | a0001c0001t0005g0194 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.725-859C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44653041 | ||||||
chr19:44653107
|
C | T | 8 | a0001c0001t0008g0227a0001c0001t0057g0228a0001c0001t0058g0233others(5): Show | 8 | HG01123.hp1 HG03130.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.725-793C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44653107 | ||||||
chr19:44653108
|
G | A | 2 | a0001c0001t0120g0149a0002c0002t0085g0064 | 2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.725-792G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44653108 | ||||||
chr19:44653155
|
A | C | 1 | a0009c0011t0002g0234 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.725-745A>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44653155 | ||||||
chr19:44653156
|
C | A | 1 | a0009c0011t0002g0234 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.725-744C>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44653156 | ||||||
chr19:44653179
|
C | T | 1 | a0001c0001t0120g0149 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.725-721C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44653179 | ||||||
chr19:44653336
|
C | T | 2 | a0001c0001t0028g0057a0001c0001t0028g0126 | 2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.725-564C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44653336 | ||||||
chr19:44653569
|
C | T | 10 | a0001c0001t0002g0021a0001c0001t0002g0044a0001c0001t0002g0158others(7): Show | 12 | HG01081.hp2 HG01106.hp1 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.725-331C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44653569 | ||||||
chr19:44653769
|
T | G | 2 | a0001c0001t0020g0028a0001c0001t0033g0028 | 3 | HG01074.hp2 HG01243.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.725-131T>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44653769 | ||||||
chr19:44653790
|
G | T | 31 | a0001c0001t0039g0148a0001c0001t0039g0150a0001c0001t0040g0152others(28): Show | 32 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.725-110G>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44653790 | ||||||
chr19:44653809
|
C | T | 1 | a0001c0001t0019g0226 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.725-91C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44653809 | ||||||
chr19:44653859
|
A | C | 1 | a0001c0001t0001g0122 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.725-41A>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44653859 | ||||||
chr19:44654074
|
G | A | 1 | a0009c0011t0002g0234 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.842+57G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654074 | ||||||
chr19:44654075
|
A | G | 1 | a0009c0011t0002g0234 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.842+58A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654075 | ||||||
chr19:44654170
|
C | A | 3 | a0001c0001t0001g0093a0001c0001t0010g0092a0001c0001t0010g0094 | 3 | HG03688.hp1 HG03710.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.842+153C>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654170 | ||||||
chr19:44654187
|
A | C | 5 | a0001c0001t0040g0152a0001c0001t0040g0153a0001c0001t0092g0155others(2): Show | 5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.842+170A>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654187 | ||||||
chr19:44654191
|
G | A | 5 | a0001c0001t0040g0152a0001c0001t0040g0153a0001c0001t0092g0155others(2): Show | 5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.842+174G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654191 | ||||||
chr19:44654199
|
G | A | 5 | a0001c0001t0040g0152a0001c0001t0040g0153a0001c0001t0092g0155others(2): Show | 5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.842+182G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654199 | ||||||
chr19:44654201
|
T | C | 5 | a0001c0001t0040g0152a0001c0001t0040g0153a0001c0001t0092g0155others(2): Show | 5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.842+184T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654201 | ||||||
chr19:44654203
|
T | C | 5 | a0001c0001t0040g0152a0001c0001t0040g0153a0001c0001t0092g0155others(2): Show | 5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.842+186T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654203 | ||||||
chr19:44654208
|
C | T | 5 | a0001c0001t0040g0152a0001c0001t0040g0153a0001c0001t0092g0155others(2): Show | 5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.842+191C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654208 | ||||||
chr19:44654215
|
A | T | 5 | a0001c0001t0040g0152a0001c0001t0040g0153a0001c0001t0092g0155others(2): Show | 5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.842+198A>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654215 | ||||||
chr19:44654221
|
A | G | 190 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(187): Show | 231 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.842+204A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654221 | ||||||
chr19:44654224
|
G | A | 5 | a0001c0001t0040g0152a0001c0001t0040g0153a0001c0001t0092g0155others(2): Show | 5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.842+207G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654224 | ||||||
chr19:44654232
|
T | TGG | 5 | a0001c0001t0040g0152a0001c0001t0040g0153a0001c0001t0092g0155others(2): Show | 5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.842+217_842+218dup others(2): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr19 | 44654232 | |||||
chr19:44654236
|
C | T | 5 | a0001c0001t0040g0152a0001c0001t0040g0153a0001c0001t0092g0155others(2): Show | 5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.842+219C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654236 | ||||||
chr19:44654236
|
CCTGGACC others(31): Show |
C | 80 | a0001c0001t0007g0013a0001c0001t0007g0061a0001c0001t0007g0062others(77): Show | 104 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(101): Show |
intron_variant | MODIFIER | c.842+246_842+283del others(38): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr19 | 44654236 | |||||
chr19:44654250
|
T | A | 5 | a0001c0001t0040g0152a0001c0001t0040g0153a0001c0001t0092g0155others(2): Show | 5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.842+233T>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654250 | ||||||
chr19:44654274
|
T | C | 5 | a0001c0001t0040g0152a0001c0001t0040g0153a0001c0001t0092g0155others(2): Show | 5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.842+257T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654274 | ||||||
chr19:44654282
|
C | G | 5 | a0001c0001t0040g0152a0001c0001t0040g0153a0001c0001t0092g0155others(2): Show | 5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.842+265C>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654282 | ||||||
chr19:44654300
|
G | T | 2 | a0001c0001t0046g0095a0001c0001t0114g0111 | 2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.842+283G>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654300 | ||||||
chr19:44654324
|
G | A | 8 | a0001c0001t0002g0024a0001c0001t0002g0184a0001c0001t0002g0190others(5): Show | 9 | HG00642.hp2 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.842+307G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654324 | ||||||
chr19:44654544
|
G | A | 2 | a0001c0001t0105g0099a0001c0001t0106g0098 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.842+527G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654544 | ||||||
chr19:44654571
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.842+554C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654571 | ||||||
chr19:44654642
|
G | A | 8 | a0001c0001t0002g0047a0001c0001t0002g0211a0001c0001t0014g0029others(5): Show | 9 | HG00423.hp2 HG02080.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.842+625G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654642 | ||||||
chr19:44654737
|
T | C | 1 | a0001c0001t0001g0119 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.842+720T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654737 | ||||||
chr19:44654770
|
T | C | 85 | a0001c0001t0007g0013a0001c0001t0007g0061a0001c0001t0007g0062others(82): Show | 109 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(106): Show |
intron_variant | MODIFIER | c.842+753T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654770 | ||||||
chr19:44654880
|
C | G | 9 | a0001c0001t0039g0148a0001c0001t0039g0150a0001c0001t0040g0152others(6): Show | 9 | HG00738.hp1 HG01884.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.842+863C>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654880 | ||||||
chr19:44655035
|
GATAATAC others(8): Show |
G | 2 | a0001c0001t0028g0057a0001c0001t0028g0126 | 2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.842+1035_842+1049d others(17): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr19 | 44655035 | |||||
chr19:44655098
|
T | A | 1 | a0001c0001t0002g0180 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.842+1081T>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44655098 | ||||||
chr19:44655144
|
C | T | 85 | a0001c0001t0007g0013a0001c0001t0007g0061a0001c0001t0007g0062others(82): Show | 109 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(106): Show |
intron_variant | MODIFIER | c.842+1127C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44655144 | ||||||
chr19:44655170
|
A | T | 2 | a0001c0001t0046g0095a0001c0001t0114g0111 | 2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.842+1153A>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44655170 | ||||||
chr19:44655186
|
G | C | 2 | a0001c0001t0001g0082a0001c0001t0010g0083 | 2 | HG02040.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.842+1169G>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44655186 | ||||||
chr19:44655228
|
G | C | 2 | a0003c0003t0007g0065a0003c0003t0007g0066 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.842+1211G>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44655228 | ||||||
chr19:44655380
|
C | T | 9 | a0001c0001t0039g0148a0001c0001t0039g0150a0001c0001t0040g0152others(6): Show | 9 | HG00738.hp1 HG01884.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.842+1363C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44655380 | ||||||
chr19:44655382
|
C | T | 2 | a0001c0001t0046g0095a0001c0001t0114g0111 | 2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.842+1365C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44655382 | ||||||
chr19:44655384
|
C | A | 1 | a0009c0011t0002g0234 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.842+1367C>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44655384 | ||||||
chr19:44655385
|
A | G | 1 | a0009c0011t0002g0234 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.842+1368A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44655385 | ||||||
chr19:44655386
|
G | A | 1 | a0009c0011t0002g0234 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.842+1369G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44655386 | ||||||
chr19:44655449
|
T | C | 1 | a0001c0001t0001g0107 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.842+1432T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44655449 | ||||||
chr19:44655484
|
GT | G | 198 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(195): Show | 242 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.842+1469delT | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr19 | 44655484 | |||||
chr19:44655608
|
G | A | 5 | a0001c0001t0007g0013a0001c0001t0007g0061a0001c0001t0007g0062others(2): Show | 7 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.842+1591G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44655608 | ||||||
chr19:44655668
|
C | A | 2 | a0001c0001t0038g0035a0001c0001t0090g0103 | 3 | HG01099.hp1 HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.842+1651C>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44655668 | ||||||
chr19:44655715
|
T | A | 1 | a0009c0011t0002g0234 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.842+1698T>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44655715 | ||||||
chr19:44655745
|
G | T | 1 | a0001c0001t0003g0213 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.842+1728G>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44655745 | ||||||
chr19:44655756
|
T | C | 85 | a0001c0001t0007g0013a0001c0001t0007g0061a0001c0001t0007g0062others(82): Show | 109 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(106): Show |
intron_variant | MODIFIER | c.842+1739T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44655756 | ||||||
chr19:44655787
|
GT | G | 3 | a0001c0001t0057g0228a0001c0001t0058g0233a0001c0001t0059g0229 | 3 | HG03195.hp1 HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.842+1773delT | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr19 | 44655787 | |||||
chr19:44655863
|
C | CT | 124 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(121): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.842+1870dupT | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr19 | 44655863 | |||||
chr19:44655863
|
C | CTT | 28 | a0001c0001t0001g0037a0001c0001t0001g0060a0001c0001t0001g0093others(25): Show | 29 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.842+1869_842+1870d others(4): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr19 | 44655863 | |||||
chr19:44655863
|
CT | C | 38 | a0001c0001t0007g0013a0001c0001t0007g0061a0001c0001t0007g0062others(35): Show | 41 | HG01109.hp2 HG01257.hp2 HG01884.hp1 others(38): Show |
intron_variant | MODIFIER | c.842+1870delT | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr19 | 44655863 | |||||
chr19:44655890
|
G | C | 2 | a0001c0001t0046g0095a0001c0001t0114g0111 | 2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.843-1872G>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44655890 | ||||||
chr19:44656338
|
G | A | 6 | a0001c0001t0011g0025a0001c0001t0011g0026a0001c0001t0011g0178others(3): Show | 9 | HG00438.hp2 HG02165.hp2 NA18949.hp2 others(6): Show |
intron_variant | MODIFIER | c.843-1424G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44656338 | ||||||
chr19:44656368
|
C | A | 85 | a0001c0001t0007g0013a0001c0001t0007g0061a0001c0001t0007g0062others(82): Show | 109 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(106): Show |
intron_variant | MODIFIER | c.843-1394C>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44656368 | ||||||
chr19:44656394
|
G | A | 4 | a0001c0001t0039g0148a0001c0001t0039g0150a0001c0001t0091g0151others(1): Show | 4 | HG00738.hp1 HG01884.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.843-1368G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44656394 | ||||||
chr19:44656463
|
C | A | 1 | a0001c0001t0008g0209 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.843-1299C>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44656463 | ||||||
chr19:44656522
|
C | T | 1 | a0001c0001t0002g0207 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.843-1240C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44656522 | ||||||
chr19:44656545
|
T | C | 1 | a0001c0001t0103g0223 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.843-1217T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44656545 | ||||||
chr19:44656577
|
A | G | 2 | a0001c0001t0046g0095a0001c0001t0114g0111 | 2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.843-1185A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44656577 | ||||||
chr19:44656668
|
C | T | 80 | a0001c0001t0028g0057a0001c0001t0028g0126a0001c0001t0039g0148others(77): Show | 102 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(99): Show |
intron_variant | MODIFIER | c.843-1094C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44656668 | ||||||
chr19:44656750
|
A | G | 6 | a0003c0003t0007g0014a0003c0003t0007g0065a0003c0003t0007g0066others(3): Show | 7 | HG01109.hp2 HG02809.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.843-1012A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44656750 | ||||||
chr19:44656993
|
AATT | A | 85 | a0001c0001t0007g0013a0001c0001t0007g0061a0001c0001t0007g0062others(82): Show | 109 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(106): Show |
intron_variant | MODIFIER | c.843-767_843-765del others(3): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr19 | 44656993 | |||||
chr19:44657123
|
G | A | 9 | a0001c0001t0039g0148a0001c0001t0039g0150a0001c0001t0040g0152others(6): Show | 9 | HG00738.hp1 HG01884.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.843-639G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44657123 | ||||||
chr19:44657196
|
C | G | 1 | a0001c0001t0002g0182 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.843-566C>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44657196 | ||||||
chr19:44657255
|
G | A | 77 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(74): Show | 91 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.843-507G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44657255 | ||||||
chr19:44657507
|
C | T | 2 | a0001c0001t0105g0099a0001c0001t0106g0098 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.843-255C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44657507 | ||||||
chr19:44657524
|
A | G | 1 | a0002c0002t0016g0144 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.843-238A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44657524 | ||||||
chr19:44657614
|
A | G | 2 | a0003c0003t0045g0096a0003c0003t0046g0097 | 2 | HG03209.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.843-148A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44657614 | ||||||
chr19:44657628
|
T | C | 180 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(177): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.843-134T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44657628 | ||||||
chr19:44657696
|
G | A | 1 | a0001c0001t0023g0115 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.843-66G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44657696 | ||||||
chr19:44657717
|
G | A | 5 | a0001c0001t0007g0013a0001c0001t0007g0061a0001c0001t0007g0062others(2): Show | 7 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.843-45G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44657717 | ||||||
chr19:44657977
|
A | C | 2 | a0001c0001t0001g0105a0001c0001t0001g0109 | 2 | NA18942.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.991+67A>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 5/7 | chr19 | 44657977 | ||||||
chr19:44658099
|
A | G | 1 | a0001c0001t0017g0205 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.991+189A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 5/7 | chr19 | 44658099 | ||||||
chr19:44658198
|
T | C | 1 | a0002c0002t0004g0145 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.991+288T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 5/7 | chr19 | 44658198 | ||||||
chr19:44658199
|
T | G | 1 | a0001c0001t0080g0206 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.991+289T>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 5/7 | chr19 | 44658199 | ||||||
chr19:44658233
|
C | A | 1 | a0001c0001t0001g0120 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.991+323C>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 5/7 | chr19 | 44658233 | ||||||
chr19:44658298
|
T | A | 190 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(187): Show | 231 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.991+388T>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 5/7 | chr19 | 44658298 | ||||||
chr19:44658490
|
A | C | 9 | a0001c0001t0039g0148a0001c0001t0039g0150a0001c0001t0040g0152others(6): Show | 9 | HG00738.hp1 HG01884.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.992-252A>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 5/7 | chr19 | 44658490 | ||||||
chr19:44658627
|
A | G | 4 | a0001c0001t0023g0115a0001c0001t0023g0116a0001c0001t0024g0038others(1): Show | 5 | HG00741.hp1 HG01192.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.992-115A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 5/7 | chr19 | 44658627 | ||||||
chr19:44658697
|
C | T | 5 | a0001c0001t0040g0152a0001c0001t0040g0153a0001c0001t0092g0155others(2): Show | 5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.992-45C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 5/7 | chr19 | 44658697 | ||||||
chr19:44658921
|
C | A | 67 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(64): Show | 81 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.1150+21C>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44658921 | ||||||
chr19:44659067
|
A | C | 7 | a0001c0001t0007g0013a0001c0001t0007g0061a0001c0001t0007g0062others(4): Show | 9 | HG02615.hp2 HG02622.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1150+167A>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44659067 | ||||||
chr19:44659101
|
C | T | 5 | a0001c0001t0007g0013a0001c0001t0007g0061a0001c0001t0007g0062others(2): Show | 7 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1150+201C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44659101 | ||||||
chr19:44659175
|
T | C | 1 | a0009c0011t0002g0234 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1150+275T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44659175 | ||||||
chr19:44659326
|
G | A | 1 | a0001c0001t0114g0111 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1150+426G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44659326 | ||||||
chr19:44659396
|
G | A | 2 | a0001c0001t0039g0150a0001c0001t0091g0151 | 2 | HG00738.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1150+496G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44659396 | ||||||
chr19:44659399
|
C | T | 37 | a0001c0001t0028g0057a0001c0001t0028g0126a0001c0001t0039g0148others(34): Show | 38 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.1150+499C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44659399 | ||||||
chr19:44659679
|
G | A | 9 | a0001c0001t0039g0148a0001c0001t0039g0150a0001c0001t0040g0152others(6): Show | 9 | HG00738.hp1 HG01884.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1150+779G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44659679 | ||||||
chr19:44659687
|
G | A | 73 | a0001c0001t0007g0013a0001c0001t0007g0061a0001c0001t0007g0062others(70): Show | 97 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(94): Show |
intron_variant | MODIFIER | c.1150+787G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44659687 | ||||||
chr19:44660006
|
G | T | 11 | a0003c0003t0007g0014a0003c0003t0007g0065a0003c0003t0007g0066others(8): Show | 12 | HG01109.hp2 HG01891.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1150+1106G>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44660006 | ||||||
chr19:44660170
|
G | A | 9 | a0001c0001t0039g0148a0001c0001t0039g0150a0001c0001t0040g0152others(6): Show | 9 | HG00738.hp1 HG01884.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1151-1122G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44660170 | ||||||
chr19:44660183
|
C | T | 1 | a0002c0002t0008g0143 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1151-1109C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44660183 | ||||||
chr19:44660184
|
G | A | 23 | a0001c0001t0048g0165a0003c0003t0007g0014a0003c0003t0007g0033others(20): Show | 24 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.1151-1108G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44660184 | ||||||
chr19:44660199
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1151-1093G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44660199 | ||||||
chr19:44660249
|
C | G | 2 | a0001c0001t0002g0184a0001c0001t0005g0185 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1151-1043C>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44660249 | ||||||
chr19:44660404
|
T | C | 86 | a0001c0001t0004g0049a0001c0001t0006g0208a0001c0001t0007g0013others(83): Show | 111 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(108): Show |
intron_variant | MODIFIER | c.1151-888T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44660404 | ||||||
chr19:44660451
|
T | C | 5 | a0001c0001t0013g0027a0001c0001t0013g0159a0001c0001t0013g0179others(2): Show | 6 | HG01070.hp2 HG01071.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.1151-841T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44660451 | ||||||
chr19:44660581
|
G | A | 2 | a0001c0001t0046g0095a0001c0001t0114g0111 | 2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1151-711G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44660581 | ||||||
chr19:44660642
|
C | T | 2 | a0001c0001t0008g0225a0001c0001t0019g0226 | 2 | HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1151-650C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44660642 | ||||||
chr19:44660673
|
C | T | 1 | a0002c0002t0016g0130 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1151-619C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44660673 | ||||||
chr19:44660721
|
G | A | 1 | a0001c0001t0003g0181 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1151-571G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44660721 | ||||||
chr19:44660725
|
T | C | 2 | a0001c0001t0002g0192a0001c0001t0005g0194 | 2 | HG00558.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1151-567T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44660725 | ||||||
chr19:44660766
|
C | T | 1 | a0002c0002t0006g0141 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1151-526C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44660766 | ||||||
chr19:44660831
|
G | A | 5 | a0001c0001t0008g0227a0001c0001t0057g0228a0001c0001t0058g0233others(2): Show | 5 | HG01123.hp1 HG03130.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1151-461G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44660831 | ||||||
chr19:44660874
|
A | C | 1 | a0002c0002t0008g0054 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1151-418A>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44660874 | ||||||
chr19:44661029
|
T | C | 1 | a0002c0002t0083g0131 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1151-263T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44661029 | ||||||
chr19:44661091
|
A | C | 8 | a0001c0001t0008g0227a0001c0001t0057g0228a0001c0001t0058g0233others(5): Show | 8 | HG01123.hp1 HG03130.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.1151-201A>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44661091 | ||||||
chr19:44661096
|
C | T | 1 | a0001c0001t0010g0055 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1151-196C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44661096 | ||||||
chr19:44661349
|
G | A | 10 | a0003c0003t0007g0033a0003c0003t0045g0034a0003c0003t0045g0096others(7): Show | 10 | HG02145.hp1 HG02258.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1182+26G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 7/7 | chr19 | 44661349 | ||||||
chr19:44661394
|
C | T | 22 | a0003c0003t0007g0014a0003c0003t0007g0033a0003c0003t0007g0065others(19): Show | 23 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.1182+71C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 7/7 | chr19 | 44661394 | ||||||
chr19:44661465
|
T | G | 85 | a0001c0001t0004g0049a0001c0001t0006g0208a0001c0001t0007g0013others(82): Show | 110 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(107): Show |
intron_variant | MODIFIER | c.1182+142T>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 7/7 | chr19 | 44661465 | ||||||
chr19:44661496
|
C | T | 2 | a0001c0001t0046g0095a0001c0001t0114g0111 | 2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1182+173C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 7/7 | chr19 | 44661496 | ||||||
chr19:44661497
|
G | A | 1 | a0003c0003t0117g0071 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1182+174G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 7/7 | chr19 | 44661497 | ||||||
chr19:44661564
|
C | A | 1 | a0001c0001t0001g0079 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1183-176C>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 7/7 | chr19 | 44661564 |