geneid | 169714 |
---|---|
ensemblid | ENSG00000165661.18 |
hgncid | 30249 |
symbol | QSOX2 |
name | quiescin sulfhydryl oxidase 2 |
refseq_nuc | NM_181701.4 |
refseq_prot | NP_859052.3 |
ensembl_nuc | ENST00000358701.10 |
ensembl_prot | ENSP00000351536.5 |
mane_status | MANE Select |
chr | chr9 |
start | 136206333 |
end | 136245812 |
strand | - |
ver | v1.2 |
region | chr9:136206333-136245812 |
region5000 | chr9:136201333-136250812 |
regionname0 | QSOX2_chr9_136206333_136245812 |
regionname5000 | QSOX2_chr9_136201333_136250812 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 698 | 326 | 89 | 64 | 122 | 11 | 38 | 86 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0002 | 0/0 | 698 | 58 | 2 | 3 | 44 | 3 | 6 | 34 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0003 | 0/0 | 698 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0004 | 0/0 | 698 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0005 | 0/0 | 698 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0006 | 0/0 | 698 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0007 | 0/0 | 698 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0008 | 0/0 | 698 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 2097 | 124 | 54 | 26 | 28 | 1 | 14 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
c0002 | 0/1 | 2097 | 120 | 17 | 21 | 60 | 4 | 17 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
c0003 | 0/0 | 2097 | 57 | 2 | 3 | 43 | 3 | 6 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
c0004 | 0/0 | 2097 | 43 | 0 | 14 | 17 | 6 | 6 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
c0005 | 0/0 | 2097 | 12 | 9 | 2 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
c0006 | 0/0 | 2097 | 10 | 0 | 0 | 10 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
c0007 | 0/0 | 2097 | 4 | 0 | 1 | 2 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
c0008 | 0/0 | 2097 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
c0009 | 0/0 | 2097 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
c0010 | 0/0 | 2097 | 2 | 0 | 0 | 0 | 2 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
c0011 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
c0012 | 0/0 | 2097 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
c0013 | 0/0 | 2097 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
c0014 | 0/0 | 2097 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
c0015 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
c0016 | 0/0 | 2097 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
c0017 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
c0018 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
c0019 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
c0020 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
c0021 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
c0022 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
c0023 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
c0024 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
c0025 | 0/0 | 2097 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
c0026 | 0/0 | 2097 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 2430 | 62 | 9 | 15 | 26 | 1 | 11 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0002 | 0/0 | 2436 | 46 | 1 | 4 | 33 | 3 | 5 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0003 | 0/0 | 2429 | 29 | 1 | 9 | 11 | 3 | 5 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0004 | 0/0 | 2429 | 25 | 1 | 11 | 11 | 0 | 2 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0005 | 0/0 | 2431 | 18 | 1 | 0 | 15 | 1 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0006 | 0/0 | 2431 | 15 | 0 | 1 | 8 | 1 | 5 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0007 | 0/0 | 2431 | 12 | 11 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0008 | 0/0 | 2435 | 9 | 5 | 2 | 0 | 0 | 2 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0009 | 0/0 | 2430 | 9 | 0 | 0 | 9 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0010 | 0/0 | 2437 | 7 | 5 | 2 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0011 | 0/0 | 2431 | 6 | 0 | 0 | 1 | 3 | 2 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0012 | 0/0 | 2428 | 6 | 1 | 4 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0013 | 0/0 | 2438 | 6 | 6 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0014 | 0/0 | 2430 | 6 | 5 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0015 | 0/0 | 2433 | 5 | 0 | 0 | 5 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0016 | 0/0 | 2437 | 5 | 5 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0017 | 0/0 | 2427 | 4 | 0 | 0 | 4 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0018 | 0/0 | 2437 | 4 | 4 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0019 | 0/0 | 2427 | 4 | 0 | 0 | 3 | 1 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0020 | 0/0 | 2438 | 4 | 0 | 0 | 3 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0021 | 0/0 | 2442 | 4 | 0 | 0 | 4 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0022 | 0/0 | 2441 | 3 | 3 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0023 | 0/0 | 2434 | 3 | 2 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0024 | 0/0 | 2436 | 3 | 3 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0025 | 0/0 | 2428 | 3 | 0 | 0 | 1 | 0 | 2 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0026 | 0/0 | 2435 | 3 | 0 | 3 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0027 | 0/0 | 2430 | 2 | 0 | 1 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0028 | 0/0 | 2439 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0029 | 0/0 | 2435 | 2 | 1 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0030 | 0/0 | 2439 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0031 | 0/0 | 2430 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0032 | 0/0 | 2432 | 2 | 0 | 0 | 0 | 2 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0033 | 0/0 | 2436 | 2 | 1 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0034 | 0/0 | 2438 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0035 | 0/0 | 2427 | 2 | 0 | 2 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0036 | 0/0 | 2430 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0037 | 0/0 | 2430 | 2 | 0 | 2 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0038 | 0/0 | 2431 | 2 | 0 | 1 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0039 | 0/0 | 2432 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0040 | 0/0 | 2440 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0041 | 0/0 | 2437 | 2 | 0 | 0 | 1 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0042 | 0/0 | 2417 | 2 | 0 | 0 | 1 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0043 | 0/0 | 2429 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0044 | 0/0 | 2429 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0045 | 0/0 | 2429 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0046 | 0/0 | 2437 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0047 | 0/0 | 2437 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0048 | 0/0 | 2439 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0049 | 0/0 | 2432 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0050 | 0/0 | 2427 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0051 | 0/0 | 2427 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0052 | 1/0 | 2405 | 1 | 0 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0053 | 0/0 | 2437 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0054 | 0/0 | 2433 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0055 | 0/0 | 2437 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0056 | 0/0 | 2441 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0057 | 0/0 | 2427 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0058 | 0/0 | 2429 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0059 | 0/0 | 2429 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0060 | 0/0 | 2438 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0061 | 0/0 | 2432 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0062 | 0/0 | 2434 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0063 | 0/0 | 2440 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0064 | 0/0 | 2429 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0065 | 0/0 | 2427 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0066 | 0/0 | 2433 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0067 | 0/0 | 2435 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0068 | 0/0 | 2439 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0069 | 0/0 | 2441 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0070 | 0/0 | 2429 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0071 | 0/0 | 2430 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0072 | 0/0 | 2424 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0073 | 0/0 | 2430 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0074 | 0/0 | 2430 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0075 | 0/0 | 2429 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0076 | 0/0 | 2430 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0077 | 0/0 | 2430 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0078 | 0/0 | 2432 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0079 | 0/0 | 2432 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0080 | 0/0 | 2436 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0081 | 0/0 | 2431 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0082 | 0/0 | 2429 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0083 | 0/1 | 2430 | 1 | 0 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0084 | 0/0 | 2431 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0085 | 0/0 | 2431 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0086 | 0/0 | 2433 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0087 | 0/0 | 2441 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0088 | 0/0 | 2431 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0089 | 0/0 | 2430 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0090 | 0/0 | 2430 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0091 | 0/0 | 2430 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0092 | 0/0 | 2427 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0093 | 0/0 | 2420 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0094 | 0/0 | 2434 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0095 | 0/0 | 2434 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0096 | 0/0 | 2446 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0097 | 0/0 | 2436 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0098 | 0/0 | 2435 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0099 | 0/0 | 2441 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0100 | 0/0 | 2438 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
t0101 | 0/0 | 2419 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0002 | 0/0 | 7 | 0 | 2 | 1 | 2 | 2 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0006 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0007 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0122 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0293 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2097 | 124 | 54 | 26 | 28 | 1 | 14 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0002 | 0/1 | 2097 | 120 | 17 | 21 | 60 | 4 | 17 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0004 | 0/0 | 2097 | 43 | 0 | 14 | 17 | 6 | 6 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0005 | 0/0 | 2097 | 12 | 9 | 2 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0006 | 0/0 | 2097 | 10 | 0 | 0 | 10 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0007 | 0/0 | 2097 | 4 | 0 | 1 | 2 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0008 | 0/0 | 2097 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0011 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0012 | 0/0 | 2097 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0013 | 0/0 | 2097 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0014 | 0/0 | 2097 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0015 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0017 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0019 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0020 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0023 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0024 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0026 | 0/0 | 2097 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0002c0003 | 0/0 | 2097 | 57 | 2 | 3 | 43 | 3 | 6 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0002c0016 | 0/0 | 2097 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0003c0010 | 0/0 | 2097 | 2 | 0 | 0 | 0 | 2 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0004c0009 | 0/0 | 2097 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0005c0025 | 0/0 | 2097 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0006c0022 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0007c0021 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0008c0018 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4526 | 5 | 1 | 3 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0001t0002 | 0/0 | 4532 | 2 | 0 | 0 | 1 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0001t0004 | 0/0 | 4525 | 19 | 1 | 10 | 7 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0001t0006 | 0/0 | 4527 | 13 | 0 | 0 | 7 | 1 | 5 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0001t0007 | 0/0 | 4527 | 11 | 10 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0001t0008 | 0/0 | 4531 | 6 | 2 | 2 | 0 | 0 | 2 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0001t0010 | 0/0 | 4533 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0001t0012 | 0/0 | 4524 | 6 | 1 | 4 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0001t0013 | 0/0 | 4534 | 5 | 5 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0001t0015 | 0/0 | 4529 | 5 | 0 | 0 | 5 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0001t0016 | 0/0 | 4533 | 5 | 5 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0001t0018 | 0/0 | 4533 | 3 | 3 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0001t0022 | 0/0 | 4537 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0001t0023 | 0/0 | 4530 | 3 | 2 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0001t0024 | 0/0 | 4532 | 3 | 3 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0001t0025 | 0/0 | 4524 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0001t0028 | 0/0 | 4535 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0001t0029 | 0/0 | 4531 | 2 | 1 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0001t0031 | 0/0 | 4526 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0001t0033 | 0/0 | 4532 | 2 | 1 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0001t0034 | 0/0 | 4534 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0001t0035 | 0/0 | 4523 | 2 | 0 | 2 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0001t0042 | 0/0 | 4513 | 2 | 0 | 0 | 1 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0001t0050 | 0/0 | 4523 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0001t0052 | 1/0 | 4501 | 1 | 0 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0001t0053 | 0/0 | 4533 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0001t0054 | 0/0 | 4529 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0001t0056 | 0/0 | 4537 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0001t0057 | 0/0 | 4523 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0001t0060 | 0/0 | 4534 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0001t0061 | 0/0 | 4528 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0001t0062 | 0/0 | 4530 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0001t0063 | 0/0 | 4536 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0001t0064 | 0/0 | 4525 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0001t0065 | 0/0 | 4523 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0001t0066 | 0/0 | 4529 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0001t0089 | 0/0 | 4526 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0001t0094 | 0/0 | 4530 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0001t0095 | 0/0 | 4530 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0001t0098 | 0/0 | 4531 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0001t0100 | 0/0 | 4534 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0001t0101 | 0/0 | 4515 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0002t0001 | 0/0 | 4526 | 54 | 6 | 12 | 24 | 1 | 11 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0002t0002 | 0/0 | 4532 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0002t0004 | 0/0 | 4525 | 3 | 0 | 1 | 1 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0002t0005 | 0/0 | 4527 | 16 | 1 | 0 | 13 | 1 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0002t0006 | 0/0 | 4527 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0002t0014 | 0/0 | 4526 | 6 | 5 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0002t0018 | 0/0 | 4533 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0002t0019 | 0/0 | 4523 | 4 | 0 | 0 | 3 | 1 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0002t0020 | 0/0 | 4534 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0002t0021 | 0/0 | 4538 | 4 | 0 | 0 | 4 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0002t0025 | 0/0 | 4524 | 2 | 0 | 0 | 1 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0002t0026 | 0/0 | 4531 | 3 | 0 | 3 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0002t0036 | 0/0 | 4526 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0002t0037 | 0/0 | 4526 | 2 | 0 | 2 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0002t0038 | 0/0 | 4527 | 2 | 0 | 1 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0002t0055 | 0/0 | 4533 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0002t0070 | 0/0 | 4525 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0002t0072 | 0/0 | 4520 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0002t0073 | 0/0 | 4526 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0002t0074 | 0/0 | 4526 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0002t0075 | 0/0 | 4525 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0002t0076 | 0/0 | 4526 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0002t0077 | 0/0 | 4526 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0002t0078 | 0/0 | 4528 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0002t0079 | 0/0 | 4528 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0002t0082 | 0/0 | 4525 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0002t0083 | 0/1 | 4526 | 1 | 0 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0002t0085 | 0/0 | 4527 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0002t0086 | 0/0 | 4529 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0002t0088 | 0/0 | 4527 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0002t0091 | 0/0 | 4526 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0002t0092 | 0/0 | 4523 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0002t0096 | 0/0 | 4542 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0004t0003 | 0/0 | 4525 | 24 | 0 | 9 | 8 | 3 | 4 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0004t0011 | 0/0 | 4527 | 6 | 0 | 0 | 1 | 3 | 2 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0004t0017 | 0/0 | 4523 | 4 | 0 | 0 | 4 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0004t0027 | 0/0 | 4526 | 2 | 0 | 1 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0004t0043 | 0/0 | 4525 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0004t0044 | 0/0 | 4525 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0004t0046 | 0/0 | 4533 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0004t0047 | 0/0 | 4533 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0004t0048 | 0/0 | 4535 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0004t0049 | 0/0 | 4528 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0004t0058 | 0/0 | 4525 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0005t0001 | 0/0 | 4526 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0005t0004 | 0/0 | 4525 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0005t0007 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0005t0008 | 0/0 | 4531 | 3 | 3 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0005t0010 | 0/0 | 4533 | 5 | 3 | 2 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0005t0068 | 0/0 | 4535 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0006t0009 | 0/0 | 4526 | 9 | 0 | 0 | 9 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0006t0084 | 0/0 | 4527 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0007t0003 | 0/0 | 4525 | 3 | 0 | 0 | 2 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0007t0006 | 0/0 | 4527 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0008t0059 | 0/0 | 4525 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0008t0081 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0011t0090 | 0/0 | 4526 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0012t0002 | 0/0 | 4532 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0013t0003 | 0/0 | 4525 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0014t0001 | 0/0 | 4526 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0015t0067 | 0/0 | 4531 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0017t0013 | 0/0 | 4534 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0019t0071 | 0/0 | 4526 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0020t0003 | 0/0 | 4525 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0023t0051 | 0/0 | 4523 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0024t0002 | 0/0 | 4532 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0001c0026t0004 | 0/0 | 4525 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0002c0003t0002 | 0/0 | 4532 | 40 | 0 | 3 | 30 | 3 | 4 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0002c0003t0004 | 0/0 | 4525 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0002c0003t0005 | 0/0 | 4527 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0002c0003t0020 | 0/0 | 4534 | 3 | 0 | 0 | 2 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0002c0003t0022 | 0/0 | 4537 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0002c0003t0039 | 0/0 | 4528 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0002c0003t0040 | 0/0 | 4536 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0002c0003t0041 | 0/0 | 4533 | 2 | 0 | 0 | 1 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0002c0003t0080 | 0/0 | 4532 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0002c0003t0087 | 0/0 | 4537 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0002c0003t0093 | 0/0 | 4516 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0002c0003t0097 | 0/0 | 4532 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0002c0003t0099 | 0/0 | 4537 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0002c0016t0040 | 0/0 | 4536 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0003c0010t0032 | 0/0 | 4528 | 2 | 0 | 0 | 0 | 2 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0004c0009t0030 | 0/0 | 4535 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0005c0025t0002 | 0/0 | 4532 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0006c0022t0069 | 0/0 | 4537 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0007c0021t0045 | 0/0 | 4525 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
a0008c0018t0001 | 0/0 | 4526 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | copy fasta | chr9 | 136201333 | 136250812 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0004g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0004g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0004g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0004g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0004g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0004g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0004g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0004g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0004g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0006g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0006g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0006g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0006g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0006g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0006g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0006g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0006g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0006g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0006g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0006g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0006g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0006g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0007g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0007g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0007g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0007g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0007g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0007g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0007g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0007g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0008g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0008g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0008g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0008g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0008g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0008g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0010g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0012g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0012g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0012g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0012g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0012g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0013g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0013g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0013g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0015g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0015g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0015g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0016g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0016g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0016g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0016g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0016g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0018g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0018g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0018g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0022g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0022g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0023g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0023g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0023g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0024g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0024g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0024g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0025g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0028g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0028g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0029g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0029g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0031g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0031g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0033g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0033g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0034g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0034g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0035g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0042g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0042g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0050g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0052g0293 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0053g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0054g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0056g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0057g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0060g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0061g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0062g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0063g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0064g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0065g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0066g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0089g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0094g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0095g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0098g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0100g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0001t0101g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0006 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0004g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0004g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0005g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0005g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0005g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0005g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0005g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0005g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0005g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0005g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0005g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0005g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0005g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0005g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0005g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0005g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0005g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0006g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0014g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0014g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0014g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0014g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0014g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0018g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0019g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0019g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0019g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0019g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0020g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0021g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0021g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0021g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0025g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0025g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0026g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0026g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0026g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0036g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0036g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0037g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0038g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0038g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0055g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0070g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0072g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0073g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0074g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0075g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0076g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0077g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0078g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0079g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0082g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0083g0122 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0085g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0086g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0088g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0091g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0092g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0002t0096g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0004t0003g0002 | 0/0 | 7 | 0 | 2 | 1 | 2 | 2 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0004t0003g0007 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0004t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0004t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0004t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0004t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0004t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0004t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0004t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0004t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0004t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0004t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0004t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0004t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0004t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0004t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0004t0011g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0004t0011g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0004t0011g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0004t0011g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0004t0011g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0004t0017g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0004t0017g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0004t0017g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0004t0027g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0004t0027g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0004t0043g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0004t0044g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0004t0046g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0004t0047g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0004t0048g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0004t0049g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0004t0058g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0005t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0005t0004g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0005t0007g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0005t0008g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0005t0008g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0005t0008g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0005t0010g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0005t0010g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0005t0010g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0005t0010g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0005t0068g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0006t0009g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0006t0009g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0006t0009g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0006t0009g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0006t0009g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0006t0084g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0007t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0007t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0007t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0007t0006g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0008t0059g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0008t0081g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0011t0090g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0012t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0013t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0014t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0015t0067g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0017t0013g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0019t0071g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0020t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0023t0051g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0024t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0001c0026t0004g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0002g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0002g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0002g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0005g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0005g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0020g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0020g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0020g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0022g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0039g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0040g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0041g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0041g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0080g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0087g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0093g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0097g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0003t0099g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0002c0016t0040g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0003c0010t0032g0031 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0004c0009t0030g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0004c0009t0030g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0005c0025t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0006c0022t0069g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0007c0021t0045g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
a0008c0018t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0004 | t0011 | g0169 | EUR | GBR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0058 | EUR | GBR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG00140 | hp1 | a0001 | c0004 | t0003 | g0127 | EUR | GBR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG00140 | hp2 | a0001 | c0002 | t0005 | g0064 | EUR | GBR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG00280 | hp1 | a0003 | c0010 | t0032 | g0031 | EUR | FIN | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG00280 | hp2 | a0001 | c0004 | t0003 | g0002 | EUR | FIN | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG00323 | hp1 | a0001 | c0001 | t0006 | g0285 | EUR | FIN | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG00323 | hp2 | a0001 | c0004 | t0003 | g0002 | EUR | FIN | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | CHS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG00408 | hp2 | a0001 | c0002 | t0006 | g0081 | EAS | CHS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG00423 | hp1 | a0001 | c0002 | t0005 | g0130 | EAS | CHS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG00423 | hp2 | a0002 | c0003 | t0097 | g0253 | EAS | CHS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG00438 | hp1 | a0001 | c0002 | t0005 | g0049 | EAS | CHS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG00438 | hp2 | a0002 | c0003 | t0002 | g0264 | EAS | CHS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG00544 | hp1 | a0002 | c0003 | t0087 | g0256 | EAS | CHS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG00544 | hp2 | a0002 | c0003 | t0002 | g0001 | EAS | CHS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | CHS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG00558 | hp2 | a0001 | c0004 | t0048 | g0142 | EAS | CHS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG00609 | hp1 | a0001 | c0001 | t0006 | g0291 | EAS | CHS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG00609 | hp2 | a0001 | c0004 | t0027 | g0136 | EAS | CHS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG00621 | hp1 | a0001 | c0002 | t0070 | g0061 | EAS | CHS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG00621 | hp2 | a0001 | c0014 | t0001 | g0150 | EAS | CHS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG00639 | hp1 | a0001 | c0004 | t0003 | g0055 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG00639 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG00642 | hp1 | a0001 | c0002 | t0037 | g0020 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG00642 | hp2 | a0001 | c0004 | t0003 | g0007 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0086 | EAS | CHS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG00673 | hp2 | a0002 | c0003 | t0002 | g0005 | EAS | CHS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG00735 | hp1 | a0001 | c0001 | t0004 | g0226 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG00735 | hp2 | a0001 | c0001 | t0012 | g0236 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG00741 | hp1 | a0001 | c0004 | t0003 | g0054 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG00741 | hp2 | a0001 | c0001 | t0060 | g0188 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0078 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01069 | hp2 | a0001 | c0001 | t0008 | g0192 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01070 | hp1 | a0001 | c0001 | t0035 | g0033 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01070 | hp2 | a0001 | c0004 | t0003 | g0138 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01074 | hp1 | a0001 | c0001 | t0012 | g0036 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01074 | hp2 | a0001 | c0001 | t0007 | g0029 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01081 | hp1 | a0001 | c0001 | t0035 | g0033 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01081 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01099 | hp1 | a0001 | c0001 | t0012 | g0229 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01099 | hp2 | a0001 | c0004 | t0027 | g0135 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01106 | hp1 | a0001 | c0001 | t0008 | g0203 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0077 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01109 | hp1 | a0001 | c0001 | t0004 | g0008 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01109 | hp2 | a0001 | c0002 | t0014 | g0010 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01167 | hp1 | a0001 | c0005 | t0010 | g0026 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01167 | hp2 | a0001 | c0001 | t0012 | g0036 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01168 | hp1 | a0002 | c0003 | t0002 | g0312 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01168 | hp2 | a0001 | c0002 | t0026 | g0146 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01169 | hp1 | a0002 | c0003 | t0002 | g0309 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01169 | hp2 | a0001 | c0005 | t0010 | g0026 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01175 | hp1 | a0005 | c0025 | t0002 | g0184 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01175 | hp2 | a0001 | c0004 | t0044 | g0129 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01192 | hp1 | a0001 | c0002 | t0088 | g0156 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01192 | hp2 | a0001 | c0004 | t0049 | g0133 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01243 | hp1 | a0001 | c0001 | t0023 | g0295 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0021 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01255 | hp1 | a0001 | c0004 | t0003 | g0053 | AMR | CLM | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01255 | hp2 | a0001 | c0002 | t0026 | g0159 | AMR | CLM | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0059 | AMR | CLM | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01258 | hp2 | a0001 | c0002 | t0001 | g0063 | AMR | CLM | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01261 | hp1 | a0001 | c0004 | t0003 | g0002 | AMR | CLM | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01261 | hp2 | a0001 | c0001 | t0098 | g0216 | AMR | CLM | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01346 | hp2 | a0002 | c0003 | t0002 | g0310 | AMR | CLM | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01358 | hp1 | a0001 | c0001 | t0004 | g0228 | AMR | CLM | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01358 | hp2 | a0001 | c0002 | t0037 | g0020 | AMR | CLM | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01361 | hp1 | a0001 | c0002 | t0026 | g0039 | AMR | CLM | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01361 | hp2 | a0001 | c0002 | t0038 | g0162 | AMR | CLM | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0163 | AMR | CLM | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01433 | hp2 | a0001 | c0002 | t0001 | g0074 | AMR | CLM | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01496 | hp1 | a0001 | c0007 | t0006 | g0172 | AMR | CLM | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01496 | hp2 | a0001 | c0001 | t0033 | g0186 | AMR | CLM | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01515 | hp1 | a0002 | c0003 | t0002 | g0306 | EUR | IBS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01515 | hp2 | a0001 | c0004 | t0011 | g0018 | EUR | IBS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01516 | hp1 | a0002 | c0003 | t0002 | g0263 | EUR | IBS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01516 | hp2 | a0003 | c0010 | t0032 | g0031 | EUR | IBS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01517 | hp1 | a0001 | c0004 | t0011 | g0018 | EUR | IBS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01517 | hp2 | a0002 | c0003 | t0002 | g0261 | EUR | IBS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01884 | hp1 | a0004 | c0009 | t0030 | g0329 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01884 | hp2 | a0001 | c0001 | t0016 | g0297 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0113 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01891 | hp2 | a0001 | c0023 | t0051 | g0322 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0173 | AMR | PEL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01928 | hp2 | a0001 | c0001 | t0004 | g0227 | AMR | PEL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01943 | hp1 | a0001 | c0001 | t0004 | g0234 | AMR | PEL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0012 | AMR | PEL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01952 | hp1 | a0001 | c0001 | t0004 | g0232 | AMR | PEL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01952 | hp2 | a0001 | c0004 | t0043 | g0056 | AMR | PEL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01978 | hp1 | a0001 | c0004 | t0003 | g0125 | AMR | PEL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01978 | hp2 | a0001 | c0004 | t0058 | g0117 | AMR | PEL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0011 | AMR | PEL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02004 | hp1 | a0001 | c0004 | t0003 | g0109 | AMR | PEL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02004 | hp2 | a0001 | c0002 | t0001 | g0012 | AMR | PEL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02015 | hp2 | a0001 | c0006 | t0009 | g0015 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0320 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02040 | hp1 | a0002 | c0003 | t0002 | g0248 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02040 | hp2 | a0002 | c0003 | t0002 | g0314 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02055 | hp1 | a0001 | c0001 | t0050 | g0202 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02055 | hp2 | a0001 | c0001 | t0007 | g0214 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02056 | hp1 | a0002 | c0003 | t0020 | g0262 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02056 | hp2 | a0001 | c0002 | t0005 | g0073 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02071 | hp1 | a0001 | c0026 | t0004 | g0330 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02071 | hp2 | a0001 | c0007 | t0003 | g0164 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02074 | hp1 | a0001 | c0002 | t0025 | g0153 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02074 | hp2 | a0002 | c0003 | t0002 | g0001 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02080 | hp1 | a0001 | c0002 | t0005 | g0090 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02080 | hp2 | a0001 | c0002 | t0005 | g0097 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02083 | hp1 | a0001 | c0005 | t0004 | g0321 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02083 | hp2 | a0001 | c0013 | t0003 | g0134 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02129 | hp1 | a0001 | c0001 | t0053 | g0319 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02129 | hp2 | a0001 | c0007 | t0003 | g0132 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02132 | hp1 | a0001 | c0002 | t0082 | g0147 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02135 | hp1 | a0001 | c0002 | t0005 | g0040 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02135 | hp2 | a0001 | c0001 | t0006 | g0280 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02145 | hp1 | a0001 | c0001 | t0028 | g0271 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02145 | hp2 | a0001 | c0002 | t0075 | g0123 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | CDX | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0152 | EAS | CDX | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02165 | hp1 | a0001 | c0001 | t0042 | g0331 | EAS | CDX | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02165 | hp2 | a0002 | c0003 | t0002 | g0255 | EAS | CDX | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02257 | hp1 | a0001 | c0002 | t0001 | g0079 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02257 | hp2 | a0001 | c0001 | t0007 | g0028 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02258 | hp1 | a0001 | c0001 | t0100 | g0327 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02258 | hp2 | a0001 | c0001 | t0034 | g0208 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02280 | hp1 | a0001 | c0002 | t0091 | g0082 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02280 | hp2 | a0006 | c0022 | t0069 | g0299 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02293 | hp1 | a0001 | c0002 | t0004 | g0100 | AMR | PEL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02293 | hp2 | a0001 | c0001 | t0004 | g0238 | AMR | PEL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0087 | AMR | PEL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02300 | hp2 | a0001 | c0001 | t0004 | g0230 | AMR | PEL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02451 | hp1 | a0001 | c0015 | t0067 | g0091 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02451 | hp2 | a0001 | c0002 | t0092 | g0121 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02523 | hp1 | a0001 | c0004 | t0003 | g0119 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02523 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02572 | hp1 | a0001 | c0001 | t0013 | g0024 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02572 | hp2 | a0001 | c0001 | t0018 | g0189 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02602 | hp1 | a0001 | c0001 | t0008 | g0191 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02602 | hp2 | a0001 | c0001 | t0025 | g0224 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02615 | hp1 | a0001 | c0017 | t0013 | g0180 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02615 | hp2 | a0001 | c0008 | t0081 | g0047 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02622 | hp1 | a0001 | c0002 | t0005 | g0114 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02622 | hp2 | a0001 | c0001 | t0094 | g0266 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0088 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02630 | hp2 | a0001 | c0002 | t0055 | g0157 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02647 | hp1 | a0001 | c0002 | t0014 | g0010 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02647 | hp2 | a0001 | c0001 | t0028 | g0269 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0006 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02683 | hp2 | a0001 | c0002 | t0001 | g0011 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02698 | hp1 | a0001 | c0004 | t0011 | g0139 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02698 | hp2 | a0001 | c0007 | t0003 | g0158 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02717 | hp1 | a0001 | c0001 | t0010 | g0037 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02717 | hp2 | a0001 | c0001 | t0023 | g0274 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02723 | hp1 | a0001 | c0002 | t0001 | g0179 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02723 | hp2 | a0001 | c0020 | t0003 | g0183 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02738 | hp1 | a0002 | c0003 | t0002 | g0260 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0072 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02809 | hp1 | a0001 | c0001 | t0008 | g0199 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02809 | hp2 | a0001 | c0002 | t0014 | g0043 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02818 | hp1 | a0001 | c0001 | t0013 | g0024 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02818 | hp2 | a0001 | c0001 | t0066 | g0301 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02886 | hp1 | a0001 | c0001 | t0024 | g0324 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02886 | hp2 | a0001 | c0001 | t0056 | g0270 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02895 | hp1 | a0001 | c0002 | t0001 | g0089 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02895 | hp2 | a0001 | c0001 | t0013 | g0023 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02896 | hp1 | a0001 | c0005 | t0010 | g0196 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02896 | hp2 | a0001 | c0001 | t0018 | g0272 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02897 | hp1 | a0001 | c0005 | t0010 | g0197 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02897 | hp2 | a0001 | c0001 | t0013 | g0023 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02922 | hp1 | a0001 | c0001 | t0024 | g0323 | AFR | ESN | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02922 | hp2 | a0007 | c0021 | t0045 | g0182 | AFR | ESN | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02965 | hp1 | a0001 | c0001 | t0016 | g0304 | AFR | ESN | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02965 | hp2 | a0001 | c0001 | t0054 | g0294 | AFR | ESN | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02970 | hp1 | a0004 | c0009 | t0030 | g0328 | AFR | ESN | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02970 | hp2 | a0001 | c0005 | t0008 | g0198 | AFR | ESN | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02976 | hp1 | a0001 | c0001 | t0016 | g0303 | AFR | ESN | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02976 | hp2 | a0001 | c0001 | t0007 | g0029 | AFR | ESN | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03041 | hp1 | a0008 | c0018 | t0001 | g0181 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03041 | hp2 | a0001 | c0001 | t0007 | g0211 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03098 | hp1 | a0001 | c0002 | t0014 | g0041 | AFR | MSL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03098 | hp2 | a0001 | c0001 | t0031 | g0209 | AFR | MSL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03130 | hp1 | a0001 | c0001 | t0016 | g0302 | AFR | ESN | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03130 | hp2 | a0001 | c0001 | t0007 | g0028 | AFR | ESN | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03139 | hp1 | a0001 | c0001 | t0022 | g0268 | AFR | ESN | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03139 | hp2 | a0001 | c0002 | t0001 | g0112 | AFR | ESN | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03195 | hp1 | a0001 | c0001 | t0007 | g0027 | AFR | ESN | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03195 | hp2 | a0001 | c0002 | t0018 | g0038 | AFR | ESN | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03209 | hp1 | a0001 | c0001 | t0004 | g0257 | AFR | MSL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03209 | hp2 | a0002 | c0003 | t0022 | g0259 | AFR | MSL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | MSL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03225 | hp2 | a0001 | c0011 | t0090 | g0128 | AFR | MSL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03239 | hp1 | a0002 | c0003 | t0002 | g0258 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03239 | hp2 | a0001 | c0004 | t0003 | g0007 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03453 | hp1 | a0001 | c0005 | t0007 | g0212 | AFR | MSL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03453 | hp2 | a0001 | c0001 | t0031 | g0305 | AFR | MSL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03486 | hp1 | a0001 | c0002 | t0014 | g0042 | AFR | MSL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03486 | hp2 | a0001 | c0005 | t0010 | g0194 | AFR | MSL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03490 | hp1 | a0001 | c0001 | t0004 | g0223 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03490 | hp2 | a0001 | c0004 | t0003 | g0002 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03492 | hp1 | a0001 | c0001 | t0065 | g0225 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0069 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03516 | hp1 | a0001 | c0001 | t0007 | g0027 | AFR | ESN | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03516 | hp2 | a0001 | c0001 | t0010 | g0037 | AFR | ESN | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03540 | hp1 | a0001 | c0001 | t0013 | g0185 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03540 | hp2 | a0001 | c0001 | t0008 | g0201 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03579 | hp1 | a0001 | c0001 | t0007 | g0219 | AFR | MSL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03579 | hp2 | a0001 | c0001 | t0016 | g0296 | AFR | MSL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0111 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03654 | hp2 | a0001 | c0002 | t0001 | g0065 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03669 | hp1 | a0001 | c0002 | t0086 | g0126 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03669 | hp2 | a0001 | c0002 | t0004 | g0068 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03688 | hp1 | a0001 | c0001 | t0006 | g0284 | SAS | STU | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03688 | hp2 | a0001 | c0004 | t0011 | g0137 | SAS | STU | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0062 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03704 | hp2 | a0001 | c0001 | t0006 | g0276 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03710 | hp1 | a0001 | c0002 | t0005 | g0161 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03710 | hp2 | a0001 | c0001 | t0006 | g0281 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03831 | hp1 | a0002 | c0003 | t0002 | g0242 | SAS | BEB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03831 | hp2 | a0001 | c0001 | t0042 | g0332 | SAS | BEB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0021 | SAS | BEB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03834 | hp2 | a0001 | c0001 | t0057 | g0290 | SAS | BEB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03927 | hp1 | a0002 | c0003 | t0020 | g0307 | SAS | BEB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03927 | hp2 | a0001 | c0004 | t0003 | g0007 | SAS | BEB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03942 | hp1 | a0002 | c0003 | t0041 | g0308 | SAS | BEB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03942 | hp2 | a0001 | c0001 | t0006 | g0282 | SAS | BEB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG04115 | hp1 | a0001 | c0002 | t0038 | g0160 | SAS | STU | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0124 | SAS | STU | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG04184 | hp1 | a0002 | c0003 | t0002 | g0311 | SAS | BEB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG04184 | hp2 | a0001 | c0004 | t0003 | g0002 | SAS | BEB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG04199 | hp1 | a0001 | c0001 | t0012 | g0235 | SAS | STU | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG04199 | hp2 | a0001 | c0001 | t0006 | g0277 | SAS | STU | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG04204 | hp1 | a0001 | c0002 | t0001 | g0066 | SAS | STU | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG04204 | hp2 | a0001 | c0002 | t0025 | g0110 | SAS | STU | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0283 | SAS | STU | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0067 | SAS | STU | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18522 | hp1 | a0001 | c0001 | t0018 | g0187 | AFR | YRI | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18522 | hp2 | a0001 | c0001 | t0029 | g0298 | AFR | YRI | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18612 | hp1 | a0001 | c0012 | t0002 | g0131 | EAS | CHB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18612 | hp2 | a0001 | c0001 | t0064 | g0231 | EAS | CHB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18906 | hp1 | a0001 | c0005 | t0008 | g0204 | AFR | YRI | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18906 | hp2 | a0001 | c0001 | t0034 | g0206 | AFR | YRI | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18940 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18940 | hp2 | a0001 | c0001 | t0006 | g0292 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18941 | hp1 | a0002 | c0003 | t0002 | g0318 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18942 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18942 | hp2 | a0001 | c0004 | t0003 | g0002 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18944 | hp1 | a0001 | c0001 | t0015 | g0035 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18944 | hp2 | a0001 | c0004 | t0047 | g0141 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18946 | hp1 | a0001 | c0004 | t0003 | g0120 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18946 | hp2 | a0001 | c0006 | t0009 | g0080 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18947 | hp1 | a0002 | c0003 | t0002 | g0244 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18947 | hp2 | a0001 | c0002 | t0005 | g0092 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18948 | hp1 | a0001 | c0001 | t0004 | g0237 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18948 | hp2 | a0001 | c0002 | t0074 | g0154 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18952 | hp1 | a0002 | c0003 | t0002 | g0005 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18952 | hp2 | a0001 | c0006 | t0084 | g0167 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18954 | hp1 | a0001 | c0004 | t0046 | g0140 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18954 | hp2 | a0001 | c0002 | t0021 | g0176 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18956 | hp1 | a0001 | c0001 | t0015 | g0035 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18956 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18959 | hp1 | a0002 | c0003 | t0002 | g0032 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18959 | hp2 | a0001 | c0001 | t0015 | g0275 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18961 | hp1 | a0002 | c0003 | t0002 | g0246 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18961 | hp2 | a0001 | c0001 | t0006 | g0278 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18962 | hp1 | a0001 | c0006 | t0009 | g0166 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18962 | hp2 | a0002 | c0016 | t0040 | g0171 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18963 | hp1 | a0001 | c0002 | t0078 | g0151 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18963 | hp2 | a0002 | c0003 | t0002 | g0317 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18964 | hp1 | a0002 | c0003 | t0002 | g0001 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18964 | hp2 | a0001 | c0002 | t0002 | g0174 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18965 | hp1 | a0001 | c0002 | t0005 | g0095 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18965 | hp2 | a0002 | c0003 | t0002 | g0315 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18966 | hp1 | a0001 | c0002 | t0096 | g0177 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18966 | hp2 | a0002 | c0003 | t0002 | g0217 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18967 | hp1 | a0002 | c0003 | t0002 | g0001 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18967 | hp2 | a0001 | c0001 | t0006 | g0286 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18968 | hp1 | a0002 | c0003 | t0002 | g0005 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18968 | hp2 | a0001 | c0002 | t0076 | g0098 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18971 | hp2 | a0001 | c0002 | t0021 | g0022 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18973 | hp1 | a0001 | c0001 | t0006 | g0279 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18973 | hp2 | a0002 | c0003 | t0002 | g0001 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18975 | hp1 | a0001 | c0002 | t0021 | g0022 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18975 | hp2 | a0001 | c0001 | t0004 | g0240 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18977 | hp1 | a0001 | c0004 | t0011 | g0116 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18977 | hp2 | a0001 | c0002 | t0019 | g0085 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18979 | hp1 | a0001 | c0004 | t0017 | g0046 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18982 | hp1 | a0001 | c0002 | t0021 | g0178 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18983 | hp1 | a0001 | c0002 | t0005 | g0148 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18983 | hp2 | a0001 | c0002 | t0005 | g0099 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18985 | hp1 | a0001 | c0002 | t0005 | g0052 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18985 | hp2 | a0001 | c0004 | t0017 | g0016 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18986 | hp1 | a0002 | c0003 | t0039 | g0034 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18986 | hp2 | a0001 | c0004 | t0003 | g0144 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18988 | hp1 | a0001 | c0006 | t0009 | g0004 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18988 | hp2 | a0002 | c0003 | t0041 | g0252 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18990 | hp1 | a0001 | c0006 | t0009 | g0004 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18990 | hp2 | a0002 | c0003 | t0002 | g0009 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18992 | hp1 | a0002 | c0003 | t0005 | g0233 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18992 | hp2 | a0002 | c0003 | t0004 | g0249 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18998 | hp1 | a0001 | c0002 | t0019 | g0083 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18998 | hp2 | a0001 | c0001 | t0015 | g0025 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19000 | hp1 | a0002 | c0003 | t0039 | g0034 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19000 | hp2 | a0001 | c0001 | t0061 | g0287 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19001 | hp2 | a0001 | c0001 | t0006 | g0288 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19004 | hp1 | a0002 | c0003 | t0002 | g0247 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19004 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19005 | hp1 | a0002 | c0003 | t0002 | g0001 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19007 | hp1 | a0001 | c0004 | t0003 | g0165 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19007 | hp2 | a0001 | c0006 | t0009 | g0004 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19009 | hp1 | a0002 | c0003 | t0040 | g0245 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19010 | hp1 | a0001 | c0006 | t0009 | g0015 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19010 | hp2 | a0001 | c0002 | t0004 | g0149 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19011 | hp2 | a0002 | c0003 | t0002 | g0001 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19030 | hp1 | a0001 | c0001 | t0089 | g0265 | AFR | LWK | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19030 | hp2 | a0001 | c0001 | t0024 | g0325 | AFR | LWK | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19043 | hp1 | a0001 | c0019 | t0071 | g0273 | AFR | LWK | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19043 | hp2 | a0001 | c0001 | t0007 | g0220 | AFR | LWK | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19054 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19054 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19057 | hp1 | a0002 | c0003 | t0002 | g0032 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19057 | hp2 | a0001 | c0001 | t0101 | g0333 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19058 | hp1 | a0001 | c0006 | t0009 | g0168 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19058 | hp2 | a0001 | c0001 | t0062 | g0190 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19064 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19064 | hp2 | a0001 | c0002 | t0019 | g0084 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19065 | hp1 | a0001 | c0001 | t0029 | g0289 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19065 | hp2 | a0001 | c0002 | t0073 | g0170 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19066 | hp1 | a0001 | c0004 | t0017 | g0118 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19066 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19067 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19067 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19068 | hp1 | a0002 | c0003 | t0002 | g0009 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19068 | hp2 | a0001 | c0002 | t0072 | g0050 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19070 | hp1 | a0002 | c0003 | t0002 | g0254 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19070 | hp2 | a0001 | c0006 | t0009 | g0004 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19077 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19077 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19078 | hp1 | a0002 | c0003 | t0099 | g0218 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19078 | hp2 | a0001 | c0002 | t0005 | g0105 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19079 | hp1 | a0001 | c0004 | t0003 | g0145 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19079 | hp2 | a0002 | c0003 | t0002 | g0005 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19080 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19080 | hp2 | a0001 | c0001 | t0015 | g0025 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19081 | hp1 | a0001 | c0004 | t0003 | g0115 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19081 | hp2 | a0001 | c0002 | t0020 | g0175 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19084 | hp1 | a0001 | c0004 | t0017 | g0016 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19084 | hp2 | a0002 | c0003 | t0005 | g0250 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19085 | hp1 | a0001 | c0004 | t0003 | g0143 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19085 | hp2 | a0002 | c0003 | t0002 | g0009 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19087 | hp1 | a0002 | c0003 | t0002 | g0241 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19087 | hp2 | a0001 | c0002 | t0036 | g0060 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19088 | hp1 | a0002 | c0003 | t0002 | g0001 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19088 | hp2 | a0001 | c0002 | t0036 | g0057 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19090 | hp1 | a0001 | c0002 | t0005 | g0104 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19090 | hp2 | a0002 | c0003 | t0020 | g0251 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19240 | hp1 | a0001 | c0001 | t0033 | g0210 | AFR | YRI | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA19240 | hp2 | a0001 | c0008 | t0059 | g0045 | AFR | YRI | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA20752 | hp1 | a0001 | c0002 | t0019 | g0155 | EUR | TSI | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA20752 | hp2 | a0001 | c0002 | t0085 | g0071 | EUR | TSI | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA20905 | hp1 | a0001 | c0001 | t0008 | g0193 | SAS | GIH | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA20905 | hp2 | a0001 | c0002 | t0077 | g0070 | SAS | GIH | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0313 | AMR | CLM | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG01123 | hp2 | a0001 | c0004 | t0003 | g0002 | AMR | CLM | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02109 | hp1 | a0001 | c0005 | t0001 | g0205 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02109 | hp2 | a0001 | c0005 | t0008 | g0200 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02486 | hp1 | a0001 | c0005 | t0068 | g0195 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02486 | hp2 | a0001 | c0001 | t0012 | g0222 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02559 | hp1 | a0001 | c0001 | t0022 | g0267 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG02559 | hp2 | a0001 | c0001 | t0063 | g0207 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03471 | hp1 | a0001 | c0001 | t0095 | g0215 | AFR | MSL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG03471 | hp2 | a0001 | c0002 | t0014 | g0044 | AFR | MSL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG06807 | hp1 | a0002 | c0003 | t0093 | g0300 | AFR | USA | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
HG06807 | hp2 | a0001 | c0001 | t0007 | g0213 | AFR | USA | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18955 | hp1 | a0001 | c0002 | t0079 | g0108 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA18955 | hp2 | a0002 | c0003 | t0080 | g0316 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA21309 | hp1 | a0001 | c0001 | t0023 | g0326 | AFR | LWK | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
NA21309 | hp2 | a0001 | c0024 | t0002 | g0243 | AFR | LWK | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0083 | g0122 | REF | REF | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0052 | g0293 | REF | REF | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:136208898
|
T | C | 1 | a0006 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.1927A>G | p.Lys643Glu | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1936/4501 | 1927/2097 | 643/698 | chr9 | 136208898 | ||
chr9:136209255
|
G | A | 1 | a0005 | 1 | HG01175.hp1 | missense_variant | MODERATE | c.1570C>T | p.Arg524Trp | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1579/4501 | 1570/2097 | 524/698 | chr9 | 136209255 | ||
chr9:136211431
|
G | A | 1 | a0007 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.1382C>T | p.Ala461Val | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/12 | 1391/4501 | 1382/2097 | 461/698 | chr9 | 136211431 | ||
chr9:136215249
|
C | T | 1 | a0004 | 2 | HG01884.hp1 HG02970.hp1 |
missense_variant | MODERATE | c.1265G>A | p.Arg422Gln | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/12 | 1274/4501 | 1265/2097 | 422/698 | chr9 | 136215249 | ||
chr9:136218710
|
G | A | 1 | a0003 | 2 | HG00280.hp1 HG01516.hp2 |
missense_variant | MODERATE | c.1055C>T | p.Thr352Met | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/12 | 1064/4501 | 1055/2097 | 352/698 | chr9 | 136218710 | ||
chr9:136226827
|
T | C | 2 | a0002a0005 | 59 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(56): Show |
missense_variant | MODERATE | c.376A>G | p.Lys126Glu | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/12 | 385/4501 | 376/2097 | 126/698 | chr9 | 136226827 | ||
chr9:136245599
|
C | G | 1 | a0008 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.205G>C | p.Gly69Arg | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/12 | 214/4501 | 205/2097 | 69/698 | chr9 | 136245599 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:136208821
|
G | A | 1 | a0001c0006 | 10 | HG02015.hp2 NA18946.hp2 NA18952.hp2 others(7): Show |
synonymous_variant | LOW | c.2004C>T | p.Tyr668Tyr | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 2013/4501 | 2004/2097 | 668/698 | chr9 | 136208821 | ||
chr9:136208887
|
G | A | 1 | a0001c0013 | 1 | HG02083.hp2 | synonymous_variant | LOW | c.1938C>T | p.Gly646Gly | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1947/4501 | 1938/2097 | 646/698 | chr9 | 136208887 | ||
chr9:136208959
|
T | C | 5 | a0001c0004a0001c0007a0001c0013others(2): Show | 50 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(47): Show |
synonymous_variant | LOW | c.1866A>G | p.Pro622Pro | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1875/4501 | 1866/2097 | 622/698 | chr9 | 136208959 | ||
chr9:136209043
|
G | A | 1 | a0001c0014 | 1 | HG00621.hp2 | synonymous_variant | LOW | c.1782C>T | p.Leu594Leu | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1791/4501 | 1782/2097 | 594/698 | chr9 | 136209043 | ||
chr9:136211406
|
G | A | 1 | a0001c0023 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.1407C>T | p.Tyr469Tyr | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/12 | 1416/4501 | 1407/2097 | 469/698 | chr9 | 136211406 | ||
chr9:136216639
|
G | A | 1 | a0001c0015 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.1170C>T | p.Pro390Pro | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 9/12 | 1179/4501 | 1170/2097 | 390/698 | chr9 | 136216639 | ||
chr9:136218808
|
C | T | 3 | a0001c0004a0001c0012a0001c0013 | 45 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(42): Show |
splice_region_variant&synonymous_variant | LOW | c.957G>A | p.Lys319Lys | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/12 | 966/4501 | 957/2097 | 319/698 | chr9 | 136218808 | ||
chr9:136219113
|
A | G | 5 | a0001c0005a0001c0008a0001c0020others(2): Show | 17 | HG01167.hp1 HG01169.hp2 HG02083.hp1 others(14): Show |
synonymous_variant | LOW | c.873T>C | p.Asp291Asp | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 7/12 | 882/4501 | 873/2097 | 291/698 | chr9 | 136219113 | ||
chr9:136219137
|
C | T | 1 | a0001c0019 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.849G>A | p.Ser283Ser | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 7/12 | 858/4501 | 849/2097 | 283/698 | chr9 | 136219137 | ||
chr9:136221813
|
C | G | 1 | a0001c0011 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.804G>C | p.Ser268Ser | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/12 | 813/4501 | 804/2097 | 268/698 | chr9 | 136221813 | ||
chr9:136224020
|
G | A | 1 | a0001c0024 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.571C>T | p.Leu191Leu | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 4/12 | 580/4501 | 571/2097 | 191/698 | chr9 | 136224020 | ||
chr9:136245561
|
C | A | 1 | a0001c0026 | 1 | HG02071.hp1 | synonymous_variant | LOW | c.243G>T | p.Ala81Ala | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/12 | 252/4501 | 243/2097 | 81/698 | chr9 | 136245561 | ||
chr9:136245699
|
C | G | 1 | a0001c0017 | 1 | HG02615.hp1 | synonymous_variant | LOW | c.105G>C | p.Arg35Arg | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/12 | 114/4501 | 105/2097 | 35/698 | chr9 | 136245699 | ||
chr9:136245780
|
C | T | 11 | a0001c0002a0001c0004a0001c0006others(8): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
synonymous_variant | LOW | c.24G>A | p.Val8Val | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/12 | 33/4501 | 24/2097 | 8/698 | chr9 | 136245780 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:136206370
|
C | T | 1 | a0001c0002t0073 | 1 | NA19065.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2358G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 2358 | chr9 | 136206370 | |||||
chr9:136206537
|
A | T | 3 | a0001c0001t0042a0001c0001t0053a0001c0001t0101 | 4 | HG02129.hp1 HG02165.hp1 HG03831.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2191T>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 2191 | chr9 | 136206537 | |||||
chr9:136206567
|
A | G | 3 | a0001c0002t0073a0001c0002t0074a0001c0002t0078 | 3 | NA18948.hp2 NA18963.hp1 NA19065.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2161T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 2161 | chr9 | 136206567 | |||||
chr9:136206624
|
T | C | 3 | a0001c0001t0013a0001c0001t0033a0001c0017t0013 | 8 | HG01496.hp2 HG02572.hp1 HG02615.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2104A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 2104 | chr9 | 136206624 | |||||
chr9:136206668
|
AC | A | 4 | a0001c0002t0037a0001c0002t0075a0001c0002t0083others(1): Show | 5 | HG00642.hp1 HG01192.hp1 HG01358.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2059delG | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 2059 | chr9 | 136206668 | |||||
chr9:136206799
|
G | A | 2 | a0001c0006t0009a0001c0006t0084 | 10 | HG02015.hp2 NA18946.hp2 NA18952.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1929C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1929 | chr9 | 136206799 | |||||
chr9:136206885
|
A | C | 3 | a0001c0001t0022a0001c0002t0055a0002c0003t0022 | 4 | HG02559.hp1 HG02630.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1843T>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1843 | chr9 | 136206885 | |||||
chr9:136207087
|
G | A | 1 | a0001c0001t0095 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1641C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1641 | chr9 | 136207087 | |||||
chr9:136207096
|
G | A | 2 | a0001c0002t0037a0001c0002t0088 | 3 | HG00642.hp1 HG01192.hp1 HG01358.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1632C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1632 | chr9 | 136207096 | |||||
chr9:136207227
|
A | G | 65 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(62): Show | 191 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(188): Show |
3_prime_UTR_variant | MODIFIER | c.*1501T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1501 | chr9 | 136207227 | |||||
chr9:136207266
|
T | C | 1 | a0001c0002t0076 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1462A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1462 | chr9 | 136207266 | |||||
chr9:136207342
|
G | A | 2 | a0001c0002t0077a0001c0002t0085 | 2 | NA20752.hp2 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1386C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1386 | chr9 | 136207342 | |||||
chr9:136207359
|
TCTCATAC others(5): Show |
T | 1 | a0001c0001t0101 | 1 | NA19057.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1357_*1368delTGTG others(8): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1357 | chr9 | 136207359 | |||||
chr9:136207359
|
TCTCATAC others(7): Show |
T | 1 | a0001c0001t0042 | 2 | HG02165.hp1 HG03831.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1355_*1368delTGTG others(10): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1355 | chr9 | 136207359 | |||||
chr9:136207364
|
T | TAC | 7 | a0001c0001t0015a0001c0001t0023a0001c0001t0054others(4): Show | 14 | HG01243.hp1 HG02451.hp1 HG02717.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1362_*1363dupGT | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1363 | chr9 | 136207364 | |||||
chr9:136207364
|
T | TACAC | 8 | a0001c0001t0010a0001c0001t0024a0001c0001t0029others(5): Show | 17 | HG01167.hp1 HG01169.hp2 HG01261.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1360_*1363dupGTGT | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1363 | chr9 | 136207364 | |||||
chr9:136207364
|
T | TACACAC | 24 | a0001c0001t0002a0001c0001t0008a0001c0001t0013others(21): Show | 83 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*1358_*1363dupGTGT others(2): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1363 | chr9 | 136207364 | |||||
chr9:136207364
|
T | TACACACA others(1): Show |
7 | a0001c0001t0028a0001c0001t0063a0001c0002t0020others(4): Show | 11 | HG00558.hp2 HG01884.hp1 HG02056.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1356_*1363dupGTGT others(4): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1363 | chr9 | 136207364 | |||||
chr9:136207364
|
T | TACACACA others(3): Show |
6 | a0001c0001t0022a0001c0001t0056a0002c0003t0022others(3): Show | 7 | HG02559.hp1 HG02886.hp2 HG03139.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1354_*1363dupGTGT others(6): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1363 | chr9 | 136207364 | |||||
chr9:136207364
|
T | TACACACA others(5): Show |
1 | a0001c0002t0021 | 4 | NA18954.hp2 NA18971.hp2 NA18975.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1352_*1363dupGTGT others(8): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1363 | chr9 | 136207364 | |||||
chr9:136207364
|
T | TACACACA others(9): Show |
1 | a0001c0002t0096 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1348_*1363dupGTGT others(12): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1363 | chr9 | 136207364 | |||||
chr9:136207364
|
TAC | T | 15 | a0001c0001t0031a0001c0002t0014a0001c0002t0078others(12): Show | 47 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1362_*1363delGT | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1362 | chr9 | 136207364 | |||||
chr9:136207364
|
TACAC | T | 37 | a0001c0001t0001a0001c0001t0004a0001c0001t0012others(34): Show | 152 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(149): Show |
3_prime_UTR_variant | MODIFIER | c.*1360_*1363delGTGT | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1360 | chr9 | 136207364 | |||||
chr9:136207364
|
TACACAC | T | 7 | a0001c0001t0025a0001c0001t0035a0001c0001t0065others(4): Show | 9 | HG01070.hp1 HG01081.hp1 HG01891.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1358_*1363delGTGT others(2): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1358 | chr9 | 136207364 | |||||
chr9:136207364
|
TACACACA others(3): Show |
T | 2 | a0001c0002t0072a0002c0003t0093 | 2 | HG06807.hp1 NA19068.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1354_*1363delGTGT others(6): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1354 | chr9 | 136207364 | |||||
chr9:136207374
|
C | T | 1 | a0001c0001t0101 | 1 | NA19057.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1354G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1354 | chr9 | 136207374 | |||||
chr9:136207376
|
C | T | 1 | a0001c0001t0042 | 2 | HG02165.hp1 HG03831.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1352G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1352 | chr9 | 136207376 | |||||
chr9:136207566
|
C | T | 1 | a0001c0002t0070 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1162G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1162 | chr9 | 136207566 | |||||
chr9:136207605
|
A | C | 126 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(123): Show | 386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
3_prime_UTR_variant | MODIFIER | c.*1123T>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1123 | chr9 | 136207605 | |||||
chr9:136207625
|
C | G | 9 | a0001c0001t0018a0001c0001t0022a0001c0001t0028others(6): Show | 13 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1103G>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1103 | chr9 | 136207625 | |||||
chr9:136207749
|
G | T | 1 | a0001c0001t0053 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*979C>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 979 | chr9 | 136207749 | |||||
chr9:136207754
|
G | C | 2 | a0001c0002t0036a0001c0002t0070 | 3 | HG00621.hp1 NA19087.hp2 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*974C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 974 | chr9 | 136207754 | |||||
chr9:136207781
|
G | A | 1 | a0001c0004t0044 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*947C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 947 | chr9 | 136207781 | |||||
chr9:136207782
|
C | T | 3 | a0001c0008t0081a0001c0011t0090a0001c0019t0071 | 3 | HG02615.hp2 HG03225.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*946G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 946 | chr9 | 136207782 | |||||
chr9:136207855
|
C | A | 1 | a0002c0003t0097 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*873G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 873 | chr9 | 136207855 | |||||
chr9:136207939
|
G | A | 1 | a0001c0001t0100 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*789C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 789 | chr9 | 136207939 | |||||
chr9:136208072
|
G | C | 1 | a0001c0004t0044 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*656C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 656 | chr9 | 136208072 | |||||
chr9:136208081
|
C | G | 6 | a0001c0001t0007a0001c0001t0042a0001c0001t0050others(3): Show | 17 | HG01074.hp2 HG02055.hp1 HG02055.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*647G>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 647 | chr9 | 136208081 | |||||
chr9:136208139
|
AAC | A | 2 | a0001c0001t0008a0001c0005t0008 | 9 | HG01069.hp2 HG01106.hp1 HG02109.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*587_*588delGT | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 587 | chr9 | 136208139 | |||||
chr9:136208192
|
C | T | 2 | a0001c0004t0046a0007c0021t0045 | 2 | HG02922.hp2 NA18954.hp1 |
3_prime_UTR_variant | MODIFIER | c.*536G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 536 | chr9 | 136208192 | |||||
chr9:136208218
|
C | A | 1 | a0001c0001t0031 | 2 | HG03098.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*510G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 510 | chr9 | 136208218 | |||||
chr9:136208242
|
C | G | 1 | a0001c0001t0064 | 1 | NA18612.hp2 | 3_prime_UTR_variant | MODIFIER | c.*486G>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 486 | chr9 | 136208242 | |||||
chr9:136208252
|
G | A | 2 | a0001c0001t0007a0001c0005t0007 | 12 | HG01074.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*476C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 476 | chr9 | 136208252 | |||||
chr9:136208284
|
A | G | 1 | a0001c0001t0031 | 2 | HG03098.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*444T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 444 | chr9 | 136208284 | |||||
chr9:136208289
|
A | AGTGGAGG others(21): Show |
1 | a0001c0023t0051 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*438_*439insCCACCT others(22): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 438 | chr9 | 136208289 | |||||
chr9:136208291
|
T | TGGAGGGT others(22): Show |
1 | a0001c0001t0089 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*436_*437insCCCCGA others(23): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 436 | chr9 | 136208291 | |||||
chr9:136208291
|
T | TGGAGGGT others(19): Show |
56 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(53): Show | 182 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*436_*437insCCACCT others(20): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 436 | chr9 | 136208291 | |||||
chr9:136208291
|
T | TGGAGGGT others(20): Show |
20 | a0001c0001t0012a0001c0001t0013a0001c0001t0023others(17): Show | 44 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*436_*437insCCCACC others(21): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 436 | chr9 | 136208291 | |||||
chr9:136208291
|
T | TGGAGGGT others(21): Show |
16 | a0001c0001t0004a0001c0001t0010a0001c0001t0035others(13): Show | 42 | HG00621.hp1 HG00639.hp2 HG00735.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*436_*437insCCCCAC others(22): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 436 | chr9 | 136208291 | |||||
chr9:136208291
|
T | TGGAGGGT others(22): Show |
1 | a0001c0011t0090 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*436_*437insGCCCCA others(23): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 436 | chr9 | 136208291 | |||||
chr9:136208291
|
T | TGGAGGGT others(22): Show |
20 | a0001c0001t0001a0001c0001t0025a0001c0002t0001others(17): Show | 87 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*436_*437insCCCCCA others(23): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 436 | chr9 | 136208291 | |||||
chr9:136208291
|
T | TGGAGGGT others(23): Show |
12 | a0001c0002t0005a0001c0002t0026a0001c0002t0037others(9): Show | 32 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*436_*437insCCCCCC others(24): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 436 | chr9 | 136208291 | |||||
chr9:136208291
|
T | TGGAGGGT others(24): Show |
1 | a0001c0002t0088 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*436_*437insCCCCCC others(25): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 436 | chr9 | 136208291 | |||||
chr9:136208294
|
G | C | 2 | a0001c0002t0038a0001c0002t0091 | 3 | HG01361.hp2 HG02280.hp1 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*434C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 434 | chr9 | 136208294 | |||||
chr9:136208313
|
G | C | 1 | a0001c0002t0092 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*415C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 415 | chr9 | 136208313 | |||||
chr9:136208314
|
G | T | 1 | a0001c0001t0050 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*414C>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 414 | chr9 | 136208314 | |||||
chr9:136208524
|
T | C | 1 | a0001c0002t0014 | 6 | HG01109.hp2 HG02647.hp1 HG02809.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*204A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 204 | chr9 | 136208524 | |||||
chr9:136208567
|
C | T | 14 | a0001c0004t0003a0001c0004t0011a0001c0004t0017others(11): Show | 48 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*161G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 161 | chr9 | 136208567 | |||||
chr9:136208568
|
GT | G | 20 | a0001c0001t0002a0001c0001t0094a0001c0001t0095others(17): Show | 67 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*159delA | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 159 | chr9 | 136208568 | |||||
chr9:136208607
|
C | T | 2 | a0001c0004t0043a0001c0004t0044 | 2 | HG01175.hp2 HG01952.hp2 |
3_prime_UTR_variant | MODIFIER | c.*121G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 121 | chr9 | 136208607 | |||||
chr9:136208628
|
T | G | 1 | a0001c0001t0100 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*100A>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 100 | chr9 | 136208628 | |||||
chr9:136208673
|
C | T | 2 | a0001c0001t0007a0001c0005t0007 | 12 | HG01074.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*55G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 55 | chr9 | 136208673 | |||||
chr9:136245807
|
G | A | 2 | a0001c0001t0042a0001c0001t0101 | 3 | HG02165.hp1 HG03831.hp2 NA19057.hp2 |
5_prime_UTR_variant | MODIFIER | c.-4C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/12 | 4 | chr9 | 136245807 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:136209329
|
C | T | 2 | a0001c0001t0006g0281a0001c0001t0006g0282 | 2 | HG03710.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1550-54G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136209329 | ||||||
chr9:136209485
|
C | T | 1 | a0001c0001t0050g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1550-210G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136209485 | ||||||
chr9:136209519
|
G | T | 1 | a0001c0001t0063g0207 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1550-244C>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136209519 | ||||||
chr9:136209528
|
C | T | 1 | a0001c0001t0100g0327 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1550-253G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136209528 | ||||||
chr9:136209543
|
C | T | 2 | a0001c0001t0031g0209a0001c0001t0031g0305 | 2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1550-268G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136209543 | ||||||
chr9:136209672
|
C | A | 9 | a0001c0001t0007g0027a0001c0001t0007g0028a0001c0001t0007g0029others(6): Show | 12 | HG01074.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1550-397G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136209672 | ||||||
chr9:136209724
|
C | T | 39 | a0001c0002t0001g0096a0001c0004t0003g0002a0001c0004t0003g0007others(36): Show | 49 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.1550-449G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136209724 | ||||||
chr9:136209737
|
G | T | 145 | a0001c0001t0001g0030a0001c0001t0001g0221a0001c0001t0001g0239others(142): Show | 175 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.1550-462C>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136209737 | ||||||
chr9:136209765
|
T | C | 9 | a0001c0001t0013g0023a0001c0001t0013g0024a0001c0001t0013g0185others(6): Show | 11 | HG01496.hp2 HG02258.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1550-490A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136209765 | ||||||
chr9:136209828
|
C | T | 2 | a0001c0001t0056g0270a0001c0001t0057g0290 | 2 | HG02886.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1550-553G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136209828 | ||||||
chr9:136209925
|
C | T | 3 | a0004c0009t0030g0328a0004c0009t0030g0329a0007c0021t0045g0182 | 3 | HG01884.hp1 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1550-650G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136209925 | ||||||
chr9:136209926
|
G | A | 120 | a0001c0001t0002g0283a0001c0001t0002g0320a0001c0001t0006g0292others(117): Show | 148 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.1550-651C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136209926 | ||||||
chr9:136209930
|
G | A | 7 | a0001c0001t0010g0037a0001c0001t0066g0301a0001c0005t0010g0026others(4): Show | 9 | HG01167.hp1 HG01169.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1550-655C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136209930 | ||||||
chr9:136209947
|
G | A | 3 | a0001c0001t0042g0331a0001c0001t0042g0332a0001c0001t0101g0333 | 3 | HG02165.hp1 HG03831.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1550-672C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136209947 | ||||||
chr9:136209963
|
G | A | 1 | a0001c0001t0031g0305 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1550-688C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136209963 | ||||||
chr9:136209990
|
A | G | 1 | a0001c0006t0009g0080 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1550-715T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136209990 | ||||||
chr9:136210101
|
G | T | 15 | a0001c0001t0010g0037a0001c0001t0031g0209a0001c0001t0031g0305others(12): Show | 17 | HG01167.hp1 HG01169.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1550-826C>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136210101 | ||||||
chr9:136210108
|
C | T | 1 | a0001c0001t0066g0301 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1550-833G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136210108 | ||||||
chr9:136210298
|
G | C | 89 | a0001c0001t0001g0030a0001c0001t0001g0221a0001c0001t0001g0239others(86): Show | 106 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.1549+966C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136210298 | ||||||
chr9:136210471
|
C | G | 58 | a0001c0001t0006g0276a0001c0001t0006g0277a0001c0001t0006g0278others(55): Show | 70 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.1549+793G>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136210471 | ||||||
chr9:136210473
|
G | C | 1 | a0001c0002t0026g0146 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1549+791C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136210473 | ||||||
chr9:136210484
|
G | C | 1 | a0001c0001t0050g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1549+780C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136210484 | ||||||
chr9:136210498
|
C | T | 1 | a0001c0002t0005g0052 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1549+766G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136210498 | ||||||
chr9:136210499
|
G | A | 1 | a0001c0005t0001g0205 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1549+765C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136210499 | ||||||
chr9:136210502
|
G | A | 6 | a0001c0001t0018g0187a0001c0001t0018g0189a0001c0001t0042g0332others(3): Show | 6 | HG00741.hp2 HG02129.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1549+762C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136210502 | ||||||
chr9:136210532
|
C | A | 1 | a0005c0025t0002g0184 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1549+732G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136210532 | ||||||
chr9:136210565
|
C | T | 1 | a0001c0004t0003g0143 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1549+699G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136210565 | ||||||
chr9:136210604
|
G | A | 23 | a0001c0001t0002g0283a0001c0001t0006g0276a0001c0001t0006g0277others(20): Show | 25 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.1549+660C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136210604 | ||||||
chr9:136210611
|
A | G | 1 | a0001c0001t0050g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1549+653T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136210611 | ||||||
chr9:136210747
|
T | C | 1 | a0001c0002t0075g0123 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1549+517A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136210747 | ||||||
chr9:136210759
|
A | G | 3 | a0001c0001t0042g0331a0001c0001t0042g0332a0001c0001t0101g0333 | 3 | HG02165.hp1 HG03831.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1549+505T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136210759 | ||||||
chr9:136210769
|
G | T | 1 | a0001c0004t0003g0115 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1549+495C>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136210769 | ||||||
chr9:136210813
|
T | C | 1 | a0001c0002t0005g0097 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1549+451A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136210813 | ||||||
chr9:136210877
|
G | A | 1 | a0001c0001t0050g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1549+387C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136210877 | ||||||
chr9:136210985
|
G | C | 40 | a0001c0004t0003g0002a0001c0004t0003g0007a0001c0004t0003g0053others(37): Show | 50 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.1549+279C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136210985 | ||||||
chr9:136211061
|
A | AAGCCGGG others(9): Show |
9 | a0001c0001t0013g0023a0001c0001t0013g0024a0001c0001t0013g0185others(6): Show | 11 | HG01496.hp2 HG02258.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1549+187_1549+202d others(18): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136211061 | ||||||
chr9:136211066
|
G | A | 1 | a0001c0002t0001g0066 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1549+198C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136211066 | ||||||
chr9:136211131
|
C | T | 1 | a0001c0002t0070g0061 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1549+133G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136211131 | ||||||
chr9:136211151
|
C | T | 1 | a0002c0003t0005g0233 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1549+113G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136211151 | ||||||
chr9:136211182
|
G | A | 17 | a0001c0001t0007g0027a0001c0001t0007g0028a0001c0001t0007g0029others(14): Show | 20 | HG00741.hp2 HG01074.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.1549+82C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136211182 | ||||||
chr9:136211480
|
C | T | 1 | a0001c0004t0003g0165 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1361-28G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136211480 | ||||||
chr9:136211536
|
A | G | 7 | a0001c0001t0023g0274a0001c0001t0023g0295a0001c0001t0023g0326others(4): Show | 7 | HG01243.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1361-84T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136211536 | ||||||
chr9:136211633
|
C | T | 1 | a0001c0004t0017g0046 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1361-181G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136211633 | ||||||
chr9:136211732
|
G | A | 1 | a0001c0001t0004g0238 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1361-280C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136211732 | ||||||
chr9:136211738
|
G | A | 1 | a0001c0008t0059g0045 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1361-286C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136211738 | ||||||
chr9:136211758
|
G | A | 7 | a0001c0001t0010g0037a0001c0001t0066g0301a0001c0005t0010g0026others(4): Show | 9 | HG01167.hp1 HG01169.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1361-306C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136211758 | ||||||
chr9:136211804
|
T | C | 1 | a0001c0001t0089g0265 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1361-352A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136211804 | ||||||
chr9:136211863
|
T | C | 1 | a0001c0001t0050g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1361-411A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136211863 | ||||||
chr9:136211938
|
G | A | 1 | a0001c0001t0050g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1361-486C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136211938 | ||||||
chr9:136212109
|
G | A | 61 | a0001c0001t0002g0283a0001c0001t0006g0276a0001c0001t0006g0277others(58): Show | 73 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.1361-657C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136212109 | ||||||
chr9:136212244
|
C | T | 2 | a0001c0004t0003g0007a0001c0004t0011g0139 | 4 | HG00642.hp2 HG02698.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1361-792G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136212244 | ||||||
chr9:136212515
|
C | T | 6 | a0001c0001t0016g0296a0001c0001t0016g0297a0001c0001t0016g0302others(3): Show | 6 | HG01884.hp2 HG02965.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1361-1063G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136212515 | ||||||
chr9:136212528
|
G | GAGAGC | 7 | a0001c0001t0023g0274a0001c0001t0023g0295a0001c0001t0023g0326others(4): Show | 7 | HG01243.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1361-1081_1361-107 others(9): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136212528 | ||||||
chr9:136212608
|
G | A | 1 | a0001c0001t0002g0320 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1361-1156C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136212608 | ||||||
chr9:136212761
|
C | A | 1 | a0001c0002t0026g0039 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1361-1309G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136212761 | ||||||
chr9:136212799
|
A | T | 3 | a0001c0001t0008g0199a0001c0001t0008g0201a0001c0001t0008g0203 | 3 | HG01106.hp1 HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1361-1347T>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136212799 | ||||||
chr9:136213147
|
G | C | 1 | a0001c0001t0004g0230 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1361-1695C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213147 | ||||||
chr9:136213216
|
C | A | 9 | a0001c0001t0007g0027a0001c0001t0007g0028a0001c0001t0007g0029others(6): Show | 12 | HG01074.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1361-1764G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213216 | ||||||
chr9:136213243
|
G | GT | 15 | a0001c0001t0013g0023a0001c0001t0013g0185a0001c0001t0033g0186others(12): Show | 16 | HG01106.hp2 HG01496.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.1361-1792dupA | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213243 | ||||||
chr9:136213243
|
GT | G | 73 | a0001c0001t0001g0030a0001c0001t0001g0221a0001c0001t0001g0239others(70): Show | 88 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.1361-1792delA | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213243 | ||||||
chr9:136213243
|
GTT | G | 63 | a0001c0001t0002g0283a0001c0001t0006g0276a0001c0001t0006g0277others(60): Show | 75 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.1361-1793_1361-179 others(6): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213243 | ||||||
chr9:136213243
|
GTTTT | G | 9 | a0001c0001t0042g0331a0001c0001t0042g0332a0001c0001t0101g0333others(6): Show | 11 | HG02165.hp1 HG02738.hp1 HG03831.hp2 others(8): Show |
intron_variant | MODIFIER | c.1361-1795_1361-179 others(8): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213243 | ||||||
chr9:136213243
|
GTTTTT | G | 49 | a0001c0001t0008g0191a0001c0001t0008g0192a0001c0001t0008g0193others(46): Show | 62 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.1361-1796_1361-179 others(9): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213243 | ||||||
chr9:136213243
|
GTTTTTT | G | 6 | a0001c0002t0005g0105a0001c0002t0021g0176a0001c0002t0021g0178others(3): Show | 6 | HG01516.hp1 NA18954.hp2 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.1361-1797_1361-179 others(10): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213243 | ||||||
chr9:136213255
|
T | G | 7 | a0001c0001t0023g0274a0001c0001t0023g0295a0001c0001t0023g0326others(4): Show | 7 | HG01243.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1361-1803A>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213255 | ||||||
chr9:136213263
|
T | C | 1 | a0001c0008t0059g0045 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1361-1811A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213263 | ||||||
chr9:136213383
|
T | C | 63 | a0001c0001t0008g0191a0001c0001t0008g0192a0001c0001t0008g0193others(60): Show | 78 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1360+1771A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213383 | ||||||
chr9:136213400
|
C | T | 1 | a0001c0001t0016g0302 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1360+1754G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213400 | ||||||
chr9:136213469
|
TTC | T | 3 | a0001c0001t0008g0199a0001c0001t0008g0201a0001c0001t0008g0203 | 3 | HG01106.hp1 HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1360+1683_1360+168 others(6): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213469 | ||||||
chr9:136213574
|
C | T | 1 | a0001c0002t0001g0179 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1360+1580G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213574 | ||||||
chr9:136213658
|
C | T | 1 | a0001c0001t0022g0267 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1360+1496G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213658 | ||||||
chr9:136213663
|
C | G | 1 | a0001c0001t0056g0270 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1360+1491G>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213663 | ||||||
chr9:136213728
|
C | T | 1 | a0002c0003t0099g0218 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1360+1426G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213728 | ||||||
chr9:136213746
|
G | A | 3 | a0001c0004t0003g0143a0001c0004t0003g0144a0001c0004t0027g0136 | 3 | HG00609.hp2 NA18986.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1360+1408C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213746 | ||||||
chr9:136213921
|
C | G | 2 | a0001c0001t0023g0274a0001c0001t0023g0295 | 2 | HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1360+1233G>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213921 | ||||||
chr9:136213967
|
A | AAC | 153 | a0001c0001t0002g0283a0001c0001t0002g0320a0001c0001t0006g0276others(150): Show | 183 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1360+1185_1360+118 others(6): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213967 | ||||||
chr9:136213988
|
C | T | 26 | a0001c0001t0001g0030a0001c0001t0001g0239a0001c0001t0004g0003others(23): Show | 35 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.1360+1166G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213988 | ||||||
chr9:136214030
|
C | T | 3 | a0001c0001t0042g0331a0001c0001t0042g0332a0001c0001t0101g0333 | 3 | HG02165.hp1 HG03831.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1360+1124G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136214030 | ||||||
chr9:136214094
|
G | A | 61 | a0001c0001t0002g0320a0001c0001t0008g0191a0001c0001t0008g0192others(58): Show | 76 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.1360+1060C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136214094 | ||||||
chr9:136214307
|
C | T | 8 | a0001c0001t0007g0219a0001c0001t0023g0274a0001c0001t0023g0295others(5): Show | 8 | HG01243.hp1 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1360+847G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136214307 | ||||||
chr9:136214341
|
C | T | 8 | a0001c0001t0007g0027a0001c0001t0007g0028a0001c0001t0007g0029others(5): Show | 11 | HG01074.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1360+813G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136214341 | ||||||
chr9:136214491
|
C | T | 1 | a0001c0014t0001g0150 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1360+663G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136214491 | ||||||
chr9:136214560
|
C | T | 1 | a0001c0004t0003g0145 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1360+594G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136214560 | ||||||
chr9:136214733
|
C | T | 2 | a0001c0001t0031g0209a0001c0001t0031g0305 | 2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1360+421G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136214733 | ||||||
chr9:136214756
|
G | A | 1 | a0002c0003t0093g0300 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1360+398C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136214756 | ||||||
chr9:136214785
|
G | A | 1 | a0001c0001t0054g0294 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1360+369C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136214785 | ||||||
chr9:136214794
|
C | T | 5 | a0001c0002t0014g0010a0001c0002t0014g0041a0001c0002t0014g0042others(2): Show | 6 | HG01109.hp2 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1360+360G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136214794 | ||||||
chr9:136214916
|
T | C | 1 | a0001c0001t0100g0327 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1360+238A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136214916 | ||||||
chr9:136214968
|
G | A | 1 | a0001c0024t0002g0243 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1360+186C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136214968 | ||||||
chr9:136214975
|
C | T | 2 | a0001c0002t0001g0066a0001c0002t0001g0072 | 2 | HG02738.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1360+179G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136214975 | ||||||
chr9:136215329
|
C | A | 1 | a0001c0002t0001g0152 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1210-25G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 9/11 | chr9 | 136215329 | ||||||
chr9:136215384
|
T | C | 86 | a0001c0001t0007g0027a0001c0001t0007g0028a0001c0001t0007g0029others(83): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.1210-80A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 9/11 | chr9 | 136215384 | ||||||
chr9:136215423
|
A | C | 1 | a0001c0002t0001g0179 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1210-119T>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 9/11 | chr9 | 136215423 | ||||||
chr9:136215793
|
G | A | 1 | a0001c0002t0086g0126 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1210-489C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 9/11 | chr9 | 136215793 | ||||||
chr9:136216012
|
C | T | 8 | a0001c0001t0007g0027a0001c0001t0007g0028a0001c0001t0007g0029others(5): Show | 11 | HG01074.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1209+588G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 9/11 | chr9 | 136216012 | ||||||
chr9:136216033
|
C | T | 105 | a0001c0001t0002g0283a0001c0001t0002g0320a0001c0001t0006g0276others(102): Show | 120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.1209+567G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 9/11 | chr9 | 136216033 | ||||||
chr9:136216037
|
A | T | 1 | a0001c0002t0001g0065 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1209+563T>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 9/11 | chr9 | 136216037 | ||||||
chr9:136216070
|
G | A | 1 | a0001c0002t0001g0089 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1209+530C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 9/11 | chr9 | 136216070 | ||||||
chr9:136216078
|
C | T | 2 | a0001c0008t0059g0045a0002c0003t0002g0306 | 2 | HG01515.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1209+522G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 9/11 | chr9 | 136216078 | ||||||
chr9:136216079
|
G | A | 39 | a0001c0002t0001g0079a0001c0004t0003g0002a0001c0004t0003g0007others(36): Show | 49 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.1209+521C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 9/11 | chr9 | 136216079 | ||||||
chr9:136216245
|
A | C | 9 | a0001c0001t0022g0267a0001c0001t0022g0268a0001c0002t0001g0112others(6): Show | 9 | HG01891.hp1 HG02451.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1209+355T>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 9/11 | chr9 | 136216245 | ||||||
chr9:136216292
|
C | T | 6 | a0001c0001t0013g0023a0001c0001t0013g0024a0001c0001t0013g0185others(3): Show | 8 | HG01496.hp2 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209+308G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 9/11 | chr9 | 136216292 | ||||||
chr9:136216462
|
G | A | 19 | a0001c0001t0002g0320a0001c0001t0008g0191a0001c0001t0008g0192others(16): Show | 19 | HG01069.hp2 HG01106.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.1209+138C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 9/11 | chr9 | 136216462 | ||||||
chr9:136216478
|
A | G | 150 | a0001c0001t0002g0283a0001c0001t0002g0320a0001c0001t0006g0276others(147): Show | 179 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.1209+122T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 9/11 | chr9 | 136216478 | ||||||
chr9:136216499
|
G | A | 1 | a0001c0001t0034g0208 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1209+101C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 9/11 | chr9 | 136216499 | ||||||
chr9:136216513
|
G | A | 39 | a0001c0002t0001g0079a0001c0004t0003g0002a0001c0004t0003g0007others(36): Show | 49 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.1209+87C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 9/11 | chr9 | 136216513 | ||||||
chr9:136216526
|
C | A | 1 | a0001c0001t0006g0285 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1209+74G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 9/11 | chr9 | 136216526 | ||||||
chr9:136216793
|
G | A | 3 | a0001c0001t0042g0331a0001c0001t0042g0332a0001c0001t0101g0333 | 3 | HG02165.hp1 HG03831.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1087-71C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136216793 | ||||||
chr9:136216852
|
A | G | 2 | a0004c0009t0030g0328a0004c0009t0030g0329 | 2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1087-130T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136216852 | ||||||
chr9:136216895
|
C | A | 2 | a0004c0009t0030g0328a0004c0009t0030g0329 | 2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1087-173G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136216895 | ||||||
chr9:136216910
|
T | C | 8 | a0001c0001t0007g0027a0001c0001t0007g0028a0001c0001t0007g0029others(5): Show | 11 | HG01074.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1087-188A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136216910 | ||||||
chr9:136217138
|
G | A | 2 | a0002c0003t0002g0309a0002c0003t0002g0312 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1087-416C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136217138 | ||||||
chr9:136217161
|
G | A | 22 | a0001c0001t0002g0283a0001c0001t0006g0276a0001c0001t0006g0277others(19): Show | 24 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.1087-439C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136217161 | ||||||
chr9:136217170
|
C | T | 3 | a0001c0001t0042g0331a0001c0001t0042g0332a0001c0001t0101g0333 | 3 | HG02165.hp1 HG03831.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1087-448G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136217170 | ||||||
chr9:136217213
|
G | C | 39 | a0001c0002t0001g0079a0001c0004t0003g0002a0001c0004t0003g0007others(36): Show | 49 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.1087-491C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136217213 | ||||||
chr9:136217229
|
C | T | 1 | a0001c0001t0004g0226 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1087-507G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136217229 | ||||||
chr9:136217234
|
T | C | 39 | a0001c0002t0001g0079a0001c0004t0003g0002a0001c0004t0003g0007others(36): Show | 49 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.1087-512A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136217234 | ||||||
chr9:136217362
|
G | A | 1 | a0002c0003t0002g0254 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1087-640C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136217362 | ||||||
chr9:136217401
|
A | G | 214 | a0001c0001t0001g0030a0001c0001t0001g0221a0001c0001t0001g0239others(211): Show | 258 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.1087-679T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136217401 | ||||||
chr9:136217417
|
G | A | 39 | a0001c0002t0001g0079a0001c0004t0003g0002a0001c0004t0003g0007others(36): Show | 49 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.1087-695C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136217417 | ||||||
chr9:136217471
|
G | A | 5 | a0001c0002t0014g0010a0001c0002t0014g0041a0001c0002t0014g0042others(2): Show | 6 | HG01109.hp2 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1087-749C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136217471 | ||||||
chr9:136217522
|
C | T | 1 | a0001c0002t0038g0160 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1087-800G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136217522 | ||||||
chr9:136217680
|
C | G | 213 | a0001c0001t0001g0030a0001c0001t0001g0221a0001c0001t0001g0239others(210): Show | 257 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.1087-958G>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136217680 | ||||||
chr9:136217727
|
G | A | 3 | a0001c0004t0011g0137a0001c0004t0043g0056a0001c0004t0044g0129 | 3 | HG01175.hp2 HG01952.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1086+952C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136217727 | ||||||
chr9:136217739
|
C | T | 10 | a0001c0001t0004g0257a0001c0001t0010g0037a0001c0001t0016g0296others(7): Show | 11 | HG01884.hp2 HG02280.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1086+940G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136217739 | ||||||
chr9:136217741
|
G | A | 1 | a0001c0001t0050g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1086+938C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136217741 | ||||||
chr9:136217972
|
C | G | 1 | a0001c0001t0056g0270 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1086+707G>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136217972 | ||||||
chr9:136218015
|
T | G | 216 | a0001c0001t0001g0030a0001c0001t0001g0221a0001c0001t0001g0239others(213): Show | 260 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.1086+664A>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136218015 | ||||||
chr9:136218024
|
T | G | 7 | a0001c0001t0023g0274a0001c0001t0023g0295a0001c0001t0023g0326others(4): Show | 7 | HG01243.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1086+655A>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136218024 | ||||||
chr9:136218065
|
C | T | 1 | a0001c0002t0001g0066 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1086+614G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136218065 | ||||||
chr9:136218304
|
C | T | 2 | a0004c0009t0030g0328a0004c0009t0030g0329 | 2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1086+375G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136218304 | ||||||
chr9:136218325
|
C | G | 26 | a0001c0001t0001g0030a0001c0001t0001g0239a0001c0001t0004g0003others(23): Show | 35 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.1086+354G>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136218325 | ||||||
chr9:136218361
|
A | C | 6 | a0001c0001t0007g0219a0001c0001t0023g0274a0001c0001t0023g0295others(3): Show | 6 | HG01243.hp1 HG02258.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1086+318T>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136218361 | ||||||
chr9:136218362
|
G | GGT | 3 | a0001c0001t0042g0331a0001c0001t0042g0332a0001c0001t0101g0333 | 3 | HG02165.hp1 HG03831.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1086+315_1086+316d others(4): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136218362 | ||||||
chr9:136218444
|
A | G | 330 | a0001c0001t0001g0030a0001c0001t0001g0221a0001c0001t0001g0239others(327): Show | 389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.1086+235T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136218444 | ||||||
chr9:136218501
|
C | T | 1 | a0001c0002t0001g0163 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1086+178G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136218501 | ||||||
chr9:136218515
|
G | A | 6 | a0001c0001t0013g0023a0001c0001t0013g0024a0001c0001t0013g0185others(3): Show | 8 | HG01496.hp2 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1086+164C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136218515 | ||||||
chr9:136218524
|
G | A | 1 | a0002c0003t0002g0310 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1086+155C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136218524 | ||||||
chr9:136218572
|
C | T | 1 | a0001c0001t0050g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1086+107G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136218572 | ||||||
chr9:136218611
|
G | A | 1 | a0001c0001t0056g0270 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1086+68C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136218611 | ||||||
chr9:136218673
|
C | T | 5 | a0001c0001t0007g0028a0001c0001t0007g0211a0001c0001t0007g0213others(2): Show | 6 | HG02055.hp2 HG02257.hp2 HG03041.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1086+6G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136218673 | ||||||
chr9:136218835
|
G | A | 2 | a0004c0009t0030g0328a0004c0009t0030g0329 | 2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.957-27C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 7/11 | chr9 | 136218835 | ||||||
chr9:136218930
|
C | G | 1 | a0001c0001t0053g0319 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.956+100G>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 7/11 | chr9 | 136218930 | ||||||
chr9:136218989
|
C | T | 1 | a0001c0001t0004g0238 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.956+41G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 7/11 | chr9 | 136218989 | ||||||
chr9:136219175
|
G | A | 1 | a0001c0002t0038g0160 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.822-11C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136219175 | ||||||
chr9:136219187
|
G | A | 23 | a0001c0001t0007g0219a0001c0001t0013g0023a0001c0001t0013g0024others(20): Show | 26 | HG00741.hp2 HG01109.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.822-23C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136219187 | ||||||
chr9:136219366
|
A | G | 5 | a0001c0002t0014g0010a0001c0002t0014g0041a0001c0002t0014g0042others(2): Show | 6 | HG01109.hp2 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.822-202T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136219366 | ||||||
chr9:136219581
|
G | A | 1 | a0001c0002t0075g0123 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.822-417C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136219581 | ||||||
chr9:136219620
|
G | A | 2 | a0001c0002t0001g0011a0001c0002t0001g0059 | 3 | HG01258.hp1 HG01993.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.822-456C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136219620 | ||||||
chr9:136219883
|
G | A | 3 | a0001c0001t0042g0331a0001c0001t0042g0332a0001c0001t0101g0333 | 3 | HG02165.hp1 HG03831.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.822-719C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136219883 | ||||||
chr9:136219911
|
C | T | 1 | a0001c0001t0024g0324 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.822-747G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136219911 | ||||||
chr9:136219979
|
G | A | 1 | a0001c0008t0081g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.822-815C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136219979 | ||||||
chr9:136219985
|
T | C | 6 | a0001c0001t0018g0272a0001c0001t0022g0267a0001c0001t0022g0268others(3): Show | 6 | HG02145.hp1 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.822-821A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136219985 | ||||||
chr9:136220024
|
G | T | 181 | a0001c0001t0001g0030a0001c0001t0001g0221a0001c0001t0001g0239others(178): Show | 215 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(212): Show |
intron_variant | MODIFIER | c.822-860C>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136220024 | ||||||
chr9:136220078
|
C | T | 1 | a0001c0002t0091g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.822-914G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136220078 | ||||||
chr9:136220127
|
G | C | 2 | a0001c0004t0003g0125a0001c0004t0003g0138 | 2 | HG01070.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.822-963C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136220127 | ||||||
chr9:136220160
|
T | C | 6 | a0001c0001t0018g0272a0001c0001t0022g0267a0001c0001t0022g0268others(3): Show | 6 | HG02145.hp1 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.822-996A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136220160 | ||||||
chr9:136220359
|
G | A | 1 | a0001c0001t0004g0232 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.822-1195C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136220359 | ||||||
chr9:136220606
|
GCCTCACG others(10): Show |
G | 180 | a0001c0001t0001g0030a0001c0001t0001g0221a0001c0001t0002g0283others(177): Show | 214 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.821+1173_821+1189d others(19): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136220606 | ||||||
chr9:136220623
|
TCCTCACG others(11): Show |
T | 1 | a0001c0001t0001g0239 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.821+1155_821+1172d others(20): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136220623 | ||||||
chr9:136220629
|
C | T | 1 | a0001c0002t0005g0095 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.821+1167G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136220629 | ||||||
chr9:136220676
|
C | A | 1 | a0002c0003t0002g0318 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.821+1120G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136220676 | ||||||
chr9:136220701
|
C | A | 2 | a0001c0002t0025g0153a0001c0002t0082g0147 | 2 | HG02074.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.821+1095G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136220701 | ||||||
chr9:136220710
|
T | A | 1 | a0002c0003t0002g0244 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.821+1086A>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136220710 | ||||||
chr9:136220749
|
C | T | 2 | a0001c0020t0003g0183a0007c0021t0045g0182 | 2 | HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.821+1047G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136220749 | ||||||
chr9:136220766
|
G | A | 3 | a0001c0001t0042g0331a0001c0001t0042g0332a0001c0001t0101g0333 | 3 | HG02165.hp1 HG03831.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.821+1030C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136220766 | ||||||
chr9:136220844
|
G | A | 2 | a0001c0001t0002g0320a0001c0001t0053g0319 | 2 | HG02027.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.821+952C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136220844 | ||||||
chr9:136220846
|
G | T | 1 | a0001c0008t0059g0045 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.821+950C>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136220846 | ||||||
chr9:136220909
|
T | C | 2 | a0001c0001t0031g0209a0001c0001t0031g0305 | 2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.821+887A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136220909 | ||||||
chr9:136221052
|
GCAGAGGC others(40): Show |
G | 3 | a0001c0001t0042g0331a0001c0001t0042g0332a0001c0001t0101g0333 | 3 | HG02165.hp1 HG03831.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.821+697_821+743del others(47): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136221052 | ||||||
chr9:136221057
|
G | C | 14 | a0001c0001t0002g0320a0001c0001t0008g0191a0001c0001t0008g0192others(11): Show | 14 | HG01069.hp2 HG01106.hp1 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.821+739C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136221057 | ||||||
chr9:136221071
|
C | G | 1 | a0001c0002t0086g0126 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.821+725G>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136221071 | ||||||
chr9:136221103
|
AGGCAAAG others(87): Show |
A | 2 | a0001c0001t0031g0209a0001c0001t0031g0305 | 2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.821+599_821+692del others(94): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136221103 | ||||||
chr9:136221104
|
G | C | 3 | a0001c0001t0042g0331a0001c0001t0042g0332a0001c0001t0101g0333 | 3 | HG02165.hp1 HG03831.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.821+692C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136221104 | ||||||
chr9:136221141
|
TCCACGCA others(87): Show |
T | 3 | a0001c0001t0022g0267a0001c0001t0022g0268a0001c0001t0056g0270 | 3 | HG02559.hp1 HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.821+561_821+654del others(94): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136221141 | ||||||
chr9:136221201
|
AAAGGGCT others(40): Show |
A | 1 | a0001c0001t0053g0319 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.821+548_821+594del others(47): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136221201 | ||||||
chr9:136221247
|
C | T | 3 | a0001c0001t0018g0272a0001c0001t0028g0269a0001c0001t0028g0271 | 3 | HG02145.hp1 HG02647.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.821+549G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136221247 | ||||||
chr9:136221299
|
G | C | 2 | a0001c0020t0003g0183a0007c0021t0045g0182 | 2 | HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.821+497C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136221299 | ||||||
chr9:136221340
|
G | A | 2 | a0002c0003t0002g0241a0002c0003t0002g0242 | 2 | HG03831.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.821+456C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136221340 | ||||||
chr9:136221495
|
C | G | 2 | a0001c0001t0001g0313a0001c0002t0001g0078 | 2 | HG01069.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.821+301G>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136221495 | ||||||
chr9:136221508
|
T | C | 1 | a0001c0002t0001g0163 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.821+288A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136221508 | ||||||
chr9:136221561
|
G | A | 3 | a0001c0001t0094g0266a0001c0001t0095g0215a0001c0001t0098g0216 | 3 | HG01261.hp2 HG02622.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.821+235C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136221561 | ||||||
chr9:136221621
|
A | C | 17 | a0001c0001t0002g0320a0001c0001t0008g0191a0001c0001t0008g0192others(14): Show | 17 | HG01069.hp2 HG01106.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.821+175T>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136221621 | ||||||
chr9:136221643
|
G | A | 6 | a0001c0001t0018g0272a0001c0001t0022g0267a0001c0001t0022g0268others(3): Show | 6 | HG02145.hp1 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.821+153C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136221643 | ||||||
chr9:136221785
|
C | T | 2 | a0001c0005t0004g0321a0001c0008t0059g0045 | 2 | HG02083.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.821+11G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136221785 | ||||||
chr9:136222096
|
T | C | 3 | a0001c0001t0004g0223a0001c0001t0025g0224a0001c0001t0065g0225 | 3 | HG02602.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.676-155A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136222096 | ||||||
chr9:136222104
|
T | TA | 102 | a0001c0001t0001g0030a0001c0001t0001g0221a0001c0001t0001g0239others(99): Show | 128 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.676-164dupT | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136222104 | ||||||
chr9:136222144
|
G | A | 1 | a0001c0001t0006g0291 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.676-203C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136222144 | ||||||
chr9:136222153
|
C | T | 1 | a0001c0005t0008g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.676-212G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136222153 | ||||||
chr9:136222317
|
G | A | 2 | a0001c0020t0003g0183a0007c0021t0045g0182 | 2 | HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.676-376C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136222317 | ||||||
chr9:136222338
|
G | A | 1 | a0002c0003t0002g0311 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.676-397C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136222338 | ||||||
chr9:136222345
|
C | T | 8 | a0001c0001t0007g0027a0001c0001t0007g0028a0001c0001t0007g0029others(5): Show | 11 | HG01074.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.676-404G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136222345 | ||||||
chr9:136222462
|
T | C | 58 | a0001c0001t0002g0283a0001c0001t0002g0320a0001c0001t0006g0276others(55): Show | 63 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.676-521A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136222462 | ||||||
chr9:136222575
|
C | T | 14 | a0001c0001t0002g0320a0001c0001t0008g0191a0001c0001t0008g0192others(11): Show | 14 | HG01069.hp2 HG01106.hp1 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.676-634G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136222575 | ||||||
chr9:136222582
|
G | A | 2 | a0001c0004t0003g0007a0001c0004t0011g0139 | 4 | HG00642.hp2 HG02698.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.676-641C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136222582 | ||||||
chr9:136222613
|
G | C | 1 | a0001c0002t0025g0153 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.676-672C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136222613 | ||||||
chr9:136222631
|
G | T | 1 | a0001c0004t0003g0119 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.676-690C>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136222631 | ||||||
chr9:136222689
|
C | CCTGCA | 3 | a0001c0001t0042g0331a0001c0001t0042g0332a0001c0001t0101g0333 | 3 | HG02165.hp1 HG03831.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.676-753_676-749dup others(5): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136222689 | ||||||
chr9:136222754
|
C | T | 2 | a0001c0020t0003g0183a0007c0021t0045g0182 | 2 | HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.676-813G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136222754 | ||||||
chr9:136222755
|
G | C | 1 | a0001c0004t0003g0145 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.676-814C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136222755 | ||||||
chr9:136222778
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.676-837C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136222778 | ||||||
chr9:136222896
|
T | C | 2 | a0001c0001t0002g0320a0001c0001t0053g0319 | 2 | HG02027.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.675+867A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136222896 | ||||||
chr9:136222900
|
G | A | 1 | a0001c0002t0092g0121 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.675+863C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136222900 | ||||||
chr9:136222954
|
G | A | 8 | a0001c0001t0007g0027a0001c0001t0007g0028a0001c0001t0007g0029others(5): Show | 11 | HG01074.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.675+809C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136222954 | ||||||
chr9:136223075
|
C | T | 1 | a0001c0004t0017g0118 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.675+688G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136223075 | ||||||
chr9:136223106
|
G | A | 1 | a0001c0002t0025g0110 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.675+657C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136223106 | ||||||
chr9:136223127
|
A | G | 1 | a0001c0001t0001g0221 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.675+636T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136223127 | ||||||
chr9:136223381
|
A | C | 2 | a0001c0001t0002g0320a0001c0001t0053g0319 | 2 | HG02027.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.675+382T>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136223381 | ||||||
chr9:136223470
|
G | A | 1 | a0002c0003t0002g0255 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.675+293C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136223470 | ||||||
chr9:136223970
|
C | T | 1 | a0001c0023t0051g0322 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.584+37G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 4/11 | chr9 | 136223970 | ||||||
chr9:136224153
|
G | A | 22 | a0001c0001t0002g0283a0001c0001t0006g0276a0001c0001t0006g0277others(19): Show | 24 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.479-41C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 3/11 | chr9 | 136224153 | ||||||
chr9:136224383
|
G | A | 1 | a0001c0001t0061g0287 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.479-271C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 3/11 | chr9 | 136224383 | ||||||
chr9:136224406
|
C | A | 5 | a0001c0002t0014g0010a0001c0002t0014g0041a0001c0002t0014g0042others(2): Show | 6 | HG01109.hp2 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.479-294G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 3/11 | chr9 | 136224406 | ||||||
chr9:136224425
|
A | ACAGGC | 3 | a0001c0001t0008g0199a0001c0001t0008g0201a0001c0001t0008g0203 | 3 | HG01106.hp1 HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.479-318_479-314dup others(5): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 3/11 | chr9 | 136224425 | ||||||
chr9:136224447
|
G | A | 2 | a0001c0005t0001g0205a0008c0018t0001g0181 | 2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.479-335C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 3/11 | chr9 | 136224447 | ||||||
chr9:136224449
|
G | A | 14 | a0001c0001t0007g0027a0001c0001t0007g0028a0001c0001t0007g0029others(11): Show | 17 | HG01074.hp2 HG02055.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.479-337C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 3/11 | chr9 | 136224449 | ||||||
chr9:136224477
|
G | A | 2 | a0001c0001t0031g0209a0001c0001t0031g0305 | 2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.479-365C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 3/11 | chr9 | 136224477 | ||||||
chr9:136224712
|
C | T | 1 | a0001c0002t0019g0155 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.478+149G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 3/11 | chr9 | 136224712 | ||||||
chr9:136224820
|
G | A | 17 | a0001c0001t0002g0320a0001c0001t0008g0191a0001c0001t0008g0192others(14): Show | 17 | HG01069.hp2 HG01106.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.478+41C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 3/11 | chr9 | 136224820 | ||||||
chr9:136224986
|
G | A | 2 | a0002c0003t0099g0218a0002c0016t0040g0171 | 2 | NA18962.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.430-77C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136224986 | ||||||
chr9:136225052
|
C | T | 8 | a0001c0001t0007g0027a0001c0001t0007g0028a0001c0001t0007g0029others(5): Show | 11 | HG01074.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.430-143G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136225052 | ||||||
chr9:136225061
|
T | G | 58 | a0001c0001t0002g0283a0001c0001t0002g0320a0001c0001t0006g0276others(55): Show | 63 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.430-152A>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136225061 | ||||||
chr9:136225100
|
A | G | 1 | a0001c0007t0006g0172 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.430-191T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136225100 | ||||||
chr9:136225255
|
G | A | 6 | a0001c0001t0018g0272a0001c0001t0022g0267a0001c0001t0022g0268others(3): Show | 6 | HG02145.hp1 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.430-346C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136225255 | ||||||
chr9:136225380
|
G | A | 1 | a0001c0002t0001g0179 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.430-471C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136225380 | ||||||
chr9:136225444
|
G | C | 1 | a0001c0002t0001g0089 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.430-535C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136225444 | ||||||
chr9:136225511
|
G | A | 1 | a0001c0005t0008g0204 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.430-602C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136225511 | ||||||
chr9:136225624
|
A | G | 1 | a0002c0003t0002g0248 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.430-715T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136225624 | ||||||
chr9:136225632
|
G | A | 1 | a0001c0002t0001g0101 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.430-723C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136225632 | ||||||
chr9:136225699
|
G | A | 1 | a0002c0003t0087g0256 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.430-790C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136225699 | ||||||
chr9:136225752
|
C | T | 71 | a0001c0001t0002g0283a0001c0001t0002g0320a0001c0001t0006g0276others(68): Show | 78 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.430-843G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136225752 | ||||||
chr9:136225801
|
G | A | 4 | a0001c0001t0018g0187a0001c0001t0018g0189a0001c0001t0060g0188others(1): Show | 4 | HG00741.hp2 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.430-892C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136225801 | ||||||
chr9:136225873
|
A | C | 17 | a0001c0001t0002g0320a0001c0001t0008g0191a0001c0001t0008g0192others(14): Show | 17 | HG01069.hp2 HG01106.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.429+901T>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136225873 | ||||||
chr9:136226013
|
T | C | 3 | a0001c0004t0003g0053a0001c0004t0003g0054a0001c0004t0003g0055 | 3 | HG00639.hp1 HG00741.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.429+761A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136226013 | ||||||
chr9:136226332
|
T | C | 8 | a0001c0002t0001g0102a0001c0002t0001g0106a0001c0002t0002g0174others(5): Show | 9 | NA18954.hp2 NA18964.hp2 NA18966.hp1 others(6): Show |
intron_variant | MODIFIER | c.429+442A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136226332 | ||||||
chr9:136226415
|
C | T | 1 | a0001c0007t0003g0132 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.429+359G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136226415 | ||||||
chr9:136226424
|
C | T | 10 | a0001c0001t0018g0187a0001c0001t0018g0189a0001c0001t0018g0272others(7): Show | 10 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.429+350G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136226424 | ||||||
chr9:136226530
|
G | A | 1 | a0001c0001t0054g0294 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.429+244C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136226530 | ||||||
chr9:136226552
|
TC | T | 23 | a0001c0001t0002g0283a0001c0001t0006g0276a0001c0001t0006g0277others(20): Show | 25 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.429+221delG | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136226552 | ||||||
chr9:136226621
|
A | G | 1 | a0001c0001t0034g0208 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.429+153T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136226621 | ||||||
chr9:136226669
|
C | T | 3 | a0001c0004t0003g0053a0001c0004t0003g0054a0001c0004t0003g0055 | 3 | HG00639.hp1 HG00741.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.429+105G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136226669 | ||||||
chr9:136226704
|
C | T | 5 | a0001c0001t0001g0239a0001c0001t0004g0003a0001c0001t0004g0237others(2): Show | 9 | HG02523.hp2 HG02559.hp2 NA18948.hp1 others(6): Show |
intron_variant | MODIFIER | c.429+70G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136226704 | ||||||
chr9:136226760
|
C | T | 12 | a0001c0001t0023g0274a0001c0001t0023g0295a0001c0001t0023g0326others(9): Show | 13 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.429+14G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136226760 | ||||||
chr9:136226959
|
C | T | 1 | a0001c0004t0003g0125 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.329-85G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136226959 | ||||||
chr9:136226989
|
C | A | 1 | a0001c0004t0003g0165 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.329-115G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136226989 | ||||||
chr9:136227196
|
C | A | 71 | a0001c0001t0002g0283a0001c0001t0002g0320a0001c0001t0006g0276others(68): Show | 78 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.329-322G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136227196 | ||||||
chr9:136227351
|
G | A | 2 | a0001c0001t0031g0209a0001c0001t0031g0305 | 2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.329-477C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136227351 | ||||||
chr9:136227369
|
A | G | 88 | a0001c0001t0001g0030a0001c0001t0001g0221a0001c0001t0001g0239others(85): Show | 113 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.329-495T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136227369 | ||||||
chr9:136227377
|
C | A | 2 | a0004c0009t0030g0328a0004c0009t0030g0329 | 2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.329-503G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136227377 | ||||||
chr9:136227391
|
G | C | 1 | a0001c0023t0051g0322 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.329-517C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136227391 | ||||||
chr9:136227593
|
A | G | 1 | a0001c0002t0005g0148 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.329-719T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136227593 | ||||||
chr9:136227601
|
C | T | 1 | a0001c0001t0006g0285 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.329-727G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136227601 | ||||||
chr9:136227716
|
T | C | 2 | a0004c0009t0030g0328a0004c0009t0030g0329 | 2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.329-842A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136227716 | ||||||
chr9:136227765
|
A | C | 5 | a0001c0005t0010g0026a0001c0005t0010g0194a0001c0005t0010g0196others(2): Show | 6 | HG01167.hp1 HG01169.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.329-891T>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136227765 | ||||||
chr9:136227847
|
C | T | 8 | a0001c0001t0007g0027a0001c0001t0007g0028a0001c0001t0007g0029others(5): Show | 11 | HG01074.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.329-973G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136227847 | ||||||
chr9:136228032
|
G | T | 1 | a0002c0003t0002g0312 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.329-1158C>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136228032 | ||||||
chr9:136228033
|
T | G | 1 | a0002c0003t0002g0312 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.329-1159A>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136228033 | ||||||
chr9:136228045
|
C | T | 1 | a0001c0004t0003g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.329-1171G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136228045 | ||||||
chr9:136228125
|
C | G | 2 | a0001c0002t0019g0083a0001c0002t0019g0084 | 2 | NA18998.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.329-1251G>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136228125 | ||||||
chr9:136228149
|
T | C | 1 | a0001c0002t0026g0159 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.329-1275A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136228149 | ||||||
chr9:136228197
|
C | G | 102 | a0001c0001t0001g0030a0001c0001t0001g0221a0001c0001t0001g0239others(99): Show | 128 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.329-1323G>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136228197 | ||||||
chr9:136228259
|
A | G | 23 | a0001c0001t0002g0283a0001c0001t0006g0276a0001c0001t0006g0277others(20): Show | 25 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.329-1385T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136228259 | ||||||
chr9:136228318
|
A | G | 27 | a0001c0001t0002g0283a0001c0001t0006g0276a0001c0001t0006g0277others(24): Show | 29 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.329-1444T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136228318 | ||||||
chr9:136228330
|
C | T | 7 | a0001c0001t0023g0274a0001c0001t0023g0295a0001c0001t0023g0326others(4): Show | 7 | HG01243.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.329-1456G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136228330 | ||||||
chr9:136228381
|
A | G | 4 | a0001c0001t0042g0331a0001c0001t0042g0332a0001c0001t0101g0333others(1): Show | 5 | HG02165.hp1 HG03831.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.329-1507T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136228381 | ||||||
chr9:136228473
|
A | G | 12 | a0001c0001t0008g0191a0001c0001t0008g0192a0001c0001t0008g0193others(9): Show | 12 | HG01069.hp2 HG01106.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.329-1599T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136228473 | ||||||
chr9:136228615
|
C | T | 1 | a0001c0002t0001g0065 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.329-1741G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136228615 | ||||||
chr9:136228771
|
G | A | 1 | a0001c0002t0038g0160 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.329-1897C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136228771 | ||||||
chr9:136228835
|
C | A | 12 | a0001c0001t0008g0191a0001c0001t0008g0192a0001c0001t0008g0193others(9): Show | 12 | HG01069.hp2 HG01106.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.329-1961G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136228835 | ||||||
chr9:136228959
|
A | G | 8 | a0001c0001t0007g0027a0001c0001t0007g0028a0001c0001t0007g0029others(5): Show | 11 | HG01074.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.329-2085T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136228959 | ||||||
chr9:136228982
|
T | C | 88 | a0001c0001t0001g0030a0001c0001t0001g0221a0001c0001t0001g0239others(85): Show | 113 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.329-2108A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136228982 | ||||||
chr9:136229012
|
C | A | 2 | a0002c0003t0002g0247a0002c0003t0002g0254 | 2 | NA19004.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.329-2138G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136229012 | ||||||
chr9:136229146
|
C | T | 7 | a0001c0001t0023g0274a0001c0001t0023g0295a0001c0001t0023g0326others(4): Show | 7 | HG01243.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.329-2272G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136229146 | ||||||
chr9:136229148
|
C | T | 1 | a0001c0001t0018g0272 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.329-2274G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136229148 | ||||||
chr9:136229216
|
C | T | 3 | a0001c0001t0042g0331a0001c0001t0042g0332a0001c0001t0101g0333 | 3 | HG02165.hp1 HG03831.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.329-2342G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136229216 | ||||||
chr9:136229227
|
C | T | 2 | a0001c0001t0002g0320a0001c0001t0053g0319 | 2 | HG02027.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.329-2353G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136229227 | ||||||
chr9:136229265
|
G | A | 2 | a0001c0020t0003g0183a0007c0021t0045g0182 | 2 | HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.329-2391C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136229265 | ||||||
chr9:136229269
|
A | C | 8 | a0001c0001t0007g0027a0001c0001t0007g0028a0001c0001t0007g0029others(5): Show | 11 | HG01074.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.329-2395T>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136229269 | ||||||
chr9:136229312
|
C | T | 3 | a0001c0001t0042g0331a0001c0001t0042g0332a0001c0001t0101g0333 | 3 | HG02165.hp1 HG03831.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.329-2438G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136229312 | ||||||
chr9:136229506
|
A | G | 3 | a0001c0001t0042g0331a0001c0001t0042g0332a0001c0001t0101g0333 | 3 | HG02165.hp1 HG03831.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.329-2632T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136229506 | ||||||
chr9:136229515
|
A | T | 23 | a0001c0001t0002g0283a0001c0001t0006g0276a0001c0001t0006g0277others(20): Show | 25 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.329-2641T>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136229515 | ||||||
chr9:136229607
|
G | A | 9 | a0001c0001t0010g0037a0001c0001t0016g0296a0001c0001t0016g0297others(6): Show | 10 | HG01884.hp2 HG02280.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.329-2733C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136229607 | ||||||
chr9:136229751
|
C | A | 2 | a0001c0005t0004g0321a0001c0008t0059g0045 | 2 | HG02083.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.329-2877G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136229751 | ||||||
chr9:136229875
|
G | C | 23 | a0001c0001t0002g0283a0001c0001t0006g0276a0001c0001t0006g0277others(20): Show | 25 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.329-3001C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136229875 | ||||||
chr9:136229894
|
A | C | 188 | a0001c0001t0001g0030a0001c0001t0001g0221a0001c0001t0001g0239others(185): Show | 222 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.329-3020T>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136229894 | ||||||
chr9:136230018
|
C | A | 2 | a0001c0001t0031g0209a0001c0001t0031g0305 | 2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.329-3144G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136230018 | ||||||
chr9:136230075
|
T | C | 2 | a0001c0001t0031g0209a0001c0001t0031g0305 | 2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.329-3201A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136230075 | ||||||
chr9:136230218
|
G | A | 12 | a0001c0001t0008g0191a0001c0001t0008g0192a0001c0001t0008g0193others(9): Show | 12 | HG01069.hp2 HG01106.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.329-3344C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136230218 | ||||||
chr9:136230257
|
G | A | 1 | a0001c0002t0005g0040 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.329-3383C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136230257 | ||||||
chr9:136230265
|
G | A | 1 | a0001c0001t0054g0294 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.329-3391C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136230265 | ||||||
chr9:136230306
|
T | G | 8 | a0001c0001t0007g0027a0001c0001t0007g0028a0001c0001t0007g0029others(5): Show | 11 | HG01074.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.329-3432A>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136230306 | ||||||
chr9:136230322
|
C | T | 1 | a0001c0007t0003g0158 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.329-3448G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136230322 | ||||||
chr9:136230329
|
G | A | 10 | a0001c0001t0018g0187a0001c0001t0018g0189a0001c0001t0018g0272others(7): Show | 10 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.329-3455C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136230329 | ||||||
chr9:136230517
|
G | A | 88 | a0001c0001t0001g0030a0001c0001t0001g0221a0001c0001t0001g0239others(85): Show | 113 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.329-3643C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136230517 | ||||||
chr9:136230683
|
C | T | 1 | a0002c0003t0002g0258 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.329-3809G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136230683 | ||||||
chr9:136230701
|
G | A | 17 | a0001c0001t0002g0320a0001c0001t0008g0191a0001c0001t0008g0192others(14): Show | 17 | HG01069.hp2 HG01106.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.329-3827C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136230701 | ||||||
chr9:136230863
|
G | A | 2 | a0001c0020t0003g0183a0007c0021t0045g0182 | 2 | HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.329-3989C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136230863 | ||||||
chr9:136230892
|
C | G | 2 | a0001c0001t0002g0320a0001c0001t0053g0319 | 2 | HG02027.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.329-4018G>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136230892 | ||||||
chr9:136230936
|
T | C | 2 | a0001c0001t0031g0209a0001c0001t0031g0305 | 2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.329-4062A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136230936 | ||||||
chr9:136230966
|
G | A | 1 | a0001c0002t0005g0052 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.329-4092C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136230966 | ||||||
chr9:136231113
|
C | G | 10 | a0001c0001t0018g0187a0001c0001t0018g0189a0001c0001t0018g0272others(7): Show | 10 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.329-4239G>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231113 | ||||||
chr9:136231135
|
G | T | 1 | a0001c0002t0092g0121 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.329-4261C>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231135 | ||||||
chr9:136231150
|
C | T | 3 | a0001c0001t0042g0331a0001c0001t0042g0332a0001c0001t0101g0333 | 3 | HG02165.hp1 HG03831.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.329-4276G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231150 | ||||||
chr9:136231178
|
G | C | 1 | a0002c0003t0002g0255 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.329-4304C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231178 | ||||||
chr9:136231195
|
G | A | 1 | a0001c0001t0006g0285 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.329-4321C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231195 | ||||||
chr9:136231219
|
C | T | 1 | a0001c0002t0092g0121 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.329-4345G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231219 | ||||||
chr9:136231225
|
T | C | 1 | a0001c0002t0025g0153 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.329-4351A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231225 | ||||||
chr9:136231316
|
C | T | 10 | a0001c0001t0018g0187a0001c0001t0018g0189a0001c0001t0018g0272others(7): Show | 10 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.329-4442G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231316 | ||||||
chr9:136231585
|
T | C | 12 | a0001c0001t0008g0191a0001c0001t0008g0192a0001c0001t0008g0193others(9): Show | 12 | HG01069.hp2 HG01106.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.329-4711A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231585 | ||||||
chr9:136231629
|
C | A | 2 | a0001c0001t0002g0320a0001c0001t0053g0319 | 2 | HG02027.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.329-4755G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231629 | ||||||
chr9:136231794
|
C | T | 1 | a0001c0001t0057g0290 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.329-4920G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231794 | ||||||
chr9:136231853
|
C | T | 5 | a0001c0001t0002g0320a0001c0001t0042g0331a0001c0001t0042g0332others(2): Show | 5 | HG02027.hp2 HG02129.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.329-4979G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231853 | ||||||
chr9:136231868
|
GC | G | 7 | a0001c0001t0023g0274a0001c0001t0023g0295a0001c0001t0023g0326others(4): Show | 7 | HG01243.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.329-4995delG | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231868 | ||||||
chr9:136231870
|
AATCCGCC others(20): Show |
A | 2 | a0001c0001t0006g0281a0001c0001t0006g0282 | 2 | HG03710.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.329-5023_329-4997d others(29): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231870 | ||||||
chr9:136231871
|
A | C | 60 | a0001c0001t0002g0283a0001c0001t0002g0320a0001c0001t0006g0276others(57): Show | 65 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.329-4997T>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231871 | ||||||
chr9:136231883
|
C | T | 1 | a0001c0002t0005g0097 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.329-5009G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231883 | ||||||
chr9:136231888
|
C | T | 1 | a0001c0001t0063g0207 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.329-5014G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231888 | ||||||
chr9:136231902
|
A | G | 2 | a0001c0001t0006g0281a0001c0001t0006g0282 | 2 | HG03710.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.329-5028T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231902 | ||||||
chr9:136231915
|
C | A | 1 | a0002c0003t0002g0255 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.329-5041G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231915 | ||||||
chr9:136231924
|
TCTCCGCC others(2): Show |
T | 6 | a0001c0001t0013g0023a0001c0001t0013g0024a0001c0001t0013g0185others(3): Show | 8 | HG01496.hp2 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.329-5059_329-5051d others(11): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231924 | ||||||
chr9:136231931
|
CTCCTCCG others(2): Show |
C | 3 | a0001c0001t0034g0206a0001c0001t0034g0208a0001c0001t0063g0207 | 3 | HG02258.hp2 HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.329-5066_329-5058d others(11): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231931 | ||||||
chr9:136231940
|
A | T | 6 | a0001c0001t0013g0023a0001c0001t0013g0024a0001c0001t0013g0185others(3): Show | 8 | HG01496.hp2 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.329-5066T>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231940 | ||||||
chr9:136232057
|
C | T | 1 | a0001c0002t0082g0147 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.329-5183G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136232057 | ||||||
chr9:136232068
|
C | T | 10 | a0001c0001t0018g0187a0001c0001t0018g0189a0001c0001t0018g0272others(7): Show | 10 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.329-5194G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136232068 | ||||||
chr9:136232187
|
G | A | 3 | a0001c0001t0004g0234a0001c0001t0031g0209a0001c0001t0031g0305 | 3 | HG01943.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.329-5313C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136232187 | ||||||
chr9:136232244
|
G | A | 7 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0005g0114others(4): Show | 7 | HG01891.hp1 HG02451.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.329-5370C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136232244 | ||||||
chr9:136232260
|
A | G | 62 | a0001c0001t0002g0283a0001c0001t0002g0320a0001c0001t0006g0276others(59): Show | 67 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.329-5386T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136232260 | ||||||
chr9:136232286
|
C | T | 3 | a0001c0001t0008g0191a0001c0001t0008g0192a0001c0001t0008g0193 | 3 | HG01069.hp2 HG02602.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.329-5412G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136232286 | ||||||
chr9:136232302
|
A | C | 17 | a0001c0001t0002g0320a0001c0001t0008g0191a0001c0001t0008g0192others(14): Show | 17 | HG01069.hp2 HG01106.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.329-5428T>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136232302 | ||||||
chr9:136232338
|
C | T | 1 | a0002c0003t0002g0247 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.329-5464G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136232338 | ||||||
chr9:136232533
|
T | C | 1 | a0002c0003t0040g0245 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.329-5659A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136232533 | ||||||
chr9:136232706
|
G | A | 10 | a0001c0001t0008g0191a0001c0001t0008g0192a0001c0001t0008g0193others(7): Show | 10 | HG01069.hp2 HG01106.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.329-5832C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136232706 | ||||||
chr9:136232917
|
C | CA | 46 | a0001c0001t0007g0214a0001c0001t0007g0219a0001c0001t0008g0191others(43): Show | 50 | HG00140.hp2 HG00741.hp2 HG01106.hp2 others(47): Show |
intron_variant | MODIFIER | c.329-6044dupT | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136232917 | ||||||
chr9:136232917
|
CA | C | 20 | a0001c0001t0002g0283a0001c0001t0006g0276a0001c0001t0006g0277others(17): Show | 21 | HG00323.hp1 HG00408.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.329-6044delT | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136232917 | ||||||
chr9:136232934
|
A | G | 2 | a0001c0020t0003g0183a0007c0021t0045g0182 | 2 | HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.329-6060T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136232934 | ||||||
chr9:136232935
|
A | AG | 84 | a0001c0001t0001g0030a0001c0001t0001g0221a0001c0001t0001g0239others(81): Show | 109 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.329-6062_329-6061i others(3): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136232935 | ||||||
chr9:136232935
|
A | G | 1 | a0002c0003t0002g0246 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.329-6061T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136232935 | ||||||
chr9:136232943
|
A | C | 10 | a0001c0001t0018g0187a0001c0001t0018g0189a0001c0001t0018g0272others(7): Show | 10 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.329-6069T>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136232943 | ||||||
chr9:136232960
|
A | G | 3 | a0001c0001t0094g0266a0001c0001t0095g0215a0001c0001t0098g0216 | 3 | HG01261.hp2 HG02622.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.329-6086T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136232960 | ||||||
chr9:136232963
|
A | G | 1 | a0001c0023t0051g0322 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.329-6089T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136232963 | ||||||
chr9:136232968
|
G | A | 1 | a0001c0002t0001g0124 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.329-6094C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136232968 | ||||||
chr9:136232975
|
G | C | 1 | a0001c0001t0034g0206 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.329-6101C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136232975 | ||||||
chr9:136233010
|
C | A | 54 | a0001c0001t0002g0283a0001c0001t0002g0320a0001c0001t0006g0276others(51): Show | 56 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.329-6136G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136233010 | ||||||
chr9:136233284
|
G | A | 1 | a0001c0004t0044g0129 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.329-6410C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136233284 | ||||||
chr9:136233320
|
G | T | 7 | a0001c0001t0023g0274a0001c0001t0023g0295a0001c0001t0023g0326others(4): Show | 7 | HG01243.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.329-6446C>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136233320 | ||||||
chr9:136233355
|
G | T | 1 | a0001c0001t0012g0235 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.329-6481C>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136233355 | ||||||
chr9:136233433
|
T | C | 1 | a0002c0003t0087g0256 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.329-6559A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136233433 | ||||||
chr9:136233503
|
T | C | 2 | a0001c0001t0023g0274a0001c0001t0023g0295 | 2 | HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.329-6629A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136233503 | ||||||
chr9:136233570
|
C | T | 5 | a0001c0005t0010g0026a0001c0005t0010g0194a0001c0005t0010g0196others(2): Show | 6 | HG01167.hp1 HG01169.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.329-6696G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136233570 | ||||||
chr9:136233703
|
C | T | 10 | a0001c0001t0018g0187a0001c0001t0018g0189a0001c0001t0018g0272others(7): Show | 10 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.329-6829G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136233703 | ||||||
chr9:136233780
|
C | T | 1 | a0008c0018t0001g0181 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.329-6906G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136233780 | ||||||
chr9:136233819
|
T | C | 17 | a0001c0001t0002g0320a0001c0001t0008g0191a0001c0001t0008g0192others(14): Show | 17 | HG01069.hp2 HG01106.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.329-6945A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136233819 | ||||||
chr9:136233850
|
T | G | 5 | a0001c0001t0006g0278a0001c0001t0006g0279a0001c0001t0006g0280others(2): Show | 6 | HG02135.hp2 NA18961.hp2 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.329-6976A>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136233850 | ||||||
chr9:136233983
|
G | A | 4 | a0001c0001t0031g0209a0001c0001t0031g0305a0001c0020t0003g0183others(1): Show | 4 | HG02723.hp2 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.329-7109C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136233983 | ||||||
chr9:136234034
|
AGGACAAA others(36): Show |
A | 7 | a0001c0001t0031g0209a0001c0001t0031g0305a0001c0002t0014g0010others(4): Show | 8 | HG01109.hp2 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.329-7203_329-7161d others(45): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234034 | ||||||
chr9:136234044
|
T | C | 321 | a0001c0001t0001g0030a0001c0001t0001g0221a0001c0001t0001g0239others(318): Show | 379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.329-7170A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234044 | ||||||
chr9:136234094
|
G | C | 1 | a0001c0002t0005g0090 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.329-7220C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234094 | ||||||
chr9:136234095
|
A | T | 2 | a0001c0020t0003g0183a0007c0021t0045g0182 | 2 | HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.329-7221T>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234095 | ||||||
chr9:136234136
|
C | T | 1 | a0001c0002t0001g0086 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.329-7262G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234136 | ||||||
chr9:136234214
|
T | C | 2 | a0004c0009t0030g0328a0004c0009t0030g0329 | 2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.329-7340A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234214 | ||||||
chr9:136234215
|
G | A | 1 | a0001c0001t0007g0219 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.329-7341C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234215 | ||||||
chr9:136234219
|
G | A | 7 | a0001c0001t0023g0274a0001c0001t0023g0295a0001c0001t0023g0326others(4): Show | 7 | HG01243.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.329-7345C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234219 | ||||||
chr9:136234231
|
G | A | 1 | a0001c0001t0004g0257 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.329-7357C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234231 | ||||||
chr9:136234247
|
C | G | 17 | a0001c0001t0002g0320a0001c0001t0008g0191a0001c0001t0008g0192others(14): Show | 17 | HG01069.hp2 HG01106.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.329-7373G>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234247 | ||||||
chr9:136234265
|
A | T | 23 | a0001c0001t0002g0283a0001c0001t0006g0276a0001c0001t0006g0277others(20): Show | 25 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.329-7391T>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234265 | ||||||
chr9:136234274
|
C | T | 173 | a0001c0001t0001g0030a0001c0001t0001g0221a0001c0001t0001g0239others(170): Show | 206 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.329-7400G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234274 | ||||||
chr9:136234297
|
G | A | 3 | a0001c0001t0042g0331a0001c0001t0042g0332a0001c0001t0101g0333 | 3 | HG02165.hp1 HG03831.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.329-7423C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234297 | ||||||
chr9:136234327
|
C | T | 3 | a0001c0001t0004g0223a0001c0001t0025g0224a0001c0001t0065g0225 | 3 | HG02602.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.329-7453G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234327 | ||||||
chr9:136234349
|
G | T | 2 | a0001c0002t0001g0011a0001c0002t0001g0059 | 3 | HG01258.hp1 HG01993.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.329-7475C>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234349 | ||||||
chr9:136234448
|
G | A | 2 | a0001c0001t0023g0274a0001c0001t0023g0295 | 2 | HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.329-7574C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234448 | ||||||
chr9:136234451
|
C | A | 2 | a0001c0002t0055g0157a0001c0002t0092g0121 | 2 | HG02451.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.329-7577G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234451 | ||||||
chr9:136234587
|
C | A | 1 | a0001c0002t0001g0086 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.329-7713G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234587 | ||||||
chr9:136234723
|
G | GGCTTGGG others(70): Show |
1 | a0001c0004t0003g0109 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.329-7850_329-7849i others(79): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | ||||||
chr9:136234723
|
G | GGCTTGGG others(147): Show |
1 | a0004c0009t0030g0328 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.329-7850_329-7849i others(156): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | ||||||
chr9:136234723
|
G | GGCTTGGG others(301): Show |
1 | a0004c0009t0030g0329 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.329-7850_329-7849i others(310): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | ||||||
chr9:136234723
|
G | GGCTTGGG others(70): Show |
1 | a0001c0002t0014g0042 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.329-7850_329-7849i others(79): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | ||||||
chr9:136234723
|
G | GGCTTGGG others(147): Show |
1 | a0001c0008t0059g0045 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.329-7850_329-7849i others(156): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | ||||||
chr9:136234723
|
G | GGCTTGGG others(148): Show |
1 | a0001c0002t0005g0104 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.329-7850_329-7849i others(157): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | ||||||
chr9:136234723
|
G | GGCTTGGG others(70): Show |
73 | a0001c0001t0001g0030a0001c0001t0001g0239a0001c0001t0001g0313others(70): Show | 91 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.329-7850_329-7849i others(79): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | ||||||
chr9:136234723
|
G | GGCTTGGG others(147): Show |
26 | a0001c0002t0001g0006a0001c0002t0001g0062a0001c0002t0001g0063others(23): Show | 33 | HG00140.hp2 HG00642.hp1 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.329-7850_329-7849i others(156): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | ||||||
chr9:136234723
|
G | GGCTTGGG others(224): Show |
9 | a0001c0002t0001g0065a0001c0002t0001g0066a0001c0002t0001g0067others(6): Show | 9 | HG02698.hp2 HG03492.hp2 HG03654.hp1 others(6): Show |
intron_variant | MODIFIER | c.329-7850_329-7849i others(233): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | ||||||
chr9:136234723
|
G | GGCTTGGG others(609): Show |
1 | a0001c0002t0001g0059 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.329-7850_329-7849i others(618): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | ||||||
chr9:136234723
|
G | GGCTTGGG others(686): Show |
1 | a0001c0002t0001g0011 | 2 | HG01993.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.329-7850_329-7849i others(695): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | ||||||
chr9:136234723
|
G | GGCTTGGG others(224): Show |
4 | a0001c0002t0001g0014a0001c0002t0001g0058a0001c0002t0001g0179others(1): Show | 5 | HG00099.hp2 HG02723.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.329-7850_329-7849i others(233): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | ||||||
chr9:136234723
|
G | GGCTTGGG others(302): Show |
1 | a0001c0002t0005g0105 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.329-7850_329-7849i others(311): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | ||||||
chr9:136234723
|
G | GGCTTGGG others(301): Show |
2 | a0001c0002t0020g0175a0001c0002t0021g0176 | 2 | NA18954.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.329-7850_329-7849i others(310): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | ||||||
chr9:136234723
|
G | GGCTTGGG others(378): Show |
3 | a0001c0002t0001g0096a0001c0002t0002g0174a0001c0002t0005g0095 | 3 | HG00408.hp1 NA18964.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.329-7850_329-7849i others(387): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | ||||||
chr9:136234723
|
G | GGCTTGGG others(302): Show |
1 | a0001c0002t0001g0072 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.329-7850_329-7849i others(311): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | ||||||
chr9:136234723
|
G | GGCTTGGG others(301): Show |
1 | a0001c0001t0031g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.329-7850_329-7849i others(310): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | ||||||
chr9:136234723
|
G | GGCTTGGG others(840): Show |
1 | a0001c0001t0031g0305 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.329-7850_329-7849i others(849): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | ||||||
chr9:136234723
|
G | GGCTTGGG others(147): Show |
15 | a0001c0001t0012g0036a0001c0001t0012g0222a0001c0001t0012g0235others(12): Show | 17 | HG00280.hp1 HG00558.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.329-7850_329-7849i others(156): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | ||||||
chr9:136234723
|
G | GGCTTGGG others(224): Show |
2 | a0001c0002t0001g0012a0001c0002t0001g0087 | 3 | HG01943.hp2 HG02004.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.329-7850_329-7849i others(233): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | ||||||
chr9:136234723
|
G | GGCTTGGG others(224): Show |
2 | a0001c0001t0001g0221a0001c0004t0003g0145 | 2 | HG03225.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.329-7850_329-7849i others(233): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | ||||||
chr9:136234723
|
G | GGCTTGGG others(455): Show |
2 | a0001c0001t0042g0331a0001c0001t0101g0333 | 2 | HG02165.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.329-7850_329-7849i others(464): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | ||||||
chr9:136234723
|
G | GGCTTGGG others(456): Show |
1 | a0001c0001t0042g0332 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.329-7850_329-7849i others(465): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | ||||||
chr9:136234723
|
G | GGCTTGGG others(147): Show |
1 | a0001c0001t0023g0326 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.329-7850_329-7849i others(156): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | ||||||
chr9:136234723
|
G | GGCTTGGG others(70): Show |
1 | a0001c0001t0016g0304 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.329-7850_329-7849i others(79): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | ||||||
chr9:136234723
|
G | GGCTTGGG others(147): Show |
1 | a0006c0022t0069g0299 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.329-7850_329-7849i others(156): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | ||||||
chr9:136234723
|
G | GGCTTGGG others(71): Show |
1 | a0001c0001t0004g0237 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.329-7850_329-7849i others(80): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | ||||||
chr9:136234723
|
G | GGCTTGGG others(73): Show |
3 | a0001c0002t0001g0017a0001c0002t0005g0130a0001c0002t0036g0057 | 4 | HG00423.hp1 NA18940.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.329-7850_329-7849i others(82): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | ||||||
chr9:136234723
|
G | GGCTTGGG others(150): Show |
6 | a0001c0002t0001g0086a0001c0002t0019g0083a0001c0002t0019g0084others(3): Show | 6 | HG00621.hp1 HG00673.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.329-7850_329-7849i others(159): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | ||||||
chr9:136234723
|
G | GGCTTGGG others(150): Show |
1 | a0001c0001t0057g0290 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.329-7850_329-7849i others(159): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | ||||||
chr9:136234723
|
G | GGCTTGGG others(227): Show |
2 | a0001c0001t0006g0280a0001c0002t0091g0082 | 2 | HG02135.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.329-7850_329-7849i others(236): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | ||||||
chr9:136234723
|
G | GGCTTGGG others(304): Show |
8 | a0001c0001t0006g0277a0001c0001t0006g0288a0001c0001t0006g0291others(5): Show | 9 | HG00408.hp2 HG00609.hp1 HG04199.hp2 others(6): Show |
intron_variant | MODIFIER | c.329-7850_329-7849i others(313): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | ||||||
chr9:136234723
|
G | GGCTTGGG others(381): Show |
5 | a0001c0001t0006g0279a0001c0001t0006g0285a0001c0001t0006g0286others(2): Show | 5 | HG00323.hp1 HG02965.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.329-7850_329-7849i others(390): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | ||||||
chr9:136234723
|
G | GGCTTGGG others(458): Show |
1 | a0001c0001t0006g0276 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.329-7850_329-7849i others(467): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | ||||||
chr9:136234723
|
G | GGCTTGGG others(535): Show |
1 | a0001c0001t0006g0278 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.329-7850_329-7849i others(544): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | ||||||
chr9:136234723
|
G | GGCTTGGG others(150): Show |
3 | a0001c0001t0006g0281a0001c0002t0001g0019a0001c0002t0005g0040 | 4 | HG02135.hp1 HG03710.hp2 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.329-7850_329-7849i others(159): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | ||||||
chr9:136234723
|
G | GGCTTGGG others(227): Show |
1 | a0001c0001t0015g0025 | 2 | NA18998.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.329-7850_329-7849i others(236): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | ||||||
chr9:136234723
|
G | GGCTTGGG others(304): Show |
2 | a0001c0001t0002g0283a0001c0001t0006g0282 | 2 | HG03942.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.329-7850_329-7849i others(313): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | ||||||
chr9:136234723
|
G | GGCTTGGG others(612): Show |
1 | a0001c0001t0006g0284 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.329-7850_329-7849i others(621): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | ||||||
chr9:136234723
|
G | GGCTTGGG others(228): Show |
1 | a0001c0001t0062g0190 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.329-7850_329-7849i others(237): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | ||||||
chr9:136234723
|
GGCTTGGG others(70): Show |
G | 26 | a0001c0001t0002g0320a0001c0001t0008g0191a0001c0001t0008g0199others(23): Show | 28 | HG00741.hp2 HG01261.hp2 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.329-7926_329-7850d others(79): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | ||||||
chr9:136234734
|
A | AAGGCTGG others(70): Show |
1 | a0001c0002t0001g0124 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.329-7861_329-7860i others(79): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234734 | ||||||
chr9:136234734
|
A | AAGGCTGG others(70): Show |
4 | a0001c0002t0014g0041a0001c0005t0004g0321a0001c0020t0003g0183others(1): Show | 4 | HG02083.hp1 HG02723.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.329-7861_329-7860i others(79): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234734 | ||||||
chr9:136234749
|
A | AAGGCCCC others(70): Show |
14 | a0001c0002t0001g0048a0001c0002t0001g0051a0001c0002t0001g0152others(11): Show | 14 | HG00621.hp2 HG01168.hp2 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.329-7952_329-7876d others(79): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234749 | ||||||
chr9:136234749
|
A | AAGGCCCC others(301): Show |
1 | a0001c0002t0005g0049 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.329-7876_329-7875i others(310): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234749 | ||||||
chr9:136234749
|
A | G | 268 | a0001c0001t0001g0030a0001c0001t0001g0221a0001c0001t0001g0239others(265): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.329-7875T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234749 | ||||||
chr9:136234752
|
G | GCCCCCCA others(148): Show |
1 | a0001c0002t0001g0107 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.329-7879_329-7878i others(157): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234752 | ||||||
chr9:136234769
|
C | T | 5 | a0001c0001t0010g0037a0001c0001t0016g0296a0001c0001t0016g0297others(2): Show | 6 | HG01884.hp2 HG02717.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.329-7895G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234769 | ||||||
chr9:136234770
|
G | A | 6 | a0001c0001t0008g0192a0001c0001t0008g0193a0001c0002t0014g0010others(3): Show | 7 | HG01069.hp2 HG01109.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.329-7896C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234770 | ||||||
chr9:136234770
|
G | GCCCGCCC others(148): Show |
1 | a0001c0006t0009g0168 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.329-7897_329-7896i others(157): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234770 | ||||||
chr9:136234770
|
G | GCCCGCCC others(70): Show |
1 | a0002c0003t0040g0245 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.329-7897_329-7896i others(79): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234770 | ||||||
chr9:136234770
|
G | GCCCGCCC others(70): Show |
1 | a0001c0023t0051g0322 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.329-7897_329-7896i others(79): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234770 | ||||||
chr9:136234773
|
C | T | 2 | a0001c0002t0075g0123a0001c0002t0083g0122 | 2 | HG02145.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.329-7899G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234773 | ||||||
chr9:136234792
|
C | CACACCCC others(70): Show |
1 | a0002c0003t0093g0300 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.329-7919_329-7918i others(79): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234792 | ||||||
chr9:136234811
|
A | AAGGCTGG others(224): Show |
1 | a0001c0019t0071g0273 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.329-7938_329-7937i others(233): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234811 | ||||||
chr9:136234811
|
A | AAGGCTGG others(224): Show |
5 | a0001c0001t0007g0028a0001c0001t0007g0211a0001c0001t0007g0213others(2): Show | 6 | HG02055.hp2 HG02257.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.329-7938_329-7937i others(233): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234811 | ||||||
chr9:136234811
|
A | AAGGCTGG others(378): Show |
1 | a0001c0001t0007g0027 | 2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.329-7938_329-7937i others(387): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234811 | ||||||
chr9:136234811
|
A | AAGGCTGG others(455): Show |
1 | a0001c0001t0007g0220 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.329-7938_329-7937i others(464): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234811 | ||||||
chr9:136234811
|
A | AAGGCTGG others(378): Show |
1 | a0001c0001t0007g0029 | 2 | HG01074.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.329-7938_329-7937i others(387): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234811 | ||||||
chr9:136234811
|
A | G | 3 | a0001c0001t0013g0185a0004c0009t0030g0329a0006c0022t0069g0299 | 3 | HG01884.hp1 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.329-7937T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234811 | ||||||
chr9:136234812
|
A | G | 1 | a0001c0002t0092g0121 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.329-7938T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234812 | ||||||
chr9:136234826
|
G | A | 3 | a0001c0002t0001g0077a0001c0002t0079g0108a0001c0006t0009g0015 | 4 | HG01106.hp2 HG02015.hp2 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.329-7952C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234826 | ||||||
chr9:136234826
|
G | GAGGCCCC others(147): Show |
1 | a0001c0005t0010g0026 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.329-7953_329-7952i others(156): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234826 | ||||||
chr9:136234826
|
G | GAGGCCCC others(224): Show |
3 | a0001c0005t0010g0196a0001c0005t0010g0197a0001c0005t0068g0195 | 3 | HG02486.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.329-7953_329-7952i others(233): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234826 | ||||||
chr9:136234847
|
G | GCCCGCCC others(70): Show |
2 | a0001c0001t0022g0267a0001c0001t0022g0268 | 2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.329-7974_329-7973i others(79): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234847 | ||||||
chr9:136234847
|
G | GCCCGCCC others(224): Show |
1 | a0001c0001t0023g0274 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.329-7974_329-7973i others(233): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234847 | ||||||
chr9:136234847
|
G | GCCCGCCC others(301): Show |
1 | a0001c0001t0023g0295 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.329-7974_329-7973i others(310): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234847 | ||||||
chr9:136234907
|
T | C | 3 | a0001c0001t0042g0331a0001c0001t0042g0332a0001c0001t0101g0333 | 3 | HG02165.hp1 HG03831.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.329-8033A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234907 | ||||||
chr9:136234926
|
C | T | 2 | a0001c0001t0034g0206a0001c0001t0063g0207 | 2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.329-8052G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234926 | ||||||
chr9:136234927
|
C | T | 16 | a0001c0001t0002g0320a0001c0001t0018g0187a0001c0001t0022g0267others(13): Show | 16 | HG00741.hp2 HG01243.hp1 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.329-8053G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234927 | ||||||
chr9:136234943
|
C | T | 33 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0058others(30): Show | 36 | HG00099.hp2 HG00140.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.329-8069G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234943 | ||||||
chr9:136235038
|
T | C | 2 | a0001c0001t0034g0208a0001c0001t0063g0207 | 2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.329-8164A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136235038 | ||||||
chr9:136235057
|
G | A | 1 | a0001c0019t0071g0273 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.329-8183C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136235057 | ||||||
chr9:136235201
|
C | T | 1 | a0002c0003t0040g0245 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.329-8327G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136235201 | ||||||
chr9:136235289
|
G | C | 10 | a0001c0001t0023g0295a0001c0001t0034g0206a0001c0002t0005g0114others(7): Show | 10 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.329-8415C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136235289 | ||||||
chr9:136235474
|
G | A | 1 | a0001c0001t0002g0320 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.329-8600C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136235474 | ||||||
chr9:136235598
|
A | T | 1 | a0002c0003t0040g0245 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.329-8724T>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136235598 | ||||||
chr9:136235628
|
G | A | 1 | a0001c0001t0101g0333 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.329-8754C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136235628 | ||||||
chr9:136235643
|
G | T | 12 | a0001c0001t0018g0187a0001c0001t0018g0189a0001c0001t0022g0267others(9): Show | 12 | HG00741.hp2 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.329-8769C>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136235643 | ||||||
chr9:136235649
|
T | G | 1 | a0001c0008t0059g0045 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.329-8775A>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136235649 | ||||||
chr9:136235719
|
G | A | 1 | a0001c0001t0031g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.329-8845C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136235719 | ||||||
chr9:136235720
|
C | A | 85 | a0001c0001t0001g0030a0001c0001t0001g0221a0001c0001t0001g0239others(82): Show | 109 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.329-8846G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136235720 | ||||||
chr9:136235721
|
G | A | 3 | a0001c0001t0023g0326a0001c0001t0024g0325a0001c0001t0100g0327 | 3 | HG02258.hp1 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.329-8847C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136235721 | ||||||
chr9:136235750
|
C | T | 5 | a0001c0001t0006g0278a0001c0001t0006g0279a0001c0001t0006g0280others(2): Show | 6 | HG02135.hp2 NA18961.hp2 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.329-8876G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136235750 | ||||||
chr9:136235761
|
A | G | 5 | a0001c0002t0014g0010a0001c0002t0014g0041a0001c0002t0014g0042others(2): Show | 6 | HG01109.hp2 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.329-8887T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136235761 | ||||||
chr9:136235763
|
A | C | 1 | a0001c0001t0024g0325 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.329-8889T>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136235763 | ||||||
chr9:136235832
|
G | A | 2 | a0001c0020t0003g0183a0007c0021t0045g0182 | 2 | HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.329-8958C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136235832 | ||||||
chr9:136235876
|
A | G | 1 | a0001c0008t0081g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.329-9002T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136235876 | ||||||
chr9:136235912
|
T | G | 1 | a0001c0001t0100g0327 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.329-9038A>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136235912 | ||||||
chr9:136236150
|
G | C | 1 | a0001c0005t0004g0321 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.329-9276C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236150 | ||||||
chr9:136236195
|
T | C | 2 | a0001c0005t0004g0321a0001c0008t0059g0045 | 2 | HG02083.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.328+9281A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236195 | ||||||
chr9:136236221
|
A | G | 19 | a0001c0001t0008g0191a0001c0001t0008g0192a0001c0001t0008g0193others(16): Show | 19 | HG00741.hp2 HG01069.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.328+9255T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236221 | ||||||
chr9:136236236
|
G | A | 2 | a0001c0001t0001g0239a0001c0001t0004g0240 | 2 | NA18975.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.328+9240C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236236 | ||||||
chr9:136236243
|
G | A | 12 | a0001c0001t0018g0187a0001c0001t0018g0189a0001c0001t0018g0272others(9): Show | 12 | HG00741.hp2 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.328+9233C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236243 | ||||||
chr9:136236268
|
G | T | 1 | a0001c0005t0008g0204 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.328+9208C>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236268 | ||||||
chr9:136236345
|
A | ATGT | 38 | a0001c0001t0002g0320a0001c0001t0008g0191a0001c0001t0008g0192others(35): Show | 42 | HG01069.hp2 HG01106.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.328+9130_328+9131i others(5): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236345 | ||||||
chr9:136236358
|
C | T | 3 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0005g0114 | 3 | HG01891.hp1 HG02622.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.328+9118G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236358 | ||||||
chr9:136236468
|
G | A | 17 | a0001c0001t0008g0191a0001c0001t0008g0192a0001c0001t0008g0193others(14): Show | 18 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.328+9008C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236468 | ||||||
chr9:136236495
|
C | T | 5 | a0001c0002t0014g0010a0001c0002t0014g0041a0001c0002t0014g0042others(2): Show | 6 | HG01109.hp2 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.328+8981G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236495 | ||||||
chr9:136236647
|
G | A | 1 | a0001c0001t0034g0208 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.328+8829C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236647 | ||||||
chr9:136236711
|
G | A | 1 | a0001c0007t0003g0164 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.328+8765C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236711 | ||||||
chr9:136236723
|
T | C | 71 | a0001c0001t0002g0283a0001c0001t0002g0320a0001c0001t0006g0276others(68): Show | 77 | HG00323.hp1 HG00609.hp1 HG00741.hp2 others(74): Show |
intron_variant | MODIFIER | c.328+8753A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236723 | ||||||
chr9:136236738
|
G | A | 1 | a0001c0004t0003g0165 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.328+8738C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236738 | ||||||
chr9:136236785
|
G | A | 32 | a0001c0002t0001g0006a0001c0002t0001g0013a0001c0002t0001g0014others(29): Show | 41 | HG00408.hp1 HG00558.hp1 HG02015.hp1 others(38): Show |
intron_variant | MODIFIER | c.328+8691C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236785 | ||||||
chr9:136236789
|
G | A | 2 | a0001c0005t0010g0196a0001c0005t0010g0197 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.328+8687C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236789 | ||||||
chr9:136236833
|
A | G | 2 | a0001c0001t0001g0221a0001c0001t0007g0220 | 2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.328+8643T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236833 | ||||||
chr9:136236901
|
AGCCCGTC others(43): Show |
A | 1 | a0001c0004t0011g0169 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.328+8525_328+8574d others(52): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236901 | ||||||
chr9:136236905
|
C | T | 22 | a0001c0001t0002g0283a0001c0001t0006g0276a0001c0001t0006g0277others(19): Show | 24 | HG00323.hp1 HG00609.hp1 HG02135.hp2 others(21): Show |
intron_variant | MODIFIER | c.328+8571G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236905 | ||||||
chr9:136236966
|
ACACCTGG others(20): Show |
A | 1 | a0001c0005t0004g0321 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.328+8483_328+8509d others(29): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236966 | ||||||
chr9:136236978
|
TGTCCTGG others(20): Show |
T | 1 | a0001c0002t0001g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.328+8471_328+8497d others(29): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236978 | ||||||
chr9:136237016
|
G | A | 2 | a0001c0005t0001g0205a0008c0018t0001g0181 | 2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.328+8460C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237016 | ||||||
chr9:136237032
|
T | TGTCCTGG others(20): Show |
1 | a0002c0003t0002g0264 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.328+8443_328+8444i others(29): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237032 | ||||||
chr9:136237032
|
T | TGTCCTGT others(16): Show |
1 | a0001c0026t0004g0330 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.328+8421_328+8443d others(25): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237032 | ||||||
chr9:136237032
|
TGTCCTGT others(16): Show |
T | 1 | a0002c0003t0002g0314 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.328+8421_328+8443d others(25): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237032 | ||||||
chr9:136237125
|
A | ATCCTGGG others(20): Show |
2 | a0001c0001t0006g0276a0001c0001t0006g0277 | 2 | HG03704.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.328+8324_328+8350d others(29): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237125 | ||||||
chr9:136237138
|
G | A | 1 | a0001c0001t0006g0291 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.328+8338C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237138 | ||||||
chr9:136237278
|
C | T | 2 | a0001c0001t0012g0036a0001c0001t0012g0222 | 3 | HG01074.hp1 HG01167.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.328+8198G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237278 | ||||||
chr9:136237293
|
TCACCTGG others(170): Show |
T | 2 | a0001c0001t0012g0036a0001c0001t0012g0222 | 3 | HG01074.hp1 HG01167.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.328+8006_328+8182d others(2): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237293 | ||||||
chr9:136237405
|
T | C | 2 | a0001c0001t0031g0209a0001c0004t0003g0109 | 2 | HG02004.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.328+8071A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237405 | ||||||
chr9:136237433
|
GTCCTGTG others(16): Show |
G | 1 | a0001c0004t0043g0056 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.328+8020_328+8042d others(25): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237433 | ||||||
chr9:136237456
|
A | ATCCTGTG others(20): Show |
1 | a0001c0002t0001g0111 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.328+8019_328+8020i others(29): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237456 | ||||||
chr9:136237456
|
A | ATCCTGTG others(20): Show |
87 | a0001c0001t0008g0199a0001c0001t0008g0201a0001c0001t0008g0203others(84): Show | 96 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.328+7993_328+8019d others(29): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237456 | ||||||
chr9:136237456
|
A | ATCCTGTG others(47): Show |
9 | a0001c0001t0013g0023a0001c0001t0013g0024a0001c0001t0013g0185others(6): Show | 11 | HG01496.hp2 HG02258.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.328+7966_328+8019d others(56): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237456 | ||||||
chr9:136237456
|
A | ATCCTGTG others(74): Show |
3 | a0001c0001t0008g0191a0001c0001t0008g0192a0001c0001t0008g0193 | 3 | HG01069.hp2 HG02602.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.328+7939_328+8019d others(83): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237456 | ||||||
chr9:136237456
|
A | G | 1 | a0001c0002t0025g0110 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.328+8020T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237456 | ||||||
chr9:136237456
|
ATCCTGTG others(20): Show |
A | 72 | a0001c0001t0001g0221a0001c0001t0001g0313a0001c0001t0004g0257others(69): Show | 89 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.328+7993_328+8019d others(29): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237456 | ||||||
chr9:136237456
|
ATCCTGTG others(47): Show |
A | 24 | a0001c0001t0001g0030a0001c0001t0001g0239a0001c0001t0004g0003others(21): Show | 32 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.328+7966_328+8019d others(56): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237456 | ||||||
chr9:136237492
|
CGGCG | C | 2 | a0001c0001t0012g0036a0001c0001t0012g0222 | 3 | HG01074.hp1 HG01167.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.328+7980_328+7983d others(6): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237492 | ||||||
chr9:136237495
|
C | T | 1 | a0001c0001t0016g0296 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.328+7981G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237495 | ||||||
chr9:136237510
|
G | A | 2 | a0001c0001t0012g0036a0001c0001t0012g0222 | 3 | HG01074.hp1 HG01167.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.328+7966C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237510 | ||||||
chr9:136237519
|
C | T | 1 | a0001c0005t0004g0321 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.328+7957G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237519 | ||||||
chr9:136237524
|
A | ACACCTGG others(97): Show |
1 | a0001c0017t0013g0180 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.328+7951_328+7952i others(106): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237524 | ||||||
chr9:136237524
|
ACACCTGG others(43): Show |
A | 1 | a0001c0002t0073g0170 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.328+7902_328+7951d others(52): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237524 | ||||||
chr9:136237545
|
CCACACCT others(16): Show |
C | 10 | a0001c0001t0018g0187a0001c0001t0018g0189a0001c0001t0018g0272others(7): Show | 10 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.328+7908_328+7930d others(25): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237545 | ||||||
chr9:136237568
|
G | C | 62 | a0001c0001t0002g0283a0001c0001t0002g0320a0001c0001t0006g0276others(59): Show | 68 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(65): Show |
intron_variant | MODIFIER | c.328+7908C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237568 | ||||||
chr9:136237569
|
C | T | 23 | a0001c0001t0002g0320a0001c0001t0008g0191a0001c0001t0008g0192others(20): Show | 24 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.328+7907G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237569 | ||||||
chr9:136237610
|
A | G | 1 | a0001c0017t0013g0180 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.328+7866T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237610 | ||||||
chr9:136237695
|
C | T | 7 | a0001c0002t0014g0010a0001c0002t0014g0041a0001c0002t0014g0042others(4): Show | 8 | HG01109.hp2 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.328+7781G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237695 | ||||||
chr9:136237698
|
C | T | 9 | a0001c0001t0013g0023a0001c0001t0013g0024a0001c0001t0013g0185others(6): Show | 11 | HG01496.hp2 HG02258.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.328+7778G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237698 | ||||||
chr9:136237720
|
G | A | 1 | a0001c0001t0031g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.328+7756C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237720 | ||||||
chr9:136237795
|
C | T | 3 | a0001c0004t0003g0053a0001c0004t0003g0054a0001c0004t0003g0055 | 3 | HG00639.hp1 HG00741.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.328+7681G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237795 | ||||||
chr9:136237914
|
G | A | 2 | a0001c0001t0001g0221a0001c0001t0007g0220 | 2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.328+7562C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237914 | ||||||
chr9:136237973
|
A | G | 1 | a0001c0001t0034g0206 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.328+7503T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237973 | ||||||
chr9:136237974
|
T | C | 1 | a0001c0001t0008g0193 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.328+7502A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237974 | ||||||
chr9:136238129
|
G | A | 1 | a0001c0023t0051g0322 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.328+7347C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136238129 | ||||||
chr9:136238244
|
C | T | 1 | a0001c0001t0015g0275 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.328+7232G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136238244 | ||||||
chr9:136238252
|
C | G | 5 | a0001c0001t0094g0266a0001c0001t0095g0215a0001c0001t0098g0216others(2): Show | 5 | HG01261.hp2 HG02622.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.328+7224G>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136238252 | ||||||
chr9:136238380
|
G | A | 1 | a0001c0001t0031g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.328+7096C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136238380 | ||||||
chr9:136238392
|
CCAAA | C | 5 | a0001c0005t0010g0026a0001c0005t0010g0194a0001c0005t0010g0196others(2): Show | 6 | HG01167.hp1 HG01169.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.328+7080_328+7083d others(6): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136238392 | ||||||
chr9:136238489
|
G | C | 10 | a0001c0001t0018g0187a0001c0001t0018g0189a0001c0001t0018g0272others(7): Show | 10 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.328+6987C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136238489 | ||||||
chr9:136238518
|
G | A | 88 | a0001c0001t0001g0030a0001c0001t0001g0239a0001c0001t0001g0313others(85): Show | 113 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.328+6958C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136238518 | ||||||
chr9:136238536
|
G | A | 25 | a0001c0001t0001g0030a0001c0001t0001g0239a0001c0001t0004g0003others(22): Show | 34 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.328+6940C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136238536 | ||||||
chr9:136238613
|
C | G | 9 | a0001c0001t0013g0023a0001c0001t0013g0024a0001c0001t0013g0185others(6): Show | 11 | HG01496.hp2 HG02258.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.328+6863G>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136238613 | ||||||
chr9:136238663
|
C | T | 1 | a0001c0001t0034g0206 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.328+6813G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136238663 | ||||||
chr9:136238664
|
G | A | 1 | a0001c0023t0051g0322 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.328+6812C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136238664 | ||||||
chr9:136238693
|
A | G | 2 | a0002c0003t0002g0241a0002c0003t0002g0242 | 2 | HG03831.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.328+6783T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136238693 | ||||||
chr9:136238771
|
G | A | 6 | a0001c0001t0013g0023a0001c0001t0013g0024a0001c0001t0013g0185others(3): Show | 8 | HG01496.hp2 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.328+6705C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136238771 | ||||||
chr9:136238901
|
C | T | 1 | a0001c0002t0005g0052 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.328+6575G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136238901 | ||||||
chr9:136239096
|
C | A | 1 | a0001c0023t0051g0322 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.328+6380G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136239096 | ||||||
chr9:136239145
|
T | G | 2 | a0001c0001t0023g0326a0001c0001t0024g0325 | 2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.328+6331A>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136239145 | ||||||
chr9:136239431
|
G | C | 3 | a0002c0003t0002g0317a0002c0003t0002g0318a0002c0003t0080g0316 | 3 | NA18941.hp1 NA18955.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.328+6045C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136239431 | ||||||
chr9:136239469
|
C | T | 25 | a0001c0001t0001g0030a0001c0001t0001g0239a0001c0001t0004g0003others(22): Show | 34 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.328+6007G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136239469 | ||||||
chr9:136239791
|
C | CCGAG | 4 | a0001c0002t0001g0048a0001c0002t0001g0051a0001c0002t0005g0049others(1): Show | 4 | HG00438.hp1 HG02132.hp2 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.328+5681_328+5684d others(6): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136239791 | ||||||
chr9:136239799
|
A | G | 10 | a0001c0001t0018g0187a0001c0001t0018g0189a0001c0001t0018g0272others(7): Show | 10 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.328+5677T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136239799 | ||||||
chr9:136239847
|
C | T | 1 | a0001c0005t0004g0321 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.328+5629G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136239847 | ||||||
chr9:136240100
|
T | TG | 181 | a0001c0001t0001g0030a0001c0001t0001g0221a0001c0001t0001g0239others(178): Show | 215 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(212): Show |
intron_variant | MODIFIER | c.328+5375dupC | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136240100 | ||||||
chr9:136240166
|
G | A | 1 | a0001c0001t0001g0313 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.328+5310C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136240166 | ||||||
chr9:136240216
|
G | C | 1 | a0001c0001t0100g0327 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.328+5260C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136240216 | ||||||
chr9:136240394
|
C | A | 87 | a0001c0001t0001g0030a0001c0001t0001g0239a0001c0001t0001g0313others(84): Show | 112 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.328+5082G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136240394 | ||||||
chr9:136240449
|
G | A | 27 | a0001c0001t0013g0023a0001c0001t0013g0024a0001c0001t0013g0185others(24): Show | 30 | HG00741.hp2 HG01109.hp2 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.328+5027C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136240449 | ||||||
chr9:136240454
|
T | C | 28 | a0001c0001t0007g0029a0001c0001t0013g0023a0001c0001t0013g0024others(25): Show | 32 | HG00741.hp2 HG01074.hp2 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.328+5022A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136240454 | ||||||
chr9:136240454
|
T | G | 1 | a0001c0001t0006g0292 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.328+5022A>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136240454 | ||||||
chr9:136240744
|
T | C | 1 | a0001c0007t0006g0172 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.328+4732A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136240744 | ||||||
chr9:136240762
|
G | A | 3 | a0001c0001t0094g0266a0001c0001t0095g0215a0001c0001t0098g0216 | 3 | HG01261.hp2 HG02622.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.328+4714C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136240762 | ||||||
chr9:136240910
|
C | T | 1 | a0001c0001t0054g0294 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.328+4566G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136240910 | ||||||
chr9:136240933
|
G | GCAGTGCT others(20): Show |
1 | a0002c0003t0099g0218 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.328+4516_328+4542d others(29): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136240933 | ||||||
chr9:136241187
|
A | G | 78 | a0001c0001t0002g0283a0001c0001t0002g0320a0001c0001t0006g0276others(75): Show | 87 | HG00323.hp1 HG00609.hp1 HG00741.hp2 others(84): Show |
intron_variant | MODIFIER | c.328+4289T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136241187 | ||||||
chr9:136241256
|
C | A | 7 | a0001c0001t0007g0027a0001c0001t0007g0028a0001c0001t0007g0029others(4): Show | 10 | HG01074.hp2 HG02055.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.328+4220G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136241256 | ||||||
chr9:136241299
|
G | T | 1 | a0001c0001t0034g0206 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.328+4177C>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136241299 | ||||||
chr9:136241391
|
C | T | 1 | a0002c0003t0002g0217 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.328+4085G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136241391 | ||||||
chr9:136241521
|
A | G | 3 | a0001c0001t0034g0206a0001c0001t0034g0208a0001c0001t0063g0207 | 3 | HG02258.hp2 HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.328+3955T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136241521 | ||||||
chr9:136241691
|
G | A | 1 | a0001c0002t0001g0173 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.328+3785C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136241691 | ||||||
chr9:136241772
|
G | A | 6 | a0001c0002t0002g0174a0001c0002t0020g0175a0001c0002t0021g0022others(3): Show | 7 | NA18954.hp2 NA18964.hp2 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.328+3704C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136241772 | ||||||
chr9:136241897
|
G | A | 1 | a0001c0001t0054g0294 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.328+3579C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136241897 | ||||||
chr9:136241901
|
G | C | 11 | a0001c0001t0010g0037a0001c0001t0016g0296a0001c0001t0016g0297others(8): Show | 12 | HG01884.hp2 HG02280.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.328+3575C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136241901 | ||||||
chr9:136242038
|
A | C | 2 | a0001c0001t0002g0320a0001c0001t0053g0319 | 2 | HG02027.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.328+3438T>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136242038 | ||||||
chr9:136242043
|
T | C | 3 | a0001c0001t0042g0331a0001c0001t0042g0332a0001c0001t0101g0333 | 3 | HG02165.hp1 HG03831.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.328+3433A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136242043 | ||||||
chr9:136242086
|
T | G | 7 | a0001c0001t0007g0027a0001c0001t0007g0028a0001c0001t0007g0029others(4): Show | 10 | HG01074.hp2 HG02055.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.328+3390A>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136242086 | ||||||
chr9:136242095
|
C | G | 17 | a0001c0001t0008g0191a0001c0001t0008g0192a0001c0001t0008g0193others(14): Show | 18 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.328+3381G>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136242095 | ||||||
chr9:136242291
|
T | C | 5 | a0001c0001t0002g0320a0001c0001t0042g0331a0001c0001t0042g0332others(2): Show | 5 | HG02027.hp2 HG02129.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.328+3185A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136242291 | ||||||
chr9:136242303
|
C | T | 3 | a0001c0001t0008g0191a0001c0001t0008g0192a0001c0001t0008g0193 | 3 | HG01069.hp2 HG02602.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.328+3173G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136242303 | ||||||
chr9:136242369
|
C | T | 5 | a0001c0002t0014g0010a0001c0002t0014g0041a0001c0002t0014g0042others(2): Show | 6 | HG01109.hp2 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.328+3107G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136242369 | ||||||
chr9:136242382
|
G | A | 7 | a0001c0001t0007g0027a0001c0001t0007g0028a0001c0001t0007g0029others(4): Show | 10 | HG01074.hp2 HG02055.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.328+3094C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136242382 | ||||||
chr9:136242599
|
C | T | 1 | a0001c0008t0081g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.328+2877G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136242599 | ||||||
chr9:136242613
|
G | A | 2 | a0004c0009t0030g0328a0004c0009t0030g0329 | 2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.328+2863C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136242613 | ||||||
chr9:136242623
|
C | T | 2 | a0001c0001t0095g0215a0001c0001t0098g0216 | 2 | HG01261.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.328+2853G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136242623 | ||||||
chr9:136242628
|
T | C | 99 | a0001c0001t0001g0030a0001c0001t0001g0221a0001c0001t0001g0239others(96): Show | 124 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.328+2848A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136242628 | ||||||
chr9:136242673
|
A | G | 1 | a0001c0001t0023g0274 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.328+2803T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136242673 | ||||||
chr9:136242702
|
A | C | 17 | a0001c0001t0008g0191a0001c0001t0008g0192a0001c0001t0008g0193others(14): Show | 18 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.328+2774T>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136242702 | ||||||
chr9:136242832
|
C | T | 2 | a0001c0001t0016g0296a0001c0001t0016g0297 | 2 | HG01884.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.328+2644G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136242832 | ||||||
chr9:136242833
|
G | A | 10 | a0001c0001t0018g0187a0001c0001t0018g0189a0001c0001t0018g0272others(7): Show | 10 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.328+2643C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136242833 | ||||||
chr9:136242839
|
T | C | 18 | a0001c0001t0008g0191a0001c0001t0008g0192a0001c0001t0008g0193others(15): Show | 19 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.328+2637A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136242839 | ||||||
chr9:136243005
|
C | T | 1 | a0001c0004t0017g0046 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.328+2471G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136243005 | ||||||
chr9:136243006
|
G | A | 1 | a0001c0019t0071g0273 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.328+2470C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136243006 | ||||||
chr9:136243135
|
A | G | 147 | a0001c0001t0001g0030a0001c0001t0001g0221a0001c0001t0001g0239others(144): Show | 179 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.328+2341T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136243135 | ||||||
chr9:136243307
|
C | T | 1 | a0001c0002t0005g0040 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.328+2169G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136243307 | ||||||
chr9:136243308
|
G | A | 1 | a0001c0001t0012g0036 | 2 | HG01074.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.328+2168C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136243308 | ||||||
chr9:136243470
|
T | C | 2 | a0001c0005t0001g0205a0008c0018t0001g0181 | 2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.328+2006A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136243470 | ||||||
chr9:136243920
|
C | T | 1 | a0001c0002t0026g0039 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.328+1556G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136243920 | ||||||
chr9:136243949
|
T | C | 17 | a0001c0001t0008g0191a0001c0001t0008g0192a0001c0001t0008g0193others(14): Show | 18 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.328+1527A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136243949 | ||||||
chr9:136244008
|
T | C | 11 | a0001c0001t0010g0037a0001c0001t0016g0296a0001c0001t0016g0297others(8): Show | 12 | HG01884.hp2 HG02280.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.328+1468A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136244008 | ||||||
chr9:136244118
|
T | G | 8 | a0001c0001t0001g0313a0002c0003t0002g0306a0002c0003t0002g0309others(5): Show | 8 | HG01123.hp1 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.328+1358A>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136244118 | ||||||
chr9:136244133
|
A | T | 2 | a0001c0001t0002g0320a0001c0001t0053g0319 | 2 | HG02027.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.328+1343T>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136244133 | ||||||
chr9:136244551
|
A | T | 17 | a0001c0001t0008g0191a0001c0001t0008g0192a0001c0001t0008g0193others(14): Show | 18 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.328+925T>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136244551 | ||||||
chr9:136244694
|
C | T | 2 | a0001c0001t0015g0025a0001c0001t0062g0190 | 3 | NA18998.hp2 NA19058.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.328+782G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136244694 | ||||||
chr9:136244884
|
A | T | 4 | a0001c0001t0018g0187a0001c0001t0018g0189a0001c0001t0060g0188others(1): Show | 4 | HG00741.hp2 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.328+592T>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136244884 | ||||||
chr9:136244895
|
G | A | 6 | a0002c0003t0002g0005a0002c0003t0002g0314a0002c0003t0002g0315others(3): Show | 9 | HG00673.hp2 HG02040.hp2 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.328+581C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136244895 | ||||||
chr9:136244982
|
A | G | 5 | a0001c0001t0013g0023a0001c0001t0013g0024a0001c0001t0013g0185others(2): Show | 7 | HG01496.hp2 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.328+494T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136244982 | ||||||
chr9:136244997
|
C | T | 1 | a0005c0025t0002g0184 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.328+479G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136244997 | ||||||
chr9:136245132
|
T | C | 5 | a0001c0001t0002g0320a0001c0001t0042g0331a0001c0001t0042g0332others(2): Show | 5 | HG02027.hp2 HG02129.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.328+344A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136245132 | ||||||
chr9:136245324
|
C | T | 2 | a0001c0020t0003g0183a0007c0021t0045g0182 | 2 | HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.328+152G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136245324 | ||||||
chr9:136245331
|
C | T | 2 | a0001c0020t0003g0183a0007c0021t0045g0182 | 2 | HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.328+145G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136245331 | ||||||
chr9:136245358
|
G | A | 167 | a0001c0001t0023g0326a0001c0001t0024g0323a0001c0001t0024g0324others(164): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.328+118C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136245358 |