geneid | 5660 |
---|---|
ensemblid | ENSG00000197746.15 |
hgncid | 9498 |
symbol | PSAP |
name | prosaposin |
refseq_nuc | NM_002778.4 |
refseq_prot | NP_002769.1 |
ensembl_nuc | ENST00000394936.8 |
ensembl_prot | ENSP00000378394.3 |
mane_status | MANE Select |
chr | chr10 |
start | 71816298 |
end | 71851251 |
strand | - |
ver | v1.2 |
region | chr10:71816298-71851251 |
region5000 | chr10:71811298-71856251 |
regionname0 | PSAP_chr10_71816298_71851251 |
regionname5000 | PSAP_chr10_71811298_71856251 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 524 | 419 | 91 | 71 | 199 | 14 | 42 | 153 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
a0002 | 0/0 | 524 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
a0003 | 0/0 | 524 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
a0004 | 0/0 | 524 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
a0005 | 0/0 | 524 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
a0006 | 0/0 | 524 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1575 | 414 | 88 | 70 | 199 | 14 | 41 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
c0002 | 0/0 | 1575 | 5 | 5 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
c0003 | 0/0 | 1575 | 3 | 3 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
c0004 | 0/0 | 1575 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
c0005 | 0/0 | 1575 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
c0006 | 0/0 | 1575 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
c0007 | 0/0 | 1575 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
c0008 | 0/0 | 1575 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
c0009 | 0/0 | 1575 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
c0010 | 0/0 | 1575 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
c0011 | 0/0 | 1575 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1174 | 195 | 39 | 33 | 84 | 7 | 30 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
t0002 | 0/0 | 1174 | 145 | 44 | 27 | 65 | 2 | 7 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
t0003 | 0/0 | 1174 | 68 | 1 | 9 | 49 | 4 | 5 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
t0004 | 0/0 | 1174 | 8 | 8 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
t0005 | 0/0 | 1174 | 5 | 3 | 2 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
t0006 | 0/0 | 1174 | 3 | 1 | 0 | 2 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
t0007 | 0/0 | 1174 | 2 | 1 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
t0008 | 0/0 | 1174 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
t0009 | 0/0 | 1174 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
t0010 | 0/0 | 1174 | 1 | 0 | 0 | 0 | 1 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
t0011 | 0/0 | 1174 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 24 | 0 | 0 | 24 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0002 | 0/0 | 21 | 0 | 2 | 16 | 2 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0003 | 0/0 | 10 | 1 | 0 | 9 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0004 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0005 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0006 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0009 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0011 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0012 | 1/0 | 4 | 0 | 3 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0014 | 0/1 | 4 | 0 | 0 | 0 | 1 | 2 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0020 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0023 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0024 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0025 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0041 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0046 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0051 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0055 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0056 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0057 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0058 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1575 | 414 | 88 | 70 | 199 | 14 | 41 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
a0001c0006 | 0/0 | 1575 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
a0001c0007 | 0/0 | 1575 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
a0001c0009 | 0/0 | 1575 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
a0001c0010 | 0/0 | 1575 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
a0001c0011 | 0/0 | 1575 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
a0002c0002 | 0/0 | 1575 | 5 | 5 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
a0003c0003 | 0/0 | 1575 | 3 | 3 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
a0004c0004 | 0/0 | 1575 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
a0005c0005 | 0/0 | 1575 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
a0006c0008 | 0/0 | 1575 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2748 | 191 | 37 | 32 | 84 | 7 | 29 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
a0001c0001t0002 | 0/0 | 2748 | 141 | 42 | 26 | 64 | 2 | 7 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
a0001c0001t0003 | 0/0 | 2748 | 68 | 1 | 9 | 49 | 4 | 5 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
a0001c0001t0004 | 0/0 | 2748 | 2 | 2 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
a0001c0001t0005 | 0/0 | 2748 | 4 | 2 | 2 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
a0001c0001t0006 | 0/0 | 2748 | 3 | 1 | 0 | 2 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
a0001c0001t0007 | 0/0 | 2748 | 2 | 1 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
a0001c0001t0009 | 0/0 | 2748 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
a0001c0001t0010 | 0/0 | 2748 | 1 | 0 | 0 | 0 | 1 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
a0001c0001t0011 | 0/0 | 2748 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
a0001c0006t0005 | 0/0 | 2748 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
a0001c0007t0001 | 0/0 | 2748 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
a0001c0009t0001 | 0/0 | 2748 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
a0001c0010t0001 | 0/0 | 2748 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
a0001c0011t0008 | 0/0 | 2748 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
a0002c0002t0004 | 0/0 | 2748 | 5 | 5 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
a0003c0003t0002 | 0/0 | 2748 | 2 | 2 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
a0003c0003t0004 | 0/0 | 2748 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
a0004c0004t0002 | 0/0 | 2748 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
a0005c0005t0001 | 0/0 | 2748 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
a0006c0008t0002 | 0/0 | 2748 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | copy fasta | chr10 | 71811298 | 71856251 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0005 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0012 | 1/0 | 4 | 0 | 3 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0014 | 0/1 | 4 | 0 | 0 | 0 | 1 | 2 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0023 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0024 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0025 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0046 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0002 | 0/0 | 21 | 0 | 2 | 16 | 2 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0003 | 0/0 | 10 | 1 | 0 | 9 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0006 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0009 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0011 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0003g0001 | 0/0 | 24 | 0 | 0 | 24 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0003g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0003g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0003g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0003g0055 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0003g0056 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0003g0057 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0003g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0004g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0005g0058 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0005g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0005g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0006g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0006g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0006g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0007g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0007g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0009g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0010g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0001t0011g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0006t0005g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0007t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0009t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0010t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0001c0011t0008g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0002c0002t0004g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0002c0002t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0002c0002t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0002c0002t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0003c0003t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0003c0003t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0003c0003t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0004c0004t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0005c0005t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
a0006c0008t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | GBR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0041 | EUR | GBR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0057 | EUR | GBR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | GBR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG00280 | hp1 | a0001 | c0001 | t0010 | g0092 | EUR | FIN | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | CHS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | CHS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | CHS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | CHS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG00639 | hp1 | a0001 | c0001 | t0007 | g0273 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG00642 | hp2 | a0001 | c0001 | t0005 | g0276 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | CHS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0265 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0056 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0056 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0267 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0261 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0182 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0268 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0271 | AMR | CLM | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | CLM | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01433 | hp2 | a0001 | c0010 | t0001 | g0095 | AMR | CLM | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | CLM | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0051 | EUR | IBS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0240 | EUR | IBS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0055 | EUR | IBS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0051 | EUR | IBS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PEL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | PEL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0191 | AMR | PEL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0170 | AMR | PEL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | PEL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0087 | AMR | PEL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PEL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PEL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0068 | AMR | PEL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02004 | hp1 | a0004 | c0004 | t0002 | g0148 | AMR | PEL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0084 | AMR | PEL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | KHV | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | KHV | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02040 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | KHV | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02145 | hp1 | a0003 | c0003 | t0002 | g0238 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0247 | EAS | CDX | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CDX | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0209 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02280 | hp1 | a0002 | c0002 | t0004 | g0100 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0249 | AMR | PEL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0078 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02451 | hp2 | a0001 | c0001 | t0004 | g0044 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0077 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0219 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0159 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0217 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0030 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0179 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02698 | hp2 | a0001 | c0009 | t0001 | g0192 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0263 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0220 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0166 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02895 | hp1 | a0001 | c0011 | t0008 | g0094 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0164 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02922 | hp1 | a0002 | c0002 | t0004 | g0036 | AFR | ESN | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0083 | AFR | ESN | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0074 | AFR | ESN | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | ESN | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02976 | hp1 | a0001 | c0001 | t0005 | g0058 | AFR | ESN | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | ESN | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0167 | AFR | MSL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | MSL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03130 | hp1 | a0005 | c0005 | t0001 | g0139 | AFR | ESN | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03130 | hp2 | a0001 | c0001 | t0007 | g0274 | AFR | ESN | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | MSL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03209 | hp2 | a0001 | c0001 | t0004 | g0044 | AFR | MSL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03225 | hp2 | a0002 | c0002 | t0004 | g0099 | AFR | MSL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0153 | AFR | MSL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0245 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0246 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03516 | hp1 | a0001 | c0001 | t0005 | g0058 | AFR | ESN | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | ESN | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03579 | hp1 | a0003 | c0003 | t0004 | g0239 | AFR | MSL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0236 | AFR | MSL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0244 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | STU | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | STU | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | BEB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0176 | SAS | BEB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | BEB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | STU | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | STU | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0243 | SAS | BEB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | STU | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | STU | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | STU | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0085 | SAS | STU | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18522 | hp2 | a0002 | c0002 | t0004 | g0098 | AFR | YRI | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | CHB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CHB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | CHB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | CHB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18906 | hp1 | a0001 | c0001 | t0009 | g0168 | AFR | YRI | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | YRI | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18942 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18943 | hp1 | a0001 | c0001 | t0006 | g0255 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18957 | hp2 | a0006 | c0008 | t0002 | g0089 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18959 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18961 | hp2 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18963 | hp1 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18965 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0270 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0256 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18985 | hp1 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18989 | hp2 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18992 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18997 | hp1 | a0001 | c0001 | t0003 | g0264 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19001 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | LWK | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | LWK | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19043 | hp1 | a0003 | c0003 | t0002 | g0237 | AFR | LWK | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19043 | hp2 | a0001 | c0006 | t0005 | g0275 | AFR | LWK | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19055 | hp1 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19067 | hp1 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19080 | hp2 | a0001 | c0001 | t0006 | g0269 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19087 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | YRI | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ASW | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA20129 | hp2 | a0002 | c0002 | t0004 | g0036 | AFR | ASW | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | TSI | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0125 | EUR | TSI | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0266 | EUR | TSI | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | TSI | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0076 | SAS | GIH | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | GIH | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01123 | hp1 | a0001 | c0001 | t0005 | g0272 | AMR | CLM | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG01123 | hp2 | a0001 | c0001 | t0003 | g0055 | AMR | CLM | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02109 | hp1 | a0001 | c0001 | t0011 | g0135 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02109 | hp2 | a0001 | c0001 | t0006 | g0242 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0248 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0165 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | MSL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | MSL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | USA | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | USA | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA20300 | hp1 | a0001 | c0007 | t0001 | g0061 | AFR | USA | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | USA | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | LWK | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0113 | AFR | LWK | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0014 | REF | REF | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0012 | REF | REF | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:71818618
|
T | C | 1 | a0005 | 1 | HG03130.hp1 | missense_variant&splice_region_variant | MODERATE | c.1538A>G | p.Asn513Ser | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 13/14 | 1568/2748 | 1538/1575 | 513/524 | chr10 | 71818618 | ||
chr10:71828039
|
C | T | 1 | a0004 | 1 | HG02004.hp1 | missense_variant | MODERATE | c.695G>A | p.Arg232His | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/14 | 725/2748 | 695/1575 | 232/524 | chr10 | 71828039 | ||
chr10:71828883
|
C | A | 1 | a0002 | 5 | HG02280.hp1 HG02922.hp1 HG03225.hp2 others(2): Show |
missense_variant | MODERATE | c.570G>T | p.Gln190His | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 5/14 | 600/2748 | 570/1575 | 190/524 | chr10 | 71828883 | ||
chr10:71828888
|
G | A | 1 | a0006 | 1 | NA18957.hp2 | missense_variant | MODERATE | c.565C>T | p.Pro189Ser | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 5/14 | 595/2748 | 565/1575 | 189/524 | chr10 | 71828888 | ||
chr10:71851206
|
G | A | 1 | a0003 | 3 | HG02145.hp1 HG03579.hp1 NA19043.hp1 |
missense_variant | MODERATE | c.16C>T | p.Leu6Phe | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/14 | 46/2748 | 16/1575 | 6/524 | chr10 | 71851206 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:71818704
|
C | T | 1 | a0002c0002 | 5 | HG02280.hp1 HG02922.hp1 HG03225.hp2 others(2): Show |
synonymous_variant | LOW | c.1452G>A | p.Ser484Ser | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 13/14 | 1482/2748 | 1452/1575 | 484/524 | chr10 | 71818704 | ||
chr10:71819082
|
G | A | 1 | a0001c0006 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.1380C>T | p.Pro460Pro | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 12/14 | 1410/2748 | 1380/1575 | 460/524 | chr10 | 71819082 | ||
chr10:71819889
|
G | A | 1 | a0001c0007 | 1 | NA20300.hp1 | synonymous_variant | LOW | c.1017C>T | p.Leu339Leu | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 10/14 | 1047/2748 | 1017/1575 | 339/524 | chr10 | 71819889 | ||
chr10:71831165
|
G | A | 1 | a0001c0009 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.336C>T | p.Ser112Ser | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/14 | 366/2748 | 336/1575 | 112/524 | chr10 | 71831165 | ||
chr10:71834426
|
G | A | 1 | a0001c0011 | 1 | HG02895.hp1 | synonymous_variant | LOW | c.120C>T | p.Ser40Ser | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/14 | 150/2748 | 120/1575 | 40/524 | chr10 | 71834426 | ||
chr10:71834468
|
G | A | 2 | a0001c0010a0001c0011 | 2 | HG01433.hp2 HG02895.hp1 |
synonymous_variant | LOW | c.78C>T | p.Thr26Thr | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/14 | 108/2748 | 78/1575 | 26/524 | chr10 | 71834468 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:71816370
|
T | C | 2 | a0001c0001t0009a0001c0011t0008 | 2 | HG02895.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1071A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 14/14 | 1071 | chr10 | 71816370 | |||||
chr10:71816550
|
C | T | 9 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(6): Show | 220 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*891G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 14/14 | 891 | chr10 | 71816550 | |||||
chr10:71816644
|
T | C | 1 | a0001c0001t0010 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*797A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 14/14 | 797 | chr10 | 71816644 | |||||
chr10:71816666
|
C | T | 3 | a0001c0001t0004a0002c0002t0004a0003c0003t0004 | 8 | HG02280.hp1 HG02451.hp2 HG02922.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*775G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 14/14 | 775 | chr10 | 71816666 | |||||
chr10:71817319
|
G | C | 1 | a0001c0001t0011 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*122C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 14/14 | 122 | chr10 | 71817319 | |||||
chr10:71851225
|
G | A | 2 | a0001c0001t0003a0001c0001t0006 | 71 | HG00140.hp1 HG00558.hp1 HG00597.hp1 others(68): Show |
5_prime_UTR_variant | MODIFIER | c.-4C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/14 | 4 | chr10 | 71851225 | |||||
chr10:71851231
|
T | C | 3 | a0001c0001t0005a0001c0001t0007a0001c0006t0005 | 7 | HG00639.hp1 HG00642.hp2 HG01123.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-10A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/14 | 10 | chr10 | 71851231 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:71817510
|
G | A | 60 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0010others(57): Show | 112 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.1540-34C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 13/13 | chr10 | 71817510 | ||||||
chr10:71817747
|
AC | A | 66 | a0001c0001t0002g0006a0001c0001t0002g0009a0001c0001t0002g0022others(63): Show | 108 | HG00140.hp1 HG00597.hp1 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.1540-272delG | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 13/13 | chr10 | 71817747 | ||||||
chr10:71817754
|
A | G | 3 | a0001c0001t0001g0026a0001c0001t0001g0197a0001c0001t0001g0215 | 5 | NA18970.hp1 NA18984.hp2 NA19058.hp2 others(2): Show |
intron_variant | MODIFIER | c.1540-278T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 13/13 | chr10 | 71817754 | ||||||
chr10:71817778
|
G | A | 1 | a0001c0001t0001g0110 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1540-302C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 13/13 | chr10 | 71817778 | ||||||
chr10:71817795
|
C | T | 6 | a0001c0001t0002g0009a0001c0001t0002g0209a0001c0001t0002g0217others(3): Show | 10 | HG01243.hp1 HG01891.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1540-319G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 13/13 | chr10 | 71817795 | ||||||
chr10:71817854
|
T | A | 1 | a0001c0001t0001g0136 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1540-378A>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 13/13 | chr10 | 71817854 | ||||||
chr10:71817869
|
A | T | 79 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(76): Show | 111 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.1540-393T>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 13/13 | chr10 | 71817869 | ||||||
chr10:71818024
|
T | C | 1 | a0001c0011t0008g0094 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1540-548A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 13/13 | chr10 | 71818024 | ||||||
chr10:71818077
|
T | C | 1 | a0001c0011t0008g0094 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1539+540A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 13/13 | chr10 | 71818077 | ||||||
chr10:71818088
|
G | A | 2 | a0001c0001t0001g0053a0003c0003t0004g0239 | 3 | HG02922.hp2 HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1539+529C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 13/13 | chr10 | 71818088 | ||||||
chr10:71818337
|
T | A | 2 | a0001c0001t0002g0075a0001c0001t0002g0082 | 2 | HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1539+280A>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 13/13 | chr10 | 71818337 | ||||||
chr10:71818375
|
C | CA | 7 | a0001c0001t0001g0013a0001c0001t0001g0046a0001c0001t0001g0051others(4): Show | 12 | HG00140.hp2 HG01167.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.1539+241dupT | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 13/13 | chr10 | 71818375 | ||||||
chr10:71818395
|
T | A | 57 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0010others(54): Show | 108 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.1539+222A>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 13/13 | chr10 | 71818395 | ||||||
chr10:71818402
|
A | T | 63 | a0001c0001t0002g0006a0001c0001t0002g0009a0001c0001t0002g0022others(60): Show | 105 | HG00140.hp1 HG00597.hp1 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.1539+215T>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 13/13 | chr10 | 71818402 | ||||||
chr10:71818425
|
T | G | 2 | a0003c0003t0002g0237a0003c0003t0002g0238 | 2 | HG02145.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1539+192A>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 13/13 | chr10 | 71818425 | ||||||
chr10:71818746
|
G | A | 127 | a0001c0001t0001g0053a0001c0001t0002g0002a0001c0001t0002g0003others(124): Show | 222 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.1432-22C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 12/13 | chr10 | 71818746 | ||||||
chr10:71818753
|
G | C | 2 | a0001c0001t0001g0053a0001c0011t0008g0094 | 3 | HG02895.hp1 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1432-29C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 12/13 | chr10 | 71818753 | ||||||
chr10:71818773
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1432-49G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 12/13 | chr10 | 71818773 | ||||||
chr10:71818871
|
C | T | 6 | a0001c0001t0004g0044a0002c0002t0004g0036a0002c0002t0004g0098others(3): Show | 8 | HG02280.hp1 HG02451.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1432-147G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 12/13 | chr10 | 71818871 | ||||||
chr10:71818915
|
G | A | 68 | a0001c0001t0001g0053a0001c0001t0002g0006a0001c0001t0002g0009others(65): Show | 111 | HG00140.hp1 HG00597.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.1431+116C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 12/13 | chr10 | 71818915 | ||||||
chr10:71818926
|
C | T | 1 | a0001c0011t0008g0094 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1431+105G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 12/13 | chr10 | 71818926 | ||||||
chr10:71818947
|
AAGTCTC | A | 79 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(76): Show | 111 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.1431+78_1431+83del others(6): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 12/13 | chr10 | 71818947 | ||||||
chr10:71819125
|
T | C | 129 | a0001c0001t0001g0053a0001c0001t0001g0067a0001c0001t0001g0071others(126): Show | 224 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.1351-14A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 11/13 | chr10 | 71819125 | ||||||
chr10:71819460
|
C | T | 53 | a0001c0001t0002g0006a0001c0001t0002g0022a0001c0001t0002g0073others(50): Show | 90 | HG00140.hp1 HG00597.hp1 HG00597.hp2 others(87): Show |
splice_region_variant&intron_variant | LOW | c.1350+5G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 11/13 | chr10 | 71819460 | ||||||
chr10:71819640
|
G | A | 1 | a0001c0001t0001g0188 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1193-18C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 10/13 | chr10 | 71819640 | ||||||
chr10:71819648
|
C | T | 53 | a0001c0001t0002g0006a0001c0001t0002g0022a0001c0001t0002g0073others(50): Show | 90 | HG00140.hp1 HG00597.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.1193-26G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 10/13 | chr10 | 71819648 | ||||||
chr10:71819921
|
G | A | 7 | a0001c0001t0002g0029a0001c0001t0002g0059a0001c0001t0002g0060others(4): Show | 9 | HG00741.hp2 HG01069.hp1 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.1006-21C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 9/13 | chr10 | 71819921 | ||||||
chr10:71819948
|
G | C | 1 | a0001c0001t0003g0241 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1006-48C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 9/13 | chr10 | 71819948 | ||||||
chr10:71820030
|
A | G | 3 | a0001c0001t0001g0020a0001c0001t0001g0136a0001c0001t0001g0145 | 5 | HG01167.hp2 HG02056.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1006-130T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 9/13 | chr10 | 71820030 | ||||||
chr10:71820030
|
A | T | 3 | a0001c0001t0003g0057a0001c0001t0003g0267a0001c0001t0003g0271 | 4 | HG00140.hp1 HG01109.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.1006-130T>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 9/13 | chr10 | 71820030 | ||||||
chr10:71820085
|
G | T | 1 | a0001c0001t0002g0075 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1005+155C>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 9/13 | chr10 | 71820085 | ||||||
chr10:71820111
|
C | T | 6 | a0001c0001t0001g0020a0001c0001t0001g0117a0001c0001t0001g0136others(3): Show | 8 | HG01167.hp2 HG01433.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1005+129G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 9/13 | chr10 | 71820111 | ||||||
chr10:71820196
|
G | A | 5 | a0001c0001t0004g0044a0002c0002t0004g0036a0002c0002t0004g0098others(2): Show | 7 | HG02280.hp1 HG02451.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1005+44C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 9/13 | chr10 | 71820196 | ||||||
chr10:71820198
|
G | C | 1 | a0001c0006t0005g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1005+42C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 9/13 | chr10 | 71820198 | ||||||
chr10:71820222
|
G | A | 61 | a0001c0001t0001g0067a0001c0001t0002g0002a0001c0001t0002g0003others(58): Show | 113 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.1005+18C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 9/13 | chr10 | 71820222 | ||||||
chr10:71820432
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.910-97C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 8/13 | chr10 | 71820432 | ||||||
chr10:71820440
|
A | G | 7 | a0001c0001t0001g0048a0001c0001t0001g0169a0001c0001t0001g0172others(4): Show | 8 | HG00621.hp2 HG00673.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.910-105T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 8/13 | chr10 | 71820440 | ||||||
chr10:71820518
|
C | A | 4 | a0001c0001t0001g0042a0001c0001t0001g0101a0001c0001t0001g0116others(1): Show | 5 | HG00642.hp1 HG01081.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.910-183G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 8/13 | chr10 | 71820518 | ||||||
chr10:71820525
|
C | T | 1 | a0001c0001t0003g0253 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.910-190G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 8/13 | chr10 | 71820525 | ||||||
chr10:71820640
|
T | C | 1 | a0001c0001t0002g0210 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.910-305A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 8/13 | chr10 | 71820640 | ||||||
chr10:71820644
|
C | T | 1 | a0001c0006t0005g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.910-309G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 8/13 | chr10 | 71820644 | ||||||
chr10:71820710
|
G | GA | 128 | a0001c0001t0001g0053a0001c0001t0001g0067a0001c0001t0002g0002others(125): Show | 223 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.910-376dupT | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 8/13 | chr10 | 71820710 | ||||||
chr10:71820720
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.910-385G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 8/13 | chr10 | 71820720 | ||||||
chr10:71821011
|
T | C | 5 | a0001c0001t0002g0133a0001c0001t0002g0134a0001c0001t0003g0054others(2): Show | 6 | HG00558.hp1 NA18940.hp2 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.910-676A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 8/13 | chr10 | 71821011 | ||||||
chr10:71821048
|
G | A | 1 | a0001c0001t0002g0070 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.910-713C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 8/13 | chr10 | 71821048 | ||||||
chr10:71821115
|
C | T | 3 | a0001c0001t0002g0028a0003c0003t0002g0237a0003c0003t0002g0238 | 4 | HG02145.hp1 HG02145.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.909+761G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 8/13 | chr10 | 71821115 | ||||||
chr10:71821319
|
C | A | 79 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(76): Show | 111 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.909+557G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 8/13 | chr10 | 71821319 | ||||||
chr10:71821417
|
T | G | 6 | a0001c0001t0002g0009a0001c0001t0002g0209a0001c0001t0002g0217others(3): Show | 10 | HG01243.hp1 HG01891.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.909+459A>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 8/13 | chr10 | 71821417 | ||||||
chr10:71821420
|
G | A | 1 | a0001c0001t0001g0112 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.909+456C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 8/13 | chr10 | 71821420 | ||||||
chr10:71821803
|
A | T | 64 | a0001c0001t0002g0006a0001c0001t0002g0009a0001c0001t0002g0022others(61): Show | 106 | HG00140.hp1 HG00597.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.909+73T>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 8/13 | chr10 | 71821803 | ||||||
chr10:71821844
|
C | A | 5 | a0001c0001t0001g0041a0001c0001t0001g0141a0001c0001t0001g0142others(2): Show | 6 | HG00099.hp2 HG00423.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.909+32G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 8/13 | chr10 | 71821844 | ||||||
chr10:71822090
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.778-83G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71822090 | ||||||
chr10:71822126
|
C | T | 1 | a0001c0001t0002g0228 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.778-119G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71822126 | ||||||
chr10:71822129
|
CT | C | 6 | a0001c0001t0002g0009a0001c0001t0002g0209a0001c0001t0002g0217others(3): Show | 10 | HG01243.hp1 HG01891.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.778-123delA | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71822129 | ||||||
chr10:71822271
|
C | G | 1 | a0001c0001t0001g0042 | 2 | HG02622.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.778-264G>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71822271 | ||||||
chr10:71822276
|
C | T | 3 | a0001c0001t0002g0028a0003c0003t0002g0237a0003c0003t0002g0238 | 4 | HG02145.hp1 HG02145.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.778-269G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71822276 | ||||||
chr10:71822277
|
G | A | 6 | a0001c0001t0001g0181a0001c0001t0001g0184a0001c0001t0001g0186others(3): Show | 6 | HG00735.hp2 HG01106.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-270C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71822277 | ||||||
chr10:71822286
|
T | C | 1 | a0001c0001t0001g0200 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.778-279A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71822286 | ||||||
chr10:71822540
|
T | C | 3 | a0001c0001t0001g0230a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01175.hp1 HG03654.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.778-533A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71822540 | ||||||
chr10:71822684
|
G | A | 2 | a0001c0001t0001g0190a0001c0001t0001g0201 | 2 | HG03654.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.778-677C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71822684 | ||||||
chr10:71822950
|
A | AAAAT | 61 | a0001c0001t0001g0053a0001c0001t0001g0067a0001c0001t0002g0002others(58): Show | 114 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.778-947_778-944dup others(4): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71822950 | ||||||
chr10:71822950
|
AAAATAAA others(1): Show |
A | 7 | a0001c0001t0001g0048a0001c0001t0001g0169a0001c0001t0001g0172others(4): Show | 8 | HG00621.hp2 HG00673.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.778-951_778-944del others(8): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71822950 | ||||||
chr10:71822985
|
C | T | 1 | a0001c0001t0002g0153 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.778-978G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71822985 | ||||||
chr10:71822995
|
T | A | 128 | a0001c0001t0001g0053a0001c0001t0001g0067a0001c0001t0002g0002others(125): Show | 223 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.778-988A>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71822995 | ||||||
chr10:71823011
|
G | GA | 6 | a0001c0001t0001g0108a0001c0001t0002g0028a0001c0001t0002g0113others(3): Show | 7 | HG00597.hp2 HG02145.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.778-1005dupT | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71823011 | ||||||
chr10:71823024
|
G | T | 65 | a0001c0001t0002g0006a0001c0001t0002g0009a0001c0001t0002g0022others(62): Show | 107 | HG00140.hp1 HG00597.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.778-1017C>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71823024 | ||||||
chr10:71823221
|
G | A | 1 | a0001c0001t0002g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.778-1214C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71823221 | ||||||
chr10:71823380
|
G | T | 1 | a0001c0001t0001g0222 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.778-1373C>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71823380 | ||||||
chr10:71823542
|
T | C | 3 | a0001c0001t0002g0073a0001c0001t0002g0088a0001c0001t0002g0091 | 3 | NA18939.hp2 NA18950.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.778-1535A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71823542 | ||||||
chr10:71823615
|
T | G | 1 | a0001c0001t0002g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.778-1608A>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71823615 | ||||||
chr10:71823681
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.778-1674C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71823681 | ||||||
chr10:71823763
|
G | C | 206 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(203): Show | 332 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.778-1756C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71823763 | ||||||
chr10:71823816
|
C | CA | 90 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(87): Show | 125 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.778-1810dupT | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71823816 | ||||||
chr10:71823844
|
G | C | 1 | a0001c0001t0003g0244 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.778-1837C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71823844 | ||||||
chr10:71824142
|
C | G | 1 | a0003c0003t0004g0239 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.777+1695G>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71824142 | ||||||
chr10:71824160
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.777+1677C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71824160 | ||||||
chr10:71824191
|
TG | T | 60 | a0001c0001t0001g0020a0001c0001t0001g0117a0001c0001t0001g0136others(57): Show | 100 | HG00140.hp1 HG00597.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.777+1645delC | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71824191 | ||||||
chr10:71824258
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.777+1579C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71824258 | ||||||
chr10:71824331
|
G | C | 1 | a0001c0001t0003g0252 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.777+1506C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71824331 | ||||||
chr10:71824332
|
G | C | 1 | a0001c0001t0002g0077 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.777+1505C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71824332 | ||||||
chr10:71824358
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.777+1479C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71824358 | ||||||
chr10:71824488
|
G | C | 42 | a0001c0001t0002g0022a0001c0001t0002g0073a0001c0001t0002g0077others(39): Show | 74 | HG00140.hp1 HG00597.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.777+1349C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71824488 | ||||||
chr10:71824498
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.777+1339A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71824498 | ||||||
chr10:71824504
|
T | G | 2 | a0001c0001t0001g0147a0001c0001t0006g0255 | 2 | NA18943.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.777+1333A>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71824504 | ||||||
chr10:71824513
|
C | G | 1 | a0001c0001t0001g0071 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.777+1324G>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71824513 | ||||||
chr10:71824598
|
T | G | 1 | a0001c0001t0001g0071 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.777+1239A>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71824598 | ||||||
chr10:71824658
|
G | A | 1 | a0001c0001t0002g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.777+1179C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71824658 | ||||||
chr10:71824669
|
T | C | 78 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(75): Show | 109 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.777+1168A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71824669 | ||||||
chr10:71824716
|
A | C | 208 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(205): Show | 335 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.777+1121T>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71824716 | ||||||
chr10:71824764
|
T | C | 2 | a0001c0001t0002g0059a0001c0001t0002g0060 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.777+1073A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71824764 | ||||||
chr10:71824826
|
G | C | 1 | a0001c0001t0002g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.777+1011C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71824826 | ||||||
chr10:71824927
|
G | C | 1 | a0001c0001t0002g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.777+910C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71824927 | ||||||
chr10:71825032
|
T | C | 1 | a0001c0001t0002g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.777+805A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71825032 | ||||||
chr10:71825191
|
T | G | 2 | a0001c0001t0002g0075a0001c0001t0002g0082 | 2 | HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.777+646A>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71825191 | ||||||
chr10:71825268
|
C | T | 213 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(210): Show | 339 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.777+569G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71825268 | ||||||
chr10:71825276
|
A | G | 2 | a0001c0001t0001g0053a0003c0003t0004g0239 | 3 | HG02922.hp2 HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.777+561T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71825276 | ||||||
chr10:71825420
|
C | T | 2 | a0001c0001t0001g0171a0001c0001t0001g0185 | 2 | HG02132.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.777+417G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71825420 | ||||||
chr10:71825437
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.777+400G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71825437 | ||||||
chr10:71825567
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.777+270A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71825567 | ||||||
chr10:71825567
|
TGGCTGGC others(7): Show |
T | 5 | a0001c0001t0002g0187a0001c0001t0003g0055a0001c0001t0003g0240others(2): Show | 6 | HG01081.hp2 HG01123.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.777+256_777+269del others(14): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71825567 | ||||||
chr10:71825580
|
C | T | 1 | a0001c0007t0001g0061 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.777+257G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71825580 | ||||||
chr10:71825655
|
G | A | 1 | a0001c0001t0001g0112 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.777+182C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71825655 | ||||||
chr10:71825678
|
G | T | 1 | a0001c0001t0001g0232 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.777+159C>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71825678 | ||||||
chr10:71825734
|
G | C | 1 | a0001c0001t0001g0071 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.777+103C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71825734 | ||||||
chr10:71825769
|
A | G | 80 | a0001c0001t0001g0031a0001c0001t0001g0053a0001c0001t0001g0064others(77): Show | 138 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.777+68T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71825769 | ||||||
chr10:71826073
|
G | A | 2 | a0001c0001t0001g0147a0001c0001t0006g0255 | 2 | NA18943.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.721-180C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71826073 | ||||||
chr10:71826082
|
A | C | 3 | a0001c0001t0001g0053a0001c0001t0009g0168a0001c0011t0008g0094 | 4 | HG02895.hp1 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.721-189T>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71826082 | ||||||
chr10:71826180
|
G | C | 50 | a0001c0001t0002g0006a0001c0001t0002g0022a0001c0001t0002g0073others(47): Show | 87 | HG00140.hp1 HG00597.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.721-287C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71826180 | ||||||
chr10:71826402
|
A | G | 1 | a0001c0001t0002g0086 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.721-509T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71826402 | ||||||
chr10:71826561
|
T | C | 1 | a0001c0001t0002g0028 | 2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.721-668A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71826561 | ||||||
chr10:71826576
|
A | G | 2 | a0001c0001t0001g0102a0001c0001t0001g0144 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.721-683T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71826576 | ||||||
chr10:71826743
|
G | GA | 208 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(205): Show | 335 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.721-851dupT | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71826743 | ||||||
chr10:71826782
|
C | T | 2 | a0002c0002t0004g0098a0002c0002t0004g0100 | 2 | HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.721-889G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71826782 | ||||||
chr10:71826828
|
A | G | 222 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(219): Show | 351 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(348): Show |
intron_variant | MODIFIER | c.721-935T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71826828 | ||||||
chr10:71826959
|
G | A | 6 | a0001c0001t0001g0041a0001c0001t0001g0141a0001c0001t0001g0142others(3): Show | 7 | HG00099.hp2 HG00423.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.720+1055C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71826959 | ||||||
chr10:71827002
|
G | A | 1 | a0001c0001t0002g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.720+1012C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71827002 | ||||||
chr10:71827036
|
C | T | 130 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(127): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.720+978G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71827036 | ||||||
chr10:71827044
|
C | T | 1 | a0001c0001t0002g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.720+970G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71827044 | ||||||
chr10:71827255
|
C | T | 3 | a0001c0001t0001g0033a0001c0001t0001g0081a0001c0001t0001g0152 | 4 | HG03453.hp1 HG03540.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+759G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71827255 | ||||||
chr10:71827315
|
C | G | 7 | a0001c0001t0001g0048a0001c0001t0001g0169a0001c0001t0001g0172others(4): Show | 8 | HG00621.hp2 HG00673.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.720+699G>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71827315 | ||||||
chr10:71827327
|
A | C | 1 | a0001c0001t0001g0125 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.720+687T>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71827327 | ||||||
chr10:71827405
|
G | GA | 48 | a0001c0001t0002g0022a0001c0001t0002g0028a0001c0001t0002g0073others(45): Show | 82 | HG00140.hp1 HG00597.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.720+608dupT | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71827405 | ||||||
chr10:71827405
|
G | GAA | 77 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(74): Show | 108 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.720+607_720+608dup others(2): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71827405 | ||||||
chr10:71827408
|
A | AG | 4 | a0001c0001t0002g0006a0001c0001t0002g0074a0001c0001t0002g0078others(1): Show | 8 | HG00735.hp1 HG01891.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.720+605_720+606ins others(1): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71827408 | ||||||
chr10:71827418
|
G | C | 1 | a0001c0001t0005g0058 | 2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.720+596C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71827418 | ||||||
chr10:71827455
|
A | T | 42 | a0001c0001t0001g0031a0001c0001t0001g0064a0001c0001t0002g0002others(39): Show | 85 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.720+559T>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71827455 | ||||||
chr10:71827619
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.720+395G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71827619 | ||||||
chr10:71827726
|
C | CA | 10 | a0001c0001t0001g0071a0001c0001t0001g0162a0001c0001t0001g0222others(7): Show | 10 | HG00639.hp1 HG01346.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.720+287dupT | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71827726 | ||||||
chr10:71827726
|
CA | C | 6 | a0001c0001t0001g0141a0001c0001t0001g0202a0001c0001t0001g0223others(3): Show | 6 | HG01074.hp2 HG03490.hp2 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.720+287delT | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71827726 | ||||||
chr10:71827754
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.720+260T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71827754 | ||||||
chr10:71827785
|
G | C | 1 | a0001c0001t0001g0196 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.720+229C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71827785 | ||||||
chr10:71827910
|
T | G | 1 | a0001c0001t0001g0071 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.720+104A>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71827910 | ||||||
chr10:71827923
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.720+91T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71827923 | ||||||
chr10:71828167
|
A | G | 1 | a0001c0001t0003g0250 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.577-10T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 5/13 | chr10 | 71828167 | ||||||
chr10:71828179
|
T | A | 1 | a0001c0001t0002g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.577-22A>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 5/13 | chr10 | 71828179 | ||||||
chr10:71828213
|
C | T | 13 | a0001c0001t0002g0021a0001c0001t0002g0045a0001c0001t0002g0158others(10): Show | 17 | HG00642.hp2 HG01243.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.577-56G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 5/13 | chr10 | 71828213 | ||||||
chr10:71828310
|
G | A | 1 | a0001c0006t0005g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.577-153C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 5/13 | chr10 | 71828310 | ||||||
chr10:71828436
|
G | A | 6 | a0001c0001t0004g0044a0002c0002t0004g0036a0002c0002t0004g0098others(3): Show | 8 | HG02280.hp1 HG02451.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.577-279C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 5/13 | chr10 | 71828436 | ||||||
chr10:71828542
|
G | A | 49 | a0001c0001t0002g0006a0001c0001t0002g0022a0001c0001t0002g0073others(46): Show | 86 | HG00140.hp1 HG00597.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.576+335C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 5/13 | chr10 | 71828542 | ||||||
chr10:71828605
|
A | G | 1 | a0001c0001t0001g0203 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.576+272T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 5/13 | chr10 | 71828605 | ||||||
chr10:71828662
|
ATT | A | 8 | a0001c0001t0002g0010a0001c0001t0002g0052a0001c0001t0002g0226others(5): Show | 13 | HG00558.hp2 HG02145.hp1 NA18612.hp1 others(10): Show |
intron_variant | MODIFIER | c.576+213_576+214del others(2): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 5/13 | chr10 | 71828662 | ||||||
chr10:71828717
|
C | G | 5 | a0001c0001t0004g0044a0002c0002t0004g0036a0002c0002t0004g0098others(2): Show | 7 | HG02280.hp1 HG02451.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.576+160G>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 5/13 | chr10 | 71828717 | ||||||
chr10:71828727
|
C | T | 1 | a0001c0001t0001g0053 | 2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.576+150G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 5/13 | chr10 | 71828727 | ||||||
chr10:71828797
|
A | C | 1 | a0001c0001t0002g0133 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.576+80T>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 5/13 | chr10 | 71828797 | ||||||
chr10:71828799
|
G | A | 1 | a0001c0001t0002g0037 | 2 | NA18964.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.576+78C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 5/13 | chr10 | 71828799 | ||||||
chr10:71829252
|
G | A | 1 | a0001c0001t0003g0266 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.376-175C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71829252 | ||||||
chr10:71829486
|
A | G | 3 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0002g0085 | 3 | HG04204.hp2 NA18948.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.376-409T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71829486 | ||||||
chr10:71829534
|
A | G | 1 | a0001c0001t0001g0033 | 2 | HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.376-457T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71829534 | ||||||
chr10:71829541
|
A | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0071 | 5 | HG00099.hp1 HG02735.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.376-464T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71829541 | ||||||
chr10:71829565
|
C | G | 1 | a0001c0001t0001g0063 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.376-488G>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71829565 | ||||||
chr10:71829661
|
T | C | 136 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0025others(133): Show | 242 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.376-584A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71829661 | ||||||
chr10:71829678
|
T | C | 1 | a0001c0001t0002g0160 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.376-601A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71829678 | ||||||
chr10:71829770
|
G | A | 10 | a0001c0001t0001g0155a0001c0001t0001g0227a0001c0001t0002g0010others(7): Show | 15 | HG00558.hp2 HG02145.hp1 NA18612.hp1 others(12): Show |
intron_variant | MODIFIER | c.376-693C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71829770 | ||||||
chr10:71829774
|
G | A | 1 | a0002c0002t0004g0099 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.376-697C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71829774 | ||||||
chr10:71829896
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.376-819C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71829896 | ||||||
chr10:71829952
|
G | A | 1 | a0001c0001t0003g0056 | 2 | HG00741.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.376-875C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71829952 | ||||||
chr10:71829975
|
C | T | 3 | a0001c0001t0001g0227a0001c0001t0002g0052a0001c0001t0002g0229 | 4 | HG00558.hp2 NA18747.hp2 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.376-898G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71829975 | ||||||
chr10:71830038
|
T | C | 11 | a0001c0001t0002g0021a0001c0001t0002g0045a0001c0001t0002g0164others(8): Show | 16 | HG00642.hp2 HG01243.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.376-961A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71830038 | ||||||
chr10:71830096
|
G | A | 10 | a0001c0001t0002g0021a0001c0001t0002g0045a0001c0001t0002g0164others(7): Show | 15 | HG00642.hp2 HG01243.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.376-1019C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71830096 | ||||||
chr10:71830284
|
C | T | 3 | a0001c0001t0002g0028a0001c0001t0002g0059a0001c0001t0002g0060 | 4 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.375+842G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71830284 | ||||||
chr10:71830294
|
A | G | 1 | a0003c0003t0004g0239 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.375+832T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71830294 | ||||||
chr10:71830364
|
A | G | 4 | a0001c0001t0001g0026a0001c0001t0001g0197a0001c0001t0001g0215others(1): Show | 6 | NA18946.hp2 NA18970.hp1 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.375+762T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71830364 | ||||||
chr10:71830428
|
A | C | 2 | a0001c0001t0002g0176a0001c0001t0002g0182 | 2 | HG01175.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.375+698T>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71830428 | ||||||
chr10:71830545
|
G | T | 1 | a0001c0001t0001g0184 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.375+581C>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71830545 | ||||||
chr10:71830591
|
C | T | 11 | a0001c0001t0001g0018a0001c0001t0001g0103a0001c0001t0001g0104others(8): Show | 13 | HG02074.hp2 NA18612.hp2 NA18950.hp2 others(10): Show |
intron_variant | MODIFIER | c.375+535G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71830591 | ||||||
chr10:71830593
|
C | A | 5 | a0001c0001t0001g0222a0001c0001t0002g0028a0001c0001t0002g0059others(2): Show | 6 | HG01346.hp1 HG02145.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.375+533G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71830593 | ||||||
chr10:71830713
|
C | T | 3 | a0001c0001t0007g0273a0001c0001t0007g0274a0001c0006t0005g0275 | 3 | HG00639.hp1 HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.375+413G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71830713 | ||||||
chr10:71830762
|
C | A | 3 | a0001c0001t0002g0028a0001c0001t0002g0059a0001c0001t0002g0060 | 4 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.375+364G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71830762 | ||||||
chr10:71830773
|
A | C | 1 | a0001c0001t0002g0016 | 3 | NA18946.hp1 NA18959.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.375+353T>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71830773 | ||||||
chr10:71830794
|
AG | A | 2 | a0001c0001t0003g0056a0001c0001t0003g0261 | 3 | HG00741.hp2 HG01070.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.375+331delC | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71830794 | ||||||
chr10:71830813
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.375+313A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71830813 | ||||||
chr10:71830824
|
G | A | 1 | a0001c0001t0002g0131 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.375+302C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71830824 | ||||||
chr10:71830900
|
C | T | 74 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(71): Show | 101 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.375+226G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71830900 | ||||||
chr10:71830918
|
C | T | 4 | a0001c0001t0005g0272a0001c0001t0007g0273a0001c0001t0007g0274others(1): Show | 4 | HG00639.hp1 HG01123.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.375+208G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71830918 | ||||||
chr10:71830919
|
G | A | 6 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0109others(3): Show | 6 | HG02074.hp2 NA18612.hp2 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.375+207C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71830919 | ||||||
chr10:71830921
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.375+205T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71830921 | ||||||
chr10:71830934
|
C | A | 2 | a0001c0001t0004g0044a0001c0001t0009g0168 | 3 | HG02451.hp2 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.375+192G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71830934 | ||||||
chr10:71831033
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.375+93G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71831033 | ||||||
chr10:71831392
|
T | C | 93 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(90): Show | 131 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.250-141A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 3/13 | chr10 | 71831392 | ||||||
chr10:71831473
|
G | A | 4 | a0001c0001t0001g0040a0001c0001t0001g0132a0001c0001t0001g0150others(1): Show | 5 | HG02040.hp1 NA19054.hp1 NA19080.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-222C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 3/13 | chr10 | 71831473 | ||||||
chr10:71831490
|
T | G | 1 | a0001c0001t0003g0267 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.250-239A>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 3/13 | chr10 | 71831490 | ||||||
chr10:71831497
|
A | T | 2 | a0001c0001t0004g0044a0001c0001t0009g0168 | 3 | HG02451.hp2 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.250-246T>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 3/13 | chr10 | 71831497 | ||||||
chr10:71831520
|
A | G | 1 | a0001c0001t0002g0153 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.250-269T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 3/13 | chr10 | 71831520 | ||||||
chr10:71831570
|
G | A | 1 | a0003c0003t0004g0239 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.249+276C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 3/13 | chr10 | 71831570 | ||||||
chr10:71831654
|
A | G | 3 | a0001c0001t0001g0230a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01175.hp1 HG03654.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.249+192T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 3/13 | chr10 | 71831654 | ||||||
chr10:71831665
|
T | C | 1 | a0001c0001t0001g0206 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.249+181A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 3/13 | chr10 | 71831665 | ||||||
chr10:71831698
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.249+148T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 3/13 | chr10 | 71831698 | ||||||
chr10:71831773
|
G | A | 14 | a0001c0001t0001g0053a0001c0001t0001g0101a0001c0001t0001g0102others(11): Show | 17 | HG01346.hp1 HG01433.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.249+73C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 3/13 | chr10 | 71831773 | ||||||
chr10:71831809
|
C | T | 1 | a0001c0001t0002g0193 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.249+37G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 3/13 | chr10 | 71831809 | ||||||
chr10:71831821
|
A | G | 4 | a0001c0001t0001g0147a0001c0001t0001g0149a0001c0001t0001g0155others(1): Show | 4 | HG00408.hp1 NA18948.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.249+25T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 3/13 | chr10 | 71831821 | ||||||
chr10:71831939
|
G | T | 1 | a0001c0001t0001g0125 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.175-19C>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71831939 | ||||||
chr10:71832003
|
G | A | 2 | a0001c0001t0002g0029a0001c0001t0002g0062 | 3 | HG01069.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.175-83C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71832003 | ||||||
chr10:71832022
|
G | T | 11 | a0001c0001t0002g0021a0001c0001t0002g0045a0001c0001t0002g0164others(8): Show | 16 | HG00642.hp2 HG01243.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.175-102C>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71832022 | ||||||
chr10:71832037
|
G | A | 31 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0053others(28): Show | 40 | HG00639.hp1 HG00733.hp2 HG01123.hp1 others(37): Show |
intron_variant | MODIFIER | c.175-117C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71832037 | ||||||
chr10:71832060
|
T | G | 11 | a0001c0001t0002g0021a0001c0001t0002g0045a0001c0001t0002g0164others(8): Show | 16 | HG00642.hp2 HG01243.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.175-140A>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71832060 | ||||||
chr10:71832072
|
G | A | 74 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(71): Show | 101 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.175-152C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71832072 | ||||||
chr10:71832089
|
G | A | 2 | a0001c0010t0001g0095a0001c0011t0008g0094 | 2 | HG01433.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.175-169C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71832089 | ||||||
chr10:71832337
|
C | T | 11 | a0001c0001t0002g0021a0001c0001t0002g0045a0001c0001t0002g0164others(8): Show | 16 | HG00642.hp2 HG01243.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.175-417G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71832337 | ||||||
chr10:71832648
|
T | C | 5 | a0001c0001t0001g0101a0002c0002t0004g0036a0002c0002t0004g0098others(2): Show | 6 | HG02280.hp1 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.175-728A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71832648 | ||||||
chr10:71832737
|
A | G | 1 | a0001c0001t0001g0231 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.175-817T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71832737 | ||||||
chr10:71832758
|
G | A | 1 | a0001c0001t0004g0044 | 2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.175-838C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71832758 | ||||||
chr10:71832874
|
G | A | 1 | a0001c0001t0002g0075 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.175-954C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71832874 | ||||||
chr10:71832946
|
G | C | 18 | a0001c0001t0001g0053a0001c0001t0001g0223a0001c0001t0001g0224others(15): Show | 29 | HG00423.hp1 HG00558.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.175-1026C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71832946 | ||||||
chr10:71833016
|
C | CAAAAAA | 30 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0023others(27): Show | 46 | HG00140.hp2 HG00673.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.175-1102_175-1097d others(8): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833016 | ||||||
chr10:71833016
|
C | CAAAAAAA | 21 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0025others(18): Show | 31 | HG00099.hp1 HG00609.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.175-1103_175-1097d others(9): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833016 | ||||||
chr10:71833016
|
C | CAAAAAAA others(1): Show |
10 | a0001c0001t0001g0178a0001c0001t0001g0180a0001c0001t0001g0194others(7): Show | 10 | HG00621.hp2 HG01106.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.175-1104_175-1097d others(10): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833016 | ||||||
chr10:71833016
|
C | CAAAAAAA others(2): Show |
6 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199others(3): Show | 6 | HG01175.hp1 HG01256.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.175-1105_175-1097d others(11): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833016 | ||||||
chr10:71833016
|
C | CAAAAAAA others(3): Show |
2 | a0001c0001t0001g0047a0001c0001t0001g0162 | 3 | HG02258.hp1 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.175-1106_175-1097d others(12): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833016 | ||||||
chr10:71833016
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0175 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.175-1107_175-1097d others(13): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833016 | ||||||
chr10:71833016
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0174 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.175-1108_175-1097d others(14): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833016 | ||||||
chr10:71833027
|
AAAAAC | A | 11 | a0001c0001t0001g0053a0001c0001t0001g0181a0001c0001t0001g0223others(8): Show | 17 | HG00423.hp1 HG00735.hp2 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.175-1112_175-1108d others(7): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833027 | ||||||
chr10:71833028
|
AAAAC | A | 16 | a0001c0001t0001g0227a0001c0001t0002g0010a0001c0001t0002g0021others(13): Show | 25 | HG00558.hp2 HG00642.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.175-1112_175-1109d others(6): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833028 | ||||||
chr10:71833032
|
C | A | 121 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(118): Show | 182 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.175-1112G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833032 | ||||||
chr10:71833033
|
A | C | 37 | a0001c0001t0002g0093a0001c0001t0003g0001a0001c0001t0003g0015others(34): Show | 69 | HG00140.hp1 HG00558.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.175-1113T>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833033 | ||||||
chr10:71833039
|
C | A | 92 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(89): Show | 130 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.175-1119G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833039 | ||||||
chr10:71833126
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.175-1206A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833126 | ||||||
chr10:71833189
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.174+1183G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833189 | ||||||
chr10:71833240
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.174+1132G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833240 | ||||||
chr10:71833284
|
C | A | 13 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0064others(10): Show | 19 | HG00733.hp2 HG01256.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.174+1088G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833284 | ||||||
chr10:71833434
|
G | C | 4 | a0001c0001t0005g0272a0001c0001t0007g0273a0001c0001t0007g0274others(1): Show | 4 | HG00639.hp1 HG01123.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.174+938C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833434 | ||||||
chr10:71833501
|
G | C | 1 | a0001c0001t0002g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.174+871C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833501 | ||||||
chr10:71833530
|
T | C | 5 | a0001c0001t0002g0009a0001c0001t0002g0217a0001c0001t0002g0218others(2): Show | 9 | HG01243.hp1 HG01891.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.174+842A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833530 | ||||||
chr10:71833596
|
A | T | 1 | a0003c0003t0004g0239 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.174+776T>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833596 | ||||||
chr10:71833621
|
G | A | 1 | a0001c0001t0001g0042 | 2 | HG02622.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.174+751C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833621 | ||||||
chr10:71833686
|
T | C | 107 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(104): Show | 150 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.174+686A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833686 | ||||||
chr10:71833707
|
A | G | 1 | a0001c0001t0001g0222 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.174+665T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833707 | ||||||
chr10:71833760
|
C | A | 17 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0064others(14): Show | 23 | HG00639.hp1 HG00733.hp2 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.174+612G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833760 | ||||||
chr10:71833796
|
T | C | 2 | a0001c0001t0001g0121a0001c0001t0001g0124 | 2 | HG02683.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.174+576A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833796 | ||||||
chr10:71833935
|
G | A | 1 | a0001c0001t0002g0220 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.174+437C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833935 | ||||||
chr10:71833975
|
C | G | 1 | a0001c0001t0002g0084 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.174+397G>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833975 | ||||||
chr10:71834029
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.174+343G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71834029 | ||||||
chr10:71834038
|
C | T | 13 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0064others(10): Show | 19 | HG00733.hp2 HG01256.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.174+334G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71834038 | ||||||
chr10:71834057
|
G | A | 1 | a0003c0003t0004g0239 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.174+315C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71834057 | ||||||
chr10:71834071
|
G | A | 5 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(2): Show | 6 | HG00423.hp1 HG01069.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.174+301C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71834071 | ||||||
chr10:71834156
|
A | G | 75 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(72): Show | 102 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.174+216T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71834156 | ||||||
chr10:71834208
|
G | A | 18 | a0001c0001t0001g0053a0001c0001t0001g0223a0001c0001t0001g0224others(15): Show | 29 | HG00423.hp1 HG00558.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.174+164C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71834208 | ||||||
chr10:71834522
|
C | T | 2 | a0001c0001t0001g0154a0001c0001t0002g0153 | 2 | HG00642.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.41-17G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71834522 | ||||||
chr10:71834558
|
G | A | 11 | a0001c0001t0002g0021a0001c0001t0002g0045a0001c0001t0002g0164others(8): Show | 16 | HG00642.hp2 HG01243.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.41-53C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71834558 | ||||||
chr10:71834601
|
C | T | 74 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(71): Show | 101 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.41-96G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71834601 | ||||||
chr10:71834674
|
A | G | 1 | a0003c0003t0004g0239 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.41-169T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71834674 | ||||||
chr10:71834702
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.41-197T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71834702 | ||||||
chr10:71834742
|
G | A | 135 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(132): Show | 186 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.41-237C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71834742 | ||||||
chr10:71834757
|
T | C | 9 | a0001c0001t0002g0021a0001c0001t0002g0045a0001c0001t0002g0164others(6): Show | 13 | HG00642.hp2 HG01243.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.41-252A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71834757 | ||||||
chr10:71834891
|
A | G | 1 | a0001c0001t0003g0249 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.41-386T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71834891 | ||||||
chr10:71834894
|
T | C | 4 | a0001c0001t0005g0272a0001c0001t0007g0273a0001c0001t0007g0274others(1): Show | 4 | HG00639.hp1 HG01123.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-389A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71834894 | ||||||
chr10:71834940
|
T | A | 1 | a0003c0003t0004g0239 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.41-435A>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71834940 | ||||||
chr10:71834965
|
G | A | 4 | a0001c0001t0002g0158a0001c0001t0002g0159a0001c0001t0002g0160others(1): Show | 4 | HG02055.hp1 HG02630.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-460C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71834965 | ||||||
chr10:71835021
|
C | G | 1 | a0001c0001t0001g0222 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.41-516G>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835021 | ||||||
chr10:71835080
|
C | CA | 4 | a0001c0001t0001g0050a0001c0001t0001g0202a0001c0001t0001g0213others(1): Show | 5 | HG02896.hp2 NA18940.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.41-576dupT | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835080 | ||||||
chr10:71835134
|
C | T | 93 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(90): Show | 131 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.41-629G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835134 | ||||||
chr10:71835160
|
T | C | 2 | a0001c0001t0002g0029a0001c0001t0002g0062 | 3 | HG01069.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.41-655A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835160 | ||||||
chr10:71835208
|
C | T | 28 | a0001c0001t0001g0090a0001c0001t0002g0002a0001c0001t0002g0003others(25): Show | 67 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.41-703G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835208 | ||||||
chr10:71835219
|
A | AAAAT | 49 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0064others(46): Show | 81 | HG00140.hp1 HG00558.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.41-718_41-715dupAT others(2): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835219 | ||||||
chr10:71835219
|
A | AAAATAAA others(1): Show |
7 | a0001c0001t0002g0009a0001c0001t0002g0217a0001c0001t0002g0218others(4): Show | 14 | HG01243.hp1 HG01891.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.41-722_41-715dupAT others(6): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835219 | ||||||
chr10:71835219
|
AAAAT | A | 86 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(83): Show | 118 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(115): Show |
intron_variant | MODIFIER | c.41-718_41-715delAT others(2): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835219 | ||||||
chr10:71835219
|
AAAATAAA others(1): Show |
A | 7 | a0001c0001t0001g0222a0001c0001t0002g0028a0001c0001t0002g0059others(4): Show | 8 | HG01346.hp1 HG02145.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.41-722_41-715delAT others(6): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835219 | ||||||
chr10:71835219
|
AAAATAAA others(5): Show |
A | 28 | a0001c0001t0001g0090a0001c0001t0002g0002a0001c0001t0002g0003others(25): Show | 67 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.41-726_41-715delAT others(10): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835219 | ||||||
chr10:71835253
|
A | T | 1 | a0001c0001t0001g0053 | 2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.41-748T>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835253 | ||||||
chr10:71835377
|
C | T | 1 | a0001c0001t0001g0053 | 2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.41-872G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835377 | ||||||
chr10:71835429
|
G | A | 12 | a0001c0001t0002g0021a0001c0001t0002g0045a0001c0001t0002g0164others(9): Show | 17 | HG00642.hp2 HG01243.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.41-924C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835429 | ||||||
chr10:71835464
|
C | T | 75 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(72): Show | 102 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.41-959G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835464 | ||||||
chr10:71835521
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.41-1016C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835521 | ||||||
chr10:71835647
|
A | G | 2 | a0001c0001t0001g0154a0001c0001t0002g0153 | 2 | HG00642.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.41-1142T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835647 | ||||||
chr10:71835712
|
A | G | 11 | a0001c0001t0002g0021a0001c0001t0002g0045a0001c0001t0002g0164others(8): Show | 16 | HG00642.hp2 HG01243.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.41-1207T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835712 | ||||||
chr10:71835719
|
T | C | 1 | a0001c0001t0001g0051 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.41-1214A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835719 | ||||||
chr10:71835728
|
AG | A | 4 | a0001c0001t0002g0028a0001c0001t0002g0059a0001c0001t0002g0060others(1): Show | 5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.41-1224delC | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835728 | ||||||
chr10:71835821
|
G | GA | 9 | a0001c0001t0001g0043a0001c0001t0001g0223a0001c0001t0002g0009others(6): Show | 15 | HG01069.hp1 HG01074.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.41-1317dupT | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835821 | ||||||
chr10:71835821
|
G | GAA | 13 | a0001c0001t0001g0053a0001c0001t0001g0224a0001c0001t0001g0225others(10): Show | 19 | HG00423.hp1 HG00558.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.41-1318_41-1317dup others(2): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835821 | ||||||
chr10:71835821
|
GA | G | 19 | a0001c0001t0001g0018a0001c0001t0001g0038a0001c0001t0001g0103others(16): Show | 22 | HG01070.hp1 HG01071.hp2 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.41-1317delT | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835821 | ||||||
chr10:71835838
|
AAC | A | 26 | a0001c0001t0001g0090a0001c0001t0001g0177a0001c0001t0002g0002others(23): Show | 64 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.41-1335_41-1334del others(2): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835838 | ||||||
chr10:71835839
|
AC | A | 151 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(148): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.41-1335delG | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835839 | ||||||
chr10:71835840
|
C | A | 51 | a0001c0001t0001g0053a0001c0001t0001g0096a0001c0001t0001g0116others(48): Show | 67 | HG00423.hp1 HG00558.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.41-1335G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835840 | ||||||
chr10:71835844
|
A | AAC | 10 | a0001c0001t0002g0021a0001c0001t0002g0164a0001c0001t0002g0165others(7): Show | 14 | HG00642.hp2 HG01243.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.41-1340_41-1339ins others(2): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835844 | ||||||
chr10:71835845
|
C | A | 11 | a0001c0001t0002g0021a0001c0001t0002g0045a0001c0001t0002g0164others(8): Show | 16 | HG00642.hp2 HG01243.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.41-1340G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835845 | ||||||
chr10:71835925
|
G | A | 1 | a0001c0001t0003g0243 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.41-1420C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835925 | ||||||
chr10:71835979
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.41-1474G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835979 | ||||||
chr10:71835981
|
A | G | 97 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(94): Show | 135 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.41-1476T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835981 | ||||||
chr10:71836066
|
T | C | 183 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(180): Show | 267 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.41-1561A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71836066 | ||||||
chr10:71836118
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.41-1613G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71836118 | ||||||
chr10:71836148
|
A | G | 2 | a0003c0003t0002g0237a0003c0003t0002g0238 | 2 | HG02145.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.41-1643T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71836148 | ||||||
chr10:71836273
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.41-1768G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71836273 | ||||||
chr10:71836371
|
G | T | 1 | a0001c0001t0006g0269 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.41-1866C>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71836371 | ||||||
chr10:71836385
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.41-1880C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71836385 | ||||||
chr10:71836607
|
A | G | 46 | a0001c0001t0001g0033a0001c0001t0001g0081a0001c0001t0001g0096others(43): Show | 79 | HG00140.hp1 HG00558.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.41-2102T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71836607 | ||||||
chr10:71836877
|
A | C | 1 | a0001c0010t0001g0095 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.41-2372T>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71836877 | ||||||
chr10:71837116
|
G | A | 13 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0222others(10): Show | 15 | HG01346.hp1 HG01433.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.41-2611C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71837116 | ||||||
chr10:71837251
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.41-2746G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71837251 | ||||||
chr10:71837283
|
C | T | 5 | a0001c0001t0002g0003a0001c0001t0002g0017a0001c0001t0002g0079others(2): Show | 16 | HG00438.hp1 HG00544.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.41-2778G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71837283 | ||||||
chr10:71837420
|
G | A | 1 | a0003c0003t0004g0239 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.41-2915C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71837420 | ||||||
chr10:71837595
|
C | T | 75 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(72): Show | 102 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.41-3090G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71837595 | ||||||
chr10:71837596
|
G | A | 2 | a0001c0001t0001g0154a0001c0001t0002g0153 | 2 | HG00642.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.41-3091C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71837596 | ||||||
chr10:71837721
|
G | A | 4 | a0002c0002t0004g0036a0002c0002t0004g0098a0002c0002t0004g0099others(1): Show | 5 | HG02280.hp1 HG02922.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.41-3216C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71837721 | ||||||
chr10:71837759
|
T | C | 1 | a0001c0001t0003g0260 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.41-3254A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71837759 | ||||||
chr10:71837896
|
C | A | 1 | a0001c0001t0001g0162 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.41-3391G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71837896 | ||||||
chr10:71838107
|
G | C | 1 | a0001c0001t0002g0133 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.41-3602C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71838107 | ||||||
chr10:71838196
|
C | A | 2 | a0001c0001t0004g0044a0001c0001t0009g0168 | 3 | HG02451.hp2 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.41-3691G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71838196 | ||||||
chr10:71838203
|
A | G | 93 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(90): Show | 131 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.41-3698T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71838203 | ||||||
chr10:71838208
|
C | G | 1 | a0001c0001t0001g0053 | 2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.41-3703G>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71838208 | ||||||
chr10:71838374
|
C | G | 1 | a0001c0011t0008g0094 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.41-3869G>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71838374 | ||||||
chr10:71838434
|
G | A | 93 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(90): Show | 131 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.41-3929C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71838434 | ||||||
chr10:71838435
|
C | CAT | 120 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(117): Show | 169 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.41-3931_41-3930ins others(2): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71838435 | ||||||
chr10:71838464
|
G | A | 3 | a0001c0001t0002g0074a0001c0001t0002g0078a0001c0001t0002g0221 | 3 | HG02451.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.41-3959C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71838464 | ||||||
chr10:71838614
|
C | G | 1 | a0003c0003t0004g0239 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.41-4109G>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71838614 | ||||||
chr10:71838982
|
A | G | 5 | a0001c0001t0002g0009a0001c0001t0002g0217a0001c0001t0002g0218others(2): Show | 9 | HG01243.hp1 HG01891.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.41-4477T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71838982 | ||||||
chr10:71839132
|
A | G | 208 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(205): Show | 331 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.41-4627T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71839132 | ||||||
chr10:71839147
|
A | G | 71 | a0001c0001t0001g0033a0001c0001t0001g0081a0001c0001t0001g0090others(68): Show | 143 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.41-4642T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71839147 | ||||||
chr10:71839168
|
C | T | 12 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(9): Show | 18 | HG00423.hp1 HG00558.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.41-4663G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71839168 | ||||||
chr10:71839178
|
GGCAAATT others(2): Show |
G | 75 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(72): Show | 102 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.41-4682_41-4674del others(9): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71839178 | ||||||
chr10:71839353
|
C | T | 24 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0064others(21): Show | 35 | HG00642.hp2 HG00733.hp2 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.41-4848G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71839353 | ||||||
chr10:71839396
|
T | C | 13 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0064others(10): Show | 19 | HG00733.hp2 HG01256.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.41-4891A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71839396 | ||||||
chr10:71839429
|
A | G | 211 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(208): Show | 334 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.41-4924T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71839429 | ||||||
chr10:71839671
|
C | T | 120 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(117): Show | 169 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.41-5166G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71839671 | ||||||
chr10:71839769
|
G | A | 1 | a0001c0010t0001g0095 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.41-5264C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71839769 | ||||||
chr10:71839784
|
G | A | 3 | a0003c0003t0002g0237a0003c0003t0002g0238a0003c0003t0004g0239 | 3 | HG02145.hp1 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.41-5279C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71839784 | ||||||
chr10:71839841
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.41-5336C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71839841 | ||||||
chr10:71840141
|
T | C | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG02572.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.41-5636A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71840141 | ||||||
chr10:71840148
|
G | A | 1 | a0001c0001t0002g0134 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.41-5643C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71840148 | ||||||
chr10:71840211
|
G | A | 1 | a0001c0001t0002g0074 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.41-5706C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71840211 | ||||||
chr10:71840339
|
G | A | 13 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0064others(10): Show | 19 | HG00733.hp2 HG01256.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.41-5834C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71840339 | ||||||
chr10:71840342
|
C | T | 1 | a0001c0001t0001g0053 | 2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.41-5837G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71840342 | ||||||
chr10:71840343
|
G | A | 6 | a0001c0001t0001g0066a0001c0001t0002g0011a0001c0001t0002g0065others(3): Show | 9 | HG01258.hp2 HG01361.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.41-5838C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71840343 | ||||||
chr10:71840398
|
G | A | 71 | a0001c0001t0001g0033a0001c0001t0001g0081a0001c0001t0001g0090others(68): Show | 143 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.41-5893C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71840398 | ||||||
chr10:71840463
|
T | C | 9 | a0001c0001t0002g0021a0001c0001t0002g0045a0001c0001t0002g0164others(6): Show | 13 | HG00642.hp2 HG01243.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.41-5958A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71840463 | ||||||
chr10:71840559
|
A | G | 75 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(72): Show | 102 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.41-6054T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71840559 | ||||||
chr10:71840591
|
T | C | 1 | a0001c0001t0004g0044 | 2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.41-6086A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71840591 | ||||||
chr10:71840747
|
G | A | 88 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(85): Show | 122 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.41-6242C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71840747 | ||||||
chr10:71840763
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.41-6258A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71840763 | ||||||
chr10:71840862
|
C | A | 13 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0064others(10): Show | 19 | HG00733.hp2 HG01256.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.41-6357G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71840862 | ||||||
chr10:71840888
|
T | C | 12 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(9): Show | 18 | HG00423.hp1 HG00558.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.41-6383A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71840888 | ||||||
chr10:71840893
|
TG | T | 24 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0064others(21): Show | 35 | HG00642.hp2 HG00733.hp2 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.41-6389delC | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71840893 | ||||||
chr10:71840937
|
A | G | 2 | a0001c0001t0001g0154a0001c0001t0002g0153 | 2 | HG00642.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.41-6432T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71840937 | ||||||
chr10:71841045
|
T | G | 5 | a0001c0001t0002g0009a0001c0001t0002g0217a0001c0001t0002g0218others(2): Show | 9 | HG01243.hp1 HG01891.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.41-6540A>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71841045 | ||||||
chr10:71841094
|
C | T | 2 | a0001c0001t0002g0078a0001c0001t0002g0221 | 2 | HG02451.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.41-6589G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71841094 | ||||||
chr10:71841199
|
A | G | 120 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(117): Show | 169 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.41-6694T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71841199 | ||||||
chr10:71841341
|
C | T | 210 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(207): Show | 333 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.41-6836G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71841341 | ||||||
chr10:71841487
|
C | T | 3 | a0003c0003t0002g0237a0003c0003t0002g0238a0003c0003t0004g0239 | 3 | HG02145.hp1 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.41-6982G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71841487 | ||||||
chr10:71841488
|
G | A | 88 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(85): Show | 122 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.41-6983C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71841488 | ||||||
chr10:71841517
|
G | A | 75 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(72): Show | 102 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.41-7012C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71841517 | ||||||
chr10:71841804
|
G | A | 1 | a0001c0001t0002g0017 | 3 | NA19001.hp1 NA19068.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.41-7299C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71841804 | ||||||
chr10:71841862
|
C | T | 13 | a0001c0001t0001g0053a0001c0001t0001g0223a0001c0001t0001g0224others(10): Show | 20 | HG00423.hp1 HG00558.hp2 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.41-7357G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71841862 | ||||||
chr10:71841932
|
C | T | 3 | a0001c0001t0001g0102a0001c0010t0001g0095a0001c0011t0008g0094 | 3 | HG01433.hp2 HG02818.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.41-7427G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71841932 | ||||||
chr10:71841954
|
C | T | 4 | a0002c0002t0004g0036a0002c0002t0004g0098a0002c0002t0004g0099others(1): Show | 5 | HG02280.hp1 HG02922.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.41-7449G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71841954 | ||||||
chr10:71841973
|
T | G | 93 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(90): Show | 131 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.41-7468A>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71841973 | ||||||
chr10:71842000
|
C | T | 1 | a0001c0001t0002g0120 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.41-7495G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71842000 | ||||||
chr10:71842005
|
T | TA | 73 | a0001c0001t0001g0033a0001c0001t0001g0081a0001c0001t0001g0090others(70): Show | 145 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.41-7501dupT | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71842005 | ||||||
chr10:71842005
|
T | TAA | 5 | a0001c0001t0002g0009a0001c0001t0002g0217a0001c0001t0002g0218others(2): Show | 9 | HG01243.hp1 HG01891.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.41-7502_41-7501dup others(2): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71842005 | ||||||
chr10:71842195
|
C | T | 1 | a0001c0001t0001g0063 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.41-7690G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71842195 | ||||||
chr10:71842254
|
T | G | 1 | a0001c0001t0001g0071 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.41-7749A>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71842254 | ||||||
chr10:71842434
|
C | A | 1 | a0001c0001t0010g0092 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.41-7929G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71842434 | ||||||
chr10:71842483
|
C | T | 75 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(72): Show | 102 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.41-7978G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71842483 | ||||||
chr10:71842572
|
C | G | 1 | a0001c0001t0004g0044 | 2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.41-8067G>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71842572 | ||||||
chr10:71842695
|
T | C | 120 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(117): Show | 169 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.41-8190A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71842695 | ||||||
chr10:71842794
|
C | T | 1 | a0001c0001t0002g0077 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.41-8289G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71842794 | ||||||
chr10:71842892
|
A | G | 18 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0041others(15): Show | 26 | HG00099.hp2 HG01081.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.40+8290T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71842892 | ||||||
chr10:71842900
|
C | T | 5 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(2): Show | 6 | HG00423.hp1 HG01069.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.40+8282G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71842900 | ||||||
chr10:71842936
|
A | G | 1 | a0001c0001t0002g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.40+8246T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71842936 | ||||||
chr10:71843015
|
G | A | 1 | a0001c0001t0002g0216 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.40+8167C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71843015 | ||||||
chr10:71843038
|
C | T | 1 | a0001c0001t0002g0179 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.40+8144G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71843038 | ||||||
chr10:71843056
|
C | A | 1 | a0001c0001t0001g0207 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.40+8126G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71843056 | ||||||
chr10:71843125
|
C | G | 208 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(205): Show | 331 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.40+8057G>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71843125 | ||||||
chr10:71843177
|
G | C | 88 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(85): Show | 122 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.40+8005C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71843177 | ||||||
chr10:71843221
|
G | A | 2 | a0001c0001t0003g0056a0001c0001t0003g0261 | 3 | HG00741.hp2 HG01070.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.40+7961C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71843221 | ||||||
chr10:71843304
|
G | T | 24 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0064others(21): Show | 35 | HG00642.hp2 HG00733.hp2 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.40+7878C>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71843304 | ||||||
chr10:71843331
|
C | G | 2 | a0001c0001t0003g0245a0001c0001t0003g0246 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.40+7851G>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71843331 | ||||||
chr10:71843339
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.40+7843G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71843339 | ||||||
chr10:71843340
|
A | G | 229 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(226): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.40+7842T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71843340 | ||||||
chr10:71843357
|
C | T | 2 | a0001c0001t0003g0244a0001c0001t0003g0263 | 2 | HG02738.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.40+7825G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71843357 | ||||||
chr10:71843392
|
C | T | 1 | a0001c0001t0002g0158 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.40+7790G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71843392 | ||||||
chr10:71843425
|
A | ACT | 8 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0010t0001g0095others(5): Show | 9 | HG01433.hp2 HG02280.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.40+7755_40+7756dup others(2): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71843425 | ||||||
chr10:71843457
|
C | CTA | 3 | a0001c0001t0002g0028a0001c0001t0002g0059a0001c0001t0002g0060 | 4 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.40+7723_40+7724dup others(2): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71843457 | ||||||
chr10:71843548
|
T | C | 1 | a0001c0001t0001g0019 | 3 | HG00621.hp1 NA18961.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.40+7634A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71843548 | ||||||
chr10:71843583
|
T | G | 1 | a0001c0001t0002g0097 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.40+7599A>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71843583 | ||||||
chr10:71843713
|
T | G | 13 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0064others(10): Show | 19 | HG00733.hp2 HG01256.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.40+7469A>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71843713 | ||||||
chr10:71844172
|
G | A | 2 | a0001c0001t0004g0044a0001c0001t0009g0168 | 3 | HG02451.hp2 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.40+7010C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71844172 | ||||||
chr10:71844181
|
T | C | 1 | a0001c0001t0011g0135 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.40+7001A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71844181 | ||||||
chr10:71844303
|
C | G | 1 | a0001c0001t0001g0104 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.40+6879G>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71844303 | ||||||
chr10:71844450
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.40+6732C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71844450 | ||||||
chr10:71844558
|
C | T | 1 | a0003c0003t0004g0239 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.40+6624G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71844558 | ||||||
chr10:71844659
|
C | G | 1 | a0001c0001t0003g0243 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.40+6523G>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71844659 | ||||||
chr10:71844680
|
C | T | 210 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(207): Show | 333 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.40+6502G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71844680 | ||||||
chr10:71844696
|
T | C | 1 | a0001c0001t0002g0075 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.40+6486A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71844696 | ||||||
chr10:71844763
|
C | T | 2 | a0001c0001t0002g0029a0001c0001t0002g0062 | 3 | HG01069.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.40+6419G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71844763 | ||||||
chr10:71844780
|
A | G | 117 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(114): Show | 166 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.40+6402T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71844780 | ||||||
chr10:71845080
|
G | A | 1 | a0001c0001t0001g0053 | 2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.40+6102C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71845080 | ||||||
chr10:71845160
|
T | C | 1 | a0001c0001t0002g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.40+6022A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71845160 | ||||||
chr10:71845209
|
A | G | 1 | a0001c0001t0001g0119 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.40+5973T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71845209 | ||||||
chr10:71845300
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.40+5882C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71845300 | ||||||
chr10:71845326
|
T | TGGC | 5 | a0001c0001t0001g0222a0001c0001t0002g0028a0001c0001t0002g0059others(2): Show | 6 | HG01346.hp1 HG02145.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.40+5853_40+5855dup others(3): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71845326 | ||||||
chr10:71845383
|
G | A | 39 | a0001c0001t0002g0093a0001c0001t0003g0001a0001c0001t0003g0015others(36): Show | 71 | HG00140.hp1 HG00558.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.40+5799C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71845383 | ||||||
chr10:71845529
|
C | T | 1 | a0001c0010t0001g0095 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.40+5653G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71845529 | ||||||
chr10:71845569
|
G | T | 1 | a0001c0001t0002g0037 | 2 | NA18964.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.40+5613C>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71845569 | ||||||
chr10:71845636
|
T | C | 13 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0222others(10): Show | 15 | HG01346.hp1 HG01433.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.40+5546A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71845636 | ||||||
chr10:71845639
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.40+5543G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71845639 | ||||||
chr10:71845703
|
G | A | 5 | a0001c0001t0002g0009a0001c0001t0002g0217a0001c0001t0002g0218others(2): Show | 9 | HG01243.hp1 HG01891.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.40+5479C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71845703 | ||||||
chr10:71845733
|
A | G | 120 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(117): Show | 169 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.40+5449T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71845733 | ||||||
chr10:71845786
|
G | T | 1 | a0001c0001t0001g0171 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.40+5396C>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71845786 | ||||||
chr10:71845819
|
T | C | 1 | a0001c0010t0001g0095 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.40+5363A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71845819 | ||||||
chr10:71846074
|
T | C | 24 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0064others(21): Show | 35 | HG00642.hp2 HG00733.hp2 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.40+5108A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71846074 | ||||||
chr10:71846096
|
G | C | 229 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(226): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.40+5086C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71846096 | ||||||
chr10:71846099
|
TACTA | T | 6 | a0001c0001t0001g0101a0001c0001t0002g0176a0002c0002t0004g0036others(3): Show | 7 | HG02280.hp1 HG02818.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.40+5079_40+5082del others(4): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71846099 | ||||||
chr10:71846169
|
G | T | 191 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(188): Show | 312 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.40+5013C>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71846169 | ||||||
chr10:71846425
|
T | TA | 35 | a0001c0001t0001g0117a0001c0001t0001g0146a0001c0001t0001g0208others(32): Show | 49 | HG00423.hp1 HG00558.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.40+4756dupT | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71846425 | ||||||
chr10:71846425
|
TA | T | 12 | a0001c0001t0001g0047a0001c0001t0001g0096a0001c0001t0001g0103others(9): Show | 13 | HG00642.hp1 HG01975.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.40+4756delT | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71846425 | ||||||
chr10:71846463
|
G | A | 4 | a0001c0001t0005g0272a0001c0001t0007g0273a0001c0001t0007g0274others(1): Show | 4 | HG00639.hp1 HG01123.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.40+4719C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71846463 | ||||||
chr10:71846468
|
T | G | 2 | a0001c0001t0001g0208a0001c0001t0002g0209 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.40+4714A>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71846468 | ||||||
chr10:71846504
|
C | A | 71 | a0001c0001t0001g0033a0001c0001t0001g0081a0001c0001t0001g0090others(68): Show | 143 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.40+4678G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71846504 | ||||||
chr10:71846567
|
A | G | 3 | a0003c0003t0002g0237a0003c0003t0002g0238a0003c0003t0004g0239 | 3 | HG02145.hp1 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.40+4615T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71846567 | ||||||
chr10:71846600
|
C | A | 2 | a0003c0003t0002g0237a0003c0003t0002g0238 | 2 | HG02145.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.40+4582G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71846600 | ||||||
chr10:71846635
|
G | A | 17 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0222others(14): Show | 19 | HG00639.hp1 HG01123.hp1 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.40+4547C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71846635 | ||||||
chr10:71846656
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.40+4526G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71846656 | ||||||
chr10:71846731
|
CA | C | 12 | a0001c0001t0001g0043a0001c0001t0001g0064a0001c0001t0001g0066others(9): Show | 16 | HG01496.hp1 HG01496.hp2 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.40+4450delT | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71846731 | ||||||
chr10:71846731
|
CAA | C | 143 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(140): Show | 247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.40+4449_40+4450del others(2): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71846731 | ||||||
chr10:71846731
|
CAAA | C | 94 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(91): Show | 128 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.40+4448_40+4450del others(3): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71846731 | ||||||
chr10:71846731
|
CAAAA | C | 15 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0223others(12): Show | 19 | HG01074.hp2 HG01243.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.40+4447_40+4450del others(4): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71846731 | ||||||
chr10:71846778
|
C | A | 1 | a0001c0001t0001g0149 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.40+4404G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71846778 | ||||||
chr10:71846997
|
A | C | 5 | a0001c0001t0002g0009a0001c0001t0002g0217a0001c0001t0002g0218others(2): Show | 9 | HG01243.hp1 HG01891.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.40+4185T>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71846997 | ||||||
chr10:71847223
|
G | A | 70 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(67): Show | 97 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.40+3959C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71847223 | ||||||
chr10:71847257
|
C | A | 1 | a0001c0001t0001g0150 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.40+3925G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71847257 | ||||||
chr10:71847260
|
G | A | 1 | a0001c0001t0001g0072 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.40+3922C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71847260 | ||||||
chr10:71847370
|
A | C | 1 | a0001c0001t0001g0169 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.40+3812T>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71847370 | ||||||
chr10:71847417
|
G | A | 4 | a0001c0001t0005g0272a0001c0001t0007g0273a0001c0001t0007g0274others(1): Show | 4 | HG00639.hp1 HG01123.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.40+3765C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71847417 | ||||||
chr10:71847453
|
T | C | 120 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(117): Show | 169 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.40+3729A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71847453 | ||||||
chr10:71847549
|
A | G | 2 | a0001c0001t0001g0046a0001c0001t0002g0216 | 3 | HG00140.hp2 HG01192.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.40+3633T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71847549 | ||||||
chr10:71847568
|
C | T | 120 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(117): Show | 169 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.40+3614G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71847568 | ||||||
chr10:71847605
|
G | A | 4 | a0001c0001t0005g0272a0001c0001t0007g0273a0001c0001t0007g0274others(1): Show | 4 | HG00639.hp1 HG01123.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.40+3577C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71847605 | ||||||
chr10:71847612
|
T | C | 5 | a0001c0001t0001g0101a0002c0002t0004g0036a0002c0002t0004g0098others(2): Show | 6 | HG02280.hp1 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.40+3570A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71847612 | ||||||
chr10:71847865
|
T | G | 5 | a0001c0001t0001g0101a0002c0002t0004g0036a0002c0002t0004g0098others(2): Show | 6 | HG02280.hp1 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.40+3317A>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71847865 | ||||||
chr10:71847937
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.40+3245C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71847937 | ||||||
chr10:71847964
|
C | A | 1 | a0001c0001t0001g0214 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.40+3218G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71847964 | ||||||
chr10:71847997
|
T | C | 24 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0064others(21): Show | 35 | HG00642.hp2 HG00733.hp2 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.40+3185A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71847997 | ||||||
chr10:71848011
|
C | A | 5 | a0001c0001t0001g0222a0001c0001t0002g0028a0001c0001t0002g0059others(2): Show | 6 | HG01346.hp1 HG02145.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.40+3171G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71848011 | ||||||
chr10:71848103
|
C | A | 1 | a0001c0001t0001g0102 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.40+3079G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71848103 | ||||||
chr10:71848193
|
G | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0215 | 4 | NA18970.hp1 NA18984.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.40+2989C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71848193 | ||||||
chr10:71848315
|
A | G | 3 | a0001c0001t0002g0028a0001c0001t0002g0059a0001c0001t0002g0060 | 4 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.40+2867T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71848315 | ||||||
chr10:71848343
|
T | C | 1 | a0001c0001t0002g0216 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.40+2839A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71848343 | ||||||
chr10:71848641
|
A | G | 3 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225 | 3 | HG00423.hp1 HG01074.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.40+2541T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71848641 | ||||||
chr10:71848810
|
A | C | 1 | a0001c0001t0001g0114 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.40+2372T>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71848810 | ||||||
chr10:71848966
|
A | G | 211 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(208): Show | 334 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.40+2216T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71848966 | ||||||
chr10:71849244
|
T | G | 1 | a0001c0001t0003g0265 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.40+1938A>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71849244 | ||||||
chr10:71849302
|
G | C | 69 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(66): Show | 96 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.40+1880C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71849302 | ||||||
chr10:71849525
|
CG | C | 5 | a0001c0001t0002g0009a0001c0001t0002g0217a0001c0001t0002g0218others(2): Show | 9 | HG01243.hp1 HG01891.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.40+1656delC | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71849525 | ||||||
chr10:71849534
|
G | A | 2 | a0001c0001t0001g0154a0001c0001t0002g0153 | 2 | HG00642.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.40+1648C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71849534 | ||||||
chr10:71849562
|
T | G | 1 | a0001c0001t0003g0268 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.40+1620A>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71849562 | ||||||
chr10:71849607
|
A | G | 3 | a0003c0003t0002g0237a0003c0003t0002g0238a0003c0003t0004g0239 | 3 | HG02145.hp1 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.40+1575T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71849607 | ||||||
chr10:71849624
|
AAAAC | A | 5 | a0001c0001t0002g0009a0001c0001t0002g0217a0001c0001t0002g0218others(2): Show | 9 | HG01243.hp1 HG01891.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.40+1554_40+1557del others(4): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71849624 | ||||||
chr10:71849646
|
A | C | 5 | a0001c0001t0002g0009a0001c0001t0002g0217a0001c0001t0002g0218others(2): Show | 9 | HG01243.hp1 HG01891.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.40+1536T>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71849646 | ||||||
chr10:71849658
|
G | A | 1 | a0001c0001t0002g0235 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.40+1524C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71849658 | ||||||
chr10:71849660
|
G | T | 11 | a0001c0001t0001g0018a0001c0001t0001g0103a0001c0001t0001g0104others(8): Show | 13 | HG02074.hp2 NA18612.hp2 NA18950.hp2 others(10): Show |
intron_variant | MODIFIER | c.40+1522C>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71849660 | ||||||
chr10:71849690
|
T | C | 3 | a0003c0003t0002g0237a0003c0003t0002g0238a0003c0003t0004g0239 | 3 | HG02145.hp1 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.40+1492A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71849690 | ||||||
chr10:71849771
|
T | C | 5 | a0001c0001t0003g0057a0001c0001t0003g0266a0001c0001t0003g0267others(2): Show | 6 | HG00140.hp1 HG01109.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.40+1411A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71849771 | ||||||
chr10:71849805
|
A | G | 210 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(207): Show | 333 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.40+1377T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71849805 | ||||||
chr10:71849861
|
C | G | 1 | a0001c0001t0002g0217 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.40+1321G>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71849861 | ||||||
chr10:71849903
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.40+1279G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71849903 | ||||||
chr10:71850057
|
G | GA | 105 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(102): Show | 148 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.40+1124dupT | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71850057 | ||||||
chr10:71850265
|
GCTCT | G | 5 | a0001c0001t0002g0009a0001c0001t0002g0217a0001c0001t0002g0218others(2): Show | 9 | HG01243.hp1 HG01891.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.40+913_40+916delAG others(2): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71850265 | ||||||
chr10:71850284
|
T | C | 17 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0064others(14): Show | 23 | HG00642.hp1 HG00733.hp2 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.40+898A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71850284 | ||||||
chr10:71850298
|
G | A | 97 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(94): Show | 135 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.40+884C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71850298 | ||||||
chr10:71850362
|
T | C | 1 | a0001c0001t0003g0270 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.40+820A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71850362 | ||||||
chr10:71850450
|
T | G | 5 | a0001c0001t0002g0009a0001c0001t0002g0217a0001c0001t0002g0218others(2): Show | 9 | HG01243.hp1 HG01891.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.40+732A>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71850450 | ||||||
chr10:71850479
|
T | C | 1 | a0001c0001t0002g0221 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.40+703A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71850479 | ||||||
chr10:71850499
|
T | C | 20 | a0001c0001t0001g0014a0001c0001t0001g0053a0001c0001t0001g0222others(17): Show | 30 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.40+683A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71850499 | ||||||
chr10:71850580
|
C | T | 13 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0064others(10): Show | 19 | HG00733.hp2 HG01256.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.40+602G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71850580 | ||||||
chr10:71850837
|
T | C | 1 | a0001c0001t0003g0271 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.40+345A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71850837 | ||||||
chr10:71850916
|
C | T | 1 | a0001c0001t0001g0063 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.40+266G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71850916 | ||||||
chr10:71850982
|
C | T | 2 | a0001c0001t0002g0029a0001c0001t0002g0062 | 3 | HG01069.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.40+200G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71850982 | ||||||
chr10:71851017
|
C | CCCAGAGA others(3): Show |
6 | a0001c0001t0002g0028a0001c0001t0002g0059a0001c0001t0002g0060others(3): Show | 7 | HG02145.hp1 HG02145.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.40+155_40+164dupCT others(8): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71851017 | ||||||
chr10:71851101
|
G | C | 1 | a0001c0001t0002g0236 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.40+81C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71851101 |