geneid | 192670 |
---|---|
ensemblid | ENSG00000134698.11 |
hgncid | 18424 |
symbol | AGO4 |
name | argonaute RISC component 4 |
refseq_nuc | NM_017629.4 |
refseq_prot | NP_060099.2 |
ensembl_nuc | ENST00000373210.4 |
ensembl_prot | ENSP00000362306.3 |
mane_status | MANE Select |
chr | chr1 |
start | 35808016 |
end | 35857890 |
strand | + |
ver | v1.2 |
region | chr1:35808016-35857890 |
region5000 | chr1:35803016-35862890 |
regionname0 | AGO4_chr1_35808016_35857890 |
regionname5000 | AGO4_chr1_35803016_35862890 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2586 | 176 | 75 | 26 | 59 | 3 | 11 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
c0002 | 0/0 | 2586 | 86 | 10 | 16 | 42 | 7 | 11 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
c0003 | 0/0 | 2586 | 6 | 6 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
c0004 | 0/0 | 2586 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
c0005 | 0/0 | 2586 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 4685 | 87 | 27 | 15 | 32 | 7 | 6 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
t0002 | 0/0 | 4688 | 75 | 10 | 13 | 48 | 1 | 3 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
t0003 | 0/1 | 4684 | 29 | 18 | 3 | 5 | 0 | 2 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
t0004 | 0/0 | 4684 | 14 | 5 | 0 | 3 | 2 | 4 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
t0005 | 0/0 | 4686 | 12 | 6 | 1 | 1 | 0 | 4 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
t0006 | 0/0 | 4685 | 6 | 3 | 0 | 2 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
t0007 | 0/0 | 4693 | 4 | 4 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
t0008 | 0/0 | 4686 | 4 | 2 | 1 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
t0009 | 0/0 | 4685 | 4 | 2 | 2 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
t0010 | 0/0 | 4689 | 3 | 1 | 0 | 2 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
t0011 | 0/0 | 4687 | 2 | 2 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
t0012 | 0/0 | 4687 | 2 | 2 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
t0013 | 0/0 | 4685 | 2 | 2 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
t0014 | 0/0 | 4685 | 2 | 0 | 2 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
t0015 | 0/0 | 4687 | 2 | 2 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
t0016 | 0/0 | 4684 | 2 | 0 | 2 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
t0017 | 0/0 | 4694 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
t0018 | 0/0 | 4690 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
t0019 | 0/0 | 4689 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
t0020 | 0/0 | 4690 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
t0021 | 0/0 | 4685 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
t0022 | 0/0 | 4688 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
t0023 | 0/0 | 4686 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
t0024 | 0/0 | 4685 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
t0025 | 0/0 | 4686 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
t0026 | 1/0 | 4687 | 1 | 0 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
t0027 | 0/0 | 4685 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
t0028 | 0/0 | 4687 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
t0029 | 0/0 | 4687 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
t0030 | 0/0 | 4685 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
t0031 | 0/0 | 4685 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
t0032 | 0/0 | 4685 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
t0033 | 0/0 | 4684 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
t0034 | 0/0 | 4686 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
t0035 | 0/0 | 4685 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
t0036 | 0/0 | 4685 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0046 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0247 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2586 | 176 | 75 | 26 | 59 | 3 | 11 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0002 | 0/0 | 2586 | 86 | 10 | 16 | 42 | 7 | 11 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0003 | 0/0 | 2586 | 6 | 6 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0005 | 0/0 | 2586 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0002c0004 | 0/0 | 2586 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 7270 | 20 | 17 | 3 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0001t0002 | 0/0 | 7273 | 74 | 10 | 13 | 47 | 1 | 3 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0001t0003 | 0/1 | 7269 | 29 | 18 | 3 | 5 | 0 | 2 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0001t0004 | 0/0 | 7269 | 7 | 1 | 0 | 0 | 2 | 4 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0001t0005 | 0/0 | 7271 | 6 | 6 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0001t0006 | 0/0 | 7270 | 6 | 3 | 0 | 2 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0001t0007 | 0/0 | 7278 | 4 | 4 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0001t0008 | 0/0 | 7271 | 2 | 1 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0001t0009 | 0/0 | 7270 | 4 | 2 | 2 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0001t0010 | 0/0 | 7274 | 3 | 1 | 0 | 2 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0001t0011 | 0/0 | 7272 | 2 | 2 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0001t0012 | 0/0 | 7272 | 2 | 2 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0001t0015 | 0/0 | 7272 | 2 | 2 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0001t0016 | 0/0 | 7269 | 2 | 0 | 2 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0001t0018 | 0/0 | 7275 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0001t0019 | 0/0 | 7274 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0001t0020 | 0/0 | 7275 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0001t0022 | 0/0 | 7273 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0001t0023 | 0/0 | 7271 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0001t0025 | 0/0 | 7271 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0001t0026 | 1/0 | 7272 | 1 | 0 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0001t0028 | 0/0 | 7272 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0001t0030 | 0/0 | 7270 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0001t0033 | 0/0 | 7269 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0001t0034 | 0/0 | 7271 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0001t0035 | 0/0 | 7270 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0001t0036 | 0/0 | 7270 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0002t0001 | 0/0 | 7270 | 66 | 9 | 12 | 32 | 7 | 6 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0002t0004 | 0/0 | 7269 | 3 | 0 | 0 | 3 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0002t0005 | 0/0 | 7271 | 6 | 0 | 1 | 1 | 0 | 4 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0002t0008 | 0/0 | 7271 | 2 | 1 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0002t0014 | 0/0 | 7270 | 2 | 0 | 2 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0002t0017 | 0/0 | 7279 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0002t0021 | 0/0 | 7270 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0002t0024 | 0/0 | 7270 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0002t0027 | 0/0 | 7270 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0002t0029 | 0/0 | 7272 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0002t0031 | 0/0 | 7270 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0002t0032 | 0/0 | 7270 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0003t0001 | 0/0 | 7270 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0003t0004 | 0/0 | 7269 | 3 | 3 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0003t0013 | 0/0 | 7270 | 2 | 2 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0001c0005t0004 | 0/0 | 7269 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
a0002c0004t0002 | 0/0 | 7273 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | copy fasta | chr1 | 35803016 | 35862890 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0001 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0046 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0004g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0004g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0005g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0005g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0005g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0005g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0006g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0006g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0006g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0006g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0006g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0006g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0007g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0007g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0007g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0007g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0008g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0008g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0009g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0009g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0009g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0009g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0010g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0010g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0010g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0011g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0012g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0012g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0015g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0015g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0016g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0016g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0018g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0019g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0020g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0022g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0023g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0025g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0026g0247 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0028g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0030g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0033g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0034g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0035g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0036g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0005g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0005g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0005g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0005g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0005g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0005g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0008g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0008g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0014g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0014g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0017g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0021g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0024g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0027g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0029g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0031g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0032g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0003t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0003t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0003t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0003t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0003t0013g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0003t0013g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0005t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0002c0004t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0002 | t0001 | g0180 | EUR | GBR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0087 | EUR | GBR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG00280 | hp1 | a0001 | c0002 | t0001 | g0208 | EUR | FIN | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG00280 | hp2 | a0001 | c0001 | t0004 | g0012 | EUR | FIN | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0202 | EUR | FIN | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG00323 | hp2 | a0001 | c0001 | t0004 | g0012 | EUR | FIN | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG00438 | hp1 | a0001 | c0001 | t0006 | g0048 | EAS | CHS | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG00438 | hp2 | a0001 | c0001 | t0010 | g0107 | EAS | CHS | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | CHS | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | CHS | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0178 | AMR | PUR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0094 | AMR | PUR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG00673 | hp1 | a0001 | c0001 | t0010 | g0013 | EAS | CHS | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG00673 | hp2 | a0001 | c0002 | t0005 | g0197 | EAS | CHS | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0179 | AMR | PUR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01069 | hp1 | a0001 | c0001 | t0009 | g0055 | AMR | PUR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0245 | AMR | PUR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0184 | AMR | PUR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01071 | hp2 | a0001 | c0001 | t0009 | g0056 | AMR | PUR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01074 | hp1 | a0001 | c0002 | t0001 | g0163 | AMR | PUR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0134 | AMR | PUR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0174 | AMR | PUR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01168 | hp1 | a0001 | c0001 | t0016 | g0252 | AMR | PUR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01168 | hp2 | a0001 | c0002 | t0014 | g0203 | AMR | PUR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01169 | hp1 | a0001 | c0001 | t0016 | g0250 | AMR | PUR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01175 | hp1 | a0001 | c0002 | t0005 | g0175 | AMR | PUR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0023 | AMR | PUR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01243 | hp1 | a0001 | c0001 | t0008 | g0172 | AMR | PUR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0045 | AMR | PUR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0181 | AMR | CLM | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01255 | hp2 | a0001 | c0001 | t0022 | g0251 | AMR | CLM | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0081 | AMR | CLM | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0030 | AMR | CLM | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0079 | AMR | CLM | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0239 | AMR | CLM | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | CLM | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01433 | hp2 | a0001 | c0002 | t0014 | g0207 | AMR | CLM | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01516 | hp1 | a0001 | c0002 | t0001 | g0170 | EUR | IBS | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01516 | hp2 | a0001 | c0002 | t0001 | g0221 | EUR | IBS | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0220 | EUR | IBS | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01517 | hp2 | a0001 | c0002 | t0001 | g0228 | EUR | IBS | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0117 | AFR | ACB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01891 | hp2 | a0001 | c0003 | t0004 | g0157 | AFR | ACB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0241 | AMR | PEL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01928 | hp2 | a0001 | c0001 | t0019 | g0098 | AMR | PEL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | PEL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0125 | AMR | PEL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01943 | hp2 | a0001 | c0002 | t0021 | g0168 | AMR | PEL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0190 | AMR | PEL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | PEL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0232 | EAS | KHV | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02055 | hp1 | a0001 | c0001 | t0006 | g0040 | AFR | ACB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02055 | hp2 | a0001 | c0003 | t0013 | g0156 | AFR | ACB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0210 | EAS | KHV | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02056 | hp2 | a0001 | c0001 | t0020 | g0130 | EAS | KHV | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0236 | EAS | KHV | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02129 | hp2 | a0001 | c0001 | t0030 | g0071 | EAS | KHV | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02145 | hp1 | a0001 | c0001 | t0007 | g0015 | AFR | ACB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02145 | hp2 | a0001 | c0001 | t0015 | g0074 | AFR | ACB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | CDX | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0230 | EAS | CDX | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02258 | hp1 | a0001 | c0001 | t0007 | g0016 | AFR | ACB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02258 | hp2 | a0001 | c0002 | t0001 | g0204 | AFR | ACB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0213 | AMR | PEL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0116 | AFR | ACB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02280 | hp2 | a0001 | c0001 | t0009 | g0054 | AFR | ACB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02300 | hp2 | a0001 | c0002 | t0001 | g0183 | AMR | PEL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | ACB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02451 | hp2 | a0001 | c0001 | t0009 | g0057 | AFR | ACB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02572 | hp1 | a0001 | c0001 | t0010 | g0246 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02602 | hp1 | a0001 | c0001 | t0018 | g0133 | SAS | PJL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0014 | SAS | PJL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02615 | hp1 | a0001 | c0001 | t0007 | g0018 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02630 | hp2 | a0001 | c0001 | t0008 | g0143 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0214 | SAS | PJL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0223 | SAS | PJL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0041 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02717 | hp2 | a0001 | c0005 | t0004 | g0069 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02723 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0039 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02809 | hp2 | a0001 | c0001 | t0005 | g0058 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02818 | hp1 | a0001 | c0001 | t0015 | g0073 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02886 | hp1 | a0001 | c0003 | t0013 | g0158 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0242 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02922 | hp1 | a0001 | c0003 | t0004 | g0159 | AFR | ESN | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0049 | AFR | ESN | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0127 | AFR | ESN | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02970 | hp1 | a0001 | c0001 | t0012 | g0154 | AFR | ESN | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02970 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | ESN | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03017 | hp1 | a0001 | c0002 | t0031 | g0216 | SAS | PJL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03017 | hp2 | a0001 | c0001 | t0004 | g0253 | SAS | PJL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03041 | hp1 | a0001 | c0002 | t0001 | g0234 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03098 | hp2 | a0001 | c0001 | t0011 | g0006 | AFR | MSL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03130 | hp1 | a0001 | c0001 | t0007 | g0017 | AFR | ESN | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03130 | hp2 | a0001 | c0001 | t0006 | g0021 | AFR | ESN | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03139 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | ESN | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03195 | hp1 | a0001 | c0001 | t0005 | g0249 | AFR | ESN | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03195 | hp2 | a0001 | c0002 | t0001 | g0212 | AFR | ESN | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | MSL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03209 | hp2 | a0001 | c0001 | t0006 | g0028 | AFR | MSL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03453 | hp1 | a0001 | c0001 | t0012 | g0256 | AFR | MSL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0062 | AFR | MSL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0051 | AFR | MSL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03486 | hp2 | a0001 | c0001 | t0011 | g0006 | AFR | MSL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0124 | SAS | PJL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0182 | SAS | PJL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03491 | hp1 | a0001 | c0002 | t0001 | g0201 | SAS | PJL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03491 | hp2 | a0001 | c0001 | t0004 | g0053 | SAS | PJL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03516 | hp1 | a0001 | c0002 | t0008 | g0199 | AFR | ESN | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03516 | hp2 | a0001 | c0003 | t0004 | g0155 | AFR | ESN | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0224 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03579 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | MSL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03579 | hp2 | a0001 | c0001 | t0023 | g0063 | AFR | MSL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03654 | hp1 | a0001 | c0002 | t0005 | g0240 | SAS | PJL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03654 | hp2 | a0001 | c0002 | t0005 | g0162 | SAS | PJL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0191 | SAS | PJL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03704 | hp2 | a0001 | c0001 | t0004 | g0254 | SAS | PJL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0235 | SAS | BEB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0077 | SAS | BEB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03927 | hp1 | a0001 | c0002 | t0005 | g0219 | SAS | BEB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0047 | SAS | BEB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG04199 | hp1 | a0001 | c0002 | t0005 | g0237 | SAS | STU | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG04199 | hp2 | a0001 | c0001 | t0006 | g0020 | SAS | STU | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | YRI | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | YRI | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | CHB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | CHB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | YRI | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0050 | AFR | YRI | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18941 | hp1 | a0001 | c0002 | t0004 | g0186 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18946 | hp1 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18954 | hp1 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18960 | hp1 | a0001 | c0002 | t0027 | g0008 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18964 | hp1 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18968 | hp2 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18969 | hp2 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18972 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18975 | hp2 | a0001 | c0001 | t0006 | g0033 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18978 | hp2 | a0001 | c0002 | t0032 | g0196 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18982 | hp2 | a0001 | c0002 | t0004 | g0165 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18989 | hp2 | a0001 | c0002 | t0017 | g0217 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18991 | hp1 | a0001 | c0002 | t0029 | g0171 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18994 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18995 | hp2 | a0001 | c0001 | t0034 | g0034 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19000 | hp1 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19030 | hp1 | a0001 | c0003 | t0001 | g0153 | AFR | LWK | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | LWK | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | LWK | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19043 | hp2 | a0001 | c0002 | t0001 | g0164 | AFR | LWK | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19057 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19060 | hp1 | a0001 | c0002 | t0024 | g0231 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19062 | hp1 | a0001 | c0002 | t0004 | g0167 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19063 | hp1 | a0002 | c0004 | t0002 | g0095 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19063 | hp2 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19066 | hp1 | a0001 | c0002 | t0008 | g0227 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19068 | hp2 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19075 | hp1 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19086 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | YRI | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19240 | hp2 | a0001 | c0001 | t0035 | g0176 | AFR | YRI | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | ASW | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ASW | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA20905 | hp1 | a0001 | c0001 | t0004 | g0255 | SAS | GIH | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0123 | SAS | GIH | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0238 | AMR | CLM | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0113 | AMR | CLM | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02109 | hp1 | a0001 | c0002 | t0001 | g0225 | AFR | ACB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02109 | hp2 | a0001 | c0001 | t0025 | g0146 | AFR | ACB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0243 | AFR | ACB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02486 | hp2 | a0001 | c0002 | t0001 | g0187 | AFR | ACB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0244 | AFR | ACB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03471 | hp1 | a0001 | c0001 | t0036 | g0070 | AFR | MSL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0042 | AFR | MSL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG06807 | hp1 | a0001 | c0001 | t0028 | g0072 | AFR | USA | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG06807 | hp2 | a0001 | c0001 | t0033 | g0052 | AFR | USA | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | USA | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | USA | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA21309 | hp1 | a0001 | c0001 | t0005 | g0248 | AFR | LWK | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0118 | AFR | LWK | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0046 | REF | REF | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0026 | g0247 | REF | REF | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:35834036
|
C | T | 1 | a0002 | 1 | NA19063.hp1 | missense_variant | MODERATE | c.1426C>T | p.Pro476Ser | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 12/18 | 1827/7272 | 1426/2586 | 476/861 | chr1 | 35834036 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:35825688
|
A | G | 1 | a0001c0005 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.498A>G | p.Pro166Pro | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 5/18 | 899/7272 | 498/2586 | 166/861 | chr1 | 35825688 | ||
chr1:35841300
|
C | T | 1 | a0001c0003 | 6 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(3): Show |
synonymous_variant | LOW | c.1860C>T | p.Thr620Thr | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 14/18 | 2261/7272 | 1860/2586 | 620/861 | chr1 | 35841300 | ||
chr1:35850970
|
A | C | 1 | a0001c0002 | 86 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(83): Show |
synonymous_variant | LOW | c.2394A>C | p.Ser798Ser | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/18 | 2795/7272 | 2394/2586 | 798/861 | chr1 | 35850970 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:35808170
|
T | TGGC | 6 | a0001c0001t0002a0001c0001t0010a0001c0001t0018others(3): Show | 81 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(78): Show |
5_prime_UTR_variant | MODIFIER | c.-223_-221dupCGG | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/18 | 220 | INFO_REALIGN_3_PRIME | chr1 | 35808170 | ||||
chr1:35808170
|
T | TGGCGGCG others(2): Show |
2 | a0001c0001t0007a0001c0002t0017 | 5 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-229_-221dupCGGCGG others(3): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/18 | 220 | INFO_REALIGN_3_PRIME | chr1 | 35808170 | ||||
chr1:35853672
|
C | T | 1 | a0001c0001t0036 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*67C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 67 | chr1 | 35853672 | |||||
chr1:35854402
|
A | G | 1 | a0001c0001t0016 | 2 | HG01168.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*797A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 797 | chr1 | 35854402 | |||||
chr1:35854484
|
C | G | 1 | a0001c0001t0035 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*879C>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 879 | chr1 | 35854484 | |||||
chr1:35854557
|
G | A | 1 | a0001c0002t0021 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*952G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 952 | chr1 | 35854557 | |||||
chr1:35854592
|
T | C | 1 | a0001c0001t0022 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*987T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 987 | chr1 | 35854592 | |||||
chr1:35855300
|
G | T | 5 | a0001c0001t0003a0001c0001t0006a0001c0001t0007others(2): Show | 41 | HG00438.hp1 HG00558.hp1 HG01175.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1695G>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 1695 | chr1 | 35855300 | |||||
chr1:35855375
|
C | G | 1 | a0001c0002t0032 | 1 | NA18978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1770C>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 1770 | chr1 | 35855375 | |||||
chr1:35855466
|
C | G | 1 | a0001c0002t0031 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1861C>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 1861 | chr1 | 35855466 | |||||
chr1:35855513
|
A | G | 1 | a0001c0001t0030 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1908A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 1908 | chr1 | 35855513 | |||||
chr1:35855547
|
C | T | 1 | a0001c0001t0009 | 4 | HG01069.hp1 HG01071.hp2 HG02280.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1942C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 1942 | chr1 | 35855547 | |||||
chr1:35855652
|
C | CT | 5 | a0001c0001t0008a0001c0001t0019a0001c0001t0020others(2): Show | 7 | HG01243.hp1 HG01928.hp2 HG02056.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2065dupT | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 2066 | INFO_REALIGN_3_PRIME | chr1 | 35855652 | ||||
chr1:35855652
|
CT | C | 15 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(12): Show | 65 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*2065delT | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 2065 | INFO_REALIGN_3_PRIME | chr1 | 35855652 | ||||
chr1:35855694
|
C | G | 1 | a0001c0001t0030 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2089C>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 2089 | chr1 | 35855694 | |||||
chr1:35855720
|
T | G | 1 | a0001c0002t0024 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2115T>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 2115 | chr1 | 35855720 | |||||
chr1:35855748
|
A | G | 1 | a0001c0001t0028 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2143A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 2143 | chr1 | 35855748 | |||||
chr1:35856022
|
T | A | 3 | a0001c0001t0011a0001c0001t0012a0001c0001t0022 | 5 | HG01255.hp2 HG02970.hp1 HG03098.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2417T>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 2417 | chr1 | 35856022 | |||||
chr1:35856201
|
G | A | 1 | a0001c0001t0036 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2596G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 2596 | chr1 | 35856201 | |||||
chr1:35856430
|
G | T | 1 | a0001c0002t0027 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2825G>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 2825 | chr1 | 35856430 | |||||
chr1:35856830
|
AG | A | 11 | a0001c0001t0005a0001c0001t0006a0001c0001t0010others(8): Show | 29 | HG00438.hp1 HG00438.hp2 HG00673.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*3237delG | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 3237 | INFO_REALIGN_3_PRIME | chr1 | 35856830 | ||||
chr1:35856830
|
AGG | A | 28 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(25): Show | 235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
3_prime_UTR_variant | MODIFIER | c.*3236_*3237delGG | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 3236 | INFO_REALIGN_3_PRIME | chr1 | 35856830 | ||||
chr1:35856836
|
G | C | 2 | a0001c0001t0011a0001c0002t0014 | 4 | HG01168.hp2 HG01433.hp2 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3231G>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 3231 | chr1 | 35856836 | |||||
chr1:35856842
|
G | A | 1 | a0001c0001t0022 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3237G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 3237 | chr1 | 35856842 | |||||
chr1:35856880
|
A | G | 2 | a0001c0001t0015a0001c0001t0028 | 3 | HG02145.hp2 HG02818.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3275A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 3275 | chr1 | 35856880 | |||||
chr1:35856906
|
G | A | 1 | a0001c0001t0033 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3301G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 3301 | chr1 | 35856906 | |||||
chr1:35856936
|
A | AACT | 3 | a0001c0001t0011a0001c0001t0012a0001c0001t0022 | 5 | HG01255.hp2 HG02970.hp1 HG03098.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3333_*3335dupCTA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 3336 | INFO_REALIGN_3_PRIME | chr1 | 35856936 | ||||
chr1:35857456
|
C | T | 1 | a0001c0001t0025 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3851C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 3851 | chr1 | 35857456 | |||||
chr1:35857727
|
G | A | 1 | a0001c0001t0030 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4122G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 4122 | chr1 | 35857727 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:35808459
|
G | GCGGGACC others(7): Show |
1 | a0001c0001t0010g0013 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.19+36_19+49dupACCC others(10): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 35808459 | |||||
chr1:35808529
|
G | A | 40 | a0001c0001t0003g0003a0001c0001t0003g0014a0001c0001t0003g0019others(37): Show | 41 | HG00438.hp1 HG00558.hp1 HG01175.hp2 others(38): Show |
intron_variant | MODIFIER | c.19+94G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35808529 | ||||||
chr1:35808651
|
G | A | 1 | a0001c0001t0004g0053 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.19+216G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35808651 | ||||||
chr1:35808778
|
C | G | 1 | a0001c0001t0012g0256 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.19+343C>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35808778 | ||||||
chr1:35809023
|
C | T | 8 | a0001c0001t0004g0012a0001c0001t0004g0053a0001c0001t0004g0253others(5): Show | 9 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+588C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35809023 | ||||||
chr1:35809042
|
T | C | 252 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0064others(249): Show | 263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.19+607T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35809042 | ||||||
chr1:35809275
|
T | C | 4 | a0001c0001t0009g0054a0001c0001t0009g0055a0001c0001t0009g0056others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.19+840T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35809275 | ||||||
chr1:35809511
|
G | A | 118 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0064others(115): Show | 124 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.19+1076G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35809511 | ||||||
chr1:35809587
|
A | G | 40 | a0001c0001t0003g0003a0001c0001t0003g0014a0001c0001t0003g0019others(37): Show | 41 | HG00438.hp1 HG00558.hp1 HG01175.hp2 others(38): Show |
intron_variant | MODIFIER | c.19+1152A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35809587 | ||||||
chr1:35809783
|
G | A | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0005g0058 | 3 | HG02809.hp2 HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.19+1348G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35809783 | ||||||
chr1:35809790
|
A | G | 2 | a0001c0001t0002g0160a0001c0001t0002g0161 | 2 | NA18944.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.19+1355A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35809790 | ||||||
chr1:35809967
|
G | A | 1 | a0001c0001t0002g0061 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.19+1532G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35809967 | ||||||
chr1:35810027
|
C | CT | 24 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0141others(21): Show | 25 | HG01109.hp1 HG01891.hp2 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.19+1604dupT | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 35810027 | |||||
chr1:35810032
|
T | G | 1 | a0001c0002t0005g0162 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.19+1597T>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35810032 | ||||||
chr1:35810036
|
T | G | 95 | a0001c0001t0001g0177a0001c0001t0002g0242a0001c0001t0002g0243others(92): Show | 99 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.19+1601T>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35810036 | ||||||
chr1:35810036
|
T | TG | 38 | a0001c0001t0003g0003a0001c0001t0003g0019a0001c0001t0003g0022others(35): Show | 39 | HG00438.hp1 HG00558.hp1 HG01175.hp2 others(36): Show |
intron_variant | MODIFIER | c.19+1601_19+1602ins others(1): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35810036 | ||||||
chr1:35810037
|
T | G | 1 | a0001c0001t0004g0062 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.19+1602T>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35810037 | ||||||
chr1:35810166
|
G | T | 8 | a0001c0001t0004g0012a0001c0001t0004g0053a0001c0001t0004g0253others(5): Show | 9 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+1731G>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35810166 | ||||||
chr1:35810303
|
T | C | 1 | a0001c0001t0007g0015 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.19+1868T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35810303 | ||||||
chr1:35810393
|
C | T | 9 | a0001c0001t0011g0006a0001c0001t0012g0154a0001c0001t0012g0256others(6): Show | 10 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.19+1958C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35810393 | ||||||
chr1:35810438
|
C | T | 5 | a0001c0001t0002g0242a0001c0001t0002g0243a0001c0001t0002g0244others(2): Show | 5 | HG01069.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.19+2003C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35810438 | ||||||
chr1:35810601
|
G | C | 2 | a0001c0002t0001g0007a0001c0002t0001g0163 | 3 | HG01074.hp1 HG02723.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.19+2166G>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35810601 | ||||||
chr1:35810798
|
C | T | 91 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0076others(88): Show | 95 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.19+2363C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35810798 | ||||||
chr1:35810961
|
G | A | 3 | a0001c0001t0007g0016a0001c0001t0007g0017a0001c0001t0007g0018 | 3 | HG02258.hp1 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.19+2526G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35810961 | ||||||
chr1:35810967
|
A | ACTAAAAA others(16): Show |
1 | a0001c0002t0001g0164 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.19+2556_19+2578dup others(23): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 35810967 | |||||
chr1:35811083
|
G | A | 2 | a0001c0001t0015g0073a0001c0001t0028g0072 | 2 | HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.19+2648G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35811083 | ||||||
chr1:35811150
|
C | CA | 7 | a0001c0001t0002g0242a0001c0001t0015g0073a0001c0001t0015g0074others(4): Show | 7 | HG01074.hp1 HG02145.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.19+2724dupA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 35811150 | |||||
chr1:35811150
|
CA | C | 8 | a0001c0001t0004g0012a0001c0001t0004g0053a0001c0001t0004g0253others(5): Show | 9 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+2724delA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 35811150 | |||||
chr1:35811156
|
A | C | 8 | a0001c0001t0004g0012a0001c0001t0004g0053a0001c0001t0004g0253others(5): Show | 9 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+2721A>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35811156 | ||||||
chr1:35811160
|
C | A | 1 | a0001c0001t0003g0019 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.19+2725C>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35811160 | ||||||
chr1:35811290
|
G | A | 3 | a0001c0001t0002g0243a0001c0001t0002g0244a0001c0001t0002g0245 | 3 | HG01069.hp2 HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.19+2855G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35811290 | ||||||
chr1:35811470
|
C | A | 1 | a0001c0002t0001g0166 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.19+3035C>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35811470 | ||||||
chr1:35811470
|
C | CA | 32 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0064others(29): Show | 32 | HG01109.hp1 HG01169.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.19+3046dupA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 35811470 | |||||
chr1:35811548
|
T | G | 1 | a0001c0001t0002g0078 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.19+3113T>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35811548 | ||||||
chr1:35811585
|
G | A | 1 | a0001c0001t0006g0020 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.19+3150G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35811585 | ||||||
chr1:35811598
|
C | T | 1 | a0001c0001t0011g0006 | 2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.19+3163C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35811598 | ||||||
chr1:35811599
|
G | A | 1 | a0001c0001t0033g0052 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.19+3164G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35811599 | ||||||
chr1:35811606
|
G | T | 1 | a0001c0001t0030g0071 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.19+3171G>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35811606 | ||||||
chr1:35811657
|
G | A | 1 | a0001c0002t0001g0170 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.19+3222G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35811657 | ||||||
chr1:35811727
|
C | T | 2 | a0001c0001t0002g0139a0001c0001t0002g0140 | 2 | NA18972.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.19+3292C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35811727 | ||||||
chr1:35811746
|
G | A | 1 | a0001c0001t0033g0052 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.19+3311G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35811746 | ||||||
chr1:35811848
|
C | T | 1 | a0001c0002t0001g0241 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.19+3413C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35811848 | ||||||
chr1:35811987
|
A | G | 1 | a0001c0002t0005g0240 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.19+3552A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35811987 | ||||||
chr1:35812016
|
G | A | 16 | a0001c0001t0002g0075a0001c0001t0002g0079a0001c0001t0002g0080others(13): Show | 16 | HG00140.hp2 HG00558.hp2 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.19+3581G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35812016 | ||||||
chr1:35812057
|
G | C | 1 | a0001c0001t0036g0070 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.19+3622G>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35812057 | ||||||
chr1:35812209
|
GA | G | 33 | a0001c0001t0003g0003a0001c0001t0003g0014a0001c0001t0003g0022others(30): Show | 34 | HG00438.hp1 HG00558.hp1 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.19+3784delA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 35812209 | |||||
chr1:35812559
|
A | C | 1 | a0001c0002t0001g0239 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.19+4124A>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35812559 | ||||||
chr1:35812886
|
C | G | 1 | a0001c0001t0002g0138 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.20-3996C>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35812886 | ||||||
chr1:35813266
|
G | A | 1 | a0001c0001t0036g0070 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.20-3616G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35813266 | ||||||
chr1:35813281
|
C | T | 1 | a0001c0002t0001g0238 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.20-3601C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35813281 | ||||||
chr1:35813333
|
C | T | 6 | a0001c0003t0001g0153a0001c0003t0004g0155a0001c0003t0004g0157others(3): Show | 6 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.20-3549C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35813333 | ||||||
chr1:35813408
|
C | CA | 8 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(5): Show | 8 | HG01884.hp2 HG02896.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.20-3460dupA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 35813408 | |||||
chr1:35813455
|
T | G | 39 | a0001c0001t0003g0003a0001c0001t0003g0014a0001c0001t0003g0019others(36): Show | 40 | HG00438.hp1 HG00558.hp1 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.20-3427T>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35813455 | ||||||
chr1:35813582
|
C | T | 2 | a0001c0001t0012g0154a0001c0001t0012g0256 | 2 | HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.20-3300C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35813582 | ||||||
chr1:35813727
|
C | T | 8 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(5): Show | 8 | HG01884.hp2 HG02717.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.20-3155C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35813727 | ||||||
chr1:35813741
|
C | G | 1 | a0001c0002t0005g0237 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.20-3141C>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35813741 | ||||||
chr1:35813778
|
A | G | 3 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0051 | 3 | HG02922.hp2 HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.20-3104A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35813778 | ||||||
chr1:35813790
|
AGAAGGAA others(4): Show |
A | 6 | a0001c0003t0001g0153a0001c0003t0004g0155a0001c0003t0004g0157others(3): Show | 6 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.20-3076_20-3066del others(11): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 35813790 | |||||
chr1:35813838
|
G | A | 1 | a0001c0001t0030g0071 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.20-3044G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35813838 | ||||||
chr1:35814007
|
G | A | 1 | a0001c0001t0008g0172 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.20-2875G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35814007 | ||||||
chr1:35814037
|
T | C | 28 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0061others(25): Show | 31 | HG00438.hp2 HG00642.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.20-2845T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35814037 | ||||||
chr1:35814074
|
C | CA | 6 | a0001c0003t0001g0153a0001c0003t0004g0155a0001c0003t0004g0157others(3): Show | 6 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.20-2796dupA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 35814074 | |||||
chr1:35814147
|
A | G | 1 | a0001c0001t0002g0137 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.20-2735A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35814147 | ||||||
chr1:35814282
|
A | G | 1 | a0001c0001t0012g0154 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.20-2600A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35814282 | ||||||
chr1:35814339
|
A | G | 257 | a0001c0001t0001g0010a0001c0001t0001g0059a0001c0001t0001g0060others(254): Show | 269 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.20-2543A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35814339 | ||||||
chr1:35814460
|
C | G | 1 | a0001c0002t0001g0236 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.20-2422C>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35814460 | ||||||
chr1:35815664
|
T | C | 252 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0064others(249): Show | 263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.20-1218T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35815664 | ||||||
chr1:35815698
|
A | T | 1 | a0001c0001t0006g0048 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.20-1184A>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35815698 | ||||||
chr1:35815735
|
A | G | 110 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0076others(107): Show | 116 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.20-1147A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35815735 | ||||||
chr1:35815767
|
C | T | 1 | a0001c0001t0003g0047 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.20-1115C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35815767 | ||||||
chr1:35815781
|
C | T | 1 | a0001c0001t0002g0092 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.20-1101C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35815781 | ||||||
chr1:35816216
|
C | G | 1 | a0001c0002t0005g0240 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.20-666C>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35816216 | ||||||
chr1:35816288
|
T | C | 4 | a0001c0001t0009g0054a0001c0001t0009g0055a0001c0001t0009g0056others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.20-594T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35816288 | ||||||
chr1:35816408
|
G | A | 1 | a0001c0001t0033g0052 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.20-474G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35816408 | ||||||
chr1:35816798
|
CAAAAAAA others(6): Show |
C | 88 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0076others(85): Show | 92 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.20-73_20-61delAAAA others(9): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 35816798 | |||||
chr1:35816812
|
A | G | 1 | a0001c0002t0001g0235 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.20-70A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35816812 | ||||||
chr1:35816816
|
A | AG | 6 | a0001c0001t0001g0177a0001c0001t0009g0054a0001c0001t0035g0176others(3): Show | 6 | HG01109.hp2 HG01169.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.20-66_20-65insG | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35816816 | ||||||
chr1:35816816
|
A | G | 88 | a0001c0001t0002g0242a0001c0001t0002g0243a0001c0001t0002g0244others(85): Show | 92 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.20-66A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35816816 | ||||||
chr1:35816818
|
A | G | 32 | a0001c0001t0003g0003a0001c0001t0003g0014a0001c0001t0003g0023others(29): Show | 33 | HG00438.hp1 HG00558.hp1 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.20-64A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35816818 | ||||||
chr1:35817215
|
C | T | 1 | a0001c0001t0003g0047 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.185+168C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35817215 | ||||||
chr1:35817346
|
G | A | 1 | a0001c0001t0003g0049 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.185+299G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35817346 | ||||||
chr1:35817411
|
G | GTA | 36 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0064others(33): Show | 36 | HG00140.hp1 HG00642.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.185+380_185+381dup others(2): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35817411 | |||||
chr1:35817429
|
C | A | 1 | a0001c0001t0002g0116 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.185+382C>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35817429 | ||||||
chr1:35817506
|
G | A | 1 | a0001c0002t0001g0185 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.185+459G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35817506 | ||||||
chr1:35817643
|
G | C | 2 | a0001c0001t0015g0073a0001c0001t0028g0072 | 2 | HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.185+596G>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35817643 | ||||||
chr1:35817784
|
G | A | 1 | a0001c0002t0001g0178 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.185+737G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35817784 | ||||||
chr1:35817844
|
G | A | 1 | a0001c0002t0004g0186 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.185+797G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35817844 | ||||||
chr1:35818026
|
A | G | 6 | a0001c0003t0001g0153a0001c0003t0004g0155a0001c0003t0004g0157others(3): Show | 6 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.185+979A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35818026 | ||||||
chr1:35818067
|
T | C | 1 | a0001c0001t0004g0062 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.185+1020T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35818067 | ||||||
chr1:35818151
|
A | T | 1 | a0001c0001t0002g0078 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.185+1104A>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35818151 | ||||||
chr1:35818248
|
T | C | 1 | a0001c0001t0006g0021 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.185+1201T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35818248 | ||||||
chr1:35818349
|
C | T | 2 | a0001c0001t0002g0115a0001c0002t0001g0178 | 2 | HG00642.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.185+1302C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35818349 | ||||||
chr1:35818353
|
A | G | 118 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0064others(115): Show | 124 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.185+1306A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35818353 | ||||||
chr1:35818625
|
AAAAG | A | 49 | a0001c0001t0001g0064a0001c0001t0001g0076a0001c0001t0001g0142others(46): Show | 53 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.185+1611_185+1614d others(6): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818625 | |||||
chr1:35818625
|
AAAAGAAA others(1): Show |
A | 13 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0141others(10): Show | 13 | HG00642.hp1 HG00741.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.185+1607_185+1614d others(10): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818625 | |||||
chr1:35818642
|
A | AAAGG | 7 | a0001c0001t0002g0089a0001c0001t0002g0090a0001c0001t0002g0091others(4): Show | 7 | HG01123.hp2 NA18944.hp2 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.185+1598_185+1599i others(6): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818642 | |||||
chr1:35818646
|
A | G | 35 | a0001c0001t0001g0151a0001c0001t0002g0004a0001c0001t0002g0075others(32): Show | 36 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.185+1599A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35818646 | ||||||
chr1:35818646
|
AAAGAAAG others(9): Show |
A | 1 | a0001c0005t0004g0069 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.185+1607_185+1622d others(18): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818646 | |||||
chr1:35818650
|
A | AAAGG | 29 | a0001c0001t0002g0245a0001c0001t0008g0172a0001c0001t0009g0057others(26): Show | 32 | HG01069.hp2 HG01243.hp1 HG01516.hp2 others(29): Show |
intron_variant | MODIFIER | c.185+1606_185+1607i others(6): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818650 | |||||
chr1:35818650
|
A | G | 61 | a0001c0001t0001g0076a0001c0001t0001g0142a0001c0001t0001g0144others(58): Show | 65 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.185+1603A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35818650 | ||||||
chr1:35818650
|
AAAGAAAG others(5): Show |
A | 3 | a0001c0001t0002g0078a0001c0001t0002g0118a0001c0001t0004g0053 | 3 | HG03491.hp2 NA19074.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.185+1611_185+1622d others(14): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818650 | |||||
chr1:35818654
|
A | AAAGGAAG others(5): Show |
1 | a0001c0003t0004g0159 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.185+1610_185+1611i others(14): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818654 | |||||
chr1:35818654
|
A | G | 121 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0065others(118): Show | 124 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.185+1607A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35818654 | ||||||
chr1:35818658
|
A | AAAGAAAG others(141): Show |
1 | a0001c0001t0003g0023 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.185+1614_185+1615i others(150): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | |||||
chr1:35818658
|
A | AAAGAAAG others(197): Show |
1 | a0001c0001t0003g0024 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.185+1614_185+1615i others(206): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | |||||
chr1:35818658
|
A | AAAGAAAG others(45): Show |
1 | a0001c0001t0003g0025 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.185+1614_185+1615i others(54): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | |||||
chr1:35818658
|
A | AAAGAAAG others(53): Show |
1 | a0001c0001t0006g0021 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.185+1614_185+1615i others(62): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | |||||
chr1:35818658
|
A | AAAGAAAG others(41): Show |
1 | a0001c0001t0003g0026 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.185+1614_185+1615i others(50): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | |||||
chr1:35818658
|
A | AAAGAAAG others(37): Show |
1 | a0001c0001t0003g0027 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.185+1614_185+1615i others(46): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | |||||
chr1:35818658
|
A | AAAGAAAG others(37): Show |
1 | a0001c0001t0006g0028 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.185+1614_185+1615i others(46): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | |||||
chr1:35818658
|
A | AAAGAAAG others(25): Show |
1 | a0001c0001t0007g0016 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.185+1614_185+1615i others(34): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | |||||
chr1:35818658
|
A | AAAGAAAG others(21): Show |
1 | a0001c0001t0006g0020 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+1614_185+1615i others(30): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | |||||
chr1:35818658
|
A | AAAGAAAG others(25): Show |
1 | a0001c0001t0003g0029 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.185+1614_185+1615i others(34): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | |||||
chr1:35818658
|
A | AAAGAAAG others(17): Show |
2 | a0001c0001t0003g0030a0001c0001t0006g0048 | 2 | HG00438.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.185+1614_185+1615i others(26): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | |||||
chr1:35818658
|
A | AAAGAAAG others(21): Show |
1 | a0001c0001t0003g0031 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.185+1614_185+1615i others(30): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | |||||
chr1:35818658
|
A | AAAGAAAG others(25): Show |
2 | a0001c0001t0003g0032a0001c0001t0003g0050 | 2 | NA18906.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.185+1614_185+1615i others(34): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | |||||
chr1:35818658
|
A | AAAGAAAG others(31): Show |
1 | a0001c0001t0006g0033 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.185+1614_185+1615i others(40): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | |||||
chr1:35818658
|
A | AAAGAAAG others(9): Show |
4 | a0001c0001t0003g0014a0001c0001t0003g0035a0001c0001t0007g0015others(1): Show | 4 | HG02145.hp1 HG02155.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.185+1614_185+1615i others(18): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | |||||
chr1:35818658
|
A | AAAGAAAG others(13): Show |
4 | a0001c0001t0003g0036a0001c0001t0003g0047a0001c0001t0003g0049others(1): Show | 4 | HG00558.hp1 HG02922.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.185+1614_185+1615i others(22): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | |||||
chr1:35818658
|
A | AAAGAAAG others(17): Show |
7 | a0001c0001t0003g0003a0001c0001t0003g0019a0001c0001t0003g0022others(4): Show | 8 | HG01884.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.185+1614_185+1615i others(26): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | |||||
chr1:35818658
|
A | AAAGAAAG others(21): Show |
7 | a0001c0001t0003g0041a0001c0001t0003g0042a0001c0001t0003g0043others(4): Show | 7 | HG02055.hp1 HG02451.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.185+1614_185+1615i others(30): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | |||||
chr1:35818658
|
A | AAAGAAAG others(25): Show |
1 | a0001c0001t0003g0045 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.185+1614_185+1615i others(34): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | |||||
chr1:35818658
|
A | AAAGGAAG others(1): Show |
10 | a0001c0001t0001g0177a0001c0001t0022g0251a0001c0002t0001g0185others(7): Show | 10 | HG01123.hp1 HG01169.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.185+1618_185+1619i others(10): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | |||||
chr1:35818658
|
A | AAAGGAAG others(5): Show |
6 | a0001c0001t0009g0054a0001c0002t0001g0229a0001c0002t0001g0230others(3): Show | 6 | HG01943.hp2 HG02155.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.185+1618_185+1619i others(14): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | |||||
chr1:35818658
|
A | AAAGGAAG others(9): Show |
1 | a0001c0002t0024g0231 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.185+1618_185+1619i others(18): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | |||||
chr1:35818658
|
A | AAAGGAAG others(13): Show |
1 | a0001c0002t0001g0169 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.185+1618_185+1619i others(22): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | |||||
chr1:35818658
|
A | G | 123 | a0001c0001t0001g0076a0001c0001t0001g0142a0001c0001t0001g0144others(120): Show | 132 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.185+1611A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35818658 | ||||||
chr1:35818658
|
AAAGGAAG others(5): Show |
A | 6 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(3): Show | 6 | HG01884.hp2 HG01928.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.185+1619_185+1630d others(14): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | |||||
chr1:35818662
|
G | A | 1 | a0001c0001t0005g0011 | 2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.185+1615G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35818662 | ||||||
chr1:35818662
|
GAAGA | G | 19 | a0001c0001t0002g0243a0001c0001t0004g0062a0001c0002t0001g0170others(16): Show | 19 | HG00140.hp1 HG00673.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.185+1619_185+1622d others(6): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818662 | |||||
chr1:35818666
|
A | AAAGGAAG others(13): Show |
1 | a0001c0001t0003g0046 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.185+1638_185+1657d others(22): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818666 | |||||
chr1:35818666
|
A | G | 222 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0076others(219): Show | 234 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.185+1619A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35818666 | ||||||
chr1:35818674
|
G | A | 1 | a0001c0005t0004g0069 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.185+1627G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35818674 | ||||||
chr1:35818811
|
G | T | 1 | a0001c0002t0005g0197 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.185+1764G>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35818811 | ||||||
chr1:35819416
|
C | T | 1 | a0001c0001t0003g0044 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.185+2369C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35819416 | ||||||
chr1:35819451
|
G | A | 1 | a0001c0002t0004g0167 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.185+2404G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35819451 | ||||||
chr1:35819457
|
G | A | 6 | a0001c0003t0001g0153a0001c0003t0004g0155a0001c0003t0004g0157others(3): Show | 6 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.185+2410G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35819457 | ||||||
chr1:35819712
|
G | A | 94 | a0001c0001t0001g0177a0001c0001t0002g0242a0001c0001t0002g0243others(91): Show | 98 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.185+2665G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35819712 | ||||||
chr1:35819732
|
C | CA | 174 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0076others(171): Show | 182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.185+2703dupA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35819732 | |||||
chr1:35819732
|
C | CAA | 12 | a0001c0001t0002g0094a0001c0001t0002g0139a0001c0001t0009g0055others(9): Show | 12 | HG00642.hp2 HG01069.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.185+2702_185+2703d others(4): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35819732 | |||||
chr1:35819732
|
CA | C | 20 | a0001c0001t0001g0068a0001c0001t0004g0012a0001c0001t0004g0053others(17): Show | 22 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.185+2703delA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35819732 | |||||
chr1:35819799
|
T | TA | 8 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(5): Show | 8 | HG01175.hp2 HG01884.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.185+2768dupA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35819799 | |||||
chr1:35820004
|
A | T | 1 | a0001c0001t0036g0070 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.186-2858A>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35820004 | ||||||
chr1:35820269
|
A | T | 40 | a0001c0001t0003g0003a0001c0001t0003g0014a0001c0001t0003g0019others(37): Show | 41 | HG00438.hp1 HG00558.hp1 HG01175.hp2 others(38): Show |
intron_variant | MODIFIER | c.186-2593A>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35820269 | ||||||
chr1:35820337
|
A | G | 1 | a0001c0002t0001g0228 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.186-2525A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35820337 | ||||||
chr1:35820424
|
C | T | 1 | a0001c0001t0033g0052 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.186-2438C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35820424 | ||||||
chr1:35820453
|
G | A | 1 | a0001c0001t0036g0070 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.186-2409G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35820453 | ||||||
chr1:35820701
|
A | T | 1 | a0001c0002t0001g0223 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.186-2161A>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35820701 | ||||||
chr1:35820861
|
G | A | 4 | a0001c0002t0001g0174a0001c0002t0001g0180a0001c0002t0001g0181others(1): Show | 4 | HG00140.hp1 HG01109.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-2001G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35820861 | ||||||
chr1:35820937
|
T | C | 1 | a0001c0001t0035g0176 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.186-1925T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35820937 | ||||||
chr1:35821483
|
A | G | 4 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(1): Show | 4 | HG01884.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.186-1379A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35821483 | ||||||
chr1:35821511
|
T | C | 1 | a0001c0001t0033g0052 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.186-1351T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35821511 | ||||||
chr1:35821520
|
G | A | 1 | a0001c0001t0035g0176 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.186-1342G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35821520 | ||||||
chr1:35821819
|
C | A | 1 | a0001c0001t0003g0029 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.186-1043C>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35821819 | ||||||
chr1:35821822
|
A | T | 1 | a0001c0002t0008g0227 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.186-1040A>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35821822 | ||||||
chr1:35821893
|
A | AT | 13 | a0001c0001t0002g0088a0001c0001t0002g0139a0001c0001t0004g0012others(10): Show | 15 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.186-955dupT | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35821893 | |||||
chr1:35821950
|
C | T | 39 | a0001c0001t0003g0003a0001c0001t0003g0014a0001c0001t0003g0019others(36): Show | 40 | HG00438.hp1 HG00558.hp1 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.186-912C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35821950 | ||||||
chr1:35821997
|
C | T | 72 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(69): Show | 76 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.186-865C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35821997 | ||||||
chr1:35822072
|
G | T | 1 | a0001c0001t0003g0039 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.186-790G>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35822072 | ||||||
chr1:35822128
|
C | T | 1 | a0001c0002t0004g0167 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.186-734C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35822128 | ||||||
chr1:35822152
|
T | C | 1 | a0001c0002t0001g0224 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.186-710T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35822152 | ||||||
chr1:35822170
|
A | G | 11 | a0001c0001t0004g0012a0001c0001t0004g0053a0001c0001t0004g0253others(8): Show | 13 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.186-692A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35822170 | ||||||
chr1:35822261
|
C | CT | 6 | a0001c0003t0001g0153a0001c0003t0004g0155a0001c0003t0004g0157others(3): Show | 6 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.186-593dupT | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35822261 | |||||
chr1:35822351
|
G | A | 71 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(68): Show | 75 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.186-511G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35822351 | ||||||
chr1:35822533
|
C | T | 2 | a0001c0001t0003g0030a0001c0001t0003g0046 | 2 | HG01261.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.186-329C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35822533 | ||||||
chr1:35823034
|
G | A | 1 | a0001c0002t0001g0225 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.306+52G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35823034 | ||||||
chr1:35823164
|
A | C | 1 | a0001c0001t0030g0071 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.306+182A>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35823164 | ||||||
chr1:35823252
|
A | AT | 12 | a0001c0001t0001g0152a0001c0001t0002g0087a0001c0001t0002g0136others(9): Show | 12 | HG00140.hp2 HG01109.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.306+288dupT | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr1 | 35823252 | |||||
chr1:35823252
|
AT | A | 6 | a0001c0001t0002g0082a0001c0001t0002g0131a0001c0001t0006g0021others(3): Show | 6 | HG02451.hp2 HG03130.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.306+288delT | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr1 | 35823252 | |||||
chr1:35823287
|
CTG | C | 6 | a0001c0003t0001g0153a0001c0003t0004g0155a0001c0003t0004g0157others(3): Show | 6 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.306+307_306+308del others(2): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr1 | 35823287 | |||||
chr1:35823388
|
G | T | 1 | a0001c0001t0002g0086 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.306+406G>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35823388 | ||||||
chr1:35823496
|
G | T | 91 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0076others(88): Show | 95 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.306+514G>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35823496 | ||||||
chr1:35823528
|
C | T | 1 | a0001c0001t0002g0081 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.306+546C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35823528 | ||||||
chr1:35823571
|
G | A | 1 | a0001c0001t0002g0078 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.306+589G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35823571 | ||||||
chr1:35823755
|
T | A | 130 | a0001c0001t0001g0177a0001c0001t0002g0083a0001c0001t0002g0089others(127): Show | 135 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.306+773T>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35823755 | ||||||
chr1:35823758
|
T | A | 1 | a0001c0001t0003g0019 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.306+776T>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35823758 | ||||||
chr1:35823881
|
C | T | 2 | a0001c0002t0001g0220a0001c0002t0001g0221 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.306+899C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35823881 | ||||||
chr1:35824223
|
C | T | 1 | a0001c0001t0008g0172 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.307-1090C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35824223 | ||||||
chr1:35824280
|
A | G | 5 | a0001c0001t0002g0242a0001c0001t0002g0243a0001c0001t0002g0244others(2): Show | 5 | HG01069.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.307-1033A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35824280 | ||||||
chr1:35824448
|
TA | T | 5 | a0001c0001t0002g0093a0001c0001t0002g0101a0001c0001t0002g0102others(2): Show | 5 | NA18946.hp2 NA18973.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.307-864delA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35824448 | ||||||
chr1:35824537
|
G | A | 1 | a0001c0001t0002g0132 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.307-776G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35824537 | ||||||
chr1:35824539
|
C | G | 1 | a0001c0002t0005g0219 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.307-774C>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35824539 | ||||||
chr1:35824602
|
C | A | 1 | a0001c0001t0001g0142 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.307-711C>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35824602 | ||||||
chr1:35824740
|
A | G | 1 | a0001c0002t0008g0227 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.307-573A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35824740 | ||||||
chr1:35824792
|
C | T | 6 | a0001c0003t0001g0153a0001c0003t0004g0155a0001c0003t0004g0157others(3): Show | 6 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-521C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35824792 | ||||||
chr1:35824809
|
C | A | 8 | a0001c0001t0030g0071a0001c0001t0036g0070a0001c0003t0001g0153others(5): Show | 8 | HG01891.hp2 HG02055.hp2 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.307-504C>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35824809 | ||||||
chr1:35824908
|
C | T | 6 | a0001c0003t0001g0153a0001c0003t0004g0155a0001c0003t0004g0157others(3): Show | 6 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-405C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35824908 | ||||||
chr1:35824997
|
A | G | 1 | a0001c0001t0030g0071 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.307-316A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35824997 | ||||||
chr1:35825178
|
G | T | 2 | a0001c0001t0023g0063a0001c0005t0004g0069 | 2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.307-135G>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35825178 | ||||||
chr1:35825503
|
C | T | 1 | a0001c0002t0014g0207 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.488+9C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 4/17 | chr1 | 35825503 | ||||||
chr1:35826149
|
G | A | 11 | a0001c0001t0004g0012a0001c0001t0004g0053a0001c0001t0004g0253others(8): Show | 13 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.760+89G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 6/17 | chr1 | 35826149 | ||||||
chr1:35826290
|
A | G | 2 | a0001c0002t0001g0218a0001c0002t0017g0217 | 2 | NA18955.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.760+230A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 6/17 | chr1 | 35826290 | ||||||
chr1:35826489
|
G | A | 1 | a0001c0002t0024g0231 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.761-259G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 6/17 | chr1 | 35826489 | ||||||
chr1:35826657
|
A | G | 11 | a0001c0001t0004g0012a0001c0001t0004g0053a0001c0001t0004g0253others(8): Show | 13 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.761-91A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 6/17 | chr1 | 35826657 | ||||||
chr1:35827034
|
T | C | 1 | a0001c0001t0036g0070 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.848+199T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35827034 | ||||||
chr1:35827063
|
G | A | 6 | a0001c0003t0001g0153a0001c0003t0004g0155a0001c0003t0004g0157others(3): Show | 6 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.848+228G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35827063 | ||||||
chr1:35827502
|
A | G | 1 | a0001c0001t0002g0078 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.848+667A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35827502 | ||||||
chr1:35827609
|
T | C | 95 | a0001c0001t0001g0177a0001c0001t0002g0242a0001c0001t0002g0243others(92): Show | 99 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.848+774T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35827609 | ||||||
chr1:35827790
|
CTT | C | 230 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0064others(227): Show | 239 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.848+974_848+975del others(2): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr1 | 35827790 | |||||
chr1:35827790
|
CTTT | C | 9 | a0001c0001t0002g0245a0001c0001t0030g0071a0001c0001t0036g0070others(6): Show | 9 | HG01069.hp2 HG01891.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.848+973_848+975del others(3): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr1 | 35827790 | |||||
chr1:35827790
|
CTTTT | C | 11 | a0001c0001t0004g0012a0001c0001t0004g0053a0001c0001t0004g0253others(8): Show | 13 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.848+972_848+975del others(4): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr1 | 35827790 | |||||
chr1:35827883
|
T | C | 2 | a0001c0001t0023g0063a0001c0005t0004g0069 | 2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.848+1048T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35827883 | ||||||
chr1:35828012
|
T | C | 1 | a0001c0001t0003g0019 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.848+1177T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35828012 | ||||||
chr1:35828082
|
A | G | 3 | a0001c0001t0015g0073a0001c0001t0015g0074a0001c0001t0028g0072 | 3 | HG02145.hp2 HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.848+1247A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35828082 | ||||||
chr1:35828290
|
G | A | 8 | a0001c0001t0004g0012a0001c0001t0004g0053a0001c0001t0004g0253others(5): Show | 9 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.848+1455G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35828290 | ||||||
chr1:35828470
|
A | G | 1 | a0001c0001t0002g0082 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.848+1635A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35828470 | ||||||
chr1:35828474
|
G | T | 7 | a0001c0002t0001g0173a0001c0002t0001g0187a0001c0002t0001g0206others(4): Show | 7 | HG02486.hp2 HG03041.hp1 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.848+1639G>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35828474 | ||||||
chr1:35828539
|
G | T | 1 | a0001c0001t0002g0093 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.848+1704G>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35828539 | ||||||
chr1:35828581
|
G | A | 1 | a0001c0001t0002g0101 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.848+1746G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35828581 | ||||||
chr1:35828712
|
G | A | 1 | a0001c0001t0001g0064 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.848+1877G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35828712 | ||||||
chr1:35828712
|
G | C | 1 | a0001c0001t0002g0079 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.848+1877G>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35828712 | ||||||
chr1:35828881
|
G | T | 1 | a0001c0001t0003g0022 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.848+2046G>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35828881 | ||||||
chr1:35829029
|
C | A | 10 | a0001c0001t0002g0119a0001c0001t0007g0015a0001c0001t0007g0016others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.848+2194C>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35829029 | ||||||
chr1:35829031
|
C | A | 229 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0064others(226): Show | 238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.848+2196C>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35829031 | ||||||
chr1:35829031
|
C | CA | 8 | a0001c0001t0001g0177a0001c0001t0002g0138a0001c0001t0003g0047others(5): Show | 8 | HG00642.hp1 HG00741.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.848+2196_848+2197i others(3): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35829031 | ||||||
chr1:35829036
|
C | A | 2 | a0001c0002t0001g0174a0001c0002t0001g0180 | 2 | HG00140.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.848+2201C>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35829036 | ||||||
chr1:35829086
|
G | T | 2 | a0001c0001t0003g0031a0001c0001t0003g0032 | 2 | NA18969.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.848+2251G>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35829086 | ||||||
chr1:35829309
|
GA | G | 11 | a0001c0001t0001g0010a0001c0001t0003g0019a0001c0001t0005g0010others(8): Show | 11 | HG01891.hp2 HG01943.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.849-2102delA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr1 | 35829309 | |||||
chr1:35829475
|
A | G | 2 | a0001c0001t0002g0160a0001c0001t0002g0161 | 2 | NA18944.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.849-1952A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35829475 | ||||||
chr1:35829552
|
C | T | 2 | a0001c0001t0009g0055a0001c0001t0009g0056 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.849-1875C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35829552 | ||||||
chr1:35829809
|
C | T | 6 | a0001c0003t0001g0153a0001c0003t0004g0155a0001c0003t0004g0157others(3): Show | 6 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.849-1618C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35829809 | ||||||
chr1:35829840
|
T | TA | 81 | a0001c0001t0001g0177a0001c0001t0002g0113a0001c0001t0002g0120others(78): Show | 85 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.849-1561dupA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr1 | 35829840 | |||||
chr1:35829840
|
T | TAA | 10 | a0001c0002t0001g0008a0001c0002t0001g0192a0001c0002t0001g0198others(7): Show | 10 | HG02040.hp1 HG02109.hp1 HG03516.hp1 others(7): Show |
intron_variant | MODIFIER | c.849-1562_849-1561d others(4): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr1 | 35829840 | |||||
chr1:35829840
|
TA | T | 7 | a0001c0001t0001g0068a0001c0001t0003g0003a0001c0001t0003g0030others(4): Show | 9 | HG00280.hp2 HG00323.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.849-1561delA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr1 | 35829840 | |||||
chr1:35829840
|
TAA | T | 13 | a0001c0001t0004g0053a0001c0001t0004g0253a0001c0001t0004g0255others(10): Show | 13 | HG01169.hp1 HG01255.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.849-1562_849-1561d others(4): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr1 | 35829840 | |||||
chr1:35830143
|
CA | C | 146 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0076others(143): Show | 152 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.849-1265delA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr1 | 35830143 | |||||
chr1:35830143
|
CAA | C | 100 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(97): Show | 104 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(101): Show |
intron_variant | MODIFIER | c.849-1266_849-1265d others(4): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr1 | 35830143 | |||||
chr1:35830574
|
T | A | 5 | a0001c0001t0002g0242a0001c0001t0002g0243a0001c0001t0002g0244others(2): Show | 5 | HG01069.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.849-853T>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35830574 | ||||||
chr1:35830691
|
T | C | 1 | a0001c0001t0030g0071 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.849-736T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35830691 | ||||||
chr1:35830724
|
C | T | 1 | a0001c0001t0002g0128 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.849-703C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35830724 | ||||||
chr1:35830827
|
T | C | 13 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0037others(10): Show | 14 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.849-600T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35830827 | ||||||
chr1:35830840
|
C | T | 1 | a0001c0001t0003g0047 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.849-587C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35830840 | ||||||
chr1:35830843
|
G | A | 1 | a0001c0001t0030g0071 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.849-584G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35830843 | ||||||
chr1:35830850
|
T | C | 1 | a0001c0001t0003g0039 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.849-577T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35830850 | ||||||
chr1:35830973
|
C | CA | 15 | a0001c0001t0002g0084a0001c0001t0002g0100a0001c0001t0002g0138others(12): Show | 15 | HG01069.hp2 HG02486.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.849-435dupA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr1 | 35830973 | |||||
chr1:35831099
|
C | T | 1 | a0001c0002t0001g0228 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.849-328C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35831099 | ||||||
chr1:35831369
|
A | T | 1 | a0001c0002t0001g0194 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.849-58A>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35831369 | ||||||
chr1:35831998
|
T | C | 1 | a0001c0001t0003g0047 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1117-59T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 9/17 | chr1 | 35831998 | ||||||
chr1:35832747
|
G | C | 91 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0076others(88): Show | 95 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.1379+177G>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 11/17 | chr1 | 35832747 | ||||||
chr1:35832824
|
C | T | 6 | a0001c0003t0001g0153a0001c0003t0004g0155a0001c0003t0004g0157others(3): Show | 6 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1379+254C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 11/17 | chr1 | 35832824 | ||||||
chr1:35833150
|
G | A | 3 | a0001c0001t0011g0006a0001c0001t0012g0154a0001c0001t0012g0256 | 4 | HG02970.hp1 HG03098.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1379+580G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 11/17 | chr1 | 35833150 | ||||||
chr1:35833256
|
C | T | 1 | a0001c0002t0001g0204 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1379+686C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 11/17 | chr1 | 35833256 | ||||||
chr1:35833269
|
C | T | 1 | a0001c0002t0001g0230 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1379+699C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 11/17 | chr1 | 35833269 | ||||||
chr1:35833271
|
G | C | 118 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0064others(115): Show | 124 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.1379+701G>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 11/17 | chr1 | 35833271 | ||||||
chr1:35833273
|
G | A | 17 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0076others(14): Show | 17 | HG01109.hp1 HG01934.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1379+703G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 11/17 | chr1 | 35833273 | ||||||
chr1:35833371
|
A | G | 1 | a0001c0001t0030g0071 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1380-619A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 11/17 | chr1 | 35833371 | ||||||
chr1:35833429
|
C | T | 252 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0064others(249): Show | 263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.1380-561C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 11/17 | chr1 | 35833429 | ||||||
chr1:35834316
|
T | C | 1 | a0001c0001t0002g0121 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1564+142T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 12/17 | chr1 | 35834316 | ||||||
chr1:35834366
|
C | T | 4 | a0001c0001t0003g0023a0001c0001t0003g0024a0001c0001t0003g0025others(1): Show | 4 | HG01175.hp2 HG02572.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1564+192C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 12/17 | chr1 | 35834366 | ||||||
chr1:35834527
|
C | T | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1564+353C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 12/17 | chr1 | 35834527 | ||||||
chr1:35834727
|
GCT | G | 40 | a0001c0001t0003g0003a0001c0001t0003g0014a0001c0001t0003g0019others(37): Show | 41 | HG00438.hp1 HG00558.hp1 HG01175.hp2 others(38): Show |
intron_variant | MODIFIER | c.1564+556_1564+557d others(4): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 35834727 | |||||
chr1:35834750
|
C | T | 2 | a0001c0001t0016g0250a0001c0001t0016g0252 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1564+576C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 12/17 | chr1 | 35834750 | ||||||
chr1:35834812
|
C | G | 1 | a0001c0002t0001g0009 | 2 | NA18970.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1564+638C>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 12/17 | chr1 | 35834812 | ||||||
chr1:35834820
|
C | G | 7 | a0001c0001t0036g0070a0001c0003t0001g0153a0001c0003t0004g0155others(4): Show | 7 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1564+646C>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 12/17 | chr1 | 35834820 | ||||||
chr1:35834974
|
G | A | 1 | a0001c0001t0003g0030 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1564+800G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 12/17 | chr1 | 35834974 | ||||||
chr1:35835006
|
C | CT | 24 | a0001c0001t0001g0150a0001c0001t0002g0092a0001c0001t0002g0112others(21): Show | 25 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.1565-806dupT | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 35835006 | |||||
chr1:35835006
|
C | CTT | 83 | a0001c0001t0001g0177a0001c0001t0002g0242a0001c0001t0002g0244others(80): Show | 87 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.1565-807_1565-806d others(4): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 35835006 | |||||
chr1:35835006
|
C | CTTT | 9 | a0001c0002t0001g0183a0001c0002t0001g0184a0001c0002t0001g0188others(6): Show | 9 | HG01071.hp1 HG01175.hp1 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.1565-808_1565-806d others(5): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 35835006 | |||||
chr1:35835006
|
CT | C | 34 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0024others(31): Show | 35 | HG00558.hp1 HG01255.hp2 HG01261.hp2 others(32): Show |
intron_variant | MODIFIER | c.1565-806delT | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 35835006 | |||||
chr1:35835204
|
G | A | 1 | a0001c0001t0033g0052 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1565-630G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 12/17 | chr1 | 35835204 | ||||||
chr1:35835248
|
G | C | 4 | a0001c0001t0009g0054a0001c0001t0009g0055a0001c0001t0009g0056others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1565-586G>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 12/17 | chr1 | 35835248 | ||||||
chr1:35835303
|
C | G | 1 | a0001c0001t0004g0062 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1565-531C>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 12/17 | chr1 | 35835303 | ||||||
chr1:35835621
|
G | A | 1 | a0001c0001t0018g0133 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1565-213G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 12/17 | chr1 | 35835621 | ||||||
chr1:35836202
|
G | A | 11 | a0001c0001t0004g0012a0001c0001t0004g0053a0001c0001t0004g0253others(8): Show | 13 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.1724+209G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35836202 | ||||||
chr1:35836571
|
G | A | 1 | a0001c0001t0030g0071 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1724+578G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35836571 | ||||||
chr1:35836571
|
G | T | 1 | a0001c0001t0002g0061 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1724+578G>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35836571 | ||||||
chr1:35836602
|
G | A | 2 | a0001c0001t0001g0141a0001c0001t0001g0144 | 2 | HG02559.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1724+609G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35836602 | ||||||
chr1:35836688
|
C | T | 1 | a0001c0001t0015g0074 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1724+695C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35836688 | ||||||
chr1:35837375
|
C | T | 1 | a0001c0005t0004g0069 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1724+1382C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35837375 | ||||||
chr1:35837446
|
A | G | 1 | a0001c0002t0014g0203 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1724+1453A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35837446 | ||||||
chr1:35837620
|
T | C | 1 | a0001c0002t0001g0212 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1724+1627T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35837620 | ||||||
chr1:35838102
|
C | T | 1 | a0001c0001t0033g0052 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1724+2109C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35838102 | ||||||
chr1:35838138
|
C | T | 7 | a0001c0001t0036g0070a0001c0003t0001g0153a0001c0003t0004g0155others(4): Show | 7 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1724+2145C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35838138 | ||||||
chr1:35838174
|
T | C | 1 | a0001c0001t0030g0071 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1724+2181T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35838174 | ||||||
chr1:35838294
|
A | G | 2 | a0001c0002t0001g0220a0001c0002t0001g0221 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1724+2301A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35838294 | ||||||
chr1:35838631
|
G | A | 1 | a0001c0002t0008g0199 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1725-2534G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35838631 | ||||||
chr1:35838920
|
C | CT | 28 | a0001c0001t0001g0076a0001c0001t0001g0142a0001c0001t0001g0147others(25): Show | 29 | HG00280.hp2 HG00323.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1725-2235dupT | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 35838920 | |||||
chr1:35839301
|
C | T | 2 | a0001c0002t0001g0187a0001c0002t0001g0234 | 2 | HG02486.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1725-1864C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35839301 | ||||||
chr1:35839417
|
C | T | 2 | a0001c0001t0003g0046a0001c0001t0018g0133 | 2 | HG02602.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1725-1748C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35839417 | ||||||
chr1:35839518
|
T | C | 1 | a0001c0002t0005g0240 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1725-1647T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35839518 | ||||||
chr1:35839762
|
T | C | 1 | a0001c0002t0001g0187 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1725-1403T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35839762 | ||||||
chr1:35839966
|
C | CA | 18 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0076others(15): Show | 18 | HG01109.hp1 HG01934.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1725-1183dupA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 35839966 | |||||
chr1:35839966
|
CA | C | 6 | a0001c0001t0002g0081a0001c0001t0016g0252a0001c0001t0030g0071others(3): Show | 6 | HG01168.hp1 HG01261.hp1 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.1725-1183delA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 35839966 | |||||
chr1:35840105
|
C | T | 5 | a0001c0002t0001g0173a0001c0002t0001g0206a0001c0002t0004g0165others(2): Show | 5 | NA18941.hp1 NA18972.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.1725-1060C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35840105 | ||||||
chr1:35840152
|
C | T | 1 | a0001c0001t0004g0062 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1725-1013C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35840152 | ||||||
chr1:35840166
|
T | G | 20 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(17): Show | 20 | HG01074.hp2 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1725-999T>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35840166 | ||||||
chr1:35840595
|
G | C | 1 | a0001c0001t0002g0131 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1725-570G>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35840595 | ||||||
chr1:35841149
|
C | T | 1 | a0001c0005t0004g0069 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1725-16C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35841149 | ||||||
chr1:35841519
|
G | A | 5 | a0001c0002t0001g0201a0001c0002t0001g0204a0001c0002t0001g0213others(2): Show | 5 | HG02258.hp2 HG02273.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.2040+39G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 14/17 | chr1 | 35841519 | ||||||
chr1:35841532
|
A | T | 1 | a0001c0001t0002g0125 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2040+52A>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 14/17 | chr1 | 35841532 | ||||||
chr1:35841572
|
T | C | 1 | a0001c0001t0030g0071 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2041-44T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 14/17 | chr1 | 35841572 | ||||||
chr1:35841811
|
C | CATAT | 10 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(7): Show | 10 | HG01884.hp2 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.2175+85_2175+88dup others(4): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35841811 | |||||
chr1:35841811
|
C | CATATATA others(5): Show |
1 | a0001c0001t0012g0154 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2175+77_2175+88dup others(12): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35841811 | |||||
chr1:35841811
|
C | CATATATA others(9): Show |
2 | a0001c0001t0016g0250a0001c0001t0016g0252 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2175+73_2175+88dup others(16): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35841811 | |||||
chr1:35841811
|
C | CATATATA others(11): Show |
4 | a0001c0001t0004g0253a0001c0001t0011g0006a0001c0001t0012g0256others(1): Show | 5 | HG01255.hp2 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2175+71_2175+88dup others(18): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35841811 | |||||
chr1:35841811
|
C | CATATATA others(17): Show |
1 | a0001c0001t0004g0254 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2175+80_2175+81ins others(24): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35841811 | |||||
chr1:35841811
|
C | CATATATA others(19): Show |
1 | a0001c0001t0004g0012 | 2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.2175+80_2175+81ins others(26): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35841811 | |||||
chr1:35841811
|
C | CATATATA others(13): Show |
2 | a0001c0001t0004g0053a0001c0001t0004g0255 | 2 | HG03491.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2175+69_2175+88dup others(20): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35841811 | |||||
chr1:35841811
|
CAT | C | 114 | a0001c0001t0001g0010a0001c0001t0001g0142a0001c0001t0001g0148others(111): Show | 118 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.2175+87_2175+88del others(2): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35841811 | |||||
chr1:35841811
|
CATAT | C | 92 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0076others(89): Show | 96 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.2175+85_2175+88del others(4): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35841811 | |||||
chr1:35841811
|
CATATATA others(5): Show |
C | 3 | a0001c0001t0015g0073a0001c0001t0015g0074a0001c0001t0028g0072 | 3 | HG02145.hp2 HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2175+77_2175+88del others(12): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35841811 | |||||
chr1:35841839
|
C | T | 8 | a0001c0001t0004g0012a0001c0001t0004g0053a0001c0001t0004g0253others(5): Show | 9 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.2175+89C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35841839 | ||||||
chr1:35841848
|
T | A | 1 | a0001c0001t0030g0071 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2175+98T>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35841848 | ||||||
chr1:35842160
|
C | T | 1 | a0001c0001t0028g0072 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2175+410C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35842160 | ||||||
chr1:35842166
|
C | G | 2 | a0001c0002t0001g0228a0001c0002t0001g0238 | 2 | HG01123.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2175+416C>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35842166 | ||||||
chr1:35842296
|
A | G | 91 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0076others(88): Show | 95 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.2175+546A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35842296 | ||||||
chr1:35842350
|
T | G | 2 | a0001c0001t0008g0143a0001c0001t0025g0146 | 2 | HG02109.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2175+600T>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35842350 | ||||||
chr1:35842577
|
C | T | 1 | a0001c0003t0004g0159 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2175+827C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35842577 | ||||||
chr1:35842663
|
G | A | 7 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(4): Show | 7 | HG01884.hp2 HG02717.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.2175+913G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35842663 | ||||||
chr1:35842750
|
C | T | 94 | a0001c0001t0001g0177a0001c0001t0002g0242a0001c0001t0002g0243others(91): Show | 98 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.2175+1000C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35842750 | ||||||
chr1:35842762
|
A | G | 3 | a0001c0001t0015g0073a0001c0001t0015g0074a0001c0001t0028g0072 | 3 | HG02145.hp2 HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2175+1012A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35842762 | ||||||
chr1:35842863
|
T | A | 1 | a0001c0001t0030g0071 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2175+1113T>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35842863 | ||||||
chr1:35843249
|
T | G | 1 | a0001c0001t0033g0052 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2175+1499T>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35843249 | ||||||
chr1:35843397
|
G | A | 4 | a0001c0001t0009g0054a0001c0001t0009g0055a0001c0001t0009g0056others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.2175+1647G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35843397 | ||||||
chr1:35843659
|
GA | G | 7 | a0001c0001t0002g0091a0001c0003t0001g0153a0001c0003t0004g0155others(4): Show | 7 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2175+1919delA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35843659 | |||||
chr1:35844336
|
A | G | 1 | a0001c0001t0002g0077 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2175+2586A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35844336 | ||||||
chr1:35844436
|
T | C | 4 | a0001c0001t0009g0054a0001c0001t0009g0055a0001c0001t0009g0056others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.2175+2686T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35844436 | ||||||
chr1:35844533
|
C | G | 3 | a0001c0001t0015g0073a0001c0001t0015g0074a0001c0001t0028g0072 | 3 | HG02145.hp2 HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2175+2783C>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35844533 | ||||||
chr1:35844662
|
C | T | 1 | a0001c0001t0004g0254 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2175+2912C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35844662 | ||||||
chr1:35844720
|
G | C | 1 | a0001c0001t0002g0122 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2175+2970G>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35844720 | ||||||
chr1:35844901
|
A | C | 1 | a0001c0002t0001g0229 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2175+3151A>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35844901 | ||||||
chr1:35845102
|
TTGTAATC others(35): Show |
T | 17 | a0001c0001t0004g0012a0001c0001t0004g0053a0001c0001t0004g0254others(14): Show | 19 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.2175+3381_2175+342 others(46): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35845102 | |||||
chr1:35845113
|
CT | C | 219 | a0001c0001t0001g0060a0001c0001t0001g0064a0001c0001t0001g0065others(216): Show | 227 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.2175+3381delT | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35845113 | |||||
chr1:35845113
|
CTT | C | 11 | a0001c0001t0001g0059a0001c0001t0002g0005a0001c0001t0002g0092others(8): Show | 12 | HG01934.hp1 HG01943.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.2175+3380_2175+338 others(6): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35845113 | |||||
chr1:35845113
|
CTTTTTTT others(36): Show |
C | 2 | a0001c0001t0004g0253a0001c0003t0004g0159 | 2 | HG02922.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.2175+3380_2175+342 others(47): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35845113 | |||||
chr1:35845114
|
T | C | 1 | a0001c0001t0002g0123 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2175+3364T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35845114 | ||||||
chr1:35845114
|
T | G | 1 | a0001c0001t0004g0062 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2175+3364T>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35845114 | ||||||
chr1:35845131
|
T | G | 1 | a0001c0001t0002g0104 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2175+3381T>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35845131 | ||||||
chr1:35845155
|
C | CT | 16 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(13): Show | 16 | HG00642.hp2 HG00741.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.2175+3422dupT | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35845155 | |||||
chr1:35845155
|
CT | C | 6 | a0001c0001t0002g0106a0001c0001t0003g0038a0001c0001t0028g0072others(3): Show | 6 | HG03491.hp1 HG06807.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.2175+3422delT | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35845155 | |||||
chr1:35845196
|
CT | C | 56 | a0001c0001t0003g0003a0001c0001t0003g0014a0001c0001t0003g0019others(53): Show | 59 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.2175+3462delT | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35845196 | |||||
chr1:35845196
|
CTT | C | 101 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0064others(98): Show | 105 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.2175+3461_2175+346 others(6): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35845196 | |||||
chr1:35845212
|
TG | T | 92 | a0001c0001t0001g0177a0001c0001t0002g0242a0001c0001t0002g0243others(89): Show | 96 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.2175+3463delG | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35845212 | ||||||
chr1:35845294
|
G | A | 1 | a0001c0001t0009g0057 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2175+3544G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35845294 | ||||||
chr1:35845386
|
T | C | 2 | a0001c0001t0004g0012a0001c0001t0004g0254 | 3 | HG00280.hp2 HG00323.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.2175+3636T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35845386 | ||||||
chr1:35845426
|
C | T | 1 | a0001c0001t0006g0021 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2175+3676C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35845426 | ||||||
chr1:35845459
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2175+3709G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35845459 | ||||||
chr1:35845466
|
C | G | 40 | a0001c0001t0003g0003a0001c0001t0003g0014a0001c0001t0003g0019others(37): Show | 41 | HG00438.hp1 HG00558.hp1 HG01175.hp2 others(38): Show |
intron_variant | MODIFIER | c.2175+3716C>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35845466 | ||||||
chr1:35845472
|
G | A | 4 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(1): Show | 4 | HG01884.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2175+3722G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35845472 | ||||||
chr1:35845542
|
T | G | 11 | a0001c0001t0004g0012a0001c0001t0004g0053a0001c0001t0004g0253others(8): Show | 13 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.2175+3792T>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35845542 | ||||||
chr1:35845591
|
T | C | 1 | a0001c0001t0010g0107 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2175+3841T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35845591 | ||||||
chr1:35845748
|
A | C | 1 | a0001c0002t0005g0240 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2175+3998A>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35845748 | ||||||
chr1:35846051
|
G | A | 6 | a0001c0003t0001g0153a0001c0003t0004g0155a0001c0003t0004g0157others(3): Show | 6 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2176-4106G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35846051 | ||||||
chr1:35846117
|
T | C | 5 | a0001c0001t0002g0242a0001c0001t0002g0243a0001c0001t0002g0244others(2): Show | 5 | HG01069.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.2176-4040T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35846117 | ||||||
chr1:35846381
|
A | G | 2 | a0001c0001t0003g0031a0001c0001t0003g0032 | 2 | NA18969.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.2176-3776A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35846381 | ||||||
chr1:35846401
|
T | C | 1 | a0001c0001t0001g0177 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2176-3756T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35846401 | ||||||
chr1:35846604
|
GAT | G | 35 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0076others(32): Show | 36 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.2176-3528_2176-352 others(6): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35846604 | |||||
chr1:35846604
|
GATAT | G | 200 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(197): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.2176-3530_2176-352 others(8): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35846604 | |||||
chr1:35846675
|
C | T | 1 | a0001c0002t0001g0178 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2176-3482C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35846675 | ||||||
chr1:35846724
|
A | G | 6 | a0001c0003t0001g0153a0001c0003t0004g0155a0001c0003t0004g0157others(3): Show | 6 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2176-3433A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35846724 | ||||||
chr1:35846864
|
A | G | 1 | a0001c0001t0036g0070 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2176-3293A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35846864 | ||||||
chr1:35846865
|
C | T | 1 | a0001c0002t0005g0162 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2176-3292C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35846865 | ||||||
chr1:35847012
|
A | G | 5 | a0001c0002t0001g0173a0001c0002t0001g0206a0001c0002t0004g0165others(2): Show | 5 | NA18941.hp1 NA18972.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.2176-3145A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35847012 | ||||||
chr1:35847057
|
A | ACATCCTC others(137): Show |
1 | a0001c0001t0036g0070 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2176-3082_2176-308 others(148): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35847057 | |||||
chr1:35847059
|
A | G | 1 | a0001c0002t0005g0162 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2176-3098A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35847059 | ||||||
chr1:35847254
|
G | C | 1 | a0001c0002t0001g0170 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2176-2903G>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35847254 | ||||||
chr1:35847285
|
G | A | 1 | a0001c0002t0001g0181 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2176-2872G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35847285 | ||||||
chr1:35847440
|
G | A | 1 | a0001c0002t0001g0210 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2176-2717G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35847440 | ||||||
chr1:35847685
|
TAA | T | 131 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0076others(128): Show | 136 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.2176-2471_2176-247 others(6): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35847685 | ||||||
chr1:35847742
|
A | G | 1 | a0001c0002t0001g0202 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2176-2415A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35847742 | ||||||
chr1:35847968
|
T | TAAAGAAT others(324): Show |
1 | a0001c0001t0012g0256 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2176-2173_2176-217 others(335): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35847968 | |||||
chr1:35847968
|
T | TAAAGAAT others(326): Show |
1 | a0001c0001t0012g0154 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2176-2173_2176-217 others(337): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35847968 | |||||
chr1:35847968
|
T | TAAAGAAT others(328): Show |
1 | a0001c0001t0011g0006 | 2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2176-2173_2176-217 others(339): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35847968 | |||||
chr1:35848064
|
G | A | 11 | a0001c0001t0004g0012a0001c0001t0004g0053a0001c0001t0004g0253others(8): Show | 13 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.2176-2093G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35848064 | ||||||
chr1:35848127
|
T | C | 16 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0076others(13): Show | 16 | HG01109.hp1 HG01934.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.2176-2030T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35848127 | ||||||
chr1:35848253
|
T | C | 1 | a0001c0001t0003g0046 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2176-1904T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35848253 | ||||||
chr1:35848273
|
C | G | 1 | a0001c0002t0001g0234 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2176-1884C>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35848273 | ||||||
chr1:35848402
|
A | G | 88 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0076others(85): Show | 92 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.2176-1755A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35848402 | ||||||
chr1:35848451
|
CT | C | 90 | a0001c0001t0001g0177a0001c0001t0002g0242a0001c0001t0002g0243others(87): Show | 94 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.2176-1702delT | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35848451 | |||||
chr1:35848598
|
G | A | 90 | a0001c0001t0001g0177a0001c0001t0002g0242a0001c0001t0002g0243others(87): Show | 94 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.2176-1559G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35848598 | ||||||
chr1:35848637
|
GT | G | 8 | a0001c0001t0002g0109a0001c0001t0002g0245a0001c0001t0003g0023others(5): Show | 8 | HG01069.hp2 HG01175.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.2176-1506delT | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35848637 | |||||
chr1:35848852
|
A | G | 6 | a0001c0003t0001g0153a0001c0003t0004g0155a0001c0003t0004g0157others(3): Show | 6 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2176-1305A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35848852 | ||||||
chr1:35848865
|
A | G | 57 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0061others(54): Show | 60 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.2176-1292A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35848865 | ||||||
chr1:35849026
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2176-1131A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35849026 | ||||||
chr1:35849087
|
G | A | 11 | a0001c0001t0004g0012a0001c0001t0004g0053a0001c0001t0004g0253others(8): Show | 13 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.2176-1070G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35849087 | ||||||
chr1:35849114
|
T | G | 1 | a0001c0002t0001g0195 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2176-1043T>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35849114 | ||||||
chr1:35849128
|
A | G | 1 | a0001c0003t0004g0159 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2176-1029A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35849128 | ||||||
chr1:35849260
|
A | G | 90 | a0001c0001t0001g0177a0001c0001t0002g0242a0001c0001t0002g0243others(87): Show | 94 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.2176-897A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35849260 | ||||||
chr1:35849518
|
C | CA | 25 | a0001c0001t0002g0129a0001c0001t0003g0023a0001c0001t0003g0031others(22): Show | 26 | HG00280.hp2 HG00323.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.2176-619dupA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35849518 | |||||
chr1:35849518
|
C | CAA | 6 | a0001c0001t0004g0062a0001c0001t0011g0006a0001c0001t0012g0154others(3): Show | 7 | HG02129.hp2 HG02970.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.2176-620_2176-619d others(4): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35849518 | |||||
chr1:35849518
|
CA | C | 10 | a0001c0001t0001g0065a0001c0001t0001g0067a0001c0001t0002g0090others(7): Show | 11 | HG01069.hp2 HG01884.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.2176-619delA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35849518 | |||||
chr1:35849686
|
C | CA | 10 | a0001c0001t0001g0064a0001c0001t0004g0012a0001c0001t0004g0053others(7): Show | 11 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.2176-452dupA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35849686 | |||||
chr1:35849686
|
CA | C | 69 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(66): Show | 73 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.2176-452delA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35849686 | |||||
chr1:35849793
|
G | C | 1 | a0001c0001t0036g0070 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2176-364G>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35849793 | ||||||
chr1:35849823
|
C | T | 1 | a0001c0002t0001g0234 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2176-334C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35849823 | ||||||
chr1:35849850
|
C | G | 1 | a0001c0001t0001g0150 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2176-307C>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35849850 | ||||||
chr1:35850032
|
G | C | 4 | a0001c0001t0009g0054a0001c0001t0009g0055a0001c0001t0009g0056others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.2176-125G>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35850032 | ||||||
chr1:35850330
|
C | A | 8 | a0001c0001t0030g0071a0001c0001t0036g0070a0001c0003t0001g0153others(5): Show | 8 | HG01891.hp2 HG02055.hp2 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.2277+72C>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 16/17 | chr1 | 35850330 | ||||||
chr1:35850703
|
G | C | 252 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0064others(249): Show | 263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.2278-151G>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 16/17 | chr1 | 35850703 | ||||||
chr1:35850736
|
G | A | 1 | a0001c0001t0002g0093 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2278-118G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 16/17 | chr1 | 35850736 | ||||||
chr1:35850780
|
C | CA | 89 | a0001c0001t0001g0010a0001c0001t0001g0177a0001c0001t0002g0001others(86): Show | 95 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.2278-55dupA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr1 | 35850780 | |||||
chr1:35850780
|
C | CAA | 19 | a0001c0001t0002g0082a0001c0001t0002g0091a0001c0001t0002g0096others(16): Show | 19 | HG00673.hp1 HG02056.hp1 HG02602.hp2 others(16): Show |
intron_variant | MODIFIER | c.2278-56_2278-55dup others(2): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr1 | 35850780 | |||||
chr1:35850780
|
CA | C | 6 | a0001c0002t0001g0211a0001c0003t0001g0153a0001c0003t0004g0155others(3): Show | 6 | HG02055.hp2 HG02886.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2278-55delA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr1 | 35850780 | |||||
chr1:35850794
|
A | C | 1 | a0001c0002t0004g0165 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2278-60A>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 16/17 | chr1 | 35850794 | ||||||
chr1:35850795
|
A | C | 5 | a0001c0001t0002g0242a0001c0001t0002g0243a0001c0001t0002g0244others(2): Show | 5 | HG01069.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.2278-59A>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 16/17 | chr1 | 35850795 | ||||||
chr1:35850800
|
C | A | 49 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(46): Show | 50 | HG00438.hp1 HG00558.hp1 HG01175.hp2 others(47): Show |
intron_variant | MODIFIER | c.2278-54C>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 16/17 | chr1 | 35850800 | ||||||
chr1:35850801
|
A | C | 1 | a0001c0001t0002g0140 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2278-53A>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 16/17 | chr1 | 35850801 | ||||||
chr1:35850817
|
C | CA | 250 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0064others(247): Show | 261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.2278-27dupA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr1 | 35850817 | |||||
chr1:35851077
|
G | C | 33 | a0001c0001t0003g0003a0001c0001t0003g0014a0001c0001t0003g0022others(30): Show | 34 | HG00438.hp1 HG00558.hp1 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.2477+24G>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35851077 | ||||||
chr1:35851103
|
A | T | 1 | a0001c0001t0002g0117 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2477+50A>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35851103 | ||||||
chr1:35851126
|
A | G | 1 | a0001c0001t0036g0070 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2477+73A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35851126 | ||||||
chr1:35851410
|
G | C | 1 | a0001c0001t0011g0006 | 2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2477+357G>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35851410 | ||||||
chr1:35851440
|
G | C | 99 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0064others(96): Show | 103 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.2477+387G>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35851440 | ||||||
chr1:35851779
|
C | T | 10 | a0001c0001t0004g0012a0001c0001t0004g0053a0001c0001t0004g0253others(7): Show | 12 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.2477+726C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35851779 | ||||||
chr1:35851854
|
T | A | 252 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0064others(249): Show | 263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.2477+801T>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35851854 | ||||||
chr1:35851870
|
G | C | 18 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(15): Show | 20 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.2477+817G>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35851870 | ||||||
chr1:35851888
|
G | A | 1 | a0001c0001t0035g0176 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2477+835G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35851888 | ||||||
chr1:35852234
|
C | T | 39 | a0001c0001t0003g0003a0001c0001t0003g0014a0001c0001t0003g0019others(36): Show | 40 | HG00438.hp1 HG00558.hp1 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.2477+1181C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35852234 | ||||||
chr1:35852290
|
G | A | 1 | a0001c0001t0002g0096 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2478-1207G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35852290 | ||||||
chr1:35852309
|
G | C | 2 | a0001c0001t0023g0063a0001c0005t0004g0069 | 2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2478-1188G>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35852309 | ||||||
chr1:35852564
|
G | A | 252 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0064others(249): Show | 263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.2478-933G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35852564 | ||||||
chr1:35852858
|
A | G | 1 | a0001c0005t0004g0069 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2478-639A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35852858 | ||||||
chr1:35852862
|
A | C | 1 | a0001c0001t0036g0070 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2478-635A>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35852862 | ||||||
chr1:35852950
|
T | C | 252 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0064others(249): Show | 263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.2478-547T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35852950 | ||||||
chr1:35852976
|
C | T | 2 | a0001c0002t0001g0220a0001c0002t0001g0221 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2478-521C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35852976 | ||||||
chr1:35853033
|
G | A | 1 | a0001c0001t0005g0248 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2478-464G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35853033 | ||||||
chr1:35853047
|
G | A | 1 | a0001c0001t0036g0070 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2478-450G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35853047 | ||||||
chr1:35853066
|
T | C | 1 | a0001c0001t0030g0071 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2478-431T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35853066 | ||||||
chr1:35853067
|
G | A | 1 | a0001c0001t0030g0071 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2478-430G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35853067 | ||||||
chr1:35853110
|
G | A | 6 | a0001c0003t0001g0153a0001c0003t0004g0155a0001c0003t0004g0157others(3): Show | 6 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2478-387G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35853110 | ||||||
chr1:35853119
|
C | A | 251 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0064others(248): Show | 262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.2478-378C>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35853119 | ||||||
chr1:35853120
|
G | A | 1 | a0001c0002t0001g0183 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2478-377G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35853120 | ||||||
chr1:35853207
|
C | T | 3 | a0001c0001t0015g0073a0001c0001t0015g0074a0001c0001t0028g0072 | 3 | HG02145.hp2 HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2478-290C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35853207 | ||||||
chr1:35853248
|
C | CA | 42 | a0001c0001t0002g0083a0001c0001t0002g0118a0001c0001t0002g0131others(39): Show | 43 | HG00438.hp1 HG00558.hp1 HG01123.hp1 others(40): Show |
intron_variant | MODIFIER | c.2478-229dupA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 35853248 | |||||
chr1:35853265
|
A | G | 11 | a0001c0001t0004g0012a0001c0001t0004g0053a0001c0001t0004g0253others(8): Show | 13 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.2478-232A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35853265 |