geneid | 151246 |
---|---|
ensemblid | ENSG00000163535.18 |
hgncid | 30812 |
symbol | SGO2 |
name | shugoshin 2 |
refseq_nuc | NM_152524.6 |
refseq_prot | NP_689737.4 |
ensembl_nuc | ENST00000357799.9 |
ensembl_prot | ENSP00000350447.4 |
mane_status | MANE Select |
chr | chr2 |
start | 200526207 |
end | 200584096 |
strand | + |
ver | v1.2 |
region | chr2:200526207-200584096 |
region5000 | chr2:200521207-200589096 |
regionname0 | SGO2_chr2_200526207_200584096 |
regionname5000 | SGO2_chr2_200521207_200589096 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 1265 | 295 | 49 | 61 | 137 | 14 | 33 | 108 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0002 | 0/1 | 1265 | 29 | 0 | 9 | 17 | 2 | 0 | 15 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0003 | 0/0 | 1265 | 17 | 7 | 6 | 0 | 0 | 4 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0004 | 0/0 | 1265 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0005 | 0/0 | 1265 | 9 | 7 | 2 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0006 | 0/0 | 1265 | 6 | 0 | 0 | 6 | 0 | 0 | 6 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0007 | 0/0 | 1265 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0008 | 0/0 | 1265 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0009 | 0/0 | 1265 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0010 | 0/0 | 1265 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0011 | 0/0 | 1265 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0012 | 0/0 | 1265 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0013 | 0/0 | 1258 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0014 | 0/0 | 1265 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0015 | 0/0 | 1265 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0016 | 0/0 | 1265 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0017 | 0/0 | 1265 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0018 | 0/0 | 1265 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0019 | 0/0 | 1265 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 3798 | 100 | 14 | 18 | 54 | 4 | 10 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
c0002 | 0/0 | 3798 | 87 | 15 | 13 | 48 | 5 | 6 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
c0003 | 1/0 | 3798 | 54 | 11 | 19 | 13 | 2 | 8 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
c0004 | 0/0 | 3798 | 47 | 8 | 8 | 19 | 3 | 9 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
c0005 | 0/1 | 3798 | 29 | 0 | 9 | 17 | 2 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
c0006 | 0/0 | 3798 | 17 | 7 | 6 | 0 | 0 | 4 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
c0007 | 0/0 | 3798 | 9 | 9 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
c0008 | 0/0 | 3798 | 9 | 7 | 2 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
c0009 | 0/0 | 3798 | 6 | 0 | 0 | 6 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
c0010 | 0/0 | 3798 | 5 | 5 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
c0011 | 0/0 | 3798 | 3 | 0 | 0 | 3 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
c0012 | 0/0 | 3798 | 2 | 0 | 2 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
c0013 | 0/0 | 3798 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
c0014 | 0/0 | 3798 | 2 | 2 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
c0015 | 0/0 | 3798 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
c0016 | 0/0 | 3798 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
c0017 | 0/0 | 3798 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
c0018 | 0/0 | 3798 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
c0019 | 0/0 | 3798 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
c0020 | 0/0 | 3798 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
c0021 | 0/0 | 3798 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
c0022 | 0/0 | 3798 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
c0023 | 0/0 | 3798 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
c0024 | 0/0 | 3798 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
c0025 | 0/0 | 3777 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
c0026 | 0/0 | 3798 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 681 | 287 | 73 | 48 | 123 | 12 | 30 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
t0002 | 0/0 | 681 | 61 | 12 | 20 | 19 | 2 | 8 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
t0003 | 0/1 | 682 | 32 | 0 | 10 | 19 | 2 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
t0004 | 0/0 | 681 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
t0005 | 0/0 | 681 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
t0006 | 0/0 | 681 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
t0007 | 0/0 | 682 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0003 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0007 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0008 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0010 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0023 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0043 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0099 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0254 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 3798 | 100 | 14 | 18 | 54 | 4 | 10 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0001c0002 | 0/0 | 3798 | 87 | 15 | 13 | 48 | 5 | 6 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0001c0003 | 1/0 | 3798 | 54 | 11 | 19 | 13 | 2 | 8 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0001c0004 | 0/0 | 3798 | 47 | 8 | 8 | 19 | 3 | 9 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0001c0011 | 0/0 | 3798 | 3 | 0 | 0 | 3 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0001c0012 | 0/0 | 3798 | 2 | 0 | 2 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0001c0016 | 0/0 | 3798 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0001c0022 | 0/0 | 3798 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0002c0005 | 0/1 | 3798 | 29 | 0 | 9 | 17 | 2 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0003c0006 | 0/0 | 3798 | 17 | 7 | 6 | 0 | 0 | 4 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0004c0007 | 0/0 | 3798 | 9 | 9 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0005c0008 | 0/0 | 3798 | 9 | 7 | 2 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0006c0009 | 0/0 | 3798 | 6 | 0 | 0 | 6 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0007c0010 | 0/0 | 3798 | 5 | 5 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0008c0014 | 0/0 | 3798 | 2 | 2 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0009c0013 | 0/0 | 3798 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0010c0015 | 0/0 | 3798 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0011c0026 | 0/0 | 3798 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0012c0024 | 0/0 | 3798 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0013c0025 | 0/0 | 3777 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0014c0019 | 0/0 | 3798 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0015c0018 | 0/0 | 3798 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0016c0021 | 0/0 | 3798 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0017c0017 | 0/0 | 3798 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0018c0020 | 0/0 | 3798 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0019c0023 | 0/0 | 3798 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4478 | 97 | 14 | 18 | 51 | 4 | 10 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0001c0001t0003 | 0/0 | 4479 | 3 | 0 | 0 | 3 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0001c0002t0001 | 0/0 | 4478 | 87 | 15 | 13 | 48 | 5 | 6 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0001c0003t0001 | 1/0 | 4478 | 1 | 0 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0001c0003t0002 | 0/0 | 4478 | 53 | 11 | 19 | 13 | 2 | 8 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0001c0004t0001 | 0/0 | 4478 | 47 | 8 | 8 | 19 | 3 | 9 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0001c0011t0001 | 0/0 | 4478 | 3 | 0 | 0 | 3 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0001c0012t0001 | 0/0 | 4478 | 2 | 0 | 2 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0001c0016t0001 | 0/0 | 4478 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0001c0022t0002 | 0/0 | 4478 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0002c0005t0003 | 0/1 | 4479 | 28 | 0 | 9 | 16 | 2 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0002c0005t0007 | 0/0 | 4479 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0003c0006t0001 | 0/0 | 4478 | 16 | 7 | 5 | 0 | 0 | 4 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0003c0006t0003 | 0/0 | 4479 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0004c0007t0001 | 0/0 | 4478 | 9 | 9 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0005c0008t0001 | 0/0 | 4478 | 9 | 7 | 2 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0006c0009t0002 | 0/0 | 4478 | 6 | 0 | 0 | 6 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0007c0010t0001 | 0/0 | 4478 | 4 | 4 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0007c0010t0004 | 0/0 | 4478 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0008c0014t0001 | 0/0 | 4478 | 2 | 2 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0009c0013t0001 | 0/0 | 4478 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0010c0015t0006 | 0/0 | 4478 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0011c0026t0001 | 0/0 | 4478 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0012c0024t0001 | 0/0 | 4478 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0013c0025t0001 | 0/0 | 4457 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0014c0019t0001 | 0/0 | 4478 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0015c0018t0005 | 0/0 | 4478 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0016c0021t0001 | 0/0 | 4478 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0017c0017t0001 | 0/0 | 4478 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0018c0020t0001 | 0/0 | 4478 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
a0019c0023t0002 | 0/0 | 4478 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | copy fasta | chr2 | 200521207 | 200589096 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0001 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0010 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0043 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0001g0254 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0023 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0003t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0004t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0004t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0004t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0004t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0004t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0004t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0004t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0004t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0004t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0004t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0004t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0004t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0004t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0004t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0004t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0004t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0004t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0004t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0004t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0004t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0004t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0004t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0004t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0004t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0004t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0004t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0004t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0004t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0004t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0004t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0004t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0004t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0004t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0004t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0004t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0004t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0004t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0004t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0004t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0004t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0004t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0011t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0011t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0011t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0012t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0016t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0001c0022t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0002c0005t0003g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0002c0005t0003g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0002c0005t0003g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0002c0005t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0002c0005t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0002c0005t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0002c0005t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0002c0005t0003g0099 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0002c0005t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0002c0005t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0002c0005t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0002c0005t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0002c0005t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0002c0005t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0002c0005t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0002c0005t0003g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0002c0005t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0002c0005t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0002c0005t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0002c0005t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0002c0005t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0002c0005t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0002c0005t0007g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0003c0006t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0003c0006t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0003c0006t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0003c0006t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0003c0006t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0003c0006t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0003c0006t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0003c0006t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0003c0006t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0003c0006t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0003c0006t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0003c0006t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0003c0006t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0003c0006t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0003c0006t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0003c0006t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0004c0007t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0004c0007t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0004c0007t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0004c0007t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0004c0007t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0004c0007t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0004c0007t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0004c0007t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0004c0007t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0005c0008t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0005c0008t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0005c0008t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0005c0008t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0005c0008t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0005c0008t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0005c0008t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0005c0008t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0006c0009t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0006c0009t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0006c0009t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0006c0009t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0007c0010t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0007c0010t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0007c0010t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0007c0010t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0007c0010t0004g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0008c0014t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0008c0014t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0009c0013t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0009c0013t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0010c0015t0006g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0011c0026t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0012c0024t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0013c0025t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0014c0019t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0015c0018t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0016c0021t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0017c0017t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0018c0020t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
a0019c0023t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0283 | EUR | GBR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0262 | EUR | GBR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0195 | EUR | GBR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0196 | EUR | FIN | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG00280 | hp2 | a0001 | c0004 | t0001 | g0075 | EUR | FIN | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG00323 | hp1 | a0002 | c0005 | t0003 | g0103 | EUR | FIN | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG00323 | hp2 | a0002 | c0005 | t0003 | g0121 | EUR | FIN | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0281 | EAS | CHS | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG00408 | hp2 | a0001 | c0004 | t0001 | g0077 | EAS | CHS | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG00423 | hp2 | a0001 | c0002 | t0001 | g0312 | EAS | CHS | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | CHS | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG00544 | hp2 | a0009 | c0013 | t0001 | g0204 | EAS | CHS | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0290 | EAS | CHS | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG00597 | hp2 | a0001 | c0003 | t0002 | g0021 | EAS | CHS | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG00609 | hp1 | a0002 | c0005 | t0003 | g0147 | EAS | CHS | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG00639 | hp1 | a0001 | c0003 | t0002 | g0025 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG00639 | hp2 | a0003 | c0006 | t0001 | g0030 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0292 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0303 | EAS | CHS | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG00733 | hp1 | a0001 | c0002 | t0001 | g0269 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG00738 | hp1 | a0002 | c0005 | t0003 | g0104 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG00741 | hp1 | a0002 | c0005 | t0003 | g0102 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0264 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01070 | hp1 | a0001 | c0012 | t0001 | g0037 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01071 | hp1 | a0001 | c0012 | t0001 | g0037 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01081 | hp2 | a0001 | c0003 | t0002 | g0050 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01099 | hp1 | a0001 | c0004 | t0001 | g0076 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01099 | hp2 | a0001 | c0003 | t0002 | g0149 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01106 | hp1 | a0001 | c0004 | t0001 | g0015 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01106 | hp2 | a0001 | c0003 | t0002 | g0024 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01109 | hp2 | a0005 | c0008 | t0001 | g0085 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01167 | hp2 | a0003 | c0006 | t0001 | g0169 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01169 | hp1 | a0003 | c0006 | t0003 | g0030 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01169 | hp2 | a0001 | c0003 | t0002 | g0115 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01175 | hp1 | a0001 | c0003 | t0002 | g0150 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01192 | hp1 | a0001 | c0003 | t0002 | g0005 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01243 | hp1 | a0003 | c0006 | t0001 | g0170 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01243 | hp2 | a0005 | c0008 | t0001 | g0086 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0263 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01256 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01256 | hp2 | a0001 | c0003 | t0002 | g0025 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01257 | hp1 | a0003 | c0006 | t0001 | g0165 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01257 | hp2 | a0002 | c0005 | t0003 | g0019 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01258 | hp1 | a0002 | c0005 | t0003 | g0019 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01258 | hp2 | a0001 | c0002 | t0001 | g0036 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01261 | hp1 | a0001 | c0004 | t0001 | g0069 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01346 | hp1 | a0001 | c0003 | t0002 | g0131 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01358 | hp1 | a0001 | c0004 | t0001 | g0015 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01358 | hp2 | a0001 | c0003 | t0002 | g0094 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01361 | hp1 | a0001 | c0003 | t0002 | g0022 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0036 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01433 | hp1 | a0001 | c0022 | t0002 | g0026 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01433 | hp2 | a0001 | c0002 | t0001 | g0265 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01496 | hp1 | a0001 | c0004 | t0001 | g0066 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01515 | hp1 | a0001 | c0003 | t0002 | g0023 | EUR | IBS | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01515 | hp2 | a0001 | c0004 | t0001 | g0079 | EUR | IBS | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01517 | hp1 | a0001 | c0004 | t0001 | g0052 | EUR | IBS | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01517 | hp2 | a0001 | c0003 | t0002 | g0023 | EUR | IBS | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01884 | hp1 | a0018 | c0020 | t0001 | g0093 | AFR | ACB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0044 | AFR | ACB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01891 | hp2 | a0001 | c0003 | t0002 | g0130 | AFR | ACB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01934 | hp1 | a0001 | c0004 | t0001 | g0078 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01934 | hp2 | a0001 | c0003 | t0002 | g0005 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01943 | hp1 | a0001 | c0003 | t0002 | g0111 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01952 | hp1 | a0001 | c0003 | t0002 | g0142 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01952 | hp2 | a0001 | c0004 | t0001 | g0057 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01975 | hp1 | a0001 | c0003 | t0002 | g0026 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01975 | hp2 | a0002 | c0005 | t0003 | g0096 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01978 | hp1 | a0002 | c0005 | t0003 | g0098 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0043 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01981 | hp2 | a0003 | c0006 | t0001 | g0168 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02004 | hp2 | a0002 | c0005 | t0003 | g0101 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02015 | hp2 | a0001 | c0004 | t0001 | g0065 | EAS | KHV | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0315 | EAS | KHV | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02055 | hp1 | a0003 | c0006 | t0001 | g0171 | AFR | ACB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02055 | hp2 | a0004 | c0007 | t0001 | g0152 | AFR | ACB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0318 | EAS | KHV | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02056 | hp2 | a0001 | c0004 | t0001 | g0060 | EAS | KHV | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02071 | hp2 | a0001 | c0003 | t0002 | g0024 | EAS | KHV | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02083 | hp2 | a0001 | c0004 | t0001 | g0058 | EAS | KHV | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0306 | EAS | KHV | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02129 | hp2 | a0001 | c0004 | t0001 | g0089 | EAS | KHV | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02132 | hp1 | a0002 | c0005 | t0003 | g0124 | EAS | KHV | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0285 | EAS | KHV | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02145 | hp2 | a0007 | c0010 | t0001 | g0322 | AFR | ACB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02148 | hp1 | a0002 | c0005 | t0003 | g0097 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02148 | hp2 | a0001 | c0003 | t0002 | g0022 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0041 | EAS | CDX | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CDX | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02258 | hp1 | a0011 | c0026 | t0001 | g0323 | AFR | ACB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02258 | hp2 | a0001 | c0002 | t0001 | g0304 | AFR | ACB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02273 | hp1 | a0001 | c0003 | t0002 | g0136 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02280 | hp2 | a0001 | c0002 | t0001 | g0046 | AFR | ACB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02293 | hp1 | a0002 | c0005 | t0003 | g0100 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02300 | hp1 | a0001 | c0004 | t0001 | g0056 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02300 | hp2 | a0001 | c0003 | t0002 | g0005 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02523 | hp2 | a0001 | c0004 | t0001 | g0067 | EAS | KHV | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02602 | hp1 | a0001 | c0004 | t0001 | g0092 | SAS | PJL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02602 | hp2 | a0001 | c0003 | t0002 | g0129 | SAS | PJL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02615 | hp1 | a0001 | c0002 | t0001 | g0288 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02615 | hp2 | a0005 | c0008 | t0001 | g0017 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02622 | hp1 | a0001 | c0003 | t0002 | g0139 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02622 | hp2 | a0001 | c0003 | t0002 | g0107 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02647 | hp2 | a0003 | c0006 | t0001 | g0174 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02683 | hp1 | a0003 | c0006 | t0001 | g0172 | SAS | PJL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02683 | hp2 | a0001 | c0002 | t0001 | g0279 | SAS | PJL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02723 | hp1 | a0004 | c0007 | t0001 | g0159 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02723 | hp2 | a0007 | c0010 | t0001 | g0321 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02735 | hp1 | a0003 | c0006 | t0001 | g0167 | SAS | PJL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02735 | hp2 | a0001 | c0002 | t0001 | g0317 | SAS | PJL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02738 | hp1 | a0001 | c0004 | t0001 | g0080 | SAS | PJL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02738 | hp2 | a0003 | c0006 | t0001 | g0166 | SAS | PJL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02809 | hp1 | a0001 | c0004 | t0001 | g0074 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02818 | hp1 | a0003 | c0006 | t0001 | g0162 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02818 | hp2 | a0001 | c0002 | t0001 | g0266 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02886 | hp1 | a0007 | c0010 | t0001 | g0320 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02886 | hp2 | a0013 | c0025 | t0001 | g0260 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02895 | hp1 | a0003 | c0006 | t0001 | g0029 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02895 | hp2 | a0007 | c0010 | t0001 | g0324 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02896 | hp1 | a0001 | c0004 | t0001 | g0013 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02896 | hp2 | a0005 | c0008 | t0001 | g0083 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02897 | hp1 | a0001 | c0004 | t0001 | g0013 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02897 | hp2 | a0003 | c0006 | t0001 | g0029 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02922 | hp1 | a0014 | c0019 | t0001 | g0181 | AFR | ESN | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02922 | hp2 | a0004 | c0007 | t0001 | g0155 | AFR | ESN | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02965 | hp1 | a0004 | c0007 | t0001 | g0157 | AFR | ESN | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | ESN | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02970 | hp1 | a0001 | c0004 | t0001 | g0073 | AFR | ESN | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02970 | hp2 | a0001 | c0003 | t0002 | g0006 | AFR | ESN | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02976 | hp2 | a0001 | c0003 | t0002 | g0116 | AFR | ESN | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03041 | hp1 | a0007 | c0010 | t0004 | g0319 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03041 | hp2 | a0005 | c0008 | t0001 | g0088 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ESN | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03130 | hp2 | a0004 | c0007 | t0001 | g0156 | AFR | ESN | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | ESN | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03139 | hp2 | a0001 | c0004 | t0001 | g0072 | AFR | ESN | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03195 | hp1 | a0001 | c0016 | t0001 | g0246 | AFR | ESN | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03209 | hp1 | a0001 | c0003 | t0002 | g0006 | AFR | MSL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03209 | hp2 | a0001 | c0003 | t0002 | g0109 | AFR | MSL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03225 | hp1 | a0005 | c0008 | t0001 | g0087 | AFR | MSL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03225 | hp2 | a0004 | c0007 | t0001 | g0151 | AFR | MSL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03453 | hp1 | a0003 | c0006 | t0001 | g0163 | AFR | MSL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03453 | hp2 | a0012 | c0024 | t0001 | g0259 | AFR | MSL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03486 | hp1 | a0003 | c0006 | t0001 | g0164 | AFR | MSL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03486 | hp2 | a0001 | c0002 | t0001 | g0273 | AFR | MSL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03491 | hp1 | a0003 | c0006 | t0001 | g0173 | SAS | PJL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03491 | hp2 | a0001 | c0004 | t0001 | g0016 | SAS | PJL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03492 | hp1 | a0001 | c0004 | t0001 | g0016 | SAS | PJL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03516 | hp1 | a0001 | c0003 | t0002 | g0006 | AFR | ESN | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03516 | hp2 | a0001 | c0002 | t0001 | g0310 | AFR | ESN | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03540 | hp1 | a0001 | c0003 | t0002 | g0108 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03540 | hp2 | a0004 | c0007 | t0001 | g0158 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03579 | hp1 | a0001 | c0002 | t0001 | g0287 | AFR | MSL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03579 | hp2 | a0019 | c0023 | t0002 | g0118 | AFR | MSL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03654 | hp2 | a0001 | c0004 | t0001 | g0258 | SAS | PJL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03669 | hp1 | a0001 | c0003 | t0002 | g0134 | SAS | PJL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | STU | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03688 | hp2 | a0001 | c0003 | t0002 | g0146 | SAS | STU | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03704 | hp1 | a0001 | c0004 | t0001 | g0257 | SAS | PJL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0267 | SAS | PJL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03710 | hp1 | a0001 | c0003 | t0002 | g0105 | SAS | PJL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03710 | hp2 | a0001 | c0002 | t0001 | g0294 | SAS | PJL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | BEB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03831 | hp2 | a0001 | c0004 | t0001 | g0091 | SAS | BEB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03834 | hp1 | a0001 | c0003 | t0002 | g0143 | SAS | BEB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | BEB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03927 | hp1 | a0001 | c0003 | t0002 | g0095 | SAS | BEB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | BEB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | BEB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0291 | SAS | BEB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG04115 | hp1 | a0001 | c0003 | t0002 | g0110 | SAS | STU | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG04115 | hp2 | a0017 | c0017 | t0001 | g0302 | SAS | STU | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0271 | SAS | STU | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG04199 | hp2 | a0001 | c0004 | t0001 | g0090 | SAS | STU | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG04228 | hp1 | a0001 | c0004 | t0001 | g0055 | SAS | STU | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | STU | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18522 | hp1 | a0001 | c0004 | t0001 | g0059 | AFR | YRI | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | YRI | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | CHB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18747 | hp2 | a0001 | c0003 | t0002 | g0144 | EAS | CHB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0286 | AFR | YRI | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18906 | hp2 | a0001 | c0003 | t0002 | g0126 | AFR | YRI | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18939 | hp1 | a0002 | c0005 | t0003 | g0020 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0275 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18940 | hp1 | a0002 | c0005 | t0003 | g0122 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18942 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18942 | hp2 | a0001 | c0003 | t0002 | g0112 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18943 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18943 | hp2 | a0002 | c0005 | t0003 | g0123 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18944 | hp1 | a0002 | c0005 | t0003 | g0002 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18944 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18945 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18947 | hp1 | a0006 | c0009 | t0002 | g0027 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18947 | hp2 | a0001 | c0011 | t0001 | g0241 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18948 | hp2 | a0006 | c0009 | t0002 | g0137 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18949 | hp1 | a0001 | c0003 | t0002 | g0113 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18949 | hp2 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18952 | hp1 | a0001 | c0002 | t0001 | g0301 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18952 | hp2 | a0006 | c0009 | t0002 | g0027 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18956 | hp1 | a0001 | c0002 | t0001 | g0316 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18957 | hp1 | a0002 | c0005 | t0003 | g0002 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18960 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18961 | hp1 | a0009 | c0013 | t0001 | g0220 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18961 | hp2 | a0002 | c0005 | t0003 | g0125 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18963 | hp1 | a0001 | c0002 | t0001 | g0276 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18963 | hp2 | a0002 | c0005 | t0007 | g0119 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18965 | hp1 | a0001 | c0003 | t0002 | g0114 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18965 | hp2 | a0001 | c0004 | t0001 | g0081 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18966 | hp1 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18967 | hp1 | a0001 | c0002 | t0001 | g0280 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18969 | hp2 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18974 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18975 | hp1 | a0001 | c0011 | t0001 | g0228 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18975 | hp2 | a0001 | c0004 | t0001 | g0070 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18977 | hp2 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18978 | hp1 | a0001 | c0003 | t0002 | g0135 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18978 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18979 | hp1 | a0001 | c0004 | t0001 | g0061 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18979 | hp2 | a0002 | c0005 | t0003 | g0002 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0296 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18985 | hp1 | a0001 | c0003 | t0002 | g0021 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18987 | hp2 | a0001 | c0003 | t0002 | g0106 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18988 | hp1 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18988 | hp2 | a0002 | c0005 | t0003 | g0117 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18989 | hp2 | a0002 | c0005 | t0003 | g0002 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18992 | hp1 | a0001 | c0002 | t0001 | g0311 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18994 | hp1 | a0002 | c0005 | t0003 | g0020 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18998 | hp1 | a0001 | c0003 | t0002 | g0140 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18999 | hp2 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19001 | hp1 | a0002 | c0005 | t0003 | g0120 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0305 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19004 | hp2 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19005 | hp1 | a0002 | c0005 | t0003 | g0018 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19005 | hp2 | a0001 | c0004 | t0001 | g0062 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19007 | hp1 | a0001 | c0003 | t0002 | g0128 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0299 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19010 | hp2 | a0002 | c0005 | t0003 | g0018 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19011 | hp2 | a0001 | c0003 | t0002 | g0141 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19030 | hp1 | a0008 | c0014 | t0001 | g0153 | AFR | LWK | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19030 | hp2 | a0001 | c0002 | t0001 | g0044 | AFR | LWK | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19043 | hp1 | a0004 | c0007 | t0001 | g0161 | AFR | LWK | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | LWK | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19055 | hp1 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19055 | hp2 | a0006 | c0009 | t0002 | g0028 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19056 | hp1 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19056 | hp2 | a0001 | c0004 | t0001 | g0014 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19057 | hp1 | a0001 | c0004 | t0001 | g0063 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19060 | hp2 | a0001 | c0002 | t0001 | g0314 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19064 | hp1 | a0006 | c0009 | t0002 | g0028 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0278 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19066 | hp1 | a0001 | c0002 | t0001 | g0308 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19066 | hp2 | a0001 | c0004 | t0001 | g0053 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19067 | hp1 | a0001 | c0002 | t0001 | g0309 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0307 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19072 | hp1 | a0002 | c0005 | t0003 | g0145 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19072 | hp2 | a0001 | c0002 | t0001 | g0289 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0284 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19078 | hp2 | a0001 | c0002 | t0001 | g0300 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19082 | hp2 | a0001 | c0004 | t0001 | g0014 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19084 | hp2 | a0001 | c0003 | t0002 | g0127 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19085 | hp1 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19085 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19087 | hp2 | a0001 | c0004 | t0001 | g0054 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19088 | hp1 | a0001 | c0004 | t0001 | g0064 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19089 | hp2 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0274 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19091 | hp1 | a0001 | c0002 | t0001 | g0282 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19091 | hp2 | a0001 | c0011 | t0001 | g0230 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19240 | hp1 | a0001 | c0002 | t0001 | g0295 | AFR | YRI | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA19240 | hp2 | a0005 | c0008 | t0001 | g0082 | AFR | YRI | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0277 | EUR | TSI | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0261 | EUR | TSI | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0010 | EUR | TSI | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA20905 | hp1 | a0001 | c0003 | t0002 | g0133 | SAS | GIH | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | GIH | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0270 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG01123 | hp2 | a0001 | c0003 | t0002 | g0132 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02109 | hp1 | a0008 | c0014 | t0001 | g0154 | AFR | ACB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02109 | hp2 | a0004 | c0007 | t0001 | g0160 | AFR | ACB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0298 | AFR | ACB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02486 | hp2 | a0010 | c0015 | t0006 | g0047 | AFR | ACB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02559 | hp1 | a0001 | c0003 | t0002 | g0051 | AFR | ACB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG02559 | hp2 | a0005 | c0008 | t0001 | g0084 | AFR | ACB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03471 | hp1 | a0005 | c0008 | t0001 | g0017 | AFR | MSL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG03471 | hp2 | a0015 | c0018 | t0005 | g0048 | AFR | MSL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG06807 | hp1 | a0016 | c0021 | t0001 | g0148 | AFR | USA | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
HG06807 | hp2 | a0001 | c0002 | t0001 | g0297 | AFR | USA | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18955 | hp1 | a0006 | c0009 | t0002 | g0138 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0313 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA20300 | hp1 | a0001 | c0004 | t0001 | g0071 | AFR | USA | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0293 | AFR | USA | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA21309 | hp1 | a0001 | c0002 | t0001 | g0272 | AFR | LWK | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
NA21309 | hp2 | a0001 | c0004 | t0001 | g0068 | AFR | LWK | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
homoSapiens_chm13v2 | hp1 | a0002 | c0005 | t0003 | g0099 | REF | REF | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
homoSapiens_grch38 | hp1 | a0001 | c0003 | t0001 | g0254 | REF | REF | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:200533001
|
G | A | 1 | a0002 | 29 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(26): Show |
missense_variant | MODERATE | c.26G>A | p.Gly9Asp | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/9 | 74/4478 | 26/3798 | 9/1265 | chr2 | 200533001 | ||
chr2:200571173
|
G | A | 1 | a0010 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.827G>A | p.Arg276His | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 875/4478 | 827/3798 | 276/1265 | chr2 | 200571173 | ||
chr2:200571292
|
A | G | 1 | a0008 | 2 | HG02109.hp1 NA19030.hp1 |
missense_variant | MODERATE | c.946A>G | p.Asn316Asp | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 994/4478 | 946/3798 | 316/1265 | chr2 | 200571292 | ||
chr2:200571374
|
A | C | 2 | a0007a0011 | 6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
missense_variant | MODERATE | c.1028A>C | p.Glu343Ala | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 1076/4478 | 1028/3798 | 343/1265 | chr2 | 200571374 | ||
chr2:200571375
|
G | T | 1 | a0008 | 2 | HG02109.hp1 NA19030.hp1 |
missense_variant | MODERATE | c.1029G>T | p.Glu343Asp | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 1077/4478 | 1029/3798 | 343/1265 | chr2 | 200571375 | ||
chr2:200571431
|
A | C | 2 | a0012a0013 | 2 | HG02886.hp2 HG03453.hp2 |
missense_variant | MODERATE | c.1085A>C | p.Asp362Ala | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 1133/4478 | 1085/3798 | 362/1265 | chr2 | 200571431 | ||
chr2:200571602
|
A | T | 1 | a0010 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.1256A>T | p.Asn419Ile | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 1304/4478 | 1256/3798 | 419/1265 | chr2 | 200571602 | ||
chr2:200571705
|
TAATGAAC others(14): Show |
T | 1 | a0013 | 1 | HG02886.hp2 | conservative_inframe_deletion | MODERATE | c.1378_1398delATGAAT others(15): Show |
p.Met460_Gln466del | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 1426/4478 | 1378/3798 | 460/1265 | INFO_REALIGN_3_PRIME | chr2 | 200571705 | |
chr2:200571832
|
A | G | 2 | a0003a0005 | 26 | HG00639.hp2 HG01109.hp2 HG01167.hp2 others(23): Show |
missense_variant | MODERATE | c.1486A>G | p.Ile496Val | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 1534/4478 | 1486/3798 | 496/1265 | chr2 | 200571832 | ||
chr2:200572106
|
A | G | 1 | a0019 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.1760A>G | p.His587Arg | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 1808/4478 | 1760/3798 | 587/1265 | chr2 | 200572106 | ||
chr2:200572325
|
A | G | 1 | a0003 | 17 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(14): Show |
missense_variant | MODERATE | c.1979A>G | p.Asn660Ser | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 2027/4478 | 1979/3798 | 660/1265 | chr2 | 200572325 | ||
chr2:200572612
|
G | A | 1 | a0009 | 2 | HG00544.hp2 NA18961.hp1 |
missense_variant | MODERATE | c.2266G>A | p.Gly756Arg | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 2314/4478 | 2266/3798 | 756/1265 | chr2 | 200572612 | ||
chr2:200572727
|
T | C | 1 | a0018 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.2381T>C | p.Met794Thr | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 2429/4478 | 2381/3798 | 794/1265 | chr2 | 200572727 | ||
chr2:200572784
|
G | A | 1 | a0010 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.2438G>A | p.Cys813Tyr | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 2486/4478 | 2438/3798 | 813/1265 | chr2 | 200572784 | ||
chr2:200572801
|
A | C | 1 | a0017 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.2455A>C | p.Ile819Leu | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 2503/4478 | 2455/3798 | 819/1265 | chr2 | 200572801 | ||
chr2:200573094
|
A | G | 1 | a0006 | 6 | NA18947.hp1 NA18948.hp2 NA18952.hp2 others(3): Show |
missense_variant | MODERATE | c.2748A>G | p.Ile916Met | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 2796/4478 | 2748/3798 | 916/1265 | chr2 | 200573094 | ||
chr2:200573363
|
C | T | 1 | a0016 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.3017C>T | p.Ala1006Val | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 3065/4478 | 3017/3798 | 1006/1265 | chr2 | 200573363 | ||
chr2:200573420
|
A | C | 1 | a0011 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.3074A>C | p.His1025Pro | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 3122/4478 | 3074/3798 | 1025/1265 | chr2 | 200573420 | ||
chr2:200573426
|
C | T | 1 | a0014 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.3080C>T | p.Thr1027Ile | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 3128/4478 | 3080/3798 | 1027/1265 | chr2 | 200573426 | ||
chr2:200573668
|
A | G | 1 | a0015 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.3322A>G | p.Thr1108Ala | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 3370/4478 | 3322/3798 | 1108/1265 | chr2 | 200573668 | ||
chr2:200573774
|
A | G | 3 | a0004a0008a0016 | 12 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
missense_variant | MODERATE | c.3428A>G | p.His1143Arg | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 3476/4478 | 3428/3798 | 1143/1265 | chr2 | 200573774 | ||
chr2:200573845
|
G | A | 1 | a0010 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.3499G>A | p.Gly1167Ser | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 3547/4478 | 3499/3798 | 1167/1265 | chr2 | 200573845 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:200569726
|
T | C | 1 | a0010c0015 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.537T>C | p.Asn179Asn | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/9 | 585/4478 | 537/3798 | 179/1265 | chr2 | 200569726 | ||
chr2:200571615
|
C | T | 1 | a0013c0025 | 1 | HG02886.hp2 | synonymous_variant | LOW | c.1269C>T | p.Val423Val | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 1317/4478 | 1269/3798 | 423/1265 | chr2 | 200571615 | ||
chr2:200571756
|
A | C | 1 | a0008c0014 | 2 | HG02109.hp1 NA19030.hp1 |
synonymous_variant | LOW | c.1410A>C | p.Leu470Leu | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 1458/4478 | 1410/3798 | 470/1265 | chr2 | 200571756 | ||
chr2:200572491
|
A | G | 1 | a0001c0004 | 47 | HG00280.hp2 HG00408.hp2 HG01099.hp1 others(44): Show |
synonymous_variant | LOW | c.2145A>G | p.Lys715Lys | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 2193/4478 | 2145/3798 | 715/1265 | chr2 | 200572491 | ||
chr2:200572587
|
G | A | 1 | a0001c0016 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.2241G>A | p.Thr747Thr | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 2289/4478 | 2241/3798 | 747/1265 | chr2 | 200572587 | ||
chr2:200572587
|
G | T | 1 | a0010c0015 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.2241G>T | p.Thr747Thr | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 2289/4478 | 2241/3798 | 747/1265 | chr2 | 200572587 | ||
chr2:200572605
|
C | A | 3 | a0001c0002a0001c0012a0017c0017 | 90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
synonymous_variant | LOW | c.2259C>A | p.Ile753Ile | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 2307/4478 | 2259/3798 | 753/1265 | chr2 | 200572605 | ||
chr2:200572611
|
T | C | 17 | a0001c0001a0001c0002a0001c0004others(14): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
synonymous_variant | LOW | c.2265T>C | p.Pro755Pro | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 2313/4478 | 2265/3798 | 755/1265 | chr2 | 200572611 | ||
chr2:200572695
|
A | G | 1 | a0001c0022 | 1 | HG01433.hp1 | synonymous_variant | LOW | c.2349A>G | p.Gln783Gln | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 2397/4478 | 2349/3798 | 783/1265 | chr2 | 200572695 | ||
chr2:200572770
|
T | G | 1 | a0001c0011 | 3 | NA18947.hp2 NA18975.hp1 NA19091.hp2 |
synonymous_variant | LOW | c.2424T>G | p.Pro808Pro | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 2472/4478 | 2424/3798 | 808/1265 | chr2 | 200572770 | ||
chr2:200573379
|
A | G | 1 | a0001c0012 | 2 | HG01070.hp1 HG01071.hp1 |
synonymous_variant | LOW | c.3033A>G | p.Glu1011Glu | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 3081/4478 | 3033/3798 | 1011/1265 | chr2 | 200573379 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:200526228
|
G | A | 4 | a0001c0003t0002a0001c0022t0002a0006c0009t0002others(1): Show | 61 | HG00597.hp2 HG00639.hp1 HG01081.hp2 others(58): Show |
5_prime_UTR_variant | MODIFIER | c.-27G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/9 | 6748 | chr2 | 200526228 | |||||
chr2:200583560
|
G | GT | 4 | a0001c0001t0003a0002c0005t0003a0002c0005t0007others(1): Show | 33 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*106dupT | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 9/9 | 107 | INFO_REALIGN_3_PRIME | chr2 | 200583560 | ||||
chr2:200583602
|
G | C | 1 | a0007c0010t0004 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*138G>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 9/9 | 138 | chr2 | 200583602 | |||||
chr2:200583801
|
T | C | 1 | a0015c0018t0005 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*337T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 9/9 | 337 | chr2 | 200583801 | |||||
chr2:200583963
|
T | G | 1 | a0002c0005t0007 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*499T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 9/9 | 499 | chr2 | 200583963 | |||||
chr2:200584034
|
T | C | 1 | a0010c0015t0006 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*570T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 9/9 | 570 | chr2 | 200584034 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:200526438
|
T | C | 1 | a0001c0002t0001g0046 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-3+186T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200526438 | ||||||
chr2:200526591
|
C | T | 6 | a0007c0010t0001g0320a0007c0010t0001g0321a0007c0010t0001g0322others(3): Show | 6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3+339C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200526591 | ||||||
chr2:200526768
|
A | G | 72 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(69): Show | 90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.-3+516A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200526768 | ||||||
chr2:200526826
|
G | T | 2 | a0012c0024t0001g0259a0013c0025t0001g0260 | 2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-3+574G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200526826 | ||||||
chr2:200527086
|
T | A | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-3+834T>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200527086 | ||||||
chr2:200527365
|
C | G | 1 | a0013c0025t0001g0260 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-3+1113C>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200527365 | ||||||
chr2:200527412
|
G | T | 1 | a0001c0002t0001g0318 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-3+1160G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200527412 | ||||||
chr2:200527848
|
G | A | 1 | a0015c0018t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-3+1596G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200527848 | ||||||
chr2:200528091
|
T | C | 3 | a0007c0010t0001g0320a0007c0010t0001g0321a0007c0010t0004g0319 | 3 | HG02723.hp2 HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-3+1839T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200528091 | ||||||
chr2:200528107
|
G | T | 1 | a0001c0004t0001g0258 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-3+1855G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200528107 | ||||||
chr2:200528345
|
G | C | 72 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(69): Show | 90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.-3+2093G>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200528345 | ||||||
chr2:200528490
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-3+2238G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200528490 | ||||||
chr2:200528498
|
T | A | 2 | a0012c0024t0001g0259a0013c0025t0001g0260 | 2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-3+2246T>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200528498 | ||||||
chr2:200528540
|
G | T | 1 | a0001c0004t0001g0257 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-3+2288G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200528540 | ||||||
chr2:200528541
|
G | A | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-3+2289G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200528541 | ||||||
chr2:200528584
|
G | A | 1 | a0001c0001t0001g0012 | 2 | HG00733.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.-3+2332G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200528584 | ||||||
chr2:200528603
|
C | A | 233 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(230): Show | 276 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.-3+2351C>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200528603 | ||||||
chr2:200528900
|
A | C | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-3+2648A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200528900 | ||||||
chr2:200529062
|
T | C | 1 | a0001c0003t0002g0050 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-3+2810T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200529062 | ||||||
chr2:200529284
|
T | C | 234 | a0001c0001t0001g0175a0001c0002t0001g0001a0001c0002t0001g0010others(231): Show | 277 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.-3+3032T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200529284 | ||||||
chr2:200529325
|
C | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0255a0001c0001t0001g0256 | 4 | NA18956.hp2 NA18974.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+3073C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200529325 | ||||||
chr2:200529360
|
C | A | 324 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(321): Show | 382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.-3+3108C>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200529360 | ||||||
chr2:200529504
|
C | CGTTTT | 72 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(69): Show | 90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.-3+3268_-3+3272dup others(5): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 200529504 | |||||
chr2:200529504
|
C | T | 1 | a0001c0001t0003g0252 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-3+3252C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200529504 | ||||||
chr2:200529510
|
GTTTTGTT others(5): Show |
G | 16 | a0003c0006t0001g0029a0003c0006t0001g0030a0003c0006t0001g0162others(13): Show | 17 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.-3+3268_-3+3279del others(12): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 200529510 | |||||
chr2:200529612
|
C | T | 1 | a0015c0018t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-3+3360C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200529612 | ||||||
chr2:200529626
|
A | G | 11 | a0004c0007t0001g0151a0004c0007t0001g0152a0004c0007t0001g0155others(8): Show | 11 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-2-3348A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200529626 | ||||||
chr2:200529667
|
C | T | 1 | a0001c0002t0001g0317 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-2-3307C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200529667 | ||||||
chr2:200529668
|
G | A | 9 | a0007c0010t0001g0320a0007c0010t0001g0321a0007c0010t0001g0322others(6): Show | 9 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-2-3306G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200529668 | ||||||
chr2:200529720
|
G | T | 1 | a0001c0001t0001g0251 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-2-3254G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200529720 | ||||||
chr2:200529970
|
G | A | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.-2-3004G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200529970 | ||||||
chr2:200529973
|
C | T | 6 | a0007c0010t0001g0320a0007c0010t0001g0321a0007c0010t0001g0322others(3): Show | 6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2-3001C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200529973 | ||||||
chr2:200530047
|
C | T | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-2-2927C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200530047 | ||||||
chr2:200530129
|
T | C | 1 | a0001c0003t0002g0051 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-2-2845T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200530129 | ||||||
chr2:200530438
|
A | C | 234 | a0001c0001t0001g0175a0001c0002t0001g0001a0001c0002t0001g0010others(231): Show | 277 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.-2-2536A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200530438 | ||||||
chr2:200530480
|
T | C | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-2-2494T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200530480 | ||||||
chr2:200530509
|
A | G | 8 | a0007c0010t0001g0320a0007c0010t0001g0321a0007c0010t0001g0322others(5): Show | 8 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-2-2465A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200530509 | ||||||
chr2:200530587
|
G | A | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-2-2387G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200530587 | ||||||
chr2:200530671
|
T | A | 16 | a0003c0006t0001g0029a0003c0006t0001g0030a0003c0006t0001g0162others(13): Show | 17 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.-2-2303T>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200530671 | ||||||
chr2:200530922
|
G | T | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-2-2052G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200530922 | ||||||
chr2:200531107
|
T | A | 1 | a0001c0001t0001g0178 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-2-1867T>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200531107 | ||||||
chr2:200531108
|
T | A | 1 | a0001c0001t0001g0178 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-2-1866T>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200531108 | ||||||
chr2:200531110
|
AGGAGGCA others(10): Show |
A | 86 | a0001c0001t0001g0175a0001c0003t0002g0005a0001c0003t0002g0006others(83): Show | 103 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.-2-1860_-2-1844del others(17): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 200531110 | |||||
chr2:200531287
|
T | C | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-2-1687T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200531287 | ||||||
chr2:200531320
|
G | C | 48 | a0001c0004t0001g0004a0001c0004t0001g0013a0001c0004t0001g0014others(45): Show | 55 | HG00280.hp2 HG00408.hp2 HG01099.hp1 others(52): Show |
intron_variant | MODIFIER | c.-2-1654G>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200531320 | ||||||
chr2:200531368
|
C | T | 1 | a0001c0002t0001g0316 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-2-1606C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200531368 | ||||||
chr2:200531430
|
A | G | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-2-1544A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200531430 | ||||||
chr2:200531440
|
G | A | 50 | a0001c0003t0002g0094a0001c0004t0001g0004a0001c0004t0001g0013others(47): Show | 57 | HG00280.hp2 HG00408.hp2 HG01099.hp1 others(54): Show |
intron_variant | MODIFIER | c.-2-1534G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200531440 | ||||||
chr2:200531525
|
G | A | 1 | a0015c0018t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-2-1449G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200531525 | ||||||
chr2:200531838
|
A | T | 1 | a0013c0025t0001g0260 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-2-1136A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200531838 | ||||||
chr2:200531905
|
A | G | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-2-1069A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200531905 | ||||||
chr2:200531965
|
A | G | 3 | a0001c0003t0002g0050a0001c0003t0002g0149a0001c0003t0002g0150 | 3 | HG01081.hp2 HG01099.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.-2-1009A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200531965 | ||||||
chr2:200531969
|
C | A | 1 | a0018c0020t0001g0093 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-2-1005C>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200531969 | ||||||
chr2:200532122
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-2-852G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532122 | ||||||
chr2:200532182
|
A | G | 72 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(69): Show | 90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.-2-792A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532182 | ||||||
chr2:200532263
|
G | C | 8 | a0001c0002t0001g0010a0001c0002t0001g0036a0001c0002t0001g0261others(5): Show | 12 | HG00140.hp1 HG00741.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2-711G>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532263 | ||||||
chr2:200532265
|
GTTTTTTG others(4): Show |
G | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-2-702_-2-692delGT others(9): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 200532265 | |||||
chr2:200532271
|
TG | T | 2 | a0001c0012t0001g0037a0015c0018t0005g0048 | 3 | HG01070.hp1 HG01071.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-2-702delG | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532271 | ||||||
chr2:200532272
|
G | GTT | 7 | a0004c0007t0001g0155a0004c0007t0001g0156a0004c0007t0001g0157others(4): Show | 7 | HG02109.hp2 HG02723.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-692_-2-691dupTT | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 200532272 | |||||
chr2:200532272
|
G | T | 18 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0243others(15): Show | 18 | HG01884.hp1 HG01884.hp2 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.-2-702G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532272 | ||||||
chr2:200532272
|
GT | G | 132 | a0001c0001t0001g0175a0001c0003t0002g0005a0001c0003t0002g0006others(129): Show | 157 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.-2-691delT | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 200532272 | |||||
chr2:200532273
|
T | G | 2 | a0001c0001t0001g0179a0001c0001t0001g0180 | 2 | HG01192.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.-2-701T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532273 | ||||||
chr2:200532278
|
T | G | 4 | a0001c0001t0001g0176a0001c0001t0001g0243a0001c0001t0001g0244others(1): Show | 4 | HG01884.hp2 HG02280.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-696T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532278 | ||||||
chr2:200532278
|
T | TG | 5 | a0007c0010t0001g0320a0007c0010t0001g0321a0007c0010t0001g0322others(2): Show | 5 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2-696_-2-695insG | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532278 | ||||||
chr2:200532279
|
T | G | 1 | a0015c0018t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-2-695T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532279 | ||||||
chr2:200532281
|
T | G | 10 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0243others(7): Show | 10 | HG01884.hp2 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-2-693T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532281 | ||||||
chr2:200532283
|
T | G | 6 | a0001c0003t0002g0146a0001c0003t0002g0150a0001c0004t0001g0089others(3): Show | 6 | HG01175.hp1 HG02129.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2-691T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532283 | ||||||
chr2:200532283
|
TG | T | 51 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(48): Show | 64 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.-2-690delG | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532283 | ||||||
chr2:200532284
|
G | GT | 11 | a0001c0001t0001g0035a0001c0001t0001g0235a0001c0001t0001g0237others(8): Show | 12 | HG03831.hp1 NA18940.hp2 NA18947.hp2 others(9): Show |
intron_variant | MODIFIER | c.-2-675dupT | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 200532284 | |||||
chr2:200532284
|
G | T | 49 | a0001c0002t0001g0036a0001c0002t0001g0043a0001c0002t0001g0044others(46): Show | 54 | HG00423.hp2 HG00544.hp1 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.-2-690G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532284 | ||||||
chr2:200532285
|
T | G | 5 | a0007c0010t0001g0320a0007c0010t0001g0321a0007c0010t0001g0322others(2): Show | 5 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2-689T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532285 | ||||||
chr2:200532286
|
T | G | 1 | a0001c0001t0001g0182 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-2-688T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532286 | ||||||
chr2:200532287
|
T | G | 10 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0243others(7): Show | 10 | HG01884.hp2 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-2-687T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532287 | ||||||
chr2:200532289
|
T | G | 1 | a0015c0018t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-2-685T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532289 | ||||||
chr2:200532290
|
T | G | 1 | a0001c0001t0001g0243 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-2-684T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532290 | ||||||
chr2:200532295
|
T | G | 12 | a0001c0003t0002g0095a0002c0005t0003g0018a0002c0005t0003g0019others(9): Show | 14 | HG00323.hp1 HG00738.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.-2-679T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532295 | ||||||
chr2:200532402
|
T | C | 1 | a0001c0002t0001g0266 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-2-572T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532402 | ||||||
chr2:200532440
|
C | T | 8 | a0005c0008t0001g0017a0005c0008t0001g0082a0005c0008t0001g0083others(5): Show | 9 | HG01109.hp2 HG01243.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-2-534C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532440 | ||||||
chr2:200532519
|
C | T | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-2-455C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532519 | ||||||
chr2:200532527
|
G | A | 11 | a0004c0007t0001g0151a0004c0007t0001g0152a0004c0007t0001g0155others(8): Show | 11 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-2-447G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532527 | ||||||
chr2:200532531
|
T | C | 9 | a0007c0010t0001g0320a0007c0010t0001g0321a0007c0010t0001g0322others(6): Show | 9 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-2-443T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532531 | ||||||
chr2:200532622
|
T | C | 72 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(69): Show | 90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.-2-352T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532622 | ||||||
chr2:200532727
|
T | C | 12 | a0004c0007t0001g0151a0004c0007t0001g0152a0004c0007t0001g0155others(9): Show | 12 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.-2-247T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532727 | ||||||
chr2:200532746
|
A | G | 1 | a0001c0002t0001g0314 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-2-228A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532746 | ||||||
chr2:200532757
|
A | G | 1 | a0005c0008t0001g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-2-217A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532757 | ||||||
chr2:200532846
|
G | A | 234 | a0001c0001t0001g0175a0001c0002t0001g0001a0001c0002t0001g0010others(231): Show | 277 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.-2-128G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532846 | ||||||
chr2:200532860
|
ATACT | A | 6 | a0004c0007t0001g0151a0004c0007t0001g0155a0004c0007t0001g0156others(3): Show | 6 | HG02723.hp1 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2-111_-2-108delCT others(2): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 200532860 | |||||
chr2:200532924
|
A | C | 222 | a0001c0001t0001g0175a0001c0002t0001g0001a0001c0002t0001g0010others(219): Show | 265 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.-2-50A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532924 | ||||||
chr2:200533359
|
C | G | 1 | a0003c0006t0001g0174 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.133+251C>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | chr2 | 200533359 | ||||||
chr2:200533365
|
C | T | 6 | a0007c0010t0001g0320a0007c0010t0001g0321a0007c0010t0001g0322others(3): Show | 6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.133+257C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | chr2 | 200533365 | ||||||
chr2:200533432
|
A | G | 2 | a0008c0014t0001g0153a0008c0014t0001g0154 | 2 | HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.133+324A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | chr2 | 200533432 | ||||||
chr2:200533515
|
GTA | G | 16 | a0003c0006t0001g0029a0003c0006t0001g0030a0003c0006t0001g0162others(13): Show | 17 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.133+411_133+412del others(2): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 200533515 | |||||
chr2:200533519
|
A | ATG | 12 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0003t0002g0050others(9): Show | 12 | HG00738.hp1 HG01081.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.133+439_133+440dup others(2): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 200533519 | |||||
chr2:200533519
|
A | G | 50 | a0001c0001t0001g0234a0001c0004t0001g0004a0001c0004t0001g0013others(47): Show | 57 | HG00280.hp2 HG00408.hp2 HG01099.hp1 others(54): Show |
intron_variant | MODIFIER | c.133+411A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | chr2 | 200533519 | ||||||
chr2:200533519
|
ATG | A | 30 | a0001c0001t0001g0182a0001c0001t0001g0222a0001c0001t0001g0224others(27): Show | 32 | HG02145.hp2 HG02258.hp1 HG02486.hp1 others(29): Show |
intron_variant | MODIFIER | c.133+439_133+440del others(2): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 200533519 | |||||
chr2:200533519
|
ATGTG | A | 130 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(127): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.133+437_133+440del others(4): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 200533519 | |||||
chr2:200533547
|
G | A | 16 | a0003c0006t0001g0029a0003c0006t0001g0030a0003c0006t0001g0162others(13): Show | 17 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.133+439G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | chr2 | 200533547 | ||||||
chr2:200533547
|
G | GTGTGTGT others(3): Show |
13 | a0001c0004t0001g0004a0001c0004t0001g0014a0001c0004t0001g0053others(10): Show | 16 | HG01952.hp2 HG02056.hp2 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.133+440_133+441ins others(10): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 200533547 | |||||
chr2:200533547
|
G | GTGTGTGT others(3): Show |
25 | a0001c0004t0001g0015a0001c0004t0001g0062a0001c0004t0001g0063others(22): Show | 27 | HG00280.hp2 HG01099.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.133+440_133+441ins others(10): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 200533547 | |||||
chr2:200533547
|
G | GTGTGTGT others(5): Show |
1 | a0001c0004t0001g0077 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.133+440_133+441ins others(12): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 200533547 | |||||
chr2:200533547
|
G | GTGTGTGT others(5): Show |
4 | a0001c0004t0001g0016a0001c0004t0001g0078a0001c0004t0001g0079others(1): Show | 5 | HG01515.hp2 HG01934.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.133+440_133+441ins others(12): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 200533547 | |||||
chr2:200533547
|
G | GTGTGTGT others(7): Show |
1 | a0001c0004t0001g0080 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.133+440_133+441ins others(14): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 200533547 | |||||
chr2:200533547
|
G | GTGTGTGT others(7): Show |
2 | a0001c0004t0001g0081a0001c0004t0001g0258 | 2 | HG03654.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.133+440_133+441ins others(14): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 200533547 | |||||
chr2:200533641
|
CA | C | 10 | a0001c0002t0001g0316a0007c0010t0001g0320a0007c0010t0001g0321others(7): Show | 10 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.133+543delA | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 200533641 | |||||
chr2:200534033
|
A | G | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.133+925A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | chr2 | 200534033 | ||||||
chr2:200534204
|
A | C | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.134-792A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | chr2 | 200534204 | ||||||
chr2:200534335
|
C | T | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.134-661C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | chr2 | 200534335 | ||||||
chr2:200534463
|
A | G | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.134-533A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | chr2 | 200534463 | ||||||
chr2:200534521
|
G | A | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.134-475G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | chr2 | 200534521 | ||||||
chr2:200534695
|
A | G | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.134-301A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | chr2 | 200534695 | ||||||
chr2:200534817
|
A | G | 1 | a0015c0018t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.134-179A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | chr2 | 200534817 | ||||||
chr2:200534877
|
C | G | 12 | a0004c0007t0001g0151a0004c0007t0001g0152a0004c0007t0001g0155others(9): Show | 12 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.134-119C>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | chr2 | 200534877 | ||||||
chr2:200534919
|
C | T | 1 | a0001c0001t0001g0221 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.134-77C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | chr2 | 200534919 | ||||||
chr2:200535194
|
G | T | 11 | a0003c0006t0001g0030a0003c0006t0001g0165a0003c0006t0001g0166others(8): Show | 11 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.309+23G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 3/8 | chr2 | 200535194 | ||||||
chr2:200535251
|
T | C | 1 | a0001c0003t0002g0110 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.309+80T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 3/8 | chr2 | 200535251 | ||||||
chr2:200535495
|
G | A | 1 | a0012c0024t0001g0259 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.309+324G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 3/8 | chr2 | 200535495 | ||||||
chr2:200535693
|
G | T | 16 | a0003c0006t0001g0029a0003c0006t0001g0030a0003c0006t0001g0162others(13): Show | 17 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.310-372G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 3/8 | chr2 | 200535693 | ||||||
chr2:200535728
|
G | A | 1 | a0016c0021t0001g0148 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.310-337G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 3/8 | chr2 | 200535728 | ||||||
chr2:200535962
|
A | G | 16 | a0003c0006t0001g0029a0003c0006t0001g0030a0003c0006t0001g0162others(13): Show | 17 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.310-103A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 3/8 | chr2 | 200535962 | ||||||
chr2:200536008
|
T | C | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.310-57T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 3/8 | chr2 | 200536008 | ||||||
chr2:200536326
|
A | T | 2 | a0003c0006t0001g0172a0003c0006t0001g0173 | 2 | HG02683.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.387+184A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200536326 | ||||||
chr2:200536484
|
A | G | 1 | a0002c0005t0003g0019 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.387+342A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200536484 | ||||||
chr2:200536571
|
A | G | 1 | a0016c0021t0001g0148 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.387+429A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200536571 | ||||||
chr2:200536602
|
T | A | 72 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(69): Show | 90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.387+460T>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200536602 | ||||||
chr2:200536603
|
T | C | 1 | a0001c0002t0001g0264 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.387+461T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200536603 | ||||||
chr2:200536615
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.387+473G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200536615 | ||||||
chr2:200536654
|
C | G | 41 | a0001c0004t0001g0004a0001c0004t0001g0013a0001c0004t0001g0014others(38): Show | 47 | HG00280.hp2 HG00408.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.387+512C>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200536654 | ||||||
chr2:200536813
|
G | A | 42 | a0001c0003t0002g0140a0001c0004t0001g0004a0001c0004t0001g0013others(39): Show | 48 | HG00280.hp2 HG00408.hp2 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.387+671G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200536813 | ||||||
chr2:200536870
|
C | A | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.387+728C>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200536870 | ||||||
chr2:200537026
|
A | G | 1 | a0001c0003t0002g0139 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.387+884A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200537026 | ||||||
chr2:200537216
|
T | G | 1 | a0001c0001t0001g0183 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.387+1074T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200537216 | ||||||
chr2:200537323
|
C | T | 10 | a0007c0010t0001g0320a0007c0010t0001g0321a0007c0010t0001g0322others(7): Show | 10 | HG02145.hp2 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.387+1181C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200537323 | ||||||
chr2:200537338
|
C | T | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.387+1196C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200537338 | ||||||
chr2:200537517
|
T | C | 3 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186 | 3 | HG02015.hp1 NA18948.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.387+1375T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200537517 | ||||||
chr2:200537546
|
A | T | 1 | a0001c0003t0002g0144 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.387+1404A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200537546 | ||||||
chr2:200537669
|
T | C | 1 | a0001c0003t0002g0111 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.387+1527T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200537669 | ||||||
chr2:200537706
|
T | C | 3 | a0001c0003t0002g0112a0001c0003t0002g0113a0001c0003t0002g0114 | 3 | NA18942.hp2 NA18949.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.387+1564T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200537706 | ||||||
chr2:200538048
|
T | G | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.387+1906T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200538048 | ||||||
chr2:200538103
|
A | G | 1 | a0009c0013t0001g0220 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.387+1961A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200538103 | ||||||
chr2:200538270
|
A | G | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.387+2128A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200538270 | ||||||
chr2:200538283
|
A | G | 1 | a0001c0004t0001g0089 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.387+2141A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200538283 | ||||||
chr2:200538536
|
C | T | 6 | a0007c0010t0001g0320a0007c0010t0001g0321a0007c0010t0001g0322others(3): Show | 6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.387+2394C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200538536 | ||||||
chr2:200538684
|
A | G | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.387+2542A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200538684 | ||||||
chr2:200538700
|
C | A | 1 | a0001c0001t0001g0187 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.387+2558C>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200538700 | ||||||
chr2:200539098
|
G | T | 1 | a0001c0002t0001g0294 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.387+2956G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200539098 | ||||||
chr2:200539257
|
A | C | 72 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(69): Show | 90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.387+3115A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200539257 | ||||||
chr2:200539435
|
A | G | 11 | a0002c0005t0003g0018a0002c0005t0003g0019a0002c0005t0003g0096others(8): Show | 13 | HG00323.hp1 HG00738.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.388-3144A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200539435 | ||||||
chr2:200539456
|
A | G | 1 | a0001c0001t0001g0183 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.388-3123A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200539456 | ||||||
chr2:200539628
|
A | C | 6 | a0007c0010t0001g0320a0007c0010t0001g0321a0007c0010t0001g0322others(3): Show | 6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.388-2951A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200539628 | ||||||
chr2:200539628
|
A | T | 1 | a0002c0005t0003g0103 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.388-2951A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200539628 | ||||||
chr2:200539761
|
A | G | 1 | a0001c0002t0001g0293 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.388-2818A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200539761 | ||||||
chr2:200539971
|
C | T | 158 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(155): Show | 193 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.388-2608C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200539971 | ||||||
chr2:200539975
|
C | T | 65 | a0001c0004t0001g0004a0001c0004t0001g0013a0001c0004t0001g0014others(62): Show | 73 | HG00280.hp2 HG00408.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.388-2604C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200539975 | ||||||
chr2:200540055
|
C | T | 4 | a0006c0009t0002g0027a0006c0009t0002g0028a0006c0009t0002g0137others(1): Show | 6 | NA18947.hp1 NA18948.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.388-2524C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200540055 | ||||||
chr2:200540224
|
C | T | 85 | a0001c0003t0002g0005a0001c0003t0002g0006a0001c0003t0002g0021others(82): Show | 102 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.388-2355C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200540224 | ||||||
chr2:200540253
|
G | T | 1 | a0001c0002t0001g0263 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.388-2326G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200540253 | ||||||
chr2:200540275
|
G | T | 3 | a0001c0004t0001g0014a0001c0004t0001g0061a0001c0004t0001g0077 | 4 | HG00408.hp2 NA18979.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.388-2304G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200540275 | ||||||
chr2:200540290
|
A | T | 1 | a0001c0002t0001g0292 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.388-2289A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200540290 | ||||||
chr2:200540434
|
G | A | 72 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(69): Show | 90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.388-2145G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200540434 | ||||||
chr2:200540450
|
G | A | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.388-2129G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200540450 | ||||||
chr2:200540513
|
T | C | 233 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(230): Show | 276 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.388-2066T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200540513 | ||||||
chr2:200540514
|
G | A | 6 | a0007c0010t0001g0320a0007c0010t0001g0321a0007c0010t0001g0322others(3): Show | 6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.388-2065G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200540514 | ||||||
chr2:200540524
|
A | T | 2 | a0012c0024t0001g0259a0013c0025t0001g0260 | 2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.388-2055A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200540524 | ||||||
chr2:200540570
|
G | A | 6 | a0007c0010t0001g0320a0007c0010t0001g0321a0007c0010t0001g0322others(3): Show | 6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.388-2009G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200540570 | ||||||
chr2:200540665
|
T | C | 233 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(230): Show | 276 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.388-1914T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200540665 | ||||||
chr2:200540679
|
G | A | 65 | a0001c0004t0001g0004a0001c0004t0001g0013a0001c0004t0001g0014others(62): Show | 73 | HG00280.hp2 HG00408.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.388-1900G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200540679 | ||||||
chr2:200540837
|
G | T | 233 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(230): Show | 276 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.388-1742G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200540837 | ||||||
chr2:200540994
|
G | T | 2 | a0012c0024t0001g0259a0013c0025t0001g0260 | 2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.388-1585G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200540994 | ||||||
chr2:200541034
|
A | AG | 233 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(230): Show | 276 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.388-1543dupG | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 200541034 | |||||
chr2:200541072
|
T | G | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.388-1507T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200541072 | ||||||
chr2:200541242
|
G | A | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.388-1337G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200541242 | ||||||
chr2:200541339
|
A | G | 1 | a0015c0018t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.388-1240A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200541339 | ||||||
chr2:200541697
|
G | C | 1 | a0002c0005t0003g0096 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.388-882G>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200541697 | ||||||
chr2:200541870
|
C | G | 1 | a0012c0024t0001g0259 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.388-709C>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200541870 | ||||||
chr2:200541939
|
C | T | 1 | a0001c0003t0002g0136 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.388-640C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200541939 | ||||||
chr2:200542006
|
T | C | 85 | a0001c0003t0002g0005a0001c0003t0002g0006a0001c0003t0002g0021others(82): Show | 102 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.388-573T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200542006 | ||||||
chr2:200542034
|
A | G | 2 | a0001c0003t0002g0108a0001c0003t0002g0109 | 2 | HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.388-545A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200542034 | ||||||
chr2:200542194
|
C | T | 2 | a0001c0001t0001g0245a0001c0001t0001g0250 | 2 | HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.388-385C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200542194 | ||||||
chr2:200542501
|
G | C | 6 | a0007c0010t0001g0320a0007c0010t0001g0321a0007c0010t0001g0322others(3): Show | 6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.388-78G>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200542501 | ||||||
chr2:200542538
|
A | T | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.388-41A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200542538 | ||||||
chr2:200542554
|
TTTTC | T | 6 | a0007c0010t0001g0320a0007c0010t0001g0321a0007c0010t0001g0322others(3): Show | 6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.388-21_388-18delCT others(2): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 200542554 | |||||
chr2:200543030
|
C | T | 4 | a0001c0004t0001g0052a0001c0004t0001g0075a0001c0004t0001g0076others(1): Show | 4 | HG00280.hp2 HG01099.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.473+366C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200543030 | ||||||
chr2:200543087
|
G | A | 1 | a0001c0003t0002g0115 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.473+423G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200543087 | ||||||
chr2:200543252
|
C | T | 2 | a0012c0024t0001g0259a0013c0025t0001g0260 | 2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.473+588C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200543252 | ||||||
chr2:200543269
|
G | A | 22 | a0001c0004t0001g0015a0001c0004t0001g0016a0001c0004t0001g0052others(19): Show | 24 | HG00280.hp2 HG01099.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.473+605G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200543269 | ||||||
chr2:200543773
|
T | C | 1 | a0001c0001t0001g0251 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.473+1109T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200543773 | ||||||
chr2:200543940
|
C | T | 49 | a0001c0004t0001g0004a0001c0004t0001g0013a0001c0004t0001g0014others(46): Show | 56 | HG00280.hp2 HG00408.hp2 HG01099.hp1 others(53): Show |
intron_variant | MODIFIER | c.473+1276C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200543940 | ||||||
chr2:200543983
|
C | T | 41 | a0001c0004t0001g0004a0001c0004t0001g0013a0001c0004t0001g0014others(38): Show | 47 | HG00280.hp2 HG00408.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.473+1319C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200543983 | ||||||
chr2:200544099
|
A | G | 1 | a0001c0002t0001g0293 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.473+1435A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200544099 | ||||||
chr2:200544111
|
A | G | 6 | a0007c0010t0001g0320a0007c0010t0001g0321a0007c0010t0001g0322others(3): Show | 6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.473+1447A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200544111 | ||||||
chr2:200544134
|
T | G | 17 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0188others(14): Show | 20 | HG00140.hp2 HG00280.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.473+1470T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200544134 | ||||||
chr2:200544341
|
G | A | 1 | a0001c0001t0001g0222 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.473+1677G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200544341 | ||||||
chr2:200544408
|
A | G | 1 | a0001c0001t0001g0243 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.473+1744A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200544408 | ||||||
chr2:200544486
|
T | G | 2 | a0001c0002t0001g0267a0001c0002t0001g0294 | 2 | HG03704.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.473+1822T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200544486 | ||||||
chr2:200544497
|
A | G | 10 | a0007c0010t0001g0320a0007c0010t0001g0321a0007c0010t0001g0322others(7): Show | 10 | HG02145.hp2 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.473+1833A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200544497 | ||||||
chr2:200544568
|
C | A | 65 | a0001c0004t0001g0004a0001c0004t0001g0013a0001c0004t0001g0014others(62): Show | 73 | HG00280.hp2 HG00408.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.473+1904C>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200544568 | ||||||
chr2:200544691
|
A | AGATC | 20 | a0001c0003t0002g0021a0001c0003t0002g0126a0001c0003t0002g0127others(17): Show | 26 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.473+2028_473+2031d others(6): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200544691 | |||||
chr2:200544692
|
G | GATCGATC others(1): Show |
8 | a0001c0003t0002g0116a0002c0005t0003g0018a0002c0005t0003g0097others(5): Show | 9 | HG00738.hp1 HG01978.hp1 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.473+2031_473+2032i others(10): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200544692 | |||||
chr2:200544692
|
G | GATCT | 115 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(112): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.473+2069_473+2072d others(6): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200544692 | |||||
chr2:200544692
|
G | GATCTATC others(1): Show |
77 | a0001c0001t0001g0031a0001c0001t0001g0035a0001c0001t0001g0179others(74): Show | 80 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.473+2065_473+2072d others(10): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200544692 | |||||
chr2:200544692
|
G | GATCTATC others(5): Show |
12 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(9): Show | 13 | HG01081.hp1 HG01255.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.473+2061_473+2072d others(14): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200544692 | |||||
chr2:200544692
|
G | GATCTATC others(9): Show |
1 | a0001c0002t0001g0267 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.473+2057_473+2072d others(18): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200544692 | |||||
chr2:200544692
|
GATCT | G | 39 | a0001c0001t0001g0219a0001c0003t0002g0005a0001c0003t0002g0006others(36): Show | 48 | HG00609.hp2 HG00639.hp1 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.473+2069_473+2072d others(6): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200544692 | |||||
chr2:200544692
|
GATCTATC others(1): Show |
G | 3 | a0001c0001t0001g0199a0001c0003t0002g0105a0006c0009t0002g0138 | 3 | HG03710.hp1 NA18955.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.473+2065_473+2072d others(10): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200544692 | |||||
chr2:200544696
|
T | G | 9 | a0001c0003t0002g0106a0001c0003t0002g0110a0001c0003t0002g0112others(6): Show | 10 | HG02602.hp2 HG04115.hp1 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.473+2032T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200544696 | ||||||
chr2:200544700
|
T | G | 34 | a0001c0003t0002g0005a0001c0003t0002g0006a0001c0003t0002g0022others(31): Show | 43 | HG00639.hp1 HG01081.hp2 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.473+2036T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200544700 | ||||||
chr2:200544704
|
T | G | 2 | a0001c0003t0002g0105a0006c0009t0002g0138 | 2 | HG03710.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.473+2040T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200544704 | ||||||
chr2:200544804
|
A | G | 1 | a0018c0020t0001g0093 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.473+2140A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200544804 | ||||||
chr2:200545437
|
G | A | 6 | a0007c0010t0001g0320a0007c0010t0001g0321a0007c0010t0001g0322others(3): Show | 6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.473+2773G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200545437 | ||||||
chr2:200545445
|
G | A | 86 | a0001c0003t0002g0005a0001c0003t0002g0006a0001c0003t0002g0021others(83): Show | 103 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.473+2781G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200545445 | ||||||
chr2:200545500
|
C | T | 8 | a0005c0008t0001g0017a0005c0008t0001g0082a0005c0008t0001g0083others(5): Show | 9 | HG01109.hp2 HG01243.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.473+2836C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200545500 | ||||||
chr2:200545600
|
A | C | 233 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(230): Show | 276 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.473+2936A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200545600 | ||||||
chr2:200545623
|
C | T | 233 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(230): Show | 276 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.473+2959C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200545623 | ||||||
chr2:200545681
|
A | G | 1 | a0001c0002t0001g0298 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.473+3017A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200545681 | ||||||
chr2:200545693
|
C | T | 1 | a0001c0004t0001g0004 | 3 | NA18949.hp2 NA19004.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.473+3029C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200545693 | ||||||
chr2:200545755
|
A | G | 1 | a0001c0001t0001g0178 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.473+3091A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200545755 | ||||||
chr2:200545814
|
G | A | 2 | a0012c0024t0001g0259a0013c0025t0001g0260 | 2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.473+3150G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200545814 | ||||||
chr2:200545975
|
A | T | 1 | a0001c0002t0001g0297 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.473+3311A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200545975 | ||||||
chr2:200546094
|
C | G | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+3430C>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200546094 | ||||||
chr2:200546106
|
C | G | 3 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0016t0001g0246 | 3 | HG03130.hp1 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.473+3442C>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200546106 | ||||||
chr2:200546178
|
T | TA | 10 | a0001c0001t0001g0238a0007c0010t0001g0320a0007c0010t0001g0321others(7): Show | 10 | HG02145.hp2 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.473+3530dupA | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200546178 | |||||
chr2:200546178
|
TA | T | 216 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(213): Show | 259 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.473+3530delA | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200546178 | |||||
chr2:200546178
|
TAA | T | 6 | a0004c0007t0001g0151a0004c0007t0001g0155a0004c0007t0001g0156others(3): Show | 6 | HG02723.hp1 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+3529_473+3530d others(4): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200546178 | |||||
chr2:200546330
|
G | A | 1 | a0001c0003t0002g0116 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.473+3666G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200546330 | ||||||
chr2:200546339
|
C | T | 41 | a0001c0004t0001g0004a0001c0004t0001g0013a0001c0004t0001g0014others(38): Show | 47 | HG00280.hp2 HG00408.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.473+3675C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200546339 | ||||||
chr2:200546353
|
G | GA | 42 | a0001c0001t0001g0192a0001c0001t0001g0201a0001c0001t0001g0202others(39): Show | 43 | HG00408.hp1 HG00639.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.473+3716dupA | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200546353 | |||||
chr2:200546353
|
GA | G | 26 | a0001c0001t0001g0180a0001c0001t0001g0207a0001c0001t0001g0243others(23): Show | 28 | HG00323.hp2 HG01070.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.473+3716delA | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200546353 | |||||
chr2:200546353
|
GAA | G | 110 | a0001c0003t0002g0005a0001c0003t0002g0006a0001c0003t0002g0021others(107): Show | 132 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.473+3715_473+3716d others(4): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200546353 | |||||
chr2:200546353
|
GAAAAAAA others(8): Show |
G | 2 | a0015c0018t0005g0048a0018c0020t0001g0093 | 2 | HG01884.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.473+3702_473+3716d others(17): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200546353 | |||||
chr2:200546503
|
G | A | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+3839G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200546503 | ||||||
chr2:200546517
|
A | G | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+3853A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200546517 | ||||||
chr2:200546567
|
T | G | 10 | a0007c0010t0001g0320a0007c0010t0001g0321a0007c0010t0001g0322others(7): Show | 10 | HG02145.hp2 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.473+3903T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200546567 | ||||||
chr2:200546659
|
A | G | 1 | a0001c0002t0001g0314 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.473+3995A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200546659 | ||||||
chr2:200546867
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.473+4203G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200546867 | ||||||
chr2:200546899
|
A | T | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.473+4235A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200546899 | ||||||
chr2:200546931
|
A | G | 6 | a0007c0010t0001g0320a0007c0010t0001g0321a0007c0010t0001g0322others(3): Show | 6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.473+4267A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200546931 | ||||||
chr2:200546944
|
A | G | 8 | a0005c0008t0001g0017a0005c0008t0001g0082a0005c0008t0001g0083others(5): Show | 9 | HG01109.hp2 HG01243.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.473+4280A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200546944 | ||||||
chr2:200547120
|
C | T | 2 | a0012c0024t0001g0259a0013c0025t0001g0260 | 2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.473+4456C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200547120 | ||||||
chr2:200547131
|
A | C | 4 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0198others(1): Show | 4 | HG01255.hp1 NA18957.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.473+4467A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200547131 | ||||||
chr2:200547145
|
A | G | 1 | a0001c0002t0001g0268 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.473+4481A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200547145 | ||||||
chr2:200547146
|
C | T | 234 | a0001c0001t0001g0175a0001c0002t0001g0001a0001c0002t0001g0010others(231): Show | 277 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.473+4482C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200547146 | ||||||
chr2:200547245
|
A | G | 2 | a0001c0002t0001g0268a0001c0002t0001g0280 | 2 | NA18966.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.473+4581A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200547245 | ||||||
chr2:200547247
|
G | A | 234 | a0001c0001t0001g0175a0001c0002t0001g0001a0001c0002t0001g0010others(231): Show | 277 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.473+4583G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200547247 | ||||||
chr2:200547322
|
A | T | 1 | a0001c0001t0001g0256 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.473+4658A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200547322 | ||||||
chr2:200547361
|
G | A | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+4697G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200547361 | ||||||
chr2:200547362
|
A | T | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+4698A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200547362 | ||||||
chr2:200547427
|
A | G | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+4763A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200547427 | ||||||
chr2:200547479
|
A | G | 3 | a0001c0003t0002g0107a0001c0003t0002g0108a0001c0003t0002g0109 | 3 | HG02622.hp2 HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.473+4815A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200547479 | ||||||
chr2:200547563
|
C | T | 2 | a0012c0024t0001g0259a0013c0025t0001g0260 | 2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.473+4899C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200547563 | ||||||
chr2:200547702
|
C | T | 1 | a0015c0018t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.473+5038C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200547702 | ||||||
chr2:200547888
|
A | G | 41 | a0001c0004t0001g0004a0001c0004t0001g0013a0001c0004t0001g0014others(38): Show | 47 | HG00280.hp2 HG00408.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.473+5224A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200547888 | ||||||
chr2:200547905
|
G | T | 6 | a0007c0010t0001g0320a0007c0010t0001g0321a0007c0010t0001g0322others(3): Show | 6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.473+5241G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200547905 | ||||||
chr2:200547932
|
A | G | 4 | a0001c0002t0001g0261a0001c0002t0001g0263a0001c0002t0001g0265others(1): Show | 5 | HG01070.hp1 HG01071.hp1 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.473+5268A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200547932 | ||||||
chr2:200548028
|
C | T | 20 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0184others(17): Show | 23 | HG00140.hp2 HG00280.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.473+5364C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200548028 | ||||||
chr2:200548037
|
A | G | 86 | a0001c0001t0001g0175a0001c0003t0002g0005a0001c0003t0002g0006others(83): Show | 103 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.473+5373A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200548037 | ||||||
chr2:200548050
|
G | C | 41 | a0001c0004t0001g0004a0001c0004t0001g0013a0001c0004t0001g0014others(38): Show | 47 | HG00280.hp2 HG00408.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.473+5386G>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200548050 | ||||||
chr2:200548082
|
A | T | 1 | a0001c0002t0001g0290 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.473+5418A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200548082 | ||||||
chr2:200548201
|
G | T | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+5537G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200548201 | ||||||
chr2:200548228
|
G | A | 1 | a0003c0006t0001g0165 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.473+5564G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200548228 | ||||||
chr2:200548403
|
G | A | 234 | a0001c0001t0001g0175a0001c0002t0001g0001a0001c0002t0001g0010others(231): Show | 277 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.473+5739G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200548403 | ||||||
chr2:200548529
|
A | G | 1 | a0001c0004t0001g0053 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.473+5865A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200548529 | ||||||
chr2:200548761
|
A | G | 1 | a0001c0003t0002g0127 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.473+6097A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200548761 | ||||||
chr2:200548855
|
T | C | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+6191T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200548855 | ||||||
chr2:200549195
|
C | T | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+6531C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200549195 | ||||||
chr2:200549294
|
G | T | 1 | a0001c0003t0002g0135 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.473+6630G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200549294 | ||||||
chr2:200549392
|
A | T | 1 | a0001c0002t0001g0291 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.473+6728A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200549392 | ||||||
chr2:200549447
|
C | T | 2 | a0001c0003t0002g0134a0002c0005t0003g0121 | 2 | HG00323.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.473+6783C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200549447 | ||||||
chr2:200549535
|
C | T | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+6871C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200549535 | ||||||
chr2:200549538
|
T | C | 6 | a0007c0010t0001g0320a0007c0010t0001g0321a0007c0010t0001g0322others(3): Show | 6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.473+6874T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200549538 | ||||||
chr2:200549701
|
A | C | 1 | a0005c0008t0001g0087 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.473+7037A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200549701 | ||||||
chr2:200549727
|
A | C | 1 | a0002c0005t0003g0102 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.473+7063A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200549727 | ||||||
chr2:200549876
|
A | T | 2 | a0001c0003t0002g0140a0001c0003t0002g0141 | 2 | NA18998.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.473+7212A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200549876 | ||||||
chr2:200549981
|
G | A | 1 | a0012c0024t0001g0259 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.473+7317G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200549981 | ||||||
chr2:200550105
|
C | A | 233 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(230): Show | 276 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.473+7441C>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200550105 | ||||||
chr2:200550139
|
C | G | 72 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(69): Show | 90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.473+7475C>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200550139 | ||||||
chr2:200550184
|
T | C | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+7520T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200550184 | ||||||
chr2:200550294
|
A | G | 1 | a0001c0003t0002g0134 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.473+7630A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200550294 | ||||||
chr2:200550334
|
A | T | 74 | a0001c0001t0001g0175a0001c0003t0002g0005a0001c0003t0002g0006others(71): Show | 91 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.473+7670A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200550334 | ||||||
chr2:200550381
|
C | G | 6 | a0001c0004t0001g0015a0001c0004t0001g0066a0001c0004t0001g0068others(3): Show | 7 | HG01106.hp1 HG01261.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.473+7717C>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200550381 | ||||||
chr2:200550624
|
G | A | 8 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0245others(5): Show | 8 | HG02280.hp1 HG02572.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.473+7960G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200550624 | ||||||
chr2:200550892
|
G | A | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+8228G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200550892 | ||||||
chr2:200550926
|
G | T | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+8262G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200550926 | ||||||
chr2:200550991
|
C | A | 6 | a0007c0010t0001g0320a0007c0010t0001g0321a0007c0010t0001g0322others(3): Show | 6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.473+8327C>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200550991 | ||||||
chr2:200550991
|
C | CA | 155 | a0001c0001t0001g0175a0001c0002t0001g0001a0001c0002t0001g0010others(152): Show | 189 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.473+8339dupA | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200550991 | |||||
chr2:200551276
|
A | G | 1 | a0012c0024t0001g0259 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.473+8612A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200551276 | ||||||
chr2:200551284
|
G | A | 72 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(69): Show | 90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.473+8620G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200551284 | ||||||
chr2:200551380
|
G | A | 10 | a0007c0010t0001g0320a0007c0010t0001g0321a0007c0010t0001g0322others(7): Show | 10 | HG02145.hp2 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.473+8716G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200551380 | ||||||
chr2:200551514
|
A | T | 1 | a0001c0004t0001g0074 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.473+8850A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200551514 | ||||||
chr2:200551525
|
G | A | 234 | a0001c0001t0001g0175a0001c0002t0001g0001a0001c0002t0001g0010others(231): Show | 277 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.473+8861G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200551525 | ||||||
chr2:200551718
|
T | C | 3 | a0002c0005t0003g0020a0002c0005t0003g0117a0002c0005t0003g0122 | 4 | NA18939.hp1 NA18940.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.473+9054T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200551718 | ||||||
chr2:200551989
|
C | T | 1 | a0015c0018t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.473+9325C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200551989 | ||||||
chr2:200552059
|
G | T | 1 | a0004c0007t0001g0151 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.473+9395G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200552059 | ||||||
chr2:200552251
|
G | C | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+9587G>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200552251 | ||||||
chr2:200552255
|
T | C | 16 | a0003c0006t0001g0029a0003c0006t0001g0030a0003c0006t0001g0162others(13): Show | 17 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.473+9591T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200552255 | ||||||
chr2:200552484
|
C | T | 1 | a0002c0005t0003g0101 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.473+9820C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200552484 | ||||||
chr2:200552510
|
G | A | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+9846G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200552510 | ||||||
chr2:200552892
|
C | A | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+10228C>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200552892 | ||||||
chr2:200552944
|
C | T | 1 | a0001c0001t0001g0242 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.473+10280C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200552944 | ||||||
chr2:200553113
|
G | A | 10 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0243others(7): Show | 10 | HG01884.hp2 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.473+10449G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200553113 | ||||||
chr2:200553156
|
T | C | 3 | a0001c0002t0001g0269a0001c0002t0001g0270a0001c0002t0001g0272 | 3 | HG00733.hp1 HG01123.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.473+10492T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200553156 | ||||||
chr2:200553189
|
G | A | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+10525G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200553189 | ||||||
chr2:200553426
|
T | C | 1 | a0001c0001t0001g0221 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.473+10762T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200553426 | ||||||
chr2:200553780
|
G | A | 2 | a0012c0024t0001g0259a0013c0025t0001g0260 | 2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.473+11116G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200553780 | ||||||
chr2:200553821
|
C | G | 9 | a0007c0010t0001g0320a0007c0010t0001g0321a0007c0010t0001g0322others(6): Show | 9 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.473+11157C>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200553821 | ||||||
chr2:200553976
|
T | C | 1 | a0001c0003t0002g0144 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.473+11312T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200553976 | ||||||
chr2:200554041
|
A | G | 1 | a0001c0001t0003g0252 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.473+11377A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200554041 | ||||||
chr2:200554102
|
C | T | 1 | a0001c0004t0001g0059 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.473+11438C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200554102 | ||||||
chr2:200554111
|
A | C | 1 | a0003c0006t0001g0165 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.473+11447A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200554111 | ||||||
chr2:200554115
|
T | C | 72 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(69): Show | 90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.473+11451T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200554115 | ||||||
chr2:200554399
|
C | G | 1 | a0018c0020t0001g0093 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.473+11735C>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200554399 | ||||||
chr2:200554586
|
C | T | 10 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0243others(7): Show | 10 | HG01884.hp2 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.473+11922C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200554586 | ||||||
chr2:200554611
|
A | G | 1 | a0003c0006t0001g0029 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.473+11947A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200554611 | ||||||
chr2:200554815
|
A | G | 12 | a0004c0007t0001g0151a0004c0007t0001g0152a0004c0007t0001g0155others(9): Show | 12 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.473+12151A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200554815 | ||||||
chr2:200554945
|
T | A | 16 | a0003c0006t0001g0029a0003c0006t0001g0030a0003c0006t0001g0162others(13): Show | 17 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.473+12281T>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200554945 | ||||||
chr2:200555003
|
A | G | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+12339A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200555003 | ||||||
chr2:200555018
|
A | G | 1 | a0001c0003t0002g0126 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.473+12354A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200555018 | ||||||
chr2:200555020
|
C | G | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+12356C>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200555020 | ||||||
chr2:200555063
|
G | A | 85 | a0001c0003t0002g0005a0001c0003t0002g0006a0001c0003t0002g0021others(82): Show | 102 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.473+12399G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200555063 | ||||||
chr2:200555103
|
C | T | 233 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(230): Show | 276 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.473+12439C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200555103 | ||||||
chr2:200555107
|
C | G | 16 | a0003c0006t0001g0029a0003c0006t0001g0030a0003c0006t0001g0162others(13): Show | 17 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.473+12443C>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200555107 | ||||||
chr2:200555237
|
G | A | 86 | a0001c0003t0002g0005a0001c0003t0002g0006a0001c0003t0002g0021others(83): Show | 103 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.473+12573G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200555237 | ||||||
chr2:200555307
|
C | T | 3 | a0001c0003t0002g0050a0001c0003t0002g0149a0001c0003t0002g0150 | 3 | HG01081.hp2 HG01099.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.473+12643C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200555307 | ||||||
chr2:200555312
|
G | A | 2 | a0001c0003t0002g0108a0001c0003t0002g0109 | 2 | HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.473+12648G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200555312 | ||||||
chr2:200555484
|
C | T | 1 | a0001c0001t0001g0197 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.473+12820C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200555484 | ||||||
chr2:200555591
|
A | G | 1 | a0001c0001t0001g0206 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.473+12927A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200555591 | ||||||
chr2:200555673
|
G | A | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+13009G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200555673 | ||||||
chr2:200555683
|
A | G | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+13019A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200555683 | ||||||
chr2:200555955
|
T | C | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+13291T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200555955 | ||||||
chr2:200555959
|
C | T | 1 | a0013c0025t0001g0260 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.473+13295C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200555959 | ||||||
chr2:200555962
|
T | G | 1 | a0015c0018t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.473+13298T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200555962 | ||||||
chr2:200556013
|
G | A | 4 | a0001c0002t0001g0011a0001c0002t0001g0299a0001c0002t0001g0300others(1): Show | 6 | NA18942.hp1 NA18943.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+13349G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200556013 | ||||||
chr2:200556194
|
G | A | 1 | a0001c0001t0001g0198 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.474-13469G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200556194 | ||||||
chr2:200556230
|
T | C | 8 | a0005c0008t0001g0017a0005c0008t0001g0082a0005c0008t0001g0083others(5): Show | 9 | HG01109.hp2 HG01243.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.474-13433T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200556230 | ||||||
chr2:200556303
|
T | C | 1 | a0001c0001t0001g0222 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.474-13360T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200556303 | ||||||
chr2:200556328
|
A | G | 3 | a0001c0004t0001g0075a0001c0004t0001g0076a0001c0004t0001g0079 | 3 | HG00280.hp2 HG01099.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.474-13335A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200556328 | ||||||
chr2:200556415
|
A | G | 1 | a0013c0025t0001g0260 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.474-13248A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200556415 | ||||||
chr2:200556481
|
T | C | 1 | a0001c0002t0001g0306 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.474-13182T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200556481 | ||||||
chr2:200556600
|
C | T | 41 | a0001c0004t0001g0004a0001c0004t0001g0013a0001c0004t0001g0014others(38): Show | 47 | HG00280.hp2 HG00408.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.474-13063C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200556600 | ||||||
chr2:200556678
|
G | A | 1 | a0002c0005t0003g0147 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.474-12985G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200556678 | ||||||
chr2:200556711
|
A | G | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.474-12952A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200556711 | ||||||
chr2:200556821
|
G | A | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.474-12842G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200556821 | ||||||
chr2:200556865
|
G | A | 1 | a0001c0003t0002g0131 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.474-12798G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200556865 | ||||||
chr2:200557086
|
T | C | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.474-12577T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200557086 | ||||||
chr2:200557370
|
C | G | 3 | a0001c0004t0001g0072a0001c0004t0001g0073a0001c0004t0001g0074 | 3 | HG02809.hp1 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.474-12293C>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200557370 | ||||||
chr2:200557469
|
A | C | 1 | a0015c0018t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.474-12194A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200557469 | ||||||
chr2:200557470
|
A | G | 4 | a0001c0003t0002g0140a0001c0003t0002g0141a0001c0003t0002g0144others(1): Show | 4 | HG03688.hp2 NA18747.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-12193A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200557470 | ||||||
chr2:200557788
|
C | T | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.474-11875C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200557788 | ||||||
chr2:200557798
|
ATTTG | A | 6 | a0007c0010t0001g0320a0007c0010t0001g0321a0007c0010t0001g0322others(3): Show | 6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.474-11849_474-1184 others(8): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200557798 | |||||
chr2:200557864
|
AC | A | 2 | a0001c0004t0001g0016a0001c0004t0001g0258 | 3 | HG03491.hp2 HG03492.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.474-11798delC | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200557864 | ||||||
chr2:200557865
|
C | CT | 73 | a0001c0002t0001g0001a0001c0002t0001g0011a0001c0002t0001g0038others(70): Show | 87 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.474-11781dupT | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200557865 | |||||
chr2:200557865
|
CT | C | 48 | a0001c0001t0001g0238a0001c0004t0001g0004a0001c0004t0001g0013others(45): Show | 54 | HG00280.hp2 HG00408.hp2 HG01099.hp1 others(51): Show |
intron_variant | MODIFIER | c.474-11781delT | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200557865 | |||||
chr2:200557933
|
G | A | 1 | a0015c0018t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.474-11730G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200557933 | ||||||
chr2:200557989
|
G | A | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.474-11674G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200557989 | ||||||
chr2:200558020
|
C | T | 1 | a0012c0024t0001g0259 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.474-11643C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200558020 | ||||||
chr2:200558021
|
A | G | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.474-11642A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200558021 | ||||||
chr2:200558115
|
C | T | 1 | a0007c0010t0004g0319 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.474-11548C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200558115 | ||||||
chr2:200558159
|
G | A | 12 | a0004c0007t0001g0151a0004c0007t0001g0152a0004c0007t0001g0155others(9): Show | 12 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.474-11504G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200558159 | ||||||
chr2:200558246
|
T | C | 1 | a0008c0014t0001g0154 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.474-11417T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200558246 | ||||||
chr2:200558352
|
A | C | 1 | a0001c0003t0002g0143 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.474-11311A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200558352 | ||||||
chr2:200558361
|
A | G | 3 | a0002c0005t0003g0120a0002c0005t0003g0124a0002c0005t0003g0125 | 3 | HG02132.hp1 NA18961.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.474-11302A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200558361 | ||||||
chr2:200558363
|
C | T | 1 | a0001c0001t0001g0234 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.474-11300C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200558363 | ||||||
chr2:200558527
|
A | C | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.474-11136A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200558527 | ||||||
chr2:200558658
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.474-11005G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200558658 | ||||||
chr2:200558664
|
C | T | 233 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(230): Show | 276 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.474-10999C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200558664 | ||||||
chr2:200558687
|
G | A | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.474-10976G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200558687 | ||||||
chr2:200558805
|
C | CT | 6 | a0001c0001t0001g0219a0001c0001t0003g0223a0012c0024t0001g0259others(3): Show | 6 | HG00609.hp2 HG01884.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.474-10844dupT | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200558805 | |||||
chr2:200558805
|
C | CTT | 7 | a0007c0010t0001g0320a0007c0010t0001g0321a0007c0010t0001g0322others(4): Show | 7 | HG02145.hp2 HG02258.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.474-10845_474-1084 others(6): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200558805 | |||||
chr2:200558862
|
G | A | 6 | a0001c0003t0002g0005a0001c0003t0002g0022a0001c0003t0002g0094others(3): Show | 9 | HG01192.hp1 HG01358.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.474-10801G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200558862 | ||||||
chr2:200558929
|
A | C | 1 | a0001c0003t0002g0134 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.474-10734A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200558929 | ||||||
chr2:200558960
|
G | A | 1 | a0001c0002t0001g0268 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.474-10703G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200558960 | ||||||
chr2:200559205
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.474-10458A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200559205 | ||||||
chr2:200559281
|
T | C | 1 | a0004c0007t0001g0151 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.474-10382T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200559281 | ||||||
chr2:200559409
|
T | G | 1 | a0015c0018t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.474-10254T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200559409 | ||||||
chr2:200559458
|
C | T | 3 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0016t0001g0246 | 3 | HG03130.hp1 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.474-10205C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200559458 | ||||||
chr2:200559539
|
A | G | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.474-10124A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200559539 | ||||||
chr2:200559597
|
T | C | 2 | a0001c0004t0001g0062a0001c0004t0001g0063 | 2 | NA19005.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.474-10066T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200559597 | ||||||
chr2:200559958
|
T | A | 1 | a0004c0007t0001g0151 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.474-9705T>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200559958 | ||||||
chr2:200559974
|
A | G | 5 | a0001c0001t0001g0244a0001c0001t0001g0247a0001c0001t0001g0248others(2): Show | 5 | HG02572.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.474-9689A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200559974 | ||||||
chr2:200560006
|
G | T | 233 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(230): Show | 276 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.474-9657G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200560006 | ||||||
chr2:200560022
|
C | T | 1 | a0001c0004t0001g0066 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.474-9641C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200560022 | ||||||
chr2:200560263
|
A | G | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.474-9400A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200560263 | ||||||
chr2:200560378
|
T | G | 1 | a0002c0005t0003g0117 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.474-9285T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200560378 | ||||||
chr2:200560488
|
T | G | 1 | a0001c0004t0001g0066 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.474-9175T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200560488 | ||||||
chr2:200560895
|
T | C | 49 | a0001c0004t0001g0004a0001c0004t0001g0013a0001c0004t0001g0014others(46): Show | 56 | HG00280.hp2 HG00408.hp2 HG01099.hp1 others(53): Show |
intron_variant | MODIFIER | c.474-8768T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200560895 | ||||||
chr2:200561206
|
A | C | 233 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(230): Show | 276 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.474-8457A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200561206 | ||||||
chr2:200561311
|
T | A | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.474-8352T>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200561311 | ||||||
chr2:200561314
|
A | G | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.474-8349A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200561314 | ||||||
chr2:200561355
|
C | T | 1 | a0001c0002t0001g0298 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.474-8308C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200561355 | ||||||
chr2:200561405
|
C | T | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.474-8258C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200561405 | ||||||
chr2:200561538
|
T | C | 1 | a0001c0002t0001g0273 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.474-8125T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200561538 | ||||||
chr2:200561741
|
G | A | 6 | a0007c0010t0001g0320a0007c0010t0001g0321a0007c0010t0001g0322others(3): Show | 6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.474-7922G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200561741 | ||||||
chr2:200561744
|
C | T | 1 | a0005c0008t0001g0086 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.474-7919C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200561744 | ||||||
chr2:200561768
|
G | A | 1 | a0001c0001t0001g0232 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.474-7895G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200561768 | ||||||
chr2:200562173
|
G | GT | 29 | a0001c0003t0002g0006a0001c0003t0002g0021a0001c0003t0002g0025others(26): Show | 35 | HG00597.hp2 HG00639.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.474-7484dupT | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200562173 | |||||
chr2:200562247
|
G | A | 233 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(230): Show | 276 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.474-7416G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200562247 | ||||||
chr2:200562274
|
T | C | 1 | a0001c0004t0001g0091 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.474-7389T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200562274 | ||||||
chr2:200562410
|
G | A | 16 | a0003c0006t0001g0029a0003c0006t0001g0030a0003c0006t0001g0162others(13): Show | 17 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.474-7253G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200562410 | ||||||
chr2:200562418
|
C | G | 1 | a0001c0002t0001g0263 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.474-7245C>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200562418 | ||||||
chr2:200562467
|
G | A | 1 | a0015c0018t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.474-7196G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200562467 | ||||||
chr2:200562617
|
G | A | 2 | a0008c0014t0001g0153a0008c0014t0001g0154 | 2 | HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.474-7046G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200562617 | ||||||
chr2:200562780
|
G | A | 1 | a0018c0020t0001g0093 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.474-6883G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200562780 | ||||||
chr2:200562782
|
A | G | 6 | a0007c0010t0001g0320a0007c0010t0001g0321a0007c0010t0001g0322others(3): Show | 6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.474-6881A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200562782 | ||||||
chr2:200562829
|
A | G | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.474-6834A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200562829 | ||||||
chr2:200562864
|
G | A | 9 | a0007c0010t0001g0320a0007c0010t0001g0321a0007c0010t0001g0322others(6): Show | 9 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.474-6799G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200562864 | ||||||
chr2:200563041
|
T | A | 1 | a0002c0005t0003g0121 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.474-6622T>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200563041 | ||||||
chr2:200563074
|
T | G | 1 | a0016c0021t0001g0148 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.474-6589T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200563074 | ||||||
chr2:200563300
|
C | T | 1 | a0001c0004t0001g0071 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.474-6363C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200563300 | ||||||
chr2:200563357
|
C | T | 18 | a0001c0003t0002g0021a0001c0003t0002g0025a0001c0003t0002g0026others(15): Show | 22 | HG00597.hp2 HG00639.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.474-6306C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200563357 | ||||||
chr2:200563376
|
G | A | 2 | a0001c0004t0001g0068a0001c0004t0001g0091 | 2 | HG03831.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.474-6287G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200563376 | ||||||
chr2:200563472
|
A | G | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.474-6191A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200563472 | ||||||
chr2:200563515
|
T | A | 1 | a0012c0024t0001g0259 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.474-6148T>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200563515 | ||||||
chr2:200563650
|
T | G | 8 | a0005c0008t0001g0017a0005c0008t0001g0082a0005c0008t0001g0083others(5): Show | 9 | HG01109.hp2 HG01243.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.474-6013T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200563650 | ||||||
chr2:200563746
|
G | A | 1 | a0001c0001t0001g0244 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.474-5917G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200563746 | ||||||
chr2:200563811
|
A | T | 1 | a0001c0001t0001g0206 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.474-5852A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200563811 | ||||||
chr2:200563975
|
G | T | 1 | a0013c0025t0001g0260 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.474-5688G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200563975 | ||||||
chr2:200564345
|
T | G | 16 | a0003c0006t0001g0029a0003c0006t0001g0030a0003c0006t0001g0162others(13): Show | 17 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.474-5318T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200564345 | ||||||
chr2:200564452
|
A | C | 49 | a0001c0004t0001g0004a0001c0004t0001g0013a0001c0004t0001g0014others(46): Show | 56 | HG00280.hp2 HG00408.hp2 HG01099.hp1 others(53): Show |
intron_variant | MODIFIER | c.474-5211A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200564452 | ||||||
chr2:200564533
|
T | G | 85 | a0001c0003t0002g0005a0001c0003t0002g0006a0001c0003t0002g0021others(82): Show | 102 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.474-5130T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200564533 | ||||||
chr2:200564787
|
G | T | 9 | a0001c0002t0001g0010a0001c0002t0001g0036a0001c0002t0001g0261others(6): Show | 13 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.474-4876G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200564787 | ||||||
chr2:200564964
|
T | C | 1 | a0001c0011t0001g0230 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.474-4699T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200564964 | ||||||
chr2:200564995
|
TG | T | 7 | a0001c0002t0001g0045a0001c0002t0001g0289a0001c0002t0001g0305others(4): Show | 8 | HG00423.hp2 HG00544.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.474-4665delG | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200564995 | |||||
chr2:200565039
|
C | T | 1 | a0018c0020t0001g0093 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.474-4624C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200565039 | ||||||
chr2:200565040
|
C | T | 1 | a0001c0003t0002g0131 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.474-4623C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200565040 | ||||||
chr2:200565223
|
C | T | 1 | a0004c0007t0001g0161 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.474-4440C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200565223 | ||||||
chr2:200565235
|
G | C | 1 | a0001c0001t0001g0215 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.474-4428G>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200565235 | ||||||
chr2:200565271
|
G | A | 1 | a0009c0013t0001g0220 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.474-4392G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200565271 | ||||||
chr2:200565361
|
C | A | 86 | a0001c0003t0002g0005a0001c0003t0002g0006a0001c0003t0002g0021others(83): Show | 103 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.474-4302C>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200565361 | ||||||
chr2:200565646
|
C | T | 1 | a0001c0004t0001g0071 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.474-4017C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200565646 | ||||||
chr2:200565861
|
C | T | 1 | a0001c0004t0001g0016 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.474-3802C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200565861 | ||||||
chr2:200565912
|
A | T | 1 | a0001c0003t0002g0114 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.474-3751A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200565912 | ||||||
chr2:200565940
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.474-3723T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200565940 | ||||||
chr2:200566104
|
G | A | 72 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(69): Show | 90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.474-3559G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200566104 | ||||||
chr2:200566215
|
G | T | 1 | a0018c0020t0001g0093 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.474-3448G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200566215 | ||||||
chr2:200566244
|
G | T | 3 | a0003c0006t0001g0167a0003c0006t0001g0172a0003c0006t0001g0173 | 3 | HG02683.hp1 HG02735.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.474-3419G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200566244 | ||||||
chr2:200566264
|
T | C | 1 | a0001c0003t0002g0127 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.474-3399T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200566264 | ||||||
chr2:200566331
|
G | A | 1 | a0019c0023t0002g0118 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.474-3332G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200566331 | ||||||
chr2:200566381
|
C | G | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.474-3282C>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200566381 | ||||||
chr2:200566419
|
C | T | 1 | a0018c0020t0001g0093 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.474-3244C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200566419 | ||||||
chr2:200566474
|
G | A | 41 | a0001c0004t0001g0004a0001c0004t0001g0013a0001c0004t0001g0014others(38): Show | 47 | HG00280.hp2 HG00408.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.474-3189G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200566474 | ||||||
chr2:200566481
|
A | G | 1 | a0018c0020t0001g0093 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.474-3182A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200566481 | ||||||
chr2:200566576
|
G | C | 6 | a0007c0010t0001g0320a0007c0010t0001g0321a0007c0010t0001g0322others(3): Show | 6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.474-3087G>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200566576 | ||||||
chr2:200566580
|
G | C | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.474-3083G>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200566580 | ||||||
chr2:200566717
|
C | T | 5 | a0003c0006t0001g0029a0003c0006t0001g0162a0003c0006t0001g0163others(2): Show | 6 | HG02647.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-2946C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200566717 | ||||||
chr2:200566779
|
G | A | 42 | a0001c0004t0001g0004a0001c0004t0001g0013a0001c0004t0001g0014others(39): Show | 48 | HG00280.hp2 HG00408.hp2 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.474-2884G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200566779 | ||||||
chr2:200566849
|
G | T | 70 | a0001c0003t0002g0005a0001c0003t0002g0006a0001c0003t0002g0021others(67): Show | 87 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.474-2814G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200566849 | ||||||
chr2:200566857
|
G | T | 1 | a0015c0018t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.474-2806G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200566857 | ||||||
chr2:200566877
|
G | A | 12 | a0004c0007t0001g0151a0004c0007t0001g0152a0004c0007t0001g0155others(9): Show | 12 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.474-2786G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200566877 | ||||||
chr2:200567028
|
G | A | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.474-2635G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200567028 | ||||||
chr2:200567046
|
A | G | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.474-2617A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200567046 | ||||||
chr2:200567147
|
G | A | 7 | a0007c0010t0001g0320a0007c0010t0001g0321a0007c0010t0001g0322others(4): Show | 7 | HG02145.hp2 HG02258.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.474-2516G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200567147 | ||||||
chr2:200567149
|
C | T | 86 | a0001c0003t0002g0005a0001c0003t0002g0006a0001c0003t0002g0021others(83): Show | 103 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.474-2514C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200567149 | ||||||
chr2:200567156
|
A | G | 72 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(69): Show | 90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.474-2507A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200567156 | ||||||
chr2:200567391
|
G | C | 2 | a0001c0001t0001g0245a0001c0001t0001g0250 | 2 | HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.474-2272G>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200567391 | ||||||
chr2:200567618
|
AC | A | 8 | a0007c0010t0001g0320a0007c0010t0001g0321a0007c0010t0001g0322others(5): Show | 8 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.474-2039delC | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200567618 | |||||
chr2:200567622
|
C | G | 3 | a0001c0004t0001g0075a0001c0004t0001g0076a0001c0004t0001g0079 | 3 | HG00280.hp2 HG01099.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.474-2041C>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200567622 | ||||||
chr2:200567623
|
C | G | 1 | a0001c0003t0002g0116 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.474-2040C>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200567623 | ||||||
chr2:200567824
|
G | A | 322 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(319): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.474-1839G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200567824 | ||||||
chr2:200568071
|
C | T | 1 | a0012c0024t0001g0259 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.474-1592C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200568071 | ||||||
chr2:200568072
|
G | T | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.474-1591G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200568072 | ||||||
chr2:200568122
|
T | C | 1 | a0001c0002t0001g0304 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.474-1541T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200568122 | ||||||
chr2:200568359
|
A | G | 1 | a0001c0003t0002g0144 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.474-1304A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200568359 | ||||||
chr2:200568382
|
A | C | 1 | a0016c0021t0001g0148 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.474-1281A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200568382 | ||||||
chr2:200568515
|
C | G | 8 | a0005c0008t0001g0017a0005c0008t0001g0082a0005c0008t0001g0083others(5): Show | 9 | HG01109.hp2 HG01243.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.474-1148C>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200568515 | ||||||
chr2:200568759
|
C | T | 9 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0244others(6): Show | 9 | HG01884.hp2 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.474-904C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200568759 | ||||||
chr2:200568817
|
A | T | 1 | a0004c0007t0001g0159 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.474-846A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200568817 | ||||||
chr2:200568909
|
TTATTTTT others(5): Show |
T | 72 | a0001c0003t0002g0005a0001c0003t0002g0006a0001c0003t0002g0021others(69): Show | 88 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.474-753_474-742del others(12): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200568909 | ||||||
chr2:200568913
|
T | A | 1 | a0002c0005t0003g0018 | 2 | NA19005.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.474-750T>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200568913 | ||||||
chr2:200568914
|
TTTGTTAA others(8): Show |
T | 1 | a0002c0005t0003g0018 | 2 | NA19005.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.474-748_474-734del others(15): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200568914 | ||||||
chr2:200568923
|
TTG | T | 72 | a0001c0003t0002g0005a0001c0003t0002g0006a0001c0003t0002g0021others(69): Show | 88 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.474-738_474-737del others(2): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200568923 | |||||
chr2:200568926
|
T | A | 72 | a0001c0003t0002g0005a0001c0003t0002g0006a0001c0003t0002g0021others(69): Show | 88 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.474-737T>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200568926 | ||||||
chr2:200568928
|
T | A | 72 | a0001c0003t0002g0005a0001c0003t0002g0006a0001c0003t0002g0021others(69): Show | 88 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.474-735T>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200568928 | ||||||
chr2:200569093
|
C | T | 41 | a0001c0004t0001g0004a0001c0004t0001g0013a0001c0004t0001g0014others(38): Show | 47 | HG00280.hp2 HG00408.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.474-570C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200569093 | ||||||
chr2:200569127
|
T | C | 1 | a0001c0001t0003g0223 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.474-536T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200569127 | ||||||
chr2:200570006
|
G | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0255a0001c0001t0001g0256 | 4 | NA18956.hp2 NA18974.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.703+114G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | chr2 | 200570006 | ||||||
chr2:200570153
|
A | G | 1 | a0001c0004t0001g0058 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.703+261A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | chr2 | 200570153 | ||||||
chr2:200570180
|
C | T | 41 | a0001c0004t0001g0004a0001c0004t0001g0013a0001c0004t0001g0014others(38): Show | 47 | HG00280.hp2 HG00408.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.703+288C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | chr2 | 200570180 | ||||||
chr2:200570186
|
A | G | 1 | a0015c0018t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.703+294A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | chr2 | 200570186 | ||||||
chr2:200570355
|
A | G | 16 | a0003c0006t0001g0029a0003c0006t0001g0030a0003c0006t0001g0162others(13): Show | 17 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.703+463A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | chr2 | 200570355 | ||||||
chr2:200570405
|
A | G | 2 | a0012c0024t0001g0259a0013c0025t0001g0260 | 2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.703+513A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | chr2 | 200570405 | ||||||
chr2:200570431
|
A | G | 1 | a0001c0004t0001g0071 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.703+539A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | chr2 | 200570431 | ||||||
chr2:200570478
|
A | ATG | 26 | a0001c0002t0001g0010a0001c0002t0001g0036a0001c0002t0001g0261others(23): Show | 32 | HG00099.hp1 HG00741.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.704-541_704-540dup others(2): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 200570478 | |||||
chr2:200570478
|
A | ATGTG | 63 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0187others(60): Show | 78 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.704-543_704-540dup others(4): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 200570478 | |||||
chr2:200570478
|
A | ATGTGTG | 52 | a0001c0001t0001g0183a0001c0001t0001g0192a0001c0001t0001g0193others(49): Show | 58 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.704-545_704-540dup others(6): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 200570478 | |||||
chr2:200570478
|
A | ATGTGTGT others(1): Show |
62 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(59): Show | 76 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.704-547_704-540dup others(8): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 200570478 | |||||
chr2:200570478
|
A | ATGTGTGT others(3): Show |
18 | a0001c0001t0001g0033a0001c0001t0001g0182a0001c0001t0001g0190others(15): Show | 19 | HG01255.hp1 HG03130.hp1 HG03492.hp2 others(16): Show |
intron_variant | MODIFIER | c.704-549_704-540dup others(10): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 200570478 | |||||
chr2:200570478
|
A | ATGTGTGT others(5): Show |
3 | a0001c0001t0001g0208a0001c0001t0001g0248a0001c0016t0001g0246 | 3 | HG00642.hp1 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.704-551_704-540dup others(12): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 200570478 | |||||
chr2:200570478
|
A | ATGTGTGT others(7): Show |
2 | a0001c0001t0001g0245a0001c0001t0001g0250 | 2 | HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.704-553_704-540dup others(14): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 200570478 | |||||
chr2:200570478
|
ATG | A | 11 | a0001c0003t0002g0023a0002c0005t0003g0098a0004c0007t0001g0152others(8): Show | 12 | HG01515.hp1 HG01517.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.704-541_704-540del others(2): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 200570478 | |||||
chr2:200570478
|
ATGTG | A | 5 | a0001c0003t0002g0108a0001c0003t0002g0109a0001c0003t0002g0143others(2): Show | 5 | HG01243.hp2 HG03209.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.704-543_704-540del others(4): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 200570478 | |||||
chr2:200570494
|
G | GTGTGTGT others(3): Show |
1 | a0001c0001t0001g0244 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.704-547_704-546ins others(10): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 200570494 | |||||
chr2:200570510
|
G | GTGTGTGT others(4): Show |
1 | a0001c0001t0001g0225 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.704-540_704-539ins others(11): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | chr2 | 200570510 | ||||||
chr2:200570552
|
TAC | T | 72 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(69): Show | 90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.704-492_704-491del others(2): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 200570552 | |||||
chr2:200570631
|
CAT | C | 65 | a0001c0004t0001g0004a0001c0004t0001g0013a0001c0004t0001g0014others(62): Show | 73 | HG00280.hp2 HG00408.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.704-414_704-413del others(2): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 200570631 | |||||
chr2:200570698
|
A | G | 6 | a0007c0010t0001g0320a0007c0010t0001g0321a0007c0010t0001g0322others(3): Show | 6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-352A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | chr2 | 200570698 | ||||||
chr2:200570732
|
A | C | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.704-318A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | chr2 | 200570732 | ||||||
chr2:200570778
|
C | A | 1 | a0001c0002t0001g0273 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.704-272C>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | chr2 | 200570778 | ||||||
chr2:200570872
|
T | C | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.704-178T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | chr2 | 200570872 | ||||||
chr2:200570886
|
C | T | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.704-164C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | chr2 | 200570886 | ||||||
chr2:200574058
|
G | A | 1 | a0015c0018t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3631+81G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/8 | chr2 | 200574058 | ||||||
chr2:200574279
|
A | G | 1 | a0015c0018t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3631+302A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/8 | chr2 | 200574279 | ||||||
chr2:200574501
|
C | T | 1 | a0004c0007t0001g0158 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3631+524C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/8 | chr2 | 200574501 | ||||||
chr2:200574536
|
T | A | 1 | a0003c0006t0001g0170 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3631+559T>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/8 | chr2 | 200574536 | ||||||
chr2:200574557
|
A | G | 65 | a0001c0004t0001g0004a0001c0004t0001g0013a0001c0004t0001g0014others(62): Show | 73 | HG00280.hp2 HG00408.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.3631+580A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/8 | chr2 | 200574557 | ||||||
chr2:200574570
|
A | G | 12 | a0004c0007t0001g0151a0004c0007t0001g0152a0004c0007t0001g0155others(9): Show | 12 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.3631+593A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/8 | chr2 | 200574570 | ||||||
chr2:200574890
|
C | T | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3632-421C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/8 | chr2 | 200574890 | ||||||
chr2:200574911
|
G | A | 73 | a0001c0001t0001g0225a0001c0002t0001g0001a0001c0002t0001g0010others(70): Show | 91 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.3632-400G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/8 | chr2 | 200574911 | ||||||
chr2:200574923
|
T | TA | 2 | a0001c0001t0001g0012a0001c0001t0001g0208 | 3 | HG00642.hp1 HG00733.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.3632-384dupA | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 200574923 | |||||
chr2:200575081
|
C | G | 1 | a0016c0021t0001g0148 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3632-230C>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/8 | chr2 | 200575081 | ||||||
chr2:200575099
|
T | C | 1 | a0001c0004t0001g0072 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3632-212T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/8 | chr2 | 200575099 | ||||||
chr2:200575145
|
A | G | 325 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(322): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.3632-166A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/8 | chr2 | 200575145 | ||||||
chr2:200575287
|
G | C | 2 | a0001c0002t0001g0039a0001c0002t0001g0303 | 3 | HG00673.hp2 NA18944.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.3632-24G>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/8 | chr2 | 200575287 | ||||||
chr2:200575576
|
A | G | 72 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(69): Show | 90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.3782+115A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200575576 | ||||||
chr2:200575581
|
A | G | 8 | a0005c0008t0001g0017a0005c0008t0001g0082a0005c0008t0001g0083others(5): Show | 9 | HG01109.hp2 HG01243.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.3782+120A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200575581 | ||||||
chr2:200575643
|
G | A | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3782+182G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200575643 | ||||||
chr2:200575698
|
T | TCTA | 65 | a0001c0004t0001g0004a0001c0004t0001g0013a0001c0004t0001g0014others(62): Show | 73 | HG00280.hp2 HG00408.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.3782+243_3782+245d others(5): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 200575698 | |||||
chr2:200575857
|
C | T | 1 | a0001c0011t0001g0228 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.3782+396C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200575857 | ||||||
chr2:200575913
|
G | A | 4 | a0001c0001t0001g0032a0001c0001t0001g0201a0001c0001t0001g0207others(1): Show | 5 | HG00423.hp1 HG01070.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.3782+452G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200575913 | ||||||
chr2:200575934
|
T | C | 1 | a0001c0004t0001g0060 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.3782+473T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200575934 | ||||||
chr2:200576145
|
A | C | 1 | a0001c0003t0002g0132 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3782+684A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200576145 | ||||||
chr2:200576216
|
CT | C | 92 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(89): Show | 107 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.3782+765delT | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 200576216 | |||||
chr2:200576223
|
TTTTC | T | 8 | a0005c0008t0001g0017a0005c0008t0001g0082a0005c0008t0001g0083others(5): Show | 9 | HG01109.hp2 HG01243.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.3782+766_3782+769d others(6): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 200576223 | |||||
chr2:200576225
|
TTC | T | 55 | a0001c0004t0001g0004a0001c0004t0001g0013a0001c0004t0001g0014others(52): Show | 62 | HG00280.hp2 HG00408.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.3782+766_3782+767d others(4): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 200576225 | |||||
chr2:200576237
|
T | C | 1 | a0003c0006t0001g0168 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3782+776T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200576237 | ||||||
chr2:200576240
|
T | C | 6 | a0007c0010t0001g0320a0007c0010t0001g0321a0007c0010t0001g0322others(3): Show | 6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.3782+779T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200576240 | ||||||
chr2:200576310
|
T | A | 1 | a0018c0020t0001g0093 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3782+849T>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200576310 | ||||||
chr2:200576410
|
T | C | 17 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0182others(14): Show | 20 | HG00140.hp2 HG00280.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.3782+949T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200576410 | ||||||
chr2:200576449
|
G | A | 92 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(89): Show | 107 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.3782+988G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200576449 | ||||||
chr2:200576499
|
T | C | 252 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(249): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.3782+1038T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200576499 | ||||||
chr2:200576530
|
T | C | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3782+1069T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200576530 | ||||||
chr2:200576560
|
C | A | 252 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(249): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.3782+1099C>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200576560 | ||||||
chr2:200576586
|
A | T | 2 | a0012c0024t0001g0259a0013c0025t0001g0260 | 2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3782+1125A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200576586 | ||||||
chr2:200576706
|
C | T | 65 | a0001c0004t0001g0004a0001c0004t0001g0013a0001c0004t0001g0014others(62): Show | 73 | HG00280.hp2 HG00408.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.3782+1245C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200576706 | ||||||
chr2:200576717
|
A | G | 1 | a0016c0021t0001g0148 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3782+1256A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200576717 | ||||||
chr2:200576833
|
T | C | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3782+1372T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200576833 | ||||||
chr2:200576856
|
A | G | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3782+1395A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200576856 | ||||||
chr2:200576902
|
T | A | 5 | a0003c0006t0001g0029a0003c0006t0001g0162a0003c0006t0001g0163others(2): Show | 6 | HG02647.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3782+1441T>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200576902 | ||||||
chr2:200576903
|
C | A | 5 | a0003c0006t0001g0029a0003c0006t0001g0162a0003c0006t0001g0163others(2): Show | 6 | HG02647.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3782+1442C>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200576903 | ||||||
chr2:200576910
|
G | A | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3782+1449G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200576910 | ||||||
chr2:200576966
|
T | C | 1 | a0008c0014t0001g0154 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3782+1505T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200576966 | ||||||
chr2:200576971
|
C | T | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3782+1510C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200576971 | ||||||
chr2:200577038
|
T | G | 1 | a0001c0004t0001g0060 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.3782+1577T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200577038 | ||||||
chr2:200577061
|
C | T | 1 | a0001c0001t0001g0240 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3782+1600C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200577061 | ||||||
chr2:200577080
|
A | C | 24 | a0003c0006t0001g0029a0003c0006t0001g0030a0003c0006t0001g0162others(21): Show | 26 | HG00639.hp2 HG01109.hp2 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.3782+1619A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200577080 | ||||||
chr2:200577151
|
C | A | 2 | a0012c0024t0001g0259a0013c0025t0001g0260 | 2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3782+1690C>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200577151 | ||||||
chr2:200577186
|
C | T | 1 | a0001c0001t0001g0213 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3782+1725C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200577186 | ||||||
chr2:200577212
|
T | C | 41 | a0001c0004t0001g0004a0001c0004t0001g0013a0001c0004t0001g0014others(38): Show | 47 | HG00280.hp2 HG00408.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.3782+1751T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200577212 | ||||||
chr2:200577252
|
GT | G | 72 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(69): Show | 90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.3782+1795delT | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 200577252 | |||||
chr2:200577300
|
A | G | 1 | a0001c0002t0001g0044 | 2 | HG01891.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3782+1839A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200577300 | ||||||
chr2:200577321
|
G | A | 92 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(89): Show | 107 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.3782+1860G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200577321 | ||||||
chr2:200577466
|
C | A | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3782+2005C>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200577466 | ||||||
chr2:200577538
|
A | G | 1 | a0013c0025t0001g0260 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3782+2077A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200577538 | ||||||
chr2:200577678
|
CT | C | 7 | a0003c0006t0001g0169a0007c0010t0001g0320a0007c0010t0001g0321others(4): Show | 7 | HG01167.hp2 HG02145.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.3782+2231delT | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 200577678 | |||||
chr2:200577699
|
T | G | 1 | a0001c0001t0001g0251 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3782+2238T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200577699 | ||||||
chr2:200577748
|
A | G | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3782+2287A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200577748 | ||||||
chr2:200577787
|
G | T | 1 | a0015c0018t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3782+2326G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200577787 | ||||||
chr2:200577861
|
G | A | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3782+2400G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200577861 | ||||||
chr2:200577863
|
G | A | 6 | a0007c0010t0001g0320a0007c0010t0001g0321a0007c0010t0001g0322others(3): Show | 6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.3782+2402G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200577863 | ||||||
chr2:200577941
|
A | C | 1 | a0001c0003t0002g0109 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3782+2480A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200577941 | ||||||
chr2:200577979
|
T | C | 1 | a0016c0021t0001g0148 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3782+2518T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200577979 | ||||||
chr2:200578150
|
C | CTATAGA | 19 | a0001c0002t0001g0286a0001c0003t0002g0025a0001c0003t0002g0131others(16): Show | 24 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.3782+2718_3782+272 others(10): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 200578150 | |||||
chr2:200578150
|
C | CTATAGAT others(5): Show |
20 | a0001c0001t0001g0243a0002c0005t0003g0120a0002c0005t0003g0123others(17): Show | 21 | HG01243.hp2 HG01257.hp1 HG02615.hp2 others(18): Show |
intron_variant | MODIFIER | c.3782+2712_3782+272 others(16): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 200578150 | |||||
chr2:200578150
|
C | CTATAGAT others(11): Show |
35 | a0001c0001t0001g0012a0001c0001t0001g0211a0001c0001t0001g0212others(32): Show | 41 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.3782+2706_3782+272 others(22): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 200578150 | |||||
chr2:200578150
|
C | CTATAGAT others(17): Show |
63 | a0001c0001t0001g0003a0001c0001t0001g0031a0001c0001t0001g0032others(60): Show | 72 | HG00423.hp1 HG00609.hp2 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.3782+2700_3782+272 others(28): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 200578150 | |||||
chr2:200578150
|
C | CTATAGAT others(23): Show |
73 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(70): Show | 93 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.3782+2694_3782+272 others(34): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 200578150 | |||||
chr2:200578150
|
C | CTATAGAT others(29): Show |
41 | a0001c0001t0001g0049a0001c0001t0001g0176a0001c0001t0001g0180others(38): Show | 44 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.3782+2723_3782+272 others(40): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 200578150 | |||||
chr2:200578150
|
C | CTATAGAT others(35): Show |
6 | a0001c0001t0001g0242a0001c0001t0001g0251a0001c0002t0001g0276others(3): Show | 6 | HG00423.hp2 NA18747.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.3782+2723_3782+272 others(46): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 200578150 | |||||
chr2:200578150
|
C | CTATAGAT others(41): Show |
5 | a0001c0002t0001g0040a0001c0002t0001g0267a0001c0002t0001g0275others(2): Show | 6 | HG01934.hp1 HG03704.hp2 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.3782+2723_3782+272 others(52): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 200578150 | |||||
chr2:200578163
|
T | TATAGATA others(16): Show |
1 | a0001c0001t0001g0209 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.3782+2723_3782+272 others(27): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 200578163 | |||||
chr2:200578177
|
T | TAGATATA others(11): Show |
1 | a0001c0004t0001g0056 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.3782+2723_3782+272 others(22): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 200578177 | |||||
chr2:200578177
|
T | TAGATATA others(17): Show |
3 | a0001c0004t0001g0014a0001c0004t0001g0053a0001c0004t0001g0057 | 4 | HG01952.hp2 NA19056.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.3782+2723_3782+272 others(28): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 200578177 | |||||
chr2:200578177
|
T | TAGATATA others(23): Show |
3 | a0001c0004t0001g0054a0001c0004t0001g0061a0001c0004t0001g0077 | 3 | HG00408.hp2 NA18979.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.3782+2723_3782+272 others(34): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 200578177 | |||||
chr2:200578330
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3782+2869A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200578330 | ||||||
chr2:200578416
|
G | T | 8 | a0005c0008t0001g0017a0005c0008t0001g0082a0005c0008t0001g0083others(5): Show | 9 | HG01109.hp2 HG01243.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.3782+2955G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200578416 | ||||||
chr2:200578450
|
G | C | 5 | a0003c0006t0001g0029a0003c0006t0001g0162a0003c0006t0001g0163others(2): Show | 6 | HG02647.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3782+2989G>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200578450 | ||||||
chr2:200578620
|
G | A | 2 | a0001c0002t0001g0039a0001c0002t0001g0303 | 3 | HG00673.hp2 NA18944.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.3782+3159G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200578620 | ||||||
chr2:200578675
|
A | C | 6 | a0007c0010t0001g0320a0007c0010t0001g0321a0007c0010t0001g0322others(3): Show | 6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.3782+3214A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200578675 | ||||||
chr2:200578708
|
A | G | 92 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(89): Show | 107 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.3782+3247A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200578708 | ||||||
chr2:200578761
|
T | C | 63 | a0001c0002t0001g0001a0001c0002t0001g0011a0001c0002t0001g0038others(60): Show | 77 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.3782+3300T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200578761 | ||||||
chr2:200578772
|
A | G | 1 | a0004c0007t0001g0161 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3782+3311A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200578772 | ||||||
chr2:200578775
|
G | A | 2 | a0012c0024t0001g0259a0013c0025t0001g0260 | 2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3782+3314G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200578775 | ||||||
chr2:200578909
|
G | A | 11 | a0003c0006t0001g0030a0003c0006t0001g0165a0003c0006t0001g0166others(8): Show | 11 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.3782+3448G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200578909 | ||||||
chr2:200579065
|
A | G | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.3782+3604A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200579065 | ||||||
chr2:200579141
|
T | C | 3 | a0001c0003t0002g0006a0001c0003t0002g0051a0001c0003t0002g0139 | 5 | HG02559.hp1 HG02622.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.3782+3680T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200579141 | ||||||
chr2:200579179
|
A | G | 2 | a0001c0001t0001g0227a0004c0007t0001g0159 | 2 | HG02723.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.3782+3718A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200579179 | ||||||
chr2:200579322
|
T | C | 1 | a0001c0002t0001g0293 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3782+3861T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200579322 | ||||||
chr2:200579575
|
G | T | 9 | a0004c0007t0001g0151a0004c0007t0001g0152a0004c0007t0001g0155others(6): Show | 9 | HG02055.hp2 HG02109.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.3783-3874G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200579575 | ||||||
chr2:200579718
|
C | T | 252 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(249): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.3783-3731C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200579718 | ||||||
chr2:200580082
|
G | T | 8 | a0005c0008t0001g0017a0005c0008t0001g0082a0005c0008t0001g0083others(5): Show | 9 | HG01109.hp2 HG01243.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.3783-3367G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200580082 | ||||||
chr2:200580096
|
G | C | 5 | a0003c0006t0001g0029a0003c0006t0001g0162a0003c0006t0001g0163others(2): Show | 6 | HG02647.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3783-3353G>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200580096 | ||||||
chr2:200580263
|
C | A | 1 | a0001c0001t0001g0190 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3783-3186C>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200580263 | ||||||
chr2:200580429
|
C | T | 167 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(164): Show | 190 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.3783-3020C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200580429 | ||||||
chr2:200580478
|
T | A | 9 | a0007c0010t0001g0320a0007c0010t0001g0321a0007c0010t0001g0322others(6): Show | 9 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.3783-2971T>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200580478 | ||||||
chr2:200580545
|
T | C | 1 | a0015c0018t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3783-2904T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200580545 | ||||||
chr2:200580591
|
G | A | 23 | a0002c0005t0003g0002a0002c0005t0003g0018a0002c0005t0003g0019others(20): Show | 29 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.3783-2858G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200580591 | ||||||
chr2:200580860
|
A | C | 2 | a0001c0001t0001g0255a0015c0018t0005g0048 | 2 | HG03471.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.3783-2589A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200580860 | ||||||
chr2:200580865
|
AT | A | 7 | a0007c0010t0001g0320a0007c0010t0001g0321a0007c0010t0001g0322others(4): Show | 7 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.3783-2575delT | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 200580865 | |||||
chr2:200580866
|
T | A | 76 | a0001c0001t0001g0196a0001c0002t0001g0001a0001c0002t0001g0010others(73): Show | 94 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.3783-2583T>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200580866 | ||||||
chr2:200580894
|
A | G | 1 | a0001c0002t0001g0285 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3783-2555A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200580894 | ||||||
chr2:200581038
|
T | C | 6 | a0004c0007t0001g0151a0004c0007t0001g0155a0004c0007t0001g0156others(3): Show | 6 | HG02723.hp1 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.3783-2411T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200581038 | ||||||
chr2:200581175
|
T | C | 1 | a0001c0002t0001g0283 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3783-2274T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200581175 | ||||||
chr2:200581379
|
G | T | 1 | a0001c0001t0001g0209 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.3783-2070G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200581379 | ||||||
chr2:200581575
|
A | G | 1 | a0007c0010t0001g0321 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3783-1874A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200581575 | ||||||
chr2:200581660
|
A | G | 1 | a0001c0001t0001g0191 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.3783-1789A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200581660 | ||||||
chr2:200582053
|
TA | T | 3 | a0001c0004t0001g0072a0001c0004t0001g0073a0001c0004t0001g0074 | 3 | HG02809.hp1 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.3783-1392delA | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 200582053 | |||||
chr2:200582065
|
A | G | 1 | a0003c0006t0001g0166 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3783-1384A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200582065 | ||||||
chr2:200582075
|
A | T | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3783-1374A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200582075 | ||||||
chr2:200582165
|
T | C | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3783-1284T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200582165 | ||||||
chr2:200582362
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3783-1087G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200582362 | ||||||
chr2:200582568
|
C | T | 1 | a0001c0002t0001g0308 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.3783-881C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200582568 | ||||||
chr2:200582637
|
C | T | 2 | a0001c0002t0001g0011a0001c0002t0001g0300 | 4 | NA18942.hp1 NA18943.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.3783-812C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200582637 | ||||||
chr2:200582821
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3783-628G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200582821 | ||||||
chr2:200583041
|
A | G | 12 | a0004c0007t0001g0151a0004c0007t0001g0152a0004c0007t0001g0155others(9): Show | 12 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.3783-408A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200583041 | ||||||
chr2:200583047
|
T | A | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3783-402T>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200583047 | ||||||
chr2:200583063
|
G | A | 1 | a0018c0020t0001g0093 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3783-386G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200583063 | ||||||
chr2:200583180
|
C | T | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3783-269C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200583180 | ||||||
chr2:200583212
|
A | G | 1 | a0010c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3783-237A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200583212 | ||||||
chr2:200583212
|
A | T | 1 | a0001c0001t0001g0202 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.3783-237A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200583212 | ||||||
chr2:200583393
|
C | G | 1 | a0002c0005t0003g0099 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3783-56C>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200583393 |