geneid | 112869 |
---|---|
ensemblid | ENSG00000176476.9 |
hgncid | 25156 |
symbol | SGF29 |
name | SAGA complex associated factor 29 |
refseq_nuc | NM_138414.3 |
refseq_prot | NP_612423.1 |
ensembl_nuc | ENST00000317058.8 |
ensembl_prot | ENSP00000316114.3 |
mane_status | MANE Select |
chr | chr16 |
start | 28553920 |
end | 28591790 |
strand | + |
ver | v1.2 |
region | chr16:28553920-28591790 |
region5000 | chr16:28548920-28596790 |
regionname0 | SGF29_chr16_28553920_28591790 |
regionname5000 | SGF29_chr16_28548920_28596790 |
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 | 1/1 | 293 | 345 | 90 | 64 | 139 | 10 | 40 | 102 | SGF29_chr16_28548920_28596790 | SGF29 | copy fasta | chr16 | 28548920 | 28596790 |
a0002 | 0/0 | 293 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | copy fasta | chr16 | 28548920 | 28596790 |
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 | 1/1 | 882 | 275 | 75 | 49 | 112 | 6 | 31 | SGF29_chr16_28548920_28596790 | SGF29 | copy fasta | chr16 | 28548920 | 28596790 |
c0002 | 0/0 | 882 | 51 | 10 | 10 | 26 | 1 | 4 | SGF29_chr16_28548920_28596790 | SGF29 | copy fasta | chr16 | 28548920 | 28596790 |
c0003 | 0/0 | 882 | 17 | 3 | 5 | 1 | 3 | 5 | SGF29_chr16_28548920_28596790 | SGF29 | copy fasta | chr16 | 28548920 | 28596790 |
c0004 | 0/0 | 882 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | copy fasta | chr16 | 28548920 | 28596790 |
c0005 | 0/0 | 882 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | copy fasta | chr16 | 28548920 | 28596790 |
c0006 | 0/0 | 882 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | copy fasta | chr16 | 28548920 | 28596790 |
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 | 278 | 186 | 45 | 23 | 86 | 3 | 28 | SGF29_chr16_28548920_28596790 | SGF29 | copy fasta | chr16 | 28548920 | 28596790 |
t0002 | 0/1 | 277 | 136 | 39 | 33 | 44 | 7 | 12 | SGF29_chr16_28548920_28596790 | SGF29 | copy fasta | chr16 | 28548920 | 28596790 |
t0003 | 0/0 | 277 | 15 | 0 | 8 | 7 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | copy fasta | chr16 | 28548920 | 28596790 |
t0004 | 0/0 | 277 | 3 | 3 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | copy fasta | chr16 | 28548920 | 28596790 |
t0005 | 0/0 | 277 | 2 | 2 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | copy fasta | chr16 | 28548920 | 28596790 |
t0006 | 0/0 | 278 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | copy fasta | chr16 | 28548920 | 28596790 |
t0007 | 0/0 | 278 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | copy fasta | chr16 | 28548920 | 28596790 |
t0008 | 0/0 | 278 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | copy fasta | chr16 | 28548920 | 28596790 |
t0009 | 0/0 | 277 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | copy fasta | chr16 | 28548920 | 28596790 |
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 | 6 | 0 | 0 | 6 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0002 | 0/0 | 6 | 0 | 0 | 3 | 1 | 2 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0003 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0005 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0022 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0025 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0095 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0270 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
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 | 1/1 | 882 | 275 | 75 | 49 | 112 | 6 | 31 | SGF29_chr16_28548920_28596790 | SGF29 | copy fasta | chr16 | 28548920 | 28596790 |
a0001c0002 | 0/0 | 882 | 51 | 10 | 10 | 26 | 1 | 4 | SGF29_chr16_28548920_28596790 | SGF29 | copy fasta | chr16 | 28548920 | 28596790 |
a0001c0003 | 0/0 | 882 | 17 | 3 | 5 | 1 | 3 | 5 | SGF29_chr16_28548920_28596790 | SGF29 | copy fasta | chr16 | 28548920 | 28596790 |
a0001c0005 | 0/0 | 882 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | copy fasta | chr16 | 28548920 | 28596790 |
a0001c0006 | 0/0 | 882 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | copy fasta | chr16 | 28548920 | 28596790 |
a0002c0004 | 0/0 | 882 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | copy fasta | chr16 | 28548920 | 28596790 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 1159 | 184 | 45 | 22 | 85 | 3 | 28 | SGF29_chr16_28548920_28596790 | SGF29 | copy fasta | chr16 | 28548920 | 28596790 |
a0001c0001t0002 | 0/1 | 1158 | 81 | 24 | 25 | 25 | 3 | 3 | SGF29_chr16_28548920_28596790 | SGF29 | copy fasta | chr16 | 28548920 | 28596790 |
a0001c0001t0003 | 0/0 | 1158 | 2 | 0 | 2 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | copy fasta | chr16 | 28548920 | 28596790 |
a0001c0001t0004 | 0/0 | 1158 | 3 | 3 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | copy fasta | chr16 | 28548920 | 28596790 |
a0001c0001t0005 | 0/0 | 1158 | 2 | 2 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | copy fasta | chr16 | 28548920 | 28596790 |
a0001c0001t0006 | 0/0 | 1159 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | copy fasta | chr16 | 28548920 | 28596790 |
a0001c0001t0007 | 0/0 | 1159 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | copy fasta | chr16 | 28548920 | 28596790 |
a0001c0001t0008 | 0/0 | 1159 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | copy fasta | chr16 | 28548920 | 28596790 |
a0001c0002t0002 | 0/0 | 1158 | 37 | 10 | 4 | 18 | 1 | 4 | SGF29_chr16_28548920_28596790 | SGF29 | copy fasta | chr16 | 28548920 | 28596790 |
a0001c0002t0003 | 0/0 | 1158 | 13 | 0 | 6 | 7 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | copy fasta | chr16 | 28548920 | 28596790 |
a0001c0002t0009 | 0/0 | 1158 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | copy fasta | chr16 | 28548920 | 28596790 |
a0001c0003t0001 | 0/0 | 1159 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | copy fasta | chr16 | 28548920 | 28596790 |
a0001c0003t0002 | 0/0 | 1158 | 16 | 3 | 4 | 1 | 3 | 5 | SGF29_chr16_28548920_28596790 | SGF29 | copy fasta | chr16 | 28548920 | 28596790 |
a0001c0005t0002 | 0/0 | 1158 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | copy fasta | chr16 | 28548920 | 28596790 |
a0001c0006t0002 | 0/0 | 1158 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | copy fasta | chr16 | 28548920 | 28596790 |
a0002c0004t0001 | 0/0 | 1159 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | copy fasta | chr16 | 28548920 | 28596790 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0002 | 0/0 | 6 | 0 | 0 | 3 | 1 | 2 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0270 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0003 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0095 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0004g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0005g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0005g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0006g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0007g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0001t0008g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0002t0002g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0002t0002g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0002t0002g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0002t0002g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0002t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0002t0002g0025 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0002t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0002t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0002t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0002t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0002t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0002t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0002t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0002t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0002t0003g0005 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0002t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0002t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0002t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0002t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0002t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0002t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0002t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0002t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0002t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0002t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0002t0009g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0003t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0003t0002g0022 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0003t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0003t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0003t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0003t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0003t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0003t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0003t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0003t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0003t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0003t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0003t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0003t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0003t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0003t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0005t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0001c0006t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
a0002c0004t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0002 | g0025 | EUR | GBR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0242 | EUR | FIN | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0098 | EUR | FIN | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG00609 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | CHS | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG00642 | hp1 | a0001 | c0003 | t0002 | g0219 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG00735 | hp1 | a0001 | c0002 | t0002 | g0009 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG00738 | hp2 | a0001 | c0003 | t0002 | g0224 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0056 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01074 | hp1 | a0001 | c0002 | t0002 | g0052 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0097 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0289 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01106 | hp2 | a0001 | c0003 | t0002 | g0227 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01109 | hp1 | a0001 | c0002 | t0002 | g0278 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0079 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01175 | hp1 | a0001 | c0003 | t0001 | g0171 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01192 | hp1 | a0001 | c0002 | t0003 | g0030 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | CLM | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | CLM | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0036 | AMR | CLM | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01261 | hp1 | a0001 | c0002 | t0003 | g0005 | AMR | CLM | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01261 | hp2 | a0001 | c0003 | t0002 | g0225 | AMR | CLM | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | CLM | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01346 | hp2 | a0001 | c0002 | t0003 | g0005 | AMR | CLM | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | CLM | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | CLM | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0044 | AMR | CLM | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01433 | hp2 | a0001 | c0002 | t0002 | g0008 | AMR | CLM | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0066 | EUR | IBS | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0261 | EUR | IBS | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01884 | hp1 | a0001 | c0001 | t0004 | g0296 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01884 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0283 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0074 | AMR | PEL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0082 | AMR | PEL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG01978 | hp2 | a0001 | c0002 | t0003 | g0038 | AMR | PEL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02004 | hp2 | a0001 | c0002 | t0003 | g0032 | AMR | PEL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0295 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02056 | hp2 | a0001 | c0003 | t0002 | g0226 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02071 | hp1 | a0002 | c0004 | t0001 | g0132 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02071 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02080 | hp2 | a0001 | c0002 | t0003 | g0033 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02083 | hp2 | a0001 | c0002 | t0003 | g0029 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02132 | hp1 | a0001 | c0002 | t0002 | g0035 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02135 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0090 | AMR | PEL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02148 | hp2 | a0001 | c0002 | t0003 | g0028 | AMR | PEL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CDX | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02155 | hp2 | a0001 | c0002 | t0002 | g0305 | EAS | CDX | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CDX | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02165 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | CDX | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0291 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0306 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0301 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0290 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0083 | AMR | PEL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0300 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02572 | hp2 | a0001 | c0002 | t0002 | g0280 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02602 | hp2 | a0001 | c0003 | t0002 | g0223 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02698 | hp2 | a0001 | c0002 | t0002 | g0091 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02735 | hp2 | a0001 | c0003 | t0002 | g0265 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02809 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02895 | hp1 | a0001 | c0002 | t0002 | g0281 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02896 | hp2 | a0001 | c0001 | t0005 | g0108 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02897 | hp1 | a0001 | c0001 | t0005 | g0107 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02897 | hp2 | a0001 | c0002 | t0002 | g0276 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | ESN | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0302 | AFR | ESN | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0279 | AFR | MSL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | MSL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ESN | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03130 | hp2 | a0001 | c0002 | t0002 | g0277 | AFR | ESN | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0285 | AFR | ESN | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0294 | AFR | ESN | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03209 | hp1 | a0001 | c0002 | t0002 | g0004 | AFR | MSL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0292 | AFR | MSL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0287 | AFR | MSL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0299 | AFR | MSL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0297 | AFR | MSL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03491 | hp1 | a0001 | c0002 | t0002 | g0027 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03492 | hp2 | a0001 | c0002 | t0002 | g0026 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ESN | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03540 | hp2 | a0001 | c0005 | t0002 | g0286 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0073 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03669 | hp1 | a0001 | c0003 | t0002 | g0228 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | STU | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03704 | hp2 | a0001 | c0003 | t0002 | g0222 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | BEB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | BEB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03927 | hp1 | a0001 | c0002 | t0002 | g0304 | SAS | BEB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | BEB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | BEB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG04184 | hp1 | a0001 | c0003 | t0002 | g0220 | SAS | BEB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | BEB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | STU | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0011 | SAS | STU | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | STU | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0282 | AFR | YRI | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18522 | hp2 | a0001 | c0003 | t0002 | g0218 | AFR | YRI | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18906 | hp1 | a0001 | c0006 | t0002 | g0106 | AFR | YRI | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | YRI | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18943 | hp1 | a0001 | c0001 | t0006 | g0250 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18944 | hp1 | a0001 | c0002 | t0002 | g0050 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18947 | hp1 | a0001 | c0001 | t0008 | g0111 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18952 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18953 | hp1 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18960 | hp1 | a0001 | c0002 | t0003 | g0031 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18961 | hp1 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18962 | hp2 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18971 | hp1 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18975 | hp1 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18977 | hp1 | a0001 | c0002 | t0002 | g0048 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18980 | hp2 | a0001 | c0002 | t0003 | g0037 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18983 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18991 | hp2 | a0001 | c0002 | t0003 | g0046 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18994 | hp1 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19005 | hp1 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | LWK | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19030 | hp2 | a0001 | c0001 | t0007 | g0208 | AFR | LWK | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | LWK | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19077 | hp2 | a0001 | c0002 | t0002 | g0051 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19080 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19087 | hp1 | a0001 | c0002 | t0003 | g0034 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19091 | hp2 | a0001 | c0002 | t0009 | g0042 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | YRI | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | YRI | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0076 | AFR | ASW | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA20129 | hp2 | a0001 | c0002 | t0002 | g0275 | AFR | ASW | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA20752 | hp1 | a0001 | c0003 | t0002 | g0221 | EUR | TSI | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA20752 | hp2 | a0001 | c0003 | t0002 | g0022 | EUR | TSI | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA20805 | hp1 | a0001 | c0003 | t0002 | g0022 | EUR | TSI | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0077 | EUR | TSI | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | GIH | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | GIH | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02109 | hp1 | a0001 | c0003 | t0002 | g0216 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0303 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0288 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0284 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG03471 | hp2 | a0001 | c0003 | t0002 | g0217 | AFR | MSL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG06807 | hp1 | a0001 | c0002 | t0002 | g0025 | AFR | USA | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | USA | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA20300 | hp1 | a0001 | c0001 | t0004 | g0298 | AFR | USA | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0293 | AFR | USA | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | LWK | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
NA21309 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | LWK | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0095 | REF | REF | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0270 | REF | REF | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:28585692
|
G | A | 1 | a0002 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.196G>A | p.Ala66Thr | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/10 | 389/1159 | 196/882 | 66/293 | chr16 | 28585692 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:28591646
|
C | G | 1 | a0001c0006 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.822C>G | p.Ser274Ser | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 10/10 | 1015/1159 | 822/882 | 274/293 | chr16 | 28591646 | ||
chr16:28591670
|
A | G | 3 | a0001c0002a0001c0003a0001c0006 | 69 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(66): Show |
synonymous_variant | LOW | c.846A>G | p.Arg282Arg | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 10/10 | 1039/1159 | 846/882 | 282/293 | chr16 | 28591670 | ||
chr16:28591673
|
C | T | 1 | a0001c0005 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.849C>T | p.Tyr283Tyr | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 10/10 | 1042/1159 | 849/882 | 283/293 | chr16 | 28591673 | ||
chr16:28591691
|
A | G | 2 | a0001c0003a0001c0006 | 18 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(15): Show |
synonymous_variant | LOW | c.867A>G | p.Glu289Glu | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 10/10 | 1060/1159 | 867/882 | 289/293 | chr16 | 28591691 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:28553947
|
G | C | 1 | a0001c0001t0006 | 1 | NA18943.hp1 | 5_prime_UTR_variant | MODIFIER | c.-166G>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/10 | 27123 | chr16 | 28553947 | |||||
chr16:28553948
|
GA | G | 10 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(7): Show | 157 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(154): Show |
5_prime_UTR_variant | MODIFIER | c.-157delA | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/10 | 27114 | INFO_REALIGN_3_PRIME | chr16 | 28553948 | ||||
chr16:28554004
|
G | C | 1 | a0001c0001t0004 | 3 | HG01884.hp1 HG03486.hp2 NA20300.hp1 |
5_prime_UTR_variant | MODIFIER | c.-109G>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/10 | 27066 | chr16 | 28554004 | |||||
chr16:28554006
|
T | G | 2 | a0001c0001t0003a0001c0002t0003 | 15 | HG01192.hp1 HG01258.hp2 HG01261.hp1 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-107T>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/10 | 27064 | chr16 | 28554006 | |||||
chr16:28591710
|
C | T | 1 | a0001c0002t0009 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 10/10 | 4 | chr16 | 28591710 | |||||
chr16:28591736
|
C | T | 1 | a0001c0001t0008 | 1 | NA18947.hp1 | 3_prime_UTR_variant | MODIFIER | c.*30C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 10/10 | 30 | chr16 | 28591736 | |||||
chr16:28591761
|
C | T | 1 | a0001c0001t0007 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*55C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 10/10 | 55 | chr16 | 28591761 | |||||
chr16:28591762
|
G | A | 1 | a0001c0001t0005 | 2 | HG02896.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*56G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 10/10 | 56 | chr16 | 28591762 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:28554124
|
G | A | 32 | a0001c0001t0002g0045a0001c0001t0003g0036a0001c0001t0003g0044others(29): Show | 39 | HG00609.hp1 HG00735.hp1 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.-16+27G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28554124 | ||||||
chr16:28554168
|
G | A | 55 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0053others(52): Show | 59 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.-16+71G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28554168 | ||||||
chr16:28554172
|
C | G | 1 | a0001c0001t0002g0105 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-16+75C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28554172 | ||||||
chr16:28554176
|
G | T | 1 | a0001c0001t0002g0306 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-16+79G>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28554176 | ||||||
chr16:28554182
|
G | T | 3 | a0001c0002t0002g0025a0001c0002t0002g0304a0001c0002t0002g0305 | 4 | HG00099.hp1 HG02155.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+85G>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28554182 | ||||||
chr16:28554266
|
G | A | 3 | a0001c0001t0005g0107a0001c0001t0005g0108a0001c0006t0002g0106 | 3 | HG02896.hp2 HG02897.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-16+169G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28554266 | ||||||
chr16:28554305
|
C | T | 1 | a0001c0001t0002g0303 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-16+208C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28554305 | ||||||
chr16:28554346
|
C | G | 125 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0024others(122): Show | 141 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(138): Show |
intron_variant | MODIFIER | c.-16+249C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28554346 | ||||||
chr16:28554350
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-16+253G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28554350 | ||||||
chr16:28554351
|
A | C | 1 | a0001c0001t0001g0274 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-16+254A>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28554351 | ||||||
chr16:28554352
|
G | C | 2 | a0001c0002t0002g0026a0001c0002t0002g0027 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-16+255G>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28554352 | ||||||
chr16:28554353
|
G | A | 2 | a0001c0001t0001g0112a0001c0001t0008g0111 | 2 | HG01934.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.-16+256G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28554353 | ||||||
chr16:28554456
|
C | T | 1 | a0001c0002t0002g0025 | 2 | HG00099.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-16+359C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28554456 | ||||||
chr16:28554632
|
A | G | 80 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0024others(77): Show | 85 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.-16+535A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28554632 | ||||||
chr16:28554658
|
T | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | HG02040.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.-16+561T>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28554658 | ||||||
chr16:28554687
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-16+590G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28554687 | ||||||
chr16:28554837
|
G | T | 125 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0024others(122): Show | 141 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(138): Show |
intron_variant | MODIFIER | c.-16+740G>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28554837 | ||||||
chr16:28555054
|
T | C | 298 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(295): Show | 336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.-16+957T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28555054 | ||||||
chr16:28555171
|
A | G | 1 | a0001c0006t0002g0106 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-16+1074A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28555171 | ||||||
chr16:28555215
|
GCACTTTG others(3): Show |
G | 1 | a0001c0001t0002g0104 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-16+1119_-16+1128d others(12): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28555215 | ||||||
chr16:28555230
|
G | A | 4 | a0001c0001t0002g0053a0001c0001t0002g0054a0001c0001t0002g0055others(1): Show | 4 | HG00639.hp1 HG00642.hp2 HG01070.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16+1133G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28555230 | ||||||
chr16:28555301
|
T | TA | 34 | a0001c0001t0002g0045a0001c0001t0002g0057a0001c0001t0002g0058others(31): Show | 41 | HG00609.hp1 HG00735.hp1 HG01192.hp1 others(38): Show |
intron_variant | MODIFIER | c.-16+1221dupA | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28555301 | |||||
chr16:28555301
|
TA | T | 15 | a0001c0001t0001g0114a0001c0001t0001g0260a0001c0001t0001g0261others(12): Show | 15 | HG01099.hp1 HG01167.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.-16+1221delA | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28555301 | |||||
chr16:28555332
|
C | T | 4 | a0001c0002t0002g0006a0001c0002t0002g0049a0001c0002t0002g0050others(1): Show | 6 | HG00609.hp1 NA18944.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16+1235C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28555332 | ||||||
chr16:28555347
|
A | G | 4 | a0001c0001t0002g0303a0001c0002t0002g0025a0001c0002t0002g0304others(1): Show | 5 | HG00099.hp1 HG02155.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16+1250A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28555347 | ||||||
chr16:28555380
|
G | T | 4 | a0001c0001t0001g0023a0001c0001t0001g0257a0001c0001t0001g0258others(1): Show | 5 | NA18967.hp2 NA18970.hp2 NA18997.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16+1283G>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28555380 | ||||||
chr16:28555477
|
A | G | 1 | a0001c0001t0001g0256 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-16+1380A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28555477 | ||||||
chr16:28555508
|
C | T | 1 | a0001c0001t0002g0302 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-16+1411C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28555508 | ||||||
chr16:28555612
|
A | G | 32 | a0001c0001t0001g0023a0001c0001t0001g0229a0001c0001t0001g0230others(29): Show | 33 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.-16+1515A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28555612 | ||||||
chr16:28555683
|
A | G | 15 | a0001c0003t0002g0022a0001c0003t0002g0216a0001c0003t0002g0217others(12): Show | 16 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.-16+1586A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28555683 | ||||||
chr16:28556042
|
T | C | 1 | a0001c0001t0002g0303 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-16+1945T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28556042 | ||||||
chr16:28556263
|
G | A | 6 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(3): Show | 6 | HG01891.hp2 HG02451.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16+2166G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28556263 | ||||||
chr16:28556339
|
T | C | 1 | a0001c0002t0002g0275 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-16+2242T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28556339 | ||||||
chr16:28556368
|
C | G | 1 | a0001c0001t0001g0215 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-16+2271C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28556368 | ||||||
chr16:28556368
|
C | T | 1 | a0001c0002t0002g0280 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-16+2271C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28556368 | ||||||
chr16:28556433
|
C | T | 1 | a0001c0001t0002g0098 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-16+2336C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28556433 | ||||||
chr16:28556479
|
C | G | 1 | a0001c0001t0001g0214 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-16+2382C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28556479 | ||||||
chr16:28556743
|
A | T | 1 | a0001c0001t0002g0011 | 2 | HG00741.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-16+2646A>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28556743 | ||||||
chr16:28556747
|
G | A | 3 | a0001c0002t0002g0025a0001c0002t0002g0304a0001c0002t0002g0305 | 4 | HG00099.hp1 HG02155.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+2650G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28556747 | ||||||
chr16:28556757
|
C | A | 1 | a0001c0001t0002g0104 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-16+2660C>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28556757 | ||||||
chr16:28556809
|
A | G | 4 | a0001c0001t0002g0095a0001c0001t0002g0096a0001c0001t0002g0097others(1): Show | 4 | HG01081.hp1 HG01099.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16+2712A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28556809 | ||||||
chr16:28556839
|
G | A | 3 | a0001c0001t0005g0107a0001c0001t0005g0108a0001c0006t0002g0106 | 3 | HG02896.hp2 HG02897.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-16+2742G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28556839 | ||||||
chr16:28556894
|
C | T | 32 | a0001c0001t0002g0045a0001c0001t0003g0036a0001c0001t0003g0044others(29): Show | 39 | HG00609.hp1 HG00735.hp1 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.-16+2797C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28556894 | ||||||
chr16:28556900
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-16+2803G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28556900 | ||||||
chr16:28557010
|
T | C | 3 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231 | 3 | NA18939.hp1 NA19000.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.-16+2913T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28557010 | ||||||
chr16:28557046
|
G | T | 2 | a0001c0001t0001g0212a0001c0001t0001g0213 | 2 | HG00735.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.-16+2949G>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28557046 | ||||||
chr16:28557357
|
C | T | 15 | a0001c0003t0002g0022a0001c0003t0002g0216a0001c0003t0002g0217others(12): Show | 16 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.-16+3260C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28557357 | ||||||
chr16:28557649
|
C | T | 1 | a0001c0001t0002g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-16+3552C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28557649 | ||||||
chr16:28557733
|
A | G | 1 | a0001c0001t0002g0011 | 2 | HG00741.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-16+3636A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28557733 | ||||||
chr16:28557824
|
C | G | 4 | a0001c0001t0002g0303a0001c0002t0002g0025a0001c0002t0002g0304others(1): Show | 5 | HG00099.hp1 HG02155.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16+3727C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28557824 | ||||||
chr16:28557965
|
G | GT | 46 | a0001c0001t0001g0021a0001c0001t0001g0184a0001c0001t0001g0185others(43): Show | 47 | HG00544.hp2 HG00558.hp2 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.-16+3894dupT | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28557965 | |||||
chr16:28557965
|
GT | G | 62 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(59): Show | 72 | HG00609.hp1 HG00642.hp1 HG00738.hp2 others(69): Show |
intron_variant | MODIFIER | c.-16+3894delT | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28557965 | |||||
chr16:28557966
|
T | G | 1 | a0001c0001t0002g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-16+3869T>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28557966 | ||||||
chr16:28557967
|
T | G | 1 | a0001c0001t0002g0282 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-16+3870T>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28557967 | ||||||
chr16:28557991
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-16+3894T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28557991 | ||||||
chr16:28557992
|
C | T | 1 | a0001c0002t0002g0091 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-16+3895C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28557992 | ||||||
chr16:28558184
|
C | T | 6 | a0001c0001t0001g0021a0001c0001t0001g0207a0001c0001t0001g0209others(3): Show | 7 | HG02615.hp2 HG02895.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-16+4087C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28558184 | ||||||
chr16:28558199
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-16+4102G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28558199 | ||||||
chr16:28558200
|
G | A | 1 | a0001c0001t0002g0303 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-16+4103G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28558200 | ||||||
chr16:28558272
|
A | AT | 22 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(19): Show | 25 | HG02080.hp1 HG02145.hp1 HG02698.hp1 others(22): Show |
intron_variant | MODIFIER | c.-16+4190dupT | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28558272 | |||||
chr16:28558443
|
G | C | 55 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0053others(52): Show | 59 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.-16+4346G>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28558443 | ||||||
chr16:28558455
|
C | T | 1 | a0001c0001t0002g0303 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-16+4358C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28558455 | ||||||
chr16:28558523
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-16+4426T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28558523 | ||||||
chr16:28558536
|
G | A | 3 | a0001c0003t0002g0216a0001c0003t0002g0217a0001c0003t0002g0218 | 3 | HG02109.hp1 HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-16+4439G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28558536 | ||||||
chr16:28558556
|
G | A | 1 | a0001c0001t0002g0045 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-16+4459G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28558556 | ||||||
chr16:28558684
|
C | T | 78 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0024others(75): Show | 83 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.-16+4587C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28558684 | ||||||
chr16:28558701
|
A | G | 1 | a0001c0001t0002g0300 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-16+4604A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28558701 | ||||||
chr16:28558729
|
A | G | 43 | a0001c0001t0002g0045a0001c0001t0002g0279a0001c0001t0003g0036others(40): Show | 53 | HG00609.hp1 HG00735.hp1 HG01074.hp1 others(50): Show |
intron_variant | MODIFIER | c.-16+4632A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28558729 | ||||||
chr16:28558901
|
G | A | 1 | a0001c0001t0002g0061 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-16+4804G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28558901 | ||||||
chr16:28558951
|
A | G | 3 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0202 | 3 | HG02280.hp1 HG02615.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-16+4854A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28558951 | ||||||
chr16:28559000
|
A | G | 298 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(295): Show | 336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.-16+4903A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28559000 | ||||||
chr16:28559007
|
T | C | 1 | a0001c0002t0002g0049 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-16+4910T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28559007 | ||||||
chr16:28559300
|
A | G | 14 | a0001c0001t0001g0023a0001c0001t0001g0229a0001c0001t0001g0230others(11): Show | 15 | HG00558.hp1 HG02132.hp2 NA18939.hp1 others(12): Show |
intron_variant | MODIFIER | c.-16+5203A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28559300 | ||||||
chr16:28559318
|
C | T | 2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-16+5221C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28559318 | ||||||
chr16:28559382
|
TTTG | T | 80 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0024others(77): Show | 85 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.-16+5300_-16+5302d others(5): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28559382 | |||||
chr16:28559401
|
T | A | 4 | a0001c0001t0002g0303a0001c0002t0002g0025a0001c0002t0002g0304others(1): Show | 5 | HG00099.hp1 HG02155.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16+5304T>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28559401 | ||||||
chr16:28559414
|
C | T | 1 | a0001c0001t0002g0045 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-16+5317C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28559414 | ||||||
chr16:28559709
|
C | A | 11 | a0001c0002t0003g0005a0001c0002t0003g0028a0001c0002t0003g0029others(8): Show | 13 | HG01192.hp1 HG01261.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.-16+5612C>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28559709 | ||||||
chr16:28559772
|
C | G | 1 | a0001c0001t0001g0206 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-16+5675C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28559772 | ||||||
chr16:28560102
|
C | T | 1 | a0001c0001t0002g0299 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-16+6005C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28560102 | ||||||
chr16:28560235
|
C | A | 6 | a0001c0001t0002g0303a0001c0002t0002g0025a0001c0002t0002g0304others(3): Show | 7 | HG00099.hp1 HG02109.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.-16+6138C>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28560235 | ||||||
chr16:28560370
|
C | T | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-16+6273C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28560370 | ||||||
chr16:28560435
|
T | A | 298 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(295): Show | 336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.-16+6338T>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28560435 | ||||||
chr16:28560480
|
T | G | 2 | a0001c0001t0002g0284a0001c0001t0002g0285 | 2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-16+6383T>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28560480 | ||||||
chr16:28560552
|
G | A | 4 | a0001c0001t0002g0303a0001c0002t0002g0025a0001c0002t0002g0304others(1): Show | 5 | HG00099.hp1 HG02155.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16+6455G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28560552 | ||||||
chr16:28560565
|
G | T | 4 | a0001c0001t0002g0303a0001c0002t0002g0025a0001c0002t0002g0304others(1): Show | 5 | HG00099.hp1 HG02155.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16+6468G>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28560565 | ||||||
chr16:28560575
|
C | G | 3 | a0001c0002t0002g0043a0001c0002t0002g0048a0001c0002t0009g0042 | 3 | NA18962.hp2 NA18977.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-16+6478C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28560575 | ||||||
chr16:28560684
|
C | T | 31 | a0001c0001t0001g0121a0001c0001t0002g0045a0001c0002t0002g0006others(28): Show | 38 | HG00609.hp1 HG00735.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.-16+6587C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28560684 | ||||||
chr16:28560700
|
G | A | 33 | a0001c0001t0001g0023a0001c0001t0001g0184a0001c0001t0001g0229others(30): Show | 34 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.-16+6603G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28560700 | ||||||
chr16:28560830
|
G | A | 1 | a0001c0002t0002g0035 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-16+6733G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28560830 | ||||||
chr16:28560960
|
C | CA | 61 | a0001c0001t0001g0113a0001c0001t0001g0126a0001c0001t0001g0229others(58): Show | 65 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.-16+6879dupA | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28560960 | |||||
chr16:28560974
|
AAAG | A | 8 | a0001c0001t0002g0279a0001c0002t0002g0004a0001c0002t0002g0275others(5): Show | 11 | HG01109.hp1 HG01884.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-16+6878_-16+6880d others(5): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28560974 | ||||||
chr16:28561031
|
A | G | 1 | a0001c0001t0001g0172 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-16+6934A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28561031 | ||||||
chr16:28561162
|
C | T | 2 | a0001c0001t0002g0299a0001c0001t0002g0300 | 2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-16+7065C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28561162 | ||||||
chr16:28561273
|
G | A | 6 | a0001c0001t0002g0279a0001c0002t0002g0004a0001c0002t0002g0276others(3): Show | 9 | HG01109.hp1 HG01884.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-16+7176G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28561273 | ||||||
chr16:28561527
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-16+7430C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28561527 | ||||||
chr16:28561652
|
C | T | 2 | a0001c0003t0002g0216a0001c0003t0002g0217 | 2 | HG02109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-16+7555C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28561652 | ||||||
chr16:28561915
|
C | G | 3 | a0001c0001t0004g0296a0001c0001t0004g0297a0001c0001t0004g0298 | 3 | HG01884.hp1 HG03486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-16+7818C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28561915 | ||||||
chr16:28561926
|
A | G | 1 | a0001c0002t0002g0280 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-16+7829A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28561926 | ||||||
chr16:28562010
|
A | G | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-16+7913A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28562010 | ||||||
chr16:28562042
|
G | C | 5 | a0001c0001t0001g0001a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 10 | HG00408.hp1 NA18943.hp2 NA18953.hp2 others(7): Show |
intron_variant | MODIFIER | c.-16+7945G>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28562042 | ||||||
chr16:28562058
|
C | T | 1 | a0001c0001t0001g0200 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-16+7961C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28562058 | ||||||
chr16:28562237
|
C | T | 1 | a0001c0002t0002g0025 | 2 | HG00099.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-16+8140C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28562237 | ||||||
chr16:28562291
|
T | G | 1 | a0001c0001t0002g0303 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-16+8194T>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28562291 | ||||||
chr16:28562402
|
G | A | 1 | a0001c0002t0002g0275 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-16+8305G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28562402 | ||||||
chr16:28562417
|
A | T | 1 | a0001c0001t0002g0295 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-16+8320A>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28562417 | ||||||
chr16:28562642
|
C | T | 19 | a0001c0001t0005g0107a0001c0001t0005g0108a0001c0003t0001g0171others(16): Show | 20 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.-16+8545C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28562642 | ||||||
chr16:28562670
|
A | T | 3 | a0001c0001t0001g0021a0001c0001t0001g0210a0001c0001t0001g0211 | 4 | HG02895.hp2 HG02970.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16+8573A>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28562670 | ||||||
chr16:28562688
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-16+8591C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28562688 | ||||||
chr16:28562756
|
T | C | 1 | a0001c0001t0002g0303 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-16+8659T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28562756 | ||||||
chr16:28562826
|
C | T | 3 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0088 | 3 | HG02015.hp1 NA18970.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.-16+8729C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28562826 | ||||||
chr16:28562903
|
C | CA | 94 | a0001c0001t0001g0110a0001c0001t0001g0122a0001c0001t0001g0131others(91): Show | 103 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(100): Show |
intron_variant | MODIFIER | c.-16+8830dupA | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28562903 | |||||
chr16:28562903
|
C | CAA | 22 | a0001c0001t0001g0109a0001c0001t0001g0130a0001c0001t0001g0237others(19): Show | 22 | HG00280.hp2 HG00438.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.-16+8829_-16+8830d others(4): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28562903 | |||||
chr16:28562903
|
CA | C | 28 | a0001c0001t0001g0118a0001c0001t0002g0024a0001c0001t0002g0282others(25): Show | 30 | HG00099.hp1 HG01106.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.-16+8830delA | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28562903 | |||||
chr16:28563008
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-16+8911G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28563008 | ||||||
chr16:28563033
|
A | G | 1 | a0001c0001t0001g0273 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-16+8936A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28563033 | ||||||
chr16:28563294
|
A | G | 147 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0121others(144): Show | 164 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.-16+9197A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28563294 | ||||||
chr16:28563316
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-16+9219T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28563316 | ||||||
chr16:28563338
|
C | T | 2 | a0001c0001t0001g0123a0001c0001t0001g0169 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-16+9241C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28563338 | ||||||
chr16:28563350
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-16+9253G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28563350 | ||||||
chr16:28563715
|
C | CT | 87 | a0001c0001t0001g0018a0001c0001t0001g0112a0001c0001t0001g0116others(84): Show | 93 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.-16+9641dupT | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28563715 | |||||
chr16:28563715
|
C | CTT | 11 | a0001c0001t0002g0057a0001c0001t0002g0058a0001c0001t0002g0067others(8): Show | 11 | HG01175.hp2 HG01255.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.-16+9640_-16+9641d others(4): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28563715 | |||||
chr16:28563715
|
CT | C | 19 | a0001c0001t0001g0110a0001c0001t0005g0107a0001c0001t0005g0108others(16): Show | 20 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.-16+9641delT | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28563715 | |||||
chr16:28563781
|
C | T | 3 | a0001c0002t0002g0025a0001c0002t0002g0304a0001c0002t0002g0305 | 4 | HG00099.hp1 HG02155.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+9684C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28563781 | ||||||
chr16:28563998
|
C | T | 1 | a0001c0001t0002g0300 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-16+9901C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28563998 | ||||||
chr16:28564023
|
A | G | 2 | a0001c0001t0001g0121a0001c0001t0002g0045 | 2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-16+9926A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564023 | ||||||
chr16:28564214
|
G | C | 1 | a0001c0001t0001g0173 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-16+10117G>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564214 | ||||||
chr16:28564431
|
A | G | 1 | a0001c0001t0001g0213 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-16+10334A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564431 | ||||||
chr16:28564479
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-16+10382C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564479 | ||||||
chr16:28564511
|
A | G | 1 | a0001c0001t0002g0061 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-16+10414A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564511 | ||||||
chr16:28564517
|
ATATGTGT others(3): Show |
A | 3 | a0001c0002t0002g0025a0001c0002t0002g0304a0001c0002t0002g0305 | 4 | HG00099.hp1 HG02155.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+10424_-16+1043 others(14): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564517 | |||||
chr16:28564521
|
G | A | 1 | a0001c0001t0002g0303 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-16+10424G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564521 | ||||||
chr16:28564523
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-16+10426G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564523 | ||||||
chr16:28564525
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-16+10428G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564525 | ||||||
chr16:28564526
|
T | TGTATATA others(17): Show |
1 | a0001c0001t0001g0178 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-16+10442_-16+1046 others(28): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564526 | |||||
chr16:28564527
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-16+10430G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564527 | ||||||
chr16:28564529
|
A | ATACGTAT others(11): Show |
2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-16+10434_-16+1043 others(22): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564529 | |||||
chr16:28564529
|
A | G | 2 | a0001c0001t0001g0212a0001c0001t0001g0213 | 2 | HG00735.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.-16+10432A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564529 | ||||||
chr16:28564535
|
A | G | 3 | a0001c0002t0002g0025a0001c0002t0002g0304a0001c0002t0002g0305 | 4 | HG00099.hp1 HG02155.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+10438A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564535 | ||||||
chr16:28564537
|
A | G | 3 | a0001c0002t0002g0025a0001c0002t0002g0304a0001c0002t0002g0305 | 4 | HG00099.hp1 HG02155.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+10440A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564537 | ||||||
chr16:28564538
|
T | C | 4 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0002g0068others(1): Show | 4 | HG01346.hp1 HG02486.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16+10441T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564538 | ||||||
chr16:28564538
|
TGTATATA others(33): Show |
T | 1 | a0001c0001t0004g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-16+10442_-16+1048 others(44): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564538 | ||||||
chr16:28564541
|
A | G | 2 | a0001c0001t0001g0121a0001c0001t0002g0045 | 2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-16+10444A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564541 | ||||||
chr16:28564549
|
A | G | 1 | a0001c0001t0002g0080 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-16+10452A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564549 | ||||||
chr16:28564549
|
ACG | A | 70 | a0001c0001t0002g0024a0001c0001t0002g0279a0001c0001t0002g0282others(67): Show | 81 | HG00609.hp1 HG00642.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.-16+10453_-16+1045 others(6): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564549 | ||||||
chr16:28564550
|
C | T | 70 | a0001c0001t0001g0121a0001c0001t0001g0196a0001c0001t0001g0237others(67): Show | 75 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-16+10453C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564550 | ||||||
chr16:28564551
|
G | A | 3 | a0001c0001t0001g0121a0001c0001t0002g0045a0001c0001t0002g0080 | 3 | HG02257.hp2 HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-16+10454G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564551 | ||||||
chr16:28564551
|
GTA | G | 32 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(29): Show | 39 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.-16+10467_-16+1046 others(6): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564551 | |||||
chr16:28564552
|
T | TGTGTGTA others(21): Show |
1 | a0001c0001t0001g0196 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-16+10455_-16+1045 others(32): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564552 | ||||||
chr16:28564553
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0002g0080 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-16+10464_-16+1046 others(14): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564553 | |||||
chr16:28564553
|
A | ATATATAT others(5): Show |
51 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0053others(48): Show | 55 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.-16+10466_-16+1046 others(16): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564553 | |||||
chr16:28564553
|
A | ATATATAT others(19): Show |
4 | a0001c0001t0002g0095a0001c0001t0002g0096a0001c0001t0002g0097others(1): Show | 4 | HG01081.hp1 HG01099.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16+10466_-16+1046 others(30): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564553 | |||||
chr16:28564553
|
A | G | 73 | a0001c0001t0001g0121a0001c0001t0001g0196a0001c0001t0002g0024others(70): Show | 84 | HG00544.hp2 HG00609.hp1 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.-16+10456A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564553 | ||||||
chr16:28564554
|
T | TATATATA others(5): Show |
2 | a0001c0001t0002g0089a0001c0001t0002g0100 | 2 | NA18941.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.-16+10466_-16+1046 others(16): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564554 | |||||
chr16:28564555
|
A | ATATATAT others(19): Show |
3 | a0001c0001t0001g0162a0001c0001t0001g0188a0001c0001t0001g0189 | 3 | HG03195.hp2 HG03516.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-16+10470_-16+1049 others(30): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564555 | |||||
chr16:28564555
|
A | ATATATAT others(45): Show |
1 | a0001c0001t0001g0163 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-16+10495_-16+1049 others(56): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564555 | |||||
chr16:28564558
|
T | TATATACG others(41): Show |
1 | a0001c0001t0002g0093 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-16+10466_-16+1046 others(52): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564558 | |||||
chr16:28564562
|
TATAC | T | 3 | a0001c0002t0002g0025a0001c0002t0002g0304a0001c0002t0002g0305 | 4 | HG00099.hp1 HG02155.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+10466_-16+1046 others(8): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564562 | ||||||
chr16:28564564
|
TACGTATA others(7): Show |
T | 6 | a0001c0001t0001g0237a0001c0001t0001g0240a0001c0002t0002g0010others(3): Show | 7 | HG00438.hp2 HG02165.hp2 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.-16+10484_-16+1049 others(18): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564564 | |||||
chr16:28564566
|
C | T | 1 | a0001c0001t0002g0093 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-16+10469C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564566 | ||||||
chr16:28564569
|
A | G | 1 | a0001c0001t0002g0093 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-16+10472A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564569 | ||||||
chr16:28564578
|
C | T | 135 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0121others(132): Show | 151 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(148): Show |
intron_variant | MODIFIER | c.-16+10481C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564578 | ||||||
chr16:28564580
|
C | CATATATA others(1): Show |
4 | a0001c0001t0002g0095a0001c0001t0002g0096a0001c0001t0002g0097others(1): Show | 4 | HG01081.hp1 HG01099.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16+10483_-16+1048 others(12): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564580 | ||||||
chr16:28564581
|
G | A | 1 | a0001c0001t0002g0303 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-16+10484G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564581 | ||||||
chr16:28564582
|
T | C | 1 | a0001c0001t0002g0303 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-16+10485T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564582 | ||||||
chr16:28564583
|
A | G | 4 | a0001c0001t0002g0095a0001c0001t0002g0096a0001c0001t0002g0097others(1): Show | 4 | HG01081.hp1 HG01099.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16+10486A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564583 | ||||||
chr16:28564592
|
C | G | 1 | a0001c0001t0001g0130 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-16+10495C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564592 | ||||||
chr16:28564594
|
CACATATA others(17): Show |
C | 1 | a0001c0001t0002g0294 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-16+10499_-16+1052 others(28): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564594 | |||||
chr16:28564596
|
C | T | 80 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0024others(77): Show | 85 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.-16+10499C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564596 | ||||||
chr16:28564597
|
A | G | 1 | a0001c0001t0002g0303 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-16+10500A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564597 | ||||||
chr16:28564599
|
A | G | 1 | a0001c0001t0002g0303 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-16+10502A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564599 | ||||||
chr16:28564601
|
ATGTGTAT others(35): Show |
A | 1 | a0001c0001t0002g0045 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-16+10508_-16+1054 others(46): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564601 | |||||
chr16:28564603
|
G | A | 1 | a0001c0001t0002g0303 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-16+10506G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564603 | ||||||
chr16:28564604
|
TGTATATA others(55): Show |
T | 1 | a0001c0001t0001g0121 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-16+10508_-16+1056 others(66): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564604 | ||||||
chr16:28564605
|
G | A | 1 | a0001c0001t0002g0303 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-16+10508G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564605 | ||||||
chr16:28564617
|
A | G | 3 | a0001c0002t0002g0025a0001c0002t0002g0304a0001c0002t0002g0305 | 4 | HG00099.hp1 HG02155.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+10520A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564617 | ||||||
chr16:28564624
|
C | T | 2 | a0001c0002t0002g0304a0001c0002t0002g0305 | 2 | HG02155.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-16+10527C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564624 | ||||||
chr16:28564626
|
T | C | 2 | a0001c0001t0002g0282a0001c0001t0002g0283 | 2 | HG01891.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-16+10529T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564626 | ||||||
chr16:28564635
|
G | A | 4 | a0001c0003t0002g0219a0001c0003t0002g0221a0001c0003t0002g0226others(1): Show | 4 | HG00642.hp1 HG02056.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+10538G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564635 | ||||||
chr16:28564641
|
A | ATG | 7 | a0001c0003t0001g0171a0001c0003t0002g0022a0001c0003t0002g0220others(4): Show | 8 | HG00738.hp2 HG01106.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.-16+10548_-16+1054 others(6): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564641 | |||||
chr16:28564641
|
A | G | 4 | a0001c0003t0002g0219a0001c0003t0002g0221a0001c0003t0002g0226others(1): Show | 4 | HG00642.hp1 HG02056.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+10544A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564641 | ||||||
chr16:28564645
|
G | A | 4 | a0001c0003t0002g0219a0001c0003t0002g0221a0001c0003t0002g0226others(1): Show | 4 | HG00642.hp1 HG02056.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+10548G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564645 | ||||||
chr16:28564645
|
G | GTA | 8 | a0001c0001t0005g0107a0001c0001t0005g0108a0001c0003t0002g0216others(5): Show | 8 | HG02109.hp1 HG02602.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-16+10555_-16+1055 others(6): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564645 | |||||
chr16:28564654
|
C | T | 1 | a0001c0001t0002g0045 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-16+10557C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564654 | ||||||
chr16:28564665
|
G | A | 2 | a0001c0001t0001g0212a0001c0001t0001g0213 | 2 | HG00735.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.-16+10568G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564665 | ||||||
chr16:28564666
|
C | CATATATG others(1): Show |
77 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0053others(74): Show | 85 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.-16+10575_-16+1057 others(12): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564666 | |||||
chr16:28564666
|
C | T | 1 | a0001c0001t0002g0045 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-16+10569C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564666 | ||||||
chr16:28564666
|
CAT | C | 27 | a0001c0001t0002g0024a0001c0001t0002g0069a0001c0001t0002g0070others(24): Show | 28 | HG01106.hp1 HG01884.hp1 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.-16+10576_-16+1057 others(6): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564666 | |||||
chr16:28564667
|
A | G | 1 | a0001c0001t0002g0045 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-16+10570A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564667 | ||||||
chr16:28564671
|
ATATGTAT others(7): Show |
A | 35 | a0001c0001t0001g0237a0001c0001t0001g0240a0001c0001t0002g0303others(32): Show | 43 | HG00099.hp1 HG00438.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.-16+10576_-16+1058 others(18): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564671 | |||||
chr16:28564675
|
G | A | 2 | a0001c0001t0002g0102a0001c0001t0002g0300 | 2 | HG01099.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-16+10578G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564675 | ||||||
chr16:28564677
|
A | G | 2 | a0001c0001t0002g0102a0001c0001t0002g0300 | 2 | HG01099.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-16+10580A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564677 | ||||||
chr16:28564683
|
A | G | 3 | a0001c0001t0001g0183a0001c0001t0001g0185a0001c0001t0001g0192 | 3 | HG02074.hp2 HG03942.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.-16+10586A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564683 | ||||||
chr16:28564685
|
G | A | 2 | a0001c0001t0002g0104a0001c0001t0002g0300 | 2 | HG02129.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-16+10588G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564685 | ||||||
chr16:28564685
|
GTGTATAT others(3): Show |
G | 12 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(9): Show | 12 | HG01891.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.-16+10600_-16+1060 others(14): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564685 | |||||
chr16:28564685
|
GTGTATAT others(41): Show |
G | 5 | a0001c0001t0002g0024a0001c0001t0002g0287a0001c0001t0002g0288others(2): Show | 6 | HG01106.hp1 HG02055.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-16+10590_-16+1063 others(52): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564685 | |||||
chr16:28564687
|
G | A | 64 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0045others(61): Show | 68 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.-16+10590G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564687 | ||||||
chr16:28564687
|
GTA | G | 9 | a0001c0001t0001g0121a0001c0001t0002g0279a0001c0002t0002g0004others(6): Show | 12 | HG01109.hp1 HG01884.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-16+10598_-16+1059 others(6): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564687 | |||||
chr16:28564688
|
T | C | 2 | a0001c0001t0002g0045a0001c0001t0002g0104 | 2 | HG02129.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-16+10591T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564688 | ||||||
chr16:28564695
|
A | G | 58 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0053others(55): Show | 62 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.-16+10598A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564695 | ||||||
chr16:28564695
|
ATGTATAT others(43): Show |
A | 3 | a0001c0001t0004g0296a0001c0001t0004g0297a0001c0001t0004g0298 | 3 | HG01884.hp1 HG03486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-16+10600_-16+1064 others(54): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564695 | |||||
chr16:28564696
|
T | C | 74 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(71): Show | 90 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.-16+10599T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564696 | ||||||
chr16:28564697
|
G | A | 67 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0053others(64): Show | 71 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.-16+10600G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564697 | ||||||
chr16:28564698
|
T | C | 1 | a0001c0005t0002g0286 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-16+10601T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564698 | ||||||
chr16:28564698
|
TATATATA others(3): Show |
T | 3 | a0001c0001t0005g0107a0001c0001t0005g0108a0001c0006t0002g0106 | 3 | HG02896.hp2 HG02897.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-16+10610_-16+1061 others(14): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564698 | |||||
chr16:28564704
|
TATAC | T | 3 | a0001c0002t0002g0025a0001c0002t0002g0304a0001c0002t0002g0305 | 4 | HG00099.hp1 HG02155.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+10611_-16+1061 others(8): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564704 | |||||
chr16:28564705
|
A | ATG | 5 | a0001c0003t0002g0218a0001c0003t0002g0219a0001c0003t0002g0221others(2): Show | 5 | HG00642.hp1 HG02056.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16+10609_-16+1061 others(6): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564705 | |||||
chr16:28564705
|
A | G | 1 | a0001c0001t0002g0303 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-16+10608A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564705 | ||||||
chr16:28564706
|
T | C | 4 | a0001c0001t0001g0123a0001c0001t0001g0130a0001c0001t0001g0142others(1): Show | 4 | HG02717.hp1 HG03490.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+10609T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564706 | ||||||
chr16:28564706
|
TAC | T | 10 | a0001c0001t0002g0303a0001c0003t0001g0171a0001c0003t0002g0022others(7): Show | 11 | HG00738.hp2 HG01106.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.-16+10611_-16+1061 others(6): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564706 | |||||
chr16:28564707
|
A | G | 41 | a0001c0001t0001g0187a0001c0001t0001g0232a0001c0001t0001g0237others(38): Show | 48 | HG00438.hp2 HG00609.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.-16+10610A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564707 | ||||||
chr16:28564708
|
C | CAT | 14 | a0001c0001t0001g0021a0001c0001t0001g0109a0001c0001t0001g0110others(11): Show | 15 | HG01891.hp2 HG02559.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.-16+10618_-16+1061 others(6): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564708 | |||||
chr16:28564708
|
C | T | 39 | a0001c0001t0001g0237a0001c0001t0001g0240a0001c0002t0002g0006others(36): Show | 46 | HG00438.hp2 HG00609.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.-16+10611C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564708 | ||||||
chr16:28564709
|
A | G | 45 | a0001c0001t0001g0237a0001c0001t0001g0240a0001c0002t0002g0006others(42): Show | 54 | HG00099.hp1 HG00438.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-16+10612A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564709 | ||||||
chr16:28564710
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-16+10613T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564710 | ||||||
chr16:28564711
|
A | G | 9 | a0001c0003t0001g0171a0001c0003t0002g0022a0001c0003t0002g0220others(6): Show | 10 | HG00738.hp2 HG01106.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.-16+10614A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564711 | ||||||
chr16:28564714
|
TATGTATA others(7): Show |
T | 1 | a0001c0001t0001g0211 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-16+10620_-16+1063 others(18): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564714 | |||||
chr16:28564716
|
T | C | 11 | a0001c0001t0001g0124a0001c0001t0001g0126a0001c0001t0001g0137others(8): Show | 11 | HG00639.hp2 HG01243.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.-16+10619T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564716 | ||||||
chr16:28564717
|
G | GTA | 50 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0053others(47): Show | 54 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.-16+10629_-16+1063 others(6): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564717 | |||||
chr16:28564717
|
G | GTATATAT others(27): Show |
2 | a0001c0001t0002g0062a0001c0001t0002g0066 | 2 | HG01256.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.-16+10629_-16+1063 others(38): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564717 | |||||
chr16:28564721
|
ATATATAC others(9): Show |
A | 1 | a0001c0001t0001g0261 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-16+10631_-16+1064 others(20): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564721 | |||||
chr16:28564725
|
A | G | 14 | a0001c0001t0002g0061a0001c0001t0002g0104a0001c0001t0002g0282others(11): Show | 14 | HG01891.hp1 HG02129.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-16+10628A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564725 | ||||||
chr16:28564728
|
C | CAT | 19 | a0001c0001t0005g0107a0001c0001t0005g0108a0001c0003t0001g0171others(16): Show | 20 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.-16+10638_-16+1063 others(6): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564728 | |||||
chr16:28564728
|
C | T | 14 | a0001c0001t0002g0061a0001c0001t0002g0104a0001c0001t0002g0282others(11): Show | 14 | HG01891.hp1 HG02129.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-16+10631C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564728 | ||||||
chr16:28564728
|
CATATATA others(11): Show |
C | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0013others(136): Show | 158 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.-16+10666_-16+1068 others(22): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564728 | |||||
chr16:28564735
|
A | G | 15 | a0001c0001t0001g0211a0001c0001t0002g0061a0001c0001t0002g0104others(12): Show | 15 | HG01891.hp1 HG02129.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-16+10638A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564735 | ||||||
chr16:28564736
|
T | C | 3 | a0001c0001t0002g0071a0001c0001t0002g0300a0001c0002t0002g0275 | 3 | HG02451.hp1 NA19074.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-16+10639T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564736 | ||||||
chr16:28564737
|
G | A | 20 | a0001c0001t0001g0211a0001c0001t0002g0024a0001c0001t0002g0061others(17): Show | 21 | HG01106.hp1 HG01891.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.-16+10640G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564737 | ||||||
chr16:28564745
|
G | A | 79 | a0001c0001t0001g0121a0001c0001t0001g0205a0001c0001t0001g0211others(76): Show | 88 | HG00438.hp2 HG00609.hp1 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.-16+10648G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564745 | ||||||
chr16:28564746
|
T | C | 24 | a0001c0001t0001g0211a0001c0001t0001g0261a0001c0001t0002g0024others(21): Show | 25 | HG01106.hp1 HG01515.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.-16+10649T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564746 | ||||||
chr16:28564746
|
T | TAC | 52 | a0001c0001t0001g0121a0001c0001t0001g0205a0001c0001t0001g0237others(49): Show | 60 | HG00438.hp2 HG00609.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.-16+10650_-16+1065 others(6): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564746 | |||||
chr16:28564746
|
T | TATAC | 5 | a0001c0001t0002g0063a0001c0001t0002g0072a0001c0001t0002g0089others(2): Show | 5 | HG02135.hp1 HG02523.hp2 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16+10652_-16+1065 others(8): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564746 | |||||
chr16:28564746
|
T | TATATATA others(15): Show |
6 | a0001c0001t0002g0279a0001c0002t0002g0004a0001c0002t0002g0276others(3): Show | 9 | HG01109.hp1 HG01884.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-16+10665_-16+1066 others(26): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564746 | |||||
chr16:28564746
|
T | TATATATA others(55): Show |
1 | a0001c0002t0002g0277 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-16+10665_-16+1066 others(66): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564746 | |||||
chr16:28564754
|
T | C | 1 | a0001c0001t0002g0290 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-16+10657T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564754 | ||||||
chr16:28564754
|
T | TGTATATA others(15): Show |
1 | a0001c0002t0002g0275 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-16+10665_-16+1066 others(26): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564754 | |||||
chr16:28564755
|
G | A | 19 | a0001c0001t0005g0107a0001c0001t0005g0108a0001c0003t0001g0171others(16): Show | 20 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.-16+10658G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564755 | ||||||
chr16:28564755
|
GTATATAT others(13): Show |
G | 6 | a0001c0001t0001g0012a0001c0001t0001g0119a0001c0001t0001g0130others(3): Show | 7 | HG01243.hp1 HG01496.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-16+10666_-16+1068 others(24): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564755 | |||||
chr16:28564756
|
T | C | 19 | a0001c0001t0005g0107a0001c0001t0005g0108a0001c0003t0001g0171others(16): Show | 20 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.-16+10659T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564756 | ||||||
chr16:28564757
|
ATATATGT others(9): Show |
A | 5 | a0001c0001t0001g0020a0001c0001t0001g0150a0001c0001t0001g0161others(2): Show | 6 | HG01192.hp2 HG02486.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16+10666_-16+1068 others(20): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564757 | |||||
chr16:28564759
|
ATATGTAT others(7): Show |
A | 3 | a0001c0002t0002g0025a0001c0002t0002g0304a0001c0002t0002g0305 | 4 | HG00099.hp1 HG02155.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+10666_-16+1067 others(18): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564759 | |||||
chr16:28564762
|
T | C | 1 | a0001c0006t0002g0106 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-16+10665T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564762 | ||||||
chr16:28564763
|
G | A | 55 | a0001c0001t0001g0198a0001c0001t0002g0003a0001c0001t0002g0011others(52): Show | 59 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.-16+10666G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564763 | ||||||
chr16:28564763
|
GTATATAT others(11): Show |
G | 1 | a0001c0001t0001g0236 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-16+10673_-16+1069 others(22): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564763 | |||||
chr16:28564765
|
A | ACATATAT others(3): Show |
1 | a0001c0005t0002g0286 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-16+10668_-16+1066 others(14): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564765 | ||||||
chr16:28564765
|
A | ACATATAT others(3): Show |
50 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0053others(47): Show | 54 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.-16+10668_-16+1066 others(14): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564765 | ||||||
chr16:28564768
|
TATATGTA others(17): Show |
T | 1 | a0001c0001t0001g0198 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-16+10673_-16+1069 others(28): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564768 | |||||
chr16:28564773
|
GTA | G | 51 | a0001c0001t0001g0121a0001c0001t0001g0237a0001c0001t0001g0240others(48): Show | 59 | HG00438.hp2 HG00609.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.-16+10689_-16+1069 others(6): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564773 | |||||
chr16:28564773
|
GTATA | G | 21 | a0001c0001t0002g0024a0001c0001t0002g0104a0001c0001t0002g0282others(18): Show | 22 | HG01106.hp1 HG01884.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.-16+10687_-16+1069 others(8): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564773 | |||||
chr16:28564775
|
A | G | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-16+10678A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564775 | ||||||
chr16:28564777
|
A | ATATATAC others(27): Show |
6 | a0001c0001t0002g0061a0001c0001t0002g0063a0001c0001t0002g0072others(3): Show | 6 | HG02135.hp1 HG02523.hp2 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.-16+10686_-16+1068 others(38): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564777 | |||||
chr16:28564777
|
A | ATATATG | 50 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0053others(47): Show | 54 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.-16+10685_-16+1068 others(10): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564777 | |||||
chr16:28564777
|
A | ATATGTAT others(45): Show |
2 | a0001c0001t0002g0067a0001c0001t0002g0080 | 2 | HG01255.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-16+10683_-16+1068 others(56): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564777 | |||||
chr16:28564777
|
A | G | 1 | a0001c0002t0002g0041 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-16+10680A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564777 | ||||||
chr16:28564782
|
T | C | 3 | a0001c0002t0002g0025a0001c0002t0002g0304a0001c0002t0002g0305 | 4 | HG00099.hp1 HG02155.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+10685T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564782 | ||||||
chr16:28564783
|
A | G | 1 | a0001c0001t0002g0300 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-16+10686A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564783 | ||||||
chr16:28564784
|
T | C | 4 | a0001c0001t0002g0303a0001c0002t0002g0025a0001c0002t0002g0304others(1): Show | 5 | HG00099.hp1 HG02155.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16+10687T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564784 | ||||||
chr16:28564786
|
T | C | 24 | a0001c0001t0001g0020a0001c0001t0001g0113a0001c0001t0001g0116others(21): Show | 29 | HG00099.hp1 HG00738.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.-16+10689T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564786 | ||||||
chr16:28564788
|
C | T | 2 | a0001c0001t0001g0151a0001c0001t0002g0300 | 2 | HG01243.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-16+10691C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564788 | ||||||
chr16:28564790
|
C | T | 1 | a0001c0001t0002g0300 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-16+10693C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564790 | ||||||
chr16:28564792
|
C | T | 1 | a0001c0001t0002g0300 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-16+10695C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564792 | ||||||
chr16:28564806
|
C | A | 1 | a0001c0001t0002g0294 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-16+10709C>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564806 | ||||||
chr16:28564807
|
A | C | 1 | a0001c0001t0001g0129 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-16+10710A>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564807 | ||||||
chr16:28564808
|
A | C | 1 | a0001c0001t0002g0294 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-16+10711A>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564808 | ||||||
chr16:28564824
|
T | C | 3 | a0001c0001t0002g0284a0001c0001t0002g0285a0001c0001t0002g0291 | 3 | HG02257.hp1 HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-16+10727T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564824 | ||||||
chr16:28564880
|
T | C | 8 | a0001c0001t0002g0279a0001c0002t0002g0004a0001c0002t0002g0275others(5): Show | 11 | HG01109.hp1 HG01884.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-16+10783T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564880 | ||||||
chr16:28564921
|
T | C | 3 | a0001c0002t0002g0025a0001c0002t0002g0304a0001c0002t0002g0305 | 4 | HG00099.hp1 HG02155.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+10824T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564921 | ||||||
chr16:28565048
|
G | A | 19 | a0001c0001t0005g0107a0001c0001t0005g0108a0001c0003t0001g0171others(16): Show | 20 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.-16+10951G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28565048 | ||||||
chr16:28565099
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-16+11002A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28565099 | ||||||
chr16:28565116
|
C | T | 2 | a0001c0001t0001g0125a0001c0001t0001g0177 | 2 | HG01496.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-16+11019C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28565116 | ||||||
chr16:28565186
|
C | T | 16 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0115others(13): Show | 18 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(15): Show |
intron_variant | MODIFIER | c.-16+11089C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28565186 | ||||||
chr16:28565260
|
C | A | 1 | a0001c0001t0002g0024 | 2 | HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-16+11163C>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28565260 | ||||||
chr16:28565397
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-16+11300G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28565397 | ||||||
chr16:28565575
|
G | A | 1 | a0001c0001t0002g0092 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-16+11478G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28565575 | ||||||
chr16:28565585
|
C | T | 1 | a0001c0001t0001g0252 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-16+11488C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28565585 | ||||||
chr16:28565733
|
C | T | 4 | a0001c0001t0002g0303a0001c0002t0002g0025a0001c0002t0002g0304others(1): Show | 5 | HG00099.hp1 HG02155.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16+11636C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28565733 | ||||||
chr16:28565769
|
G | A | 1 | a0001c0001t0001g0144 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-16+11672G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28565769 | ||||||
chr16:28565995
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-16+11898C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28565995 | ||||||
chr16:28566089
|
C | T | 2 | a0001c0001t0001g0248a0001c0001t0001g0251 | 2 | HG00558.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.-16+11992C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28566089 | ||||||
chr16:28566149
|
C | T | 1 | a0001c0001t0002g0289 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-16+12052C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28566149 | ||||||
chr16:28566158
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-16+12061C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28566158 | ||||||
chr16:28566273
|
C | CA | 6 | a0001c0001t0001g0248a0001c0001t0001g0251a0001c0001t0002g0303others(3): Show | 7 | HG00099.hp1 HG00558.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.-16+12187dupA | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28566273 | |||||
chr16:28566279
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-16+12182A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28566279 | ||||||
chr16:28566610
|
T | C | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(81): Show | 101 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.-16+12513T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28566610 | ||||||
chr16:28566641
|
C | T | 8 | a0001c0001t0002g0279a0001c0002t0002g0004a0001c0002t0002g0275others(5): Show | 11 | HG01109.hp1 HG01884.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-16+12544C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28566641 | ||||||
chr16:28566813
|
G | A | 1 | a0001c0003t0002g0226 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-16+12716G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28566813 | ||||||
chr16:28566959
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-16+12862C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28566959 | ||||||
chr16:28566999
|
T | G | 18 | a0001c0001t0002g0024a0001c0001t0002g0282a0001c0001t0002g0283others(15): Show | 19 | HG01106.hp1 HG01891.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-16+12902T>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28566999 | ||||||
chr16:28567510
|
CT | C | 3 | a0001c0001t0004g0296a0001c0001t0004g0297a0001c0001t0004g0298 | 3 | HG01884.hp1 HG03486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-16+13414delT | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28567510 | ||||||
chr16:28567761
|
A | C | 31 | a0001c0001t0001g0237a0001c0001t0001g0240a0001c0002t0002g0006others(28): Show | 38 | HG00438.hp2 HG00609.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-15-13294A>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28567761 | ||||||
chr16:28568146
|
C | G | 1 | a0001c0001t0001g0149 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-15-12909C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28568146 | ||||||
chr16:28568186
|
G | A | 3 | a0001c0002t0002g0025a0001c0002t0002g0304a0001c0002t0002g0305 | 4 | HG00099.hp1 HG02155.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15-12869G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28568186 | ||||||
chr16:28568313
|
C | CA | 143 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0021others(140): Show | 161 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.-15-12718dupA | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28568313 | |||||
chr16:28568313
|
C | CAA | 7 | a0001c0001t0001g0121a0001c0001t0001g0167a0001c0001t0002g0057others(4): Show | 7 | HG01099.hp1 HG02135.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15-12719_-15-1271 others(6): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28568313 | |||||
chr16:28568313
|
CA | C | 7 | a0001c0001t0001g0020a0001c0001t0001g0128a0001c0001t0001g0133others(4): Show | 8 | HG01167.hp1 HG01243.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15-12718delA | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28568313 | |||||
chr16:28568515
|
AT | A | 16 | a0001c0003t0001g0171a0001c0003t0002g0022a0001c0003t0002g0216others(13): Show | 17 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.-15-12538delT | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28568515 | |||||
chr16:28568594
|
GT | G | 95 | a0001c0001t0001g0139a0001c0001t0002g0003a0001c0001t0002g0011others(92): Show | 102 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(99): Show |
intron_variant | MODIFIER | c.-15-12459delT | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28568594 | |||||
chr16:28568596
|
T | G | 51 | a0001c0001t0001g0121a0001c0001t0001g0237a0001c0001t0001g0240others(48): Show | 61 | HG00438.hp2 HG00609.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.-15-12459T>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28568596 | ||||||
chr16:28568597
|
G | C | 8 | a0001c0001t0002g0279a0001c0002t0002g0004a0001c0002t0002g0275others(5): Show | 11 | HG01109.hp1 HG01884.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-15-12458G>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28568597 | ||||||
chr16:28568619
|
A | C | 1 | a0001c0001t0002g0078 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-15-12436A>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28568619 | ||||||
chr16:28568710
|
C | T | 31 | a0001c0001t0001g0237a0001c0001t0001g0240a0001c0002t0002g0006others(28): Show | 38 | HG00438.hp2 HG00609.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-15-12345C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28568710 | ||||||
chr16:28568919
|
G | GA | 43 | a0001c0001t0001g0237a0001c0001t0001g0240a0001c0001t0002g0061others(40): Show | 54 | HG00099.hp1 HG00438.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-15-12124dupA | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28568919 | |||||
chr16:28568949
|
G | A | 1 | a0001c0001t0001g0145 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-15-12106G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28568949 | ||||||
chr16:28568956
|
C | T | 1 | a0001c0001t0002g0303 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-15-12099C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28568956 | ||||||
chr16:28569012
|
T | C | 143 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0237others(140): Show | 160 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.-15-12043T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28569012 | ||||||
chr16:28569123
|
T | G | 2 | a0001c0001t0002g0054a0001c0001t0002g0056 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-15-11932T>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28569123 | ||||||
chr16:28569247
|
T | C | 1 | a0001c0001t0002g0074 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-15-11808T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28569247 | ||||||
chr16:28569277
|
A | G | 5 | a0001c0001t0001g0184a0001c0001t0001g0246a0001c0001t0001g0247others(2): Show | 5 | NA18961.hp2 NA18971.hp2 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15-11778A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28569277 | ||||||
chr16:28569364
|
A | G | 57 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0053others(54): Show | 61 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.-15-11691A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28569364 | ||||||
chr16:28569393
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-15-11662C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28569393 | ||||||
chr16:28569428
|
G | A | 1 | a0001c0002t0002g0280 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-15-11627G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28569428 | ||||||
chr16:28569508
|
C | T | 80 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0024others(77): Show | 85 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.-15-11547C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28569508 | ||||||
chr16:28569562
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-15-11493G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28569562 | ||||||
chr16:28569652
|
A | G | 1 | a0001c0001t0002g0067 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-15-11403A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28569652 | ||||||
chr16:28569717
|
G | C | 57 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0053others(54): Show | 61 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.-15-11338G>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28569717 | ||||||
chr16:28569751
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-15-11304A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28569751 | ||||||
chr16:28569917
|
C | A | 1 | a0001c0001t0001g0207 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-15-11138C>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28569917 | ||||||
chr16:28570390
|
T | C | 4 | a0001c0001t0001g0013a0001c0001t0001g0131a0001c0001t0001g0138others(1): Show | 5 | NA18966.hp1 NA18991.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15-10665T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28570390 | ||||||
chr16:28570406
|
A | G | 3 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0263 | 5 | HG01074.hp2 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15-10649A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28570406 | ||||||
chr16:28570419
|
C | T | 1 | a0001c0001t0002g0303 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-15-10636C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28570419 | ||||||
chr16:28570544
|
T | TTTTA | 55 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(52): Show | 65 | HG00280.hp2 HG00544.hp2 HG00741.hp1 others(62): Show |
intron_variant | MODIFIER | c.-15-10466_-15-1046 others(8): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28570544 | |||||
chr16:28570544
|
T | TTTTATTT others(1): Show |
17 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0001g0157others(14): Show | 17 | HG00408.hp1 HG01081.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.-15-10470_-15-1046 others(12): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28570544 | |||||
chr16:28570544
|
TTTTA | T | 85 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0021others(82): Show | 91 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.-15-10466_-15-1046 others(8): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28570544 | |||||
chr16:28570544
|
TTTTATTT others(1): Show |
T | 8 | a0001c0001t0001g0122a0001c0001t0001g0135a0001c0001t0001g0158others(5): Show | 8 | HG02129.hp2 NA18906.hp1 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15-10470_-15-1046 others(12): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28570544 | |||||
chr16:28570544
|
TTTTATTT others(5): Show |
T | 18 | a0001c0001t0005g0107a0001c0001t0005g0108a0001c0003t0001g0171others(15): Show | 19 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.-15-10474_-15-1046 others(16): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28570544 | |||||
chr16:28570544
|
TTTTATTT others(9): Show |
T | 1 | a0001c0001t0001g0155 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-15-10478_-15-1046 others(20): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28570544 | |||||
chr16:28570544
|
TTTTATTT others(13): Show |
T | 33 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0237others(30): Show | 40 | HG00438.hp2 HG00609.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.-15-10482_-15-1046 others(24): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28570544 | |||||
chr16:28570780
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-15-10275G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28570780 | ||||||
chr16:28570821
|
G | T | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(128): Show | 151 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.-15-10234G>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28570821 | ||||||
chr16:28571216
|
C | T | 3 | a0001c0002t0002g0025a0001c0002t0002g0304a0001c0002t0002g0305 | 4 | HG00099.hp1 HG02155.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15-9839C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28571216 | ||||||
chr16:28571528
|
A | G | 144 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0130others(141): Show | 161 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.-15-9527A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28571528 | ||||||
chr16:28571591
|
T | TA | 32 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0001g0152others(29): Show | 33 | HG00639.hp1 HG00642.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.-15-9446dupA | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28571591 | |||||
chr16:28571591
|
T | TAA | 56 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0053others(53): Show | 64 | HG00099.hp1 HG00642.hp2 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.-15-9447_-15-9446d others(4): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28571591 | |||||
chr16:28571591
|
T | TAAA | 41 | a0001c0001t0001g0237a0001c0001t0001g0240a0001c0001t0002g0061others(38): Show | 48 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.-15-9448_-15-9446d others(5): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28571591 | |||||
chr16:28571620
|
C | A | 84 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0024others(81): Show | 90 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.-15-9435C>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28571620 | ||||||
chr16:28571685
|
C | T | 1 | a0001c0001t0002g0063 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-15-9370C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28571685 | ||||||
chr16:28571817
|
T | C | 1 | a0001c0002t0003g0034 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-15-9238T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28571817 | ||||||
chr16:28571894
|
G | A | 19 | a0001c0001t0005g0107a0001c0001t0005g0108a0001c0003t0001g0171others(16): Show | 20 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.-15-9161G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28571894 | ||||||
chr16:28571926
|
A | C | 1 | a0001c0001t0001g0206 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-15-9129A>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28571926 | ||||||
chr16:28572041
|
A | G | 84 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0024others(81): Show | 90 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.-15-9014A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28572041 | ||||||
chr16:28572268
|
G | A | 31 | a0001c0001t0001g0237a0001c0001t0001g0240a0001c0002t0002g0006others(28): Show | 38 | HG00438.hp2 HG00609.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-15-8787G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28572268 | ||||||
chr16:28572289
|
C | T | 84 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0024others(81): Show | 90 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.-15-8766C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28572289 | ||||||
chr16:28572377
|
C | A | 3 | a0001c0001t0004g0296a0001c0001t0004g0297a0001c0001t0004g0298 | 3 | HG01884.hp1 HG03486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-15-8678C>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28572377 | ||||||
chr16:28572377
|
C | T | 1 | a0001c0001t0001g0256 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-15-8678C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28572377 | ||||||
chr16:28572416
|
C | T | 2 | a0001c0001t0001g0121a0001c0001t0002g0045 | 2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-15-8639C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28572416 | ||||||
chr16:28572520
|
C | T | 1 | a0001c0003t0002g0226 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-15-8535C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28572520 | ||||||
chr16:28572544
|
C | T | 84 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0024others(81): Show | 90 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.-15-8511C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28572544 | ||||||
chr16:28572547
|
G | A | 1 | a0001c0001t0001g0158 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-15-8508G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28572547 | ||||||
chr16:28572561
|
G | A | 3 | a0001c0002t0002g0025a0001c0002t0002g0304a0001c0002t0002g0305 | 4 | HG00099.hp1 HG02155.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15-8494G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28572561 | ||||||
chr16:28572665
|
G | A | 1 | a0001c0001t0002g0085 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-15-8390G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28572665 | ||||||
chr16:28572779
|
G | A | 7 | a0001c0002t0002g0004a0001c0002t0002g0275a0001c0002t0002g0276others(4): Show | 10 | HG01109.hp1 HG01884.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-15-8276G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28572779 | ||||||
chr16:28572824
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-15-8231G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28572824 | ||||||
chr16:28572827
|
G | T | 3 | a0001c0002t0002g0025a0001c0002t0002g0304a0001c0002t0002g0305 | 4 | HG00099.hp1 HG02155.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15-8228G>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28572827 | ||||||
chr16:28572869
|
T | C | 1 | a0001c0001t0002g0104 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-15-8186T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28572869 | ||||||
chr16:28572870
|
T | C | 1 | a0001c0001t0001g0206 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-15-8185T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28572870 | ||||||
chr16:28572891
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-15-8164A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28572891 | ||||||
chr16:28572912
|
C | T | 8 | a0001c0001t0002g0060a0001c0001t0002g0065a0001c0001t0002g0075others(5): Show | 8 | HG02015.hp1 HG02129.hp2 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15-8143C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28572912 | ||||||
chr16:28573057
|
A | G | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0120 | 3 | HG01891.hp2 HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-15-7998A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28573057 | ||||||
chr16:28573212
|
G | A | 1 | a0001c0001t0002g0299 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-15-7843G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28573212 | ||||||
chr16:28573241
|
C | G | 7 | a0001c0002t0002g0004a0001c0002t0002g0275a0001c0002t0002g0276others(4): Show | 10 | HG01109.hp1 HG01884.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-15-7814C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28573241 | ||||||
chr16:28573357
|
G | A | 1 | a0001c0001t0004g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-15-7698G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28573357 | ||||||
chr16:28573616
|
G | A | 17 | a0001c0003t0001g0171a0001c0003t0002g0022a0001c0003t0002g0216others(14): Show | 18 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.-15-7439G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28573616 | ||||||
chr16:28573724
|
A | G | 3 | a0001c0001t0002g0292a0001c0001t0002g0302a0001c0001t0002g0306 | 3 | HG02258.hp1 HG02922.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-15-7331A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28573724 | ||||||
chr16:28573898
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-15-7157C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28573898 | ||||||
chr16:28574300
|
T | C | 31 | a0001c0001t0001g0237a0001c0001t0001g0240a0001c0002t0002g0006others(28): Show | 38 | HG00438.hp2 HG00609.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-15-6755T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28574300 | ||||||
chr16:28574315
|
C | T | 79 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0053others(76): Show | 84 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.-15-6740C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28574315 | ||||||
chr16:28574376
|
G | C | 1 | a0001c0001t0001g0170 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-15-6679G>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28574376 | ||||||
chr16:28574474
|
G | A | 1 | a0001c0001t0002g0303 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-15-6581G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28574474 | ||||||
chr16:28574500
|
A | G | 3 | a0001c0003t0002g0216a0001c0003t0002g0217a0001c0003t0002g0218 | 3 | HG02109.hp1 HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-15-6555A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28574500 | ||||||
chr16:28574611
|
T | C | 8 | a0001c0001t0002g0303a0001c0002t0002g0004a0001c0002t0002g0275others(5): Show | 11 | HG01109.hp1 HG01884.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-15-6444T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28574611 | ||||||
chr16:28574683
|
G | A | 1 | a0001c0002t0003g0038 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-15-6372G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28574683 | ||||||
chr16:28574735
|
T | G | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-15-6320T>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28574735 | ||||||
chr16:28574784
|
G | C | 3 | a0001c0002t0002g0025a0001c0002t0002g0304a0001c0002t0002g0305 | 4 | HG00099.hp1 HG02155.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15-6271G>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28574784 | ||||||
chr16:28574806
|
T | C | 81 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0024others(78): Show | 86 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.-15-6249T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28574806 | ||||||
chr16:28575546
|
T | C | 2 | a0001c0001t0002g0282a0001c0001t0002g0283 | 2 | HG01891.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-15-5509T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28575546 | ||||||
chr16:28575652
|
T | C | 1 | a0001c0002t0002g0041 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-15-5403T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28575652 | ||||||
chr16:28575844
|
C | T | 3 | a0001c0001t0002g0077a0001c0001t0002g0084a0001c0001t0002g0099 | 3 | HG01168.hp1 HG01169.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-15-5211C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28575844 | ||||||
chr16:28575994
|
T | C | 3 | a0001c0001t0001g0146a0001c0001t0001g0193a0001c0001t0001g0203 | 3 | HG01070.hp1 HG01109.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.-15-5061T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28575994 | ||||||
chr16:28576068
|
T | C | 84 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0024others(81): Show | 90 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.-15-4987T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28576068 | ||||||
chr16:28576070
|
G | A | 1 | a0001c0001t0002g0279 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-15-4985G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28576070 | ||||||
chr16:28576163
|
TA | T | 18 | a0001c0001t0002g0024a0001c0001t0002g0282a0001c0001t0002g0283others(15): Show | 19 | HG01106.hp1 HG01891.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-15-4884delA | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28576163 | |||||
chr16:28576276
|
G | T | 81 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0024others(78): Show | 86 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.-15-4779G>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28576276 | ||||||
chr16:28576277
|
C | T | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-15-4778C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28576277 | ||||||
chr16:28576327
|
A | T | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-15-4728A>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28576327 | ||||||
chr16:28576346
|
A | T | 18 | a0001c0001t0002g0024a0001c0001t0002g0282a0001c0001t0002g0283others(15): Show | 19 | HG01106.hp1 HG01891.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-15-4709A>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28576346 | ||||||
chr16:28576470
|
G | T | 1 | a0001c0001t0001g0148 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-15-4585G>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28576470 | ||||||
chr16:28576728
|
A | C | 81 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0024others(78): Show | 86 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.-15-4327A>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28576728 | ||||||
chr16:28576738
|
C | G | 11 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0156others(8): Show | 13 | HG02698.hp1 HG02738.hp1 HG03017.hp1 others(10): Show |
intron_variant | MODIFIER | c.-15-4317C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28576738 | ||||||
chr16:28576795
|
C | T | 2 | a0001c0001t0001g0121a0001c0001t0002g0045 | 2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-15-4260C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28576795 | ||||||
chr16:28576995
|
G | A | 2 | a0001c0001t0001g0172a0001c0001t0001g0201 | 2 | HG06807.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-15-4060G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28576995 | ||||||
chr16:28577073
|
C | G | 1 | a0001c0001t0001g0209 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-15-3982C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28577073 | ||||||
chr16:28577074
|
A | C | 81 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0024others(78): Show | 86 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.-15-3981A>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28577074 | ||||||
chr16:28577107
|
G | A | 5 | a0001c0001t0001g0021a0001c0001t0001g0209a0001c0001t0001g0210others(2): Show | 6 | HG02895.hp2 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-3948G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28577107 | ||||||
chr16:28577122
|
C | T | 84 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0024others(81): Show | 90 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.-15-3933C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28577122 | ||||||
chr16:28577350
|
C | CA | 9 | a0001c0001t0002g0060a0001c0001t0002g0065a0001c0001t0002g0075others(6): Show | 9 | HG02015.hp1 HG02055.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.-15-3693dupA | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28577350 | |||||
chr16:28577414
|
C | A | 1 | a0001c0001t0001g0206 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-15-3641C>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28577414 | ||||||
chr16:28577662
|
A | C | 1 | a0001c0001t0001g0209 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-15-3393A>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28577662 | ||||||
chr16:28577759
|
A | C | 1 | a0001c0001t0001g0165 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-15-3296A>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28577759 | ||||||
chr16:28577846
|
T | G | 1 | a0001c0001t0002g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-15-3209T>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28577846 | ||||||
chr16:28578052
|
G | T | 1 | a0001c0001t0001g0149 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-15-3003G>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28578052 | ||||||
chr16:28578078
|
C | A | 1 | a0001c0001t0001g0151 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-15-2977C>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28578078 | ||||||
chr16:28578134
|
G | A | 80 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0024others(77): Show | 85 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.-15-2921G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28578134 | ||||||
chr16:28578331
|
C | T | 4 | a0001c0001t0001g0156a0001c0001t0001g0180a0001c0001t0001g0182others(1): Show | 4 | HG02698.hp1 HG03017.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15-2724C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28578331 | ||||||
chr16:28578398
|
A | G | 16 | a0001c0003t0001g0171a0001c0003t0002g0022a0001c0003t0002g0216others(13): Show | 17 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.-15-2657A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28578398 | ||||||
chr16:28578637
|
G | A | 1 | a0001c0002t0002g0275 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-15-2418G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28578637 | ||||||
chr16:28578684
|
TA | T | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(277): Show | 318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.-15-2353delA | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28578684 | |||||
chr16:28578684
|
TAA | T | 16 | a0001c0001t0001g0114a0001c0001t0001g0125a0001c0001t0001g0153others(13): Show | 16 | HG01070.hp2 HG01168.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.-15-2354_-15-2353d others(4): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28578684 | |||||
chr16:28578688
|
A | G | 7 | a0001c0002t0002g0004a0001c0002t0002g0275a0001c0002t0002g0276others(4): Show | 10 | HG01109.hp1 HG01884.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-15-2367A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28578688 | ||||||
chr16:28578709
|
G | A | 84 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0024others(81): Show | 90 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.-15-2346G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28578709 | ||||||
chr16:28578786
|
C | G | 2 | a0001c0002t0002g0035a0001c0002t0002g0039 | 2 | HG02132.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.-15-2269C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28578786 | ||||||
chr16:28578836
|
G | A | 3 | a0001c0003t0002g0219a0001c0003t0002g0221a0001c0003t0002g0228 | 3 | HG00642.hp1 HG03669.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-15-2219G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28578836 | ||||||
chr16:28579087
|
T | A | 1 | a0001c0002t0003g0029 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-15-1968T>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28579087 | ||||||
chr16:28579197
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-15-1858C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28579197 | ||||||
chr16:28579257
|
C | CT | 11 | a0001c0001t0001g0122a0001c0001t0001g0180a0001c0001t0001g0198others(8): Show | 11 | HG01175.hp2 HG01978.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.-15-1779dupT | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28579257 | |||||
chr16:28579257
|
CT | C | 7 | a0001c0001t0001g0018a0001c0001t0001g0142a0001c0001t0001g0256others(4): Show | 8 | HG00741.hp2 HG01081.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.-15-1779delT | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28579257 | |||||
chr16:28579259
|
T | C | 1 | a0001c0005t0002g0286 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-15-1796T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28579259 | ||||||
chr16:28579272
|
T | G | 1 | a0001c0005t0002g0286 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-15-1783T>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28579272 | ||||||
chr16:28579281
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-15-1774C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28579281 | ||||||
chr16:28579508
|
G | A | 1 | a0001c0001t0002g0069 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-15-1547G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28579508 | ||||||
chr16:28579541
|
C | T | 84 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0024others(81): Show | 90 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.-15-1514C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28579541 | ||||||
chr16:28579657
|
G | A | 31 | a0001c0001t0001g0237a0001c0001t0001g0240a0001c0002t0002g0006others(28): Show | 38 | HG00438.hp2 HG00609.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-15-1398G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28579657 | ||||||
chr16:28579668
|
C | T | 57 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0053others(54): Show | 61 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.-15-1387C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28579668 | ||||||
chr16:28579887
|
C | T | 6 | a0001c0001t0002g0063a0001c0001t0002g0072a0001c0001t0002g0089others(3): Show | 6 | HG02135.hp1 HG02523.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15-1168C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28579887 | ||||||
chr16:28580091
|
A | G | 1 | a0001c0002t0002g0278 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-15-964A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28580091 | ||||||
chr16:28580119
|
G | A | 1 | a0001c0006t0002g0106 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-15-936G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28580119 | ||||||
chr16:28580209
|
G | A | 55 | a0001c0001t0001g0237a0001c0001t0001g0240a0001c0002t0002g0004others(52): Show | 66 | HG00438.hp2 HG00609.hp1 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.-15-846G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28580209 | ||||||
chr16:28580258
|
G | A | 31 | a0001c0001t0001g0237a0001c0001t0001g0240a0001c0002t0002g0006others(28): Show | 38 | HG00438.hp2 HG00609.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-15-797G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28580258 | ||||||
chr16:28580425
|
C | G | 1 | a0001c0001t0002g0300 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-15-630C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28580425 | ||||||
chr16:28580434
|
G | A | 31 | a0001c0001t0001g0237a0001c0001t0001g0240a0001c0002t0002g0006others(28): Show | 38 | HG00438.hp2 HG00609.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-15-621G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28580434 | ||||||
chr16:28580438
|
G | A | 2 | a0001c0001t0001g0209a0001c0001t0007g0208 | 2 | HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-15-617G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28580438 | ||||||
chr16:28580446
|
G | A | 3 | a0001c0002t0002g0025a0001c0002t0002g0304a0001c0002t0002g0305 | 4 | HG00099.hp1 HG02155.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15-609G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28580446 | ||||||
chr16:28580510
|
T | TC | 31 | a0001c0001t0001g0237a0001c0001t0001g0240a0001c0002t0002g0006others(28): Show | 38 | HG00438.hp2 HG00609.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-15-543dupC | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28580510 | |||||
chr16:28580523
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-15-532G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28580523 | ||||||
chr16:28580664
|
A | G | 1 | a0001c0006t0002g0106 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-15-391A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28580664 | ||||||
chr16:28580785
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-15-270G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28580785 | ||||||
chr16:28580806
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15-249C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28580806 | ||||||
chr16:28581377
|
A | T | 1 | a0001c0001t0002g0095 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.75+233A>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28581377 | ||||||
chr16:28581386
|
A | G | 1 | a0001c0001t0001g0242 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.75+242A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28581386 | ||||||
chr16:28581388
|
C | T | 2 | a0001c0001t0001g0115a0001c0001t0001g0167 | 2 | HG00544.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.75+244C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28581388 | ||||||
chr16:28581523
|
C | G | 1 | a0001c0001t0002g0288 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.75+379C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28581523 | ||||||
chr16:28581568
|
C | T | 7 | a0001c0001t0001g0235a0001c0001t0001g0239a0001c0001t0001g0243others(4): Show | 7 | HG01358.hp2 HG02074.hp1 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+424C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28581568 | ||||||
chr16:28581599
|
G | A | 1 | a0001c0001t0001g0149 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.75+455G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28581599 | ||||||
chr16:28581617
|
C | G | 305 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(302): Show | 345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.75+473C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28581617 | ||||||
chr16:28581621
|
T | C | 305 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(302): Show | 345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.75+477T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28581621 | ||||||
chr16:28581626
|
C | G | 3 | a0001c0001t0001g0135a0001c0001t0001g0158a0001c0001t0001g0214 | 3 | NA18942.hp2 NA18955.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.75+482C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28581626 | ||||||
chr16:28581630
|
G | T | 1 | a0001c0001t0001g0121 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.75+486G>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28581630 | ||||||
chr16:28581810
|
T | G | 31 | a0001c0001t0001g0237a0001c0001t0001g0240a0001c0002t0002g0006others(28): Show | 38 | HG00438.hp2 HG00609.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.75+666T>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28581810 | ||||||
chr16:28581876
|
G | A | 1 | a0001c0001t0001g0186 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.75+732G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28581876 | ||||||
chr16:28581918
|
C | CA | 81 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0024others(78): Show | 87 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.75+787dupA | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 28581918 | |||||
chr16:28581995
|
T | C | 7 | a0001c0002t0002g0004a0001c0002t0002g0275a0001c0002t0002g0276others(4): Show | 10 | HG01109.hp1 HG01884.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.75+851T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28581995 | ||||||
chr16:28582026
|
T | C | 84 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0024others(81): Show | 90 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.75+882T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28582026 | ||||||
chr16:28582027
|
G | A | 18 | a0001c0001t0002g0024a0001c0001t0002g0282a0001c0001t0002g0283others(15): Show | 19 | HG01106.hp1 HG01891.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.75+883G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28582027 | ||||||
chr16:28582172
|
A | G | 3 | a0001c0001t0001g0135a0001c0001t0001g0158a0001c0001t0001g0214 | 3 | NA18942.hp2 NA18955.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.75+1028A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28582172 | ||||||
chr16:28582276
|
G | A | 81 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0024others(78): Show | 86 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.75+1132G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28582276 | ||||||
chr16:28582295
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.75+1151C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28582295 | ||||||
chr16:28582373
|
C | T | 2 | a0001c0001t0005g0107a0001c0001t0005g0108 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.75+1229C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28582373 | ||||||
chr16:28582376
|
T | C | 1 | a0001c0001t0001g0122 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.75+1232T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28582376 | ||||||
chr16:28582379
|
T | TG | 80 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0024others(77): Show | 85 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.75+1241dupG | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 28582379 | |||||
chr16:28582380
|
G | T | 2 | a0001c0001t0001g0267a0001c0001t0001g0268 | 2 | HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.75+1236G>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28582380 | ||||||
chr16:28582681
|
T | C | 3 | a0001c0001t0004g0296a0001c0001t0004g0297a0001c0001t0004g0298 | 3 | HG01884.hp1 HG03486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.75+1537T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28582681 | ||||||
chr16:28582900
|
A | C | 1 | a0001c0001t0002g0299 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.75+1756A>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28582900 | ||||||
chr16:28582914
|
G | A | 3 | a0001c0001t0001g0146a0001c0001t0001g0193a0001c0001t0001g0203 | 3 | HG01070.hp1 HG01109.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.75+1770G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28582914 | ||||||
chr16:28582916
|
CAA | C | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0120 | 3 | HG01891.hp2 HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.75+1773_75+1774del others(2): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28582916 | ||||||
chr16:28583023
|
A | G | 7 | a0001c0001t0001g0017a0001c0001t0001g0115a0001c0001t0001g0136others(4): Show | 8 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+1879A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28583023 | ||||||
chr16:28583107
|
C | T | 2 | a0001c0001t0002g0292a0001c0001t0002g0306 | 2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.76-1806C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28583107 | ||||||
chr16:28583228
|
A | G | 84 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0024others(81): Show | 90 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.76-1685A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28583228 | ||||||
chr16:28583362
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.76-1551G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28583362 | ||||||
chr16:28583390
|
C | G | 2 | a0001c0001t0005g0107a0001c0001t0005g0108 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.76-1523C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28583390 | ||||||
chr16:28583390
|
C | T | 16 | a0001c0003t0001g0171a0001c0003t0002g0022a0001c0003t0002g0216others(13): Show | 17 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.76-1523C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28583390 | ||||||
chr16:28583443
|
A | G | 2 | a0001c0001t0005g0107a0001c0001t0005g0108 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.76-1470A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28583443 | ||||||
chr16:28584028
|
C | CT | 7 | a0001c0002t0002g0004a0001c0002t0002g0276a0001c0002t0002g0277others(4): Show | 10 | HG01109.hp1 HG01884.hp2 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.76-869dupT | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 28584028 | |||||
chr16:28584028
|
CT | C | 10 | a0001c0001t0001g0131a0001c0001t0001g0161a0001c0001t0001g0175others(7): Show | 10 | HG01169.hp1 HG01515.hp1 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.76-869delT | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 28584028 | |||||
chr16:28584101
|
C | A | 1 | a0001c0001t0001g0207 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.76-812C>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28584101 | ||||||
chr16:28584133
|
C | T | 1 | a0001c0002t0003g0032 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.76-780C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28584133 | ||||||
chr16:28584188
|
A | G | 1 | a0001c0001t0001g0206 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.76-725A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28584188 | ||||||
chr16:28584379
|
A | G | 84 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0024others(81): Show | 90 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.76-534A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28584379 | ||||||
chr16:28584382
|
C | T | 1 | a0001c0003t0002g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.76-531C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28584382 | ||||||
chr16:28584489
|
C | G | 84 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0024others(81): Show | 90 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.76-424C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28584489 | ||||||
chr16:28584515
|
C | T | 1 | a0001c0006t0002g0106 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.76-398C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28584515 | ||||||
chr16:28584616
|
C | T | 2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.76-297C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28584616 | ||||||
chr16:28584621
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.76-292C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28584621 | ||||||
chr16:28584668
|
A | G | 4 | a0001c0001t0001g0123a0001c0001t0001g0147a0001c0001t0001g0169others(1): Show | 4 | HG02602.hp1 HG02683.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-245A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28584668 | ||||||
chr16:28584788
|
CA | C | 52 | a0001c0001t0001g0211a0001c0001t0001g0234a0001c0001t0002g0003others(49): Show | 56 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.76-106delA | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 28584788 | |||||
chr16:28584788
|
CAA | C | 29 | a0001c0001t0002g0024a0001c0001t0002g0056a0001c0001t0002g0060others(26): Show | 30 | HG01070.hp2 HG01106.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.76-107_76-106delAA | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 28584788 | |||||
chr16:28585053
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.151+65G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 3/9 | chr16 | 28585053 | ||||||
chr16:28585383
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.152-265G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 3/9 | chr16 | 28585383 | ||||||
chr16:28585409
|
A | T | 5 | a0001c0002t0002g0004a0001c0002t0002g0276a0001c0002t0002g0277others(2): Show | 8 | HG01109.hp1 HG01884.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.152-239A>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 3/9 | chr16 | 28585409 | ||||||
chr16:28585563
|
G | A | 17 | a0001c0003t0001g0171a0001c0003t0002g0022a0001c0003t0002g0216others(14): Show | 18 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.152-85G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 3/9 | chr16 | 28585563 | ||||||
chr16:28585765
|
G | A | 1 | a0001c0001t0002g0053 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.224+45G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28585765 | ||||||
chr16:28585775
|
T | G | 1 | a0001c0001t0002g0069 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.224+55T>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28585775 | ||||||
chr16:28585847
|
T | A | 2 | a0001c0001t0001g0195a0001c0001t0001g0201 | 2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.224+127T>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28585847 | ||||||
chr16:28585848
|
C | A | 2 | a0001c0001t0001g0195a0001c0001t0001g0201 | 2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.224+128C>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28585848 | ||||||
chr16:28585944
|
A | G | 5 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(2): Show | 5 | HG01891.hp2 HG03225.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.224+224A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28585944 | ||||||
chr16:28586506
|
C | CA | 6 | a0001c0001t0001g0144a0001c0001t0001g0229a0001c0001t0001g0241others(3): Show | 6 | HG02056.hp1 NA18950.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.224+802dupA | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr16 | 28586506 | |||||
chr16:28586506
|
CA | C | 32 | a0001c0001t0001g0191a0001c0002t0002g0006a0001c0002t0002g0008others(29): Show | 40 | HG00099.hp1 HG00609.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.224+802delA | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr16 | 28586506 | |||||
chr16:28586618
|
C | G | 1 | a0001c0001t0001g0130 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.224+898C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28586618 | ||||||
chr16:28586653
|
T | G | 1 | a0001c0002t0002g0275 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.224+933T>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28586653 | ||||||
chr16:28587011
|
T | G | 1 | a0001c0002t0002g0305 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.224+1291T>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28587011 | ||||||
chr16:28587083
|
C | G | 2 | a0001c0001t0005g0107a0001c0001t0005g0108 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.224+1363C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28587083 | ||||||
chr16:28587657
|
T | C | 1 | a0001c0001t0001g0145 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.225-1443T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28587657 | ||||||
chr16:28587749
|
C | T | 3 | a0001c0001t0004g0296a0001c0001t0004g0297a0001c0001t0004g0298 | 3 | HG01884.hp1 HG03486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.225-1351C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28587749 | ||||||
chr16:28587799
|
G | A | 2 | a0001c0001t0005g0107a0001c0001t0005g0108 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.225-1301G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28587799 | ||||||
chr16:28587878
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.225-1222C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28587878 | ||||||
chr16:28587949
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.225-1151G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28587949 | ||||||
chr16:28588090
|
A | G | 84 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0024others(81): Show | 90 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.225-1010A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28588090 | ||||||
chr16:28588639
|
A | G | 1 | a0001c0001t0002g0082 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.225-461A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28588639 | ||||||
chr16:28588681
|
C | CA | 37 | a0001c0002t0002g0004a0001c0002t0002g0006a0001c0002t0002g0008others(34): Show | 47 | HG00609.hp1 HG00735.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.225-418dupA | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr16 | 28588681 | |||||
chr16:28588695
|
G | C | 7 | a0001c0002t0002g0004a0001c0002t0002g0275a0001c0002t0002g0276others(4): Show | 10 | HG01109.hp1 HG01884.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.225-405G>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28588695 | ||||||
chr16:28588700
|
G | A | 2 | a0001c0001t0001g0123a0001c0001t0001g0169 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.225-400G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28588700 | ||||||
chr16:28588720
|
G | A | 7 | a0001c0002t0002g0004a0001c0002t0002g0275a0001c0002t0002g0276others(4): Show | 10 | HG01109.hp1 HG01884.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.225-380G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28588720 | ||||||
chr16:28588770
|
C | T | 80 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0024others(77): Show | 85 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.225-330C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28588770 | ||||||
chr16:28588880
|
G | GT | 83 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0024others(80): Show | 89 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.225-217dupT | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr16 | 28588880 | |||||
chr16:28588956
|
C | T | 37 | a0001c0002t0002g0004a0001c0002t0002g0006a0001c0002t0002g0008others(34): Show | 47 | HG00609.hp1 HG00735.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.225-144C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28588956 | ||||||
chr16:28588961
|
G | T | 9 | a0001c0003t0001g0171a0001c0003t0002g0022a0001c0003t0002g0220others(6): Show | 10 | HG00738.hp2 HG01106.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.225-139G>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28588961 | ||||||
chr16:28589060
|
C | T | 18 | a0001c0001t0002g0024a0001c0001t0002g0282a0001c0001t0002g0283others(15): Show | 19 | HG01106.hp1 HG01891.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.225-40C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28589060 | ||||||
chr16:28589061
|
G | A | 1 | a0001c0001t0001g0235 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.225-39G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28589061 | ||||||
chr16:28589067
|
C | G | 1 | a0001c0001t0001g0273 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.225-33C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28589067 | ||||||
chr16:28589194
|
C | G | 1 | a0001c0002t0003g0031 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.289+30C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 5/9 | chr16 | 28589194 | ||||||
chr16:28589222
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.289+58C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 5/9 | chr16 | 28589222 | ||||||
chr16:28589351
|
G | A | 1 | a0001c0002t0002g0280 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.289+187G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 5/9 | chr16 | 28589351 | ||||||
chr16:28589436
|
C | T | 2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.289+272C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 5/9 | chr16 | 28589436 | ||||||
chr16:28589483
|
T | C | 1 | a0001c0002t0002g0049 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.289+319T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 5/9 | chr16 | 28589483 | ||||||
chr16:28589699
|
G | T | 1 | a0001c0001t0002g0303 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.290-397G>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 5/9 | chr16 | 28589699 | ||||||
chr16:28589865
|
G | C | 17 | a0001c0003t0001g0171a0001c0003t0002g0022a0001c0003t0002g0216others(14): Show | 18 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.290-231G>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 5/9 | chr16 | 28589865 | ||||||
chr16:28589935
|
G | A | 1 | a0001c0001t0002g0085 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.290-161G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 5/9 | chr16 | 28589935 | ||||||
chr16:28590242
|
C | T | 1 | a0001c0001t0001g0260 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.419+17C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 6/9 | chr16 | 28590242 | ||||||
chr16:28590278
|
C | T | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.420-18C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 6/9 | chr16 | 28590278 | ||||||
chr16:28590481
|
G | A | 36 | a0001c0002t0002g0004a0001c0002t0002g0006a0001c0002t0002g0008others(33): Show | 46 | HG00609.hp1 HG00735.hp1 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.566+39G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 7/9 | chr16 | 28590481 | ||||||
chr16:28590491
|
G | A | 3 | a0001c0002t0002g0025a0001c0002t0002g0304a0001c0002t0002g0305 | 4 | HG00099.hp1 HG02155.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.566+49G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 7/9 | chr16 | 28590491 | ||||||
chr16:28591128
|
T | G | 30 | a0001c0002t0002g0006a0001c0002t0002g0008a0001c0002t0002g0009others(27): Show | 37 | HG00609.hp1 HG00735.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.765+193T>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 9/9 | chr16 | 28591128 | ||||||
chr16:28591162
|
G | C | 3 | a0001c0002t0002g0025a0001c0002t0002g0304a0001c0002t0002g0305 | 4 | HG00099.hp1 HG02155.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.765+227G>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 9/9 | chr16 | 28591162 | ||||||
chr16:28591366
|
C | G | 1 | a0001c0001t0001g0206 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.766-224C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 9/9 | chr16 | 28591366 | ||||||
chr16:28591367
|
C | T | 1 | a0001c0006t0002g0106 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.766-223C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 9/9 | chr16 | 28591367 | ||||||
chr16:28591429
|
A | T | 1 | a0001c0001t0001g0130 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.766-161A>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 9/9 | chr16 | 28591429 | ||||||
chr16:28591518
|
G | C | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.766-72G>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 9/9 | chr16 | 28591518 |