geneid | 2356 |
---|---|
ensemblid | ENSG00000136877.15 |
hgncid | 3824 |
symbol | FPGS |
name | folylpolyglutamate synthase |
refseq_nuc | NM_004957.6 |
refseq_prot | NP_004948.4 |
ensembl_nuc | ENST00000373247.7 |
ensembl_prot | ENSP00000362344.2 |
mane_status | MANE Select |
chr | chr9 |
start | 127802882 |
end | 127814081 |
strand | + |
ver | v1.2 |
region | chr9:127802882-127814081 |
region5000 | chr9:127797882-127819081 |
regionname0 | FPGS_chr9_127802882_127814081 |
regionname5000 | FPGS_chr9_127797882_127819081 |
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 | 0/1 | 587 | 340 | 81 | 50 | 174 | 5 | 29 | 128 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
a0002 | 1/0 | 587 | 58 | 13 | 16 | 6 | 7 | 15 | 6 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
a0003 | 0/0 | 587 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
a0004 | 0/0 | 587 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
a0005 | 0/0 | 587 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
a0006 | 0/0 | 568 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
a0007 | 0/0 | 587 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1764 | 306 | 57 | 50 | 170 | 5 | 23 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
c0002 | 1/0 | 1764 | 58 | 13 | 16 | 6 | 7 | 15 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
c0003 | 0/0 | 1764 | 26 | 22 | 0 | 1 | 0 | 3 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
c0004 | 0/0 | 1764 | 2 | 0 | 2 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
c0005 | 0/0 | 1764 | 2 | 0 | 0 | 0 | 0 | 2 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
c0006 | 0/0 | 1764 | 2 | 0 | 2 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
c0007 | 0/0 | 1764 | 2 | 0 | 0 | 2 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
c0008 | 0/0 | 1764 | 2 | 0 | 0 | 2 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
c0009 | 0/0 | 1764 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
c0010 | 0/0 | 1795 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
c0011 | 0/0 | 1764 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
c0012 | 0/0 | 1764 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
c0013 | 0/0 | 1764 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
c0014 | 0/0 | 1764 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
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 | 0/0 | 521 | 194 | 26 | 40 | 113 | 4 | 11 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
t0002 | 1/1 | 521 | 183 | 47 | 31 | 68 | 8 | 27 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
t0003 | 0/0 | 519 | 25 | 21 | 0 | 1 | 0 | 3 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
t0004 | 0/0 | 521 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
t0005 | 0/0 | 521 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
t0006 | 0/0 | 521 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
t0007 | 0/0 | 521 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
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 | 96 | 3 | 29 | 53 | 3 | 8 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0002 | 0/0 | 73 | 14 | 7 | 41 | 1 | 10 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0003 | 0/0 | 38 | 8 | 13 | 5 | 2 | 10 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0004 | 0/0 | 13 | 0 | 0 | 13 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0005 | 0/0 | 10 | 7 | 0 | 1 | 0 | 2 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0006 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0009 | 0/0 | 5 | 1 | 0 | 4 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0010 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0012 | 0/1 | 4 | 0 | 3 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0013 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0017 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0018 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0019 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0029 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1764 | 306 | 57 | 50 | 170 | 5 | 23 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
a0001c0003 | 0/0 | 1764 | 26 | 22 | 0 | 1 | 0 | 3 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
a0001c0005 | 0/0 | 1764 | 2 | 0 | 0 | 0 | 0 | 2 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
a0001c0008 | 0/0 | 1764 | 2 | 0 | 0 | 2 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
a0001c0011 | 0/0 | 1764 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
a0001c0012 | 0/0 | 1764 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
a0001c0013 | 0/0 | 1764 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
a0001c0014 | 0/0 | 1764 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
a0002c0002 | 1/0 | 1764 | 58 | 13 | 16 | 6 | 7 | 15 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
a0003c0006 | 0/0 | 1764 | 2 | 0 | 2 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
a0004c0004 | 0/0 | 1764 | 2 | 0 | 2 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
a0005c0007 | 0/0 | 1764 | 2 | 0 | 0 | 2 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
a0006c0010 | 0/0 | 1795 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
a0007c0009 | 0/0 | 1764 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2284 | 183 | 23 | 37 | 109 | 3 | 11 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
a0001c0001t0002 | 0/1 | 2284 | 120 | 33 | 12 | 61 | 2 | 11 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
a0001c0001t0003 | 0/0 | 2282 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
a0001c0001t0004 | 0/0 | 2284 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
a0001c0001t0006 | 0/0 | 2284 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
a0001c0003t0001 | 0/0 | 2284 | 2 | 2 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
a0001c0003t0003 | 0/0 | 2282 | 24 | 20 | 0 | 1 | 0 | 3 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
a0001c0005t0002 | 0/0 | 2284 | 2 | 0 | 0 | 0 | 0 | 2 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
a0001c0008t0001 | 0/0 | 2284 | 2 | 0 | 0 | 2 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
a0001c0011t0002 | 0/0 | 2284 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
a0001c0012t0002 | 0/0 | 2284 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
a0001c0013t0001 | 0/0 | 2284 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
a0001c0014t0002 | 0/0 | 2284 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
a0002c0002t0001 | 0/0 | 2284 | 1 | 0 | 0 | 0 | 1 | 0 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
a0002c0002t0002 | 1/0 | 2284 | 55 | 13 | 16 | 6 | 6 | 13 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
a0002c0002t0005 | 0/0 | 2284 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
a0002c0002t0007 | 0/0 | 2284 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
a0003c0006t0001 | 0/0 | 2284 | 2 | 0 | 2 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
a0004c0004t0002 | 0/0 | 2284 | 2 | 0 | 2 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
a0005c0007t0001 | 0/0 | 2284 | 2 | 0 | 0 | 2 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
a0006c0010t0001 | 0/0 | 2315 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
a0007c0009t0002 | 0/0 | 2284 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | copy fasta | chr9 | 127797882 | 127819081 |
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 | 91 | 3 | 27 | 51 | 3 | 7 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0004 | 0/0 | 13 | 0 | 0 | 13 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0006 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0010 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0013 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0002g0002 | 0/0 | 70 | 14 | 7 | 40 | 1 | 8 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0002g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0002g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0002g0009 | 0/0 | 5 | 1 | 0 | 4 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0002g0012 | 0/1 | 4 | 0 | 3 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0004g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0001t0006g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0003t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0003t0003g0005 | 0/0 | 10 | 7 | 0 | 1 | 0 | 2 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0003t0003g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0003t0003g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0003t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0003t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0003t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0003t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0003t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0003t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0003t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0003t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0005t0002g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0008t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0011t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0012t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0013t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0001c0014t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0002c0002t0002g0003 | 0/0 | 33 | 8 | 10 | 5 | 2 | 8 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0002c0002t0002g0019 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0002c0002t0002g0029 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0002c0002t0002g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0002c0002t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0002c0002t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0002c0002t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0002c0002t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0002c0002t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0002c0002t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0002c0002t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0002c0002t0005g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0002c0002t0007g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0003c0006t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0003c0006t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0004c0004t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0005c0007t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0006c0010t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
a0007c0009t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG00099 | hp2 | a0002 | c0002 | t0002 | g0029 | EUR | GBR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG00140 | hp1 | a0002 | c0002 | t0002 | g0090 | EUR | GBR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG00140 | hp2 | a0002 | c0002 | t0002 | g0095 | EUR | GBR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG00323 | hp2 | a0002 | c0002 | t0002 | g0003 | EUR | FIN | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG00408 | hp2 | a0005 | c0007 | t0001 | g0001 | EAS | CHS | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | CHS | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG00544 | hp1 | a0001 | c0008 | t0001 | g0026 | EAS | CHS | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | CHS | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG00639 | hp1 | a0002 | c0002 | t0002 | g0030 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG00642 | hp1 | a0007 | c0009 | t0002 | g0089 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG00738 | hp1 | a0006 | c0010 | t0001 | g0068 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG00738 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01070 | hp1 | a0004 | c0004 | t0002 | g0003 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01071 | hp1 | a0004 | c0004 | t0002 | g0003 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01081 | hp2 | a0002 | c0002 | t0002 | g0096 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01106 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0120 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01167 | hp2 | a0002 | c0002 | t0002 | g0091 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01169 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01192 | hp1 | a0001 | c0001 | t0006 | g0001 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01243 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01255 | hp1 | a0003 | c0006 | t0001 | g0001 | AMR | CLM | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01256 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | CLM | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01346 | hp2 | a0002 | c0002 | t0002 | g0030 | AMR | CLM | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01433 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | CLM | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01433 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | CLM | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0034 | EUR | IBS | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01884 | hp1 | a0001 | c0013 | t0001 | g0051 | AFR | ACB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01884 | hp2 | a0002 | c0002 | t0002 | g0003 | AFR | ACB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01928 | hp1 | a0003 | c0006 | t0001 | g0018 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01952 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01975 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01993 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02056 | hp2 | a0005 | c0007 | t0001 | g0001 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02080 | hp2 | a0001 | c0003 | t0003 | g0005 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02145 | hp1 | a0002 | c0002 | t0002 | g0003 | AFR | ACB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02148 | hp1 | a0002 | c0002 | t0002 | g0103 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CDX | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02257 | hp2 | a0002 | c0002 | t0002 | g0003 | AFR | ACB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02258 | hp1 | a0001 | c0003 | t0003 | g0045 | AFR | ACB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02258 | hp2 | a0001 | c0003 | t0003 | g0015 | AFR | ACB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02280 | hp1 | a0001 | c0003 | t0003 | g0005 | AFR | ACB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02280 | hp2 | a0001 | c0003 | t0003 | g0014 | AFR | ACB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02300 | hp1 | a0002 | c0002 | t0002 | g0100 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02451 | hp1 | a0002 | c0002 | t0002 | g0094 | AFR | ACB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02602 | hp1 | a0002 | c0002 | t0002 | g0003 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02615 | hp2 | a0001 | c0003 | t0003 | g0005 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02622 | hp1 | a0001 | c0003 | t0003 | g0005 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02622 | hp2 | a0002 | c0002 | t0002 | g0093 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02630 | hp1 | a0001 | c0003 | t0003 | g0046 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02647 | hp2 | a0002 | c0002 | t0002 | g0003 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02683 | hp1 | a0001 | c0003 | t0003 | g0042 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02683 | hp2 | a0002 | c0002 | t0002 | g0003 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02698 | hp1 | a0002 | c0002 | t0007 | g0003 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02723 | hp1 | a0001 | c0003 | t0003 | g0044 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0112 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02735 | hp2 | a0002 | c0002 | t0002 | g0097 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02809 | hp1 | a0001 | c0012 | t0002 | g0041 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0119 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02886 | hp1 | a0001 | c0003 | t0003 | g0014 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02895 | hp1 | a0002 | c0002 | t0002 | g0003 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | ESN | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02965 | hp1 | a0001 | c0003 | t0001 | g0033 | AFR | ESN | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02965 | hp2 | a0001 | c0003 | t0003 | g0005 | AFR | ESN | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02976 | hp1 | a0002 | c0002 | t0002 | g0003 | AFR | ESN | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03017 | hp1 | a0002 | c0002 | t0002 | g0104 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03041 | hp1 | a0001 | c0003 | t0001 | g0033 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03041 | hp2 | a0002 | c0002 | t0002 | g0098 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | MSL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | MSL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03130 | hp2 | a0001 | c0003 | t0003 | g0015 | AFR | ESN | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03139 | hp1 | a0001 | c0003 | t0003 | g0005 | AFR | ESN | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0115 | AFR | ESN | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03195 | hp2 | a0002 | c0002 | t0002 | g0003 | AFR | ESN | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03209 | hp1 | a0001 | c0003 | t0003 | g0048 | AFR | MSL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | MSL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03225 | hp2 | a0002 | c0002 | t0002 | g0019 | AFR | MSL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03239 | hp1 | a0002 | c0002 | t0002 | g0003 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03239 | hp2 | a0001 | c0003 | t0003 | g0005 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03453 | hp1 | a0001 | c0003 | t0003 | g0047 | AFR | MSL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | MSL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | MSL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | MSL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0031 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03516 | hp2 | a0001 | c0003 | t0003 | g0043 | AFR | ESN | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03540 | hp2 | a0001 | c0003 | t0003 | g0014 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03579 | hp1 | a0001 | c0003 | t0003 | g0005 | AFR | MSL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | MSL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03654 | hp1 | a0002 | c0002 | t0002 | g0003 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03669 | hp1 | a0001 | c0001 | t0004 | g0001 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03669 | hp2 | a0002 | c0002 | t0002 | g0029 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | STU | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | STU | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03704 | hp1 | a0001 | c0003 | t0003 | g0005 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03831 | hp1 | a0001 | c0005 | t0002 | g0002 | SAS | BEB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03831 | hp2 | a0002 | c0002 | t0005 | g0003 | SAS | BEB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03834 | hp2 | a0002 | c0002 | t0002 | g0101 | SAS | BEB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03927 | hp1 | a0002 | c0002 | t0002 | g0003 | SAS | BEB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03927 | hp2 | a0002 | c0002 | t0002 | g0003 | SAS | BEB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | STU | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | STU | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG04184 | hp1 | a0002 | c0002 | t0002 | g0003 | SAS | BEB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG04184 | hp2 | a0001 | c0011 | t0002 | g0117 | SAS | BEB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG04199 | hp1 | a0002 | c0002 | t0002 | g0105 | SAS | STU | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | STU | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0035 | SAS | STU | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG04228 | hp2 | a0001 | c0005 | t0002 | g0002 | SAS | STU | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | YRI | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | YRI | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | CHB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | CHB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | YRI | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18941 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18946 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18969 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18971 | hp1 | a0001 | c0008 | t0001 | g0026 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18983 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | LWK | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | LWK | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19043 | hp1 | a0001 | c0003 | t0003 | g0049 | AFR | LWK | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19043 | hp2 | a0001 | c0003 | t0003 | g0015 | AFR | LWK | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19057 | hp2 | a0001 | c0014 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19063 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19068 | hp1 | a0002 | c0002 | t0002 | g0102 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | YRI | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA19240 | hp2 | a0001 | c0003 | t0003 | g0005 | AFR | YRI | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0076 | AFR | ASW | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA20752 | hp2 | a0002 | c0002 | t0002 | g0092 | EUR | TSI | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA20805 | hp1 | a0002 | c0002 | t0002 | g0003 | EUR | TSI | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA20805 | hp2 | a0002 | c0002 | t0001 | g0099 | EUR | TSI | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA20905 | hp2 | a0002 | c0002 | t0002 | g0003 | SAS | GIH | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | ACB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0077 | AFR | MSL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG03471 | hp2 | a0002 | c0002 | t0002 | g0019 | AFR | MSL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG06807 | hp1 | a0002 | c0002 | t0002 | g0003 | AFR | USA | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | USA | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | USA | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | LWK | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | LWK | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0012 | REF | REF | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0002 | g0019 | REF | REF | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:127802988
|
A | G | 6 | a0001a0003a0004others(3): Show | 348 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(345): Show |
missense_variant | MODERATE | c.64A>G | p.Ile22Val | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 1/15 | 107/2284 | 64/1764 | 22/587 | chr9 | 127802988 | ||
chr9:127809767
|
G | A | 1 | a0007 | 1 | HG00642.hp1 | missense_variant | MODERATE | c.1144G>A | p.Ala382Thr | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 12/15 | 1187/2284 | 1144/1764 | 382/587 | chr9 | 127809767 | ||
chr9:127813236
|
C | T | 1 | a0007 | 1 | HG00642.hp1 | missense_variant | MODERATE | c.1396C>T | p.Arg466Cys | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 15/15 | 1439/2284 | 1396/1764 | 466/587 | chr9 | 127813236 | ||
chr9:127813306
|
C | T | 1 | a0005 | 2 | HG00408.hp2 HG02056.hp2 |
missense_variant | MODERATE | c.1466C>T | p.Ala489Val | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 15/15 | 1509/2284 | 1466/1764 | 489/587 | chr9 | 127813306 | ||
chr9:127813336
|
C | T | 1 | a0003 | 2 | HG01255.hp1 HG01928.hp1 |
missense_variant | MODERATE | c.1496C>T | p.Ser499Phe | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 15/15 | 1539/2284 | 1496/1764 | 499/587 | chr9 | 127813336 | ||
chr9:127813339
|
T | C | 1 | a0004 | 2 | HG01070.hp1 HG01071.hp1 |
missense_variant | MODERATE | c.1499T>C | p.Leu500Pro | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 15/15 | 1542/2284 | 1499/1764 | 500/587 | chr9 | 127813339 | ||
chr9:127813461
|
C | CCAAAGGG others(24): Show |
1 | a0006 | 1 | HG00738.hp1 | frameshift_variant | HIGH | c.1624_1654dupAAGGGC others(25): Show |
p.Ser552fs | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 15/15 | 1698/2284 | 1655/1764 | 552/587 | INFO_REALIGN_3_PRIME | chr9 | 127813461 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:127803047
|
G | A | 1 | a0001c0003 | 26 | HG02080.hp2 HG02258.hp1 HG02258.hp2 others(23): Show |
synonymous_variant | LOW | c.123G>A | p.Pro41Pro | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 1/15 | 166/2284 | 123/1764 | 41/587 | chr9 | 127803047 | ||
chr9:127804290
|
C | T | 1 | a0001c0014 | 1 | NA19057.hp2 | synonymous_variant | LOW | c.144C>T | p.Ala48Ala | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 2/15 | 187/2284 | 144/1764 | 48/587 | chr9 | 127804290 | ||
chr9:127804389
|
G | A | 1 | a0007c0009 | 1 | HG00642.hp1 | synonymous_variant | LOW | c.243G>A | p.Leu81Leu | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 2/15 | 286/2284 | 243/1764 | 81/587 | chr9 | 127804389 | ||
chr9:127804516
|
G | T | 1 | a0001c0013 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.285G>T | p.Arg95Arg | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 3/15 | 328/2284 | 285/1764 | 95/587 | chr9 | 127804516 | ||
chr9:127804531
|
C | T | 1 | a0001c0012 | 1 | HG02809.hp1 | synonymous_variant | LOW | c.300C>T | p.His100His | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 3/15 | 343/2284 | 300/1764 | 100/587 | chr9 | 127804531 | ||
chr9:127808593
|
C | T | 1 | a0001c0008 | 2 | HG00544.hp1 NA18971.hp1 |
synonymous_variant | LOW | c.858C>T | p.Leu286Leu | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 10/15 | 901/2284 | 858/1764 | 286/587 | chr9 | 127808593 | ||
chr9:127808888
|
C | T | 1 | a0001c0011 | 1 | HG04184.hp2 | splice_region_variant&synonymous_variant | LOW | c.1059C>T | p.Leu353Leu | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 11/15 | 1102/2284 | 1059/1764 | 353/587 | chr9 | 127808888 | ||
chr9:127813338
|
C | T | 1 | a0001c0005 | 2 | HG03831.hp1 HG04228.hp2 |
synonymous_variant | LOW | c.1498C>T | p.Leu500Leu | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 15/15 | 1541/2284 | 1498/1764 | 500/587 | chr9 | 127813338 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:127802888
|
C | T | 1 | a0002c0002t0007 | 1 | HG02698.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-37C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 1/15 | chr9 | 127802888 | ||||||
chr9:127813643
|
G | T | 1 | a0001c0001t0006 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*39G>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 15/15 | 39 | chr9 | 127813643 | |||||
chr9:127813796
|
T | C | 12 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(9): Show | 221 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(218): Show |
3_prime_UTR_variant | MODIFIER | c.*192T>C | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 15/15 | 192 | chr9 | 127813796 | |||||
chr9:127813840
|
A | C | 1 | a0002c0002t0005 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*236A>C | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 15/15 | 236 | chr9 | 127813840 | |||||
chr9:127813941
|
C | T | 1 | a0001c0001t0004 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*337C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 15/15 | 337 | chr9 | 127813941 | |||||
chr9:127814045
|
CTT | C | 2 | a0001c0001t0003a0001c0003t0003 | 25 | HG02080.hp2 HG02258.hp1 HG02258.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*443_*444delTT | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 15/15 | 443 | INFO_REALIGN_3_PRIME | chr9 | 127814045 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:127803090
|
G | A | 2 | a0001c0001t0002g0034a0001c0001t0002g0035 | 2 | HG01517.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.138+28G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 1/14 | chr9 | 127803090 | ||||||
chr9:127803168
|
C | T | 1 | a0001c0001t0001g0013 | 4 | HG01099.hp2 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.138+106C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 1/14 | chr9 | 127803168 | ||||||
chr9:127803273
|
A | G | 2 | a0001c0001t0002g0121a0001c0001t0002g0122 | 2 | NA18993.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.138+211A>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 1/14 | chr9 | 127803273 | ||||||
chr9:127803286
|
C | G | 1 | a0001c0003t0001g0033 | 2 | HG02965.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.138+224C>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 1/14 | chr9 | 127803286 | ||||||
chr9:127803360
|
C | T | 1 | a0001c0001t0002g0120 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.138+298C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 1/14 | chr9 | 127803360 | ||||||
chr9:127803396
|
G | A | 1 | a0001c0001t0001g0036 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.138+334G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 1/14 | chr9 | 127803396 | ||||||
chr9:127803598
|
C | T | 26 | a0001c0001t0002g0002a0001c0001t0002g0009a0001c0001t0002g0012others(23): Show | 105 | HG00323.hp1 HG00423.hp1 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.138+536C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 1/14 | chr9 | 127803598 | ||||||
chr9:127803676
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.139-609C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 1/14 | chr9 | 127803676 | ||||||
chr9:127803746
|
T | G | 1 | a0001c0001t0001g0037 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.139-539T>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 1/14 | chr9 | 127803746 | ||||||
chr9:127803906
|
G | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(106): Show | 345 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(342): Show |
intron_variant | MODIFIER | c.139-379G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 1/14 | chr9 | 127803906 | ||||||
chr9:127803968
|
G | A | 5 | a0001c0001t0002g0007a0001c0001t0002g0038a0001c0001t0002g0039others(2): Show | 9 | HG02486.hp2 HG02572.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.139-317G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 1/14 | chr9 | 127803968 | ||||||
chr9:127803988
|
G | A | 12 | a0001c0003t0001g0033a0001c0003t0003g0005a0001c0003t0003g0014others(9): Show | 26 | HG02080.hp2 HG02258.hp1 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.139-297G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 1/14 | chr9 | 127803988 | ||||||
chr9:127804030
|
G | A | 1 | a0001c0001t0002g0106 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.139-255G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 1/14 | chr9 | 127804030 | ||||||
chr9:127804179
|
G | A | 1 | a0002c0002t0002g0090 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.139-106G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 1/14 | chr9 | 127804179 | ||||||
chr9:127804260
|
A | G | 13 | a0001c0003t0001g0033a0001c0003t0003g0005a0001c0003t0003g0014others(10): Show | 27 | HG00642.hp1 HG02080.hp2 HG02258.hp1 others(24): Show |
intron_variant | MODIFIER | c.139-25A>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 1/14 | chr9 | 127804260 | ||||||
chr9:127804863
|
A | G | 1 | a0001c0001t0002g0119 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.386+163A>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127804863 | ||||||
chr9:127804890
|
A | AT | 17 | a0001c0001t0001g0087a0001c0001t0002g0027a0001c0001t0002g0028others(14): Show | 33 | HG02080.hp2 HG02258.hp1 HG02258.hp2 others(30): Show |
intron_variant | MODIFIER | c.386+206dupT | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr9 | 127804890 | |||||
chr9:127804890
|
A | ATT | 3 | a0001c0001t0001g0011a0001c0001t0001g0088a0001c0003t0003g0049 | 6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.386+205_386+206dup others(2): Show |
FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr9 | 127804890 | |||||
chr9:127804890
|
AT | A | 7 | a0001c0001t0001g0020a0001c0001t0001g0052a0001c0001t0002g0009others(4): Show | 12 | HG01167.hp2 HG01884.hp1 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.386+206delT | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr9 | 127804890 | |||||
chr9:127804925
|
A | G | 1 | a0001c0003t0003g0048 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.386+225A>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127804925 | ||||||
chr9:127805108
|
C | T | 12 | a0001c0003t0001g0033a0001c0003t0003g0005a0001c0003t0003g0014others(9): Show | 26 | HG02080.hp2 HG02258.hp1 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.386+408C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127805108 | ||||||
chr9:127805146
|
C | T | 1 | a0002c0002t0002g0104 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.386+446C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127805146 | ||||||
chr9:127805232
|
T | A | 1 | a0001c0001t0001g0053 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.386+532T>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127805232 | ||||||
chr9:127805328
|
G | A | 1 | a0007c0009t0002g0089 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.386+628G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127805328 | ||||||
chr9:127805377
|
A | T | 130 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(127): Show | 401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.386+677A>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127805377 | ||||||
chr9:127805393
|
G | A | 1 | a0001c0001t0002g0107 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.386+693G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127805393 | ||||||
chr9:127805409
|
T | TA | 13 | a0001c0001t0001g0054a0001c0003t0001g0033a0001c0003t0003g0005others(10): Show | 27 | HG01993.hp1 HG02080.hp2 HG02258.hp1 others(24): Show |
intron_variant | MODIFIER | c.386+721dupA | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr9 | 127805409 | |||||
chr9:127805476
|
A | G | 1 | a0001c0001t0001g0085 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.386+776A>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127805476 | ||||||
chr9:127805579
|
C | T | 5 | a0001c0001t0002g0007a0001c0001t0002g0038a0001c0001t0002g0039others(2): Show | 9 | HG02486.hp2 HG02572.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.386+879C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127805579 | ||||||
chr9:127805658
|
A | G | 2 | a0001c0001t0002g0034a0001c0001t0002g0035 | 2 | HG01517.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.386+958A>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127805658 | ||||||
chr9:127805697
|
A | G | 2 | a0001c0001t0002g0121a0001c0001t0002g0122 | 2 | NA18993.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.386+997A>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127805697 | ||||||
chr9:127805823
|
A | C | 12 | a0001c0003t0001g0033a0001c0003t0003g0005a0001c0003t0003g0014others(9): Show | 26 | HG02080.hp2 HG02258.hp1 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.386+1123A>C | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127805823 | ||||||
chr9:127805880
|
C | T | 5 | a0001c0001t0001g0006a0001c0001t0001g0082a0001c0001t0001g0083others(2): Show | 15 | HG00438.hp1 HG00544.hp1 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.387-1093C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127805880 | ||||||
chr9:127805881
|
C | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0081 | 5 | HG01167.hp1 HG02723.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.387-1092C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127805881 | ||||||
chr9:127805912
|
T | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0055a0001c0001t0001g0057others(3): Show | 18 | HG00408.hp1 HG00558.hp1 HG02132.hp2 others(15): Show |
intron_variant | MODIFIER | c.387-1061T>C | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127805912 | ||||||
chr9:127805929
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.387-1044G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127805929 | ||||||
chr9:127806050
|
C | T | 1 | a0001c0001t0001g0080 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.387-923C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127806050 | ||||||
chr9:127806134
|
C | T | 1 | a0001c0001t0002g0116 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.387-839C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127806134 | ||||||
chr9:127806135
|
G | A | 3 | a0001c0003t0003g0014a0001c0003t0003g0043a0001c0003t0003g0048 | 5 | HG02280.hp2 HG02886.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.387-838G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127806135 | ||||||
chr9:127806303
|
C | G | 1 | a0001c0001t0001g0079 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.387-670C>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127806303 | ||||||
chr9:127806366
|
C | T | 1 | a0001c0003t0003g0043 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.387-607C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127806366 | ||||||
chr9:127806379
|
G | C | 1 | a0002c0002t0002g0095 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.387-594G>C | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127806379 | ||||||
chr9:127806397
|
T | G | 1 | a0001c0001t0001g0060 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.387-576T>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127806397 | ||||||
chr9:127806403
|
G | A | 3 | a0001c0003t0003g0014a0001c0003t0003g0043a0001c0003t0003g0048 | 5 | HG02280.hp2 HG02886.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.387-570G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127806403 | ||||||
chr9:127806407
|
G | A | 10 | a0001c0003t0001g0033a0001c0003t0003g0005a0001c0003t0003g0014others(7): Show | 22 | HG02080.hp2 HG02258.hp1 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.387-566G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127806407 | ||||||
chr9:127806420
|
C | T | 1 | a0001c0001t0001g0013 | 4 | HG01099.hp2 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.387-553C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127806420 | ||||||
chr9:127806454
|
C | T | 1 | a0007c0009t0002g0089 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.387-519C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127806454 | ||||||
chr9:127806484
|
C | T | 1 | a0001c0001t0001g0078 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.387-489C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127806484 | ||||||
chr9:127806583
|
G | A | 1 | a0001c0001t0002g0121 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.387-390G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127806583 | ||||||
chr9:127806719
|
G | A | 1 | a0001c0001t0002g0061 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.387-254G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127806719 | ||||||
chr9:127806838
|
G | T | 1 | a0001c0003t0003g0047 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.387-135G>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127806838 | ||||||
chr9:127806882
|
G | T | 1 | a0001c0001t0001g0059 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.387-91G>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127806882 | ||||||
chr9:127806926
|
C | T | 1 | a0002c0002t0002g0103 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.387-47C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127806926 | ||||||
chr9:127807288
|
T | C | 1 | a0002c0002t0002g0096 | 1 | HG01081.hp2 | splice_donor_variant&intron_variant | HIGH | c.579+2T>C | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 6/14 | chr9 | 127807288 | ||||||
chr9:127807523
|
C | T | 1 | a0001c0001t0002g0035 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.641+41C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 7/14 | chr9 | 127807523 | ||||||
chr9:127807533
|
C | T | 1 | a0001c0001t0001g0013 | 4 | HG01099.hp2 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.641+51C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 7/14 | chr9 | 127807533 | ||||||
chr9:127807554
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.642-32G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 7/14 | chr9 | 127807554 | ||||||
chr9:127807896
|
C | T | 1 | a0001c0001t0001g0008 | 5 | HG02027.hp2 NA18963.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.744+208C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 8/14 | chr9 | 127807896 | ||||||
chr9:127807935
|
G | C | 1 | a0002c0002t0002g0029 | 2 | HG00099.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.744+247G>C | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 8/14 | chr9 | 127807935 | ||||||
chr9:127807948
|
A | C | 1 | a0001c0001t0002g0115 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.744+260A>C | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 8/14 | chr9 | 127807948 | ||||||
chr9:127808024
|
C | T | 13 | a0001c0001t0003g0077a0001c0003t0001g0033a0001c0003t0003g0005others(10): Show | 27 | HG02080.hp2 HG02258.hp1 HG02258.hp2 others(24): Show |
intron_variant | MODIFIER | c.745-210C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 8/14 | chr9 | 127808024 | ||||||
chr9:127808105
|
C | A | 13 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0021others(10): Show | 25 | HG01099.hp2 HG01884.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.745-129C>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 8/14 | chr9 | 127808105 | ||||||
chr9:127808330
|
G | A | 5 | a0001c0001t0001g0006a0001c0001t0001g0082a0001c0001t0001g0083others(2): Show | 15 | HG00438.hp1 HG00544.hp1 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.822+19G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 9/14 | chr9 | 127808330 | ||||||
chr9:127808358
|
T | C | 1 | a0001c0001t0001g0063 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.822+47T>C | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 9/14 | chr9 | 127808358 | ||||||
chr9:127808359
|
C | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0063 | 3 | HG01168.hp2 HG01169.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.822+48C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 9/14 | chr9 | 127808359 | ||||||
chr9:127808432
|
G | T | 1 | a0001c0001t0001g0053 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.822+121G>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 9/14 | chr9 | 127808432 | ||||||
chr9:127808434
|
C | T | 1 | a0001c0001t0001g0053 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.822+123C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 9/14 | chr9 | 127808434 | ||||||
chr9:127808771
|
G | A | 5 | a0001c0001t0002g0007a0001c0001t0002g0038a0001c0001t0002g0039others(2): Show | 9 | HG02486.hp2 HG02572.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.971-29G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 10/14 | chr9 | 127808771 | ||||||
chr9:127808946
|
A | AT | 26 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0018others(23): Show | 52 | HG00438.hp1 HG00544.hp1 HG01928.hp1 others(49): Show |
intron_variant | MODIFIER | c.1060+77dupT | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr9 | 127808946 | |||||
chr9:127808946
|
AT | A | 7 | a0001c0001t0001g0016a0001c0001t0001g0055a0001c0001t0002g0031others(4): Show | 10 | HG00642.hp1 HG02735.hp2 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.1060+77delT | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr9 | 127808946 | |||||
chr9:127809010
|
A | G | 1 | a0001c0001t0002g0113 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1060+121A>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 11/14 | chr9 | 127809010 | ||||||
chr9:127809076
|
T | C | 3 | a0001c0003t0003g0014a0001c0003t0003g0043a0001c0003t0003g0048 | 5 | HG02280.hp2 HG02886.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060+187T>C | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 11/14 | chr9 | 127809076 | ||||||
chr9:127809078
|
T | A | 3 | a0001c0003t0003g0014a0001c0003t0003g0043a0001c0003t0003g0048 | 5 | HG02280.hp2 HG02886.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060+189T>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 11/14 | chr9 | 127809078 | ||||||
chr9:127809079
|
T | A | 3 | a0001c0003t0003g0014a0001c0003t0003g0043a0001c0003t0003g0048 | 5 | HG02280.hp2 HG02886.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060+190T>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 11/14 | chr9 | 127809079 | ||||||
chr9:127809080
|
C | A | 3 | a0001c0003t0003g0014a0001c0003t0003g0043a0001c0003t0003g0048 | 5 | HG02280.hp2 HG02886.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060+191C>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 11/14 | chr9 | 127809080 | ||||||
chr9:127809081
|
T | G | 3 | a0001c0003t0003g0014a0001c0003t0003g0043a0001c0003t0003g0048 | 5 | HG02280.hp2 HG02886.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060+192T>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 11/14 | chr9 | 127809081 | ||||||
chr9:127809082
|
C | T | 3 | a0001c0003t0003g0014a0001c0003t0003g0043a0001c0003t0003g0048 | 5 | HG02280.hp2 HG02886.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060+193C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 11/14 | chr9 | 127809082 | ||||||
chr9:127809084
|
T | G | 3 | a0001c0003t0003g0014a0001c0003t0003g0043a0001c0003t0003g0048 | 5 | HG02280.hp2 HG02886.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060+195T>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 11/14 | chr9 | 127809084 | ||||||
chr9:127809085
|
C | A | 3 | a0001c0003t0003g0014a0001c0003t0003g0043a0001c0003t0003g0048 | 5 | HG02280.hp2 HG02886.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060+196C>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 11/14 | chr9 | 127809085 | ||||||
chr9:127809137
|
C | T | 1 | a0001c0001t0002g0112 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1060+248C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 11/14 | chr9 | 127809137 | ||||||
chr9:127809279
|
T | G | 1 | a0001c0001t0001g0064 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1060+390T>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 11/14 | chr9 | 127809279 | ||||||
chr9:127809555
|
G | C | 1 | a0001c0008t0001g0026 | 2 | HG00544.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1061-129G>C | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 11/14 | chr9 | 127809555 | ||||||
chr9:127809594
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1061-90G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 11/14 | chr9 | 127809594 | ||||||
chr9:127809839
|
G | A | 2 | a0001c0001t0002g0027a0001c0001t0002g0086 | 3 | HG02647.hp1 HG02818.hp2 HG03098.hp1 |
splice_region_variant&intron_variant | LOW | c.1211+5G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 12/14 | chr9 | 127809839 | ||||||
chr9:127809844
|
A | G | 69 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(66): Show | 219 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.1211+10A>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 12/14 | chr9 | 127809844 | ||||||
chr9:127809898
|
A | G | 2 | a0001c0001t0001g0021a0001c0013t0001g0051 | 3 | HG01884.hp1 HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1211+64A>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 12/14 | chr9 | 127809898 | ||||||
chr9:127809942
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1212-89G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 12/14 | chr9 | 127809942 | ||||||
chr9:127809975
|
G | A | 1 | a0001c0001t0001g0067 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1212-56G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 12/14 | chr9 | 127809975 | ||||||
chr9:127810026
|
C | G | 3 | a0001c0001t0002g0111a0001c0001t0002g0121a0001c0001t0002g0122 | 3 | NA18966.hp2 NA18993.hp2 NA19012.hp1 |
splice_region_variant&intron_variant | LOW | c.1212-5C>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 12/14 | chr9 | 127810026 | ||||||
chr9:127810161
|
C | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0075 | 3 | HG00621.hp1 HG02056.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.1287+55C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 13/14 | chr9 | 127810161 | ||||||
chr9:127810178
|
G | T | 1 | a0001c0001t0001g0013 | 4 | HG01099.hp2 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1287+72G>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 13/14 | chr9 | 127810178 | ||||||
chr9:127810420
|
A | G | 1 | a0002c0002t0002g0101 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1287+314A>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 13/14 | chr9 | 127810420 | ||||||
chr9:127810427
|
C | T | 1 | a0002c0002t0002g0093 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1287+321C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 13/14 | chr9 | 127810427 | ||||||
chr9:127810744
|
C | T | 1 | a0001c0003t0003g0046 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1288-201C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 13/14 | chr9 | 127810744 | ||||||
chr9:127810830
|
C | T | 1 | a0001c0001t0002g0076 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1288-115C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 13/14 | chr9 | 127810830 | ||||||
chr9:127810871
|
C | T | 1 | a0001c0001t0001g0078 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1288-74C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 13/14 | chr9 | 127810871 | ||||||
chr9:127811069
|
G | C | 1 | a0001c0001t0001g0081 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1354+58G>C | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127811069 | ||||||
chr9:127811070
|
G | T | 1 | a0001c0001t0001g0081 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1354+59G>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127811070 | ||||||
chr9:127811092
|
G | A | 1 | a0001c0001t0001g0021 | 2 | HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1354+81G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127811092 | ||||||
chr9:127811095
|
GTAGGAAA others(24): Show |
G | 1 | a0006c0010t0001g0068 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1354+85_1354+115de others(32): Show |
FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127811095 | ||||||
chr9:127811132
|
T | C | 2 | a0001c0001t0003g0077a0001c0003t0001g0033 | 3 | HG02965.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1354+121T>C | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127811132 | ||||||
chr9:127811134
|
G | A | 1 | a0006c0010t0001g0068 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1354+123G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127811134 | ||||||
chr9:127811313
|
CA | C | 4 | a0001c0001t0001g0011a0001c0001t0001g0062a0001c0001t0001g0087others(1): Show | 7 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1354+312delA | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr9 | 127811313 | |||||
chr9:127811406
|
C | T | 1 | a0001c0013t0001g0051 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1354+395C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127811406 | ||||||
chr9:127811450
|
C | T | 1 | a0001c0013t0001g0051 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1354+439C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127811450 | ||||||
chr9:127811480
|
C | CA | 14 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0017others(11): Show | 29 | HG00438.hp1 HG00544.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.1354+483dupA | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr9 | 127811480 | |||||
chr9:127811480
|
C | CAA | 38 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(35): Show | 156 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.1354+482_1354+483d others(4): Show |
FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr9 | 127811480 | |||||
chr9:127811617
|
C | T | 28 | a0001c0001t0002g0002a0001c0001t0002g0009a0001c0001t0002g0028others(25): Show | 105 | HG00323.hp1 HG00423.hp1 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.1354+606C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127811617 | ||||||
chr9:127811619
|
G | T | 1 | a0001c0001t0002g0114 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1354+608G>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127811619 | ||||||
chr9:127811693
|
C | T | 1 | a0001c0001t0001g0074 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1354+682C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127811693 | ||||||
chr9:127811829
|
C | T | 1 | a0001c0001t0001g0023 | 2 | NA19001.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1354+818C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127811829 | ||||||
chr9:127811843
|
C | A | 3 | a0001c0001t0001g0022a0001c0001t0001g0054a0001c0001t0001g0069 | 4 | HG01928.hp2 HG01981.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1354+832C>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127811843 | ||||||
chr9:127811888
|
G | A | 1 | a0001c0001t0001g0053 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1354+877G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127811888 | ||||||
chr9:127812082
|
T | TA | 13 | a0001c0001t0003g0077a0001c0003t0001g0033a0001c0003t0003g0005others(10): Show | 27 | HG02080.hp2 HG02258.hp1 HG02258.hp2 others(24): Show |
intron_variant | MODIFIER | c.1354+1080dupA | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr9 | 127812082 | |||||
chr9:127812322
|
A | AT | 32 | a0001c0001t0001g0011a0001c0001t0001g0062a0001c0001t0001g0073others(29): Show | 74 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.1355-857dupT | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr9 | 127812322 | |||||
chr9:127812322
|
AT | A | 15 | a0001c0001t0001g0070a0001c0001t0001g0085a0001c0001t0002g0061others(12): Show | 28 | HG02080.hp2 HG02258.hp1 HG02258.hp2 others(25): Show |
intron_variant | MODIFIER | c.1355-857delT | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr9 | 127812322 | |||||
chr9:127812348
|
G | T | 1 | a0001c0001t0001g0084 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1355-847G>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127812348 | ||||||
chr9:127812352
|
C | G | 4 | a0001c0001t0001g0011a0001c0001t0001g0062a0001c0001t0001g0087others(1): Show | 7 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1355-843C>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127812352 | ||||||
chr9:127812403
|
T | C | 4 | a0001c0001t0001g0022a0001c0001t0001g0054a0001c0001t0001g0069others(1): Show | 5 | HG01928.hp2 HG01934.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.1355-792T>C | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127812403 | ||||||
chr9:127812463
|
C | T | 1 | a0002c0002t0002g0100 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1355-732C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127812463 | ||||||
chr9:127812479
|
C | T | 1 | a0001c0001t0002g0110 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1355-716C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127812479 | ||||||
chr9:127812643
|
A | G | 1 | a0001c0001t0002g0118 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1355-552A>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127812643 | ||||||
chr9:127812648
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1355-547C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127812648 | ||||||
chr9:127812699
|
G | GT | 43 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(40): Show | 172 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.1355-495dupT | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr9 | 127812699 | |||||
chr9:127812700
|
T | G | 13 | a0001c0001t0003g0077a0001c0003t0001g0033a0001c0003t0003g0005others(10): Show | 27 | HG02080.hp2 HG02258.hp1 HG02258.hp2 others(24): Show |
intron_variant | MODIFIER | c.1355-495T>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127812700 | ||||||
chr9:127812701
|
G | T | 71 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(68): Show | 223 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.1355-494G>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127812701 | ||||||
chr9:127812924
|
G | T | 1 | a0002c0002t0002g0094 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1355-271G>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127812924 | ||||||
chr9:127813006
|
T | A | 2 | a0002c0002t0002g0030a0002c0002t0002g0097 | 3 | HG00639.hp1 HG01346.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1355-189T>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127813006 | ||||||
chr9:127813080
|
A | T | 3 | a0001c0001t0001g0011a0001c0001t0001g0062a0001c0001t0001g0088 | 6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1355-115A>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127813080 | ||||||
chr9:127813120
|
C | T | 1 | a0001c0003t0003g0045 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1355-75C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127813120 | ||||||
chr9:127813121
|
A | T | 1 | a0007c0009t0002g0089 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1355-74A>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127813121 |