geneid | 59345 |
---|---|
ensemblid | ENSG00000114450.11 |
hgncid | 20731 |
symbol | GNB4 |
name | G protein subunit beta 4 |
refseq_nuc | NM_021629.4 |
refseq_prot | NP_067642.1 |
ensembl_nuc | ENST00000232564.8 |
ensembl_prot | ENSP00000232564.3 |
mane_status | MANE Select |
chr | chr3 |
start | 179396088 |
end | 179451470 |
strand | - |
ver | v1.2 |
region | chr3:179396088-179451470 |
region5000 | chr3:179391088-179456470 |
regionname0 | GNB4_chr3_179396088_179451470 |
regionname5000 | GNB4_chr3_179391088_179456470 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 340 | 397 | 92 | 78 | 169 | 10 | 46 | 130 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0002 | 0/0 | 58 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0003 | 0/0 | 340 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0004 | 0/0 | 340 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1023 | 199 | 42 | 36 | 98 | 1 | 20 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
c0002 | 0/0 | 1023 | 190 | 48 | 38 | 71 | 9 | 24 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
c0003 | 0/0 | 1023 | 8 | 2 | 4 | 0 | 0 | 2 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
c0004 | 0/0 | 1023 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
c0005 | 0/0 | 1006 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
c0006 | 0/0 | 1023 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 5289 | 71 | 2 | 17 | 46 | 2 | 4 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0002 | 1/1 | 5293 | 70 | 7 | 18 | 33 | 0 | 10 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0003 | 0/0 | 5285 | 39 | 4 | 2 | 27 | 0 | 6 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0004 | 0/0 | 5289 | 37 | 5 | 9 | 12 | 5 | 6 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0005 | 0/0 | 5285 | 17 | 6 | 3 | 8 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0006 | 0/0 | 5289 | 12 | 0 | 2 | 9 | 1 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0007 | 0/0 | 5289 | 9 | 9 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0008 | 0/0 | 5293 | 8 | 0 | 0 | 8 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0009 | 0/0 | 5293 | 8 | 2 | 4 | 0 | 0 | 2 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0010 | 0/0 | 5288 | 8 | 5 | 3 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0011 | 0/0 | 5285 | 7 | 1 | 4 | 0 | 1 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0012 | 0/0 | 5293 | 6 | 0 | 0 | 6 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0013 | 0/0 | 5289 | 6 | 3 | 1 | 1 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0014 | 0/0 | 5288 | 6 | 4 | 2 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0015 | 0/0 | 5289 | 5 | 3 | 2 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0016 | 0/0 | 5288 | 5 | 5 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0017 | 0/0 | 5286 | 4 | 1 | 0 | 3 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0018 | 0/0 | 5289 | 4 | 0 | 0 | 0 | 0 | 4 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0019 | 0/0 | 5288 | 4 | 4 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0020 | 0/0 | 5285 | 4 | 0 | 0 | 4 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0021 | 0/0 | 5289 | 4 | 0 | 0 | 1 | 0 | 3 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0022 | 0/0 | 5289 | 3 | 2 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0023 | 0/0 | 5289 | 2 | 2 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0024 | 0/0 | 5285 | 2 | 0 | 1 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0025 | 0/0 | 5293 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0026 | 0/0 | 5289 | 2 | 2 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0027 | 0/0 | 5293 | 2 | 0 | 2 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0028 | 0/0 | 5294 | 2 | 2 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0029 | 0/0 | 5289 | 2 | 1 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0030 | 0/0 | 5289 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0031 | 0/0 | 5289 | 2 | 0 | 0 | 0 | 0 | 2 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0032 | 0/0 | 5290 | 2 | 2 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0033 | 0/0 | 5289 | 2 | 2 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0034 | 0/0 | 5289 | 2 | 2 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0035 | 0/0 | 5289 | 2 | 2 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0036 | 0/0 | 5285 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0037 | 0/0 | 5289 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0038 | 0/0 | 5285 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0039 | 0/0 | 5289 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0040 | 0/0 | 5290 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0041 | 0/0 | 5289 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0042 | 0/0 | 5289 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0043 | 0/0 | 5289 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0044 | 0/0 | 5293 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0045 | 0/0 | 5293 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0046 | 0/0 | 5292 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0047 | 0/0 | 5289 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0048 | 0/0 | 5293 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0049 | 0/0 | 5289 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0050 | 0/0 | 5289 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0051 | 0/0 | 5289 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0052 | 0/0 | 5289 | 1 | 0 | 0 | 0 | 1 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0053 | 0/0 | 5288 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0054 | 0/0 | 5289 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0055 | 0/0 | 5285 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0056 | 0/0 | 5286 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0057 | 0/0 | 5286 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0058 | 0/0 | 5368 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0059 | 0/0 | 5293 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0060 | 0/0 | 5285 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0061 | 0/0 | 5289 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0062 | 0/0 | 5293 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0063 | 0/0 | 5289 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0064 | 0/0 | 5288 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0065 | 0/0 | 5290 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0066 | 0/0 | 5288 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0067 | 0/0 | 5288 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0068 | 0/0 | 5288 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0069 | 0/0 | 5285 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0070 | 0/0 | 5285 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0071 | 0/0 | 5288 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
t0072 | 0/0 | 5293 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0002 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0007 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0011 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0016 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0040 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0052 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1023 | 199 | 42 | 36 | 98 | 1 | 20 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0002 | 0/0 | 1023 | 190 | 48 | 38 | 71 | 9 | 24 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0003 | 0/0 | 1023 | 8 | 2 | 4 | 0 | 0 | 2 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0002c0005 | 0/0 | 1006 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0003c0004 | 0/0 | 1023 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0004c0006 | 0/0 | 1023 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6311 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0001t0002 | 1/1 | 6315 | 68 | 7 | 18 | 31 | 0 | 10 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0001t0003 | 0/0 | 6307 | 39 | 4 | 2 | 27 | 0 | 6 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0001t0004 | 0/0 | 6311 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0001t0005 | 0/0 | 6307 | 16 | 6 | 3 | 7 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0001t0008 | 0/0 | 6315 | 8 | 0 | 0 | 8 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0001t0009 | 0/0 | 6315 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0001t0010 | 0/0 | 6310 | 8 | 5 | 3 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0001t0011 | 0/0 | 6307 | 7 | 1 | 4 | 0 | 1 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0001t0012 | 0/0 | 6315 | 6 | 0 | 0 | 6 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0001t0014 | 0/0 | 6310 | 4 | 4 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0001t0017 | 0/0 | 6308 | 4 | 1 | 0 | 3 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0001t0019 | 0/0 | 6310 | 4 | 4 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0001t0020 | 0/0 | 6307 | 4 | 0 | 0 | 4 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0001t0024 | 0/0 | 6307 | 2 | 0 | 1 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0001t0025 | 0/0 | 6315 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0001t0027 | 0/0 | 6315 | 2 | 0 | 2 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0001t0028 | 0/0 | 6316 | 2 | 2 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0001t0036 | 0/0 | 6307 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0001t0037 | 0/0 | 6311 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0001t0038 | 0/0 | 6307 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0001t0044 | 0/0 | 6315 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0001t0045 | 0/0 | 6315 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0001t0046 | 0/0 | 6314 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0001t0048 | 0/0 | 6315 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0001t0053 | 0/0 | 6310 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0001t0054 | 0/0 | 6311 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0001t0055 | 0/0 | 6307 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0001t0056 | 0/0 | 6308 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0001t0057 | 0/0 | 6308 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0001t0058 | 0/0 | 6390 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0001t0060 | 0/0 | 6307 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0001t0061 | 0/0 | 6311 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0001t0067 | 0/0 | 6310 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0001t0069 | 0/0 | 6307 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0001t0070 | 0/0 | 6307 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0001t0071 | 0/0 | 6310 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0001t0072 | 0/0 | 6315 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0002t0001 | 0/0 | 6311 | 69 | 2 | 17 | 44 | 2 | 4 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0002t0002 | 0/0 | 6315 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0002t0004 | 0/0 | 6311 | 36 | 5 | 9 | 12 | 5 | 5 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0002t0005 | 0/0 | 6307 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0002t0006 | 0/0 | 6311 | 12 | 0 | 2 | 9 | 1 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0002t0007 | 0/0 | 6311 | 9 | 9 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0002t0013 | 0/0 | 6311 | 6 | 3 | 1 | 1 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0002t0014 | 0/0 | 6310 | 2 | 0 | 2 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0002t0015 | 0/0 | 6311 | 5 | 3 | 2 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0002t0016 | 0/0 | 6310 | 5 | 5 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0002t0018 | 0/0 | 6311 | 4 | 0 | 0 | 0 | 0 | 4 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0002t0021 | 0/0 | 6311 | 4 | 0 | 0 | 1 | 0 | 3 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0002t0022 | 0/0 | 6311 | 3 | 2 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0002t0023 | 0/0 | 6311 | 2 | 2 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0002t0026 | 0/0 | 6311 | 2 | 2 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0002t0029 | 0/0 | 6311 | 2 | 1 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0002t0030 | 0/0 | 6311 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0002t0031 | 0/0 | 6311 | 2 | 0 | 0 | 0 | 0 | 2 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0002t0032 | 0/0 | 6312 | 2 | 2 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0002t0033 | 0/0 | 6311 | 2 | 2 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0002t0034 | 0/0 | 6311 | 2 | 2 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0002t0035 | 0/0 | 6311 | 2 | 2 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0002t0039 | 0/0 | 6311 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0002t0040 | 0/0 | 6312 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0002t0041 | 0/0 | 6311 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0002t0042 | 0/0 | 6311 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0002t0043 | 0/0 | 6311 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0002t0047 | 0/0 | 6311 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0002t0049 | 0/0 | 6311 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0002t0050 | 0/0 | 6311 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0002t0051 | 0/0 | 6311 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0002t0052 | 0/0 | 6311 | 1 | 0 | 0 | 0 | 1 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0002t0063 | 0/0 | 6311 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0002t0064 | 0/0 | 6310 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0002t0065 | 0/0 | 6312 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0002t0066 | 0/0 | 6310 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0002t0068 | 0/0 | 6310 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0003t0009 | 0/0 | 6315 | 7 | 1 | 4 | 0 | 0 | 2 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0001c0003t0062 | 0/0 | 6315 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0002c0005t0002 | 0/0 | 6298 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0003c0004t0001 | 0/0 | 6311 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
a0004c0006t0059 | 0/0 | 6315 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | copy fasta | chr3 | 179391088 | 179456470 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0007 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0016 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0052 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0003g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0003g0011 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0003g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0003g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0003g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0003g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0003g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0003g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0005g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0005g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0005g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0005g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0005g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0005g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0005g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0005g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0005g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0005g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0005g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0005g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0005g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0008g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0008g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0008g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0008g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0008g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0009g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0010g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0010g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0010g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0010g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0010g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0010g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0011g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0011g0040 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0011g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0011g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0011g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0012g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0012g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0012g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0014g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0014g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0017g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0017g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0019g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0019g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0019g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0019g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0020g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0020g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0020g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0024g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0024g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0025g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0025g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0027g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0027g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0028g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0036g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0037g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0038g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0044g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0045g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0046g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0048g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0053g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0054g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0055g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0056g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0057g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0058g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0060g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0061g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0067g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0069g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0070g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0071g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0001t0072g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0002 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0004g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0004g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0004g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0004g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0004g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0004g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0004g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0004g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0004g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0004g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0004g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0004g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0004g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0004g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0004g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0004g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0005g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0006g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0006g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0006g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0006g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0006g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0006g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0006g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0006g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0006g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0006g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0006g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0007g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0007g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0007g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0007g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0007g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0007g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0007g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0013g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0013g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0013g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0013g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0013g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0013g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0014g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0014g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0015g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0015g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0015g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0015g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0015g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0016g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0016g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0016g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0016g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0018g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0018g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0018g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0018g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0021g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0021g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0021g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0021g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0022g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0022g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0022g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0023g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0023g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0026g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0029g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0030g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0030g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0031g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0031g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0032g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0032g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0033g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0033g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0034g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0034g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0035g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0035g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0039g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0040g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0041g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0042g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0043g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0047g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0049g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0050g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0051g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0052g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0063g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0064g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0065g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0066g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0002t0068g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0003t0009g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0003t0009g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0003t0009g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0003t0009g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0003t0009g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0003t0009g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0003t0009g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0001c0003t0062g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0002c0005t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0003c0004t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
a0004c0006t0059g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0002 | t0004 | g0178 | EUR | GBR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG00140 | hp2 | a0001 | c0002 | t0052 | g0092 | EUR | GBR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG00280 | hp1 | a0001 | c0002 | t0004 | g0251 | EUR | FIN | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG00280 | hp2 | a0001 | c0002 | t0006 | g0088 | EUR | FIN | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG00323 | hp1 | a0001 | c0002 | t0004 | g0250 | EUR | FIN | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG00323 | hp2 | a0001 | c0002 | t0004 | g0231 | EUR | FIN | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | CHS | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0300 | EAS | CHS | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0288 | EAS | CHS | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG00423 | hp2 | a0003 | c0004 | t0001 | g0090 | EAS | CHS | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | CHS | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG00438 | hp2 | a0001 | c0002 | t0004 | g0241 | EAS | CHS | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG00544 | hp1 | a0001 | c0002 | t0006 | g0086 | EAS | CHS | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG00544 | hp2 | a0001 | c0001 | t0008 | g0186 | EAS | CHS | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0276 | EAS | CHS | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | CHS | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | CHS | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG00597 | hp2 | a0001 | c0001 | t0012 | g0024 | EAS | CHS | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | CHS | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0304 | EAS | CHS | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG00621 | hp1 | a0001 | c0002 | t0004 | g0240 | EAS | CHS | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG00621 | hp2 | a0001 | c0001 | t0012 | g0024 | EAS | CHS | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG00639 | hp1 | a0001 | c0001 | t0011 | g0040 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0067 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0299 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0077 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG00733 | hp2 | a0001 | c0001 | t0011 | g0303 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG00735 | hp1 | a0001 | c0002 | t0015 | g0217 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG00735 | hp2 | a0001 | c0003 | t0009 | g0325 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG00738 | hp1 | a0001 | c0001 | t0024 | g0222 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0193 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG00741 | hp1 | a0001 | c0002 | t0040 | g0179 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01069 | hp1 | a0001 | c0002 | t0029 | g0035 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01069 | hp2 | a0001 | c0001 | t0010 | g0012 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01070 | hp2 | a0001 | c0002 | t0004 | g0032 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01071 | hp1 | a0001 | c0001 | t0010 | g0012 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01071 | hp2 | a0001 | c0002 | t0004 | g0032 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01074 | hp1 | a0001 | c0002 | t0001 | g0094 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01081 | hp1 | a0001 | c0001 | t0027 | g0254 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0069 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01106 | hp1 | a0001 | c0001 | t0027 | g0255 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01106 | hp2 | a0001 | c0001 | t0058 | g0272 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01167 | hp1 | a0001 | c0002 | t0063 | g0306 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01167 | hp2 | a0001 | c0002 | t0014 | g0260 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01168 | hp1 | a0001 | c0002 | t0041 | g0081 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01169 | hp1 | a0001 | c0002 | t0014 | g0262 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01175 | hp1 | a0001 | c0001 | t0010 | g0012 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01175 | hp2 | a0001 | c0002 | t0001 | g0018 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01192 | hp1 | a0001 | c0002 | t0013 | g0297 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01192 | hp2 | a0001 | c0001 | t0038 | g0176 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01243 | hp1 | a0001 | c0002 | t0004 | g0246 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0102 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0103 | AMR | CLM | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0123 | AMR | CLM | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01256 | hp1 | a0001 | c0003 | t0009 | g0327 | AMR | CLM | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01256 | hp2 | a0001 | c0002 | t0001 | g0105 | AMR | CLM | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0137 | AMR | CLM | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01257 | hp2 | a0001 | c0002 | t0006 | g0161 | AMR | CLM | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01258 | hp2 | a0001 | c0003 | t0009 | g0328 | AMR | CLM | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01261 | hp1 | a0001 | c0002 | t0004 | g0036 | AMR | CLM | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0070 | AMR | CLM | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01346 | hp2 | a0001 | c0001 | t0005 | g0205 | AMR | CLM | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01358 | hp1 | a0001 | c0002 | t0004 | g0235 | AMR | CLM | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | CLM | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01361 | hp1 | a0001 | c0001 | t0011 | g0038 | AMR | CLM | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0048 | AMR | CLM | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01433 | hp1 | a0001 | c0002 | t0015 | g0197 | AMR | CLM | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01433 | hp2 | a0001 | c0002 | t0022 | g0188 | AMR | CLM | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01496 | hp1 | a0001 | c0003 | t0009 | g0322 | AMR | CLM | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01496 | hp2 | a0001 | c0001 | t0005 | g0203 | AMR | CLM | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01515 | hp1 | a0001 | c0002 | t0004 | g0221 | EUR | IBS | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01515 | hp2 | a0001 | c0002 | t0001 | g0110 | EUR | IBS | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01517 | hp1 | a0001 | c0001 | t0011 | g0040 | EUR | IBS | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01517 | hp2 | a0001 | c0002 | t0001 | g0112 | EUR | IBS | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01884 | hp1 | a0001 | c0001 | t0009 | g0258 | AFR | ACB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01884 | hp2 | a0001 | c0002 | t0029 | g0035 | AFR | ACB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0122 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01928 | hp2 | a0001 | c0002 | t0004 | g0009 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01952 | hp1 | a0001 | c0002 | t0006 | g0083 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01952 | hp2 | a0001 | c0001 | t0005 | g0212 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0136 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0142 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01978 | hp1 | a0001 | c0001 | t0011 | g0267 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0167 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0140 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01993 | hp1 | a0001 | c0002 | t0004 | g0009 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02015 | hp1 | a0001 | c0001 | t0005 | g0144 | EAS | KHV | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | KHV | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02027 | hp1 | a0001 | c0001 | t0012 | g0028 | EAS | KHV | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0277 | EAS | KHV | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02040 | hp1 | a0001 | c0001 | t0017 | g0006 | EAS | KHV | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02040 | hp2 | a0001 | c0001 | t0003 | g0274 | EAS | KHV | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02055 | hp1 | a0001 | c0001 | t0011 | g0264 | AFR | ACB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02055 | hp2 | a0001 | c0002 | t0026 | g0031 | AFR | ACB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | KHV | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | KHV | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | KHV | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | KHV | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | KHV | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0271 | EAS | KHV | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | KHV | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02132 | hp1 | a0001 | c0001 | t0017 | g0006 | EAS | KHV | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02132 | hp2 | a0001 | c0001 | t0072 | g0331 | EAS | KHV | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02145 | hp1 | a0001 | c0002 | t0035 | g0263 | AFR | ACB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | ACB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02148 | hp1 | a0001 | c0002 | t0001 | g0095 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02148 | hp2 | a0001 | c0002 | t0004 | g0253 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | CDX | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0281 | EAS | CDX | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02165 | hp1 | a0001 | c0002 | t0004 | g0062 | EAS | CDX | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02165 | hp2 | a0001 | c0002 | t0006 | g0084 | EAS | CDX | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02257 | hp1 | a0001 | c0002 | t0033 | g0291 | AFR | ACB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02257 | hp2 | a0001 | c0002 | t0007 | g0008 | AFR | ACB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0114 | AFR | ACB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02258 | hp2 | a0001 | c0001 | t0019 | g0226 | AFR | ACB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0270 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02273 | hp2 | a0001 | c0002 | t0004 | g0009 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02280 | hp1 | a0001 | c0002 | t0001 | g0050 | AFR | ACB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02280 | hp2 | a0001 | c0002 | t0022 | g0187 | AFR | ACB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0065 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02300 | hp2 | a0001 | c0001 | t0060 | g0302 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | KHV | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | KHV | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02572 | hp1 | a0001 | c0001 | t0061 | g0337 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02572 | hp2 | a0001 | c0002 | t0007 | g0199 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0314 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02602 | hp2 | a0001 | c0002 | t0049 | g0245 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02615 | hp1 | a0001 | c0001 | t0019 | g0227 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02615 | hp2 | a0001 | c0001 | t0014 | g0013 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0042 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02622 | hp2 | a0001 | c0001 | t0010 | g0334 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02630 | hp1 | a0001 | c0001 | t0005 | g0027 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02630 | hp2 | a0001 | c0002 | t0007 | g0214 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02647 | hp1 | a0001 | c0002 | t0013 | g0289 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02647 | hp2 | a0001 | c0001 | t0028 | g0020 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02683 | hp1 | a0001 | c0002 | t0039 | g0163 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02683 | hp2 | a0001 | c0002 | t0004 | g0037 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0113 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0174 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02717 | hp1 | a0001 | c0002 | t0015 | g0216 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02717 | hp2 | a0001 | c0002 | t0023 | g0044 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02735 | hp1 | a0001 | c0001 | t0024 | g0209 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02735 | hp2 | a0001 | c0002 | t0004 | g0232 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02738 | hp1 | a0001 | c0002 | t0001 | g0108 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02738 | hp2 | a0001 | c0002 | t0031 | g0236 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02809 | hp2 | a0001 | c0001 | t0014 | g0338 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02818 | hp1 | a0001 | c0002 | t0007 | g0200 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02818 | hp2 | a0001 | c0001 | t0019 | g0225 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0191 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02886 | hp2 | a0001 | c0002 | t0004 | g0244 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02895 | hp1 | a0001 | c0002 | t0016 | g0034 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02895 | hp2 | a0001 | c0002 | t0068 | g0259 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02896 | hp1 | a0001 | c0001 | t0046 | g0190 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02896 | hp2 | a0001 | c0002 | t0013 | g0269 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02897 | hp1 | a0001 | c0001 | t0048 | g0189 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02897 | hp2 | a0001 | c0002 | t0016 | g0034 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02922 | hp1 | a0001 | c0002 | t0016 | g0242 | AFR | ESN | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02922 | hp2 | a0001 | c0002 | t0026 | g0031 | AFR | ESN | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02965 | hp1 | a0001 | c0002 | t0016 | g0220 | AFR | ESN | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02965 | hp2 | a0001 | c0002 | t0064 | g0292 | AFR | ESN | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0336 | AFR | ESN | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02970 | hp2 | a0001 | c0003 | t0009 | g0330 | AFR | ESN | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02976 | hp1 | a0001 | c0001 | t0069 | g0319 | AFR | ESN | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02976 | hp2 | a0001 | c0002 | t0022 | g0192 | AFR | ESN | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03017 | hp1 | a0001 | c0002 | t0043 | g0079 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03017 | hp2 | a0001 | c0001 | t0011 | g0038 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03041 | hp1 | a0001 | c0002 | t0035 | g0261 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03041 | hp2 | a0001 | c0001 | t0010 | g0320 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03098 | hp1 | a0001 | c0001 | t0019 | g0215 | AFR | MSL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03098 | hp2 | a0001 | c0002 | t0034 | g0295 | AFR | MSL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03130 | hp1 | a0001 | c0002 | t0015 | g0218 | AFR | ESN | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | ESN | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03139 | hp1 | a0001 | c0002 | t0007 | g0008 | AFR | ESN | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03139 | hp2 | a0001 | c0001 | t0005 | g0149 | AFR | ESN | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03195 | hp1 | a0001 | c0002 | t0004 | g0249 | AFR | ESN | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03195 | hp2 | a0001 | c0002 | t0007 | g0202 | AFR | ESN | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03225 | hp1 | a0001 | c0002 | t0004 | g0033 | AFR | MSL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03225 | hp2 | a0001 | c0001 | t0028 | g0020 | AFR | MSL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03239 | hp1 | a0001 | c0003 | t0009 | g0326 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0011 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03453 | hp1 | a0001 | c0002 | t0004 | g0036 | AFR | MSL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03453 | hp2 | a0001 | c0002 | t0066 | g0311 | AFR | MSL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03486 | hp1 | a0001 | c0002 | t0004 | g0033 | AFR | MSL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03486 | hp2 | a0001 | c0002 | t0007 | g0243 | AFR | MSL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03490 | hp1 | a0001 | c0001 | t0053 | g0256 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0280 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0171 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0011 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03516 | hp1 | a0001 | c0002 | t0034 | g0273 | AFR | ESN | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03516 | hp2 | a0001 | c0003 | t0062 | g0324 | AFR | ESN | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03540 | hp1 | a0001 | c0002 | t0065 | g0316 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03540 | hp2 | a0001 | c0001 | t0005 | g0027 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03579 | hp1 | a0001 | c0002 | t0023 | g0045 | AFR | MSL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0042 | AFR | MSL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0266 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03669 | hp2 | a0001 | c0002 | t0021 | g0308 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0165 | SAS | STU | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03688 | hp2 | a0001 | c0002 | t0018 | g0152 | SAS | STU | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0026 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03704 | hp2 | a0001 | c0002 | t0018 | g0154 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03710 | hp1 | a0001 | c0001 | t0004 | g0127 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03710 | hp2 | a0001 | c0002 | t0001 | g0104 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0224 | SAS | BEB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03831 | hp2 | a0001 | c0002 | t0013 | g0298 | SAS | BEB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03834 | hp1 | a0001 | c0002 | t0004 | g0229 | SAS | BEB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0169 | SAS | BEB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0054 | SAS | BEB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03927 | hp2 | a0001 | c0002 | t0004 | g0252 | SAS | BEB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03942 | hp1 | a0001 | c0002 | t0004 | g0037 | SAS | BEB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03942 | hp2 | a0001 | c0002 | t0018 | g0153 | SAS | BEB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0011 | SAS | STU | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG04115 | hp2 | a0001 | c0002 | t0047 | g0107 | SAS | STU | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG04199 | hp1 | a0001 | c0002 | t0021 | g0309 | SAS | STU | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG04199 | hp2 | a0001 | c0002 | t0021 | g0329 | SAS | STU | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0173 | SAS | STU | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG04204 | hp2 | a0001 | c0002 | t0042 | g0087 | SAS | STU | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG04228 | hp1 | a0001 | c0002 | t0018 | g0155 | SAS | STU | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG04228 | hp2 | a0001 | c0003 | t0009 | g0323 | SAS | STU | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0150 | AFR | YRI | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18522 | hp2 | a0001 | c0001 | t0010 | g0333 | AFR | YRI | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18612 | hp1 | a0001 | c0002 | t0004 | g0230 | EAS | CHB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | CHB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18906 | hp1 | a0001 | c0002 | t0007 | g0008 | AFR | YRI | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18906 | hp2 | a0001 | c0001 | t0010 | g0321 | AFR | YRI | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18939 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18940 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18940 | hp2 | a0001 | c0001 | t0044 | g0175 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18942 | hp2 | a0001 | c0002 | t0004 | g0061 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18943 | hp1 | a0001 | c0001 | t0012 | g0028 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18943 | hp2 | a0001 | c0001 | t0037 | g0208 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18944 | hp2 | a0001 | c0002 | t0006 | g0159 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18946 | hp1 | a0001 | c0002 | t0004 | g0238 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18946 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0183 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18951 | hp1 | a0001 | c0001 | t0008 | g0030 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0313 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18952 | hp1 | a0001 | c0002 | t0004 | g0237 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18952 | hp2 | a0001 | c0001 | t0005 | g0206 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18953 | hp2 | a0001 | c0002 | t0004 | g0247 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18956 | hp1 | a0001 | c0001 | t0008 | g0022 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18956 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18959 | hp1 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18959 | hp2 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18961 | hp2 | a0001 | c0001 | t0020 | g0043 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0287 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18963 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18963 | hp2 | a0001 | c0002 | t0030 | g0158 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0279 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18964 | hp2 | a0001 | c0002 | t0002 | g0185 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18965 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18967 | hp2 | a0001 | c0001 | t0057 | g0315 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18968 | hp1 | a0001 | c0002 | t0006 | g0093 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18968 | hp2 | a0001 | c0001 | t0008 | g0023 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18970 | hp2 | a0001 | c0001 | t0008 | g0023 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18972 | hp1 | a0001 | c0001 | t0003 | g0283 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0282 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18977 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18978 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18980 | hp1 | a0001 | c0001 | t0012 | g0021 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0294 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18983 | hp1 | a0001 | c0002 | t0004 | g0239 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18985 | hp1 | a0001 | c0001 | t0008 | g0030 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18985 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18986 | hp1 | a0001 | c0001 | t0005 | g0195 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18986 | hp2 | a0001 | c0002 | t0006 | g0029 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18988 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18988 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18990 | hp1 | a0001 | c0002 | t0013 | g0296 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0293 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18991 | hp1 | a0001 | c0001 | t0005 | g0194 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18994 | hp1 | a0001 | c0002 | t0006 | g0162 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18995 | hp1 | a0001 | c0001 | t0005 | g0196 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18995 | hp2 | a0001 | c0002 | t0006 | g0029 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18999 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA18999 | hp2 | a0001 | c0001 | t0008 | g0132 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19001 | hp2 | a0004 | c0006 | t0059 | g0301 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19004 | hp2 | a0001 | c0001 | t0045 | g0121 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19005 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19005 | hp2 | a0001 | c0002 | t0004 | g0228 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19012 | hp1 | a0001 | c0002 | t0030 | g0177 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19012 | hp2 | a0001 | c0001 | t0020 | g0340 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | LWK | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19030 | hp2 | a0001 | c0002 | t0013 | g0310 | AFR | LWK | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19043 | hp1 | a0001 | c0002 | t0032 | g0318 | AFR | LWK | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19043 | hp2 | a0001 | c0002 | t0015 | g0219 | AFR | LWK | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19055 | hp1 | a0001 | c0001 | t0003 | g0265 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19055 | hp2 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19058 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19058 | hp2 | a0001 | c0002 | t0021 | g0312 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19060 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19065 | hp1 | a0001 | c0001 | t0020 | g0341 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19066 | hp2 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19068 | hp2 | a0001 | c0002 | t0004 | g0223 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19070 | hp1 | a0001 | c0001 | t0008 | g0022 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19070 | hp2 | a0001 | c0001 | t0020 | g0043 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19072 | hp1 | a0001 | c0002 | t0006 | g0075 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19072 | hp2 | a0001 | c0001 | t0054 | g0278 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0284 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19075 | hp1 | a0001 | c0001 | t0055 | g0286 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19075 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19077 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19081 | hp1 | a0001 | c0001 | t0036 | g0207 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19081 | hp2 | a0001 | c0001 | t0012 | g0021 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19082 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19082 | hp2 | a0002 | c0005 | t0002 | g0126 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19083 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19083 | hp2 | a0001 | c0001 | t0005 | g0204 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19084 | hp1 | a0001 | c0002 | t0006 | g0076 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19084 | hp2 | a0001 | c0002 | t0004 | g0248 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19085 | hp1 | a0001 | c0001 | t0025 | g0120 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19085 | hp2 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19086 | hp1 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19087 | hp1 | a0001 | c0001 | t0003 | g0305 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19087 | hp2 | a0001 | c0001 | t0005 | g0145 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19088 | hp1 | a0001 | c0002 | t0005 | g0049 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19088 | hp2 | a0001 | c0001 | t0025 | g0058 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19090 | hp2 | a0001 | c0001 | t0017 | g0006 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19091 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19091 | hp2 | a0001 | c0001 | t0056 | g0285 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19240 | hp1 | a0001 | c0002 | t0007 | g0201 | AFR | YRI | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA19240 | hp2 | a0001 | c0001 | t0070 | g0339 | AFR | YRI | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA20129 | hp1 | a0001 | c0002 | t0050 | g0198 | AFR | ASW | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0335 | AFR | ASW | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA20905 | hp1 | a0001 | c0002 | t0031 | g0233 | SAS | GIH | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0015 | SAS | GIH | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02109 | hp1 | a0001 | c0001 | t0071 | g0257 | AFR | ACB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02109 | hp2 | a0001 | c0001 | t0014 | g0013 | AFR | ACB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02486 | hp1 | a0001 | c0001 | t0017 | g0151 | AFR | ACB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02486 | hp2 | a0001 | c0001 | t0010 | g0332 | AFR | ACB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02559 | hp1 | a0001 | c0002 | t0016 | g0234 | AFR | ACB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG02559 | hp2 | a0001 | c0002 | t0032 | g0317 | AFR | ACB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03471 | hp1 | a0001 | c0001 | t0014 | g0013 | AFR | MSL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG03471 | hp2 | a0001 | c0002 | t0051 | g0211 | AFR | MSL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG06807 | hp1 | a0001 | c0001 | t0067 | g0307 | AFR | USA | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
HG06807 | hp2 | a0001 | c0002 | t0001 | g0091 | AFR | USA | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA20300 | hp1 | a0001 | c0002 | t0033 | g0290 | AFR | USA | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA20300 | hp2 | a0001 | c0001 | t0005 | g0210 | AFR | USA | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | LWK | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
NA21309 | hp2 | a0001 | c0001 | t0005 | g0146 | AFR | LWK | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0052 | REF | REF | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0016 | REF | REF | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:179405303
|
T | C | 1 | a0003 | 1 | HG00423.hp2 | missense_variant | MODERATE | c.803A>G | p.Asn268Ser | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/10 | 970/6315 | 803/1023 | 268/340 | chr3 | 179405303 | ||
chr3:179413452
|
T | C | 1 | a0004 | 1 | NA19001.hp2 | missense_variant | MODERATE | c.659A>G | p.Gln220Arg | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/10 | 826/6315 | 659/1023 | 220/340 | chr3 | 179413452 | ||
chr3:179419408
|
TATCCCCA others(10): Show |
T | 1 | a0002 | 1 | NA19082.hp2 | frameshift_variant | HIGH | c.177_193delTGCTATGC others(9): Show |
p.Tyr59fs | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/10 | 360/6315 | 177/1023 | 59/340 | chr3 | 179419408 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:179419485
|
A | G | 2 | a0001c0002a0003c0004 | 191 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
synonymous_variant | LOW | c.117T>C | p.Ser39Ser | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/10 | 284/6315 | 117/1023 | 39/340 | chr3 | 179419485 | ||
chr3:179426153
|
A | G | 1 | a0001c0003 | 8 | HG00735.hp2 HG01256.hp1 HG01258.hp2 others(5): Show |
synonymous_variant | LOW | c.48T>C | p.Asn16Asn | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/10 | 215/6315 | 48/1023 | 16/340 | chr3 | 179426153 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:179396154
|
T | C | 1 | a0001c0001t0027 | 2 | HG01081.hp1 HG01106.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5059A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 5059 | chr3 | 179396154 | |||||
chr3:179396256
|
C | T | 1 | a0001c0002t0033 | 2 | HG02257.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4957G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 4957 | chr3 | 179396256 | |||||
chr3:179396492
|
A | G | 2 | a0001c0002t0018a0001c0002t0021 | 8 | HG03669.hp2 HG03688.hp2 HG03704.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4721T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 4721 | chr3 | 179396492 | |||||
chr3:179396619
|
C | T | 1 | a0001c0002t0050 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4594G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 4594 | chr3 | 179396619 | |||||
chr3:179396683
|
T | C | 21 | a0001c0001t0010a0001c0001t0014a0001c0001t0019others(18): Show | 59 | HG00735.hp1 HG01069.hp1 HG01069.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*4530A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 4530 | chr3 | 179396683 | |||||
chr3:179396726
|
G | T | 1 | a0001c0002t0063 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4487C>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 4487 | chr3 | 179396726 | |||||
chr3:179396741
|
GATTA | G | 62 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(59): Show | 294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
3_prime_UTR_variant | MODIFIER | c.*4468_*4471delTAAT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 4468 | chr3 | 179396741 | |||||
chr3:179396759
|
T | C | 2 | a0001c0001t0046a0001c0001t0048 | 2 | HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4454A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 4454 | chr3 | 179396759 | |||||
chr3:179396766
|
A | T | 3 | a0001c0002t0007a0001c0002t0034a0001c0002t0050 | 12 | HG02257.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4447T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 4447 | chr3 | 179396766 | |||||
chr3:179396887
|
T | C | 1 | a0001c0002t0033 | 2 | HG02257.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4326A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 4326 | chr3 | 179396887 | |||||
chr3:179396996
|
T | G | 9 | a0001c0002t0007a0001c0002t0015a0001c0002t0023others(6): Show | 25 | HG00735.hp1 HG01069.hp1 HG01167.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*4217A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 4217 | chr3 | 179396996 | |||||
chr3:179397026
|
T | C | 1 | a0001c0001t0061 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4187A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 4187 | chr3 | 179397026 | |||||
chr3:179397230
|
G | A | 1 | a0001c0002t0049 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3983C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 3983 | chr3 | 179397230 | |||||
chr3:179397425
|
C | T | 1 | a0001c0002t0030 | 2 | NA18963.hp2 NA19012.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3788G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 3788 | chr3 | 179397425 | |||||
chr3:179397441
|
T | C | 4 | a0001c0001t0011a0001c0001t0024a0001c0001t0038others(1): Show | 11 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3772A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 3772 | chr3 | 179397441 | |||||
chr3:179397471
|
C | A | 1 | a0001c0002t0031 | 2 | HG02738.hp2 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3742G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 3742 | chr3 | 179397471 | |||||
chr3:179397534
|
T | C | 1 | a0001c0002t0066 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3679A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 3679 | chr3 | 179397534 | |||||
chr3:179397592
|
C | T | 14 | a0001c0001t0001a0001c0001t0054a0001c0001t0061others(11): Show | 94 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*3621G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 3621 | chr3 | 179397592 | |||||
chr3:179397608
|
G | C | 2 | a0001c0001t0008a0001c0001t0044 | 9 | HG00544.hp2 NA18940.hp2 NA18951.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3605C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 3605 | chr3 | 179397608 | |||||
chr3:179397612
|
G | A | 8 | a0001c0002t0007a0001c0002t0015a0001c0002t0023others(5): Show | 24 | HG00735.hp1 HG01069.hp1 HG01167.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*3601C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 3601 | chr3 | 179397612 | |||||
chr3:179397648
|
T | C | 3 | a0001c0002t0007a0001c0002t0034a0001c0002t0050 | 12 | HG02257.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3565A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 3565 | chr3 | 179397648 | |||||
chr3:179397713
|
A | T | 9 | a0001c0001t0004a0001c0002t0004a0001c0002t0013others(6): Show | 52 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*3500T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 3500 | chr3 | 179397713 | |||||
chr3:179397759
|
C | T | 1 | a0001c0003t0062 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3454G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 3454 | chr3 | 179397759 | |||||
chr3:179397760
|
G | A | 1 | a0001c0001t0067 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3453C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 3453 | chr3 | 179397760 | |||||
chr3:179397780
|
G | A | 4 | a0001c0002t0007a0001c0002t0015a0001c0002t0034others(1): Show | 17 | HG00735.hp1 HG01433.hp1 HG02257.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*3433C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 3433 | chr3 | 179397780 | |||||
chr3:179397824
|
C | A | 2 | a0001c0001t0055a0001c0001t0056 | 2 | NA19075.hp1 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3389G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 3389 | chr3 | 179397824 | |||||
chr3:179397841
|
AT | A | 10 | a0001c0001t0010a0001c0001t0014a0001c0001t0019others(7): Show | 28 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*3371delA | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 3371 | chr3 | 179397841 | |||||
chr3:179397861
|
G | A | 12 | a0001c0001t0001a0001c0001t0054a0001c0002t0001others(9): Show | 91 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*3352C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 3352 | chr3 | 179397861 | |||||
chr3:179397892
|
G | A | 1 | a0001c0001t0012 | 6 | HG00597.hp2 HG00621.hp2 HG02027.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3321C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 3321 | chr3 | 179397892 | |||||
chr3:179398322
|
C | T | 1 | a0001c0001t0060 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2891G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 2891 | chr3 | 179398322 | |||||
chr3:179398472
|
A | G | 63 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(60): Show | 295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
3_prime_UTR_variant | MODIFIER | c.*2741T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 2741 | chr3 | 179398472 | |||||
chr3:179398523
|
T | A | 1 | a0001c0002t0041 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2690A>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 2690 | chr3 | 179398523 | |||||
chr3:179398523
|
T | TA | 4 | a0001c0001t0028a0001c0001t0057a0001c0002t0032others(1): Show | 6 | HG02559.hp2 HG02647.hp2 HG03225.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2689dupT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 2689 | chr3 | 179398523 | |||||
chr3:179398523
|
T | TAAAAAAA others(76): Show |
1 | a0001c0001t0058 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2689_*2690insTTTT others(79): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 2689 | chr3 | 179398523 | |||||
chr3:179398523
|
TA | T | 23 | a0001c0001t0010a0001c0001t0014a0001c0001t0019others(20): Show | 60 | HG00735.hp1 HG01069.hp1 HG01069.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*2689delT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 2689 | chr3 | 179398523 | |||||
chr3:179398673
|
A | G | 1 | a0001c0002t0066 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2540T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 2540 | chr3 | 179398673 | |||||
chr3:179398772
|
A | AG | 20 | a0001c0001t0010a0001c0001t0014a0001c0001t0019others(17): Show | 57 | HG00735.hp1 HG01069.hp1 HG01069.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*2440dupC | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 2440 | chr3 | 179398772 | |||||
chr3:179398835
|
TTAAA | T | 17 | a0001c0001t0003a0001c0001t0005a0001c0001t0011others(14): Show | 83 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*2374_*2377delTTTA | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 2374 | chr3 | 179398835 | |||||
chr3:179398855
|
G | A | 1 | a0001c0002t0042 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2358C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 2358 | chr3 | 179398855 | |||||
chr3:179399050
|
T | A | 1 | a0001c0002t0065 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2163A>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 2163 | chr3 | 179399050 | |||||
chr3:179399077
|
A | C | 1 | a0001c0001t0045 | 1 | NA19004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2136T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 2136 | chr3 | 179399077 | |||||
chr3:179399116
|
T | C | 4 | a0001c0002t0023a0001c0002t0029a0001c0002t0035others(1): Show | 7 | HG01069.hp1 HG01167.hp1 HG01884.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2097A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 2097 | chr3 | 179399116 | |||||
chr3:179399154
|
T | C | 1 | a0001c0001t0038 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2059A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 2059 | chr3 | 179399154 | |||||
chr3:179399181
|
T | A | 1 | a0001c0002t0043 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2032A>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 2032 | chr3 | 179399181 | |||||
chr3:179399201
|
A | AT | 4 | a0001c0001t0017a0001c0001t0055a0001c0001t0056others(1): Show | 7 | HG00741.hp1 HG02040.hp1 HG02132.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2011dupA | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 2011 | chr3 | 179399201 | |||||
chr3:179399364
|
G | A | 2 | a0001c0001t0054a0001c0002t0006 | 13 | HG00280.hp2 HG00544.hp1 HG01257.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1849C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 1849 | chr3 | 179399364 | |||||
chr3:179399736
|
C | T | 1 | a0001c0002t0066 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1477G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 1477 | chr3 | 179399736 | |||||
chr3:179399797
|
C | G | 2 | a0001c0001t0055a0001c0001t0056 | 2 | NA19075.hp1 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1416G>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 1416 | chr3 | 179399797 | |||||
chr3:179399804
|
T | A | 6 | a0001c0001t0010a0001c0001t0019a0001c0001t0053others(3): Show | 20 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1409A>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 1409 | chr3 | 179399804 | |||||
chr3:179399858
|
G | A | 12 | a0001c0001t0010a0001c0001t0014a0001c0001t0019others(9): Show | 33 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1355C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 1355 | chr3 | 179399858 | |||||
chr3:179399875
|
G | C | 8 | a0001c0001t0004a0001c0002t0004a0001c0002t0013others(5): Show | 50 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*1338C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 1338 | chr3 | 179399875 | |||||
chr3:179400115
|
T | C | 12 | a0001c0001t0010a0001c0001t0014a0001c0001t0019others(9): Show | 33 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1098A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 1098 | chr3 | 179400115 | |||||
chr3:179400239
|
G | A | 12 | a0001c0001t0010a0001c0001t0014a0001c0001t0019others(9): Show | 33 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*974C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 974 | chr3 | 179400239 | |||||
chr3:179400364
|
A | C | 2 | a0001c0001t0025a0004c0006t0059 | 3 | NA19001.hp2 NA19085.hp1 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*849T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 849 | chr3 | 179400364 | |||||
chr3:179400384
|
C | T | 1 | a0001c0002t0039 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*829G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 829 | chr3 | 179400384 | |||||
chr3:179400386
|
C | T | 1 | a0001c0001t0044 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*827G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 827 | chr3 | 179400386 | |||||
chr3:179400553
|
T | C | 1 | a0001c0001t0069 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*660A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 660 | chr3 | 179400553 | |||||
chr3:179400609
|
A | C | 12 | a0001c0001t0001a0001c0001t0054a0001c0001t0071others(9): Show | 91 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*604T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 604 | chr3 | 179400609 | |||||
chr3:179400650
|
T | C | 4 | a0001c0002t0007a0001c0002t0034a0001c0002t0050others(1): Show | 13 | HG02257.hp2 HG02572.hp2 HG02630.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*563A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 563 | chr3 | 179400650 | |||||
chr3:179400916
|
T | G | 1 | a0001c0001t0020 | 4 | NA18961.hp2 NA19012.hp2 NA19065.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*297A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 297 | chr3 | 179400916 | |||||
chr3:179400977
|
T | C | 1 | a0001c0001t0036 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*236A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 236 | chr3 | 179400977 | |||||
chr3:179400978
|
A | T | 1 | a0001c0001t0036 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*235T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 235 | chr3 | 179400978 | |||||
chr3:179401088
|
T | C | 1 | a0001c0002t0035 | 2 | HG02145.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*125A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 125 | chr3 | 179401088 | |||||
chr3:179401106
|
T | C | 1 | a0001c0002t0052 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*107A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 107 | chr3 | 179401106 | |||||
chr3:179401210
|
C | T | 16 | a0001c0001t0003a0001c0001t0005a0001c0001t0011others(13): Show | 82 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*3G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 3 | chr3 | 179401210 | |||||
chr3:179426233
|
G | A | 6 | a0001c0001t0010a0001c0001t0019a0001c0001t0053others(3): Show | 16 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-33C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/10 | 33 | chr3 | 179426233 | |||||
chr3:179451372
|
C | T | 1 | a0001c0001t0053 | 1 | HG03490.hp1 | 5_prime_UTR_variant | MODIFIER | c.-69G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/10 | 25172 | chr3 | 179451372 | |||||
chr3:179451442
|
T | G | 35 | a0001c0001t0003a0001c0001t0009a0001c0001t0010others(32): Show | 112 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(109): Show |
5_prime_UTR_variant | MODIFIER | c.-139A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/10 | 25242 | chr3 | 179451442 | |||||
chr3:179451464
|
C | T | 1 | a0001c0002t0023 | 2 | HG02717.hp2 HG03579.hp1 |
5_prime_UTR_variant | MODIFIER | c.-161G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/10 | 25264 | chr3 | 179451464 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:179401348
|
C | T | 1 | a0001c0002t0004g0251 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.917-29G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179401348 | ||||||
chr3:179401445
|
AAAT | A | 81 | a0001c0001t0001g0213a0001c0002t0001g0002a0001c0002t0001g0003others(78): Show | 91 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.917-129_917-127del others(3): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179401445 | ||||||
chr3:179401445
|
AAATAAT | A | 10 | a0001c0002t0021g0308a0001c0002t0021g0309a0001c0002t0021g0312others(7): Show | 11 | HG01069.hp1 HG01167.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.917-132_917-127del others(6): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179401445 | ||||||
chr3:179401466
|
AAAC | A | 20 | a0001c0001t0010g0012a0001c0001t0010g0320a0001c0001t0010g0321others(17): Show | 22 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.917-150_917-148del others(3): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179401466 | ||||||
chr3:179401472
|
C | G | 1 | a0001c0001t0069g0319 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.917-153G>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179401472 | ||||||
chr3:179401499
|
T | A | 1 | a0001c0001t0002g0191 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.917-180A>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179401499 | ||||||
chr3:179401512
|
G | A | 5 | a0001c0002t0022g0187a0001c0002t0022g0188a0001c0002t0022g0192others(2): Show | 5 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.917-193C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179401512 | ||||||
chr3:179401562
|
G | C | 2 | a0001c0002t0032g0317a0001c0002t0032g0318 | 2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.917-243C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179401562 | ||||||
chr3:179401585
|
C | T | 20 | a0001c0001t0010g0012a0001c0001t0010g0320a0001c0001t0010g0321others(17): Show | 22 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.917-266G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179401585 | ||||||
chr3:179401611
|
A | G | 3 | a0001c0001t0014g0013a0001c0001t0014g0338a0001c0001t0067g0307 | 5 | HG02109.hp2 HG02615.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.917-292T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179401611 | ||||||
chr3:179401618
|
G | A | 1 | a0001c0002t0066g0311 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.917-299C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179401618 | ||||||
chr3:179401800
|
A | G | 2 | a0001c0002t0032g0317a0001c0002t0032g0318 | 2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.917-481T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179401800 | ||||||
chr3:179401958
|
A | C | 1 | a0001c0001t0002g0182 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.917-639T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179401958 | ||||||
chr3:179401994
|
CAA | C | 23 | a0001c0001t0010g0012a0001c0001t0010g0320a0001c0001t0010g0321others(20): Show | 27 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.917-677_917-676del others(2): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179401994 | ||||||
chr3:179402245
|
T | C | 25 | a0001c0001t0003g0039a0001c0001t0003g0041a0001c0001t0003g0268others(22): Show | 27 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.917-926A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179402245 | ||||||
chr3:179402398
|
T | C | 2 | a0001c0001t0002g0125a0001c0001t0002g0172 | 2 | HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.917-1079A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179402398 | ||||||
chr3:179402772
|
G | C | 3 | a0001c0002t0035g0261a0001c0002t0035g0263a0001c0002t0068g0259 | 3 | HG02145.hp1 HG02895.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.917-1453C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179402772 | ||||||
chr3:179402832
|
A | T | 1 | a0001c0001t0036g0207 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.917-1513T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179402832 | ||||||
chr3:179402848
|
C | A | 3 | a0001c0002t0022g0187a0001c0002t0022g0188a0001c0002t0022g0192 | 3 | HG01433.hp2 HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.917-1529G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179402848 | ||||||
chr3:179402874
|
A | G | 5 | a0001c0002t0022g0187a0001c0002t0022g0188a0001c0002t0022g0192others(2): Show | 5 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.917-1555T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179402874 | ||||||
chr3:179402881
|
C | T | 2 | a0001c0002t0033g0290a0001c0002t0033g0291 | 2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.917-1562G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179402881 | ||||||
chr3:179402893
|
C | T | 1 | a0001c0002t0065g0316 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.917-1574G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179402893 | ||||||
chr3:179402899
|
G | A | 259 | a0001c0001t0001g0213a0001c0001t0003g0010a0001c0001t0003g0011others(256): Show | 297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.917-1580C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179402899 | ||||||
chr3:179402922
|
G | A | 1 | a0001c0002t0065g0316 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.917-1603C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179402922 | ||||||
chr3:179403038
|
T | C | 1 | a0001c0001t0019g0227 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.917-1719A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403038 | ||||||
chr3:179403194
|
C | A | 8 | a0001c0001t0004g0127a0001c0002t0004g0009a0001c0002t0004g0037others(5): Show | 11 | HG00280.hp1 HG00323.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.917-1875G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403194 | ||||||
chr3:179403195
|
G | A | 72 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0039others(69): Show | 85 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.917-1876C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403195 | ||||||
chr3:179403222
|
G | T | 1 | a0001c0001t0002g0057 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.917-1903C>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403222 | ||||||
chr3:179403249
|
T | G | 2 | a0001c0002t0033g0290a0001c0002t0033g0291 | 2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.917-1930A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403249 | ||||||
chr3:179403303
|
G | GA | 15 | a0001c0001t0002g0133a0001c0001t0010g0012a0001c0001t0010g0320others(12): Show | 17 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.916+1886dupT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403303 | ||||||
chr3:179403364
|
C | A | 1 | a0001c0001t0060g0302 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.916+1826G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403364 | ||||||
chr3:179403385
|
A | C | 1 | a0001c0001t0008g0132 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.916+1805T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403385 | ||||||
chr3:179403435
|
G | A | 1 | a0001c0001t0010g0333 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.916+1755C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403435 | ||||||
chr3:179403555
|
G | A | 2 | a0001c0002t0001g0102a0001c0002t0001g0193 | 2 | HG00738.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.916+1635C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403555 | ||||||
chr3:179403602
|
G | A | 5 | a0001c0002t0022g0187a0001c0002t0022g0188a0001c0002t0022g0192others(2): Show | 5 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.916+1588C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403602 | ||||||
chr3:179403631
|
G | A | 5 | a0001c0002t0022g0187a0001c0002t0022g0188a0001c0002t0022g0192others(2): Show | 5 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.916+1559C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403631 | ||||||
chr3:179403793
|
G | A | 2 | a0001c0001t0011g0040a0001c0001t0060g0302 | 3 | HG00639.hp1 HG01517.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.916+1397C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403793 | ||||||
chr3:179403797
|
C | CAAAAA | 75 | a0001c0001t0001g0213a0001c0001t0061g0337a0001c0002t0001g0002others(72): Show | 85 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.916+1388_916+1392d others(7): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403797 | ||||||
chr3:179403800
|
A | AAAAAT | 170 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0039others(167): Show | 197 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.916+1385_916+1389d others(7): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403800 | ||||||
chr3:179403805
|
T | A | 69 | a0001c0001t0001g0213a0001c0002t0001g0002a0001c0002t0001g0003others(66): Show | 78 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.916+1385A>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403805 | ||||||
chr3:179403806
|
A | AAAAAT | 4 | a0001c0002t0001g0069a0001c0002t0001g0091a0001c0002t0001g0094others(1): Show | 4 | HG01074.hp1 HG01081.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.916+1383_916+1384i others(7): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403806 | ||||||
chr3:179403810
|
T | A | 2 | a0001c0002t0001g0073a0001c0002t0040g0179 | 2 | HG00741.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.916+1380A>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403810 | ||||||
chr3:179403826
|
T | G | 259 | a0001c0001t0001g0213a0001c0001t0003g0010a0001c0001t0003g0011others(256): Show | 297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.916+1364A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403826 | ||||||
chr3:179403850
|
A | G | 2 | a0001c0002t0032g0317a0001c0002t0032g0318 | 2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.916+1340T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403850 | ||||||
chr3:179403855
|
A | G | 5 | a0001c0002t0022g0187a0001c0002t0022g0188a0001c0002t0022g0192others(2): Show | 5 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.916+1335T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403855 | ||||||
chr3:179403885
|
C | T | 2 | a0001c0002t0032g0317a0001c0002t0032g0318 | 2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.916+1305G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403885 | ||||||
chr3:179403963
|
C | T | 1 | a0001c0001t0008g0022 | 2 | NA18956.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.916+1227G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403963 | ||||||
chr3:179404220
|
C | T | 40 | a0001c0002t0004g0032a0001c0002t0004g0033a0001c0002t0004g0061others(37): Show | 43 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.916+970G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179404220 | ||||||
chr3:179404401
|
G | A | 2 | a0001c0002t0006g0159a0001c0002t0006g0162 | 2 | NA18944.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.916+789C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179404401 | ||||||
chr3:179404704
|
C | T | 2 | a0001c0002t0014g0260a0001c0002t0014g0262 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.916+486G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179404704 | ||||||
chr3:179404806
|
A | G | 1 | a0001c0002t0015g0218 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.916+384T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179404806 | ||||||
chr3:179404854
|
G | A | 3 | a0001c0002t0022g0187a0001c0002t0022g0188a0001c0002t0022g0192 | 3 | HG01433.hp2 HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.916+336C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179404854 | ||||||
chr3:179404919
|
C | G | 82 | a0001c0001t0001g0213a0001c0001t0061g0337a0001c0002t0001g0002others(79): Show | 92 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.916+271G>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179404919 | ||||||
chr3:179405130
|
T | C | 51 | a0001c0001t0002g0156a0001c0001t0004g0127a0001c0002t0004g0009others(48): Show | 58 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.916+60A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179405130 | ||||||
chr3:179405421
|
A | G | 1 | a0001c0001t0002g0130 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.700-15T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179405421 | ||||||
chr3:179405522
|
G | A | 1 | a0001c0002t0015g0216 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.700-116C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179405522 | ||||||
chr3:179405641
|
A | G | 5 | a0001c0002t0013g0269a0001c0002t0013g0289a0001c0002t0013g0310others(2): Show | 5 | HG02647.hp1 HG02896.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.700-235T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179405641 | ||||||
chr3:179405716
|
AAT | A | 55 | a0001c0001t0004g0127a0001c0002t0004g0009a0001c0002t0004g0032others(52): Show | 62 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.700-312_700-311del others(2): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179405716 | ||||||
chr3:179405881
|
A | C | 10 | a0001c0002t0021g0308a0001c0002t0021g0309a0001c0002t0021g0312others(7): Show | 11 | HG01069.hp1 HG01167.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.700-475T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179405881 | ||||||
chr3:179405916
|
A | G | 44 | a0001c0001t0010g0012a0001c0001t0010g0320a0001c0001t0010g0321others(41): Show | 52 | HG00735.hp1 HG01069.hp1 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.700-510T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179405916 | ||||||
chr3:179405956
|
C | A | 1 | a0001c0001t0069g0319 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.700-550G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179405956 | ||||||
chr3:179406069
|
A | G | 8 | a0001c0001t0011g0038a0001c0001t0011g0040a0001c0001t0011g0267others(5): Show | 10 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.700-663T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179406069 | ||||||
chr3:179406116
|
T | C | 1 | a0001c0001t0002g0147 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.700-710A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179406116 | ||||||
chr3:179406140
|
G | A | 24 | a0001c0002t0007g0008a0001c0002t0007g0199a0001c0002t0007g0200others(21): Show | 28 | HG00735.hp1 HG01069.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.700-734C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179406140 | ||||||
chr3:179406171
|
A | C | 1 | a0001c0001t0002g0156 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.700-765T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179406171 | ||||||
chr3:179406247
|
G | A | 4 | a0001c0002t0004g0061a0001c0002t0004g0062a0001c0002t0004g0241others(1): Show | 4 | HG00438.hp2 HG02165.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.700-841C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179406247 | ||||||
chr3:179406311
|
G | A | 1 | a0001c0001t0053g0256 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.700-905C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179406311 | ||||||
chr3:179406569
|
T | C | 1 | a0001c0003t0062g0324 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.700-1163A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179406569 | ||||||
chr3:179406635
|
CAG | C | 8 | a0001c0003t0009g0322a0001c0003t0009g0323a0001c0003t0009g0325others(5): Show | 8 | HG00735.hp2 HG01256.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.700-1231_700-1230d others(4): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179406635 | ||||||
chr3:179406700
|
C | A | 3 | a0001c0001t0014g0013a0001c0001t0014g0338a0001c0001t0067g0307 | 5 | HG02109.hp2 HG02615.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.700-1294G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179406700 | ||||||
chr3:179406925
|
T | C | 5 | a0001c0002t0013g0269a0001c0002t0013g0289a0001c0002t0013g0310others(2): Show | 5 | HG02647.hp1 HG02896.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.700-1519A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179406925 | ||||||
chr3:179406972
|
T | C | 1 | a0001c0002t0049g0245 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.700-1566A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179406972 | ||||||
chr3:179407026
|
G | T | 82 | a0001c0001t0001g0213a0001c0001t0061g0337a0001c0002t0001g0002others(79): Show | 92 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.700-1620C>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179407026 | ||||||
chr3:179407112
|
T | C | 2 | a0001c0002t0032g0317a0001c0002t0032g0318 | 2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.700-1706A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179407112 | ||||||
chr3:179407150
|
G | A | 1 | a0001c0002t0066g0311 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.700-1744C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179407150 | ||||||
chr3:179407153
|
C | T | 3 | a0001c0002t0022g0187a0001c0002t0022g0188a0001c0002t0022g0192 | 3 | HG01433.hp2 HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.700-1747G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179407153 | ||||||
chr3:179407328
|
G | A | 5 | a0001c0001t0003g0010a0001c0001t0003g0279a0001c0001t0003g0281others(2): Show | 9 | HG00558.hp2 HG00609.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.700-1922C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179407328 | ||||||
chr3:179407608
|
A | C | 259 | a0001c0001t0001g0213a0001c0001t0003g0010a0001c0001t0003g0011others(256): Show | 297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.700-2202T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179407608 | ||||||
chr3:179407655
|
G | C | 5 | a0001c0002t0013g0269a0001c0002t0013g0289a0001c0002t0013g0310others(2): Show | 5 | HG02647.hp1 HG02896.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.700-2249C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179407655 | ||||||
chr3:179407740
|
A | C | 1 | a0001c0001t0010g0321 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.700-2334T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179407740 | ||||||
chr3:179407749
|
G | A | 5 | a0001c0002t0022g0187a0001c0002t0022g0188a0001c0002t0022g0192others(2): Show | 5 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.700-2343C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179407749 | ||||||
chr3:179407777
|
G | GAA | 259 | a0001c0001t0001g0213a0001c0001t0003g0010a0001c0001t0003g0011others(256): Show | 297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.700-2372_700-2371i others(4): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179407777 | ||||||
chr3:179407797
|
G | A | 50 | a0001c0001t0004g0127a0001c0002t0004g0009a0001c0002t0004g0032others(47): Show | 57 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.700-2391C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179407797 | ||||||
chr3:179407849
|
A | C | 128 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0039others(125): Show | 148 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.700-2443T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179407849 | ||||||
chr3:179407883
|
A | G | 1 | a0001c0001t0070g0339 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.700-2477T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179407883 | ||||||
chr3:179407917
|
G | T | 2 | a0001c0001t0003g0011a0001c0001t0003g0280 | 4 | HG03239.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.700-2511C>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179407917 | ||||||
chr3:179407996
|
A | G | 1 | a0001c0002t0021g0329 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.700-2590T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179407996 | ||||||
chr3:179408168
|
C | T | 2 | a0001c0001t0003g0265a0001c0001t0003g0277 | 2 | HG02027.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.700-2762G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179408168 | ||||||
chr3:179408221
|
A | C | 6 | a0001c0002t0015g0197a0001c0002t0015g0216a0001c0002t0015g0217others(3): Show | 7 | HG00735.hp1 HG01433.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.700-2815T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179408221 | ||||||
chr3:179408303
|
C | T | 1 | a0001c0001t0005g0145 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.700-2897G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179408303 | ||||||
chr3:179408541
|
A | G | 1 | a0001c0002t0032g0317 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.700-3135T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179408541 | ||||||
chr3:179408816
|
C | CA | 82 | a0001c0001t0001g0213a0001c0001t0061g0337a0001c0002t0001g0002others(79): Show | 92 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.700-3411dupT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179408816 | ||||||
chr3:179408822
|
A | G | 1 | a0001c0001t0004g0127 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.700-3416T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179408822 | ||||||
chr3:179408943
|
C | T | 1 | a0001c0002t0004g0178 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.700-3537G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179408943 | ||||||
chr3:179408956
|
G | C | 1 | a0001c0003t0009g0323 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.700-3550C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179408956 | ||||||
chr3:179409062
|
T | G | 5 | a0001c0002t0022g0187a0001c0002t0022g0188a0001c0002t0022g0192others(2): Show | 5 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.700-3656A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409062 | ||||||
chr3:179409108
|
G | A | 70 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0039others(67): Show | 83 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.700-3702C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409108 | ||||||
chr3:179409125
|
TA | T | 221 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0039others(218): Show | 253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.700-3720delT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409125 | ||||||
chr3:179409193
|
T | C | 26 | a0001c0002t0004g0032a0001c0002t0004g0061a0001c0002t0004g0062others(23): Show | 27 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(24): Show |
intron_variant | MODIFIER | c.700-3787A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409193 | ||||||
chr3:179409239
|
A | G | 259 | a0001c0001t0001g0213a0001c0001t0003g0010a0001c0001t0003g0011others(256): Show | 297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.700-3833T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409239 | ||||||
chr3:179409252
|
T | C | 128 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0039others(125): Show | 148 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.700-3846A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409252 | ||||||
chr3:179409308
|
C | A | 1 | a0001c0002t0015g0216 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.700-3902G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409308 | ||||||
chr3:179409369
|
G | A | 82 | a0001c0001t0001g0213a0001c0001t0061g0337a0001c0002t0001g0002others(79): Show | 92 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.700-3963C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409369 | ||||||
chr3:179409404
|
C | T | 2 | a0001c0002t0014g0260a0001c0002t0014g0262 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.700-3998G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409404 | ||||||
chr3:179409431
|
G | GA | 5 | a0001c0002t0022g0187a0001c0002t0022g0188a0001c0002t0022g0192others(2): Show | 5 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.699+3980dupT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409431 | ||||||
chr3:179409517
|
A | C | 1 | a0001c0001t0069g0319 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.699+3895T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409517 | ||||||
chr3:179409518
|
C | A | 1 | a0001c0001t0069g0319 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.699+3894G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409518 | ||||||
chr3:179409523
|
A | AC | 75 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0039others(72): Show | 88 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.699+3888_699+3889i others(3): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409523 | ||||||
chr3:179409523
|
A | C | 1 | a0001c0001t0069g0319 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.699+3889T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409523 | ||||||
chr3:179409680
|
T | C | 85 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0039others(82): Show | 100 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.699+3732A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409680 | ||||||
chr3:179409680
|
T | G | 1 | a0001c0001t0002g0119 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.699+3732A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409680 | ||||||
chr3:179409682
|
C | T | 1 | a0001c0001t0009g0258 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.699+3730G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409682 | ||||||
chr3:179409704
|
G | A | 1 | a0001c0002t0043g0079 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.699+3708C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409704 | ||||||
chr3:179409808
|
C | CA | 66 | a0001c0001t0002g0114a0001c0001t0002g0147a0001c0001t0002g0172others(63): Show | 73 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.699+3603dupT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409808 | ||||||
chr3:179409828
|
C | A | 3 | a0001c0001t0014g0013a0001c0001t0014g0338a0001c0001t0067g0307 | 5 | HG02109.hp2 HG02615.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.699+3584G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409828 | ||||||
chr3:179409828
|
CA | C | 7 | a0001c0001t0003g0266a0001c0002t0001g0060a0001c0002t0001g0080others(4): Show | 7 | HG01515.hp2 HG01517.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.699+3583delT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409828 | ||||||
chr3:179409831
|
A | C | 6 | a0001c0002t0001g0017a0001c0002t0001g0063a0001c0002t0001g0113others(3): Show | 7 | HG02698.hp1 HG03688.hp1 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.699+3581T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409831 | ||||||
chr3:179409832
|
A | C | 4 | a0001c0002t0022g0187a0001c0002t0022g0188a0001c0002t0022g0192others(1): Show | 5 | HG01069.hp1 HG01433.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.699+3580T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409832 | ||||||
chr3:179409832
|
AC | A | 168 | a0001c0001t0001g0213a0001c0001t0003g0010a0001c0001t0003g0011others(165): Show | 192 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.699+3579delG | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409832 | ||||||
chr3:179409833
|
C | A | 7 | a0001c0001t0014g0013a0001c0001t0014g0338a0001c0001t0067g0307others(4): Show | 10 | HG01069.hp1 HG01433.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.699+3579G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409833 | ||||||
chr3:179409833
|
CA | C | 19 | a0001c0001t0003g0282a0001c0001t0005g0145a0001c0001t0010g0012others(16): Show | 23 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.699+3578delT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409833 | ||||||
chr3:179409835
|
A | C | 4 | a0001c0002t0014g0260a0001c0002t0014g0262a0001c0002t0032g0317others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.699+3577T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409835 | ||||||
chr3:179409862
|
G | A | 5 | a0001c0002t0022g0187a0001c0002t0022g0188a0001c0002t0022g0192others(2): Show | 5 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.699+3550C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409862 | ||||||
chr3:179410058
|
G | A | 1 | a0001c0002t0006g0088 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.699+3354C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179410058 | ||||||
chr3:179410102
|
A | G | 2 | a0001c0002t0014g0260a0001c0002t0014g0262 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.699+3310T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179410102 | ||||||
chr3:179410118
|
T | C | 81 | a0001c0001t0001g0213a0001c0002t0001g0002a0001c0002t0001g0003others(78): Show | 91 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.699+3294A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179410118 | ||||||
chr3:179410124
|
G | C | 2 | a0001c0002t0001g0019a0001c0002t0001g0071 | 3 | HG02071.hp1 HG02083.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.699+3288C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179410124 | ||||||
chr3:179410212
|
G | A | 5 | a0001c0002t0022g0187a0001c0002t0022g0188a0001c0002t0022g0192others(2): Show | 5 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.699+3200C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179410212 | ||||||
chr3:179410351
|
G | T | 1 | a0001c0001t0003g0294 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.699+3061C>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179410351 | ||||||
chr3:179410354
|
T | A | 1 | a0001c0002t0004g0239 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.699+3058A>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179410354 | ||||||
chr3:179410573
|
T | C | 1 | a0001c0002t0004g0240 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.699+2839A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179410573 | ||||||
chr3:179410592
|
T | C | 1 | a0001c0001t0003g0270 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.699+2820A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179410592 | ||||||
chr3:179410663
|
A | T | 8 | a0001c0001t0011g0038a0001c0001t0011g0040a0001c0001t0011g0267others(5): Show | 10 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.699+2749T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179410663 | ||||||
chr3:179410786
|
A | G | 1 | a0001c0001t0005g0144 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.699+2626T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179410786 | ||||||
chr3:179411026
|
T | C | 1 | a0001c0002t0043g0079 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.699+2386A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179411026 | ||||||
chr3:179411466
|
C | CA | 21 | a0001c0001t0005g0150a0001c0001t0057g0315a0001c0002t0001g0003others(18): Show | 25 | HG00609.hp1 HG01433.hp2 HG02015.hp2 others(22): Show |
intron_variant | MODIFIER | c.699+1945dupT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179411466 | ||||||
chr3:179411466
|
C | CAA | 48 | a0001c0001t0004g0127a0001c0002t0004g0009a0001c0002t0004g0032others(45): Show | 55 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.699+1944_699+1945d others(4): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179411466 | ||||||
chr3:179411466
|
CA | C | 8 | a0001c0001t0003g0335a0001c0001t0010g0332a0001c0001t0010g0333others(5): Show | 9 | HG01069.hp1 HG01884.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.699+1945delT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179411466 | ||||||
chr3:179411494
|
T | C | 5 | a0001c0002t0022g0187a0001c0002t0022g0188a0001c0002t0022g0192others(2): Show | 5 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.699+1918A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179411494 | ||||||
chr3:179411534
|
G | A | 1 | a0001c0001t0003g0335 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.699+1878C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179411534 | ||||||
chr3:179411568
|
A | G | 259 | a0001c0001t0001g0213a0001c0001t0003g0010a0001c0001t0003g0011others(256): Show | 297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.699+1844T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179411568 | ||||||
chr3:179411818
|
A | C | 5 | a0001c0002t0022g0187a0001c0002t0022g0188a0001c0002t0022g0192others(2): Show | 5 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.699+1594T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179411818 | ||||||
chr3:179411867
|
A | T | 259 | a0001c0001t0001g0213a0001c0001t0003g0010a0001c0001t0003g0011others(256): Show | 297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.699+1545T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179411867 | ||||||
chr3:179411913
|
A | G | 2 | a0001c0001t0005g0205a0001c0001t0005g0212 | 2 | HG01346.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.699+1499T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179411913 | ||||||
chr3:179411985
|
C | T | 5 | a0001c0002t0007g0199a0001c0002t0007g0200a0001c0002t0007g0202others(2): Show | 5 | HG02572.hp2 HG02630.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.699+1427G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179411985 | ||||||
chr3:179412094
|
T | C | 14 | a0001c0001t0010g0012a0001c0001t0010g0320a0001c0001t0010g0321others(11): Show | 16 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.699+1318A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179412094 | ||||||
chr3:179412146
|
G | GT | 5 | a0001c0002t0022g0187a0001c0002t0022g0188a0001c0002t0022g0192others(2): Show | 5 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.699+1265dupA | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179412146 | ||||||
chr3:179412316
|
A | AAAAC | 249 | a0001c0001t0001g0213a0001c0001t0003g0010a0001c0001t0003g0011others(246): Show | 285 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.699+1092_699+1095d others(6): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179412316 | ||||||
chr3:179412320
|
C | A | 1 | a0001c0001t0009g0258 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.699+1092G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179412320 | ||||||
chr3:179412322
|
A | AAC | 10 | a0001c0001t0011g0038a0001c0001t0011g0040a0001c0001t0011g0264others(7): Show | 12 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.699+1088_699+1089d others(4): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179412322 | ||||||
chr3:179412396
|
T | C | 2 | a0001c0003t0009g0327a0001c0003t0009g0328 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.699+1016A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179412396 | ||||||
chr3:179412469
|
C | A | 2 | a0001c0002t0032g0317a0001c0002t0032g0318 | 2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.699+943G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179412469 | ||||||
chr3:179412673
|
G | A | 1 | a0001c0001t0024g0209 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.699+739C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179412673 | ||||||
chr3:179412852
|
A | G | 14 | a0001c0001t0001g0213a0001c0002t0001g0017a0001c0002t0001g0063others(11): Show | 15 | HG00408.hp1 HG01515.hp2 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.699+560T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179412852 | ||||||
chr3:179413138
|
G | A | 1 | a0001c0001t0002g0055 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.699+274C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179413138 | ||||||
chr3:179413157
|
G | A | 2 | a0001c0003t0009g0327a0001c0003t0009g0328 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.699+255C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179413157 | ||||||
chr3:179413190
|
AT | A | 5 | a0001c0002t0022g0187a0001c0002t0022g0188a0001c0002t0022g0192others(2): Show | 5 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.699+221delA | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179413190 | ||||||
chr3:179413275
|
T | C | 6 | a0001c0002t0013g0269a0001c0002t0013g0289a0001c0002t0013g0310others(3): Show | 6 | HG02647.hp1 HG02896.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.699+137A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179413275 | ||||||
chr3:179413314
|
G | T | 1 | a0001c0001t0002g0059 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.699+98C>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179413314 | ||||||
chr3:179413362
|
C | T | 1 | a0001c0001t0020g0340 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.699+50G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179413362 | ||||||
chr3:179413806
|
T | G | 1 | a0001c0001t0044g0175 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.431-25A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 6/9 | chr3 | 179413806 | ||||||
chr3:179413830
|
T | C | 1 | a0001c0001t0002g0139 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.431-49A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 6/9 | chr3 | 179413830 | ||||||
chr3:179413864
|
A | T | 114 | a0001c0001t0001g0213a0001c0001t0044g0175a0001c0002t0001g0002others(111): Show | 128 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.431-83T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 6/9 | chr3 | 179413864 | ||||||
chr3:179413869
|
T | C | 1 | a0001c0002t0066g0311 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.431-88A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 6/9 | chr3 | 179413869 | ||||||
chr3:179413884
|
A | C | 1 | a0001c0001t0044g0175 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.431-103T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 6/9 | chr3 | 179413884 | ||||||
chr3:179413887
|
A | T | 1 | a0001c0001t0044g0175 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.431-106T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 6/9 | chr3 | 179413887 | ||||||
chr3:179413898
|
A | T | 1 | a0001c0001t0044g0175 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.431-117T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 6/9 | chr3 | 179413898 | ||||||
chr3:179413899
|
T | C | 1 | a0001c0001t0044g0175 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.431-118A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 6/9 | chr3 | 179413899 | ||||||
chr3:179414092
|
C | T | 11 | a0001c0002t0014g0260a0001c0002t0014g0262a0001c0002t0021g0308others(8): Show | 12 | HG01069.hp1 HG01167.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.431-311G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 6/9 | chr3 | 179414092 | ||||||
chr3:179414134
|
T | A | 5 | a0001c0002t0022g0187a0001c0002t0022g0188a0001c0002t0022g0192others(2): Show | 5 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.431-353A>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 6/9 | chr3 | 179414134 | ||||||
chr3:179414157
|
C | T | 5 | a0001c0002t0004g0032a0001c0002t0004g0178a0001c0002t0004g0231others(2): Show | 6 | HG00140.hp1 HG00323.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.431-376G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 6/9 | chr3 | 179414157 | ||||||
chr3:179414596
|
A | C | 1 | a0001c0001t0053g0256 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.430+289T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 6/9 | chr3 | 179414596 | ||||||
chr3:179414664
|
C | A | 2 | a0001c0002t0032g0317a0001c0002t0032g0318 | 2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.430+221G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 6/9 | chr3 | 179414664 | ||||||
chr3:179414727
|
C | CTA | 84 | a0001c0001t0001g0213a0001c0001t0055g0286a0001c0001t0056g0285others(81): Show | 94 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.430+156_430+157dup others(2): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 6/9 | chr3 | 179414727 | ||||||
chr3:179414784
|
C | T | 3 | a0001c0002t0001g0113a0001c0002t0001g0165a0001c0002t0047g0107 | 3 | HG02698.hp1 HG03688.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.430+101G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 6/9 | chr3 | 179414784 | ||||||
chr3:179415447
|
G | C | 13 | a0001c0001t0010g0012a0001c0001t0010g0320a0001c0001t0010g0321others(10): Show | 15 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.268-400C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 5/9 | chr3 | 179415447 | ||||||
chr3:179415640
|
A | AAAGT | 123 | a0001c0001t0001g0213a0001c0001t0055g0286a0001c0001t0056g0285others(120): Show | 137 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.268-594_268-593ins others(4): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 5/9 | chr3 | 179415640 | ||||||
chr3:179415728
|
A | G | 1 | a0001c0002t0066g0311 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.268-681T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 5/9 | chr3 | 179415728 | ||||||
chr3:179415980
|
CTA | C | 68 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0039others(65): Show | 81 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.267+511_267+512del others(2): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 5/9 | chr3 | 179415980 | ||||||
chr3:179416095
|
A | C | 2 | a0001c0002t0006g0159a0001c0002t0006g0162 | 2 | NA18944.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.267+398T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 5/9 | chr3 | 179416095 | ||||||
chr3:179416121
|
G | C | 13 | a0001c0001t0010g0012a0001c0001t0010g0320a0001c0001t0010g0321others(10): Show | 15 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.267+372C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 5/9 | chr3 | 179416121 | ||||||
chr3:179416220
|
A | T | 1 | a0004c0006t0059g0301 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.267+273T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 5/9 | chr3 | 179416220 | ||||||
chr3:179416559
|
A | G | 1 | a0001c0002t0001g0109 | 1 | NA18956.hp2 | splice_region_variant&intron_variant | LOW | c.204-3T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179416559 | ||||||
chr3:179416610
|
A | T | 1 | a0001c0001t0044g0175 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.204-54T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179416610 | ||||||
chr3:179416623
|
T | C | 8 | a0001c0002t0022g0187a0001c0002t0022g0188a0001c0002t0022g0192others(5): Show | 8 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.204-67A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179416623 | ||||||
chr3:179416745
|
A | G | 1 | a0001c0001t0003g0270 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.204-189T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179416745 | ||||||
chr3:179416795
|
T | A | 1 | a0001c0001t0044g0175 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.204-239A>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179416795 | ||||||
chr3:179416833
|
G | T | 1 | a0001c0001t0044g0175 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.204-277C>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179416833 | ||||||
chr3:179416846
|
G | C | 82 | a0001c0001t0001g0213a0001c0002t0001g0002a0001c0002t0001g0003others(79): Show | 92 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.204-290C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179416846 | ||||||
chr3:179416887
|
A | T | 1 | a0001c0001t0044g0175 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.204-331T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179416887 | ||||||
chr3:179416966
|
T | A | 1 | a0001c0001t0044g0175 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.204-410A>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179416966 | ||||||
chr3:179417008
|
T | A | 1 | a0001c0001t0044g0175 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.204-452A>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179417008 | ||||||
chr3:179417340
|
A | C | 1 | a0001c0002t0023g0044 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.204-784T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179417340 | ||||||
chr3:179417388
|
T | A | 1 | a0001c0001t0044g0175 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.204-832A>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179417388 | ||||||
chr3:179417388
|
T | G | 49 | a0001c0002t0004g0009a0001c0002t0004g0032a0001c0002t0004g0033others(46): Show | 56 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.204-832A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179417388 | ||||||
chr3:179417409
|
A | AT | 23 | a0001c0001t0005g0149a0001c0001t0005g0150a0001c0001t0010g0012others(20): Show | 27 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.204-854dupA | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179417409 | ||||||
chr3:179417409
|
AT | A | 53 | a0001c0002t0004g0009a0001c0002t0004g0032a0001c0002t0004g0033others(50): Show | 60 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.204-854delA | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179417409 | ||||||
chr3:179417471
|
G | A | 4 | a0001c0002t0013g0269a0001c0002t0013g0289a0001c0002t0013g0310others(1): Show | 4 | HG02647.hp1 HG02896.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.204-915C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179417471 | ||||||
chr3:179417471
|
G | T | 86 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0014others(83): Show | 96 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.204-915C>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179417471 | ||||||
chr3:179417493
|
C | T | 1 | a0001c0001t0002g0131 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.204-937G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179417493 | ||||||
chr3:179417533
|
G | A | 1 | a0001c0001t0002g0116 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.204-977C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179417533 | ||||||
chr3:179417537
|
A | T | 1 | a0001c0001t0044g0175 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.204-981T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179417537 | ||||||
chr3:179417564
|
C | T | 5 | a0001c0002t0022g0187a0001c0002t0022g0188a0001c0002t0022g0192others(2): Show | 5 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.204-1008G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179417564 | ||||||
chr3:179417831
|
C | G | 1 | a0001c0002t0004g0251 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.204-1275G>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179417831 | ||||||
chr3:179417940
|
A | G | 1 | a0001c0002t0066g0311 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.204-1384T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179417940 | ||||||
chr3:179417971
|
T | C | 1 | a0001c0001t0069g0319 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.204-1415A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179417971 | ||||||
chr3:179418194
|
G | A | 46 | a0001c0001t0069g0319a0001c0002t0004g0009a0001c0002t0004g0032others(43): Show | 52 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.203+1205C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179418194 | ||||||
chr3:179418195
|
C | T | 1 | a0001c0001t0002g0118 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.203+1204G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179418195 | ||||||
chr3:179418205
|
C | A | 1 | a0001c0002t0001g0071 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.203+1194G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179418205 | ||||||
chr3:179418253
|
T | C | 4 | a0001c0002t0013g0269a0001c0002t0013g0289a0001c0002t0013g0310others(1): Show | 4 | HG02647.hp1 HG02896.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.203+1146A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179418253 | ||||||
chr3:179418394
|
TG | T | 13 | a0001c0001t0010g0012a0001c0001t0010g0320a0001c0001t0010g0321others(10): Show | 15 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.203+1004delC | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179418394 | ||||||
chr3:179418470
|
C | CAA | 38 | a0001c0002t0004g0009a0001c0002t0004g0032a0001c0002t0004g0033others(35): Show | 45 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.203+927_203+928dup others(2): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179418470 | ||||||
chr3:179418470
|
C | CAAA | 14 | a0001c0002t0004g0229a0001c0002t0004g0231a0001c0002t0004g0235others(11): Show | 14 | HG00323.hp2 HG01243.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.203+926_203+928dup others(3): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179418470 | ||||||
chr3:179418470
|
CA | C | 157 | a0001c0001t0001g0213a0001c0001t0002g0130a0001c0001t0003g0010others(154): Show | 181 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.203+928delT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179418470 | ||||||
chr3:179418470
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0011g0303 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.203+916_203+928del others(13): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179418470 | ||||||
chr3:179418489
|
G | A | 53 | a0001c0002t0004g0009a0001c0002t0004g0032a0001c0002t0004g0033others(50): Show | 60 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.203+910C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179418489 | ||||||
chr3:179419010
|
G | A | 3 | a0001c0001t0003g0041a0001c0001t0003g0313a0001c0001t0057g0315 | 4 | NA18951.hp2 NA18967.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.203+389C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179419010 | ||||||
chr3:179419047
|
A | T | 1 | a0001c0001t0003g0276 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.203+352T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179419047 | ||||||
chr3:179419311
|
T | C | 5 | a0001c0002t0022g0187a0001c0002t0022g0188a0001c0002t0022g0192others(2): Show | 5 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.203+88A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179419311 | ||||||
chr3:179419314
|
T | C | 31 | a0001c0002t0007g0008a0001c0002t0007g0199a0001c0002t0007g0200others(28): Show | 35 | HG00735.hp1 HG01069.hp1 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.203+85A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179419314 | ||||||
chr3:179419743
|
G | T | 1 | a0001c0002t0021g0312 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.97-238C>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 3/9 | chr3 | 179419743 | ||||||
chr3:179419939
|
T | C | 1 | a0001c0001t0001g0213 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.97-434A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 3/9 | chr3 | 179419939 | ||||||
chr3:179419965
|
A | T | 51 | a0001c0002t0004g0009a0001c0002t0004g0032a0001c0002t0004g0033others(48): Show | 58 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.97-460T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 3/9 | chr3 | 179419965 | ||||||
chr3:179420064
|
A | G | 1 | a0001c0002t0004g0231 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.97-559T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 3/9 | chr3 | 179420064 | ||||||
chr3:179420277
|
C | T | 1 | a0001c0001t0053g0256 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.96+612G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 3/9 | chr3 | 179420277 | ||||||
chr3:179420303
|
G | GT | 7 | a0001c0001t0002g0182a0001c0001t0011g0264a0001c0001t0044g0175others(4): Show | 7 | HG02055.hp1 HG02976.hp1 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.96+585dupA | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 3/9 | chr3 | 179420303 | ||||||
chr3:179420303
|
GT | G | 8 | a0001c0002t0021g0308a0001c0002t0021g0309a0001c0002t0021g0312others(5): Show | 8 | HG02257.hp1 HG02559.hp2 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.96+585delA | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 3/9 | chr3 | 179420303 | ||||||
chr3:179420304
|
T | G | 50 | a0001c0002t0004g0009a0001c0002t0004g0032a0001c0002t0004g0033others(47): Show | 57 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.96+585A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 3/9 | chr3 | 179420304 | ||||||
chr3:179420331
|
G | A | 1 | a0001c0001t0009g0258 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.96+558C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 3/9 | chr3 | 179420331 | ||||||
chr3:179420467
|
TA | T | 118 | a0001c0001t0001g0213a0001c0001t0003g0010a0001c0001t0003g0011others(115): Show | 140 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.96+421delT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 3/9 | chr3 | 179420467 | ||||||
chr3:179420469
|
TA | T | 92 | a0001c0001t0005g0146a0001c0001t0024g0222a0001c0001t0067g0307others(89): Show | 102 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.96+419delT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 3/9 | chr3 | 179420469 | ||||||
chr3:179420470
|
A | AT | 13 | a0001c0001t0010g0012a0001c0001t0010g0321a0001c0001t0010g0332others(10): Show | 15 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.96+418dupA | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 3/9 | chr3 | 179420470 | ||||||
chr3:179420470
|
A | T | 131 | a0001c0001t0001g0213a0001c0001t0002g0055a0001c0001t0002g0059others(128): Show | 154 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.96+419T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 3/9 | chr3 | 179420470 | ||||||
chr3:179420472
|
T | A | 3 | a0001c0001t0028g0020a0001c0001t0046g0190a0001c0001t0048g0189 | 4 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+417A>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 3/9 | chr3 | 179420472 | ||||||
chr3:179420526
|
G | A | 81 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0014others(78): Show | 91 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.96+363C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 3/9 | chr3 | 179420526 | ||||||
chr3:179420540
|
G | C | 1 | a0001c0001t0011g0264 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.96+349C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 3/9 | chr3 | 179420540 | ||||||
chr3:179420755
|
G | A | 5 | a0001c0002t0022g0187a0001c0002t0022g0188a0001c0002t0022g0192others(2): Show | 5 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+134C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 3/9 | chr3 | 179420755 | ||||||
chr3:179420769
|
CAG | C | 3 | a0001c0001t0014g0013a0001c0001t0014g0338a0001c0001t0061g0337 | 5 | HG02109.hp2 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+118_96+119delCT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 3/9 | chr3 | 179420769 | ||||||
chr3:179420794
|
A | G | 1 | a0001c0001t0002g0129 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.96+95T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 3/9 | chr3 | 179420794 | ||||||
chr3:179420814
|
T | A | 1 | a0001c0002t0004g0062 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.96+75A>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 3/9 | chr3 | 179420814 | ||||||
chr3:179420934
|
T | TA | 6 | a0001c0002t0001g0064a0001c0002t0022g0187a0001c0002t0022g0188others(3): Show | 6 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.58-8dupT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179420934 | ||||||
chr3:179421196
|
A | G | 72 | a0001c0001t0001g0213a0001c0001t0003g0010a0001c0001t0003g0011others(69): Show | 85 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.58-269T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179421196 | ||||||
chr3:179421200
|
C | G | 1 | a0001c0001t0067g0307 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-273G>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179421200 | ||||||
chr3:179421444
|
A | G | 8 | a0001c0003t0009g0322a0001c0003t0009g0323a0001c0003t0009g0325others(5): Show | 8 | HG00735.hp2 HG01256.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.58-517T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179421444 | ||||||
chr3:179421462
|
T | C | 1 | a0001c0002t0066g0311 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.58-535A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179421462 | ||||||
chr3:179421491
|
A | C | 30 | a0001c0002t0007g0008a0001c0002t0007g0199a0001c0002t0007g0200others(27): Show | 34 | HG00735.hp1 HG01069.hp1 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.58-564T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179421491 | ||||||
chr3:179421523
|
A | C | 2 | a0001c0002t0001g0180a0001c0002t0001g0181 | 2 | NA18959.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.58-596T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179421523 | ||||||
chr3:179421656
|
A | C | 4 | a0001c0002t0013g0269a0001c0002t0013g0289a0001c0002t0013g0310others(1): Show | 4 | HG02647.hp1 HG02896.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.58-729T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179421656 | ||||||
chr3:179421672
|
C | T | 4 | a0001c0001t0003g0010a0001c0001t0003g0279a0001c0001t0003g0304others(1): Show | 8 | HG00558.hp2 HG00609.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.58-745G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179421672 | ||||||
chr3:179421831
|
A | G | 1 | a0001c0002t0065g0316 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.58-904T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179421831 | ||||||
chr3:179421916
|
T | G | 1 | a0001c0001t0067g0307 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-989A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179421916 | ||||||
chr3:179422054
|
A | C | 1 | a0001c0002t0004g0237 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.58-1127T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179422054 | ||||||
chr3:179422185
|
C | G | 258 | a0001c0001t0001g0213a0001c0001t0003g0010a0001c0001t0003g0011others(255): Show | 296 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.58-1258G>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179422185 | ||||||
chr3:179422195
|
G | GT | 7 | a0001c0002t0001g0017a0001c0002t0001g0063a0001c0002t0001g0068others(4): Show | 8 | HG00408.hp1 HG01978.hp2 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.58-1269dupA | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179422195 | ||||||
chr3:179422352
|
C | T | 1 | a0001c0003t0009g0322 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.58-1425G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179422352 | ||||||
chr3:179422444
|
C | T | 1 | a0001c0002t0001g0067 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.58-1517G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179422444 | ||||||
chr3:179422464
|
A | G | 71 | a0001c0001t0001g0213a0001c0001t0002g0170a0001c0001t0003g0010others(68): Show | 84 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.58-1537T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179422464 | ||||||
chr3:179422486
|
C | CA | 82 | a0001c0002t0004g0009a0001c0002t0004g0032a0001c0002t0004g0033others(79): Show | 93 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.58-1560dupT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179422486 | ||||||
chr3:179422583
|
T | C | 2 | a0001c0001t0055g0286a0001c0001t0056g0285 | 2 | NA19075.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.58-1656A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179422583 | ||||||
chr3:179422832
|
G | A | 70 | a0001c0001t0001g0213a0001c0001t0003g0010a0001c0001t0003g0011others(67): Show | 83 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.58-1905C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179422832 | ||||||
chr3:179422853
|
C | T | 5 | a0001c0002t0022g0187a0001c0002t0022g0188a0001c0002t0022g0192others(2): Show | 5 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.58-1926G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179422853 | ||||||
chr3:179422854
|
G | A | 3 | a0001c0001t0014g0013a0001c0001t0014g0338a0001c0001t0061g0337 | 5 | HG02109.hp2 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.58-1927C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179422854 | ||||||
chr3:179422918
|
G | A | 1 | a0001c0001t0003g0281 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.58-1991C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179422918 | ||||||
chr3:179422926
|
G | A | 1 | a0001c0001t0014g0338 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.58-1999C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179422926 | ||||||
chr3:179422950
|
G | A | 71 | a0001c0001t0001g0213a0001c0001t0003g0010a0001c0001t0003g0011others(68): Show | 84 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.58-2023C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179422950 | ||||||
chr3:179422993
|
A | G | 1 | a0001c0001t0067g0307 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-2066T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179422993 | ||||||
chr3:179423017
|
T | C | 2 | a0001c0002t0033g0290a0001c0002t0033g0291 | 2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.58-2090A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179423017 | ||||||
chr3:179423038
|
G | A | 1 | a0001c0001t0002g0128 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.58-2111C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179423038 | ||||||
chr3:179423051
|
A | G | 7 | a0001c0002t0004g0009a0001c0002t0004g0037a0001c0002t0004g0249others(4): Show | 10 | HG00280.hp1 HG00323.hp1 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.58-2124T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179423051 | ||||||
chr3:179423081
|
G | A | 1 | a0001c0001t0067g0307 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-2154C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179423081 | ||||||
chr3:179423200
|
C | T | 3 | a0001c0002t0001g0060a0001c0002t0001g0080a0001c0002t0001g0085 | 3 | HG02523.hp2 NA18962.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.58-2273G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179423200 | ||||||
chr3:179423210
|
A | G | 1 | a0001c0002t0006g0084 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.58-2283T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179423210 | ||||||
chr3:179423292
|
T | C | 3 | a0001c0001t0014g0013a0001c0001t0014g0338a0001c0001t0061g0337 | 5 | HG02109.hp2 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.58-2365A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179423292 | ||||||
chr3:179423320
|
C | T | 3 | a0001c0001t0014g0013a0001c0001t0014g0338a0001c0001t0061g0337 | 5 | HG02109.hp2 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.58-2393G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179423320 | ||||||
chr3:179423526
|
G | A | 9 | a0001c0002t0007g0008a0001c0002t0007g0199a0001c0002t0007g0200others(6): Show | 11 | HG02257.hp2 HG02572.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.58-2599C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179423526 | ||||||
chr3:179423580
|
A | C | 1 | a0001c0001t0003g0281 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.57+2564T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179423580 | ||||||
chr3:179423642
|
G | A | 1 | a0001c0002t0001g0082 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.57+2502C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179423642 | ||||||
chr3:179423653
|
T | C | 1 | a0001c0001t0003g0268 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.57+2491A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179423653 | ||||||
chr3:179423709
|
A | G | 2 | a0001c0002t0032g0317a0001c0002t0032g0318 | 2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.57+2435T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179423709 | ||||||
chr3:179423786
|
T | TA | 158 | a0001c0001t0001g0213a0001c0001t0003g0010a0001c0001t0003g0011others(155): Show | 184 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.57+2357dupT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179423786 | ||||||
chr3:179423812
|
G | C | 3 | a0001c0002t0022g0187a0001c0002t0022g0188a0001c0002t0022g0192 | 3 | HG01433.hp2 HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.57+2332C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179423812 | ||||||
chr3:179423823
|
T | C | 3 | a0001c0001t0014g0013a0001c0001t0014g0338a0001c0001t0061g0337 | 5 | HG02109.hp2 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.57+2321A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179423823 | ||||||
chr3:179423880
|
C | T | 2 | a0001c0002t0004g0033a0001c0002t0004g0229 | 3 | HG03225.hp1 HG03486.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.57+2264G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179423880 | ||||||
chr3:179423928
|
G | A | 1 | a0001c0002t0001g0078 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.57+2216C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179423928 | ||||||
chr3:179423971
|
A | G | 2 | a0001c0002t0006g0083a0001c0002t0006g0161 | 2 | HG01257.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.57+2173T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179423971 | ||||||
chr3:179424049
|
C | T | 81 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0014others(78): Show | 91 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.57+2095G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179424049 | ||||||
chr3:179424248
|
C | A | 1 | a0001c0002t0066g0311 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.57+1896G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179424248 | ||||||
chr3:179424290
|
G | A | 2 | a0001c0002t0033g0290a0001c0002t0033g0291 | 2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.57+1854C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179424290 | ||||||
chr3:179424565
|
G | A | 1 | a0001c0002t0004g0244 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.57+1579C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179424565 | ||||||
chr3:179424714
|
C | T | 1 | a0001c0002t0021g0308 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.57+1430G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179424714 | ||||||
chr3:179424769
|
T | C | 1 | a0001c0001t0067g0307 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57+1375A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179424769 | ||||||
chr3:179424861
|
G | A | 4 | a0001c0002t0004g0036a0001c0002t0004g0244a0001c0002t0007g0243others(1): Show | 5 | HG01261.hp1 HG02886.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.57+1283C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179424861 | ||||||
chr3:179425179
|
A | G | 1 | a0001c0002t0021g0312 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.57+965T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179425179 | ||||||
chr3:179425344
|
C | T | 1 | a0001c0001t0002g0174 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.57+800G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179425344 | ||||||
chr3:179425345
|
G | A | 2 | a0001c0001t0003g0011a0001c0001t0003g0280 | 4 | HG03239.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.57+799C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179425345 | ||||||
chr3:179425544
|
C | T | 1 | a0001c0002t0001g0082 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.57+600G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179425544 | ||||||
chr3:179425617
|
T | C | 248 | a0001c0001t0001g0213a0001c0001t0002g0053a0001c0001t0003g0010others(245): Show | 283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.57+527A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179425617 | ||||||
chr3:179425618
|
G | A | 248 | a0001c0001t0001g0213a0001c0001t0002g0053a0001c0001t0003g0010others(245): Show | 283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.57+526C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179425618 | ||||||
chr3:179425620
|
A | G | 248 | a0001c0001t0001g0213a0001c0001t0002g0053a0001c0001t0003g0010others(245): Show | 283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.57+524T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179425620 | ||||||
chr3:179425639
|
TTTTCTAT others(24): Show |
T | 1 | a0002c0005t0002g0126 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.57+474_57+504delGG others(29): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179425639 | ||||||
chr3:179425642
|
T | C | 12 | a0001c0002t0015g0197a0001c0002t0015g0216a0001c0002t0015g0217others(9): Show | 13 | HG00735.hp1 HG01433.hp1 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.57+502A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179425642 | ||||||
chr3:179425715
|
C | A | 2 | a0001c0001t0067g0307a0001c0002t0063g0306 | 2 | HG01167.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.57+429G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179425715 | ||||||
chr3:179425751
|
A | G | 1 | a0001c0002t0006g0093 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.57+393T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179425751 | ||||||
chr3:179425762
|
T | C | 1 | a0001c0002t0007g0201 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.57+382A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179425762 | ||||||
chr3:179425767
|
A | G | 1 | a0001c0002t0007g0201 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.57+377T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179425767 | ||||||
chr3:179425881
|
G | A | 1 | a0001c0002t0065g0316 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.57+263C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179425881 | ||||||
chr3:179426407
|
AT | A | 6 | a0001c0002t0015g0197a0001c0002t0015g0216a0001c0002t0015g0217others(3): Show | 7 | HG00735.hp1 HG01433.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-42-166delA | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179426407 | ||||||
chr3:179426640
|
G | C | 1 | a0001c0002t0065g0316 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-42-398C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179426640 | ||||||
chr3:179426646
|
G | A | 18 | a0001c0001t0009g0258a0001c0001t0014g0013a0001c0001t0014g0338others(15): Show | 21 | HG01069.hp1 HG01167.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.-42-404C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179426646 | ||||||
chr3:179426652
|
A | T | 174 | a0001c0001t0001g0213a0001c0001t0003g0010a0001c0001t0003g0011others(171): Show | 201 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.-42-410T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179426652 | ||||||
chr3:179426847
|
G | A | 157 | a0001c0001t0001g0213a0001c0001t0003g0010a0001c0001t0003g0011others(154): Show | 182 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.-42-605C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179426847 | ||||||
chr3:179426951
|
C | T | 132 | a0001c0001t0001g0213a0001c0001t0003g0010a0001c0001t0003g0011others(129): Show | 152 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.-42-709G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179426951 | ||||||
chr3:179426987
|
C | T | 2 | a0001c0001t0067g0307a0001c0002t0063g0306 | 2 | HG01167.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-42-745G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179426987 | ||||||
chr3:179426988
|
C | A | 175 | a0001c0001t0001g0213a0001c0001t0003g0010a0001c0001t0003g0011others(172): Show | 202 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.-42-746G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179426988 | ||||||
chr3:179427004
|
G | A | 14 | a0001c0001t0010g0012a0001c0001t0010g0320a0001c0001t0010g0321others(11): Show | 16 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.-42-762C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179427004 | ||||||
chr3:179427146
|
C | T | 185 | a0001c0001t0003g0042a0001c0001t0003g0335a0001c0001t0003g0336others(182): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.-42-904G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179427146 | ||||||
chr3:179427269
|
C | G | 1 | a0001c0001t0069g0319 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-42-1027G>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179427269 | ||||||
chr3:179427327
|
T | G | 43 | a0001c0001t0009g0258a0001c0001t0010g0012a0001c0001t0010g0320others(40): Show | 50 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.-42-1085A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179427327 | ||||||
chr3:179427425
|
C | T | 11 | a0001c0002t0015g0197a0001c0002t0015g0216a0001c0002t0015g0217others(8): Show | 12 | HG00735.hp1 HG01433.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.-42-1183G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179427425 | ||||||
chr3:179427469
|
G | A | 1 | a0001c0001t0069g0319 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-42-1227C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179427469 | ||||||
chr3:179427477
|
T | C | 16 | a0001c0001t0010g0012a0001c0001t0010g0320a0001c0001t0010g0321others(13): Show | 18 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.-42-1235A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179427477 | ||||||
chr3:179427541
|
G | T | 1 | a0002c0005t0002g0126 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-42-1299C>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179427541 | ||||||
chr3:179427562
|
A | T | 1 | a0002c0005t0002g0126 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-42-1320T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179427562 | ||||||
chr3:179427605
|
T | TA | 17 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0137others(14): Show | 21 | HG01069.hp2 HG01070.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.-42-1364dupT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179427605 | ||||||
chr3:179427605
|
TA | T | 139 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0007others(136): Show | 166 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-42-1364delT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179427605 | ||||||
chr3:179427605
|
TAA | T | 108 | a0001c0001t0001g0213a0001c0001t0002g0128a0001c0001t0002g0135others(105): Show | 125 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.-42-1365_-42-1364d others(4): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179427605 | ||||||
chr3:179427605
|
TAAA | T | 51 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0005g0146others(48): Show | 58 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.-42-1366_-42-1364d others(5): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179427605 | ||||||
chr3:179427719
|
C | A | 1 | a0001c0002t0013g0289 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-42-1477G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179427719 | ||||||
chr3:179427734
|
T | A | 1 | a0001c0002t0004g0178 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-42-1492A>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179427734 | ||||||
chr3:179427848
|
T | C | 2 | a0001c0001t0003g0293a0001c0001t0003g0294 | 2 | NA18982.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.-42-1606A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179427848 | ||||||
chr3:179427863
|
C | T | 15 | a0001c0001t0010g0012a0001c0001t0010g0320a0001c0001t0010g0321others(12): Show | 17 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.-42-1621G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179427863 | ||||||
chr3:179427983
|
G | C | 3 | a0001c0001t0014g0013a0001c0001t0014g0338a0001c0001t0061g0337 | 5 | HG02109.hp2 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-42-1741C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179427983 | ||||||
chr3:179428011
|
T | TGATTCCC others(6): Show |
1 | a0002c0005t0002g0126 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-42-1782_-42-1770d others(15): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179428011 | ||||||
chr3:179428045
|
G | A | 1 | a0001c0002t0001g0094 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-42-1803C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179428045 | ||||||
chr3:179428051
|
G | C | 259 | a0001c0001t0001g0213a0001c0001t0003g0010a0001c0001t0003g0011others(256): Show | 297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.-42-1809C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179428051 | ||||||
chr3:179428305
|
C | CT | 259 | a0001c0001t0001g0213a0001c0001t0003g0010a0001c0001t0003g0011others(256): Show | 297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.-42-2064dupA | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179428305 | ||||||
chr3:179428401
|
G | A | 14 | a0001c0001t0009g0258a0001c0001t0014g0013a0001c0001t0014g0338others(11): Show | 17 | HG01069.hp1 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.-42-2159C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179428401 | ||||||
chr3:179428515
|
A | G | 47 | a0001c0002t0004g0009a0001c0002t0004g0032a0001c0002t0004g0033others(44): Show | 54 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.-42-2273T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179428515 | ||||||
chr3:179428568
|
G | C | 1 | a0001c0001t0010g0321 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-42-2326C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179428568 | ||||||
chr3:179428699
|
T | C | 1 | a0001c0001t0002g0134 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-42-2457A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179428699 | ||||||
chr3:179429024
|
G | A | 8 | a0001c0001t0009g0258a0001c0002t0014g0260a0001c0002t0014g0262others(5): Show | 9 | HG01069.hp1 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.-42-2782C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179429024 | ||||||
chr3:179429031
|
G | A | 1 | a0001c0002t0066g0311 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-2789C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179429031 | ||||||
chr3:179429056
|
A | G | 86 | a0001c0001t0010g0012a0001c0001t0010g0320a0001c0001t0010g0321others(83): Show | 98 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.-42-2814T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179429056 | ||||||
chr3:179429064
|
C | A | 130 | a0001c0001t0003g0042a0001c0001t0003g0335a0001c0001t0003g0336others(127): Show | 148 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.-42-2822G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179429064 | ||||||
chr3:179429071
|
C | T | 1 | a0001c0003t0062g0324 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-42-2829G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179429071 | ||||||
chr3:179429079
|
T | C | 69 | a0001c0001t0001g0213a0001c0001t0003g0010a0001c0001t0003g0011others(66): Show | 81 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.-42-2837A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179429079 | ||||||
chr3:179429087
|
A | G | 25 | a0001c0001t0010g0012a0001c0001t0010g0320a0001c0001t0010g0321others(22): Show | 29 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.-42-2845T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179429087 | ||||||
chr3:179429188
|
G | C | 9 | a0001c0002t0007g0008a0001c0002t0007g0199a0001c0002t0007g0200others(6): Show | 11 | HG02257.hp2 HG02572.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.-42-2946C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179429188 | ||||||
chr3:179429322
|
T | A | 6 | a0001c0002t0004g0223a0001c0002t0004g0228a0001c0002t0004g0237others(3): Show | 6 | HG00621.hp1 NA18946.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.-42-3080A>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179429322 | ||||||
chr3:179429342
|
G | A | 1 | a0001c0002t0065g0316 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-42-3100C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179429342 | ||||||
chr3:179429383
|
T | C | 258 | a0001c0001t0001g0213a0001c0001t0003g0010a0001c0001t0003g0011others(255): Show | 296 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.-42-3141A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179429383 | ||||||
chr3:179429562
|
T | C | 3 | a0001c0001t0067g0307a0001c0002t0063g0306a0001c0002t0066g0311 | 3 | HG01167.hp1 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-42-3320A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179429562 | ||||||
chr3:179429691
|
G | T | 254 | a0001c0001t0001g0213a0001c0001t0003g0010a0001c0001t0003g0011others(251): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.-42-3449C>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179429691 | ||||||
chr3:179429961
|
A | G | 2 | a0001c0001t0025g0058a0001c0001t0025g0120 | 2 | NA19085.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-42-3719T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179429961 | ||||||
chr3:179429977
|
C | A | 1 | a0001c0001t0069g0319 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-42-3735G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179429977 | ||||||
chr3:179430071
|
G | C | 1 | a0001c0002t0021g0329 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-42-3829C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430071 | ||||||
chr3:179430071
|
G | GAGAC | 39 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0007others(36): Show | 50 | HG00438.hp1 HG00544.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.-42-3833_-42-3830d others(6): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430071 | ||||||
chr3:179430071
|
G | GAGACAGA others(1): Show |
3 | a0001c0001t0002g0077a0001c0001t0002g0135a0001c0002t0015g0218 | 3 | HG00733.hp1 HG03130.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.-42-3837_-42-3830d others(10): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430071 | ||||||
chr3:179430071
|
GAGAC | G | 55 | a0001c0001t0002g0123a0001c0001t0002g0172a0001c0001t0004g0127others(52): Show | 63 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.-42-3833_-42-3830d others(6): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430071 | ||||||
chr3:179430071
|
GAGACAGA others(1): Show |
G | 117 | a0001c0001t0003g0042a0001c0001t0003g0335a0001c0001t0003g0336others(114): Show | 134 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.-42-3837_-42-3830d others(10): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430071 | ||||||
chr3:179430071
|
GAGACAGA others(5): Show |
G | 4 | a0001c0001t0069g0319a0001c0002t0001g0067a0001c0002t0032g0317others(1): Show | 4 | HG00639.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-42-3841_-42-3830d others(14): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430071 | ||||||
chr3:179430073
|
GACAGAC | G | 69 | a0001c0001t0001g0213a0001c0001t0003g0010a0001c0001t0003g0011others(66): Show | 81 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.-42-3837_-42-3832d others(8): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430073 | ||||||
chr3:179430105
|
GACAGACA others(5): Show |
G | 1 | a0001c0002t0022g0187 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-42-3875_-42-3864d others(14): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430105 | ||||||
chr3:179430109
|
GACAGACA others(1): Show |
G | 4 | a0001c0002t0022g0188a0001c0002t0022g0192a0001c0002t0033g0290others(1): Show | 4 | HG01433.hp2 HG02257.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-42-3875_-42-3868d others(10): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430109 | ||||||
chr3:179430117
|
A | G | 5 | a0001c0002t0015g0197a0001c0002t0015g0216a0001c0002t0015g0217others(2): Show | 6 | HG00735.hp1 HG01433.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-42-3875T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430117 | ||||||
chr3:179430245
|
C | A | 1 | a0001c0002t0004g0248 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-42-4003G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430245 | ||||||
chr3:179430252
|
ATTTTCTT | A | 8 | a0001c0002t0015g0197a0001c0002t0015g0216a0001c0002t0015g0217others(5): Show | 9 | HG00735.hp1 HG01433.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.-42-4017_-42-4011d others(9): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430252 | ||||||
chr3:179430326
|
C | T | 2 | a0001c0002t0032g0317a0001c0002t0032g0318 | 2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-42-4084G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430326 | ||||||
chr3:179430336
|
C | T | 15 | a0001c0001t0010g0012a0001c0001t0010g0320a0001c0001t0010g0321others(12): Show | 17 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.-42-4094G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430336 | ||||||
chr3:179430378
|
C | T | 1 | a0001c0002t0065g0316 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-42-4136G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430378 | ||||||
chr3:179430544
|
C | G | 2 | a0001c0002t0001g0069a0001c0002t0001g0094 | 2 | HG01074.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.-42-4302G>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430544 | ||||||
chr3:179430620
|
A | AT | 26 | a0001c0001t0001g0213a0001c0001t0008g0186a0001c0001t0010g0012others(23): Show | 30 | HG00544.hp2 HG01069.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.-42-4379dupA | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430620 | ||||||
chr3:179430620
|
AT | A | 69 | a0001c0001t0002g0053a0001c0001t0002g0125a0001c0001t0002g0137others(66): Show | 79 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.-42-4379delA | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430620 | ||||||
chr3:179430622
|
T | A | 1 | a0001c0002t0022g0192 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-42-4380A>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430622 | ||||||
chr3:179430937
|
T | G | 15 | a0001c0001t0010g0012a0001c0001t0010g0320a0001c0001t0010g0321others(12): Show | 17 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.-42-4695A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430937 | ||||||
chr3:179430960
|
G | A | 5 | a0001c0001t0014g0013a0001c0001t0014g0338a0001c0001t0061g0337others(2): Show | 7 | HG02109.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-42-4718C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430960 | ||||||
chr3:179430960
|
G | C | 2 | a0001c0002t0001g0110a0001c0002t0001g0112 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-42-4718C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430960 | ||||||
chr3:179431012
|
T | G | 2 | a0001c0001t0067g0307a0001c0002t0063g0306 | 2 | HG01167.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-42-4770A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179431012 | ||||||
chr3:179431159
|
T | G | 3 | a0001c0001t0010g0332a0001c0001t0010g0333a0001c0001t0010g0334 | 3 | HG02486.hp2 HG02622.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-42-4917A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179431159 | ||||||
chr3:179431224
|
C | T | 4 | a0001c0002t0004g0036a0001c0002t0004g0244a0001c0002t0007g0243others(1): Show | 5 | HG01261.hp1 HG02886.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-42-4982G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179431224 | ||||||
chr3:179431261
|
G | A | 7 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0137others(4): Show | 9 | HG01070.hp1 HG01257.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-42-5019C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179431261 | ||||||
chr3:179431289
|
G | T | 3 | a0001c0002t0013g0269a0001c0002t0013g0289a0001c0002t0064g0292 | 3 | HG02647.hp1 HG02896.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-42-5047C>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179431289 | ||||||
chr3:179431388
|
C | G | 7 | a0001c0001t0010g0332a0001c0001t0010g0333a0001c0001t0010g0334others(4): Show | 7 | HG02132.hp2 HG02258.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-42-5146G>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179431388 | ||||||
chr3:179431401
|
A | G | 12 | a0001c0001t0002g0114a0001c0001t0002g0123a0001c0001t0002g0124others(9): Show | 13 | HG01081.hp1 HG01106.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.-42-5159T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179431401 | ||||||
chr3:179431450
|
T | C | 1 | a0001c0001t0002g0025 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-42-5208A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179431450 | ||||||
chr3:179431510
|
G | A | 1 | a0001c0002t0006g0093 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-42-5268C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179431510 | ||||||
chr3:179431515
|
C | T | 1 | a0001c0002t0001g0073 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-42-5273G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179431515 | ||||||
chr3:179431557
|
C | CA | 147 | a0001c0001t0001g0213a0001c0001t0003g0010a0001c0001t0003g0011others(144): Show | 171 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.-42-5316dupT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179431557 | ||||||
chr3:179431557
|
C | CAA | 6 | a0001c0001t0003g0300a0001c0001t0017g0151a0001c0001t0070g0339others(3): Show | 6 | HG00408.hp2 HG01515.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-42-5317_-42-5316d others(4): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179431557 | ||||||
chr3:179431557
|
C | CAAA | 75 | a0001c0001t0003g0042a0001c0001t0003g0335a0001c0001t0003g0336others(72): Show | 86 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.-42-5318_-42-5316d others(5): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179431557 | ||||||
chr3:179431557
|
C | CAAAA | 6 | a0001c0002t0001g0094a0001c0002t0001g0095a0001c0002t0001g0096others(3): Show | 6 | HG01074.hp1 HG01978.hp2 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.-42-5319_-42-5316d others(6): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179431557 | ||||||
chr3:179431821
|
A | C | 1 | a0001c0001t0011g0264 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-42-5579T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179431821 | ||||||
chr3:179432590
|
T | C | 2 | a0001c0001t0010g0012a0001c0001t0010g0320 | 4 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.-42-6348A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179432590 | ||||||
chr3:179432614
|
A | C | 15 | a0001c0001t0010g0012a0001c0001t0010g0320a0001c0001t0010g0321others(12): Show | 17 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.-42-6372T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179432614 | ||||||
chr3:179432726
|
A | G | 1 | a0001c0002t0004g0249 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-42-6484T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179432726 | ||||||
chr3:179433068
|
C | A | 81 | a0001c0001t0012g0024a0001c0001t0072g0331a0001c0002t0001g0002others(78): Show | 92 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.-42-6826G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179433068 | ||||||
chr3:179433181
|
G | A | 5 | a0001c0001t0014g0013a0001c0001t0014g0338a0001c0001t0061g0337others(2): Show | 7 | HG02109.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-42-6939C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179433181 | ||||||
chr3:179433192
|
C | T | 1 | a0001c0002t0021g0312 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-42-6950G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179433192 | ||||||
chr3:179433312
|
A | G | 1 | a0001c0001t0054g0278 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-42-7070T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179433312 | ||||||
chr3:179433601
|
C | T | 14 | a0001c0001t0010g0012a0001c0001t0010g0320a0001c0001t0010g0321others(11): Show | 16 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.-42-7359G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179433601 | ||||||
chr3:179433618
|
G | GA | 21 | a0001c0001t0010g0012a0001c0001t0010g0320a0001c0001t0010g0321others(18): Show | 26 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.-42-7377dupT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179433618 | ||||||
chr3:179433763
|
T | C | 1 | a0001c0001t0002g0025 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-42-7521A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179433763 | ||||||
chr3:179433776
|
A | G | 1 | a0001c0002t0066g0311 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-7534T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179433776 | ||||||
chr3:179434083
|
G | A | 1 | a0001c0001t0003g0294 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-42-7841C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179434083 | ||||||
chr3:179434175
|
A | C | 3 | a0001c0002t0022g0187a0001c0002t0022g0188a0001c0002t0022g0192 | 3 | HG01433.hp2 HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-42-7933T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179434175 | ||||||
chr3:179434685
|
C | G | 14 | a0001c0001t0010g0012a0001c0001t0010g0320a0001c0001t0010g0321others(11): Show | 16 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.-42-8443G>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179434685 | ||||||
chr3:179434786
|
C | T | 1 | a0001c0002t0001g0072 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-42-8544G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179434786 | ||||||
chr3:179434892
|
C | T | 15 | a0001c0001t0010g0012a0001c0001t0010g0320a0001c0001t0010g0321others(12): Show | 17 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.-42-8650G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179434892 | ||||||
chr3:179435053
|
G | A | 38 | a0001c0002t0004g0009a0001c0002t0004g0032a0001c0002t0004g0033others(35): Show | 44 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.-42-8811C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179435053 | ||||||
chr3:179435061
|
TAAAAATA others(4): Show |
T | 1 | a0001c0002t0001g0073 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-42-8830_-42-8820d others(13): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179435061 | ||||||
chr3:179435275
|
C | G | 1 | a0001c0002t0001g0072 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-42-9033G>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179435275 | ||||||
chr3:179435470
|
C | CA | 36 | a0001c0001t0001g0213a0001c0001t0002g0054a0001c0001t0002g0059others(33): Show | 37 | HG01167.hp1 HG01192.hp2 HG01256.hp2 others(34): Show |
intron_variant | MODIFIER | c.-42-9229dupT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179435470 | ||||||
chr3:179435470
|
C | CAA | 101 | a0001c0001t0002g0077a0001c0001t0003g0042a0001c0001t0003g0275others(98): Show | 115 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.-42-9230_-42-9229d others(4): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179435470 | ||||||
chr3:179435470
|
C | CAAA | 23 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0019others(20): Show | 28 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.-42-9231_-42-9229d others(5): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179435470 | ||||||
chr3:179435470
|
CAAAAA | C | 9 | a0001c0002t0001g0017a0001c0002t0001g0063a0001c0002t0001g0068others(6): Show | 10 | HG00408.hp1 HG01978.hp2 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.-42-9233_-42-9229d others(7): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179435470 | ||||||
chr3:179435532
|
T | C | 1 | a0001c0002t0001g0067 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-42-9290A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179435532 | ||||||
chr3:179435775
|
G | A | 1 | a0001c0001t0001g0213 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-42-9533C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179435775 | ||||||
chr3:179435879
|
T | G | 1 | a0001c0001t0005g0145 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-42-9637A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179435879 | ||||||
chr3:179436214
|
C | T | 1 | a0001c0001t0002g0171 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-42-9972G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179436214 | ||||||
chr3:179436258
|
C | T | 3 | a0001c0001t0014g0013a0001c0001t0014g0338a0001c0001t0061g0337 | 5 | HG02109.hp2 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-42-10016G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179436258 | ||||||
chr3:179436330
|
C | T | 1 | a0001c0001t0011g0264 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-42-10088G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179436330 | ||||||
chr3:179436361
|
G | A | 1 | a0001c0002t0066g0311 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-10119C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179436361 | ||||||
chr3:179436385
|
C | T | 5 | a0001c0002t0007g0199a0001c0002t0007g0200a0001c0002t0007g0202others(2): Show | 5 | HG02572.hp2 HG02630.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-42-10143G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179436385 | ||||||
chr3:179436724
|
T | C | 2 | a0001c0002t0001g0102a0001c0002t0001g0193 | 2 | HG00738.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.-42-10482A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179436724 | ||||||
chr3:179436866
|
T | C | 1 | a0001c0002t0001g0103 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-42-10624A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179436866 | ||||||
chr3:179437089
|
T | TAC | 2 | a0001c0001t0002g0026a0001c0002t0018g0154 | 3 | HG01358.hp2 HG03704.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.-42-10849_-42-1084 others(6): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179437089 | ||||||
chr3:179437117
|
C | T | 2 | a0001c0001t0070g0339a0001c0001t0071g0257 | 2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-42-10875G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179437117 | ||||||
chr3:179437137
|
T | C | 1 | a0001c0002t0001g0104 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-42-10895A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179437137 | ||||||
chr3:179437306
|
T | C | 3 | a0001c0001t0014g0013a0001c0001t0014g0338a0001c0001t0061g0337 | 5 | HG02109.hp2 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-42-11064A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179437306 | ||||||
chr3:179437464
|
C | G | 1 | a0001c0002t0001g0071 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-42-11222G>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179437464 | ||||||
chr3:179437512
|
C | T | 1 | a0001c0002t0001g0070 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-42-11270G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179437512 | ||||||
chr3:179437514
|
G | C | 1 | a0001c0001t0005g0146 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-42-11272C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179437514 | ||||||
chr3:179437562
|
C | CA | 92 | a0001c0001t0002g0077a0001c0001t0002g0141a0001c0001t0002g0142others(89): Show | 105 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.-42-11321dupT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179437562 | ||||||
chr3:179437634
|
T | C | 1 | a0001c0001t0069g0319 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-42-11392A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179437634 | ||||||
chr3:179437659
|
C | A | 1 | a0001c0001t0003g0288 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-42-11417G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179437659 | ||||||
chr3:179437845
|
T | A | 1 | a0001c0002t0051g0211 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-42-11603A>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179437845 | ||||||
chr3:179438022
|
C | T | 3 | a0001c0001t0014g0013a0001c0001t0014g0338a0001c0001t0061g0337 | 5 | HG02109.hp2 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-42-11780G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179438022 | ||||||
chr3:179438071
|
C | CA | 138 | a0001c0001t0002g0077a0001c0001t0003g0042a0001c0001t0003g0335others(135): Show | 158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.-42-11830dupT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179438071 | ||||||
chr3:179438071
|
C | T | 2 | a0001c0001t0070g0339a0001c0001t0071g0257 | 2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-42-11829G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179438071 | ||||||
chr3:179438161
|
C | T | 1 | a0001c0001t0003g0277 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-42-11919G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179438161 | ||||||
chr3:179438232
|
T | C | 8 | a0001c0001t0009g0258a0001c0002t0014g0260a0001c0002t0014g0262others(5): Show | 9 | HG01069.hp1 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.-42-11990A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179438232 | ||||||
chr3:179438237
|
A | G | 1 | a0001c0001t0002g0170 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-42-11995T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179438237 | ||||||
chr3:179438238
|
C | T | 1 | a0001c0001t0002g0170 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-42-11996G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179438238 | ||||||
chr3:179438286
|
T | C | 1 | a0001c0001t0011g0264 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-42-12044A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179438286 | ||||||
chr3:179438339
|
C | T | 1 | a0001c0003t0009g0322 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-42-12097G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179438339 | ||||||
chr3:179438349
|
C | T | 1 | a0001c0001t0003g0276 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-42-12107G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179438349 | ||||||
chr3:179438491
|
G | A | 1 | a0001c0002t0001g0105 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-42-12249C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179438491 | ||||||
chr3:179438799
|
G | C | 1 | a0001c0002t0007g0202 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-43+12547C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179438799 | ||||||
chr3:179438859
|
C | T | 43 | a0001c0001t0002g0122a0001c0002t0004g0009a0001c0002t0004g0032others(40): Show | 50 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.-43+12487G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179438859 | ||||||
chr3:179439330
|
C | A | 1 | a0001c0001t0069g0319 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-43+12016G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179439330 | ||||||
chr3:179439445
|
G | T | 1 | a0001c0001t0069g0319 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-43+11901C>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179439445 | ||||||
chr3:179439520
|
G | A | 1 | a0001c0001t0003g0266 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-43+11826C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179439520 | ||||||
chr3:179439531
|
C | G | 1 | a0001c0002t0001g0046 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-43+11815G>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179439531 | ||||||
chr3:179439579
|
T | G | 13 | a0001c0001t0010g0012a0001c0001t0010g0320a0001c0001t0010g0321others(10): Show | 15 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.-43+11767A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179439579 | ||||||
chr3:179439693
|
TAA | T | 13 | a0001c0001t0010g0012a0001c0001t0010g0320a0001c0001t0010g0321others(10): Show | 15 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.-43+11651_-43+1165 others(6): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179439693 | ||||||
chr3:179439712
|
A | C | 2 | a0001c0002t0032g0317a0001c0002t0032g0318 | 2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-43+11634T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179439712 | ||||||
chr3:179439893
|
T | C | 13 | a0001c0001t0010g0012a0001c0001t0010g0320a0001c0001t0010g0321others(10): Show | 15 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.-43+11453A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179439893 | ||||||
chr3:179440114
|
C | T | 2 | a0001c0002t0032g0317a0001c0002t0032g0318 | 2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-43+11232G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179440114 | ||||||
chr3:179440158
|
T | TA | 6 | a0001c0001t0019g0215a0001c0002t0015g0216a0001c0002t0015g0217others(3): Show | 7 | HG00735.hp1 HG02055.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43+11187dupT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179440158 | ||||||
chr3:179440346
|
T | C | 3 | a0001c0002t0022g0187a0001c0002t0022g0188a0001c0002t0022g0192 | 3 | HG01433.hp2 HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-43+11000A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179440346 | ||||||
chr3:179440534
|
T | C | 2 | a0001c0001t0010g0332a0001c0001t0010g0334 | 2 | HG02486.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-43+10812A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179440534 | ||||||
chr3:179440730
|
T | C | 1 | a0001c0002t0001g0106 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-43+10616A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179440730 | ||||||
chr3:179440842
|
C | T | 7 | a0001c0001t0002g0004a0001c0001t0002g0117a0001c0001t0002g0118others(4): Show | 9 | HG00438.hp1 HG02083.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.-43+10504G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179440842 | ||||||
chr3:179440843
|
G | A | 1 | a0001c0001t0069g0319 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-43+10503C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179440843 | ||||||
chr3:179440874
|
G | T | 2 | a0001c0001t0010g0332a0001c0001t0010g0334 | 2 | HG02486.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-43+10472C>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179440874 | ||||||
chr3:179440876
|
T | TAGAGAGA others(7): Show |
1 | a0001c0001t0010g0321 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-43+10469_-43+1047 others(18): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179440876 | ||||||
chr3:179440880
|
T | G | 3 | a0001c0001t0010g0321a0001c0002t0007g0199a0001c0002t0050g0198 | 3 | HG02572.hp2 NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-43+10466A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179440880 | ||||||
chr3:179440880
|
T | TAG | 138 | a0001c0001t0002g0077a0001c0001t0003g0042a0001c0001t0003g0335others(135): Show | 157 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.-43+10464_-43+1046 others(6): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179440880 | ||||||
chr3:179440880
|
T | TAGAGAG | 8 | a0001c0001t0067g0307a0001c0002t0007g0008a0001c0002t0007g0200others(5): Show | 10 | HG01167.hp1 HG02257.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-43+10460_-43+1046 others(10): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179440880 | ||||||
chr3:179440880
|
T | TAGAGAGA others(3): Show |
7 | a0001c0001t0014g0013a0001c0001t0014g0338a0001c0001t0061g0337others(4): Show | 9 | HG02109.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-43+10456_-43+1046 others(14): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179440880 | ||||||
chr3:179440880
|
T | TAGAGAGA others(5): Show |
6 | a0001c0001t0009g0258a0001c0001t0072g0331a0001c0002t0014g0260others(3): Show | 7 | HG01069.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43+10454_-43+1046 others(16): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179440880 | ||||||
chr3:179440880
|
T | TAGAGAGA others(7): Show |
4 | a0001c0001t0010g0012a0001c0001t0010g0320a0001c0002t0015g0197others(1): Show | 6 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43+10452_-43+1046 others(18): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179440880 | ||||||
chr3:179440880
|
T | TAGAGAGA others(9): Show |
6 | a0001c0001t0010g0332a0001c0001t0010g0333a0001c0001t0010g0334others(3): Show | 6 | HG02145.hp1 HG02486.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-43+10450_-43+1046 others(20): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179440880 | ||||||
chr3:179440880
|
T | TAGAGAGA others(11): Show |
1 | a0001c0001t0019g0226 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-43+10448_-43+1046 others(22): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179440880 | ||||||
chr3:179440880
|
T | TAGAGAGA others(13): Show |
3 | a0001c0001t0019g0227a0001c0001t0070g0339a0001c0001t0071g0257 | 3 | HG02109.hp1 HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-43+10446_-43+1046 others(24): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179440880 | ||||||
chr3:179440880
|
TAGAGAGA others(1): Show |
T | 13 | a0001c0001t0001g0213a0001c0001t0003g0314a0001c0001t0005g0194others(10): Show | 13 | HG01346.hp2 HG01496.hp2 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.-43+10458_-43+1046 others(12): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179440880 | ||||||
chr3:179440909
|
T | C | 4 | a0001c0002t0021g0308a0001c0002t0021g0309a0001c0002t0021g0312others(1): Show | 4 | HG03540.hp1 HG03669.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43+10437A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179440909 | ||||||
chr3:179441174
|
A | G | 1 | a0001c0001t0002g0116 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-43+10172T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179441174 | ||||||
chr3:179441324
|
A | T | 1 | a0001c0002t0013g0310 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-43+10022T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179441324 | ||||||
chr3:179441371
|
T | C | 65 | a0001c0001t0001g0213a0001c0001t0003g0010a0001c0001t0003g0011others(62): Show | 76 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.-43+9975A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179441371 | ||||||
chr3:179441470
|
A | T | 9 | a0001c0001t0009g0258a0001c0002t0014g0260a0001c0002t0014g0262others(6): Show | 10 | HG01069.hp1 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.-43+9876T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179441470 | ||||||
chr3:179441595
|
A | G | 1 | a0001c0002t0004g0032 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-43+9751T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179441595 | ||||||
chr3:179441625
|
G | A | 7 | a0001c0002t0013g0269a0001c0002t0013g0289a0001c0002t0013g0310others(4): Show | 7 | HG02257.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-43+9721C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179441625 | ||||||
chr3:179441693
|
A | C | 1 | a0001c0002t0001g0068 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-43+9653T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179441693 | ||||||
chr3:179441733
|
T | C | 144 | a0001c0001t0002g0077a0001c0001t0003g0042a0001c0001t0003g0335others(141): Show | 165 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.-43+9613A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179441733 | ||||||
chr3:179441751
|
C | CA | 17 | a0001c0001t0002g0147a0001c0001t0005g0194a0001c0001t0005g0196others(14): Show | 19 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.-43+9594dupT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179441751 | ||||||
chr3:179441751
|
CA | C | 153 | a0001c0001t0002g0077a0001c0001t0002g0115a0001c0001t0002g0156others(150): Show | 176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.-43+9594delT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179441751 | ||||||
chr3:179441827
|
C | T | 1 | a0001c0002t0016g0242 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-43+9519G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179441827 | ||||||
chr3:179442087
|
G | A | 80 | a0001c0001t0002g0077a0001c0002t0001g0002a0001c0002t0001g0003others(77): Show | 90 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.-43+9259C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179442087 | ||||||
chr3:179442147
|
T | C | 3 | a0001c0002t0001g0113a0001c0002t0001g0165a0001c0002t0047g0107 | 3 | HG02698.hp1 HG03688.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-43+9199A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179442147 | ||||||
chr3:179442189
|
C | T | 13 | a0001c0001t0010g0012a0001c0001t0010g0320a0001c0001t0010g0321others(10): Show | 15 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.-43+9157G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179442189 | ||||||
chr3:179442300
|
C | T | 2 | a0001c0002t0007g0243a0001c0002t0034g0295 | 2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-43+9046G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179442300 | ||||||
chr3:179442367
|
G | A | 13 | a0001c0001t0010g0012a0001c0001t0010g0320a0001c0001t0010g0321others(10): Show | 15 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.-43+8979C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179442367 | ||||||
chr3:179442737
|
C | T | 1 | a0001c0002t0066g0311 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-43+8609G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179442737 | ||||||
chr3:179442915
|
C | A | 1 | a0001c0001t0003g0274 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-43+8431G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179442915 | ||||||
chr3:179442923
|
C | T | 3 | a0001c0001t0014g0013a0001c0001t0014g0338a0001c0001t0061g0337 | 5 | HG02109.hp2 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-43+8423G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179442923 | ||||||
chr3:179442925
|
C | T | 9 | a0001c0002t0007g0008a0001c0002t0007g0199a0001c0002t0007g0200others(6): Show | 11 | HG01433.hp1 HG02257.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-43+8421G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179442925 | ||||||
chr3:179442926
|
G | A | 1 | a0001c0002t0016g0242 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-43+8420C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179442926 | ||||||
chr3:179443026
|
T | C | 9 | a0001c0001t0009g0258a0001c0002t0014g0260a0001c0002t0014g0262others(6): Show | 10 | HG01069.hp1 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.-43+8320A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179443026 | ||||||
chr3:179443152
|
C | G | 1 | a0001c0001t0009g0258 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-43+8194G>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179443152 | ||||||
chr3:179443187
|
T | C | 1 | a0001c0002t0001g0066 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-43+8159A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179443187 | ||||||
chr3:179443235
|
T | C | 1 | a0001c0001t0070g0339 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-43+8111A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179443235 | ||||||
chr3:179443433
|
C | A | 144 | a0001c0001t0002g0077a0001c0001t0002g0191a0001c0001t0019g0215others(141): Show | 164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.-43+7913G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179443433 | ||||||
chr3:179443477
|
T | C | 1 | a0001c0001t0069g0319 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-43+7869A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179443477 | ||||||
chr3:179443488
|
G | A | 4 | a0001c0002t0021g0308a0001c0002t0021g0309a0001c0002t0021g0312others(1): Show | 4 | HG03540.hp1 HG03669.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43+7858C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179443488 | ||||||
chr3:179443510
|
G | C | 3 | a0001c0001t0003g0042a0001c0001t0003g0335a0001c0001t0003g0336 | 4 | HG02622.hp1 HG02970.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43+7836C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179443510 | ||||||
chr3:179443572
|
G | C | 1 | a0001c0002t0001g0108 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-43+7774C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179443572 | ||||||
chr3:179443832
|
C | A | 3 | a0001c0001t0020g0043a0001c0001t0020g0340a0001c0001t0020g0341 | 4 | NA18961.hp2 NA19012.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43+7514G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179443832 | ||||||
chr3:179443851
|
C | T | 3 | a0001c0001t0020g0043a0001c0001t0020g0340a0001c0001t0020g0341 | 4 | NA18961.hp2 NA19012.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43+7495G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179443851 | ||||||
chr3:179443911
|
G | A | 1 | a0001c0002t0001g0109 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-43+7435C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179443911 | ||||||
chr3:179443956
|
G | A | 81 | a0001c0001t0002g0077a0001c0002t0001g0002a0001c0002t0001g0003others(78): Show | 91 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.-43+7390C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179443956 | ||||||
chr3:179443991
|
C | T | 1 | a0001c0002t0001g0066 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-43+7355G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179443991 | ||||||
chr3:179444016
|
C | T | 2 | a0001c0002t0032g0317a0001c0002t0032g0318 | 2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-43+7330G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179444016 | ||||||
chr3:179444182
|
T | C | 3 | a0001c0001t0014g0013a0001c0001t0014g0338a0001c0001t0061g0337 | 5 | HG02109.hp2 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-43+7164A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179444182 | ||||||
chr3:179444227
|
T | C | 1 | a0001c0002t0004g0221 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-43+7119A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179444227 | ||||||
chr3:179444235
|
C | T | 1 | a0001c0001t0002g0169 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-43+7111G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179444235 | ||||||
chr3:179444423
|
G | GT | 58 | a0001c0001t0003g0039a0001c0001t0003g0270a0001c0001t0003g0271others(55): Show | 66 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.-43+6922dupA | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179444423 | ||||||
chr3:179444423
|
GT | G | 8 | a0001c0001t0002g0148a0001c0002t0001g0046a0001c0002t0001g0110others(5): Show | 8 | HG01433.hp1 HG01515.hp2 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.-43+6922delA | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179444423 | ||||||
chr3:179444429
|
T | G | 4 | a0001c0001t0005g0027a0001c0001t0005g0149a0001c0001t0005g0150others(1): Show | 5 | HG02486.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-43+6917A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179444429 | ||||||
chr3:179444528
|
C | A | 175 | a0001c0001t0002g0077a0001c0001t0002g0191a0001c0001t0003g0042others(172): Show | 201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.-43+6818G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179444528 | ||||||
chr3:179444562
|
G | A | 177 | a0001c0001t0002g0077a0001c0001t0002g0191a0001c0001t0003g0042others(174): Show | 203 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.-43+6784C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179444562 | ||||||
chr3:179444569
|
C | T | 2 | a0001c0001t0027g0254a0001c0001t0027g0255 | 2 | HG01081.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.-43+6777G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179444569 | ||||||
chr3:179444705
|
C | T | 3 | a0001c0001t0003g0042a0001c0001t0003g0335a0001c0001t0003g0336 | 4 | HG02622.hp1 HG02970.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43+6641G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179444705 | ||||||
chr3:179444716
|
A | G | 2 | a0001c0001t0067g0307a0001c0002t0063g0306 | 2 | HG01167.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-43+6630T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179444716 | ||||||
chr3:179444811
|
A | C | 1 | a0001c0002t0001g0060 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-43+6535T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179444811 | ||||||
chr3:179444840
|
C | T | 1 | a0001c0001t0069g0319 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-43+6506G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179444840 | ||||||
chr3:179444841
|
G | A | 1 | a0001c0003t0009g0330 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-43+6505C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179444841 | ||||||
chr3:179444932
|
T | C | 17 | a0001c0001t0003g0042a0001c0001t0003g0335a0001c0001t0003g0336others(14): Show | 20 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.-43+6414A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179444932 | ||||||
chr3:179445003
|
A | C | 338 | a0001c0001t0001g0213a0001c0001t0002g0001a0001c0001t0002g0004others(335): Show | 396 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(393): Show |
intron_variant | MODIFIER | c.-43+6343T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179445003 | ||||||
chr3:179445023
|
G | A | 4 | a0001c0002t0018g0152a0001c0002t0018g0153a0001c0002t0018g0154others(1): Show | 4 | HG03688.hp2 HG03704.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43+6323C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179445023 | ||||||
chr3:179445047
|
A | T | 2 | a0001c0001t0067g0307a0001c0002t0063g0306 | 2 | HG01167.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-43+6299T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179445047 | ||||||
chr3:179445104
|
C | T | 5 | a0001c0001t0009g0258a0001c0002t0014g0260a0001c0002t0014g0262others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43+6242G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179445104 | ||||||
chr3:179445157
|
A | G | 1 | a0001c0001t0003g0039 | 2 | HG00597.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.-43+6189T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179445157 | ||||||
chr3:179445158
|
T | C | 1 | a0001c0001t0002g0156 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-43+6188A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179445158 | ||||||
chr3:179445374
|
T | C | 1 | a0001c0001t0002g0157 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-43+5972A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179445374 | ||||||
chr3:179445627
|
T | C | 1 | a0001c0002t0004g0178 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-43+5719A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179445627 | ||||||
chr3:179445635
|
C | T | 1 | a0001c0002t0004g0228 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-43+5711G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179445635 | ||||||
chr3:179445732
|
G | A | 162 | a0001c0001t0002g0077a0001c0001t0002g0191a0001c0001t0003g0293others(159): Show | 185 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.-43+5614C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179445732 | ||||||
chr3:179445755
|
G | A | 1 | a0001c0002t0001g0113 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-43+5591C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179445755 | ||||||
chr3:179445863
|
T | C | 184 | a0001c0001t0002g0077a0001c0001t0002g0191a0001c0001t0003g0042others(181): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.-43+5483A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179445863 | ||||||
chr3:179446249
|
C | T | 2 | a0001c0002t0001g0056a0001c0002t0001g0166 | 2 | NA19065.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-43+5097G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179446249 | ||||||
chr3:179446392
|
A | C | 4 | a0001c0001t0010g0012a0001c0001t0010g0320a0001c0001t0010g0321others(1): Show | 6 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43+4954T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179446392 | ||||||
chr3:179446598
|
G | A | 1 | a0001c0001t0003g0299 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-43+4748C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179446598 | ||||||
chr3:179446738
|
A | G | 1 | a0001c0001t0002g0114 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-43+4608T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179446738 | ||||||
chr3:179446764
|
A | G | 94 | a0001c0001t0002g0051a0001c0001t0002g0052a0001c0001t0002g0057others(91): Show | 105 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.-43+4582T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179446764 | ||||||
chr3:179446942
|
T | C | 2 | a0001c0002t0013g0310a0001c0002t0066g0311 | 2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-43+4404A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179446942 | ||||||
chr3:179447101
|
G | A | 1 | a0001c0002t0004g0178 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-43+4245C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179447101 | ||||||
chr3:179447135
|
C | T | 6 | a0001c0002t0007g0199a0001c0002t0007g0200a0001c0002t0007g0201others(3): Show | 6 | HG02572.hp2 HG02630.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43+4211G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179447135 | ||||||
chr3:179447253
|
G | A | 1 | a0001c0001t0012g0028 | 2 | HG02027.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.-43+4093C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179447253 | ||||||
chr3:179447346
|
T | TA | 280 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(277): Show | 331 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(328): Show |
intron_variant | MODIFIER | c.-43+3999dupT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179447346 | ||||||
chr3:179447346
|
T | TAA | 30 | a0001c0001t0001g0213a0001c0001t0002g0007a0001c0001t0002g0169others(27): Show | 35 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.-43+3998_-43+3999d others(4): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179447346 | ||||||
chr3:179447397
|
C | A | 1 | a0001c0001t0008g0030 | 2 | NA18951.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.-43+3949G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179447397 | ||||||
chr3:179447397
|
C | G | 3 | a0001c0001t0014g0013a0001c0001t0014g0338a0001c0001t0061g0337 | 5 | HG02109.hp2 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-43+3949G>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179447397 | ||||||
chr3:179447553
|
G | A | 1 | a0001c0002t0040g0179 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-43+3793C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179447553 | ||||||
chr3:179447717
|
T | C | 2 | a0001c0001t0070g0339a0001c0001t0071g0257 | 2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-43+3629A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179447717 | ||||||
chr3:179447769
|
T | C | 2 | a0001c0002t0001g0180a0001c0002t0001g0181 | 2 | NA18959.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-43+3577A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179447769 | ||||||
chr3:179447820
|
G | A | 1 | a0001c0002t0022g0192 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-43+3526C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179447820 | ||||||
chr3:179447962
|
C | T | 1 | a0001c0001t0011g0267 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-43+3384G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179447962 | ||||||
chr3:179448044
|
G | A | 1 | a0001c0002t0001g0193 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-43+3302C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179448044 | ||||||
chr3:179448099
|
G | A | 4 | a0001c0001t0069g0319a0001c0002t0032g0317a0001c0002t0032g0318others(1): Show | 4 | HG02559.hp2 HG02976.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43+3247C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179448099 | ||||||
chr3:179448184
|
T | C | 1 | a0001c0002t0007g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-43+3162A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179448184 | ||||||
chr3:179448295
|
G | A | 167 | a0001c0001t0001g0213a0001c0001t0002g0224a0001c0001t0003g0010others(164): Show | 192 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.-43+3051C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179448295 | ||||||
chr3:179448296
|
T | C | 9 | a0001c0002t0004g0009a0001c0002t0004g0037a0001c0002t0004g0247others(6): Show | 12 | HG00280.hp1 HG00323.hp1 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.-43+3050A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179448296 | ||||||
chr3:179448353
|
T | C | 6 | a0001c0001t0019g0215a0001c0002t0015g0216a0001c0002t0015g0217others(3): Show | 7 | HG00735.hp1 HG02055.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43+2993A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179448353 | ||||||
chr3:179448406
|
T | C | 23 | a0001c0001t0003g0042a0001c0001t0003g0335a0001c0001t0003g0336others(20): Show | 26 | HG00735.hp2 HG01069.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.-43+2940A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179448406 | ||||||
chr3:179448474
|
GT | G | 7 | a0001c0001t0002g0182a0001c0001t0009g0258a0001c0001t0069g0319others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43+2871delA | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179448474 | ||||||
chr3:179448521
|
C | T | 1 | a0001c0001t0061g0337 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-43+2825G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179448521 | ||||||
chr3:179448537
|
T | G | 24 | a0001c0001t0003g0042a0001c0001t0003g0335a0001c0001t0003g0336others(21): Show | 29 | HG00735.hp2 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.-43+2809A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179448537 | ||||||
chr3:179448539
|
T | G | 24 | a0001c0001t0003g0042a0001c0001t0003g0335a0001c0001t0003g0336others(21): Show | 29 | HG00735.hp2 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.-43+2807A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179448539 | ||||||
chr3:179448636
|
G | A | 5 | a0001c0001t0009g0258a0001c0002t0014g0260a0001c0002t0014g0262others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43+2710C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179448636 | ||||||
chr3:179448763
|
C | T | 1 | a0001c0001t0003g0266 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-43+2583G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179448763 | ||||||
chr3:179448783
|
G | A | 3 | a0001c0002t0001g0183a0001c0002t0001g0184a0001c0002t0002g0185 | 3 | NA18947.hp1 NA18964.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-43+2563C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179448783 | ||||||
chr3:179448807
|
C | T | 3 | a0001c0001t0014g0013a0001c0001t0014g0338a0001c0001t0061g0337 | 5 | HG02109.hp2 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-43+2539G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179448807 | ||||||
chr3:179448900
|
G | A | 1 | a0001c0001t0003g0304 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-43+2446C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179448900 | ||||||
chr3:179449008
|
CA | C | 6 | a0001c0001t0019g0215a0001c0002t0015g0216a0001c0002t0015g0217others(3): Show | 7 | HG00735.hp1 HG02055.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43+2337delT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179449008 | ||||||
chr3:179449178
|
A | G | 6 | a0001c0001t0009g0258a0001c0002t0014g0260a0001c0002t0014g0262others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43+2168T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179449178 | ||||||
chr3:179449422
|
C | T | 1 | a0001c0001t0003g0265 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-43+1924G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179449422 | ||||||
chr3:179449500
|
A | G | 1 | a0001c0002t0001g0050 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-43+1846T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179449500 | ||||||
chr3:179449690
|
C | G | 1 | a0001c0002t0005g0049 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-43+1656G>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179449690 | ||||||
chr3:179449866
|
T | G | 1 | a0001c0001t0008g0186 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-43+1480A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179449866 | ||||||
chr3:179450037
|
T | C | 1 | a0001c0001t0003g0305 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-43+1309A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179450037 | ||||||
chr3:179450099
|
AGAT | A | 6 | a0001c0001t0002g0191a0001c0001t0046g0190a0001c0001t0048g0189others(3): Show | 6 | HG01433.hp2 HG02280.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43+1244_-43+1246d others(5): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179450099 | ||||||
chr3:179450111
|
A | G | 2 | a0001c0001t0067g0307a0001c0002t0063g0306 | 2 | HG01167.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-43+1235T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179450111 | ||||||
chr3:179450121
|
ATTTCAG | A | 5 | a0001c0001t0003g0042a0001c0001t0003g0335a0001c0001t0003g0336others(2): Show | 6 | HG02109.hp1 HG02622.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43+1219_-43+1224d others(8): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179450121 | ||||||
chr3:179450166
|
A | T | 1 | a0001c0001t0011g0264 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-43+1180T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179450166 | ||||||
chr3:179450318
|
G | A | 3 | a0001c0001t0014g0013a0001c0001t0014g0338a0001c0001t0061g0337 | 5 | HG02109.hp2 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-43+1028C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179450318 | ||||||
chr3:179450364
|
G | A | 1 | a0001c0002t0001g0193 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-43+982C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179450364 | ||||||
chr3:179450434
|
C | T | 1 | a0001c0002t0001g0048 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-43+912G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179450434 | ||||||
chr3:179450619
|
A | C | 1 | a0001c0001t0009g0258 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-43+727T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179450619 | ||||||
chr3:179450673
|
A | G | 1 | a0001c0001t0002g0047 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-43+673T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179450673 | ||||||
chr3:179450674
|
C | T | 52 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0039others(49): Show | 61 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.-43+672G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179450674 | ||||||
chr3:179450810
|
T | C | 1 | a0001c0001t0005g0194 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-43+536A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179450810 | ||||||
chr3:179450811
|
C | T | 1 | a0001c0001t0005g0194 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-43+535G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179450811 | ||||||
chr3:179450875
|
A | C | 6 | a0001c0001t0009g0258a0001c0002t0014g0260a0001c0002t0014g0262others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43+471T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179450875 | ||||||
chr3:179450896
|
C | G | 2 | a0001c0001t0070g0339a0001c0001t0071g0257 | 2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-43+450G>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179450896 | ||||||
chr3:179450977
|
G | C | 1 | a0001c0001t0070g0339 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-43+369C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179450977 | ||||||
chr3:179451032
|
G | C | 3 | a0001c0001t0020g0043a0001c0001t0020g0340a0001c0001t0020g0341 | 4 | NA18961.hp2 NA19012.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43+314C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179451032 | ||||||
chr3:179451170
|
T | C | 167 | a0001c0001t0001g0213a0001c0001t0002g0224a0001c0001t0003g0010others(164): Show | 192 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.-43+176A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179451170 | ||||||
chr3:179451249
|
G | A | 47 | a0001c0001t0002g0224a0001c0001t0019g0215a0001c0001t0019g0225others(44): Show | 56 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.-43+97C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179451249 | ||||||
chr3:179451317
|
G | A | 2 | a0001c0001t0027g0254a0001c0001t0027g0255 | 2 | HG01081.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.-43+29C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179451317 |