geneid | 84572 |
---|---|
ensemblid | ENSG00000090581.11 |
hgncid | 23026 |
symbol | GNPTG |
name | N-acetylglucosamine-1-phosphate transferase subunit gamma |
refseq_nuc | NM_032520.5 |
refseq_prot | NP_115909.1 |
ensembl_nuc | ENST00000204679.9 |
ensembl_prot | ENSP00000204679.4 |
mane_status | MANE Select |
chr | chr16 |
start | 1351931 |
end | 1364113 |
strand | + |
ver | v1.2 |
region | chr16:1351931-1364113 |
region5000 | chr16:1346931-1369113 |
regionname0 | GNPTG_chr16_1351931_1364113 |
regionname5000 | GNPTG_chr16_1346931_1369113 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000 | 0/0 | 0 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0001 | 1/1 | 305 | 368 | 88 | 71 | 143 | 18 | 46 | 97 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0002 | 0/0 | 305 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0003 | 0/0 | 305 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0004 | 0/0 | 305 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0005 | 0/0 | 305 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0006 | 0/0 | 305 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0007 | 0/0 | 305 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0008 | 0/0 | 305 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0009 | 0/0 | 305 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 918 | 360 | 82 | 71 | 143 | 17 | 45 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
c0002 | 0/0 | 918 | 3 | 3 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
c0003 | 0/0 | 918 | 2 | 0 | 0 | 2 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
c0004 | 0/0 | 918 | 2 | 2 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
c0005 | 0/0 | 918 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
c0006 | 0/0 | 918 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
c0007 | 0/0 | 178 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
c0008 | 0/0 | 918 | 1 | 0 | 0 | 0 | 1 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
c0009 | 0/0 | 918 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
c0010 | 0/0 | 918 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
c0011 | 0/0 | 918 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
c0012 | 0/0 | 918 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
c0013 | 0/0 | 918 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
c0014 | 0/0 | 918 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
c0015 | 0/0 | 918 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 1058 | 327 | 72 | 63 | 133 | 17 | 41 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
t0002 | 0/1 | 1058 | 27 | 6 | 7 | 8 | 1 | 4 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
t0003 | 0/0 | 1058 | 6 | 5 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
t0004 | 0/0 | 1058 | 3 | 3 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
t0005 | 0/0 | 1058 | 3 | 2 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
t0006 | 0/0 | 1058 | 2 | 2 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
t0007 | 0/0 | 36 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
t0008 | 0/0 | 1058 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
t0009 | 0/0 | 1058 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
t0010 | 0/0 | 1058 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
t0011 | 0/0 | 1058 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
t0012 | 0/0 | 1026 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
t0013 | 0/0 | 1058 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
t0014 | 0/0 | 1058 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
t0015 | 0/0 | 1058 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
t0016 | 0/0 | 1058 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 26 | 0 | 10 | 12 | 1 | 3 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0002 | 0/0 | 11 | 0 | 0 | 10 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0003 | 0/0 | 11 | 0 | 1 | 10 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0004 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0005 | 1/0 | 9 | 2 | 3 | 0 | 0 | 3 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0006 | 0/0 | 9 | 0 | 3 | 5 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0007 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0008 | 0/0 | 8 | 4 | 1 | 2 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0009 | 0/0 | 7 | 2 | 0 | 0 | 1 | 4 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0010 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0011 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0012 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0013 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0014 | 0/0 | 5 | 0 | 1 | 2 | 0 | 2 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0015 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0016 | 0/0 | 5 | 0 | 1 | 3 | 1 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0017 | 0/0 | 5 | 1 | 1 | 1 | 0 | 2 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0018 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0019 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0021 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0022 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0024 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0026 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0027 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0030 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0031 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0032 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0040 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0043 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0047 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0048 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0049 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0051 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0149 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0007 | 0/0 | 178 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0001c0001 | 1/1 | 918 | 360 | 82 | 71 | 143 | 17 | 45 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0001c0002 | 0/0 | 918 | 3 | 3 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0001c0004 | 0/0 | 918 | 2 | 2 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0001c0008 | 0/0 | 918 | 1 | 0 | 0 | 0 | 1 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0001c0011 | 0/0 | 918 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0001c0014 | 0/0 | 918 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0002c0003 | 0/0 | 918 | 2 | 0 | 0 | 2 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0003c0006 | 0/0 | 918 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0004c0010 | 0/0 | 918 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0005c0013 | 0/0 | 918 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0006c0012 | 0/0 | 918 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0007c0009 | 0/0 | 918 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0008c0015 | 0/0 | 918 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0009c0005 | 0/0 | 918 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0007t0007 | 0/0 | 213 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0001c0001t0001 | 1/0 | 1975 | 316 | 65 | 62 | 131 | 16 | 41 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0001c0001t0002 | 0/1 | 1975 | 23 | 3 | 7 | 8 | 1 | 3 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0001c0001t0003 | 0/0 | 1975 | 6 | 5 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0001c0001t0004 | 0/0 | 1975 | 2 | 2 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0001c0001t0005 | 0/0 | 1975 | 3 | 2 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0001c0001t0006 | 0/0 | 1975 | 2 | 2 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0001c0001t0008 | 0/0 | 1975 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0001c0001t0009 | 0/0 | 1975 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0001c0001t0010 | 0/0 | 1975 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0001c0001t0011 | 0/0 | 1975 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0001c0001t0012 | 0/0 | 1943 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0001c0001t0013 | 0/0 | 1975 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0001c0001t0015 | 0/0 | 1975 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0001c0001t0016 | 0/0 | 1975 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0001c0002t0002 | 0/0 | 1975 | 3 | 3 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0001c0004t0001 | 0/0 | 1975 | 2 | 2 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0001c0008t0001 | 0/0 | 1975 | 1 | 0 | 0 | 0 | 1 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0001c0011t0002 | 0/0 | 1975 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0001c0014t0004 | 0/0 | 1975 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0002c0003t0001 | 0/0 | 1975 | 2 | 0 | 0 | 2 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0003c0006t0001 | 0/0 | 1975 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0004c0010t0001 | 0/0 | 1975 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0005c0013t0001 | 0/0 | 1975 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0006c0012t0001 | 0/0 | 1975 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0007c0009t0001 | 0/0 | 1975 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0008c0015t0014 | 0/0 | 1975 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
a0009c0005t0001 | 0/0 | 1975 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | copy fasta | chr16 | 1346931 | 1369113 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0007t0007g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0001 | 0/0 | 25 | 0 | 9 | 12 | 1 | 3 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0002 | 0/0 | 11 | 0 | 0 | 10 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0003 | 0/0 | 10 | 0 | 1 | 9 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0004 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0005 | 1/0 | 9 | 2 | 3 | 0 | 0 | 3 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0006 | 0/0 | 9 | 0 | 3 | 5 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0007 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0008 | 0/0 | 6 | 2 | 1 | 2 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0009 | 0/0 | 7 | 2 | 0 | 0 | 1 | 4 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0010 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0011 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0013 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0014 | 0/0 | 5 | 0 | 1 | 2 | 0 | 2 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0015 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0016 | 0/0 | 5 | 0 | 1 | 3 | 1 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0019 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0021 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0022 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0027 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0030 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0031 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0040 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0047 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0048 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0051 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0002g0012 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0002g0017 | 0/0 | 5 | 1 | 1 | 1 | 0 | 2 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0002g0026 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0002g0043 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0002g0149 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0003g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0004g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0005g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0005g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0006g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0006g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0008g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0009g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0010g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0011g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0012g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0013g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0015g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0001t0016g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0002t0002g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0002t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0004t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0004t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0008t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0011t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0001c0014t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0002c0003t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0003c0006t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0004c0010t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0005c0013t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0006c0012t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0007c0009t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0008c0015t0014g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
a0009c0005t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0137 | EUR | GBR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG00099 | hp2 | a0001 | c0008 | t0001 | g0085 | EUR | GBR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0040 | EUR | GBR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | GBR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | FIN | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0095 | EUR | FIN | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0031 | EUR | FIN | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | CHS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG00544 | hp2 | a0001 | c0001 | t0015 | g0070 | EAS | CHS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | CHS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0113 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG00673 | hp2 | a0001 | c0001 | t0011 | g0079 | EAS | CHS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0177 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01109 | hp2 | a0004 | c0010 | t0001 | g0148 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0049 | EUR | IBS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0088 | EUR | IBS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0059 | EUR | IBS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0164 | EUR | IBS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0049 | EUR | IBS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01884 | hp2 | a0001 | c0002 | t0002 | g0008 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01891 | hp1 | a0001 | c0002 | t0002 | g0008 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | KHV | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CDX | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CDX | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02273 | hp1 | a0001 | c0001 | t0012 | g0001 | AMR | PEL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02572 | hp2 | a0001 | c0001 | t0006 | g0182 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0032 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02630 | hp2 | a0003 | c0006 | t0001 | g0192 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0112 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02723 | hp1 | a0006 | c0012 | t0001 | g0068 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02818 | hp1 | a0001 | c0001 | t0006 | g0018 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0055 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02896 | hp1 | a0001 | c0001 | t0008 | g0018 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02896 | hp2 | a0001 | c0001 | t0005 | g0183 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02922 | hp1 | a0000 | c0007 | t0007 | g0056 | AFR | ESN | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02922 | hp2 | a0009 | c0005 | t0001 | g0169 | AFR | ESN | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0108 | AFR | ESN | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03209 | hp1 | a0001 | c0004 | t0001 | g0158 | AFR | MSL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03225 | hp1 | a0001 | c0001 | t0004 | g0032 | AFR | MSL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03225 | hp2 | a0001 | c0004 | t0001 | g0159 | AFR | MSL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03239 | hp2 | a0001 | c0001 | t0016 | g0109 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | STU | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03834 | hp1 | a0001 | c0011 | t0002 | g0140 | SAS | BEB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | BEB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | BEB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | STU | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | STU | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | BEB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0026 | SAS | BEB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | STU | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | STU | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0017 | SAS | STU | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | YRI | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CHB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18906 | hp2 | a0001 | c0001 | t0010 | g0019 | AFR | YRI | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18939 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18943 | hp2 | a0001 | c0001 | t0005 | g0094 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18962 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | LWK | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA19030 | hp2 | a0005 | c0013 | t0001 | g0010 | AFR | LWK | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA19043 | hp1 | a0001 | c0001 | t0009 | g0156 | AFR | LWK | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA19043 | hp2 | a0001 | c0002 | t0002 | g0142 | AFR | LWK | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA19059 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA19059 | hp2 | a0008 | c0015 | t0014 | g0157 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA19087 | hp1 | a0001 | c0001 | t0013 | g0021 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | YRI | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA20129 | hp1 | a0001 | c0014 | t0004 | g0032 | AFR | ASW | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA20129 | hp2 | a0007 | c0009 | t0001 | g0189 | AFR | ASW | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0118 | EUR | TSI | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | TSI | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0090 | EUR | TSI | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0093 | EUR | TSI | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | GIH | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | GIH | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG02559 | hp2 | a0001 | c0001 | t0005 | g0120 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | MSL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | MSL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | USA | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | USA | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | USA | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | USA | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | LWK | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | LWK | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0149 | REF | REF | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0005 | REF | REF | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:1351972
|
G | A | 1 | a0009 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.7G>A | p.Ala3Thr | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 1/11 | 42/1975 | 7/918 | 3/305 | chr16 | 1351972 | ||
chr16:1351976
|
G | C | 1 | a0002 | 2 | NA18939.hp1 NA18962.hp1 |
missense_variant | MODERATE | c.11G>C | p.Gly4Ala | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 1/11 | 46/1975 | 11/918 | 4/305 | chr16 | 1351976 | ||
chr16:1352132
|
A | C | 1 | a0008 | 1 | NA19059.hp2 | missense_variant | MODERATE | c.83A>C | p.Lys28Thr | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 2/11 | 118/1975 | 83/918 | 28/305 | chr16 | 1352132 | ||
chr16:1352241
|
T | C | 1 | a0003 | 1 | HG02630.hp2 | missense_variant&splice_region_variant | MODERATE | c.113T>C | p.Val38Ala | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/11 | 148/1975 | 113/918 | 38/305 | chr16 | 1352241 | ||
chr16:1356771
|
GTCTCCAA others(8137): Show |
G | 1 | a0000 | 1 | HG02922.hp1 | exon_loss_variant | HIGH | c.178+4467_*1825del | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr16 | 1356771 | |||||
chr16:1362244
|
T | G | 1 | a0007 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.450T>G | p.His150Gln | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 7/11 | 485/1975 | 450/918 | 150/305 | chr16 | 1362244 | ||
chr16:1362482
|
G | A | 1 | a0004 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.557G>A | p.Arg186Gln | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 8/11 | 592/1975 | 557/918 | 186/305 | chr16 | 1362482 | ||
chr16:1362897
|
A | G | 1 | a0005 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.814A>G | p.Arg272Gly | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 10/11 | 849/1975 | 814/918 | 272/305 | chr16 | 1362897 | ||
chr16:1363083
|
A | G | 1 | a0006 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.910A>G | p.Ser304Gly | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 11/11 | 945/1975 | 910/918 | 304/305 | chr16 | 1363083 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:1351993
|
T | C | 1 | a0001c0002 | 3 | HG01884.hp2 HG01891.hp1 NA19043.hp2 |
synonymous_variant | LOW | c.28T>C | p.Leu10Leu | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 1/11 | 63/1975 | 28/918 | 10/305 | chr16 | 1351993 | ||
chr16:1361893
|
G | A | 1 | a0001c0008 | 1 | HG00099.hp2 | synonymous_variant | LOW | c.255G>A | p.Pro85Pro | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 5/11 | 290/1975 | 255/918 | 85/305 | chr16 | 1361893 | ||
chr16:1362271
|
C | T | 1 | a0001c0014 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.477C>T | p.Tyr159Tyr | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 7/11 | 512/1975 | 477/918 | 159/305 | chr16 | 1362271 | ||
chr16:1362528
|
C | T | 1 | a0001c0004 | 2 | HG03209.hp1 HG03225.hp2 |
synonymous_variant | LOW | c.603C>T | p.Thr201Thr | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 8/11 | 638/1975 | 603/918 | 201/305 | chr16 | 1362528 | ||
chr16:1362703
|
T | C | 1 | a0001c0011 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.702T>C | p.Pro234Pro | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 9/11 | 737/1975 | 702/918 | 234/305 | chr16 | 1362703 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:1351962
|
C | T | 1 | a0001c0001t0016 | 1 | HG03239.hp2 | 5_prime_UTR_variant | MODIFIER | c.-4C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 1/11 | 4 | chr16 | 1351962 | |||||
chr16:1363118
|
C | T | 1 | a0001c0001t0015 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*27C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 11/11 | 27 | chr16 | 1363118 | |||||
chr16:1363159
|
G | T | 1 | a0001c0001t0005 | 3 | HG02559.hp2 HG02896.hp2 NA18943.hp2 |
3_prime_UTR_variant | MODIFIER | c.*68G>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 11/11 | 68 | chr16 | 1363159 | |||||
chr16:1363177
|
G | T | 1 | a0008c0015t0014 | 1 | NA19059.hp2 | 3_prime_UTR_variant | MODIFIER | c.*86G>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 11/11 | 86 | chr16 | 1363177 | |||||
chr16:1363315
|
T | C | 1 | a0001c0001t0003 | 6 | HG00639.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*224T>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 11/11 | 224 | chr16 | 1363315 | |||||
chr16:1363426
|
G | A | 3 | a0001c0001t0002a0001c0002t0002a0001c0011t0002 | 27 | HG00099.hp1 HG00423.hp2 HG00609.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*335G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 11/11 | 335 | chr16 | 1363426 | |||||
chr16:1363556
|
G | A | 1 | a0001c0001t0008 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*465G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 11/11 | 465 | chr16 | 1363556 | |||||
chr16:1363638
|
T | C | 1 | a0001c0001t0009 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*547T>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 11/11 | 547 | chr16 | 1363638 | |||||
chr16:1363644
|
G | A | 1 | a0001c0001t0010 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*553G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 11/11 | 553 | chr16 | 1363644 | |||||
chr16:1363695
|
G | A | 2 | a0001c0001t0004a0001c0014t0004 | 3 | HG02630.hp1 HG03225.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*604G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 11/11 | 604 | chr16 | 1363695 | |||||
chr16:1363815
|
C | T | 1 | a0001c0001t0013 | 1 | NA19087.hp1 | 3_prime_UTR_variant | MODIFIER | c.*724C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 11/11 | 724 | chr16 | 1363815 | |||||
chr16:1363905
|
C | T | 2 | a0001c0001t0006a0001c0001t0008 | 3 | HG02572.hp2 HG02818.hp1 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*814C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 11/11 | 814 | chr16 | 1363905 | |||||
chr16:1363920
|
G | C | 2 | a0001c0001t0004a0001c0014t0004 | 3 | HG02630.hp1 HG03225.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*829G>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 11/11 | 829 | chr16 | 1363920 | |||||
chr16:1363942
|
G | A | 1 | a0001c0001t0009 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*851G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 11/11 | 851 | chr16 | 1363942 | |||||
chr16:1364012
|
CGGGAGAT others(25): Show |
C | 1 | a0001c0001t0012 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*923_*954delGGAGAT others(26): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 11/11 | 923 | INFO_REALIGN_3_PRIME | chr16 | 1364012 | ||||
chr16:1364013
|
G | A | 1 | a0001c0001t0011 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*922G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 11/11 | 922 | chr16 | 1364013 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:1352386
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.178+80G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1352386 | ||||||
chr16:1352424
|
C | T | 1 | a0003c0006t0001g0192 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.178+118C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1352424 | ||||||
chr16:1352492
|
C | T | 12 | a0001c0001t0001g0010a0001c0001t0001g0050a0001c0001t0001g0051others(9): Show | 22 | HG01099.hp1 HG02109.hp1 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.178+186C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1352492 | ||||||
chr16:1352630
|
T | A | 1 | a0001c0001t0003g0055 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.178+324T>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1352630 | ||||||
chr16:1352712
|
T | C | 2 | a0000c0007t0007g0056a0001c0001t0001g0023 | 4 | HG02257.hp1 HG02922.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+406T>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1352712 | ||||||
chr16:1352753
|
A | T | 3 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187 | 3 | NA18953.hp2 NA18962.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.178+447A>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1352753 | ||||||
chr16:1352915
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.178+609A>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1352915 | ||||||
chr16:1352967
|
A | AT | 148 | a0000c0007t0007g0056a0001c0001t0001g0001a0001c0001t0001g0002others(145): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.178+680dupT | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1352967 | |||||
chr16:1352967
|
A | ATT | 37 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(34): Show | 48 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.178+679_178+680dup others(2): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1352967 | |||||
chr16:1352967
|
ATT | A | 5 | a0001c0001t0001g0050a0001c0001t0001g0188a0001c0001t0004g0032others(2): Show | 7 | HG02451.hp1 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.178+679_178+680del others(2): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1352967 | |||||
chr16:1353253
|
A | G | 3 | a0001c0001t0003g0055a0001c0001t0005g0183a0001c0001t0009g0156 | 3 | HG02818.hp2 HG02896.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.178+947A>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1353253 | ||||||
chr16:1353267
|
G | A | 1 | a0006c0012t0001g0068 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.178+961G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1353267 | ||||||
chr16:1353332
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.178+1026G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1353332 | ||||||
chr16:1353549
|
G | A | 1 | a0008c0015t0014g0157 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.178+1243G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1353549 | ||||||
chr16:1353597
|
C | T | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(182): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.178+1291C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1353597 | ||||||
chr16:1353613
|
T | C | 1 | a0001c0001t0009g0156 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.178+1307T>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1353613 | ||||||
chr16:1353664
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.178+1358C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1353664 | ||||||
chr16:1353725
|
A | G | 2 | a0000c0007t0007g0056a0001c0001t0001g0023 | 4 | HG02257.hp1 HG02922.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+1419A>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1353725 | ||||||
chr16:1353997
|
G | A | 1 | a0001c0004t0001g0158 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.178+1691G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1353997 | ||||||
chr16:1354122
|
G | A | 1 | a0001c0001t0015g0070 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.178+1816G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1354122 | ||||||
chr16:1354192
|
CTG | C | 193 | a0000c0007t0007g0056a0001c0001t0001g0001a0001c0001t0001g0002others(190): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.178+1890_178+1891d others(4): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1354192 | |||||
chr16:1354268
|
T | C | 2 | a0000c0007t0007g0056a0001c0001t0001g0023 | 4 | HG02257.hp1 HG02922.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+1962T>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1354268 | ||||||
chr16:1354321
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0071 | 3 | HG01943.hp1 HG02004.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.178+2015G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1354321 | ||||||
chr16:1354325
|
A | G | 2 | a0001c0001t0001g0153a0001c0001t0001g0154 | 2 | HG03669.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.178+2019A>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1354325 | ||||||
chr16:1354380
|
A | C | 4 | a0001c0001t0001g0019a0001c0001t0001g0151a0001c0001t0001g0152others(1): Show | 7 | HG01069.hp2 HG01071.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.178+2074A>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1354380 | ||||||
chr16:1354416
|
A | G | 1 | a0001c0001t0001g0150 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.178+2110A>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1354416 | ||||||
chr16:1354585
|
C | CA | 38 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(35): Show | 95 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.178+2303dupA | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1354585 | |||||
chr16:1354585
|
C | CAA | 24 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0024others(21): Show | 47 | HG00140.hp1 HG00140.hp2 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.178+2302_178+2303d others(4): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1354585 | |||||
chr16:1354585
|
C | CAAA | 10 | a0001c0001t0001g0021a0001c0001t0001g0046a0001c0001t0001g0051others(7): Show | 14 | HG00735.hp2 HG02486.hp2 HG02523.hp2 others(11): Show |
intron_variant | MODIFIER | c.178+2301_178+2303d others(5): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1354585 | |||||
chr16:1354585
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0168 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.178+2294_178+2303d others(12): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1354585 | |||||
chr16:1354585
|
C | CAAAAAAA others(4): Show |
7 | a0001c0001t0001g0114a0001c0001t0001g0150a0001c0001t0001g0167others(4): Show | 8 | HG00639.hp1 HG02622.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.178+2293_178+2303d others(13): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1354585 | |||||
chr16:1354585
|
C | CAAAAAAA others(5): Show |
6 | a0001c0001t0001g0050a0001c0001t0001g0110a0001c0001t0001g0111others(3): Show | 7 | HG00738.hp1 HG02451.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.178+2292_178+2303d others(14): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1354585 | |||||
chr16:1354585
|
C | CAAAAAAA others(6): Show |
13 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0102others(10): Show | 25 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.178+2291_178+2303d others(15): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1354585 | |||||
chr16:1354585
|
C | CAAAAAAA others(7): Show |
23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0034others(20): Show | 44 | HG00280.hp2 HG00597.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.178+2290_178+2303d others(16): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1354585 | |||||
chr16:1354585
|
C | CAAAAAAA others(8): Show |
15 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0071others(12): Show | 26 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.178+2289_178+2303d others(17): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1354585 | |||||
chr16:1354585
|
C | CAAAAAAA others(9): Show |
5 | a0001c0001t0001g0014a0001c0001t0001g0036a0001c0001t0001g0061others(2): Show | 10 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.178+2288_178+2303d others(18): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1354585 | |||||
chr16:1354585
|
C | CAAAAAAA others(10): Show |
6 | a0001c0001t0001g0035a0001c0001t0001g0054a0001c0001t0001g0060others(3): Show | 7 | HG02738.hp1 HG02970.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.178+2287_178+2303d others(19): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1354585 | |||||
chr16:1354585
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0075 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.178+2286_178+2303d others(20): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1354585 | |||||
chr16:1354585
|
C | CAAAAAAA others(13): Show |
2 | a0001c0001t0001g0073a0001c0001t0001g0074 | 2 | HG03654.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.178+2284_178+2303d others(22): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1354585 | |||||
chr16:1354585
|
C | CAAAAAAA others(14): Show |
1 | a0001c0001t0001g0072 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.178+2283_178+2303d others(23): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1354585 | |||||
chr16:1354585
|
C | CAAAAAAA others(15): Show |
1 | a0001c0001t0001g0160 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.178+2282_178+2303d others(24): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1354585 | |||||
chr16:1354585
|
CAAAA | C | 5 | a0001c0001t0001g0018a0001c0001t0006g0018a0001c0001t0006g0182others(2): Show | 7 | HG01109.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.178+2300_178+2303d others(6): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1354585 | |||||
chr16:1354589
|
A | G | 1 | a0001c0001t0002g0149 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.178+2283A>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1354589 | ||||||
chr16:1354594
|
A | AAAAAAAC others(8): Show |
1 | a0001c0001t0009g0156 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.178+2294_178+2295i others(17): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1354594 | |||||
chr16:1354602
|
A | C | 1 | a0001c0001t0009g0156 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.178+2296A>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1354602 | ||||||
chr16:1354610
|
C | A | 2 | a0001c0001t0009g0156a0001c0001t0011g0079 | 2 | HG00673.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.178+2304C>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1354610 | ||||||
chr16:1354695
|
T | A | 1 | a0001c0001t0001g0136 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.178+2389T>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1354695 | ||||||
chr16:1354725
|
T | C | 199 | a0000c0007t0007g0056a0001c0001t0001g0001a0001c0001t0001g0002others(196): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.178+2419T>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1354725 | ||||||
chr16:1354745
|
C | T | 2 | a0001c0001t0001g0107a0001c0001t0001g0111 | 2 | HG01074.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.178+2439C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1354745 | ||||||
chr16:1354897
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.178+2591C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1354897 | ||||||
chr16:1354929
|
C | A | 1 | a0001c0001t0002g0137 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.178+2623C>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1354929 | ||||||
chr16:1354950
|
C | T | 2 | a0001c0004t0001g0158a0001c0004t0001g0159 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.178+2644C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1354950 | ||||||
chr16:1355005
|
G | C | 1 | a0001c0001t0001g0089 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.178+2699G>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1355005 | ||||||
chr16:1355033
|
GTGCGGGG others(25): Show |
G | 1 | a0001c0001t0001g0138 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.178+2752_178+2783d others(34): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1355033 | |||||
chr16:1355043
|
G | A | 2 | a0001c0001t0001g0046a0001c0001t0001g0155 | 3 | HG02965.hp2 NA18522.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.178+2737G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1355043 | ||||||
chr16:1355085
|
GGTCTCCC others(89): Show |
G | 1 | a0001c0001t0001g0135 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.178+2794_178+2889d others(98): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1355085 | |||||
chr16:1355120
|
C | T | 1 | a0001c0001t0001g0025 | 3 | HG02145.hp2 HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.178+2814C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1355120 | ||||||
chr16:1355127
|
C | G | 1 | a0001c0001t0009g0156 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.178+2821C>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1355127 | ||||||
chr16:1355164
|
T | C | 1 | a0001c0001t0009g0156 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.178+2858T>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1355164 | ||||||
chr16:1355171
|
G | A | 1 | a0001c0001t0001g0038 | 2 | HG00741.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.178+2865G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1355171 | ||||||
chr16:1355181
|
C | T | 1 | a0001c0001t0001g0101 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.178+2875C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1355181 | ||||||
chr16:1355191
|
G | A | 5 | a0001c0001t0001g0050a0001c0001t0001g0188a0001c0001t0004g0032others(2): Show | 7 | HG02451.hp1 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.178+2885G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1355191 | ||||||
chr16:1355346
|
C | T | 1 | a0001c0001t0001g0046 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.178+3040C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1355346 | ||||||
chr16:1355375
|
C | G | 3 | a0001c0001t0001g0016a0001c0001t0001g0125a0001c0001t0001g0170 | 7 | HG00280.hp1 HG01081.hp2 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.178+3069C>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1355375 | ||||||
chr16:1355384
|
G | A | 5 | a0001c0001t0003g0037a0001c0001t0003g0055a0001c0001t0003g0108others(2): Show | 6 | HG00639.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.178+3078G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1355384 | ||||||
chr16:1355525
|
G | C | 2 | a0001c0001t0001g0028a0003c0006t0001g0192 | 4 | HG02258.hp1 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+3219G>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1355525 | ||||||
chr16:1355533
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.178+3227C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1355533 | ||||||
chr16:1355536
|
C | T | 96 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(93): Show | 163 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.178+3230C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1355536 | ||||||
chr16:1355663
|
T | C | 183 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(180): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.178+3357T>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1355663 | ||||||
chr16:1355700
|
G | C | 3 | a0001c0001t0001g0033a0001c0004t0001g0158a0001c0004t0001g0159 | 4 | HG02055.hp2 HG02723.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+3394G>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1355700 | ||||||
chr16:1355969
|
G | A | 5 | a0001c0001t0002g0017a0001c0001t0002g0026a0001c0001t0002g0066others(2): Show | 11 | HG00099.hp1 HG00741.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.178+3663G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1355969 | ||||||
chr16:1356114
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.178+3808G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1356114 | ||||||
chr16:1356138
|
A | G | 7 | a0000c0007t0007g0056a0001c0001t0001g0023a0001c0001t0001g0050others(4): Show | 11 | HG02257.hp1 HG02451.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.178+3832A>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1356138 | ||||||
chr16:1356141
|
G | A | 2 | a0000c0007t0007g0056a0001c0001t0001g0023 | 4 | HG02257.hp1 HG02922.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+3835G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1356141 | ||||||
chr16:1356242
|
C | G | 1 | a0001c0001t0001g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.178+3936C>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1356242 | ||||||
chr16:1356251
|
G | A | 5 | a0001c0001t0001g0050a0001c0001t0001g0188a0001c0001t0004g0032others(2): Show | 7 | HG02451.hp1 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.178+3945G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1356251 | ||||||
chr16:1356270
|
G | A | 3 | a0001c0001t0001g0054a0001c0001t0001g0076a0001c0001t0001g0080 | 3 | HG01069.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.178+3964G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1356270 | ||||||
chr16:1356483
|
C | T | 1 | a0001c0001t0001g0038 | 2 | HG00741.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.178+4177C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1356483 | ||||||
chr16:1356496
|
C | T | 2 | a0001c0001t0001g0088a0001c0001t0001g0164 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.178+4190C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1356496 | ||||||
chr16:1356508
|
G | A | 2 | a0001c0001t0001g0119a0008c0015t0014g0157 | 2 | NA18974.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.178+4202G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1356508 | ||||||
chr16:1356517
|
G | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0160 | 2 | HG02738.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.178+4211G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1356517 | ||||||
chr16:1356563
|
C | T | 3 | a0001c0001t0001g0050a0001c0001t0001g0188a0007c0009t0001g0189 | 4 | HG02451.hp1 HG02486.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+4257C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1356563 | ||||||
chr16:1356808
|
CG | C | 5 | a0001c0001t0003g0037a0001c0001t0003g0055a0001c0001t0003g0108others(2): Show | 6 | HG00639.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.178+4503delG | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1356808 | ||||||
chr16:1356857
|
G | A | 3 | a0001c0001t0001g0127a0001c0001t0005g0120a0001c0001t0005g0183 | 3 | HG02559.hp2 HG02896.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.178+4551G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1356857 | ||||||
chr16:1356873
|
CTGCGGGC others(35): Show |
C | 180 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(177): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.178+4602_178+4643d others(44): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1356873 | |||||
chr16:1356881
|
GGGGGTCT others(34): Show |
G | 1 | a0008c0015t0014g0157 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.178+4580_178+4620d others(43): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1356881 | |||||
chr16:1356901
|
GTGCGGGC others(34): Show |
G | 1 | a0001c0001t0001g0186 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.178+4596_178+4636d others(43): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1356901 | ||||||
chr16:1356905
|
GGGCGAGA others(34): Show |
G | 1 | a0001c0001t0001g0190 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.178+4602_178+4642d others(43): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1356905 | |||||
chr16:1356909
|
G | T | 1 | a0001c0001t0001g0023 | 3 | HG02257.hp1 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.178+4603G>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1356909 | ||||||
chr16:1356925
|
G | A | 1 | a0008c0015t0014g0157 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.178+4619G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1356925 | ||||||
chr16:1356925
|
GGGTCTGC others(21): Show |
G | 1 | a0001c0001t0001g0023 | 3 | HG02257.hp1 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.178+4631_178+4658d others(30): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1356925 | |||||
chr16:1356973
|
G | C | 1 | a0001c0001t0002g0137 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.178+4667G>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1356973 | ||||||
chr16:1357092
|
G | T | 26 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0028others(23): Show | 48 | HG00099.hp1 HG00423.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.179-4651G>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1357092 | ||||||
chr16:1357130
|
C | G | 1 | a0001c0001t0001g0166 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.179-4613C>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1357130 | ||||||
chr16:1357180
|
A | T | 1 | a0001c0001t0001g0186 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.179-4563A>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1357180 | ||||||
chr16:1357241
|
T | C | 6 | a0001c0001t0001g0050a0001c0001t0001g0144a0001c0001t0001g0188others(3): Show | 8 | HG02451.hp1 HG02486.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.179-4502T>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1357241 | ||||||
chr16:1357440
|
A | G | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(195): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.179-4303A>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1357440 | ||||||
chr16:1357483
|
T | TTTA | 19 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0030others(16): Show | 37 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.179-4235_179-4233d others(5): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1357483 | |||||
chr16:1357483
|
T | TTTATTA | 5 | a0001c0001t0001g0028a0001c0001t0001g0176a0001c0001t0004g0032others(2): Show | 8 | HG02258.hp1 HG02615.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.179-4238_179-4233d others(8): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1357483 | |||||
chr16:1357483
|
TTTA | T | 6 | a0001c0001t0001g0059a0001c0001t0003g0037a0001c0001t0003g0055others(3): Show | 7 | HG00639.hp1 HG01516.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.179-4235_179-4233d others(5): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1357483 | |||||
chr16:1357488
|
T | C | 2 | a0001c0001t0001g0100a0001c0001t0001g0106 | 2 | HG01106.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.179-4255T>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1357488 | ||||||
chr16:1357522
|
CGCTGTGT others(15): Show |
C | 3 | a0001c0001t0005g0120a0001c0001t0005g0183a0001c0011t0002g0140 | 3 | HG02559.hp2 HG02896.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.179-4196_179-4175d others(24): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1357522 | |||||
chr16:1357575
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.179-4168G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1357575 | ||||||
chr16:1357614
|
C | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.179-4129C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1357614 | ||||||
chr16:1357739
|
T | G | 4 | a0001c0001t0001g0127a0001c0001t0001g0173a0001c0001t0005g0120others(1): Show | 4 | HG02559.hp2 HG02896.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-4004T>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1357739 | ||||||
chr16:1357761
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.179-3982C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1357761 | ||||||
chr16:1357791
|
T | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.179-3952T>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1357791 | ||||||
chr16:1357791
|
T | G | 4 | a0001c0001t0001g0019a0001c0001t0001g0151a0001c0001t0001g0152others(1): Show | 7 | HG01069.hp2 HG01071.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.179-3952T>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1357791 | ||||||
chr16:1357808
|
T | C | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(196): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.179-3935T>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1357808 | ||||||
chr16:1358141
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.179-3602C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1358141 | ||||||
chr16:1358147
|
G | T | 1 | a0008c0015t0014g0157 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.179-3596G>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1358147 | ||||||
chr16:1358149
|
G | T | 1 | a0001c0001t0009g0156 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.179-3594G>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1358149 | ||||||
chr16:1358193
|
TC | T | 10 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0063others(7): Show | 17 | HG00140.hp2 HG00733.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.179-3545delC | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1358193 | |||||
chr16:1358198
|
C | G | 2 | a0001c0004t0001g0158a0001c0004t0001g0159 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.179-3545C>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1358198 | ||||||
chr16:1358250
|
T | G | 1 | a0001c0001t0001g0176 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.179-3493T>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1358250 | ||||||
chr16:1358277
|
C | A | 1 | a0001c0001t0001g0151 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.179-3466C>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1358277 | ||||||
chr16:1358336
|
A | G | 4 | a0001c0001t0001g0062a0001c0001t0001g0077a0001c0001t0001g0087others(1): Show | 4 | HG03491.hp2 HG03492.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-3407A>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1358336 | ||||||
chr16:1358352
|
T | C | 1 | a0001c0001t0001g0023 | 3 | HG02257.hp1 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.179-3391T>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1358352 | ||||||
chr16:1358359
|
C | G | 1 | a0001c0001t0001g0152 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.179-3384C>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1358359 | ||||||
chr16:1358506
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.179-3237C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1358506 | ||||||
chr16:1358741
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.179-3002C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1358741 | ||||||
chr16:1358755
|
T | A | 1 | a0001c0001t0001g0186 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.179-2988T>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1358755 | ||||||
chr16:1358823
|
T | G | 1 | a0001c0001t0001g0107 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.179-2920T>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1358823 | ||||||
chr16:1358857
|
G | T | 2 | a0001c0001t0001g0119a0008c0015t0014g0157 | 2 | NA18974.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.179-2886G>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1358857 | ||||||
chr16:1358867
|
CT | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(191): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.179-2864delT | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1358867 | |||||
chr16:1358922
|
C | T | 1 | a0001c0001t0001g0052 | 2 | HG02970.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.179-2821C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1358922 | ||||||
chr16:1358965
|
G | C | 4 | a0001c0001t0001g0016a0001c0001t0001g0042a0001c0001t0001g0125others(1): Show | 9 | HG00280.hp1 HG01081.hp2 NA18954.hp1 others(6): Show |
intron_variant | MODIFIER | c.179-2778G>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1358965 | ||||||
chr16:1358999
|
T | C | 1 | a0001c0001t0001g0023 | 3 | HG02257.hp1 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.179-2744T>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1358999 | ||||||
chr16:1359079
|
A | G | 64 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(61): Show | 137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.179-2664A>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1359079 | ||||||
chr16:1359210
|
G | T | 2 | a0001c0001t0001g0119a0008c0015t0014g0157 | 2 | NA18974.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.179-2533G>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1359210 | ||||||
chr16:1359235
|
C | G | 1 | a0001c0001t0009g0156 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.179-2508C>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1359235 | ||||||
chr16:1359261
|
C | T | 2 | a0001c0001t0003g0037a0001c0001t0003g0113 | 3 | HG00639.hp1 HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.179-2482C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1359261 | ||||||
chr16:1359331
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.179-2412A>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1359331 | ||||||
chr16:1359548
|
G | A | 1 | a0004c0010t0001g0148 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.179-2195G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1359548 | ||||||
chr16:1359583
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.179-2160A>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1359583 | ||||||
chr16:1359589
|
G | C | 1 | a0001c0001t0001g0081 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.179-2154G>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1359589 | ||||||
chr16:1359657
|
C | T | 1 | a0001c0001t0009g0156 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.179-2086C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1359657 | ||||||
chr16:1359691
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0121 | 7 | HG00733.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.179-2052C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1359691 | ||||||
chr16:1359743
|
C | T | 4 | a0001c0001t0001g0088a0001c0001t0001g0097a0001c0001t0001g0164others(1): Show | 4 | HG00099.hp2 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-2000C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1359743 | ||||||
chr16:1359759
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.179-1984G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1359759 | ||||||
chr16:1359816
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.179-1927T>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1359816 | ||||||
chr16:1359902
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.179-1841G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1359902 | ||||||
chr16:1359910
|
G | A | 1 | a0001c0001t0009g0156 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.179-1833G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1359910 | ||||||
chr16:1360086
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.179-1657G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1360086 | ||||||
chr16:1360106
|
C | CA | 9 | a0001c0001t0001g0050a0001c0001t0001g0104a0001c0001t0001g0117others(6): Show | 11 | HG00735.hp2 HG02451.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.179-1625dupA | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1360106 | |||||
chr16:1360106
|
CA | C | 5 | a0001c0001t0001g0186a0001c0001t0002g0012a0001c0001t0002g0043others(2): Show | 11 | HG00423.hp2 HG00609.hp2 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.179-1625delA | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1360106 | |||||
chr16:1360132
|
G | A | 95 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(92): Show | 193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.179-1611G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1360132 | ||||||
chr16:1360173
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.179-1570G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1360173 | ||||||
chr16:1360215
|
T | A | 1 | a0001c0001t0001g0186 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.179-1528T>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1360215 | ||||||
chr16:1360307
|
C | CCTGTTTA others(3): Show |
1 | a0001c0001t0001g0092 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.179-1433_179-1424d others(12): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1360307 | |||||
chr16:1360556
|
G | A | 1 | a0001c0001t0001g0033 | 2 | HG02055.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.179-1187G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1360556 | ||||||
chr16:1360593
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.179-1150C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1360593 | ||||||
chr16:1360641
|
T | C | 1 | a0001c0001t0003g0055 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.179-1102T>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1360641 | ||||||
chr16:1360723
|
A | G | 3 | a0001c0001t0001g0033a0001c0004t0001g0158a0001c0004t0001g0159 | 4 | HG02055.hp2 HG02723.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-1020A>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1360723 | ||||||
chr16:1360735
|
C | T | 5 | a0001c0001t0001g0009a0001c0001t0001g0031a0001c0001t0001g0041others(2): Show | 14 | HG00323.hp2 HG01255.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.179-1008C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1360735 | ||||||
chr16:1360837
|
C | T | 5 | a0001c0001t0003g0037a0001c0001t0003g0055a0001c0001t0003g0108others(2): Show | 6 | HG00639.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.179-906C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1360837 | ||||||
chr16:1360875
|
G | T | 1 | a0001c0001t0003g0113 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.179-868G>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1360875 | ||||||
chr16:1360996
|
G | T | 1 | a0001c0001t0009g0156 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.179-747G>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1360996 | ||||||
chr16:1361061
|
T | C | 1 | a0001c0001t0001g0093 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.179-682T>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1361061 | ||||||
chr16:1361082
|
G | A | 4 | a0001c0001t0003g0037a0001c0001t0003g0108a0001c0001t0003g0112others(1): Show | 5 | HG00639.hp1 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.179-661G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1361082 | ||||||
chr16:1361106
|
C | G | 1 | a0001c0001t0001g0128 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.179-637C>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1361106 | ||||||
chr16:1361125
|
A | T | 82 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(79): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.179-618A>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1361125 | ||||||
chr16:1361128
|
C | T | 94 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(91): Show | 157 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.179-615C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1361128 | ||||||
chr16:1361367
|
G | A | 2 | a0001c0001t0001g0084a0001c0001t0001g0095 | 2 | HG00280.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.179-376G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1361367 | ||||||
chr16:1361382
|
A | C | 1 | a0001c0001t0001g0151 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.179-361A>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1361382 | ||||||
chr16:1361405
|
G | A | 1 | a0008c0015t0014g0157 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.179-338G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1361405 | ||||||
chr16:1361406
|
A | G | 1 | a0008c0015t0014g0157 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.179-337A>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1361406 | ||||||
chr16:1361527
|
C | T | 1 | a0001c0001t0001g0049 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.179-216C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1361527 | ||||||
chr16:1361560
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.179-183C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1361560 | ||||||
chr16:1361653
|
G | A | 1 | a0008c0015t0014g0157 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.179-90G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1361653 | ||||||
chr16:1361804
|
G | T | 5 | a0001c0001t0003g0037a0001c0001t0003g0055a0001c0001t0003g0108others(2): Show | 6 | HG00639.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.233+7G>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 4/10 | chr16 | 1361804 | ||||||
chr16:1362004
|
C | T | 18 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(15): Show | 41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.318-34C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 5/10 | chr16 | 1362004 | ||||||
chr16:1362014
|
C | T | 1 | a0001c0001t0001g0023 | 3 | HG02257.hp1 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.318-24C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 5/10 | chr16 | 1362014 | ||||||
chr16:1362020
|
G | A | 1 | a0001c0001t0001g0046 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.318-18G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 5/10 | chr16 | 1362020 | ||||||
chr16:1362146
|
GGGAGCCC others(7): Show |
G | 1 | a0001c0001t0001g0145 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.411+18_411+31delAG others(12): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 1362146 | |||||
chr16:1362189
|
C | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0171 | 4 | HG02258.hp2 HG03041.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.412-17C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 6/10 | chr16 | 1362189 | ||||||
chr16:1362192
|
C | T | 1 | a0001c0001t0001g0091 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.412-14C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 6/10 | chr16 | 1362192 | ||||||
chr16:1362361
|
G | A | 2 | a0001c0001t0001g0046a0009c0005t0001g0169 | 3 | HG02922.hp2 HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.526+41G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 7/10 | chr16 | 1362361 | ||||||
chr16:1362751
|
T | C | 1 | a0001c0002t0002g0142 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.741+9T>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 9/10 | chr16 | 1362751 | ||||||
chr16:1362964
|
C | T | 1 | a0001c0001t0001g0023 | 3 | HG02257.hp1 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.824-33C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 10/10 | chr16 | 1362964 |