geneid | 51031 |
---|---|
ensemblid | ENSG00000167699.14 |
hgncid | 14111 |
symbol | GLOD4 |
name | glyoxalase domain containing 4 |
refseq_nuc | NM_016080.4 |
refseq_prot | NP_057164.3 |
ensembl_nuc | ENST00000301329.11 |
ensembl_prot | ENSP00000301329.6 |
mane_status | MANE Select |
chr | chr17 |
start | 759330 |
end | 782280 |
strand | - |
ver | v1.2 |
region | chr17:759330-782280 |
region5000 | chr17:754330-787280 |
regionname0 | GLOD4_chr17_759330_782280 |
regionname5000 | GLOD4_chr17_754330_787280 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 298 | 403 | 92 | 71 | 176 | 17 | 45 | 138 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
a0002 | 0/0 | 298 | 12 | 0 | 2 | 9 | 0 | 1 | 7 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
a0003 | 0/0 | 298 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
a0004 | 0/0 | 298 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
a0005 | 0/0 | 298 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
a0006 | 0/0 | 298 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 897 | 394 | 92 | 71 | 171 | 15 | 43 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
c0002 | 0/0 | 897 | 12 | 0 | 2 | 9 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
c0003 | 0/0 | 897 | 5 | 0 | 0 | 5 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
c0004 | 0/0 | 897 | 2 | 0 | 1 | 0 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
c0005 | 0/0 | 897 | 2 | 0 | 0 | 0 | 2 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
c0006 | 0/0 | 897 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
c0007 | 0/0 | 897 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
c0008 | 0/0 | 897 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
c0009 | 0/0 | 897 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
c0010 | 0/0 | 897 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 869 | 397 | 88 | 71 | 173 | 18 | 45 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
t0002 | 0/0 | 869 | 11 | 0 | 2 | 8 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
t0003 | 0/0 | 869 | 5 | 0 | 0 | 5 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
t0004 | 0/0 | 869 | 2 | 2 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
t0005 | 0/0 | 869 | 2 | 2 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
t0006 | 0/0 | 869 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
t0007 | 0/0 | 869 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
t0008 | 0/0 | 869 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 13 | 0 | 7 | 4 | 0 | 2 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0002 | 0/0 | 12 | 2 | 2 | 6 | 2 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0003 | 0/0 | 8 | 0 | 0 | 4 | 1 | 3 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0004 | 0/0 | 7 | 0 | 2 | 4 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0005 | 0/0 | 7 | 0 | 3 | 4 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0006 | 0/0 | 5 | 0 | 1 | 1 | 0 | 3 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0007 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0008 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0009 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0016 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0042 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0048 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0142 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0242 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 897 | 394 | 92 | 71 | 171 | 15 | 43 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
a0001c0003 | 0/0 | 897 | 5 | 0 | 0 | 5 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
a0001c0005 | 0/0 | 897 | 2 | 0 | 0 | 0 | 2 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
a0001c0007 | 0/0 | 897 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
a0001c0008 | 0/0 | 897 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
a0002c0002 | 0/0 | 897 | 12 | 0 | 2 | 9 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
a0003c0004 | 0/0 | 897 | 2 | 0 | 1 | 0 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
a0004c0010 | 0/0 | 897 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
a0005c0009 | 0/0 | 897 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
a0006c0006 | 0/0 | 897 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1765 | 383 | 88 | 70 | 165 | 15 | 43 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
a0001c0001t0003 | 0/0 | 1765 | 5 | 0 | 0 | 5 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
a0001c0001t0004 | 0/0 | 1765 | 2 | 2 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
a0001c0001t0005 | 0/0 | 1765 | 2 | 2 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
a0001c0001t0006 | 0/0 | 1765 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
a0001c0001t0007 | 0/0 | 1765 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
a0001c0003t0001 | 0/0 | 1765 | 5 | 0 | 0 | 5 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
a0001c0005t0001 | 0/0 | 1765 | 2 | 0 | 0 | 0 | 2 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
a0001c0007t0001 | 0/0 | 1765 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
a0001c0008t0001 | 0/0 | 1765 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
a0002c0002t0002 | 0/0 | 1765 | 11 | 0 | 2 | 8 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
a0002c0002t0008 | 0/0 | 1765 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
a0003c0004t0001 | 0/0 | 1765 | 2 | 0 | 1 | 0 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
a0004c0010t0001 | 0/0 | 1765 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
a0005c0009t0001 | 0/0 | 1765 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
a0006c0006t0001 | 0/0 | 1765 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | copy fasta | chr17 | 754330 | 787280 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 13 | 0 | 7 | 4 | 0 | 2 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0002 | 0/0 | 12 | 2 | 2 | 6 | 2 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0003 | 0/0 | 8 | 0 | 0 | 4 | 1 | 3 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0004 | 0/0 | 7 | 0 | 2 | 4 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0005 | 0/0 | 7 | 0 | 3 | 4 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0006 | 0/0 | 5 | 0 | 1 | 1 | 0 | 3 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0007 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0008 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0009 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0048 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0142 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0242 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0003g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0004g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0005g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0006g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0001t0007g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0003t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0003t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0005t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0005t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0007t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0001c0008t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0002c0002t0002g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0002c0002t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0002c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0002c0002t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0002c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0002c0002t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0002c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0002c0002t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0002c0002t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0002c0002t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0002c0002t0008g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0003c0004t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0003c0004t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0004c0010t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0005c0009t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
a0006c0006t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0003 | c0004 | t0001 | g0258 | EUR | GBR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0266 | EUR | GBR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0086 | EUR | GBR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0189 | EUR | FIN | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG00280 | hp2 | a0001 | c0005 | t0001 | g0231 | EUR | FIN | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0185 | EUR | FIN | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | CHS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0257 | EAS | CHS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | CHS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG00733 | hp2 | a0002 | c0002 | t0002 | g0303 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG00741 | hp2 | a0001 | c0001 | t0006 | g0060 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01106 | hp2 | a0003 | c0004 | t0001 | g0260 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | CLM | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01515 | hp1 | a0001 | c0005 | t0001 | g0232 | EUR | IBS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0135 | EUR | IBS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0030 | EUR | IBS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0205 | EUR | IBS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | PEL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | KHV | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | KHV | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02135 | hp2 | a0002 | c0002 | t0002 | g0051 | EAS | KHV | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CDX | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CDX | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CDX | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CDX | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02451 | hp2 | a0001 | c0001 | t0004 | g0031 | AFR | ACB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02602 | hp2 | a0002 | c0002 | t0002 | g0305 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02809 | hp1 | a0001 | c0001 | t0005 | g0090 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02896 | hp1 | a0001 | c0001 | t0004 | g0031 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | ESN | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ESN | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ESN | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ESN | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | MSL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | MSL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | MSL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | MSL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03516 | hp2 | a0001 | c0001 | t0005 | g0055 | AFR | ESN | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | MSL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03669 | hp1 | a0001 | c0008 | t0001 | g0243 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | STU | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | STU | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03704 | hp2 | a0001 | c0007 | t0001 | g0105 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | BEB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | BEB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | BEB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | BEB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | BEB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | BEB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | BEB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | STU | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | STU | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | STU | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | STU | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | STU | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | YRI | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | YRI | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18747 | hp1 | a0001 | c0003 | t0001 | g0254 | EAS | CHB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18747 | hp2 | a0002 | c0002 | t0002 | g0051 | EAS | CHB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | YRI | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18943 | hp2 | a0002 | c0002 | t0002 | g0310 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18947 | hp2 | a0006 | c0006 | t0001 | g0136 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18960 | hp1 | a0002 | c0002 | t0002 | g0309 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18961 | hp2 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18968 | hp2 | a0002 | c0002 | t0008 | g0306 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18971 | hp1 | a0001 | c0003 | t0001 | g0270 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18973 | hp1 | a0004 | c0010 | t0001 | g0244 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18979 | hp1 | a0001 | c0003 | t0001 | g0268 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18989 | hp2 | a0002 | c0002 | t0002 | g0301 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18993 | hp1 | a0005 | c0009 | t0001 | g0095 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18994 | hp2 | a0002 | c0002 | t0002 | g0307 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19007 | hp1 | a0001 | c0003 | t0001 | g0199 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19010 | hp1 | a0002 | c0002 | t0002 | g0304 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | LWK | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | LWK | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19083 | hp1 | a0001 | c0001 | t0007 | g0119 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19083 | hp2 | a0002 | c0002 | t0002 | g0302 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19090 | hp1 | a0001 | c0003 | t0001 | g0201 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | YRI | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ASW | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ASW | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0208 | EUR | TSI | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0259 | EUR | TSI | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | TSI | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | GIH | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | GIH | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01123 | hp1 | a0002 | c0002 | t0002 | g0308 | AMR | CLM | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | USA | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | USA | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | USA | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | USA | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | LWK | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0242 | REF | REF | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0142 | REF | REF | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:760228
|
G | T | 1 | a0002 | 12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
missense_variant | MODERATE | c.842C>A | p.Ala281Glu | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 9/9 | 867/1765 | 842/897 | 281/298 | chr17 | 760228 | ||
chr17:760232
|
C | A | 1 | a0003 | 2 | HG00099.hp1 HG01106.hp2 |
missense_variant | MODERATE | c.838G>T | p.Ala280Ser | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 9/9 | 863/1765 | 838/897 | 280/298 | chr17 | 760232 | ||
chr17:760233
|
C | T | 1 | a0006 | 1 | NA18947.hp2 | missense_variant | MODERATE | c.837G>A | p.Met279Ile | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 9/9 | 862/1765 | 837/897 | 279/298 | chr17 | 760233 | ||
chr17:775858
|
G | A | 1 | a0005 | 1 | NA18993.hp1 | missense_variant | MODERATE | c.323C>T | p.Thr108Met | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/9 | 348/1765 | 323/897 | 108/298 | chr17 | 775858 | ||
chr17:776905
|
T | C | 1 | a0004 | 1 | NA18973.hp1 | missense_variant | MODERATE | c.224A>G | p.Tyr75Cys | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 3/9 | 249/1765 | 224/897 | 75/298 | chr17 | 776905 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:760182
|
A | C | 1 | a0001c0007 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.888T>G | p.Ala296Ala | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 9/9 | 913/1765 | 888/897 | 296/298 | chr17 | 760182 | ||
chr17:760188
|
G | A | 1 | a0001c0003 | 5 | NA18747.hp1 NA18971.hp1 NA18979.hp1 others(2): Show |
synonymous_variant | LOW | c.882C>T | p.Pro294Pro | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 9/9 | 907/1765 | 882/897 | 294/298 | chr17 | 760188 | ||
chr17:760227
|
T | A | 1 | a0002c0002 | 12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
synonymous_variant | LOW | c.843A>T | p.Ala281Ala | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 9/9 | 868/1765 | 843/897 | 281/298 | chr17 | 760227 | ||
chr17:769950
|
T | A | 1 | a0001c0005 | 2 | HG00280.hp2 HG01515.hp1 |
synonymous_variant | LOW | c.750A>T | p.Gly250Gly | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/9 | 775/1765 | 750/897 | 250/298 | chr17 | 769950 | ||
chr17:775830
|
G | A | 1 | a0001c0008 | 1 | HG03669.hp1 | synonymous_variant | LOW | c.351C>T | p.Thr117Thr | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/9 | 376/1765 | 351/897 | 117/298 | chr17 | 775830 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:759379
|
C | T | 1 | a0001c0001t0003 | 5 | HG00558.hp1 HG00597.hp1 NA18961.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*794G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 9/9 | 794 | chr17 | 759379 | |||||
chr17:759524
|
C | G | 1 | a0001c0001t0007 | 1 | NA19083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*649G>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 9/9 | 649 | chr17 | 759524 | |||||
chr17:759657
|
T | C | 1 | a0001c0001t0004 | 2 | HG02451.hp2 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*516A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 9/9 | 516 | chr17 | 759657 | |||||
chr17:759671
|
T | G | 1 | a0002c0002t0008 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*502A>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 9/9 | 502 | chr17 | 759671 | |||||
chr17:759850
|
G | A | 2 | a0002c0002t0002a0002c0002t0008 | 12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*323C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 9/9 | 323 | chr17 | 759850 | |||||
chr17:759942
|
C | T | 1 | a0001c0001t0006 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*231G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 9/9 | 231 | chr17 | 759942 | |||||
chr17:760099
|
T | C | 1 | a0001c0001t0005 | 2 | HG02809.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*74A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 9/9 | 74 | chr17 | 760099 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:760397
|
A | T | 1 | a0001c0001t0001g0044 | 2 | HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.832-159T>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 760397 | ||||||
chr17:760580
|
GA | G | 3 | a0001c0001t0001g0064a0001c0001t0001g0068a0001c0001t0001g0108 | 3 | NA18968.hp1 NA18979.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.832-343delT | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 760580 | ||||||
chr17:760690
|
C | T | 1 | a0001c0001t0004g0031 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.832-452G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 760690 | ||||||
chr17:760730
|
C | T | 1 | a0001c0003t0001g0270 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.832-492G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 760730 | ||||||
chr17:760897
|
T | C | 18 | a0001c0001t0001g0052a0001c0001t0001g0296a0001c0001t0001g0297others(15): Show | 21 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(18): Show |
intron_variant | MODIFIER | c.832-659A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 760897 | ||||||
chr17:760924
|
T | C | 1 | a0001c0001t0001g0278 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.832-686A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 760924 | ||||||
chr17:760926
|
C | T | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 368 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(365): Show |
intron_variant | MODIFIER | c.832-688G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 760926 | ||||||
chr17:761007
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.832-769C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 761007 | ||||||
chr17:761055
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.832-817C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 761055 | ||||||
chr17:761355
|
A | T | 11 | a0002c0002t0002g0051a0002c0002t0002g0301a0002c0002t0002g0302others(8): Show | 12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.832-1117T>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 761355 | ||||||
chr17:761357
|
CTGATT | C | 3 | a0001c0001t0001g0022a0001c0001t0001g0107a0001c0001t0001g0300 | 4 | HG00438.hp1 HG02080.hp1 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-1124_832-1120d others(7): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 761357 | ||||||
chr17:761384
|
A | T | 1 | a0001c0001t0004g0031 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.832-1146T>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 761384 | ||||||
chr17:761486
|
T | G | 1 | a0001c0001t0004g0031 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.832-1248A>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 761486 | ||||||
chr17:761520
|
T | C | 1 | a0001c0001t0001g0217 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.832-1282A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 761520 | ||||||
chr17:761617
|
G | A | 2 | a0001c0001t0001g0261a0001c0001t0006g0060 | 2 | HG00741.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.832-1379C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 761617 | ||||||
chr17:761689
|
A | G | 1 | a0001c0001t0001g0078 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.832-1451T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 761689 | ||||||
chr17:761715
|
G | A | 1 | a0001c0001t0004g0031 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.832-1477C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 761715 | ||||||
chr17:761759
|
C | G | 1 | a0001c0001t0001g0091 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.832-1521G>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 761759 | ||||||
chr17:761760
|
C | T | 1 | a0001c0001t0001g0091 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.832-1522G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 761760 | ||||||
chr17:761779
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.832-1541G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 761779 | ||||||
chr17:761812
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.832-1574C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 761812 | ||||||
chr17:761889
|
C | A | 1 | a0001c0001t0001g0056 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.832-1651G>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 761889 | ||||||
chr17:762029
|
A | G | 1 | a0001c0001t0001g0284 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.832-1791T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762029 | ||||||
chr17:762246
|
C | T | 2 | a0002c0002t0002g0301a0002c0002t0002g0308 | 2 | HG01123.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.832-2008G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762246 | ||||||
chr17:762315
|
G | C | 1 | a0001c0001t0001g0192 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.832-2077C>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762315 | ||||||
chr17:762364
|
C | T | 28 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(25): Show | 43 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(40): Show |
intron_variant | MODIFIER | c.832-2126G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762364 | ||||||
chr17:762395
|
C | G | 3 | a0001c0001t0001g0029a0001c0001t0001g0128a0001c0001t0001g0147 | 4 | HG01175.hp2 HG01192.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-2157G>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762395 | ||||||
chr17:762405
|
T | A | 12 | a0001c0001t0004g0031a0002c0002t0002g0051a0002c0002t0002g0301others(9): Show | 14 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.832-2167A>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762405 | ||||||
chr17:762420
|
G | GGCCTGCA others(200): Show |
1 | a0001c0001t0001g0133 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.832-2389_832-2183d others(209): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762420 | ||||||
chr17:762424
|
TGCACCTA others(61): Show |
T | 39 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0028others(36): Show | 59 | HG00099.hp1 HG00621.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.832-2254_832-2187d others(70): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762424 | ||||||
chr17:762487
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.832-2249G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762487 | ||||||
chr17:762488
|
GGCCGGCA others(132): Show |
G | 11 | a0002c0002t0002g0051a0002c0002t0002g0301a0002c0002t0002g0302others(8): Show | 12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.832-2389_832-2251d others(2): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762488 | ||||||
chr17:762492
|
G | T | 1 | a0001c0001t0004g0031 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.832-2254C>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762492 | ||||||
chr17:762492
|
GGCACCTA others(200): Show |
G | 2 | a0001c0001t0005g0055a0001c0001t0005g0090 | 2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.832-2461_832-2255d others(2): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762492 | ||||||
chr17:762507
|
CGTGATCT others(132): Show |
C | 4 | a0001c0001t0001g0052a0001c0001t0001g0296a0001c0001t0001g0297others(1): Show | 5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.832-2408_832-2270d others(2): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762507 | ||||||
chr17:762556
|
G | T | 1 | a0001c0001t0004g0031 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.832-2318C>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762556 | ||||||
chr17:762560
|
G | T | 1 | a0001c0001t0004g0031 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.832-2322C>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762560 | ||||||
chr17:762575
|
C | T | 1 | a0001c0001t0004g0031 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.832-2337G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762575 | ||||||
chr17:762587
|
G | A | 3 | a0001c0003t0001g0199a0001c0003t0001g0201a0001c0003t0001g0268 | 3 | NA18979.hp1 NA19007.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.832-2349C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762587 | ||||||
chr17:762604
|
T | TTCATCAC others(194): Show |
1 | a0001c0001t0004g0031 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.832-2367_832-2366i others(203): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762604 | ||||||
chr17:762604
|
TATTTCAT others(129): Show |
T | 1 | a0001c0001t0001g0187 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.832-2502_832-2367d others(2): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762604 | ||||||
chr17:762617
|
T | C | 5 | a0001c0001t0001g0023a0001c0001t0001g0061a0001c0001t0001g0082others(2): Show | 6 | HG00609.hp2 HG02165.hp2 NA19000.hp2 others(3): Show |
intron_variant | MODIFIER | c.832-2379A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762617 | ||||||
chr17:762627
|
T | G | 1 | a0001c0001t0004g0031 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.832-2389A>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762627 | ||||||
chr17:762646
|
T | C | 11 | a0002c0002t0002g0051a0002c0002t0002g0301a0002c0002t0002g0302others(8): Show | 12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.832-2408A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762646 | ||||||
chr17:762652
|
C | T | 3 | a0001c0001t0001g0204a0001c0001t0001g0226a0001c0001t0001g0247 | 3 | NA18959.hp2 NA18977.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.832-2414G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762652 | ||||||
chr17:762677
|
C | A | 28 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(25): Show | 43 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(40): Show |
intron_variant | MODIFIER | c.832-2439G>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762677 | ||||||
chr17:762695
|
G | T | 15 | a0001c0001t0001g0052a0001c0001t0001g0296a0001c0001t0001g0297others(12): Show | 17 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(14): Show |
intron_variant | MODIFIER | c.832-2457C>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762695 | ||||||
chr17:762714
|
C | CGTGATCT others(61): Show |
1 | a0001c0001t0004g0031 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.832-2477_832-2476i others(70): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762714 | ||||||
chr17:762714
|
C | T | 15 | a0001c0001t0001g0052a0001c0001t0001g0296a0001c0001t0001g0297others(12): Show | 17 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(14): Show |
intron_variant | MODIFIER | c.832-2476G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762714 | ||||||
chr17:762782
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.832-2544C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762782 | ||||||
chr17:762909
|
G | A | 24 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(21): Show | 30 | HG01109.hp1 HG01243.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.832-2671C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762909 | ||||||
chr17:762952
|
G | A | 6 | a0001c0001t0001g0035a0001c0001t0001g0056a0001c0001t0001g0160others(3): Show | 7 | HG02615.hp1 HG02622.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.832-2714C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762952 | ||||||
chr17:762973
|
G | A | 4 | a0001c0001t0001g0052a0001c0001t0001g0296a0001c0001t0001g0297others(1): Show | 5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.832-2735C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762973 | ||||||
chr17:763108
|
G | A | 1 | a0001c0001t0001g0277 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.832-2870C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 763108 | ||||||
chr17:763139
|
C | T | 58 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(55): Show | 76 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.832-2901G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 763139 | ||||||
chr17:763162
|
G | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0064a0001c0001t0001g0068others(1): Show | 6 | HG00408.hp1 NA18968.hp1 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.832-2924C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 763162 | ||||||
chr17:763172
|
G | C | 1 | a0001c0001t0001g0114 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.832-2934C>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 763172 | ||||||
chr17:763178
|
G | A | 1 | a0001c0001t0004g0031 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.832-2940C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 763178 | ||||||
chr17:763181
|
T | TA | 63 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0028others(60): Show | 87 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.832-2944dupT | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 763181 | ||||||
chr17:763323
|
A | C | 18 | a0001c0001t0001g0052a0001c0001t0001g0296a0001c0001t0001g0297others(15): Show | 21 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(18): Show |
intron_variant | MODIFIER | c.832-3085T>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 763323 | ||||||
chr17:763419
|
C | T | 1 | a0001c0001t0001g0259 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.832-3181G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 763419 | ||||||
chr17:763421
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.832-3183A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 763421 | ||||||
chr17:763520
|
C | T | 1 | a0001c0001t0004g0031 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.832-3282G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 763520 | ||||||
chr17:763756
|
A | G | 2 | a0001c0001t0005g0055a0001c0001t0005g0090 | 2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.832-3518T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 763756 | ||||||
chr17:763803
|
T | C | 9 | a0001c0001t0001g0014a0001c0001t0001g0034a0001c0001t0001g0123others(6): Show | 12 | HG01952.hp2 HG02145.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.832-3565A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 763803 | ||||||
chr17:763988
|
G | A | 1 | a0001c0001t0001g0276 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.832-3750C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 763988 | ||||||
chr17:763994
|
C | T | 11 | a0002c0002t0002g0051a0002c0002t0002g0301a0002c0002t0002g0302others(8): Show | 12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.832-3756G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 763994 | ||||||
chr17:763995
|
G | A | 1 | a0001c0001t0004g0031 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.832-3757C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 763995 | ||||||
chr17:764008
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.832-3770C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764008 | ||||||
chr17:764137
|
G | A | 19 | a0001c0001t0001g0008a0001c0001t0001g0036a0001c0001t0001g0037others(16): Show | 25 | HG00280.hp1 HG00323.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.832-3899C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764137 | ||||||
chr17:764270
|
T | G | 6 | a0001c0001t0001g0019a0001c0001t0001g0074a0001c0001t0001g0080others(3): Show | 7 | HG00609.hp1 HG02132.hp2 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.832-4032A>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764270 | ||||||
chr17:764403
|
C | G | 11 | a0002c0002t0002g0051a0002c0002t0002g0301a0002c0002t0002g0302others(8): Show | 12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.832-4165G>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764403 | ||||||
chr17:764418
|
G | A | 1 | a0001c0001t0001g0036 | 2 | HG02280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.832-4180C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764418 | ||||||
chr17:764516
|
AAC | A | 4 | a0001c0001t0001g0052a0001c0001t0001g0296a0001c0001t0001g0297others(1): Show | 5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.832-4280_832-4279d others(4): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764516 | ||||||
chr17:764735
|
G | A | 4 | a0001c0001t0001g0126a0001c0001t0001g0131a0001c0001t0001g0143others(1): Show | 4 | HG00438.hp2 NA18947.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-4497C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764735 | ||||||
chr17:764736
|
C | G | 10 | a0001c0001t0001g0043a0001c0001t0001g0186a0001c0001t0001g0206others(7): Show | 11 | HG00280.hp2 HG00733.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.832-4498G>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764736 | ||||||
chr17:764742
|
C | G | 1 | a0001c0001t0001g0181 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.832-4504G>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764742 | ||||||
chr17:764747
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.832-4509T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764747 | ||||||
chr17:764751
|
GTAATCCC others(814): Show |
G | 33 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0021others(30): Show | 44 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.831+4297_832-4514d others(2): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764751 | ||||||
chr17:764755
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.832-4517A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764755 | ||||||
chr17:764762
|
C | A | 1 | a0001c0001t0001g0080 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.832-4524G>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764762 | ||||||
chr17:764773
|
C | T | 6 | a0002c0002t0002g0302a0002c0002t0002g0303a0002c0002t0002g0304others(3): Show | 6 | HG00733.hp2 HG02602.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.832-4535G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764773 | ||||||
chr17:764775
|
A | G | 28 | a0001c0001t0001g0005a0001c0001t0001g0049a0001c0001t0001g0054others(25): Show | 36 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.832-4537T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764775 | ||||||
chr17:764779
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.832-4541A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764779 | ||||||
chr17:764781
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.832-4543C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764781 | ||||||
chr17:764783
|
T | C | 3 | a0001c0001t0001g0080a0001c0001t0001g0112a0001c0001t0001g0120 | 3 | HG00621.hp1 NA18941.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.832-4545A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764783 | ||||||
chr17:764791
|
A | G | 3 | a0001c0001t0001g0052a0001c0001t0001g0112a0001c0001t0001g0120 | 4 | HG00621.hp1 HG02615.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-4553T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764791 | ||||||
chr17:764810
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.832-4572G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764810 | ||||||
chr17:764811
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.832-4573T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764811 | ||||||
chr17:764811
|
A | T | 11 | a0001c0001t0001g0043a0001c0001t0001g0184a0001c0001t0001g0206others(8): Show | 12 | HG00280.hp2 HG00733.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.832-4573T>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764811 | ||||||
chr17:764812
|
T | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0173 | 4 | HG01109.hp1 HG02818.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-4574A>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764812 | ||||||
chr17:764815
|
T | C | 4 | a0001c0001t0001g0052a0001c0001t0001g0065a0001c0001t0001g0296others(1): Show | 5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.832-4577A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764815 | ||||||
chr17:764822
|
C | G | 71 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0015others(68): Show | 97 | HG00558.hp1 HG00597.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.832-4584G>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764822 | ||||||
chr17:764824
|
C | A | 3 | a0001c0001t0001g0040a0001c0001t0001g0209a0001c0001t0001g0273 | 4 | HG01243.hp2 HG01891.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-4586G>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764824 | ||||||
chr17:764824
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.832-4586G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764824 | ||||||
chr17:764831
|
A | AC | 45 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0028others(42): Show | 68 | HG00099.hp1 HG00621.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.832-4594dupG | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764831 | ||||||
chr17:764831
|
A | AT | 25 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(22): Show | 39 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.832-4594_832-4593i others(3): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764831 | ||||||
chr17:764834
|
C | T | 44 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(41): Show | 53 | HG00423.hp2 HG00609.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.832-4596G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764834 | ||||||
chr17:764876
|
A | G | 28 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(25): Show | 43 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(40): Show |
intron_variant | MODIFIER | c.832-4638T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764876 | ||||||
chr17:764879
|
T | C | 47 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0011others(44): Show | 68 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.832-4641A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764879 | ||||||
chr17:764902
|
T | G | 5 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0062others(2): Show | 7 | HG00423.hp2 HG02717.hp1 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.832-4664A>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764902 | ||||||
chr17:764983
|
G | A | 2 | a0001c0001t0005g0055a0001c0001t0005g0090 | 2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.832-4745C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764983 | ||||||
chr17:764985
|
T | C | 26 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(23): Show | 41 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(38): Show |
intron_variant | MODIFIER | c.832-4747A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764985 | ||||||
chr17:764986
|
G | A | 26 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(23): Show | 41 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(38): Show |
intron_variant | MODIFIER | c.832-4748C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764986 | ||||||
chr17:764986
|
G | C | 1 | a0001c0001t0001g0238 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.832-4748C>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764986 | ||||||
chr17:764993
|
C | G | 1 | a0001c0001t0001g0238 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.832-4755G>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764993 | ||||||
chr17:765398
|
G | A | 2 | a0001c0001t0001g0059a0001c0001t0001g0109 | 2 | NA19007.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.831+4471C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 765398 | ||||||
chr17:765457
|
G | C | 1 | a0001c0001t0001g0230 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.831+4412C>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 765457 | ||||||
chr17:765469
|
A | G | 1 | a0001c0001t0001g0299 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.831+4400T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 765469 | ||||||
chr17:765542
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.831+4327A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 765542 | ||||||
chr17:765689
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.831+4180G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 765689 | ||||||
chr17:765715
|
G | A | 1 | a0001c0001t0001g0150 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.831+4154C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 765715 | ||||||
chr17:765778
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.831+4091T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 765778 | ||||||
chr17:765780
|
C | T | 3 | a0002c0002t0002g0302a0002c0002t0002g0304a0002c0002t0002g0310 | 3 | NA18943.hp2 NA19010.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.831+4089G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 765780 | ||||||
chr17:765912
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.831+3957G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 765912 | ||||||
chr17:766067
|
T | C | 2 | a0001c0001t0004g0031a0001c0001t0005g0055 | 3 | HG02451.hp2 HG02896.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.831+3802A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 766067 | ||||||
chr17:766068
|
G | A | 11 | a0002c0002t0002g0051a0002c0002t0002g0301a0002c0002t0002g0302others(8): Show | 12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.831+3801C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 766068 | ||||||
chr17:766126
|
C | T | 11 | a0002c0002t0002g0051a0002c0002t0002g0301a0002c0002t0002g0302others(8): Show | 12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.831+3743G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 766126 | ||||||
chr17:766134
|
G | C | 17 | a0001c0001t0001g0052a0001c0001t0001g0296a0001c0001t0001g0297others(14): Show | 20 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.831+3735C>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 766134 | ||||||
chr17:766167
|
G | A | 49 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0039others(46): Show | 70 | HG00099.hp1 HG00280.hp2 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.831+3702C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 766167 | ||||||
chr17:766306
|
A | T | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 367 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(364): Show |
intron_variant | MODIFIER | c.831+3563T>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 766306 | ||||||
chr17:766322
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.831+3547C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 766322 | ||||||
chr17:766371
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.831+3498C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 766371 | ||||||
chr17:766473
|
G | C | 4 | a0001c0001t0001g0052a0001c0001t0001g0296a0001c0001t0001g0297others(1): Show | 5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+3396C>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 766473 | ||||||
chr17:766520
|
C | T | 4 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0086others(1): Show | 4 | HG00140.hp1 HG00621.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+3349G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 766520 | ||||||
chr17:766831
|
G | A | 2 | a0001c0001t0001g0071a0001c0001t0001g0076 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.831+3038C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 766831 | ||||||
chr17:767106
|
T | A | 45 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0011others(42): Show | 66 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.831+2763A>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 767106 | ||||||
chr17:767156
|
A | C | 1 | a0001c0001t0001g0084 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.831+2713T>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 767156 | ||||||
chr17:767314
|
T | C | 9 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0128others(6): Show | 11 | HG01175.hp2 HG01192.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.831+2555A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 767314 | ||||||
chr17:767441
|
C | T | 1 | a0001c0001t0001g0222 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.831+2428G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 767441 | ||||||
chr17:767476
|
AAGAAGAA others(49): Show |
A | 9 | a0001c0001t0001g0052a0001c0001t0001g0054a0001c0001t0001g0215others(6): Show | 10 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.831+2337_831+2392d others(58): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 767476 | ||||||
chr17:767517
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.831+2352C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 767517 | ||||||
chr17:767555
|
A | G | 4 | a0001c0001t0001g0052a0001c0001t0001g0296a0001c0001t0001g0297others(1): Show | 5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+2314T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 767555 | ||||||
chr17:767673
|
G | A | 30 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0021others(27): Show | 41 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.831+2196C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 767673 | ||||||
chr17:767685
|
G | A | 3 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0004g0031 | 4 | HG02145.hp2 HG02451.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+2184C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 767685 | ||||||
chr17:767687
|
G | A | 1 | a0001c0001t0001g0045 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.831+2182C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 767687 | ||||||
chr17:767690
|
TTCAGATT others(50): Show |
T | 1 | a0001c0001t0001g0113 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.831+2122_831+2178d others(59): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 767690 | ||||||
chr17:767724
|
G | C | 2 | a0001c0001t0001g0050a0001c0001t0001g0116 | 3 | HG01891.hp2 HG01928.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.831+2145C>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 767724 | ||||||
chr17:767782
|
G | A | 1 | a0001c0003t0001g0254 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.831+2087C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 767782 | ||||||
chr17:767795
|
C | T | 1 | a0001c0001t0001g0123 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.831+2074G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 767795 | ||||||
chr17:767906
|
C | T | 17 | a0001c0001t0001g0008a0001c0001t0001g0036a0001c0001t0001g0037others(14): Show | 23 | HG00280.hp1 HG00323.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.831+1963G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 767906 | ||||||
chr17:767943
|
A | G | 3 | a0001c0001t0001g0129a0001c0001t0001g0149a0001c0001t0001g0154 | 3 | NA18944.hp1 NA18954.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.831+1926T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 767943 | ||||||
chr17:767943
|
AAG | A | 4 | a0001c0001t0001g0052a0001c0001t0001g0296a0001c0001t0001g0297others(1): Show | 5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+1924_831+1925d others(4): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 767943 | ||||||
chr17:767961
|
G | A | 8 | a0001c0001t0001g0015a0001c0001t0001g0042a0001c0001t0001g0181others(5): Show | 11 | HG00673.hp1 HG01993.hp1 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.831+1908C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 767961 | ||||||
chr17:767976
|
G | C | 11 | a0002c0002t0002g0051a0002c0002t0002g0301a0002c0002t0002g0302others(8): Show | 12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.831+1893C>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 767976 | ||||||
chr17:767996
|
TGA | T | 11 | a0002c0002t0002g0051a0002c0002t0002g0301a0002c0002t0002g0302others(8): Show | 12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.831+1871_831+1872d others(4): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 767996 | ||||||
chr17:768015
|
G | A | 1 | a0001c0001t0001g0296 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.831+1854C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768015 | ||||||
chr17:768031
|
A | AAGAAGAA others(437): Show |
2 | a0001c0001t0001g0021a0001c0001t0001g0102 | 3 | HG02080.hp2 HG02083.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.831+1394_831+1837d others(446): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768031 | ||||||
chr17:768041
|
C | G | 1 | a0001c0001t0005g0055 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.831+1828G>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768041 | ||||||
chr17:768093
|
GA | G | 4 | a0001c0001t0001g0052a0001c0001t0001g0296a0001c0001t0001g0297others(1): Show | 5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+1775delT | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768093 | ||||||
chr17:768103
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.831+1766C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768103 | ||||||
chr17:768128
|
T | C | 4 | a0001c0001t0001g0052a0001c0001t0001g0296a0001c0001t0001g0297others(1): Show | 5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+1741A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768128 | ||||||
chr17:768162
|
C | T | 6 | a0001c0001t0001g0052a0001c0001t0001g0125a0001c0001t0001g0251others(3): Show | 7 | HG01070.hp1 HG02145.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+1707G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768162 | ||||||
chr17:768178
|
G | A | 16 | a0001c0001t0001g0052a0001c0001t0001g0251a0001c0001t0001g0296others(13): Show | 18 | HG00733.hp2 HG01070.hp1 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.831+1691C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768178 | ||||||
chr17:768180
|
C | G | 4 | a0001c0001t0001g0052a0001c0001t0001g0296a0001c0001t0001g0297others(1): Show | 5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+1689G>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768180 | ||||||
chr17:768181
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.831+1688C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768181 | ||||||
chr17:768183
|
A | G | 4 | a0001c0001t0001g0052a0001c0001t0001g0296a0001c0001t0001g0297others(1): Show | 5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+1686T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768183 | ||||||
chr17:768199
|
AAGAAGAA others(47): Show |
A | 4 | a0001c0001t0001g0052a0001c0001t0001g0296a0001c0001t0001g0297others(1): Show | 5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+1616_831+1669d others(56): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768199 | ||||||
chr17:768215
|
A | G | 11 | a0002c0002t0002g0051a0002c0002t0002g0301a0002c0002t0002g0302others(8): Show | 12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.831+1654T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768215 | ||||||
chr17:768266
|
G | A | 4 | a0001c0001t0001g0052a0001c0001t0001g0296a0001c0001t0001g0297others(1): Show | 5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+1603C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768266 | ||||||
chr17:768273
|
T | C | 4 | a0001c0001t0001g0052a0001c0001t0001g0296a0001c0001t0001g0297others(1): Show | 5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+1596A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768273 | ||||||
chr17:768291
|
G | C | 4 | a0001c0001t0001g0052a0001c0001t0001g0296a0001c0001t0001g0297others(1): Show | 5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+1578C>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768291 | ||||||
chr17:768323
|
A | AAGAGGAC others(47): Show |
11 | a0002c0002t0002g0051a0002c0002t0002g0301a0002c0002t0002g0302others(8): Show | 12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.831+1545_831+1546i others(56): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768323 | ||||||
chr17:768323
|
A | G | 4 | a0001c0001t0001g0052a0001c0001t0001g0296a0001c0001t0001g0297others(1): Show | 5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+1546T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768323 | ||||||
chr17:768333
|
G | A | 4 | a0001c0001t0001g0052a0001c0001t0001g0296a0001c0001t0001g0297others(1): Show | 5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+1536C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768333 | ||||||
chr17:768338
|
AGAGAAAC others(104): Show |
A | 1 | a0001c0001t0001g0057 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.831+1420_831+1530d others(2): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768338 | ||||||
chr17:768350
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.831+1519G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768350 | ||||||
chr17:768353
|
A | G | 4 | a0001c0001t0001g0052a0001c0001t0001g0296a0001c0001t0001g0297others(1): Show | 5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+1516T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768353 | ||||||
chr17:768364
|
TAGA | T | 4 | a0001c0001t0001g0052a0001c0001t0001g0296a0001c0001t0001g0297others(1): Show | 5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+1502_831+1504d others(5): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768364 | ||||||
chr17:768388
|
G | A | 4 | a0001c0001t0001g0052a0001c0001t0001g0296a0001c0001t0001g0297others(1): Show | 5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+1481C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768388 | ||||||
chr17:768390
|
A | G | 1 | a0001c0001t0004g0031 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.831+1479T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768390 | ||||||
chr17:768395
|
A | G | 5 | a0001c0001t0001g0052a0001c0001t0001g0296a0001c0001t0001g0297others(2): Show | 7 | HG02451.hp2 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.831+1474T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768395 | ||||||
chr17:768397
|
A | G | 11 | a0002c0002t0002g0051a0002c0002t0002g0301a0002c0002t0002g0302others(8): Show | 12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.831+1472T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768397 | ||||||
chr17:768410
|
G | A | 5 | a0001c0001t0001g0052a0001c0001t0001g0296a0001c0001t0001g0297others(2): Show | 7 | HG02451.hp2 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.831+1459C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768410 | ||||||
chr17:768434
|
G | T | 1 | a0001c0001t0005g0055 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.831+1435C>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768434 | ||||||
chr17:768442
|
A | G | 5 | a0001c0001t0001g0052a0001c0001t0001g0296a0001c0001t0001g0297others(2): Show | 7 | HG02451.hp2 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.831+1427T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768442 | ||||||
chr17:768444
|
A | AAGAGGGA others(545): Show |
5 | a0001c0001t0001g0046a0001c0001t0001g0282a0001c0001t0001g0284others(2): Show | 6 | HG02074.hp1 HG02132.hp1 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.831+1424_831+1425i others(554): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768444 | ||||||
chr17:768444
|
A | AAGAGGGA others(548): Show |
1 | a0001c0001t0001g0239 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.831+1424_831+1425i others(557): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768444 | ||||||
chr17:768444
|
A | AAGAGGGA others(548): Show |
28 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0039others(25): Show | 47 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.831+1424_831+1425i others(557): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768444 | ||||||
chr17:768444
|
A | AAGAGGGA others(1707): Show |
2 | a0001c0001t0001g0241a0001c0001t0001g0252 | 2 | HG02486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.831+1424_831+1425i others(1716): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768444 | ||||||
chr17:768444
|
A | G | 5 | a0001c0001t0001g0052a0001c0001t0001g0296a0001c0001t0001g0297others(2): Show | 7 | HG02451.hp2 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.831+1425T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768444 | ||||||
chr17:768449
|
G | A | 4 | a0001c0001t0001g0052a0001c0001t0001g0296a0001c0001t0001g0297others(1): Show | 5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+1420C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768449 | ||||||
chr17:768449
|
G | GGAGAAAC others(162): Show |
1 | a0001c0001t0004g0031 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.831+1419_831+1420i others(171): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768449 | ||||||
chr17:768497
|
TGA | T | 4 | a0001c0001t0001g0052a0001c0001t0001g0296a0001c0001t0001g0297others(1): Show | 5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+1370_831+1371d others(4): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768497 | ||||||
chr17:768529
|
T | TAGA | 12 | a0001c0001t0001g0057a0002c0002t0002g0051a0002c0002t0002g0301others(9): Show | 13 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.831+1337_831+1339d others(5): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768529 | ||||||
chr17:768537
|
A | G | 16 | a0001c0001t0001g0052a0001c0001t0001g0057a0001c0001t0001g0296others(13): Show | 18 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(15): Show |
intron_variant | MODIFIER | c.831+1332T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768537 | ||||||
chr17:768549
|
C | T | 13 | a0001c0001t0001g0043a0001c0001t0001g0184a0001c0001t0001g0206others(10): Show | 14 | HG00280.hp2 HG00621.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.831+1320G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768549 | ||||||
chr17:768594
|
G | A | 16 | a0001c0001t0001g0052a0001c0001t0001g0057a0001c0001t0001g0296others(13): Show | 18 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(15): Show |
intron_variant | MODIFIER | c.831+1275C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768594 | ||||||
chr17:768614
|
A | G | 78 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(75): Show | 98 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.831+1255T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768614 | ||||||
chr17:768627
|
G | A | 5 | a0001c0001t0001g0052a0001c0001t0001g0296a0001c0001t0001g0297others(2): Show | 7 | HG02451.hp2 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.831+1242C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768627 | ||||||
chr17:768644
|
A | G | 78 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(75): Show | 98 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.831+1225T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768644 | ||||||
chr17:768651
|
A | G | 2 | a0001c0001t0001g0161a0001c0001t0001g0287 | 2 | HG00621.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.831+1218T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768651 | ||||||
chr17:768664
|
G | A | 3 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0086 | 3 | HG00140.hp1 HG01981.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.831+1205C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768664 | ||||||
chr17:768669
|
AGG | A | 78 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(75): Show | 98 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.831+1198_831+1199d others(4): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768669 | ||||||
chr17:768671
|
G | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0287 | 2 | HG00621.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.831+1198C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768671 | ||||||
chr17:768698
|
AGAG | A | 78 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(75): Show | 98 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.831+1168_831+1170d others(5): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768698 | ||||||
chr17:768700
|
A | AAGAAGAA others(102): Show |
1 | a0001c0001t0001g0161 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.831+1168_831+1169i others(111): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768700 | ||||||
chr17:768701
|
G | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0287 | 2 | HG00621.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.831+1168C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768701 | ||||||
chr17:768701
|
G | GGAAGAAA others(45): Show |
178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(175): Show | 245 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.831+1167_831+1168i others(54): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768701 | ||||||
chr17:768701
|
G | GGAAGAAA others(486): Show |
1 | a0001c0001t0001g0283 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.831+1167_831+1168i others(495): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768701 | ||||||
chr17:768701
|
G | GGAAGAAA others(216): Show |
1 | a0001c0001t0004g0031 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.831+1167_831+1168i others(225): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768701 | ||||||
chr17:768703
|
A | AAGAAATC others(597): Show |
1 | a0003c0004t0001g0260 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.831+1165_831+1166i others(606): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768703 | ||||||
chr17:768703
|
A | AAGAAATC others(654): Show |
1 | a0001c0001t0001g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.831+1165_831+1166i others(663): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768703 | ||||||
chr17:768703
|
A | AAGAAATC others(654): Show |
1 | a0001c0001t0001g0178 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.831+1165_831+1166i others(663): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768703 | ||||||
chr17:768703
|
A | AAGAAATC others(654): Show |
31 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0039others(28): Show | 51 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.831+1165_831+1166i others(663): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768703 | ||||||
chr17:768703
|
A | AAGAAATC others(654): Show |
1 | a0001c0001t0001g0237 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.831+1165_831+1166i others(663): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768703 | ||||||
chr17:768703
|
A | AAGAAATC others(654): Show |
10 | a0001c0001t0001g0043a0001c0001t0001g0184a0001c0001t0001g0206others(7): Show | 11 | HG00280.hp2 HG00735.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.831+1165_831+1166i others(663): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768703 | ||||||
chr17:768703
|
A | AAGAAATC others(654): Show |
1 | a0001c0001t0001g0228 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.831+1165_831+1166i others(663): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768703 | ||||||
chr17:768703
|
A | AAGAAATC others(654): Show |
1 | a0001c0001t0001g0229 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.831+1165_831+1166i others(663): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768703 | ||||||
chr17:768703
|
A | AAGAAATC others(1212): Show |
1 | a0001c0001t0001g0287 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.831+1165_831+1166i others(1221): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768703 | ||||||
chr17:768741
|
G | A | 307 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(304): Show | 416 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(413): Show |
intron_variant | MODIFIER | c.831+1128C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768741 | ||||||
chr17:768750
|
T | TTTTTAGA others(46): Show |
1 | a0001c0001t0001g0246 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.831+1118_831+1119i others(55): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768750 | ||||||
chr17:768774
|
T | C | 1 | a0001c0001t0001g0283 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.831+1095A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768774 | ||||||
chr17:768792
|
C | G | 22 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(19): Show | 29 | HG00423.hp2 HG00609.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.831+1077G>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768792 | ||||||
chr17:768831
|
C | T | 1 | a0001c0001t0001g0283 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.831+1038G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768831 | ||||||
chr17:768848
|
G | C | 36 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0039others(33): Show | 56 | HG00099.hp1 HG00621.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.831+1021C>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768848 | ||||||
chr17:768849
|
C | T | 1 | a0001c0001t0001g0283 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.831+1020G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768849 | ||||||
chr17:768865
|
TAGAAGAA others(50): Show |
T | 1 | a0001c0001t0001g0300 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.831+947_831+1003de others(58): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768865 | ||||||
chr17:768887
|
TGA | T | 11 | a0002c0002t0002g0051a0002c0002t0002g0301a0002c0002t0002g0302others(8): Show | 12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.831+980_831+981del others(2): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768887 | ||||||
chr17:768907
|
C | T | 1 | a0001c0005t0001g0231 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.831+962G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768907 | ||||||
chr17:768922
|
A | AAGAAGAA others(99): Show |
11 | a0002c0002t0002g0051a0002c0002t0002g0301a0002c0002t0002g0302others(8): Show | 12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.831+946_831+947ins others(106): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768922 | ||||||
chr17:769014
|
A | T | 1 | a0001c0001t0001g0057 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.831+855T>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 769014 | ||||||
chr17:769044
|
G | A | 49 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0011others(46): Show | 71 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.831+825C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 769044 | ||||||
chr17:769300
|
G | A | 1 | a0001c0001t0001g0083 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.831+569C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 769300 | ||||||
chr17:769322
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.831+547C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 769322 | ||||||
chr17:769349
|
GGAGAGCT others(67): Show |
G | 1 | a0001c0001t0001g0123 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.831+446_831+519del others(74): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 769349 | ||||||
chr17:769371
|
G | A | 8 | a0001c0001t0001g0005a0001c0001t0001g0049a0001c0001t0001g0202others(5): Show | 15 | HG01123.hp2 HG01358.hp2 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.831+498C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 769371 | ||||||
chr17:769497
|
A | AGAGAGCT others(30): Show |
2 | a0001c0001t0001g0052a0001c0001t0001g0298 | 2 | HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.831+335_831+371dup others(37): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 769497 | ||||||
chr17:769527
|
T | C | 3 | a0001c0001t0001g0126a0001c0001t0001g0131a0006c0006t0001g0136 | 3 | NA18947.hp2 NA18992.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.831+342A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 769527 | ||||||
chr17:769588
|
G | A | 2 | a0001c0001t0001g0052a0001c0001t0001g0298 | 2 | HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.831+281C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 769588 | ||||||
chr17:769588
|
G | GGATGGAG others(30): Show |
16 | a0001c0001t0001g0052a0001c0001t0001g0296a0001c0001t0001g0297others(13): Show | 18 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(15): Show |
intron_variant | MODIFIER | c.831+280_831+281ins others(37): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 769588 | ||||||
chr17:769613
|
G | C | 1 | a0001c0001t0001g0056 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.831+256C>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 769613 | ||||||
chr17:769748
|
C | T | 1 | a0001c0001t0004g0031 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.831+121G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 769748 | ||||||
chr17:770556
|
A | G | 1 | a0001c0001t0005g0055 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.544-49T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 5/8 | chr17 | 770556 | ||||||
chr17:770655
|
C | G | 271 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(268): Show | 368 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(365): Show |
intron_variant | MODIFIER | c.544-148G>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 5/8 | chr17 | 770655 | ||||||
chr17:770694
|
T | C | 81 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(78): Show | 109 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.544-187A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 5/8 | chr17 | 770694 | ||||||
chr17:770695
|
G | GT | 108 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(105): Show | 147 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.544-189dupA | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 5/8 | chr17 | 770695 | ||||||
chr17:770695
|
GT | G | 18 | a0001c0001t0001g0052a0001c0001t0001g0217a0001c0001t0001g0296others(15): Show | 21 | HG00733.hp2 HG01123.hp1 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.544-189delA | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 5/8 | chr17 | 770695 | ||||||
chr17:771117
|
T | A | 4 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 4 | HG00280.hp1 HG00323.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.543+208A>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 5/8 | chr17 | 771117 | ||||||
chr17:771135
|
A | C | 1 | a0001c0001t0001g0225 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.543+190T>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 5/8 | chr17 | 771135 | ||||||
chr17:771153
|
A | G | 17 | a0001c0001t0001g0052a0001c0001t0001g0296a0001c0001t0001g0297others(14): Show | 20 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.543+172T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 5/8 | chr17 | 771153 | ||||||
chr17:771311
|
C | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0161a0001c0001t0001g0173 | 5 | HG01109.hp1 HG02818.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.543+14G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 5/8 | chr17 | 771311 | ||||||
chr17:771580
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.407-119C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 771580 | ||||||
chr17:771885
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.407-424G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 771885 | ||||||
chr17:771961
|
C | T | 16 | a0001c0001t0001g0008a0001c0001t0001g0036a0001c0001t0001g0037others(13): Show | 22 | HG00280.hp1 HG00323.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.407-500G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 771961 | ||||||
chr17:771973
|
G | A | 6 | a0002c0002t0002g0302a0002c0002t0002g0303a0002c0002t0002g0304others(3): Show | 6 | HG00733.hp2 HG02602.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.407-512C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 771973 | ||||||
chr17:772001
|
A | G | 1 | a0001c0001t0001g0261 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.407-540T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772001 | ||||||
chr17:772013
|
C | CA | 17 | a0001c0001t0001g0014a0001c0001t0001g0034a0001c0001t0001g0052others(14): Show | 22 | HG00438.hp2 HG01952.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.407-553dupT | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772013 | ||||||
chr17:772013
|
CA | C | 150 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(147): Show | 209 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.407-553delT | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772013 | ||||||
chr17:772013
|
CAA | C | 59 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(56): Show | 85 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.407-554_407-553del others(2): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772013 | ||||||
chr17:772056
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.407-595C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772056 | ||||||
chr17:772113
|
C | T | 2 | a0001c0001t0001g0236a0001c0001t0001g0298 | 2 | HG03041.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.407-652G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772113 | ||||||
chr17:772155
|
C | T | 1 | a0001c0001t0001g0298 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.407-694G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772155 | ||||||
chr17:772187
|
G | GA | 8 | a0001c0001t0001g0052a0001c0001t0001g0057a0001c0001t0001g0127others(5): Show | 9 | HG00438.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.407-727dupT | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772187 | ||||||
chr17:772187
|
G | GAAA | 8 | a0002c0002t0002g0051a0002c0002t0002g0303a0002c0002t0002g0304others(5): Show | 9 | HG00733.hp2 HG02135.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.407-729_407-727dup others(3): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772187 | ||||||
chr17:772187
|
GA | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(218): Show | 313 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.407-727delT | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772187 | ||||||
chr17:772187
|
GAA | G | 6 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0001g0112others(3): Show | 7 | HG01070.hp1 HG01258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.407-728_407-727del others(2): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772187 | ||||||
chr17:772189
|
A | G | 2 | a0001c0001t0001g0191a0001c0001t0001g0195 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.407-728T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772189 | ||||||
chr17:772202
|
A | C | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.407-741T>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772202 | ||||||
chr17:772247
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.407-786C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772247 | ||||||
chr17:772248
|
C | T | 1 | a0001c0001t0004g0031 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.407-787G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772248 | ||||||
chr17:772323
|
G | A | 1 | a0001c0001t0001g0178 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.407-862C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772323 | ||||||
chr17:772508
|
A | G | 2 | a0001c0001t0001g0282a0001c0001t0001g0295 | 2 | HG02074.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.407-1047T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772508 | ||||||
chr17:772554
|
C | T | 2 | a0001c0001t0001g0213a0001c0001t0001g0275 | 2 | NA18941.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.407-1093G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772554 | ||||||
chr17:772800
|
C | T | 1 | a0001c0001t0005g0055 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.407-1339G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772800 | ||||||
chr17:772806
|
T | C | 1 | a0001c0001t0003g0257 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.407-1345A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772806 | ||||||
chr17:772851
|
C | T | 1 | a0001c0001t0004g0031 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.407-1390G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772851 | ||||||
chr17:772926
|
C | T | 1 | a0001c0001t0005g0055 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.407-1465G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772926 | ||||||
chr17:772938
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.407-1477A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772938 | ||||||
chr17:772964
|
T | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0203 | 4 | HG02258.hp1 HG02886.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.407-1503A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772964 | ||||||
chr17:772994
|
C | CA | 6 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0115others(3): Show | 6 | HG02738.hp2 NA18961.hp2 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.407-1534dupT | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772994 | ||||||
chr17:772994
|
CA | C | 7 | a0001c0001t0001g0056a0001c0001t0001g0145a0001c0001t0001g0167others(4): Show | 7 | HG01069.hp2 HG02976.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.407-1534delT | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772994 | ||||||
chr17:773091
|
A | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0039others(44): Show | 68 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.407-1630T>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 773091 | ||||||
chr17:773216
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.407-1755A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 773216 | ||||||
chr17:773312
|
A | G | 1 | a0001c0001t0004g0031 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.407-1851T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 773312 | ||||||
chr17:773509
|
G | GGTGTGT | 17 | a0001c0001t0001g0052a0001c0001t0001g0296a0001c0001t0001g0297others(14): Show | 20 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.407-2054_407-2049d others(8): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 773509 | ||||||
chr17:773526
|
T | C | 1 | a0001c0001t0004g0031 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.407-2065A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 773526 | ||||||
chr17:773619
|
A | G | 1 | a0001c0001t0005g0055 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.406+2156T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 773619 | ||||||
chr17:773634
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.406+2141A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 773634 | ||||||
chr17:773777
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.406+1998C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 773777 | ||||||
chr17:773818
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.406+1957G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 773818 | ||||||
chr17:773823
|
T | C | 2 | a0001c0001t0001g0123a0001c0001t0001g0125 | 2 | HG02145.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.406+1952A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 773823 | ||||||
chr17:773986
|
C | T | 52 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0010others(49): Show | 73 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.406+1789G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 773986 | ||||||
chr17:774180
|
G | A | 27 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0017others(24): Show | 38 | HG00280.hp1 HG00323.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.406+1595C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 774180 | ||||||
chr17:774195
|
A | T | 52 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0010others(49): Show | 73 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.406+1580T>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 774195 | ||||||
chr17:774219
|
A | G | 17 | a0001c0001t0001g0052a0001c0001t0001g0296a0001c0001t0001g0297others(14): Show | 20 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.406+1556T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 774219 | ||||||
chr17:774226
|
T | C | 2 | a0001c0001t0004g0031a0001c0001t0005g0055 | 3 | HG02451.hp2 HG02896.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.406+1549A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 774226 | ||||||
chr17:774365
|
C | A | 2 | a0001c0001t0001g0206a0001c0001t0001g0267 | 2 | HG03017.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.406+1410G>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 774365 | ||||||
chr17:774399
|
G | A | 2 | a0001c0001t0001g0206a0001c0001t0001g0267 | 2 | HG03017.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.406+1376C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 774399 | ||||||
chr17:774406
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.406+1369G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 774406 | ||||||
chr17:774412
|
G | A | 2 | a0001c0001t0001g0169a0001c0001t0001g0171 | 2 | HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.406+1363C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 774412 | ||||||
chr17:774565
|
G | A | 11 | a0001c0001t0001g0008a0001c0001t0001g0037a0001c0001t0001g0177others(8): Show | 16 | HG00280.hp1 HG00323.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.406+1210C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 774565 | ||||||
chr17:774790
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.406+985G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 774790 | ||||||
chr17:774807
|
G | A | 1 | a0001c0001t0004g0031 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.406+968C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 774807 | ||||||
chr17:775033
|
G | T | 1 | a0001c0001t0001g0102 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.406+742C>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 775033 | ||||||
chr17:775065
|
G | A | 7 | a0001c0001t0001g0015a0001c0001t0001g0042a0001c0001t0001g0211others(4): Show | 10 | HG01993.hp1 NA18612.hp1 NA18953.hp1 others(7): Show |
intron_variant | MODIFIER | c.406+710C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 775065 | ||||||
chr17:775106
|
T | TA | 29 | a0001c0001t0001g0036a0001c0001t0001g0050a0001c0001t0001g0056others(26): Show | 32 | HG00733.hp2 HG00735.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.406+668dupT | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 775106 | ||||||
chr17:775106
|
TA | T | 7 | a0001c0001t0001g0052a0001c0001t0001g0211a0001c0001t0001g0246others(4): Show | 8 | HG02572.hp1 HG02615.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.406+668delT | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 775106 | ||||||
chr17:775124
|
A | T | 1 | a0001c0001t0001g0157 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.406+651T>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 775124 | ||||||
chr17:775140
|
A | G | 271 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(268): Show | 368 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(365): Show |
intron_variant | MODIFIER | c.406+635T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 775140 | ||||||
chr17:775260
|
C | CA | 18 | a0001c0001t0001g0052a0001c0001t0001g0210a0001c0001t0001g0296others(15): Show | 21 | HG00733.hp2 HG01123.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.406+514dupT | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 775260 | ||||||
chr17:775548
|
A | G | 2 | a0001c0001t0001g0123a0001c0001t0001g0125 | 2 | HG02145.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.406+227T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 775548 | ||||||
chr17:775636
|
C | T | 2 | a0001c0001t0001g0132a0001c0001t0001g0144 | 2 | HG03239.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.406+139G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 775636 | ||||||
chr17:776236
|
T | A | 80 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(77): Show | 108 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.262-317A>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 3/8 | chr17 | 776236 | ||||||
chr17:776514
|
G | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0160a0001c0001t0001g0166 | 4 | HG02622.hp1 HG02723.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.261+354C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 3/8 | chr17 | 776514 | ||||||
chr17:776602
|
C | G | 1 | a0001c0001t0001g0098 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.261+266G>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 3/8 | chr17 | 776602 | ||||||
chr17:776602
|
C | T | 2 | a0001c0001t0001g0045a0001c0001t0001g0233 | 3 | HG01256.hp1 HG01258.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.261+266G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 3/8 | chr17 | 776602 | ||||||
chr17:776698
|
T | C | 1 | a0001c0001t0005g0055 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.261+170A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 3/8 | chr17 | 776698 | ||||||
chr17:776823
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.261+45G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 3/8 | chr17 | 776823 | ||||||
chr17:777021
|
A | G | 1 | a0001c0001t0001g0208 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.141-33T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 777021 | ||||||
chr17:777043
|
A | C | 1 | a0001c0001t0001g0160 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.141-55T>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 777043 | ||||||
chr17:777059
|
T | C | 35 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0039others(32): Show | 54 | HG00099.hp1 HG00099.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.141-71A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 777059 | ||||||
chr17:777072
|
A | G | 22 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0033others(19): Show | 29 | HG01109.hp1 HG01346.hp1 HG01952.hp2 others(26): Show |
intron_variant | MODIFIER | c.141-84T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 777072 | ||||||
chr17:777300
|
A | G | 11 | a0002c0002t0002g0051a0002c0002t0002g0301a0002c0002t0002g0302others(8): Show | 12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.141-312T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 777300 | ||||||
chr17:777333
|
C | G | 2 | a0001c0001t0003g0038a0001c0001t0003g0197 | 3 | HG00558.hp1 NA18989.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.141-345G>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 777333 | ||||||
chr17:777344
|
A | G | 1 | a0001c0001t0003g0193 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.141-356T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 777344 | ||||||
chr17:777578
|
G | A | 61 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0015others(58): Show | 85 | HG00558.hp1 HG00597.hp1 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.141-590C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 777578 | ||||||
chr17:777612
|
C | T | 1 | a0001c0001t0001g0208 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.141-624G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 777612 | ||||||
chr17:777857
|
T | C | 1 | a0001c0001t0001g0297 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.140+838A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 777857 | ||||||
chr17:778045
|
T | A | 1 | a0001c0001t0001g0061 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.140+650A>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 778045 | ||||||
chr17:778047
|
C | A | 1 | a0001c0001t0001g0061 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.140+648G>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 778047 | ||||||
chr17:778048
|
C | A | 1 | a0001c0001t0001g0061 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.140+647G>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 778048 | ||||||
chr17:778049
|
C | A | 1 | a0001c0001t0001g0061 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.140+646G>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 778049 | ||||||
chr17:778054
|
G | A | 1 | a0001c0001t0001g0061 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.140+641C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 778054 | ||||||
chr17:778055
|
A | ATAAAAAA others(126): Show |
1 | a0001c0001t0001g0061 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.140+639_140+640ins others(133): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 778055 | ||||||
chr17:778172
|
G | A | 11 | a0002c0002t0002g0051a0002c0002t0002g0301a0002c0002t0002g0302others(8): Show | 12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.140+523C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 778172 | ||||||
chr17:778210
|
A | C | 1 | a0001c0001t0001g0061 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.140+485T>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 778210 | ||||||
chr17:778230
|
G | A | 1 | a0001c0001t0001g0280 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.140+465C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 778230 | ||||||
chr17:778272
|
C | A | 1 | a0001c0001t0001g0057 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.140+423G>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 778272 | ||||||
chr17:778278
|
T | C | 2 | a0001c0001t0001g0169a0001c0001t0001g0171 | 2 | HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.140+417A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 778278 | ||||||
chr17:778285
|
G | A | 2 | a0001c0001t0001g0191a0001c0001t0001g0195 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.140+410C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 778285 | ||||||
chr17:778299
|
C | T | 3 | a0001c0001t0001g0194a0001c0001t0001g0262a0001c0001t0001g0263 | 3 | NA18949.hp1 NA19060.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.140+396G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 778299 | ||||||
chr17:778300
|
G | A | 1 | a0001c0001t0001g0207 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.140+395C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 778300 | ||||||
chr17:778387
|
C | T | 1 | a0001c0001t0001g0202 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.140+308G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 778387 | ||||||
chr17:778390
|
CT | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0039others(44): Show | 68 | HG00099.hp1 HG00280.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.140+304delA | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 778390 | ||||||
chr17:778498
|
TCTTAATT others(87): Show |
T | 1 | a0001c0001t0001g0101 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.140+103_140+196del others(94): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 778498 | ||||||
chr17:778607
|
C | G | 2 | a0002c0002t0002g0301a0002c0002t0002g0308 | 2 | HG01123.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.140+88G>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 778607 | ||||||
chr17:778687
|
T | G | 1 | a0001c0001t0001g0046 | 2 | NA18969.hp2 NA19012.hp2 |
splice_region_variant&intron_variant | LOW | c.140+8A>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 778687 | ||||||
chr17:778785
|
A | T | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.91-41T>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 778785 | ||||||
chr17:778915
|
G | T | 1 | a0001c0003t0001g0254 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.91-171C>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 778915 | ||||||
chr17:779039
|
G | T | 5 | a0001c0001t0001g0007a0001c0001t0001g0066a0001c0001t0001g0092others(2): Show | 9 | HG01099.hp1 HG01952.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.91-295C>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 779039 | ||||||
chr17:779144
|
G | A | 4 | a0001c0001t0001g0052a0001c0001t0001g0296a0001c0001t0001g0297others(1): Show | 5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.91-400C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 779144 | ||||||
chr17:779267
|
T | C | 2 | a0001c0001t0001g0056a0001c0001t0005g0055 | 2 | HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.91-523A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 779267 | ||||||
chr17:779270
|
T | C | 11 | a0002c0002t0002g0051a0002c0002t0002g0301a0002c0002t0002g0302others(8): Show | 12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.91-526A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 779270 | ||||||
chr17:779317
|
ATT | A | 10 | a0002c0002t0002g0051a0002c0002t0002g0301a0002c0002t0002g0302others(7): Show | 11 | HG00733.hp2 HG02135.hp2 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.91-575_91-574delAA | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 779317 | ||||||
chr17:779318
|
T | A | 1 | a0002c0002t0002g0308 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.91-574A>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 779318 | ||||||
chr17:779319
|
T | TAAA | 3 | a0001c0001t0001g0009a0001c0001t0001g0259a0003c0004t0001g0260 | 7 | HG00738.hp2 HG01081.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.91-578_91-576dupTT others(1): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 779319 | ||||||
chr17:779319
|
TA | T | 77 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(74): Show | 102 | HG00140.hp2 HG00609.hp1 HG01070.hp1 others(99): Show |
intron_variant | MODIFIER | c.91-576delT | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 779319 | ||||||
chr17:779319
|
TAA | T | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(163): Show | 240 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.91-577_91-576delTT | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 779319 | ||||||
chr17:779319
|
TAAA | T | 24 | a0001c0001t0001g0039a0001c0001t0001g0052a0001c0001t0001g0064others(21): Show | 26 | HG00323.hp2 HG01069.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.91-578_91-576delTT others(1): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 779319 | ||||||
chr17:779319
|
TAAAAAAA others(1): Show |
T | 7 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0003g0038others(4): Show | 8 | HG00558.hp1 NA18949.hp2 NA18956.hp1 others(5): Show |
intron_variant | MODIFIER | c.91-583_91-576delTT others(6): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 779319 | ||||||
chr17:779321
|
A | T | 11 | a0002c0002t0002g0051a0002c0002t0002g0301a0002c0002t0002g0302others(8): Show | 12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.91-577T>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 779321 | ||||||
chr17:779322
|
A | T | 10 | a0002c0002t0002g0051a0002c0002t0002g0301a0002c0002t0002g0302others(7): Show | 11 | HG00733.hp2 HG02135.hp2 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.91-578T>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 779322 | ||||||
chr17:779417
|
G | T | 3 | a0001c0001t0001g0056a0001c0001t0004g0031a0001c0001t0005g0055 | 4 | HG02451.hp2 HG02896.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-673C>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 779417 | ||||||
chr17:779420
|
G | A | 1 | a0001c0001t0004g0031 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.91-676C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 779420 | ||||||
chr17:779781
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.91-1037C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 779781 | ||||||
chr17:779854
|
C | T | 1 | a0001c0001t0001g0052 | 2 | HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.91-1110G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 779854 | ||||||
chr17:779900
|
C | G | 11 | a0002c0002t0002g0051a0002c0002t0002g0301a0002c0002t0002g0302others(8): Show | 12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.91-1156G>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 779900 | ||||||
chr17:779907
|
G | T | 1 | a0001c0001t0001g0061 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.91-1163C>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 779907 | ||||||
chr17:780096
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.91-1352C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780096 | ||||||
chr17:780140
|
G | A | 1 | a0001c0001t0001g0297 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.91-1396C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780140 | ||||||
chr17:780151
|
G | A | 6 | a0001c0001t0001g0194a0001c0001t0001g0262a0001c0001t0001g0263others(3): Show | 6 | NA18945.hp2 NA18949.hp1 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.91-1407C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780151 | ||||||
chr17:780400
|
T | C | 1 | a0001c0001t0004g0031 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.91-1656A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780400 | ||||||
chr17:780464
|
C | A | 1 | a0001c0001t0001g0266 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.90+1702G>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780464 | ||||||
chr17:780485
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.90+1681G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780485 | ||||||
chr17:780509
|
C | T | 11 | a0002c0002t0002g0051a0002c0002t0002g0301a0002c0002t0002g0302others(8): Show | 12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.90+1657G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780509 | ||||||
chr17:780600
|
G | T | 1 | a0001c0001t0001g0096 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.90+1566C>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780600 | ||||||
chr17:780648
|
C | A | 1 | a0001c0001t0004g0031 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.90+1518G>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780648 | ||||||
chr17:780658
|
G | T | 11 | a0002c0002t0002g0051a0002c0002t0002g0301a0002c0002t0002g0302others(8): Show | 12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.90+1508C>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780658 | ||||||
chr17:780672
|
G | A | 1 | a0001c0001t0001g0267 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.90+1494C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780672 | ||||||
chr17:780741
|
C | CA | 116 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(113): Show | 151 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.90+1424dupT | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780741 | ||||||
chr17:780741
|
C | CAA | 23 | a0001c0001t0001g0010a0001c0001t0001g0020a0001c0001t0001g0058others(20): Show | 27 | HG00140.hp1 HG00558.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.90+1423_90+1424dup others(2): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780741 | ||||||
chr17:780741
|
CA | C | 15 | a0001c0001t0001g0015a0001c0001t0001g0052a0001c0001t0001g0057others(12): Show | 19 | HG00733.hp2 HG01123.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.90+1424delT | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780741 | ||||||
chr17:780761
|
A | G | 1 | a0001c0001t0005g0055 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.90+1405T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780761 | ||||||
chr17:780862
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.90+1304A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780862 | ||||||
chr17:780868
|
C | A | 1 | a0001c0001t0001g0176 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.90+1298G>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780868 | ||||||
chr17:780917
|
C | CT | 32 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0026others(29): Show | 41 | HG00280.hp1 HG00323.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.90+1248dupA | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780917 | ||||||
chr17:780917
|
CT | C | 66 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0010others(63): Show | 88 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.90+1248delA | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780917 | ||||||
chr17:780942
|
C | T | 1 | a0001c0001t0006g0060 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.90+1224G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780942 | ||||||
chr17:780957
|
G | A | 4 | a0001c0001t0001g0052a0001c0001t0001g0296a0001c0001t0001g0297others(1): Show | 5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.90+1209C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780957 | ||||||
chr17:780965
|
G | T | 1 | a0001c0001t0001g0177 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.90+1201C>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780965 | ||||||
chr17:780980
|
G | T | 1 | a0001c0001t0001g0059 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.90+1186C>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780980 | ||||||
chr17:780990
|
G | T | 26 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0032others(23): Show | 34 | HG01109.hp1 HG01346.hp1 HG01952.hp2 others(31): Show |
intron_variant | MODIFIER | c.90+1176C>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780990 | ||||||
chr17:781021
|
G | A | 271 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(268): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.90+1145C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 781021 | ||||||
chr17:781123
|
G | A | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG02145.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.90+1043C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 781123 | ||||||
chr17:781234
|
G | T | 1 | a0001c0001t0001g0058 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.90+932C>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 781234 | ||||||
chr17:781235
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.90+931G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 781235 | ||||||
chr17:781257
|
G | T | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG02145.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.90+909C>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 781257 | ||||||
chr17:781294
|
T | C | 2 | a0001c0001t0001g0050a0001c0001t0001g0299 | 3 | HG01891.hp2 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.90+872A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 781294 | ||||||
chr17:781469
|
A | G | 1 | a0001c0001t0001g0123 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.90+697T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 781469 | ||||||
chr17:781489
|
C | T | 80 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(77): Show | 108 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.90+677G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 781489 | ||||||
chr17:781553
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.90+613G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 781553 | ||||||
chr17:781598
|
G | A | 1 | a0001c0001t0001g0300 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.90+568C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 781598 | ||||||
chr17:781783
|
G | T | 2 | a0001c0001t0001g0056a0001c0001t0005g0055 | 2 | HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.90+383C>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 781783 | ||||||
chr17:781846
|
T | C | 11 | a0002c0002t0002g0051a0002c0002t0002g0301a0002c0002t0002g0302others(8): Show | 12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.90+320A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 781846 | ||||||
chr17:781992
|
T | C | 1 | a0001c0001t0001g0052 | 2 | HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.90+174A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 781992 | ||||||
chr17:782056
|
A | G | 1 | a0001c0001t0001g0054 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.90+110T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 782056 | ||||||
chr17:782133
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.90+33G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 782133 |